iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

PSEN2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6759	snp	C/T	0.499999	0.000523047	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226882036	AGAGGATGGAGAGAA[C/T]ACTGCCCAGTGGGTA	5664
rs7961	snp	C/T	0.197703	0.244469	utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875528	CCGGGATTCAGACCT[C/T]TCTGCGGCCCCAAGT	5664
rs7962	snp	C/G	0.0158469	0.0875917	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226896066	GGAAGTGGCTTAATA[C/G]TAATATCAATAAATA	5664
rs8383	snp	C/T	0.495174	0.0488838	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895849	AAGGTCAGATTAGGG[C/T]GGGGAGAAGAGCATC	5664
rs11405	snp	C/T	0.364439	0.22227	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881976	GTCCCTAATGTCGGC[C/T]GAGAGCCCCACGCCG	5664
rs732479	snp	A/G	0.228547	0.249078	intron-variant	PSEN2	GRCh38.p7	1:226877777	TCTGGTGAGGAGGCC[A/G]CATGTATGAATGACG	5664
rs743601	snp	C/T	0.399253	0.200558	intron-variant	PSEN2	GRCh38.p7	1:226892465	ACGGTGCCTGCCTAA[C/T]ACCCAATGCCAGCCC	5664
rs743602	snp	C/T	0.255503	0.249939	intron-variant	PSEN2	GRCh38.p7	1:226892584	CCTGGTGACAGTGGC[C/T]TGGCATACAGGACTC	5664
rs1046240	snp	C/T	0.499998	0.000931757	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883824	ATACGGAGCGAAGCA[C/T]GTGATCATGCTGTTT	5664
rs1295621	snp	A/T	0.388775	0.207946	intron-variant	PSEN2	GRCh38.p7	1:226873954	TTCCCACCCTCCCTT[A/T]TGCCCCAGAGAAGCA	5664
rs1295638	snp	A/G	0.493568	0.0563433	intron-variant	PSEN2	GRCh38.p7	1:226881566	GATCTTTGGTGCATA[A/G]TAGATGCACCACAGA	5664
rs1295640	snp	C/T	0.493568	0.0563433	intron-variant	PSEN2	GRCh38.p7	1:226882677	TGTGTGGACTGTTTT[C/T]TTGCAGCCAGTCTTA	5664
rs1295641	snp	C/T	0.493568	0.0563433	intron-variant	PSEN2	GRCh38.p7	1:226882994	TTTAGCTGTTCACCT[C/T]ATTAGCAAGGCAGCC	5664
rs1295642	snp	C/T	0.27893	0.24832	intron-variant	PSEN2	GRCh38.p7	1:226883347	TATCTCCTGGCCTGT[C/T]TCCTCCCATATCAGT	5664
rs1295643	snp	A/G	0.500006	0.00227077	intron-variant	PSEN2	GRCh38.p7	1:226883663	CATGGATAGGCTGCC[A/G]TGGGGGACATTCTGC	5664
rs1295644	snp	C/T	0.399449	0.200468	intron-variant	PSEN2	GRCh38.p7	1:226883676	CCGTGGGGGACATTC[C/T]GCGGCCCTCACGATG	5664
rs1295645	snp	C/T	0.256061	0.249927	utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871336	ACAGAAGCTAGTCCC[C/T]CCTCTGAATTTTACT	5664
rs1295646	snp	C/G	0.390464	0.206809	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872038	TGTTGAAGTGCCCAT[C/G]TGCCAAGTCTTGAGT	5664
rs1295647	snp	C/T	0.493658	0.0559517	intron-variant	PSEN2	GRCh38.p7	1:226872975	CTGAGGTCGGAAGTT[C/T]GAGACCAGCCTGACC	5664
rs1295648	snp	C/T	0.257176	0.249897	intron-variant	PSEN2	GRCh38.p7	1:226873604	TATTTTTATTAGAGG[C/T]GGGGTTTCACCATGT	5664
rs1296171	snp	C/G	0.493154	0.0581045	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871905	AGAGCTGCGTCCTCA[C/G]GACGCCCACGTTGAG	5664
rs1297990	snp	C/T	0.38821	0.208322	intron-variant	PSEN2	GRCh38.p7	1:226872641	AGTGTGTGTAGGTCA[C/T]ATGCAGTGTGTCTAA	5664
rs1782530	snp	A/G	0.388964	0.20782	intron-variant	PSEN2	GRCh38.p7	1:226885130	CAGTTGCTTCAGCGG[A/G]TGGGGGTCGGGTAGT	5664
rs1794038	snp	G/T	0.492775	0.059668	intron-variant	PSEN2	GRCh38.p7	1:226886011	GCTAGGACTACAGGT[G/T]TGCACCACCATACCT	5664
rs1800675	snp	A/G	0.0154538	0.0865337	intron-variant	PSEN2	GRCh38.p7	1:226892641	GAAAGATCACTCTGC[A/G]GTGGGTCTGGAAGGA	5664
rs1800678	snp	C/T	0.471863	0.115225	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890891	CCCGTAGAGGAGAAT[C/T]GCCTGCAGCGTGGCC	5664
rs1800679	snp	C/T	0.0166325	0.0896639	intron-variant	PSEN2	GRCh38.p7	1:226888238	GCATGAGGACCTGGG[C/T]GGGGAAAGATGACCA	5664
rs1800680	snp	A/G	0.118933	0.212888	intron-variant	PSEN2	GRCh38.p7	1:226888283	TCCCCAGTGCCAGCC[A/G]TTTTGGGAACCCAGG	5664
rs1800681	snp	C/G	0.283421	0.247756	intron-variant	PSEN2	GRCh38.p7	1:226888522	TCTGTTCTATCGCCC[C/G]TTGATTTGGGATATC	5664
rs2073488	snp	A/G	0.388775	0.207946	intron-variant	PSEN2	GRCh38.p7	1:226875130	TGGGGCCTGTGGTCC[A/G]GGAGGGTGGTAGGGC	5664
rs2073489	snp	C/T	0.457504	0.139435	intron-variant	PSEN2	GRCh38.p7	1:226875970	AGAACGTAGTCTATG[C/T]TGGACACTTCCTTCT	5664
rs2105822	snp	C/T	0.446118	0.155041	intron-variant	PSEN2	GRCh38.p7	1:226893226	CTGAGCCACAGCACC[C/T]GGCCAAAATTAGTTT	5664
rs2236910	snp	C/G	0.364389	0.222519	intron-variant	PSEN2	GRCh38.p7	1:226885709	CTGCCCTCCAGCCAC[C/G]CTTCTCTCCGTCTGC	5664
rs2236912	snp	A/T	0.411242	0.191052	intron-variant	PSEN2	GRCh38.p7	1:226886040	CTGGCTAATTAAAAA[A/T]TTTTTTTTTGTGCAG	5664
rs2236913	snp	A/G	0.472147	0.114677	intron-variant	PSEN2	GRCh38.p7	1:226886424	CTGCCTATAGCTGCC[A/G]AGTAGCCCCAGGGAG	5664
rs2236914	snp	A/T	0.493201	0.0579089	intron-variant	PSEN2	GRCh38.p7	1:226891020	GATTCACCCGTGAAC[A/T]GTGAGGTCTTGGCTC	5664
rs2236915	snp	C/G	0.493247	0.0577133	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891521	TGCGGCTTGAAGATT[C/G]AGCAAGTGTTGGACC	5664
rs2246221	snp	A/G	0.496968	0.0388195	intron-variant	PSEN2	GRCh38.p7	1:226887701	TATGTTTGTCTATAT[A/G]TCATCTAACACCCCT	5664
rs2793461	snp	A/C	0.493568	0.0563433	intron-variant	PSEN2	GRCh38.p7	1:226874428	CGTTGATGGCCTTTA[A/C]GGTCCTTGCCAGCTC	5664
rs2793462	snp	C/T	0.388587	0.208071	intron-variant	PSEN2	GRCh38.p7	1:226875699	ATGTTAAGGCCAAAG[C/T]CTTTACATTTCTCTG	5664
rs2802267	snp	C/T	0.360933	0.225784	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891254	TAGCACCGCCTGAGA[C/T]GTGAACCTTTTCTCC	5664
rs2855559	snp	A/G	0.493293	0.0575177	intron-variant	PSEN2	GRCh38.p7	1:226892758	GATCCCACGGGGCCC[A/G]CAGGACTGGCCTCCC	5664
rs2855560	snp	A/C	0.493293	0.0575177	intron-variant	PSEN2	GRCh38.p7	1:226893327	CCTGGTGGGGGAAGG[A/C]GGACAGCTGGGGCCA	5664
rs2855561	snp	C/T	0.0569829	0.158885	intron-variant	PSEN2	GRCh38.p7	1:226893491	ACTAAAGAAAACAAA[C/T]GAGAGCATTTTGGAA	5664
rs2855562	snp	A/G	0.488529	0.0748607	intron-variant	PSEN2	GRCh38.p7	1:226894149	CTGGGGATGCGTCCA[A/G]CTGCCTCGTGGTGGG	5664
rs2855563	snp	A/G	0.254944	0.249951	intron-variant	PSEN2	GRCh38.p7	1:226894645	TAGTCAGTTAACGTG[A/G]CCAGATACACATAAT	5664
rs3213436	snp	A/G	0.284733	0.247575	intron-variant	PSEN2	GRCh38.p7	1:226893604	CTCTGTCTTGGTGTT[A/G]TATGGGCTTTTGAAT	5664
rs3213437	snp	G/T	0.0566069	0.158427	intron-variant	PSEN2	GRCh38.p7	1:226894366	GGTGAGGAGTGTACC[G/T]GCCCCAGCGTGGCTG	5664
rs3820649	snp	A/G	0.284209	0.247648	intron-variant	PSEN2	GRCh38.p7	1:226892751	TAGCACAGATCCCAC[A/G]GGGCCCGCAGGACTG	5664
rs3829979	snp	C/G	0.287085	0.247234	intron-variant	PSEN2	GRCh38.p7	1:226894404	AGCCTCCAGGCCGAG[C/G]ACCCAGCTGACAGCT	5664
rs3831497	in-del	-/AAG	0.492823	0.0594727	intron-variant	PSEN2	GRCh38.p7	1:226885968	CAACCTCCTGGGCTC[-/AAG]AAGTTCTCCCACCCA	5664
rs4653469	snp	A/G	0.0652144	0.168387	intron-variant	PSEN2	GRCh38.p7	1:226873721	GCGCTGGGCTGAGAT[A/G]ACCACTCTTAACATG	5664
rs4653470	snp	A/T	0.495174	0.0488838	intron-variant	PSEN2	GRCh38.p7	1:226895025	CCTGGCGGCTCTGAT[A/T]CCCTTGGTGCCAGCT	5664
rs6426553	snp	G/T	0.0217336	0.101961	synonymous-codon, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891294	TGCCATGGTGTGGAC[G/T]GTTGGCATGGCGAAG	5664
rs6426554	snp	A/G	0.373799	0.217195	intron-variant	PSEN2	GRCh38.p7	1:226894744	AGCCGTGCGCTTGGC[A/G]TCTGCCCCTTAGTGA	5664
rs6660082	snp	C/G	0.0948562	0.196037	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871112	AGACCTCCGTTGCGC[C/G]GAGTCCATTCGGCCT	5664
rs6661000	snp	A/G	0.077417	0.180873	intron-variant	PSEN2	GRCh38.p7	1:226874349	catgggacattaact[A/G]attacttttgcccct	5664
rs6665033	snp	A/G	0.0329836	0.124112	utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871273	TCAGGCATTTCCAGC[A/G]GTGAGGAGACAGCCA	5664
rs6671059	snp	C/G	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226874784	GGAAATGAGCTGTGT[C/G]AGATTAGACTGTCTG	5664
rs6673248	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226880599	CCTCTGGACAGCGAT[A/C]ACTCAGCCTCTGGAC	5664
rs6675452	snp	A/G	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226874456	CTCTGACATTGTCCT[A/G]TGGATATGTCCTTTC	5664
rs6677801	snp	A/G	0.117188	0.211804	intron-variant	PSEN2	GRCh38.p7	1:226880213	gaccctcatttctac[A/G]aaatattttaaaaat	5664
rs6677908	snp	A/G	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226880348	CACCACTGTACTCCA[A/G]CGTAAGTGACCAGTG	5664
rs6678839	snp	C/T	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226874627	AGGCTACCGTGTCCT[C/T]TCTCACTGTGTCCCT	5664
rs6678940	snp	C/T	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226874688	TTATTGAACATCTAC[C/T]GTGTGCTGGACACTT	5664
rs6680042	snp	G/T	0.113685	0.209567	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890677	tgctaggcattgggg[G/T]acccagcaggaaaga	5664
rs7512986	snp	C/G	0.0901694	0.192235	intron-variant	PSEN2	GRCh38.p7	1:226894992	CAGCCCCCACACCTG[C/G]TTCCCAGGGGCAGGT	5664
rs7519422	snp	A/G	0.0260105	0.111035	intron-variant	PSEN2	GRCh38.p7	1:226875308	AAGGTGAGCAGGGAA[A/G]CTGTGGGCAATTGTC	5664
rs7522645	snp	C/G	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226873888	AAGCAGATTTGATGG[C/G]TGTGTAGAGCATTTG	5664
rs7523790	snp	A/C	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226872789	GCCACAGCTGCGGAA[A/C]GGCGGGGGTGAGGCT	5664
rs7525819	snp	G/T	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226877272	TTGGAGATCTGCATT[G/T]TTAATAAGCAGCCTA	5664
rs7530286	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226889214	GTAAAACAGAGGGGG[G/T]TCCACTATTTCTGGA	5664
rs7537037	snp	C/G	0.113685	0.209567	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891600	GGTGGAGTGGGGGAA[C/G]CCCTGGTGTCAGGTG	5664
rs7539017	snp	C/G/T	0.000189617	0.00973532	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889033	GTGGGTCATCCTGGG[C/G/T]GCCATCTCTGTGTAT	5664
rs7539119	snp	A/C	0.0905309	0.192535	intron-variant	PSEN2	GRCh38.p7	1:226889115	AAATCGTCCCCAGTG[A/C]TGCACAAGGAGGGCA	5664
rs7539129	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226889143	GCAGGTGCTGAAGGG[C/T]TTGCATCCCTTTCTG	5664
rs7539221	snp	C/T	0.120367	0.215039	intron-variant	PSEN2	GRCh38.p7	1:226889254	GTGGTCTAGATAAAA[C/T]GCAGTAGTCACTGAG	5664
rs7543640	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226889257	GTCTAGATAAAACGC[A/G]GTAGTCACTGAGCTC	5664
rs7546338	snp	C/T	0	0	intron-variant	PSEN2	GRCh38.p7	1:226889197	CTGAGAGAGTCGCCT[C/T]TGTAAAACAGAGGGG	5664
rs7555739	snp	A/C	0.078151	0.181571	intron-variant	PSEN2	GRCh38.p7	1:226894882	ACCAGACTGCCTTAC[A/C]TGAGCCCTGCTGGCC	5664
rs10693643	in-del	-/TT	0.113685	0.209567	intron-variant	PSEN2	GRCh38.p7	1:226893099	ACCACACCTGGCTCA[-/TT]TTTATATTTTTAGTA	5664
rs10753428	snp	A/G	0.419936	0.183362	intron-variant	PSEN2	GRCh38.p7	1:226893921	GGGCTGGGCAAGAGC[A/G]GCTGGGCCTTCTGGG	5664
rs11578657	snp	A/T			intron-variant	PSEN2	GRCh38.p7	1:226892918	gcactacacttaaaa[A/T]tgcagtttgtttttt	5664
rs11582894	snp	A/C	0.5	0	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890845	AACAGCTACAGAGTT[A/C]TAGGTACCTTCATGC	5664
rs11588886	snp	A/G	0.266	0.249487	intron-variant	PSEN2	GRCh38.p7	1:226873784	TTATCTATTAAAACA[A/G]TAGAGGGAGGGAACC	5664
rs11799808	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226886676	GTAGATAGAAGTGCA[G/T]AGTGCCCAGGCTAGA	5664
rs11804915	snp	C/T	0.0577344	0.159793	intron-variant	PSEN2	GRCh38.p7	1:226890366	TCCCTGACTTCATCC[C/T]GTCCATCCTCCAGCG	5664
rs12027512	snp	A/C	0	0	intron-variant	PSEN2	GRCh38.p7	1:226873500	agctaactgcaacct[A/C]tgcttgccgggttct	5664
rs12057618	snp	A/C	0.117188	0.211804	intron-variant	PSEN2	GRCh38.p7	1:226884002	CAGCCTGTGTTGGTC[A/C]CTGTACCTGCAGCTC	5664
rs12058836	snp	G/T	0.00438332	0.0466095	intron-variant	PSEN2	GRCh38.p7	1:226886539	AGGCTTTTCTCCCAG[G/T]TAAGGGGTTGAACCC	5664
rs12069540	snp	C/T	0.157972	0.232445	intron-variant	PSEN2	GRCh38.p7	1:226886301	AGGCTCCCCTCACCC[C/T]GATACTTCCCCTGAA	5664
rs12070751	snp	A/G	0.132066	0.220435	intron-variant	PSEN2	GRCh38.p7	1:226894737	GCGTCTGAGCCGTGC[A/G]CTTGGCATCTGCCCC	5664
rs12071324	snp	C/G	0.117188	0.211804	intron-variant	PSEN2	GRCh38.p7	1:226882173	ATGATGAGGATTGGC[C/G]GAAAAGGTGGGTGGC	5664
rs12091957	snp	A/C	0.174932	0.238463	intron-variant	PSEN2	GRCh38.p7	1:226874011	ATGTGGGCACTCCCC[A/C]CCATGGAGCCAAACC	5664
rs12093600	snp	A/G	0.0295035	0.117819	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871702	AAGGAAGCCTCTGAT[A/G]CCTCTGTAGCCAATT	5664
rs12096062	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226878640	GCCTGTGGCTTTTTA[A/G]GTACAGGGACTCCCA	5664
rs12097722	snp	A/G	0.136506	0.222754	intron-variant	PSEN2	GRCh38.p7	1:226874246	AACCCTGGCCACTGG[A/G]TACGTGACCCTCACA	5664
rs12123818	snp	A/G	0.284209	0.247648	intron-variant	PSEN2	GRCh38.p7	1:226892120	GGCTAAGGAGACACG[A/G]GCAGTAATCACATAG	5664
rs12130732	snp	C/T	0.264906	0.249555	intron-variant	PSEN2	GRCh38.p7	1:226891999	AGAAGATGCCTGCAG[C/T]GCTGGGGTCTTCTCA	5664
rs12401969	snp	C/T	0.39121	0.2063	intron-variant	PSEN2	GRCh38.p7	1:226884566	TTTTAAAGTTAGGGA[C/T]TTTTGTTTCATTTCG	5664
rs12402812	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226884236	gcacgtgagtgctca[A/G]GCAAGCTGGATCCTG	5664
rs12562405	snp	C/G	0.021333	0.101051	intron-variant	PSEN2	GRCh38.p7	1:226882417	AAGCATTTTTTGGCA[C/G]ATGGCCAGACATGGT	5664
rs12563525	snp	C/G	0.0475351	0.146656	intron-variant	PSEN2	GRCh38.p7	1:226879195	CTCCTGCATTTCCAC[C/G]TGATAATTTCTCTCA	5664
rs12724361	snp	A/T			intron-variant	PSEN2	GRCh38.p7	1:226876605	CATGCAAAGATAATC[A/T]TCTTTAATGTTTTGT	5664
rs12737893	snp	A/G			intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226870666	TGAGCGGGCGGTGCC[A/G]GGGGGTGCCCAGGCC	5664
rs12738615	snp	G/T			intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871049	TGCACGTGGGTCTCT[G/T]AGGCGTGTAGCAGGC	5664
rs12742755	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226876604	CCATGCAAAGATAAT[A/C]ATCTTTAATGTTTTG	5664
rs12747261	snp	C/T	0.288386	0.247035	intron-variant	PSEN2	GRCh38.p7	1:226884300	CTGTGCCACTGATCC[C/T]TGTGTGACTGCAAAC	5664
rs12758915	snp	A/G	0.496714	0.0404017	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870643	CTGGAGCGCGGCGGC[A/G]GAGCAGGTGAGCGGG	5664
rs12760155	snp	G/T	0.23031	0.249223	intron-variant	PSEN2	GRCh38.p7	1:226874905	GACTTGCTGCTGCTT[G/T]TTTAAAAATAAATGT	5664
rs16846584	snp	G/T	0.0197687	0.0974348	intron-variant	PSEN2	GRCh38.p7	1:226876483	TTATTTTCCTTTAAA[G/T]AATTAATAGCCTAAA	5664
rs16846590	snp	A/G	0.0930568	0.194599	intron-variant	PSEN2	GRCh38.p7	1:226877019	TCTGACCAGACTCTA[A/G]GTATTCAGGAGAAAG	5664
rs16846619	snp	A/G	0.0509478	0.151255	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896115	CTTGGAGTTTGGTCC[A/G]TTGTAAATGTTGACC	5664
rs17391089	snp	A/G	0.125874	0.217008	intron-variant	PSEN2	GRCh38.p7	1:226879955	GGGGATGAAGTTAAA[A/G]TCCCTGTAGGAATAA	5664
rs28936379	snp	A/G			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888977	ATGATCAGTGCGCTC[A/G]TGGCCCTAGTGTTCA	5664
rs28936380	snp	C/G/T	1.7e-05	0.00291543	PSEN2	1	allele_origin=G(germline)/C(germline)	1:226885546	CCCTCAGCATCTACA[C/G/T]GCCATTCACTGAGGA	5664
rs34012430	in-del	-/C			intron-variant	PSEN2	GRCh38.p7	1:226877615	AGACTAGCTCTTCCC[-/C]TGATTATTCCTTAAT	5664
rs34241052	in-del	-/G			intron-variant	PSEN2	GRCh38.p7	1:226893068	TCCTGAGTAGCTGGG[-/G]ATTACAGGCACGTGC	5664
rs34468000	in-del	-/C			intron-variant	PSEN2	GRCh38.p7	1:226874975	CTCTCCCACTTCCCC[-/C]ACAAACCACCCTTTT	5664
rs34498747	in-del	-/G			intron-variant	PSEN2	GRCh38.p7	1:226878215	TTCTGAGTAGCTGGG[-/G]ATTACAGGTGCCTGC	5664
rs34844805	snp	A/C	0.375	0.216506	intron-variant	PSEN2	GRCh38.p7	1:226890441	CCTCAGCTCTCCAGG[A/C]TCTTGAGAAGGGACT	5664
rs35032481	in-del	-/T			intron-variant	PSEN2	GRCh38.p7	1:226875811	GATTCTCTAGGTCAG[-/T]ACTCCCTTGGTTTGG	5664
rs35151078	in-del	-/G			intron-variant	PSEN2	GRCh38.p7	1:226893845	GCCACTGATTTGGGG[-/G]AGGCAGCTGTCCATG	5664
rs35353885	in-del	-/T	0	0	intron-variant	PSEN2	GRCh38.p7	1:226884554	TTTTTTTTTTTTTTT[-/T]AAAGTTAGGGATTTT	5664
rs35356707	in-del	-/A			intron-variant	PSEN2	GRCh38.p7	1:226878728	AACAGAGGGAGGAGA[-/A]TCGTAGCTTCCCTGT	5664
rs35519961	snp	C/T	0.288127	0.247076	intron-variant	PSEN2	GRCh38.p7	1:226884065	AACCGCCCAGGTTCA[C/T]GGCCTGGCTCACTGC	5664
rs35775893	in-del	-/T			intron-variant	PSEN2	GRCh38.p7	1:226881339	GGAACATTGTGCCTT[-/T]CTGCCCTTCCCTCCT	5664
rs35836641	in-del	-/G			intron-variant	PSEN2	GRCh38.p7	1:226890997	CATGAGTGTCCCAGG[-/G]CTCGGGGGATTCACC	5664
rs35982836	in-del	-/G			intron-variant	PSEN2	GRCh38.p7	1:226890321	GAAAGTTAGGACAGG[-/G]AAGCAGGCATCTGCT	5664
rs41309643	snp	G/T	0.0142736	0.0832652	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890808	CTGGCGTCTGCAAGG[G/T]GGCCTGGGAAAGAGT	5664
rs41314274	snp	A/G	0.00557542	0.0525036	intron-variant	PSEN2	GRCh38.p7	1:226890527	CTTGACAGCAGCGTG[A/G]CTGATTGGCATTAAT	5664
rs45500296	snp	A/T			intron-variant	PSEN2	GRCh38.p7	1:226880688	AGGCATTGTTTGAAG[A/T]TCTTCCCAGCCCAGA	5664
rs55896489	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226884613	TTGTTGTTGTTGTTT[C/T]TTTTAAAGAAAGGAA	5664
rs56736839	snp	G/T			downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896352	AGGTCCCTGGACTCA[G/T]TTGTGCACGGTGGCA	5664
rs58663378	in-del	-/T			intron-variant	PSEN2	GRCh38.p7	1:226889294	TACTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC	5664
rs58855513	snp	A/G	0.0618563	0.164627	intron-variant	PSEN2	GRCh38.p7	1:226885139	CAGCGGATGGGGGTC[A/G]GGTAGTAGCAGGTGG	5664
rs58973334	snp	A/G	0.0195985	0.0970318	PSEN2	1	allele_origin=G(germline)/A(unknown)	1:226883748	AGGAGGACCCTGACC[A/G]CTATGTCTGTAGTGG	5664
rs59683545	snp	C/T	0.0221851	0.102958	intron-variant	PSEN2	GRCh38.p7	1:226883682	GGGACATTCTGCGGC[C/T]CTCACGATGTGGTTT	5664
rs60232264	snp	A/G	0.0349115	0.127424	intron-variant	PSEN2	GRCh38.p7	1:226889164	TCCCTTTCTGCAGAG[A/G]CCTGGGTGGGATCCC	5664
rs61730652	snp	C/T	0.0256271	0.110258	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888970	CCTCATCATGATCAG[C/T]GCGCTCATGGCCCTA	5664
rs61757781	snp	A/G	0.00126775	0.0251449	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888112	CATGGCTGGTTGATC[A/G]TGTCTTCACTGATGC	5664
rs61761208	snp	A/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885602	CTCAACTCCGTGCTG[A/T]ACACCCTCATCATGA	5664
rs61837798	snp	A/T	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226887308	CCCCTTTTGGCTGTG[A/T]GTGCAGCAGGGCCGT	5664
rs63749851	snp	A/C			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885545	TCCCTCAGCATCTAC[A/C]CGCCATTCACTGAGG	5664
rs63749884	snp	A/G			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888979	GATCAGTGCGCTCAT[A/G]GCCCTAGTGTTCATC	5664
rs63750048	snp	C/T	1.64904e-05	0.00287139	PSEN2	1	allele_origin=T(germline)/C(germline)	1:226883817	CCCTCAAATACGGAG[C/T]GAAGCACGTGATCAT	5664
rs63750110	snp	A/C	7.52828e-05	0.0061348	PSEN2	1	allele_origin=A(germline)/C(germline)	1:226895548	TGCGGCCGTTCATGG[A/C]CACCCTGGCCTCCCA	5664
rs63750197	snp	C/T	0.00128686	0.0253333	PSEN2	1	allele_origin=T(germline)/C(germline)	1:226885570	CTGAGGACACACCCT[C/T]GGTGGGCCAGCGCCT	5664
rs63750207	snp	C/G	9.885e-05	0.0070296	PSEN2	1	allele_origin=G(unknown)/C(germline)	1:226891773	ACAGTTTTGGGGAGC[C/G]TTCATACCCCGAAGT	5664
rs63750215	snp	A/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885603	TCAACTCCGTGCTGA[A/T]CACCCTCATCATGAT	5664
rs63750666	snp	C/T	6.96209e-05	0.00589963	PSEN2	1	allele_origin=T(germline)/C(germline)	1:226895521	TCTTTTACTTCTCCA[C/T]GGACAACCTGGTGCG	5664
rs63750812	snp	A/G			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885623	CTCATCATGATCAGC[A/G]TCATCGTGGTTATGA	5664
rs63750880	snp	A/T	3.29565e-05	0.00405921	PSEN2	1	allele_origin=T(unknown)/A(germline)	1:226888945	GCCCTCTGGTGCTGC[A/T]GCAGGCCTACCTCAT	5664
rs66604439	in-del	-/AAG			intron-variant	PSEN2	GRCh38.p7	1:226885969	AACCTCCTGGGCTCA[-/AAG]AGTTCTCCCACCCAG	5664
rs72756540	snp	C/G			upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870049	TGAATTTCACCTTAA[C/G]TTAAAAAAAAAAAAG	5664
rs72758660	snp	A/G	0.00557542	0.0525036	intron-variant	PSEN2	GRCh38.p7	1:226874436	GCCTTTACGGTCCTT[A/G]CCAGCTCTGACATTG	5664
rs72758667	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226885443	CAGCATGGGCATCCC[A/G]GGCACCTCCCCTAGC	5664
rs74502648	snp	C/T	0.0166325	0.0896639	intron-variant	PSEN2	GRCh38.p7	1:226886980	CCTGTGTAACTGTGA[C/T]GAGGCAGGGTTTGAA	5664
rs74521736	snp	A/T	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226886944	TCTCTAAAAAAATAA[A/T]AATAAAATAAGTAAC	5664
rs75041180	snp	C/T	0.0926964	0.194308	intron-variant	PSEN2	GRCh38.p7	1:226879758	TGTGTCCCCTCCTGT[C/T]GGGTGCATTGTCCTT	5664
rs75357954	snp	A/G	1.72653e-05	0.00293809	synonymous-codon, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891306	GACGGTTGGCATGGC[A/G]AAGCTGGACCCCTCC	5664
rs75612539	snp	C/G	0.113685	0.209567	intron-variant	PSEN2	GRCh38.p7	1:226892013	GCGCTGGGGTCTTCT[C/G]AGCAGGCCCCATGTA	5664
rs75681714	snp	G/T	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226874767	CTGCTTTTTACAGCA[G/T]AGGAAATGAGCTGTG	5664
rs75702362	snp	G/T	0.0433465	0.140692	intron-variant	PSEN2	GRCh38.p7	1:226893576	TTGTAAGGTGAAAGG[G/T]TCTTCAGAGGACCTC	5664
rs75733498	snp	C/T	0.0316077	0.121675	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890108	GGAGAGAAATGAGCC[C/T]ATATTCCCTGCCCTG	5664
rs75764929	snp	A/C	0.0926964	0.194308	intron-variant	PSEN2	GRCh38.p7	1:226874062	GGAGAGCAGAGTGAG[A/C]CCTGGGGGCAGGAGA	5664
rs75827833	snp	C/T	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226873094	AGGCAGGAGAATCGC[C/T]TGAACCCAGGAGGCG	5664
rs76153780	snp	C/T	0.0225045	0.103662	intron-variant	PSEN2	GRCh38.p7	1:226886739	TGAGCCCCCTTCCAG[C/T]GGGGGCAGCAGAGGG	5664
rs76155874	snp	A/T	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226886943	GTCTCTAAAAAAATA[A/T]TAATAAAATAAGTAA	5664
rs76157777	snp	C/T	0.00914312	0.0669923	intron-variant	PSEN2	GRCh38.p7	1:226882551	GAAAGAGTAGGATAT[C/T]GTTGGGAGAGCCACT	5664
rs76161302	snp	A/C	0.0325976	0.123435	intron-variant	PSEN2	GRCh38.p7	1:226885287	GCAGGGAGGTCATCT[A/C]GCCCTCGTCCTCACT	5664
rs76221906	snp	A/G	0.0260105	0.111035	intron-variant	PSEN2	GRCh38.p7	1:226882899	CTTTCTTGGCTGAAC[A/G]TCTAGATTGGGACTC	5664
rs76336502	snp	C/G	0.00478085	0.0486577	intron-variant	PSEN2	GRCh38.p7	1:226875664	GAAATCTGTTTCTTA[C/G]CTAGTTCCATTGGCC	5664
rs76397544	snp	A/G	0.0644693	0.167566	intron-variant	PSEN2	GRCh38.p7	1:226874901	CGCTGACTTGCTGCT[A/G]CTTGTTTAAAAATAA	5664
rs76420763	snp	A/G	0.00835141	0.0640778	intron-variant	PSEN2	GRCh38.p7	1:226892868	ACCCCCTTAGGTTCA[A/G]TAACTTGCTAGAATG	5664
rs76655190	snp	A/G	0.00723442	0.0597066	intron-variant	PSEN2	GRCh38.p7	1:226882078	CAGCTGGGGGCCTTC[A/G]AACAGGTCCCTGCGG	5664
rs76732250	snp	A/G	0.117188	0.211804	intron-variant	PSEN2	GRCh38.p7	1:226885239	AGAGAAGTGCCTAGG[A/G]AGCCTTTAATCCCTG	5664
rs76766807	snp	C/T	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226876606	ATGCAAAGATAATCA[C/T]CTTTAATGTTTTGTA	5664
rs77015702	snp	C/T	0.0178098	0.0926698	intron-variant	PSEN2	GRCh38.p7	1:226883253	TCTGCAAATTCCCAG[C/T]ATCTTAGTCACACGC	5664
rs77421307	snp	G/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890047	TAGATCTCGTGGCTG[G/T]GCTGTGTCCCAAAGG	5664
rs77467343	snp	A/G	0.0876345	0.190099	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872082	ATGTGGGGAGTGAGT[A/G]GCTTGTTCCTGTCTA	5664
rs77567779	snp	A/C	0.0372196	0.131242	intron-variant	PSEN2	GRCh38.p7	1:226894984	AGGATGGGCAGCCCC[A/C]ACACCTGCTTCCCAG	5664
rs77656347	snp	A/G	0.0869089	0.189476	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869562	CTCAAACAAATACAT[A/G]TACATGCATGTTCAT	5664
rs77754809	snp	C/T	0.0333695	0.124785	intron-variant	PSEN2	GRCh38.p7	1:226876926	TGTTTTGGGCCTTTT[C/T]CAGCCCAAGAGCTCT	5664
rs77868244	in-del	-/A	0.254664	0.249956	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869766	CCTCGAAAACATGCT[-/A]AGTGAAAGACACAAA	5664
rs77871405	snp	A/G	0.0111196	0.0737302	intron-variant	PSEN2	GRCh38.p7	1:226888579	TGGGAGGACAAGAGA[A/G]AACACTTTCCCAAGG	5664
rs77875620	snp	C/G/T	4.94241e-05	0.00497092	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890039	TGTCTTCCTAGATCT[C/G/T]GTGGCTGTGCTGTGT	5664
rs78254425	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226887465	CAGCTAAGGGACTGG[A/G]TTAGGATCAGCCCCC	5664
rs78420366	snp	A/G			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891821	CTGGCTACCCAGGGG[A/G]GGAGCTGGAGGAAGA	5664
rs78421766	snp	A/G	0.0252325	0.109451	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869668	TACACACACACACAC[A/G]CACACACATATACAT	5664
rs78439943	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226876172	GGACAGACACCTAGC[A/G]GTGTTGTTTATCTGC	5664
rs78557397	snp	A/C	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226876560	AATGCAGAAAAATAT[A/C]AAGAAAATAAAAACC	5664
rs78777332	snp	C/T	0.00716266	0.059414	intron-variant	PSEN2	GRCh38.p7	1:226881409	GAAAACATTCGTGAT[C/T]TCTGAGATTTGGTTC	5664
rs78849289	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870057	ACCTTAAGTTAAAAA[A/C/G]AAAAAAGTAAAACTA	5664
rs79121491	snp	A/C	0.0260105	0.111035	intron-variant	PSEN2	GRCh38.p7	1:226886924	CTGGGCAATGTAAGA[A/C]CCTGTCTCTAAAAAA	5664
rs79343667	snp	C/T	0.0260105	0.111035	intron-variant	PSEN2	GRCh38.p7	1:226892860	CTCCCATGACCCCCT[C/T]AGGTTCAATAACTTG	5664
rs79540408	snp	A/G	0.0295053	0.117822	intron-variant	PSEN2	GRCh38.p7	1:226880771	GTGAAACCCCACTTG[A/G]CACTGTTTTAGGGGG	5664
rs79578214	snp	C/T	0.17461	0.238362	intron-variant	PSEN2	GRCh38.p7	1:226884610	TTTTTGTTGTTGTTG[C/T]TTCTTTTAAAGAAAG	5664
rs79812497	snp	C/G	0.0341408	0.126114	intron-variant	PSEN2	GRCh38.p7	1:226882502	GGGCTTCACTGTGAT[C/G]ATTCAGCCCCCAGGG	5664
rs79822981	snp	A/G	0.151668	0.229849	intron-variant	PSEN2	GRCh38.p7	1:226888359	GGGGCTGCATGGTGG[A/G]CCACATGTTTCTGTC	5664
rs80008032	snp	C/T	0	0	intron-variant	PSEN2	GRCh38.p7	1:226892673	GAGCAGGTGCGCACC[C/T]TCCAGGCAGGCTTGG	5664
rs80125697	snp	C/T	0.095934	0.196885	intron-variant	PSEN2	GRCh38.p7	1:226892103	CCCTGGTGGGACCCA[C/T]AGGCTAAGGAGACAC	5664
rs80212838	snp	A/C	0.0948562	0.196037	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870345	AAGAAAGAGTGTCCT[A/C]GAAGCCTATGTCCTA	5664
rs111297484	snp	G/T	0.276267	0.248616	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226870739	GCGCCCTGAGGGCCC[G/T]GCCCTGCCCTCCGCA	5664
rs111366321	in-del	-/GAA	0	0	intron-variant	PSEN2	GRCh38.p7	1:226885970	ACCTCCTGGGCTCAA[-/GAA]GTTCTCCCACCCAGC	5664
rs111382438	snp	C/G	0.0325976	0.123435	intron-variant	PSEN2	GRCh38.p7	1:226881544	TTTTATCCCCAGAGC[C/G]CAGCATGATCTTTGG	5664
rs111477841	snp	A/C			upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869446	ACTCTAGGCTGGGCA[A/C]CAGAGCAAGGCTCTG	5664
rs111483776	snp	C/T	0.02016	0.0983543	intron-variant	PSEN2	GRCh38.p7	1:226883335	AAAATGTTTATTTAT[C/T]TCCTGGCCTGTTTCC	5664
rs111567390	snp	G/T	0.0775194	0.180971	intron-variant	PSEN2	GRCh38.p7	1:226880697	TTGAAGTTCTTCCCA[G/T]CCCAGAAACCTGCAT	5664
rs111643955	snp	A/G	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226885352	CAGGTCTGTGGTCAG[A/G]GTGCCAGGAAATGAG	5664
rs111777599	snp	A/G	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226885269	GTGGGGGTGGGGAAA[A/G]CAGCAGGGAGGTCAT	5664
rs111901133	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868852	GTCTAGTGTCCAGAA[C/T]ATATAAAGAACTCTT	5664
rs111906419	snp	C/T	0.119978	0.213528	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896428	CAAGTGTTCACCCTC[C/T]GCAGAAGCCTGTGAG	5664
rs111910427	snp	A/G	0.0271762	0.113356	intron-variant	PSEN2	GRCh38.p7	1:226888215	CCATGTGGCACAAGT[A/G]GACATGGGCATGAGG	5664
rs112009316	snp	A/G	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226892861	TCCCATGACCCCCTT[A/G]GGTTCAATAACTTGC	5664
rs112062360	snp	A/G	0.5	0	utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875448	GTGTTAAAAACCAGC[A/G]CTGCCCTCTTTGAAA	5664
rs112130067	in-del	-/GTT	0.5	0	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891691	TTGTTTCTCTCTCTT[-/GTT]GTCCCCTCCTCACGG	5664
rs112521487	snp	C/T			upstream-variant-2KB, nc-transcript-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870427	CTCCTTCTAAGGTCG[C/T]CGCTTAGTTCCGACG	5664
rs112809286	snp	A/T	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226886473	CATCTGGCCAGAATC[A/T]TGGGCACTGCCTGTC	5664
rs112971145	snp	A/G	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226881614	AATGAGCACACTGAC[A/G]GTTTGGAGCTGCCCT	5664
rs113061270	snp	C/G	0.0444908	0.142359	intron-variant	PSEN2	GRCh38.p7	1:226889945	AGGCATGCTCTGAGA[C/G]CTCCACCCGGGGCTC	5664
rs113149123	snp	C/T	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226892122	CTAAGGAGACACGGG[C/T]AGTAATCACATAGAC	5664
rs113235155	snp	C/G	0.00914312	0.0669923	intron-variant	PSEN2	GRCh38.p7	1:226876034	AATGGGGTGCAGGGG[C/G]TGGGAGACGGGGAAA	5664
rs113439784	snp	C/G	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226888249	TGGGCGGGGAAAGAT[C/G]ACCATCGAGCTCCAG	5664
rs113478201	snp	A/G	0.00597247	0.0543191	intron-variant	PSEN2	GRCh38.p7	1:226886210	CCACTTGAGTTCCTC[A/G]TTGCAGTGTTCCAAG	5664
rs113600895	snp	C/T	0.5	0	intron-variant	PSEN2	GRCh38.p7	1:226895377	GACTCACAGCTCCTG[C/T]CCACACCAGGGATCA	5664
rs113807334	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868910	ATTTTAAAATGGGCA[A/G]AGGACTTGAATAGGC	5664
rs113958123	snp	A/G	0.00597247	0.0543191	intron-variant	PSEN2	GRCh38.p7	1:226877673	GAAGTCTTGGTCCTC[A/G]TTGTTGTGGGCACAG	5664
rs114076393	snp	A/G	0.00557542	0.0525036	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891174	CCTGCAGGATGGAGG[A/G]TCCTGTGCAGGCTTT	5664
rs114127255	snp	C/T	0.0345262	0.126772	intron-variant	PSEN2	GRCh38.p7	1:226891972	TCCCATCAGAGGCAT[C/T]TCTGTGAAAGTAGAA	5664
rs114194538	snp	C/T	0.00557542	0.0525036	intron-variant	PSEN2	GRCh38.p7	1:226878653	TAGGTACAGGGACTC[C/T]CAGAACTGCTCCTCC	5664
rs114263106	snp	A/G	0.00676609	0.0577691	intron-variant	PSEN2	GRCh38.p7	1:226878904	TGCCCCTCTTTGAGT[A/G]AGAGTGAATTCCCCA	5664
rs114334281	snp	C/T	0.00976277	0.0691814	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885622	CCTCATCATGATCAG[C/T]GTCATCGTGGTTATG	5664
rs114543513	snp	A/G/T	0.0345262	0.126772	intron-variant	PSEN2	GRCh38.p7	1:226893140	TTTGACTTGTTGCCC[A/G/T]GGCTGGTTTCGAACT	5664
rs114778691	snp	A/G	0.0333695	0.124785	intron-variant	PSEN2	GRCh38.p7	1:226884447	TTTAGTAAAATACAT[A/G]CAGAGGCAGCAGCGT	5664
rs114815412	snp	C/T	0.0352966	0.128072	intron-variant	PSEN2	GRCh38.p7	1:226875101	AAATTCAGGAGGCCC[C/T]ATCAGAGGGCCCCTG	5664
rs114816603	snp	A/G	0.021333	0.101051	intron-variant	PSEN2	GRCh38.p7	1:226887970	CTGATCCCTTCCAGC[A/G]TAGGCATGAAGTAGC	5664
rs114982010	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871409	AGGTCGCCCAGGTAC[A/G]ATATAGCAGAGCCAG	5664
rs115016070	snp	C/T	0.0271762	0.113356	upstream-variant-2KB, nc-transcript-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870414	GGCCCGGCCTCCACT[C/T]CTTCTAAGGTCGTCG	5664
rs115236371	snp	C/T	0.0205511	0.0992634	intron-variant	PSEN2	GRCh38.p7	1:226894229	GATTTTTCATTTCTT[C/T]TCTTCCCTCTGAGGG	5664
rs115270813	snp	A/C	0.0185938	0.0946107	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868623	GCTAAAACTATAAAA[A/C]TCTTAGAAGAAAACA	5664
rs115304948	snp	C/T	0.0391387	0.134304	intron-variant	PSEN2	GRCh38.p7	1:226878881	AATGCAGCAACTCTT[C/T]GTTGTGGTGCCCCTC	5664
rs115529149	snp	A/G	0.00279162	0.0372561	intron-variant	PSEN2	GRCh38.p7	1:226874947	CTACTCCAGAGGGGC[A/G]TGCTAGGGGCTCCCT	5664
rs115598326	snp	C/T	0.0349115	0.127424	intron-variant	PSEN2	GRCh38.p7	1:226892606	ACAGGACTCCAGTGA[C/T]ACGGGAGGGGCAAGC	5664
rs115652716	snp	C/T	0.00330283	0.0405032	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894110	CACGCTGGCCTGCTT[C/T]GTGGCCATCCTCATT	5664
rs115681617	snp	A/G	0.0023933	0.0345097	intron-variant	PSEN2	GRCh38.p7	1:226882395	AAGCTTAGGATGGTA[A/G]CAGGGGAAGCATTTT	5664
rs115699328	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226893741	CTCTAAGTGCCCAAC[A/G]CTGGTTTTACCTGAG	5664
rs115752022	snp	A/G	0.0356815	0.128715	intron-variant	PSEN2	GRCh38.p7	1:226881169	TTGTCTCTGGGGGTC[A/G]CTTTCCCTCTCTGGT	5664
rs115790700	snp	A/G	0.0869089	0.189476	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869422	GTGAGCCAAGATTGC[A/G]GCCACTGCACTCTAG	5664
rs115799957	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868827	TTTGCAAAGCATATA[C/T]CTGATAAGGGTCTAG	5664
rs115851013	snp	A/C	0.0260105	0.111035	intron-variant	PSEN2	GRCh38.p7	1:226883423	AGGAAGGGGAAAGAT[A/C]TTTTGATTCATTAAC	5664
rs115974666	snp	C/T	0.00874735	0.0655527	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896498	TTTGGCCCTGGGCAC[C/T]GTGGTGGGAGAGTGG	5664
rs116003409	snp	C/T	0.00271437	0.0367399	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885604	CAACTCCGTGCTGAA[C/T]ACCCTCATCATGATC	5664
rs116171245	snp	A/G	0.0193772	0.0965046	intron-variant	PSEN2	GRCh38.p7	1:226882106	CGGCTACTGTACCTT[A/G]CAGATGAAAACCAGA	5664
rs116187190	snp	A/G	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872329	CTTGTACAGAATATT[A/G]GAATTTAAGATCTTA	5664
rs116344544	snp	A/G	0.0356815	0.128715	intron-variant	PSEN2	GRCh38.p7	1:226883307	ACTCCTCTAGCTAGT[A/G]ATTTGTCAGCCAAAA	5664
rs116407447	snp	A/G	0.0372196	0.131242	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869416	GTTGCAGTGAGCCAA[A/G]ATTGCGGCCACTGCA	5664
rs116529536	snp	A/G	0.0418186	0.138422	intron-variant	PSEN2	GRCh38.p7	1:226890417	CATTCCTGTGATCCC[A/G]CAGCCACCCCTCAGC	5664
rs116567356	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226881666	TGCCCCCTGGGATGT[A/G]AGTCACCTCAGGCCA	5664
rs116602204	snp	A/C/T	0.0310518	0.120672	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871125	GCCGAGTCCATTCGG[A/C/T]CTCTAGCACCGGGTC	5664
rs116635380	snp	A/G	0.0205511	0.0992634	intron-variant	PSEN2	GRCh38.p7	1:226891942	GGAGGAGGGCATGAG[A/G]GGAGGGGCCCCTTTT	5664
rs116728405	snp	A/G	0.0341408	0.126114	intron-variant	PSEN2	GRCh38.p7	1:226894308	ACAGGAGGTGTGCTC[A/G]CCCCTAGGTGGGCTC	5664
rs116760649	snp	C/T	0.0252325	0.109451	intron-variant	PSEN2	GRCh38.p7	1:226886346	TTTCCTTTTCCTTTT[C/T]GGGCAAGGATGTGCA	5664
rs116807339	snp	G/T	0.00874735	0.0655527	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895984	CAATGCTTTGTCCAT[G/T]ATGTCCTTGTTATTT	5664
rs117025103	snp	A/G	0.0566069	0.158427	intron-variant	PSEN2	GRCh38.p7	1:226894490	GAAAATTGCTTAAGG[A/G]CCTTGCCCATGGGCG	5664
rs117145200	snp	A/C	0.00318978	0.0398085	intron-variant	PSEN2	GRCh38.p7	1:226895266	CTGCCCTTAACACCT[A/C]AAGAGCTGTTGCAGG	5664
rs117236763	snp	C/T	0.00953873	0.0683987	intron-variant	PSEN2	GRCh38.p7	1:226878440	ACTTGATCCTGGGTC[C/T]CCTGCTTCTCCATCT	5664
rs117310559	snp	A/G	0.0517044	0.152246	intron-variant	PSEN2	GRCh38.p7	1:226886642	TTTTTTGTTCAGGCC[A/G]CTGCCATCCATGGAG	5664
rs117314062	snp	A/T	0.0566069	0.158427	intron-variant	PSEN2	GRCh38.p7	1:226893840	CCACTGGCCACTGAT[A/T]TGGGGAGGCAGCTGT	5664
rs117368833	snp	G/T	0.0520825	0.152737	intron-variant	PSEN2	GRCh38.p7	1:226876031	GAGAATGGGGTGCAG[G/T]GGGTGGGAGACGGGG	5664
rs117399735	snp	G/T	0.00716266	0.059414	intron-variant	PSEN2	GRCh38.p7	1:226889841	CCTCCATGCTTGCAG[G/T]TGCCTGCGAGGCCCT	5664
rs117456084	snp	C/T	0.0566069	0.158427	intron-variant	PSEN2	GRCh38.p7	1:226894858	ATGGTGGACCCAGGC[C/T]CCTCCACCACCAGAC	5664
rs117724727	snp	A/G	0.0520825	0.152737	intron-variant	PSEN2	GRCh38.p7	1:226883584	AGTAGCTCATAGACT[A/G]CTCCTTATATCTGGA	5664
rs117856985	snp	C/G	0.0517044	0.152246	intron-variant	PSEN2	GRCh38.p7	1:226886451	GGAGTAGTGGAAGGG[C/G]AGATCCCATCTGGCC	5664
rs118067884	snp	G/T	0.0279526	0.114869	intron-variant	PSEN2	GRCh38.p7	1:226877565	CCACCAGGCTAGGAG[G/T]GTTGTGATTAGAGGG	5664
rs118121323	snp	C/T	0.00874735	0.0655527	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870114	TCTCAACCTACCCCA[C/T]AGACCCCAAATCCTG	5664
rs118147159	snp	A/C	0.00478085	0.0486577	intron-variant	PSEN2	GRCh38.p7	1:226887663	TTTCTCCATGGCCCT[A/C]ATCATTACCTGCTGA	5664
rs137981702	snp	A/G	0.0123036	0.0774623	intron-variant	PSEN2	GRCh38.p7	1:226874727	ATCTCTAGGTTTTAC[A/G]ATAATCTTGCAAGGT	5664
rs138051819	snp	G/T	0.00279162	0.0372561	intron-variant	PSEN2	GRCh38.p7	1:226878509	ACCTTTGCTCTCTGC[G/T]TATCCATTTTTGTTG	5664
rs138251565	snp	C/T	0.00398564	0.0444627	intron-variant	PSEN2	GRCh38.p7	1:226880042	TAAGGGGATTGAAAT[C/T]GGCTGACTTGGTGGA	5664
rs138289837	in-del	-/A			upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870138	AAATCCTGGAACCAC[-/A]AACCCCCTAGGCCAA	5664
rs138316025	snp	A/G	0.00716266	0.059414	intron-variant	PSEN2	GRCh38.p7	1:226885204	TGTGGGTGGGTGGGG[A/G]AATGAGAACTGGATG	5664
rs138494303	snp	C/T	0.00136824	0.0261199	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895432	CCTGCAGGGCTTGTG[C/T]CTGACCCTCCTGCTG	5664
rs138774925	snp	A/T	0.0111196	0.0737302	intron-variant	PSEN2	GRCh38.p7	1:226874145	AGCATTTCTTGACAC[A/T]TACCTGCCCGTGGTG	5664
rs138833114	snp	C/T	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226879172	CCGAGCCACCATACC[C/T]GGCCCTTCTCCTGCA	5664
rs138836272	snp	A/G	0.000502285	0.0158395	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889016	CTCCCAGAGTGGTCC[A/G]CGTGGGTCATCCTGG	5664
rs138924167	snp	A/G/T	0.00636936	0.0560724	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896272	GTTTCCTAAGCAAAG[A/G/T]AGTTAGGAGAGCAGG	5664
rs138981581	snp	A/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885410	TGGTGCCCGCACTCC[A/T]TCAGGGCAGCATGTG	5664
rs139184944	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226886577	TGGAAAGGAAATTAA[A/G]CTGGGCATTACCTAT	5664
rs139250934	snp	C/T	0.00199481	0.0315187	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890936	ATTCCAGGCGCATTC[C/T]GAGGATGAGCGGAGA	5664
rs139309459	snp	C/T	1.65594e-05	0.0028774	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226882018	GGAGGGCAGGCAGGG[C/T]CCAGAGGATGGAGAG	5664
rs139332886	snp	C/T	0.000282723	0.0118862	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883728	GGAGAACGAGGAGGA[C/T]GGTGAGGAGGACCCT	5664
rs139498276	in-del	-/G	0.077417	0.180873	intron-variant	PSEN2	GRCh38.p7	1:226877181	ACAGTGCCAGGAAAA[-/G]TCTGACACTGGCTGA	5664
rs139573101	snp	A/G	3.30639e-05	0.00406581	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885641	ATCGTGGTTATGACC[A/G]TCTTCTTGGTGGTGC	5664
rs139576184	in-del	-/TTC	0.0154538	0.0865337	intron-variant	PSEN2	GRCh38.p7	1:226882976	GTTTCATTTGGCTTT[-/TTC]TTTAGCTGTTCACCT	5664
rs139656438	snp	A/G	0.00716266	0.059414	intron-variant	PSEN2	GRCh38.p7	1:226887942	GTGCCCTCTTTATCT[A/G]TAAGGTGGCCACCTG	5664
rs139669161	snp	G/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869546	CAAATAAAAATGGGC[G/T]CTCAAACAAATACAT	5664
rs139748552	snp	A/C	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226892889	TGCTAGAATGACTCA[A/C]AGAACTCAGGAAAGC	5664
rs139832281	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226877061	TCACTCTCTCATGTG[A/G]CAATCAAGTAGTGCC	5664
rs139972151	snp	A/G	0.000115497	0.00759837	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883771	TGTAGTGGGGTTCCC[A/G]GGCGGCCGCCAGGCC	5664
rs140221267	snp	C/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226882614	AACATCTGAATTTGC[C/G]TGAACCCTGTTCTCT	5664
rs140239784	snp	C/T	0.00279162	0.0372561	intron-variant	PSEN2	GRCh38.p7	1:226876899	TTCCACACTCTCCTC[C/T]GCAGTGGGCATTGTT	5664
rs140415143	snp	C/T	0.174932	0.238463	intron-variant	PSEN2	GRCh38.p7	1:226878153	GGTGCGATCTCAGCT[C/T]ACTGCAGCCTCCGCC	5664
rs140501902	snp	C/T	0.00669197	0.0574561	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883774	AGTGGGGTTCCCGGG[C/T]GGCCGCCAGGCCTGG	5664
rs140562931	snp	C/T	1.65704e-05	0.00287836	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889001	GTGTTCATCAAGTAC[C/T]TCCCAGAGTGGTCCG	5664
rs140812381	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226878675	TGCTCCTCCAGTCAT[A/G]GCAGAGATAAATCAC	5664
rs141267340	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872146	GGCTAGGGGCTGCTG[C/G]TGGGGTGCCTGGAGC	5664
rs141303900	snp	C/G	0.00358779	0.0422022	intron-variant	PSEN2	GRCh38.p7	1:226888432	TGTGAACCCCAGGGG[C/G]ATAGAAACCCCCCAA	5664
rs141487628	in-del	-/CCT	0.02016	0.0983543	intron-variant	PSEN2	GRCh38.p7	1:226883100	TGCCCTCCCTCGTTA[-/CCT]CCTCATTTGTGCCTG	5664
rs141577748	snp	C/G/T	0.000115359	0.00759391	intron-variant	PSEN2	GRCh38.p7	1:226890148	TGTGAGTGAGCCCCC[C/G/T]GTGCCTCTGCCTGAC	5664
rs141848347	snp	A/G	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226874462	CATTGTCCTATGGAT[A/G]TGTCCTTTCATTTGA	5664
rs141887613	snp	G/T	0.0869089	0.189476	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869285	GCCTGGCCAACATGG[G/T]GAAACCCCATCTCTA	5664
rs141941207	in-del	-/CT	0.0352966	0.128072	intron-variant	PSEN2	GRCh38.p7	1:226883289	GAGTGTCCCTGTGCA[-/CT]GACTCCTCTAGCTAG	5664
rs142086801	snp	A/G	0.00755907	0.0610114	intron-variant	PSEN2	GRCh38.p7	1:226877422	AGGATGTTTAGTGCC[A/G]GCTAAGGGCTCAGCA	5664
rs142231816	snp	C/T	0.0115144	0.0749975	intron-variant	PSEN2	GRCh38.p7	1:226892118	CAGGCTAAGGAGACA[C/T]GGGCAGTAATCACAT	5664
rs142407400	snp	C/T	0.00716266	0.059414	intron-variant	PSEN2	GRCh38.p7	1:226889369	GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC	5664
rs142421813	snp	A/G/T	0.0520825	0.152737	intron-variant	PSEN2	GRCh38.p7	1:226880526	CAGCCTCTGGACAGC[A/G/T]ATCACTCAGCCTCTG	5664
rs142444752	snp	A/G	0.00478085	0.0486577	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891127	TGGACCCCTCCCACA[A/G]CGGCCTCCTAACAAT	5664
rs142445855	snp	C/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226893283	AGCCAAATGAAGAGA[C/G]AGTGAAGAAGTAATG	5664
rs142546082	snp	C/T	0.000181517	0.00952499	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883770	CTGTAGTGGGGTTCC[C/T]GGGCGGCCGCCAGGC	5664
rs142690225	snp	A/G	0.00026466	0.0115004	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894111	ACGCTGGCCTGCTTC[A/G]TGGCCATCCTCATTG	5664
rs142772982	snp	C/T	0.000413688	0.0143761	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895535	ACGGACAACCTGGTG[C/T]GGCCGTTCATGGACA	5664
rs142892469	snp	C/T	4.96208e-05	0.00498076	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881992	GAGAGCCCCACGCCG[C/T]GCTCCTGCCAGGAGG	5664
rs142995247	snp	A/G	0.00874735	0.0655527	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890873	TGCAGTTGAGGATTC[A/G]AGCCCGTAGAGGAGA	5664
rs143059995	snp	A/G	0.00716266	0.059414	utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895699	TAAAAAATAAAGTAC[A/G]TGTTTACTTGGTGAG	5664
rs143061887	snp	C/T	4.94605e-05	0.0049727	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881960	TGTGTGATGAGCGGA[C/T]GTCCCTAATGTCGGC	5664
rs143156132	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226883381	GCCACATGAACAGAA[C/T]TGAGTGACCTCCTGA	5664
rs143227762	snp	A/T	0.00270794	0.0366965	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226882039	GGATGGAGAGAACAC[A/T]GCCCAGTGGGTAGGT	5664
rs143259081	snp	C/G	0.0049936	0.0497179	intron-variant	PSEN2	GRCh38.p7	1:226889990	AGGCTCTTCTTCAGG[C/G]GGCTGCCCGGGGATA	5664
rs143476339	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872374	ACTGAAATAGTTTAT[C/T]ATTACCTTTTTACAG	5664
rs143501870	snp	A/G	0.000440827	0.0148398	PSEN2	1	allele_origin=G(germline)/A(germline)	1:226883712	TCCCACAGAGAAGCC[A/G]GGAGAACGAGGAGGA	5664
rs143549266	snp	C/T	0.000115759	0.00760697	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894097	GGGACTGGAATACCA[C/T]GCTGGCCTGCTTCGT	5664
rs143649336	snp	C/T	0.00835141	0.0640778	intron-variant	PSEN2	GRCh38.p7	1:226894881	CACCAGACTGCCTTA[C/T]CTGAGCCCTGCTGGC	5664
rs143798253	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885234	GGGTGAGAGAAGTGC[A/C]TAGGGAGCCTTTAAT	5664
rs143876830	snp	C/G	0.000951428	0.0217901	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891394	CTAACAGCCTCTCAT[C/G]ACTGGGGGGCAGCTC	5664
rs143912759	snp	A/C	0.000148826	0.008625	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894073	GCAAGGCGGCTGCCA[A/C]GGGCAGCGGGGACTG	5664
rs144004955	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226886652	AGGCCGCTGCCATCC[A/G]TGGAGCAGGTAGATA	5664
rs144159827	snp	C/T	0.00755907	0.0610114	intron-variant	PSEN2	GRCh38.p7	1:226882832	CTTGTTTGTTATCTC[C/T]GGGAAGTTTTGTACA	5664
rs144277432	snp	C/T	0.000120444	0.00775933	missense, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891293	CTGCCATGGTGTGGA[C/T]GGTTGGCATGGCGAA	5664
rs144289421	in-del	-/G	0.0158469	0.0875917	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895796	AGCGCCTCGCTTCAC[-/G]GACAGGAAGCACAGC	5664
rs144318314	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895516	GCTCATCTTTTACTT[C/T]TCCACGGACAACCTG	5664
rs144629723	snp	C/T	0.000131822	0.00811748	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888850	GCTCAAGACCTACAA[C/T]GTGGCCATGGACTAC	5664
rs144696679	snp	A/G	1.65373e-05	0.00287548	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881988	GGCTGAGAGCCCCAC[A/G]CCGCGCTCCTGCCAG	5664
rs144791481	snp	A/G	0.00311608	0.0393488	intron-variant	PSEN2	GRCh38.p7	1:226885719	GCCACGCTTCTCTCC[A/G]TCTGCCCCACACCAT	5664
rs144928658	snp	C/G	0.0111196	0.0737302	intron-variant	PSEN2	GRCh38.p7	1:226877167	ATTATAAAGCAGAGA[C/G]AGTGCCAGGAAAAGT	5664
rs145010538	snp	C/G	0.000428393	0.0146292	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888952	GGTGCTGCAGCAGGC[C/G]TACCTCATCATGATC	5664
rs145129440	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895885	TGAGGGCTGAGATGC[A/G]CAAAGAGTGTGCTCG	5664
rs145259934	snp	G/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226892928	TAAAATTGCAGTTTG[G/T]TTTTTGTTGTCGTTT	5664
rs145400391	snp	A/G	6.64695e-05	0.00576457	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889006	CATCAAGTACCTCCC[A/G]GAGTGGTCCGCGTGG	5664
rs145498605	snp	A/G	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226874516	GCCTGGGGCTGGGCC[A/G]GGAATGGAAACTTGA	5664
rs145513230	snp	C/T	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226878328	CAGGTGATCTGCCCA[C/T]CTCAGACAGGCATGA	5664
rs145582210	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871369	TGAAGAAACTGAGGC[C/T]ACAGAGCTAAAGTGA	5664
rs145649324	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876902	CACACTCTCCTCCGC[A/C]GTGGGCATTGTTTTG	5664
rs145671982	snp	A/G	1.65299e-05	0.00287483	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894082	CTGCCACGGGCAGCG[A/G]GGACTGGAATACCAC	5664
rs145720978	snp	C/T	0.00318978	0.0398085	intron-variant	PSEN2	GRCh38.p7	1:226894201	GGTGGGGGCAGGTCT[C/T]AGGATCCCTAGGGAT	5664
rs146203177	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226886560	GGTTGAACCCCTAAC[A/G]ATGGAAAGGAAATTA	5664
rs146662886	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226877911	AGTGTGGATGATGAC[A/G]ACAGTGGTCACCAGG	5664
rs146666649	snp	C/G	0.00318978	0.0398085	intron-variant	PSEN2	GRCh38.p7	1:226882446	GTAAGTGTGAGAGGA[C/G]TCTGCCTGATACACG	5664
rs146718524	snp	C/T	4.95471e-05	0.00497705	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883857	GCCTGTCACTCTGTG[C/T]ATGATCGTGGTGGTA	5664
rs146894466	snp	C/G	0.000566308	0.0168176	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883725	CCAGGAGAACGAGGA[C/G]GACGGTGAGGAGGAC	5664
rs147050055	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885061	TGGGAAGAGTGAGGT[G/T]TGAGTGAATTGCTTC	5664
rs147066272	snp	C/T	0.0123036	0.0774623	intron-variant	PSEN2	GRCh38.p7	1:226888608	GGACCTTTCCATGTG[C/T]ACAGGGTCTTCCAGG	5664
rs147240901	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226885408	GATGGTGCCCGCACT[C/T]CATCAGGGCAGCATG	5664
rs147301577	snp	A/G	0.00755907	0.0610114	intron-variant	PSEN2	GRCh38.p7	1:226876909	TCCTCCGCAGTGGGC[A/G]TTGTTTTGGGCCTTT	5664
rs147318268	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226880350	CCACTGTACTCCAAC[A/G]TAAGTGACCAGTGAG	5664
rs147326133	snp	A/G	1.65343e-05	0.00287521	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881986	TCGGCTGAGAGCCCC[A/G]CGCCGCGCTCCTGCC	5664
rs147451039	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226876512	AAATAAACCCTACAG[A/G]TACAGTCTGTGTTTA	5664
rs147467284	snp	C/G	0.00676609	0.0577691	intron-variant	PSEN2	GRCh38.p7	1:226879641	TTCCAGAATGAGCCC[C/G]CTCCTCCAAACTCTG	5664
rs147612731	snp	A/G/T	0.00517822	0.0506191	intron-variant	PSEN2	GRCh38.p7	1:226892964	TGGAGACAGGGTCTC[A/G/T]CTCTGTTGCCCAGGC	5664
rs147693123	in-del	-/CTCAGCCTCTGGACAGCGATCA			intron-variant	PSEN2	GRCh38.p7	1:226880557	ACAGACAGCGATCAC[-/CTCAGCCTCTGGACAGCGATCA]TCAGCCTCTGGACAG	5664
rs147702142	snp	A/C/G	0.011515	0.0750031	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889018	CCCAGAGTGGTCCGC[A/C/G]TGGGTCATCCTGGGC	5664
rs148238688	snp	A/G/T	0.000224772	0.0105988	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889034	TGGGTCATCCTGGGC[A/G/T]CCATCTCTGTGTATG	5664
rs148243400	snp	G/T	0.00398564	0.0444627	intron-variant	PSEN2	GRCh38.p7	1:226883570	TTTTCATATGCCCTA[G/T]TAGCTCATAGACTGC	5664
rs148366519	in-del	-/C	0.0209421	0.100162	intron-variant	PSEN2	GRCh38.p7	1:226876251	AGGCTTCAGAGCAGA[-/C]TTAGGTGGCTTGCAA	5664
rs148547900	snp	A/G	0.00517822	0.0506191	intron-variant	PSEN2	GRCh38.p7	1:226886152	GGATTACATGTGTGA[A/G]CCATTGCATCCAGCC	5664
rs148598799	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891426	CTACCTGCACCCAGC[A/T]CTGCTCGGCCTGGCT	5664
rs148721936	snp	A/G	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226876348	CTAGGTAAATCAGAG[A/G]GGCTGAGGGACAAAT	5664
rs148774430	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226880437	TTGGAGACGAACTTT[C/G]AGCAGAGCGCACACC	5664
rs148920786	snp	C/T	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226894751	CGCTTGGCATCTGCC[C/T]CTTAGTGAAAACCCT	5664
rs148996705	snp	A/G	0.00243976	0.0348415	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885547	CCTCAGCATCTACAC[A/G]CCATTCACTGAGGAC	5664
rs149053799	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226877338	TCCAAGGGTAACCTT[A/G]AGCTAATTACTTTTT	5664
rs149106598	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226883364	CCTCCCATATCAGTA[C/T]GGCCACATGAACAGA	5664
rs149172004	snp	A/C	3.30628e-05	0.00406575	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894090	GGCAGCGGGGACTGG[A/C]ATACCACGCTGGCCT	5664
rs149354305	snp	C/T	6.61452e-05	0.0057505	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881987	CGGCTGAGAGCCCCA[C/T]GCCGCGCTCCTGCCA	5664
rs149375801	snp	C/G	0.00716266	0.059414	intron-variant	PSEN2	GRCh38.p7	1:226879571	ATTGCTCGATATTAT[C/G]AGGATAGGTTATGTT	5664
rs149428641	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885694	GGTGAGGCCCTGGCC[C/T]TGCCCTCCAGCCACG	5664
rs149590162	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875387	GTGGGACTTCTCAGA[C/T]GTCAGGAGAGTGATG	5664
rs149734051	snp	A/G	0.00835141	0.0640778	intron-variant	PSEN2	GRCh38.p7	1:226888219	GTGGCACAAGTGGAC[A/G]TGGGCATGAGGACCT	5664
rs149858236	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870301	GTGAGAACAACCGGG[A/G]GGAGGAGGGGATGTG	5664
rs149910285	snp	A/G	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226877104	GGTGAAGGTGGGTGG[A/G]TGAGGGACACTCACC	5664
rs150136828	snp	C/T	0.00755907	0.0610114	intron-variant	PSEN2	GRCh38.p7	1:226878736	GGAGGAGATCGTAGC[C/T]TCCCTGTTCATTCAC	5664
rs150207043	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226893332	TGGGGGAAGGAGGAC[A/C]GCTGGGGCCAGGAGC	5664
rs150400387	snp	C/T	0.000330447	0.0128497	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883747	GAGGAGGACCCTGAC[C/T]GCTATGTCTGTAGTG	5664
rs150475531	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890773	ATGGCGGGGCTTAAA[C/T]AGCCTGAATTTCTGG	5664
rs150618255	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869421	AGTGAGCCAAGATTG[C/T]GGCCACTGCACTCTA	5664
rs150780392	snp	A/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890101	CTGCCCAGGAGAGAA[A/G]TGAGCCCATATTCCC	5664
rs150874766	in-del	-/AC			upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869667	TGTGGCATACATGAT[-/AC]ACACACACACACACG	5664
rs150877518	snp	C/T	0.0197687	0.0974348	intron-variant	PSEN2	GRCh38.p7	1:226881656	CTATGCGTTTTGCCC[C/T]CTGGGATGTGAGTCA	5664
rs150930019	snp	C/G	0.00318978	0.0398085	intron-variant	PSEN2	GRCh38.p7	1:226886981	CTGTGTAACTGTGAC[C/G]AGGCAGGGTTTGAAC	5664
rs150931933	snp	A/T	0.0111196	0.0737302	intron-variant	PSEN2	GRCh38.p7	1:226872730	GGGGACTGATAAGAC[A/T]GCAAATATTTCTGCA	5664
rs151048692	snp	C/T	0.000200481	0.01001	missense, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895562	GACACCCTGGCCTCC[C/T]ATCAGCTCTACATCT	5664
rs151212920	snp	C/T	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226892359	GGAATCAGAGGAAGC[C/T]GGGGCGGGATGCAGA	5664
rs180685271	snp	A/T	0.0532157	0.154195	intron-variant	PSEN2	GRCh38.p7	1:226873425	ATTAGGGAAAAAAAA[A/T]TTTTTTTGAGATGGA	5664
rs180765094	snp	A/G	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226887789	AGAACAGTGCCTGGC[A/G]AGTAGGAGACACCCA	5664
rs180909178	snp	C/T	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226895359	GCCCAGGGACTAGAC[C/T]ATGACTCACAGCTCC	5664
rs181176083	snp	A/G	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226887125	AGCTGGCCCCACTGC[A/G]GGCAGTAGGTGTCTG	5664
rs181276264	snp	A/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226882547	GTTAGAAAGAGTAGG[A/T]TATCGTTGGGAGAGC	5664
rs181366732	snp	A/G	0.00993419	0.0697739	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868775	ATGAAAGGACATCAG[A/G]AAGTGAAAAAGACAA	5664
rs181423706	snp	A/G			upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869868	TAATTGCCAGGGGCT[A/G]GGGGGGAAGAGGGCA	5664
rs181533346	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226882216	ACCTTCCATCTGCAG[A/G]GTTTCATAGGACTGC	5664
rs181544023	snp	A/G	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226894854	TGGGATGGTGGACCC[A/G]GGCTCCTCCACCACC	5664
rs181905006	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870456	CGTCGGGATGACCCT[C/G]TCATCCACGCGGCGT	5664
rs182084017	snp	C/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876893	CAGTTTTTCCACACT[C/G]TCCTCCGCAGTGGGC	5664
rs182206986	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872181	GTGCATAATGTCACA[C/T]CTGTCTCCCCTCCGT	5664
rs182226938	snp	A/G	0.00517822	0.0506191	intron-variant	PSEN2	GRCh38.p7	1:226874887	CCTCTGCTTTTGACC[A/G]CTGACTTGCTGCTGC	5664
rs182357168	snp	A/G	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226880862	TTCCCCACCTCACAC[A/G]TCTGCTCTCATGGCT	5664
rs182512234	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226886129	CACCTTGGCCTCCCA[A/G]AGTTCTGGGATTACA	5664
rs182893958	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226883640	TGGTTCCAAAAATCC[A/G]TGCATTACATGGATA	5664
rs182900763	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896308	CTGACATCTGCCAGC[C/G]CTGAGCTGTAAGGCT	5664
rs182918620	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226884360	CCTGAATGTGAAACA[A/G]GGTGGTTGGACCAGA	5664
rs183044548	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226889469	TTTAGTAGAGATGGG[A/G]TTTCACCATGTTGGC	5664
rs183214129	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871783	TTGGAGTCTCGGGAT[A/G]AGCTGCTTCAGGTGT	5664
rs183504909	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226888342	CACAGGGGAGTGGAA[G/T]TGGGGCTGCATGGTG	5664
rs183557498	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871580	ATGGAGAACCTGAGA[C/G]CATTCCATAGAGACG	5664
rs183708912	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876679	CAGATGATCAGGTTC[A/G]TAAAGTTTTATGTTC	5664
rs183725807	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226880480	CCAGGGTGTGAAGCT[C/T]AGCCCTGAGGGTCTC	5664
rs184098505	snp	C/T	0.0023933	0.0345097	intron-variant	PSEN2	GRCh38.p7	1:226878006	CTACCCTCCCCAGCA[C/T]AACTATCACAGATGT	5664
rs184252827	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890930	AAGCACATTCCAGGC[A/G]CATTCCGAGGATGAG	5664
rs184316899	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885254	GAGCCTTTAATCCCT[A/G]TGGGGGTGGGGAAAG	5664
rs184551016	snp	C/T	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226878730	ACAGAGGGAGGAGAT[C/T]GTAGCTTCCCTGTTC	5664
rs184853804	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226893660	TCTGTGATTCAGACT[G/T]CATACTAAATTGTAC	5664
rs184944359	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226873296	TTGTTCATCTTTGTG[A/G]AAATTCTAGAACGGG	5664
rs185076251	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226882929	CTCTCTGCAGAGAAC[C/T]GGTACTGAAGCAACT	5664
rs185211228	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226872557	TCCACTACTGCTGGG[A/C]AAGTTTTGTGGAGTC	5664
rs185246186	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869549	ATAAAAATGGGCTCT[C/T]AAACAAATACATGTA	5664
rs185271841	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876694	GTAAAGTTTTATGTT[C/T]GGTTAAATTTAACAG	5664
rs185312343	snp	C/T	0.00716266	0.059414	intron-variant	PSEN2	GRCh38.p7	1:226887210	TCCTTGGAGGTTCCA[C/T]GATACAGGCAGATGG	5664
rs185380274	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226894547	CCCTCCTCCATGCCA[C/T]TGGGACACCACAGGG	5664
rs185396731	snp	C/G/T	0.00398564	0.0444627	intron-variant	PSEN2	GRCh38.p7	1:226881636	AGCTGCCCTGACTTT[C/G/T]GTGGCTATGCGTTTT	5664
rs185399819	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226873542	TGCCTCAGCCTCCTG[A/G]GTAGCTGGGATTACA	5664
rs185868258	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226895132	CATCCCATGTGACCA[C/T]TCCAGCCAGACAGGG	5664
rs185921179	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226882238	TAGGACTGCGCATTC[A/G]CAGCCAGAGATGGAC	5664
rs186006379	snp	C/T	0.00636936	0.0560724	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869923	ATGGGGTTTTTCTTT[C/T]GGAATGAGGAAAATG	5664
rs186151996	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226887838	AACCAGTAGAGATGG[A/G]GGGAGACCGCAAGGC	5664
rs186288674	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895711	TACGTGTTTACTTGG[C/T]GAGGAGGAGGCAGAA	5664
rs186308126	snp	C/T	0.0310518	0.120672	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870599	GGCGCCGGGTCCGGC[C/T]GGGCGCTCAGCCAGC	5664
rs186618435	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872034	TTGGTGTTGAAGTGC[C/T]CATGTGCCAAGTCTT	5664
rs186767369	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226877439	CTAAGGGCTCAGCAG[A/G]TGCTGGTCCATCTCC	5664
rs186817723	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871623	CTTAACTCAGAAGCG[A/G]CAGCCTGGGGTTGCC	5664
rs186956454	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226874925	AAAATAAATGTGTTT[C/T]TGGAGCCTACTCCAG	5664
rs187104600	snp	A/G			downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896320	AGCCCTGAGCTGTAA[A/G]GCTGTGGATGCTGAG	5664
rs187488467	snp	A/G	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226888718	AGGACAGTGAAGGTC[A/G]GGGAAGGAAATGTTA	5664
rs187630675	snp	C/T	0.00279162	0.0372561	intron-variant	PSEN2	GRCh38.p7	1:226884663	TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGAC	5664
rs187632263	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872229	CCAAGGGGGGTTTGC[C/T]TCTTGCCTACTTTGG	5664
rs187866408	snp	A/G	0	0	intron-variant, splice-acceptor-variant	PSEN2	GRCh38.p7	1:226890655	CCCCATTTTGTGACA[A/G]GCACTGTGCTAGGCA	5664
rs187967479	snp	A/G	0.00993419	0.0697739	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891164	TGAGCAGATACCTGC[A/G]GGATGGAGGGTCCTG	5664
rs188294998	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226885285	CAGCAGGGAGGTCAT[A/C]TAGCCCTCGTCCTCA	5664
rs188463784	snp	C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226880803	AGGCTTCCCTCCTGT[C/T]CCCTTGGCCTTGGCC	5664
rs188476312	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870086	TACTCAGACAACGCC[A/G]AATTATTGACAATCT	5664
rs188572962	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226879911	TGATGGAGGTGAGCA[A/G]AGGCAGTCTCTGCCT	5664
rs188598190	snp	A/G	0.000365606	0.0135155	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883729	GAGAACGAGGAGGAC[A/G]GTGAGGAGGACCCTG	5664
rs188629369	snp	C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226878047	CTGCTCACAGAACTG[C/T]TTTCCAGGGATTGTC	5664
rs188721291	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226873376	CTTACTGGACTCTTT[G/T]TAAAATAAAAGTAAT	5664
rs189129471	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226887002	GGGTTTGAACATTGC[C/T]GCTGGGAGGTTGGCA	5664
rs189333497	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226873858	GAATTTTCCTTTTAT[G/T]GAGTACTCATGGAAA	5664
rs189353108	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868705	CACCAAATGCACAAA[C/T]AACAAAAGAAAAAAC	5664
rs189372290	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226893862	GGCAGCTGTCCATGT[C/T]CCCAGTCCACATCTT	5664
rs189438491	snp	A/G	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226894733	AGGAGCGTCTGAGCC[A/G]TGCGCTTGGCATCTG	5664
rs189614935	snp	C/T	0.00398564	0.0444627	intron-variant	PSEN2	GRCh38.p7	1:226895326	CGTTATCCGACTGGT[C/T]CTCGAACAAGCTCCT	5664
rs189698229	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869754	CCTGAGGATGAACCT[C/T]GAAAACATGCTAAGT	5664
rs190032978	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226882424	TTTTGGCAGATGGCC[A/G]GACATGGTAAGTGTG	5664
rs190108721	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226872842	TTCCACTGGGCTCCA[A/G]TCCTGGAGATGGGAT	5664
rs190183646	snp	C/T	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226876794	GTAGCATTTCAGGAT[C/T]GAAAGGTATGCTGTG	5664
rs190242286	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226886005	CAAGTAGCTAGGACT[A/G]CAGGTTTGCACCACC	5664
rs190477948	snp	G/T	1.64754e-05	0.00287009	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888904	GAACTTCGGGGCAGT[G/T]GGCATGGTGTGCATC	5664
rs190645105	snp	A/C	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226881672	CTGGGATGTGAGTCA[A/C]CTCAGGCCAGCCCCA	5664
rs190951446	snp	C/T	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226883056	CAAATTCTTACAGAT[C/T]GGTTTGTGCTAGTGT	5664
rs191052430	snp	A/C	0.00517822	0.0506191	utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871314	TTTGGAGCTGAAGGA[A/C]CCTGAGACAGAAGCT	5664
rs191081231	snp	C/G	0.00597247	0.0543191	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896542	GCCTTCTCTGTACAT[C/G]AATCATGGGTTGCAA	5664
rs191115973	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226896045	GTTACGGCAGTCACA[C/T]TGCTGGGAAGTGGCT	5664
rs191119504	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872083	TGTGGGGAGTGAGTG[A/G]CTTGTTCCTGTCTAT	5664
rs191334283	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871777	CGGTAATTGGAGTCT[C/T]GGGATAAGCTGCTTC	5664
rs191440796	snp	A/C	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226887757	CAGAGACTTTGCTAG[A/C]CTTGGTTCCAGAGCC	5664
rs191744468	snp	A/G	0.00279162	0.0372561	intron-variant	PSEN2	GRCh38.p7	1:226875786	ACTGCTGACACAAGC[A/G]CGGCTGGGGAGATTC	5664
rs191770060	snp	A/G	0.00597247	0.0543191	intron-variant	PSEN2	GRCh38.p7	1:226884787	GGTGTGGTGGTACAT[A/G]CCTGTAGTCTCAGCT	5664
rs191835728	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226880127	ACTCTGTAATACCAG[C/T]GCTTTGGGAGGCTGA	5664
rs191900958	snp	A/T			intron-variant	PSEN2	GRCh38.p7	1:226894291	GCTTGAGACCAAGGC[A/T]CACAGGAGGTGTGCT	5664
rs191914317	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226887938	TTCTGTGCCCTCTTT[A/G]TCTGTAAGGTGGCCA	5664
rs192142511	snp	A/G	0.000909246	0.0213025	intron-variant	PSEN2	GRCh38.p7	1:226885507	GGAGCAGTCAGGGCC[A/G]GGAGCATCAGCCCTT	5664
rs192389510	snp	A/G	0.0023933	0.0345097	intron-variant	PSEN2	GRCh38.p7	1:226884161	TAATGGGTTGATAAC[A/G]CAGTTACTGGGAGAA	5664
rs192472758	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226893553	TAATTCCCAGTTATA[G/T]TTACCTGTTGTAAGG	5664
rs192550908	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872260	CCTTTCTCTGTTATC[A/G]ATGTTAATAATGACA	5664
rs192827066	snp	A/C	0.0158469	0.0875917	intron-variant	PSEN2	GRCh38.p7	1:226878241	CCTGCCACCATGTCC[A/C]GCTAATTTTTGTATT	5664
rs192912133	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226872920	CTGTGGCTCATGTCT[A/G]TAATCCCAGCACTTT	5664
rs192939593	snp	A/G	0.00199481	0.0315187	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890798	TTCTGGAGCTCTGGC[A/G]TCTGCAAGGTGGCCT	5664
rs193234598	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226877922	TGACGACAGTGGTCA[C/T]CAGGTCACTGTCTAG	5664
rs199532840	snp	C/T			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871333	GAGACAGAAGCTAGT[C/T]CCCCCTCTGAATTTT	5664
rs199538648	snp	C/G/T	5.21502e-05	0.00510616	intron-variant	PSEN2	GRCh38.p7	1:226880695	GTTTGAAGTTCTTCC[C/G/T]AGCCCAGAAACCTGC	5664
rs199538967	snp	A/C/T	0.000217209	0.0104191	intron-variant	PSEN2	GRCh38.p7	1:226885489	CAAGGTGGGGAGCCT[A/C/T]GAGGAGCAGTCAGGG	5664
rs199547508	snp	A/G	3.64784e-05	0.00427058	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895540	CAACCTGGTGCGGCC[A/G]TTCATGGACACCCTG	5664
rs199550349	snp	C/G			missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894086	CACGGGCAGCGGGGA[C/G]TGGAATACCACGCTG	5664
rs199571588	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895784	CCCGCTTTGGGGAGC[A/G]CCTCGCTTCACGGAC	5664
rs199573390	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226889985	AGGGCAGGCTCTTCT[G/T]CAGGGGGCTGCCCGG	5664
rs199579988	snp	A/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226896033	AGTCCTGTTCTTGTT[A/T]CGGCAGTCACACTGC	5664
rs199587016	snp	C/T	0.000876655	0.0209179	synonymous-codon, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891345	TGCCCTCCAGCTCCC[C/T]TACGACCCGGAGATG	5664
rs199632838	snp	C/T			utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875432	GACCATAGAAAGTGA[C/T]GTGTTAAAAACCAGC	5664
rs199636705	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226880545	ACTCAGCCTCTGGAC[A/G]GACAGCGATCACTCA	5664
rs199644116	snp	C/T	6.59424e-05	0.00574168	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881956	GAAGTGTGTGATGAG[C/T]GGACGTCCCTAATGT	5664
rs199645229	snp	A/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895863	GCGGGGAGAAGAGCA[A/T]CCGGCATGAGGGCTG	5664
rs199652777	snp	C/T	0.000923904	0.0214732	intron-variant	PSEN2	GRCh38.p7	1:226883678	GTGGGGGACATTCTG[C/T]GGCCCTCACGATGTG	5664
rs199654606	snp	C/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885636	GCGTCATCGTGGTTA[C/T]GACCATCTTCTTGGT	5664
rs199658654	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226881843	TCCTCCACTGCCTTT[G/T]TCTCACAGGAAAGTG	5664
rs199676786	snp	A/C	1.7585e-05	0.00296517	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895526	TACTTCTCCACGGAC[A/C]ACCTGGTGCGGCCGT	5664
rs199689738	snp	A/T	0.000197664	0.00993947	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890124	ATATTCCCTGCCCTG[A/T]TATACTCATGTGAGT	5664
rs199696668	snp	A/G			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871364	ACTGATGAAGAAACT[A/G]AGGCCACAGAGCTAA	5664
rs199699508	snp	A/T			intron-variant	PSEN2	GRCh38.p7	1:226883689	TCTGCGGCCCTCACG[A/T]TGTGGTTTCCCACAG	5664
rs199707432	snp	A/G	1.64743e-05	0.00287	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890040	GTCTTCCTAGATCTC[A/G]TGGCTGTGCTGTGTC	5664
rs199714082	snp	C/T	0.000115912	0.00761201	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894064	TGCTGGTGGGCAAGG[C/T]GGCTGCCACGGGCAG	5664
rs199732302	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226880570	CACTCAGCCTCTGGA[C/G]AGCGATCACTCAGCC	5664
rs199739625	snp	C/G			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881911	AGAGGCAGGGCTATG[C/G]TCACATTCATGGCCT	5664
rs199754073	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226890013	CGGGGATAGTTTGAC[A/G]AGGATGTCTCTGTCT	5664
rs199760083	snp	A/C/T	0.000181219	0.00951728	missense, synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888895	GACTGTCTGGAACTT[A/C/T]GGGGCAGTGGGCATG	5664
rs199762553	snp	A/G			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871313	TTTTGGAGCTGAAGG[A/G]ACCTGAGACAGAAGC	5664
rs199767316	snp	C/T	0.000140366	0.00837634	intron-variant	PSEN2	GRCh38.p7	1:226882087	GCCTTCAAACAGGTC[C/T]CTGCGGCTACTGTAC	5664
rs199791100	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895796	AGCGCCTCGCTTCAC[A/G]GACAGGAAGCACAGC	5664
rs199796978	snp	A/G			missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895484	CTGCCCGCCCTCCCC[A/G]TCTCCATCACGTTCG	5664
rs199803697	snp	C/T			utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875450	GTTAAAAACCAGCGC[C/T]GCCCTCTTTGAAAGC	5664
rs199808788	snp	C/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883891	ACCATCAAGTCTGTG[C/T]GCTTCTACACAGAGA	5664
rs199833363	snp	A/C			intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891396	AACAGCCTCTCATCA[A/C]TGGGGGGCAGCTCCC	5664
rs199844009	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226894172	GTGGTGGGGGCCCCC[A/G]GGGTCCTCATTGTGG	5664
rs199854075	snp	C/T	9.90115e-05	0.00703534	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891706	GTTGTCCCCTCCTCA[C/T]GGTGATGACGGACAT	5664
rs199859861	snp	C/T			intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871435	GCCAGGCTTCGACCC[C/T]AGTGTCCTGGCTTCT	5664
rs199862712	snp	A/T			intron-variant	PSEN2	GRCh38.p7	1:226880448	CTTTCAGCAGAGCGC[A/T]CACCTGCTATCCCTG	5664
rs199881162	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226880580	CTGGACAGCGATCAC[G/T]CAGCCTCTGGACAGC	5664
rs199881176	snp	A/G	3.29516e-05	0.00405891	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891795	CCCCGAAGTCTTTGA[A/G]CCTCCCTTGACTGGC	5664
rs199882991	snp	A/C/G	5.46128e-05	0.00522532	intron-variant	PSEN2	GRCh38.p7	1:226885517	GGGCCGGGAGCATCA[A/C/G]CCCTTTGCCTTCTCC	5664
rs199899855	in-del	-/A			intron-variant	PSEN2	GRCh38.p7	1:226886035	CATACCTGGCTAATT[-/A]AAAAATTTTTTTTTG	5664
rs199904388	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226888173	GGTAAGTGACAGATA[A/G]GCAGCAGGGTCCCTG	5664
rs199937781	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226891902	GGAGCGGAGACAGAG[A/G]GTGGAGGCTCCCTGC	5664
rs199949722	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895941	TCTGGCTGGAGAGGA[A/G]AAGCCAGTTCCCTAC	5664
rs199950587	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226890153	GTGAGCCCCCCGTGC[C/T]TCTGCCTGACTCGGG	5664
rs199963095	snp	C/T	0.000115845	0.00760981	intron-variant	PSEN2	GRCh38.p7	1:226893969	TTTCCATTCTGTGCA[C/T]GCCTCTTCAGTACGG	5664
rs199968912	snp	C/G	1.65026e-05	0.00287246	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883769	TCTGTAGTGGGGTTC[C/G]CGGGCGGCCGCCAGG	5664
rs199993849	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226888085	CGTGCAATTTCTGTT[C/G]TCTAGTTCATCCATG	5664
rs199997144	snp	C/T	0.000400997	0.0141541	intron-variant	PSEN2	GRCh38.p7	1:226885505	GAGGAGCAGTCAGGG[C/T]CGGGAGCATCAGCCC	5664
rs200016565	snp	C/T	1.65217e-05	0.00287412	utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895623	TGCAGGGAATTTTCA[C/T]TGGATGCAGTTGTAT	5664
rs200034334	snp	G/T			utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875550	GCCCCAAGTGTTCGT[G/T]GTAAGTGCAGTGACT	5664
rs200034510	snp	A/G/T	8.33007e-05	0.00645317	intron-variant	PSEN2	GRCh38.p7	1:226894144	AGTGGCTGGGGATGC[A/G/T]TCCAGCTGCCTCGTG	5664
rs200037771	snp	C/T	1.6543e-05	0.00287597	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881996	GCCCCACGCCGCGCT[C/T]CTGCCAGGAGGGCAG	5664
rs200044432	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226880595	TCAGCCTCTGGACAG[C/T]GATCACTCAGCCTCT	5664
rs200044441	snp	C/G/T			synonymous-codon, missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891765	CTCCTATGACAGTTT[C/G/T]GGGGAGCCTTCATAC	5664
rs200107519	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226880429	TGACTTACTTGGAGA[C/T]GAACTTTCAGCAGAG	5664
rs200108534	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226885727	TCTCTCCGTCTGCCC[C/T]ACACCATGGCGGCAG	5664
rs200123803	snp	A/G			upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868844	TGATAAGGGTCTAGT[A/G]TCCAGAATATATAAA	5664
rs200123982	snp	C/G	3.97614e-05	0.0044586	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891248	CACTGTTAGCACCGC[C/G]TGAGATGTGAACCTT	5664
rs200129636	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226890147	ATGTGAGTGAGCCCC[A/C]CGTGCCTCTGCCTGA	5664
rs200133314	snp	C/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888987	CGCTCATGGCCCTAG[C/T]GTTCATCAAGTACCT	5664
rs200137699	snp	A/C	0.00189636	0.030734	intron-variant	PSEN2	GRCh38.p7	1:226880621	CCTCTGGACAGCGAT[A/C]ACTCAGCCTCTGTCC	5664
rs200161165	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895899	CGCAAAGAGTGTGCT[C/T]GGGAGTGGCCCCTGG	5664
rs200164062	snp	A/G/T	6.66412e-05	0.00577208	utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895582	GCTCTACATCTGAGG[A/G/T]ACATGGTGTGCCACA	5664
rs200165480	snp	G/T			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871399	ACTTTTCCCAAGGTC[G/T]CCCAGGTACGATATA	5664
rs200169735	snp	C/G/T	3.3848e-05	0.00411376	missense, synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895498	CATCTCCATCACGTT[C/G/T]GGGCTCATCTTTTAC	5664
rs200173519	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888896	ACTGTCTGGAACTTC[A/G]GGGCAGTGGGCATGG	5664
rs200173939	snp	C/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895957	AAGCCAGTTCCCTAC[C/G]AGGAGTGTTCCCAAT	5664
rs200177715	snp	C/T	3.47349e-05	0.00416728	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891262	CCTGAGATGTGAACC[C/T]TTTCTCCTCCCCCAG	5664
rs200203079	snp	A/G			splice-acceptor-variant, intron-variant	PSEN2	GRCh38.p7	1:226894005	TGTCTCTCCTCACAC[A/G]GGGGGCGTGAAGCTT	5664
rs200210453	snp	C/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888143	TGCTGTTCCTCTTCA[C/T]CTATATCTACCTTGG	5664
rs200228068	snp	G/T	6.96791e-05	0.00590209	intron-variant	PSEN2	GRCh38.p7	1:226880634	ATAACTCAGCCTCTG[G/T]CCCCGTCTGAGATGT	5664
rs200232829	snp	A/T			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871307	GCAAGCTTTTGGAGC[A/T]GAAGGAACCTGAGAC	5664
rs200284833	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226880503	AGGGTCTCTGGACAG[C/T]GATCACTCAGCCTCT	5664
rs200296479	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895789	TTTGGGGAGCGCCTC[A/G]CTTCACGGACAGGAA	5664
rs200305467	snp	A/G			utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875433	ACCATAGAAAGTGAC[A/G]TGTTAAAAACCAGCG	5664
rs200326485	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891318	GGCGAAGCTGGACCC[C/T]TCCTCTCAGGGTGCC	5664
rs200327690	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226875348	CCTGACCTTAGCAAA[C/G]TCTTCCTTGTTTTAA	5664
rs200332829	snp	C/T	0.00016735	0.00914587	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889015	CCTCCCAGAGTGGTC[C/T]GCGTGGGTCATCCTG	5664
rs200350640	snp	C/G	6.60208e-05	0.00574509	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883842	GATCATGCTGTTTGT[C/G]CCTGTCACTCTGTGC	5664
rs200358385	snp	C/T	1.67654e-05	0.00289524	intron-variant	PSEN2	GRCh38.p7	1:226895418	CCTCCCCTCCATGTC[C/T]TGCAGGGCTTGTGTC	5664
rs200361682	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226888195	GGGTCCCTGGGAGCC[C/T]CTCTCCATGTGGCAC	5664
rs200407641	snp	A/C			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895769	CACCAGACTTTGGCT[A/C]CCGCTTTGGGGAGCG	5664
rs200409502	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226889086	TGGGGGCAGTGGGGG[C/T]GATGTCCAGGGCCAA	5664
rs200410369	snp	A/G			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888846	AAGTGCTCAAGACCT[A/G]CAATGTGGCCATGGA	5664
rs200427880	snp	C/T	1.67413e-05	0.00289316	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895472	TTCAAGAAGGCGCTG[C/T]CCGCCCTCCCCATCT	5664
rs200432520	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226893989	CTTCAGTACGGGTTA[C/G]TGTCTCTCCTCACAC	5664
rs200459699	snp	C/T	8.69089e-05	0.00659143	intron-variant	PSEN2	GRCh38.p7	1:226880671	GGACTGTCAGATTTG[C/T]CAGGCATTGTTTGAA	5664
rs200463582	snp	C/T	7.08278e-05	0.00595054	intron-variant	PSEN2	GRCh38.p7	1:226882091	TCAAACAGGTCCCTG[C/T]GGCTACTGTACCTTA	5664
rs200501733	snp	A/C/T	3.45365e-05	0.00415539	missense, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891305	GGACGGTTGGCATGG[A/C/T]GAAGCTGGACCCCTC	5664
rs200506152	snp	C/G/T	9.89114e-05	0.0070319	intron-variant	PSEN2	GRCh38.p7	1:226888049	CCTTAGAATTTGTGG[C/G/T]GCTTGGGGACACCTT	5664
rs200535276	snp	A/G			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226882037	GAGGATGGAGAGAAC[A/G]CTGCCCAGTGGGTAG	5664
rs200536369	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895993	GTCCATGATGTCCTT[A/G]TTATTTTATTGCCTT	5664
rs200555636	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226890166	GCCTCTGCCTGACTC[A/G]GGGTCAGCAGGCAGC	5664
rs200559114	snp	A/C			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895891	CTGAGATGCGCAAAG[A/C]GTGTGCTCGGGAGTG	5664
rs200565077	snp	C/T	4.95086e-05	0.00497512	intron-variant	PSEN2	GRCh38.p7	1:226881849	ACTGCCTTTGTCTCA[C/T]AGGAAAGTGGAACAA	5664
rs200568747	snp	C/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226896034	GTCCTGTTCTTGTTA[C/T]GGCAGTCACACTGCT	5664
rs200571274	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226875557	GTGTTCGTGGTAAGT[A/G]CAGTGACTCCCAACC	5664
rs200572479	snp	A/C/T	0.000490187	0.0156484	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891382	TATCTTGGGGAGCTA[A/C/T]CAGCCTCTCATCACT	5664
rs200591275	snp	A/G			utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875407	GGAGAGTGATGTGAG[A/G]GAGCTGTGTGACCAT	5664
rs200607063	snp	A/C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875489	ATCATTCATTTAGCC[A/C/T]GCTGAGAAGAAGAAA	5664
rs200610057	snp	C/T	0.000613655	0.0175057	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883899	GTCTGTGCGCTTCTA[C/T]ACAGAGAAGAATGGA	5664
rs200610385	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226896103	TCCTGTTAGAATCTT[A/G]GAGTTTGGTCCGTTG	5664
rs200615414	snp	C/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895817	GAAGCACAGCAGGTT[C/T]ATCCAGATGAACTGA	5664
rs200617488	snp	A/C/T	0.000232314	0.0107754	intron-variant	PSEN2	GRCh38.p7	1:226885718	AGCCACGCTTCTCTC[A/C/T]GTCTGCCCCACACCA	5664
rs200636353	snp	A/G	0.000943092	0.0216946	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226882007	CGCTCCTGCCAGGAG[A/G]GCAGGCAGGGCCCAG	5664
rs200641411	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895866	GGGAGAAGAGCATCC[A/G]GCATGAGGGCTGAGA	5664
rs200644982	snp	C/T			synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890045	CCTAGATCTCGTGGC[C/T]GTGCTGTGTCCCAAA	5664
rs200656386	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226880547	TCAGCCTCTGGACAG[A/C]CAGCGATCACTCAGC	5664
rs200668817	snp	C/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890131	CTGCCCTGATATACT[C/T]ATGTGAGTGAGCCCC	5664
rs200670135	snp	C/T	0.00011549	0.00759812	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888972	TCATCATGATCAGTG[C/T]GCTCATGGCCCTAGT	5664
rs200691879	snp	C/T	4.95135e-05	0.00497537	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891703	CTTGTTGTCCCCTCC[C/T]CACGGTGATGACGGA	5664
rs200694973	snp	C/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890037	TCTGTCTTCCTAGAT[C/T]TCGTGGCTGTGCTGT	5664
rs200695481	snp	C/T	0.00358779	0.0422022	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226870945	GGCCTCACTGCGTCC[C/T]CACTTCCCTGCGCCC	5664
rs200716541	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226880571	ACTCAGCCTCTGGAC[A/G]GCGATCACTCAGCCT	5664
rs200739890	snp	C/G/T	1.65127e-05	0.00287334	intron-variant	PSEN2	GRCh38.p7	1:226888798	ATGCCTCCACTGAGT[C/G/T]CCAGTCACAGGCTCC	5664
rs200745703	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895597	GACATGGTGTGCCAC[A/G]GGCTGCAAGCTGCAG	5664
rs200748438	snp	C/T	0.000228423	0.0106845	intron-variant	PSEN2	GRCh38.p7	1:226885506	AGGAGCAGTCAGGGC[C/T]GGGAGCATCAGCCCT	5664
rs200754713	snp	A/G	1.64815e-05	0.00287063	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888954	TGCTGCAGCAGGCCT[A/G]CCTCATCATGATCAG	5664
rs200801915	snp	C/T	0.000231286	0.0107513	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883863	CACTCTGTGCATGAT[C/T]GTGGTGGTAGCCACC	5664
rs200804459	snp	A/G			missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895544	CTGGTGCGGCCGTTC[A/G]TGGACACCCTGGCCT	5664
rs200819815	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226880582	GGACAGCGATCACTC[A/G]GCCTCTGGACAGCGA	5664
rs200824392	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885703	CTGGCCCTGCCCTCC[A/C]GCCACGCTTCTCTCC	5664
rs200852140	snp	G/T	0.000121449	0.00779164	intron-variant	PSEN2	GRCh38.p7	1:226894175	GTGGGGGCCCCCAGG[G/T]TCCTCATTGTGGTGG	5664
rs200853904	snp	A/G/T	3.29692e-05	0.00406001	intron-variant	PSEN2	GRCh38.p7	1:226888180	GACAGATAAGCAGCA[A/G/T]GGTCCCTGGGAGCCC	5664
rs200878942	snp	A/G	3.29723e-05	0.00406018	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881933	TCATGGCCTCTGACA[A/G]CGAGGAAGAAGTGTG	5664
rs200894274	snp	A/G	1.96254e-05	0.00313246	intron-variant	PSEN2	GRCh38.p7	1:226885490	AAGGTGGGGAGCCTC[A/G]AGGAGCAGTCAGGGC	5664
rs200918027	snp	C/T			downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896129	CGTTGTAAATGTTGA[C/T]CCCTCTCCCTGCATC	5664
rs200922381	snp	C/T	0.000104502	0.00722774	intron-variant	PSEN2	GRCh38.p7	1:226880628	ACAGCGATAACTCAG[C/T]CTCTGTCCCCGTCTG	5664
rs200923178	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895921	GGCCCCTGGCACCTG[G/T]GTGCTCTGGCTGGAG	5664
rs200924879	snp	C/T	3.32259e-05	0.00407576	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885592	CCAGCGCCTCCTCAA[C/T]TCCGTGCTGAACACC	5664
rs200931244	snp	A/C			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885668	GTGCTCTACAAGTAC[A/C]GCTGCTACAAGGTGA	5664
rs200943229	snp	A/G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895660	ACACTCTAGTGCCAT[A/G/T]TATTTTTAAGACTTT	5664
rs200954447	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875365	CTTCCTTGTTTTAAG[C/T]GAGGACGTGGGACTT	5664
rs200977587	snp	A/G	1.64898e-05	0.00287135	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891840	GCTGGAGGAAGAGGA[A/G]GAAAGTAAGGTGCCC	5664
rs200981406	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226885535	CTTTGCCTTCTCCCT[C/T]AGCATCTACACGCCA	5664
rs200982557	snp	C/T			utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875533	ATTCAGACCTCTCTG[C/T]GGCCCCAAGTGTTCG	5664
rs201018913	snp	A/G	8.24396e-05	0.00641973	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881961	GTGTGATGAGCGGAC[A/G]TCCCTAATGTCGGCT	5664
rs201032114	snp	A/G	9.92113e-05	0.00704243	intron-variant	PSEN2	GRCh38.p7	1:226893983	ACGCCTCTTCAGTAC[A/G]GGTTACTGTCTCTCC	5664
rs201055590	snp	C/G	0.000461648	0.0151859	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889043	CTGGGCGCCATCTCT[C/G]TGTATGGTAGGTGGG	5664
rs201092952	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226880504	GGGTCTCTGGACAGC[A/G]ATCACTCAGCCTCTG	5664
rs201093218	snp	C/T	0.000148472	0.00861475	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894026	CGTGAAGCTTGGCCT[C/T]GGGGACTTCATCTTC	5664
rs201102002	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226880432	CTTACTTGGAGACGA[A/G]CTTTCAGCAGAGCGC	5664
rs201106517	snp	A/G/T			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871276	GGCATTTCCAGCAGT[A/G/T]AGGAGACAGCCAGAA	5664
rs201108785	snp	A/G			intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871407	CAAGGTCGCCCAGGT[A/G]CGATATAGCAGAGCC	5664
rs201111506	snp	C/T			utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875514	AAGAAACCAAGTGTC[C/T]GGGATTCAGACCTCT	5664
rs201114015	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895955	AAAAGCCAGTTCCCT[A/G]CGAGGAGTGTTCCCA	5664
rs201117237	snp	C/T	2.01517e-05	0.00317419	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891245	AGCCACTGTTAGCAC[C/T]GCCTGAGATGTGAAC	5664
rs201119121	snp	C/T	0.000216611	0.0104047	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883911	CTACACAGAGAAGAA[C/T]GGACAGCTGTGAGTT	5664
rs201146430	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871217	GCCGCAGGCTCAAGC[C/T]TAGAGCCGGTTTCTG	5664
rs201163703	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895721	CTTGGTGAGGAGGAG[A/G]CAGAACCAGCTCTTT	5664
rs201177570	snp	G/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226896058	CACTGCTGGGAAGTG[G/T]CTTAATAGTAATATC	5664
rs201191318	snp	C/G/T	0.000165112	0.00908477	intron-variant	PSEN2	GRCh38.p7	1:226893997	CGGGTTACTGTCTCT[C/G/T]CTCACACAGGGGGCG	5664
rs201196514	snp	C/T	3.31214e-05	0.00406935	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885610	CGTGCTGAACACCCT[C/T]ATCATGATCAGCGTC	5664
rs201216228	snp	C/T			intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871441	CTTCGACCCCAGTGT[C/T]CTGGCTTCTAGATCT	5664
rs201261403	snp	C/T			synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883746	TGAGGAGGACCCTGA[C/T]CGCTATGTCTGTAGT	5664
rs201272715	snp	C/T			synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883755	CCCTGACCGCTATGT[C/T]TGTAGTGGGGTTCCC	5664
rs201292728	snp	A/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889025	TGGTCCGCGTGGGTC[A/T]TCCTGGGCGCCATCT	5664
rs201300501	snp	A/G			utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875439	GAAAGTGACGTGTTA[A/G]AAACCAGCGCTGCCC	5664
rs201316014	snp	C/T			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871391	CTAAAGTGACTTTTC[C/T]CAAGGTCGCCCAGGT	5664
rs201375480	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226880460	CGCACACCTGCTATC[C/G]CTGCCCAGGGTGTGA	5664
rs201378322	snp	C/T	0.000226144	0.0106311	intron-variant	PSEN2	GRCh38.p7	1:226880638	CTCAGCCTCTGTCCC[C/T]GTCTGAGATGTTGGC	5664
rs201390077	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226880551	CCTCTGGACAGACAG[C/T]GATCACTCAGCCTCT	5664
rs201399057	snp	A/G	0.000276358	0.0117517	utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895599	CATGGTGTGCCACAG[A/G]CTGCAAGCTGCAGGG	5664
rs201403206	snp	C/G/T	0.00010067	0.00709408	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889017	TCCCAGAGTGGTCCG[C/G/T]GTGGGTCATCCTGGG	5664
rs201403983	snp	A/G	0.00144171	0.02681	intron-variant	PSEN2	GRCh38.p7	1:226880677	TCAGATTTGCCAGGC[A/G]TTGTTTGAAGTTCTT	5664
rs201407396	snp	C/T	9.4771e-05	0.00688306	intron-variant	PSEN2	GRCh38.p7	1:226883662	ACATGGATAGGCTGC[C/T]GTGGGGGACATTCTG	5664
rs201424233	snp	C/T	1.88852e-05	0.00307282	synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895549	GCGGCCGTTCATGGA[C/T]ACCCTGGCCTCCCAT	5664
rs201488196	snp	C/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895795	GAGCGCCTCGCTTCA[C/T]GGACAGGAAGCACAG	5664
rs201494032	snp	C/T			utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875422	GGAGCTGTGTGACCA[C/T]AGAAAGTGACGTGTT	5664
rs201494033	snp	A/G			missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895475	AAGAAGGCGCTGCCC[A/G]CCCTCCCCATCTCCA	5664
rs201497323	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226880539	GCGATCACTCAGCCT[C/T]TGGACAGACAGCGAT	5664
rs201510179	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895971	CGAGGAGTGTTCCCA[A/G]TGCTTTGTCCATGAT	5664
rs201515227	snp	C/T			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871315	TTGGAGCTGAAGGAA[C/T]CTGAGACAGAAGCTA	5664
rs201552337	snp	A/G			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871360	TTTTACTGATGAAGA[A/G]ACTGAGGCCACAGAG	5664
rs201559102	snp	A/C/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895772	CAGACTTTGGCTCCC[A/C/G]CTTTGGGGAGCGCCT	5664
rs201559176	snp	A/G			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871310	AGCTTTTGGAGCTGA[A/G]GGAACCTGAGACAGA	5664
rs201563279	snp	A/G	1.72991e-05	0.00294096	intron-variant	PSEN2	GRCh38.p7	1:226882079	AGCTGGGGGCCTTCA[A/G]ACAGGTCCCTGCGGC	5664
rs201563376	snp	A/C/G	9.06875e-05	0.00673328	intron-variant	PSEN2	GRCh38.p7	1:226889087	GGGGGCAGTGGGGGC[A/C/G]ATGTCCAGGGCCAAA	5664
rs201590095	snp	A/T	3.31439e-05	0.00407073	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885605	AACTCCGTGCTGAAC[A/T]CCCTCATCATGATCA	5664
rs201591394	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226875559	GTTCGTGGTAAGTGC[A/G]GTGACTCCCAACCTG	5664
rs201603449	snp	G/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226896020	CCTTTAGAAACTGAG[G/T]CCTGTTCTTGTTACG	5664
rs201605500	snp	A/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895869	AGAAGAGCATCCGGC[A/T]TGAGGGCTGAGATGC	5664
rs201606093	snp	C/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890051	TCTCGTGGCTGTGCT[C/G]TGTCCCAAAGGGCCT	5664
rs201613477	snp	C/T	3.31576e-05	0.00407157	intron-variant	PSEN2	GRCh38.p7	1:226885700	GCCCTGGCCCTGCCC[C/T]CCAGCCACGCTTCTC	5664
rs201663855	snp	C/T	0.000230886	0.010742	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891715	TCCTCACGGTGATGA[C/T]GGACATCTTCTCTTC	5664
rs201666805	snp	C/T	0.000153988	0.00877328	intron-variant	PSEN2	GRCh38.p7	1:226889998	CTTCAGGGGGCTGCC[C/T]GGGGATAGTTTGACA	5664
rs201671829	snp	G/T			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888893	CTGACTGTCTGGAAC[G/T]TCGGGGCAGTGGGCA	5664
rs201672346	snp	A/C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226880525	TCAGCCTCTGGACAG[A/C/T]GATCACTCAGCCTCT	5664
rs201683508	snp	A/G	0.000199008	0.00997319	intron-variant	PSEN2	GRCh38.p7	1:226894136	TCATTGTGAGTGGCT[A/G]GGGATGCGTCCAGCT	5664
rs201692678	snp	C/T			synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881934	CATGGCCTCTGACAG[C/T]GAGGAAGAAGTGTGT	5664
rs201698728	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226877227	CAACCATCCCGAATG[A/C]GGATCCCTGACACTG	5664
rs201704349	in-del	-/AG			intron-variant, splice-acceptor-variant	PSEN2	GRCh38.p7	1:226891059	TGGTTCTTATGCTTT[-/AG]AGGAGGGGAGACAAA	5664
rs201715744	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226880573	TCAGCCTCTGGACAG[C/T]GATCACTCAGCCTCT	5664
rs201772526	snp	C/G			synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894083	TGCCACGGGCAGCGG[C/G]GACTGGAATACCACG	5664
rs201773209	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895892	TGAGATGCGCAAAGA[A/G]TGTGCTCGGGAGTGG	5664
rs201778576	snp	A/G			missense, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891338	CTCAGGGTGCCCTCC[A/G]GCTCCCCTACGACCC	5664
rs201788938	snp	C/T	0.000243762	0.0110373	intron-variant	PSEN2	GRCh38.p7	1:226880629	CAGCGATAACTCAGC[C/T]TCTGTCCCCGTCTGA	5664
rs201802891	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226895386	CTCCTGTCCACACCA[G/T]GGATCACCACGCTCA	5664
rs201806443	snp	C/G	3.29946e-05	0.00406155	intron-variant	PSEN2	GRCh38.p7	1:226881862	CACAGGAAAGTGGAA[C/G]AAGGTCCTTGTGCTC	5664
rs201810625	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226888190	CAGCAGGGTCCCTGG[G/T]AGCCCCTCTCCATGT	5664
rs201820913	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875534	TTCAGACCTCTCTGC[A/G]GCCCCAAGTGTTCGT	5664
rs201827429	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226880592	CACTCAGCCTCTGGA[C/G]AGCGATCACTCAGCC	5664
rs201891584	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226893998	GGGTTACTGTCTCTC[C/T]TCACACAGGGGGCGT	5664
rs201892898	snp	A/G	1.65474e-05	0.00287636	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885620	ACCCTCATCATGATC[A/G]GCGTCATCGTGGTTA	5664
rs201896763	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888129	GTCTTCACTGATGCT[A/G]CTGTTCCTCTTCACC	5664
rs201908554	snp	A/G			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888959	CAGCAGGCCTACCTC[A/G]TCATGATCAGTGCGC	5664
rs201914773	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896114	TCTTGGAGTTTGGTC[C/T]GTTGTAAATGTTGAC	5664
rs201917728	snp	A/G			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891787	CCTTCATACCCCGAA[A/G]TCTTTGAGCCTCCCT	5664
rs201919671	snp	A/G	0.000115339	0.00759318	intron-variant	PSEN2	GRCh38.p7	1:226888071	GGACACCTTGTGATC[A/G]TGCAATTTCTGTTGT	5664
rs201922151	snp	A/G	9.0569e-05	0.00672877	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895536	CGGACAACCTGGTGC[A/G]GCCGTTCATGGACAC	5664
rs201944966	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871229	AGCCTAGAGCCGGTT[C/T]CTGTTAGCAGCGGTG	5664
rs201982084	snp	A/G	0.000100331	0.00708205	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895468	TGTGTTCAAGAAGGC[A/G]CTGCCCGCCCTCCCC	5664
rs201985133	snp	A/G/T	9.91726e-05	0.00704113	intron-variant	PSEN2	GRCh38.p7	1:226893985	GCCTCTTCAGTACGG[A/G/T]TTACTGTCTCTCCTC	5664
rs201999478	snp	G/T	1.64821e-05	0.00287067	intron-variant	PSEN2	GRCh38.p7	1:226890142	TACTCATGTGAGTGA[G/T]CCCCCCGTGCCTCTG	5664
rs202003390	snp	A/G	6.59957e-05	0.005744	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888973	CATCATGATCAGTGC[A/G]CTCATGGCCCTAGTG	5664
rs202005802	snp	A/G	0.00186056	0.0304437	intron-variant	PSEN2	GRCh38.p7	1:226890149	GTGAGTGAGCCCCCC[A/G]TGCCTCTGCCTGACT	5664
rs202031936	snp	A/G	1.91448e-05	0.00309387	intron-variant	PSEN2	GRCh38.p7	1:226885504	CGAGGAGCAGTCAGG[A/G]CCGGGAGCATCAGCC	5664
rs202046558	in-del	-/A			intron-variant	PSEN2	GRCh38.p7	1:226873178	TCAAAAAAAAAAAAA[-/A]TGGTTTCACATCAGT	5664
rs202060347	snp	A/G			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871279	ATTTCCAGCAGTGAG[A/G]AGACAGCCAGAAGCA	5664
rs202063466	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226882054	TGCCCAGTGGGTAGG[C/T]CCCACCAGCAGCTGG	5664
rs202067223	snp	C/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895767	ATCACCAGACTTTGG[C/T]TCCCGCTTTGGGGAG	5664
rs202069038	snp	A/C/G	5.11769e-05	0.00505829	intron-variant	PSEN2	GRCh38.p7	1:226894160	TCCAGCTGCCTCGTG[A/C/G]TGGGGGCCCCCAGGG	5664
rs202106330	snp	A/C/G	8.31433e-05	0.00644714	intron-variant	PSEN2	GRCh38.p7	1:226891883	CCTGCTTCAGCCTAC[A/C/G]GCGGGAGCGGAGACA	5664
rs202107545	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226880478	GCCCAGGGTGTGAAG[C/G]TCAGCCCTGAGGGTC	5664
rs202111966	snp	A/G	3.47862e-05	0.00417036	intron-variant	PSEN2	GRCh38.p7	1:226880639	TCAGCCTCTGTCCCC[A/G]TCTGAGATGTTGGCA	5664
rs202112948	snp	G/T	0.000244571	0.0110556	intron-variant	PSEN2	GRCh38.p7	1:226880608	AGCGATCACTCAGCC[G/T]CTGGACAGCGATAAC	5664
rs202131206	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226875340	GGGTATCACCTGACC[G/T]TAGCAAACTCTTCCT	5664
rs202133351	snp	A/C/G/T	0.00024755	0.0111231	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883768	GTCTGTAGTGGGGTT[A/C/G/T]CCGGGCGGCCGCCAG	5664
rs202142711	snp	C/T	6.68405e-05	0.00578064	intron-variant	PSEN2	GRCh38.p7	1:226891891	AGCCTACGGCGGGAG[C/T]GGAGACAGAGGGTGG	5664
rs202160009	snp	C/T			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895956	AAAGCCAGTTCCCTA[C/T]GAGGAGTGTTCCCAA	5664
rs202176021	snp	A/C			missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888832	TTGGTCCTGCAGGGA[A/C]GTGCTCAAGACCTAC	5664
rs202178096	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895930	CACCTGGGTGCTCTG[A/G]CTGGAGAGGAAAAGC	5664
rs202178897	snp	A/G/T	0.000232352	0.0107761	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226885596	CGCCTCCTCAACTCC[A/G/T]TGCTGAACACCCTCA	5664
rs202194741	snp	A/T			upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868897	AAAAGACAACCCAAT[A/T]TTAAAATGGGCAAAG	5664
rs202195827	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226880446	AACTTTCAGCAGAGC[A/G]CACACCTGCTATCCC	5664
rs202196437	snp	C/T	1.64942e-05	0.00287173	intron-variant	PSEN2	GRCh38.p7	1:226888197	GTCCCTGGGAGCCCC[C/T]CTCCATGTGGCACAA	5664
rs202197781	snp	C/T	3.33256e-05	0.00408187	intron-variant	PSEN2	GRCh38.p7	1:226894143	GAGTGGCTGGGGATG[C/T]GTCCAGCTGCCTCGT	5664
rs202210060	snp	A/G			synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889045	GGGCGCCATCTCTGT[A/G]TATGGTAGGTGGGCA	5664
rs202239448	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895673	ATATATTTTTAAGAC[C/T]TTTCTTTCCTTAAAA	5664
rs367602636	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226893318	TGGATCACACCTGGT[G/T]GGGGAAGGAGGACAG	5664
rs367645069	snp	A/G	0.000214357	0.0103505	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881973	GACGTCCCTAATGTC[A/G]GCTGAGAGCCCCACG	5664
rs367828808	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226880059	GCTGACTTGGTGGAA[G/T]GAACCTGCCTGCTTT	5664
rs367855127	snp	C/T	3.30017e-05	0.00406199	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888974	ATCATGATCAGTGCG[C/T]TCATGGCCCTAGTGT	5664
rs367875222	snp	A/C	0.00636936	0.0560724	intron-variant	PSEN2	GRCh38.p7	1:226876306	GTAGCAGAAGTCCAT[A/C]CCAGATGCTCTGTTT	5664
rs368035858	snp	G/T	1.65696e-05	0.00287828	intron-variant	PSEN2	GRCh38.p7	1:226891874	TTCACACGGCCTGCT[G/T]CAGCCTACGGCGGGA	5664
rs368082653	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226880374	CAGTGAGACCCTGTC[C/T]CTAGAAATAAAAATA	5664
rs368237778	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226872885	AATGTCTGGAGAAAA[A/G]AATGATTTCAGGCTG	5664
rs368531790	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226879687	CTAACCTTTGCAGCT[G/T]CACATCCCTCTTACT	5664
rs368659873	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226894251	CTCTGAGGGACAAGA[G/T]CAGGGAGCGGGGCTG	5664
rs368961675	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226881608	TGAATGAATGAGCAC[A/G]CTGACAGTTTGGAGC	5664
rs369062728	in-del	-/C			intron-variant	PSEN2	GRCh38.p7	1:226882677	TGTGTGGACTGTTTT[-/C]TTGCAGCCAGTCTTA	5664
rs369268719	snp	C/T	5.32912e-05	0.00516166	intron-variant	PSEN2	GRCh38.p7	1:226883687	ATTCTGCGGCCCTCA[C/T]GATGTGGTTTCCCAC	5664
rs369274454	snp	A/G	8.26721e-05	0.00642888	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894098	GGACTGGAATACCAC[A/G]CTGGCCTGCTTCGTG	5664
rs369277606	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226884734	GCCTGGGAAATGTGG[C/T]GAGACCCTGTCTGTA	5664
rs369429245	snp	G/T	1.71781e-05	0.00293066	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889032	CGTGGGTCATCCTGG[G/T]CGCCATCTCTGTGTA	5664
rs369622085	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883778	GGGTTCCCGGGCGGC[C/T]GCCAGGCCTGGAGGA	5664
rs369697148	snp	A/G	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226876695	TAAAGTTTTATGTTC[A/G]GTTAAATTTAACAGC	5664
rs369737284	in-del	-/GTGG			intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872195	CCTGTCTCCCCTCCG[-/GTGG]TAGCTGCTCACCGTC	5664
rs369833300	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226889362	GCTGACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	5664
rs369848313	snp	A/G			intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871933	GAGCCTTGGGTTCCA[A/G]GGCAGAGACTGGAGT	5664
rs370366801	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226884100	TGGATTGTGACCTAC[C/T]TGGGCATGCTTTTAA	5664
rs370380591	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226893664	TGATTCAGACTTCAT[A/G]CTAAATTGTACAGCA	5664
rs370386801	snp	C/T	0.000153988	0.00877328	intron-variant	PSEN2	GRCh38.p7	1:226890144	CTCATGTGAGTGAGC[C/T]CCCCGTGCCTCTGCC	5664
rs370607299	snp	C/G	0.000181946	0.00953624	intron-variant	PSEN2	GRCh38.p7	1:226885688	CTACAAGGTGAGGCC[C/G]TGGCCCTGCCCTCCA	5664
rs370609490	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226893669	CAGACTTCATACTAA[A/G]TTGTACAGCAGTGCC	5664
rs370626639	in-del	-/G			intron-variant	PSEN2	GRCh38.p7	1:226883975	GAGTTGCCAGGGGGT[-/G]GGGGGGCGCAGCAGC	5664
rs370677428	snp	A/G	0.00755907	0.0610114	intron-variant	PSEN2	GRCh38.p7	1:226883978	GTTGCCAGGGGGTGG[A/G]GGGCGCAGCAGCCTG	5664
rs370808347	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226887095	CAAGCTAGAAATTGC[A/G]TGGCAGATGTGAAGA	5664
rs370856356	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226892001	AAGATGCCTGCAGCG[C/T]TGGGGTCTTCTCAGC	5664
rs370999948	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226882476	GATTGACTTTTGAGC[C/T]GGGGATATTTGGGCT	5664
rs371048308	snp	C/T			intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891271	TGAACCTTTTCTCCT[C/T]CCCCAGCTGCCATGG	5664
rs371097422	snp	G/T	1.65151e-05	0.00287355	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891694	TTTCTCTCTCTTGTT[G/T]TCCCCTCCTCACGGT	5664
rs371124752	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871987	TGAAGTGGGATGGAT[A/G]TATCAGGTTTTTGGG	5664
rs371315050	snp	A/C	1.66793e-05	0.0028878	missense, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895452	CCCTCCTGCTGCTTG[A/C]TGTGTTCAAGAAGGC	5664
rs371475270	snp	A/G	0.000248088	0.0111347	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881991	TGAGAGCCCCACGCC[A/G]CGCTCCTGCCAGGAG	5664
rs371541473	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891565	CAGCCTCTGTTGCAT[C/T]GTTCTGCTGGGCGTG	5664
rs371542146	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226892179	CCATGGGGTTGGGGA[A/G]GGGCGGCAGGAGAGC	5664
rs371562367	snp	C/G	1.65263e-05	0.00287452	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888991	CATGGCCCTAGTGTT[C/G]ATCAAGTACCTCCCA	5664
rs371574453	snp	A/C	0.0134861	0.0810011	intron-variant	PSEN2	GRCh38.p7	1:226880156	GAGGCAGGAGGATCA[A/C]TTGAGGCCAGGAGTT	5664
rs371616577	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226889098	GGGCGATGTCCAGGG[A/C]CAAATCGTCCCCAGT	5664
rs371686514	snp	C/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888158	CCTATATCTACCTTG[C/G]GTAAGTGACAGATAA	5664
rs371693894	snp	A/G	4.49661e-05	0.00474141	utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895585	CTACATCTGAGGGAC[A/G]TGGTGTGCCACAGGC	5664
rs372021951	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226873990	CTCTGTCCTCCCCAT[A/G]CCCATATGTGGGCAC	5664
rs372224790	snp	A/G	0.000153988	0.00877328	intron-variant	PSEN2	GRCh38.p7	1:226891892	GCCTACGGCGGGAGC[A/G]GAGACAGAGGGTGGA	5664
rs372253386	in-del	-/TTC	0.0023933	0.0345097	intron-variant, cds-indel, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871077	GGCGGGGGCGTTTTG[-/TTC]TTCTTCTCTCTCGCC	5664
rs372265851	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226887543	CTTTCTGAGGACCTG[C/T]TTGTAGACCTTTGGG	5664
rs372305083	snp	C/T	1.66288e-05	0.00288343	intron-variant	PSEN2	GRCh38.p7	1:226891882	GCCTGCTTCAGCCTA[C/T]GGCGGGAGCGGAGAC	5664
rs372337080	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226894960	TGCCTGCATCAGCTG[C/G]GTCAGGGGAGGATGG	5664
rs372616074	snp	C/G	5.22944e-05	0.00511317	intron-variant	PSEN2	GRCh38.p7	1:226885532	GCCCTTTGCCTTCTC[C/G]CTCAGCATCTACACG	5664
rs372895655	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226884581	TTTTTGTTTCATTTC[G/T]TGTGTGTTGGTTTTT	5664
rs373001183	snp	A/T			intron-variant	PSEN2	GRCh38.p7	1:226874147	CATTTCTTGACACAT[A/T]CCTGCCCGTGGTGAA	5664
rs373007480	snp	G/T	0.00398564	0.0444627	intron-variant	PSEN2	GRCh38.p7	1:226882296	ACTCTGCCACCTTGG[G/T]TTTACCTCTCTCATG	5664
rs373015096	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226889193	CCTCCTGAGAGAGTC[A/G]CCTTTGTAAAACAGA	5664
rs373186458	snp	C/T			intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871604	AGAGACGATTGTAGA[C/T]TAACTTAACTCAGAA	5664
rs373191922	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226885279	GGAAAGCAGCAGGGA[A/G]GTCATCTAGCCCTCG	5664
rs373254101	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885737	TGCCCCACACCATGG[C/T]GGCAGGGCCCGTGAA	5664
rs373320393	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226878551	TTGGGAGCCTAAGAA[A/G]CACAACATCCTCTGA	5664
rs373334489	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226881819	GGTCGCCTCCAGCCA[C/T]CCCCTGAGTCCTCCA	5664
rs373392465	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883864	ACTCTGTGCATGATC[A/G]TGGTGGTAGCCACCA	5664
rs373559987	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226886092	CAGGCTGGTCTCAAA[C/T]TCCTGGACTCAAGTG	5664
rs373933474	in-del	-/CTT			intron-variant	PSEN2	GRCh38.p7	1:226882978	TTCATTTGGCTTTTT[-/CTT]TAGCTGTTCACCTCA	5664
rs373934941	snp	C/T	4.94287e-05	0.00497111	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891764	ACTCCTATGACAGTT[C/T]TGGGGAGCCTTCATA	5664
rs373976810	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226876496	AAGAATTAATAGCCT[A/G]AAATAAACCCTACAG	5664
rs374055800	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890119	AGCCCATATTCCCTG[C/T]CCTGATATACTCATG	5664
rs374287861	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226881571	TTGGTGCATAATAGA[G/T]GCACCACAGATGTTT	5664
rs374399405	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226883555	TTTGTCCTCACAAAC[C/T]TTTCATATGCCCTAG	5664
rs374649333	snp	C/G/T	1.65905e-05	0.0028801	intron-variant	PSEN2	GRCh38.p7	1:226889986	GGGCAGGCTCTTCTT[C/G/T]AGGGGGCTGCCCGGG	5664
rs374667563	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226880991	GTCTTTCCCGAGACT[A/C]TCTTCTCCGGTCTTC	5664
rs374773961	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226885978	GGGCTCAAGTTCTCC[C/T]ACCCAGCCCCTCAAG	5664
rs374918606	snp	A/G	0.000153988	0.00877328	intron-variant	PSEN2	GRCh38.p7	1:226888179	TGACAGATAAGCAGC[A/G]GGGTCCCTGGGAGCC	5664
rs375011189	snp	C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226879325	GTTCCCAGAACTTCC[C/T]TGTGGCCCTGGGGCC	5664
rs375175652	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226889343	GTGTAGTGGCGCCAT[C/T]TTGGCTGACTGCAAC	5664
rs375392371	in-del	-/A			upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869465	GCAAGGCTCTGTCTC[-/A]AAAAAAAAAAAAAAA	5664
rs375424407	snp	C/T	0.000153988	0.00877328	intron-variant	PSEN2	GRCh38.p7	1:226885692	AAGGTGAGGCCCTGG[C/T]CCTGCCCTCCAGCCA	5664
rs375443581	snp	C/T	3.29571e-05	0.00405924	intron-variant	PSEN2	GRCh38.p7	1:226888059	TGTGGCGCTTGGGGA[C/T]ACCTTGTGATCGTGC	5664
rs375477273	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226877405	TAGTAGCACCTTGCT[C/G]CAGGATGTTTAGTGC	5664
rs375520284	snp	C/T	3.32973e-05	0.00408014	intron-variant	PSEN2	GRCh38.p7	1:226891885	TGCTTCAGCCTACGG[C/T]GGGAGCGGAGACAGA	5664
rs375609936	snp	C/G	3.30169e-05	0.00406293	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891699	CTCTCTTGTTGTCCC[C/G]TCCTCACGGTGATGA	5664
rs375637548	snp	A/C			intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891229	CCCAGGCCCTGCAGG[A/C]AGCCACTGTTAGCAC	5664
rs376039945	snp	A/G			upstream-variant-2KB, nc-transcript-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870420	GCCTCCACTCCTTCT[A/G]AGGTCGTCGCTTAGT	5664
rs376477022	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226879985	ATCCAGGCCATAGCC[A/G]GGGTTGCTGTCTTCA	5664
rs376667461	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226893273	ACTCAGGACCAGCCA[A/G]ATGAAGAGACAGTGA	5664
rs376697912	snp	C/T	3.37707e-05	0.00410904	intron-variant	PSEN2	GRCh38.p7	1:226895396	CACCAGGGATCACCA[C/T]GCTCACCCTCCCCTC	5664
rs376711351	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226885018	ATGGAGAGAATGCAG[C/T]CAGCGGTTTGTTTGC	5664
rs376721586	snp	A/G	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226880000	GGGGTTGCTGTCTTC[A/G]GAAAGAAGGGCAGCC	5664
rs376948097	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226874597	GATCCGTAACTTTCC[A/C]AGAGGCACATCCATA	5664
rs377096583	snp	A/C/G/T	8.62325e-05	0.00656585	intron-variant	PSEN2	GRCh38.p7	1:226883935	GTGAGTTGGGGGGCT[A/C/G/T]GGGGGAGCAGGGTGG	5664
rs377258087	snp	C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226873799	ATAGAGGGAGGGAAC[C/T]GTAGGTGAAGTTTGT	5664
rs377315285	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226879019	ACCTTACAGTTTTTT[C/G]TCTTCAATTTCTTTT	5664
rs377406802	snp	A/T	1.65203e-05	0.002874	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891692	TGTTTCTCTCTCTTG[A/T]TGTCCCCTCCTCACG	5664
rs377489312	snp	A/G	4.96792e-05	0.00498368	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894065	GCTGGTGGGCAAGGC[A/G]GCTGCCACGGGCAGC	5664
rs377494557	snp	A/G	4.95929e-05	0.00497936	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894074	CAAGGCGGCTGCCAC[A/G]GGCAGCGGGGACTGG	5664
rs377628773	snp	A/C	0.00676609	0.0577691	intron-variant	PSEN2	GRCh38.p7	1:226893866	GCTGTCCATGTCCCC[A/C]GTCCACATCTTAGCT	5664
rs386639920	multinucleotide-polymorphism	CC/GA			intron-variant	PSEN2	GRCh38.p7	1:226892786	CCCTCCAGACACCAG[CC/GA]ACAAGCTCTAGAGGG	5664
rs397803056	in-del	-/AAG			intron-variant	PSEN2	GRCh38.p7	1:226885971	CCTCCTGGGCTCAAG[-/AAG]TTCTCCCACCCAGCC	5664
rs527316021	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226894259	GACAAGAGCAGGGAG[C/T]GGGGCTGGAAGGGTC	5664
rs527645461	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871969	CTTGGGGGCATGTTG[C/T]TTTGAAGTGGGATGG	5664
rs527809286	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871487	GAGCAGACCTCACCC[C/T]TGTTTATTGCCTTAA	5664
rs527859263	snp	C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226879032	TTCTCTTCAATTTCT[C/T]TTATTTATTTATTTA	5664
rs528028837	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226882132	CCAGACATTCATTCC[C/G]TGATGCGGGAGGGAG	5664
rs528042597	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226874676	TATAACTACGACTTA[C/T]TGAACATCTACTGTG	5664
rs528056595	snp	A/T	0.0111196	0.0737302	intron-variant	PSEN2	GRCh38.p7	1:226873016	AACCCCATCTTTACT[A/T]AAAATACAAAATTAG	5664
rs528220024	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226881000	GAGACTCTCTTCTCC[A/G]GTCTTCCCTGTCTTA	5664
rs528577540	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226887318	CTGTGTGTGCAGCAG[A/G]GCCGTGGAGGCTGCT	5664
rs528617607	snp	C/T			intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890946	CATTCCGAGGATGAG[C/T]GGAGACCATGTATGG	5664
rs528769020	in-del	-/T			intron-variant	PSEN2	GRCh38.p7	1:226884539	CACCTTCTGTAAACT[-/T]TTTTTTTTTTTTTTT	5664
rs528853091	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869195	ACTGAAGGCTGGGCA[C/T]GGTGGCTCATGCCTA	5664
rs528980926	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226874731	CTAGGTTTTACGATA[A/G]TCTTGCAAGGTATGC	5664
rs529007601	snp	C/T			intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891511	GCCGGACACATGCGG[C/T]TTGAAGATTCAGCAA	5664
rs529020153	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868586	AATTATCTTAAAATG[A/G]ATCAACAACCTAAAT	5664
rs529065814	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868628	AACTATAAAACTCTT[A/T]GAAGAAAACACAGGA	5664
rs529129866	snp	C/G	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226893685	TTGTACAGCAGTGCC[C/G]AGCCCAAGGCCTTGC	5664
rs529146535	snp	C/T	0	0	intron-variant	PSEN2	GRCh38.p7	1:226887504	TTCACTCTCCCATCC[C/T]TGGCCAGGAGAAGAG	5664
rs529213252	snp	A/G			intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871472	GCTGTCCATCCCTCC[A/G]AGCAGACCTCACCCC	5664
rs529315020	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876105	CCCCACCCCCACCTG[C/T]CCGTGAGTCAGCCTC	5664
rs529330961	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226883133	CCCACCTTCCCAGAG[A/C]CTGCGTCTTCTCAGA	5664
rs529406499	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871335	GACAGAAGCTAGTCC[C/T]CCCTCTGAATTTTAC	5664
rs529561202	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226870714	GGCGCTGAGGGCCCG[A/G]GGTGGGGCTGCGCCC	5664
rs529574118	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876629	GTTTTGTAATATTTC[C/T]GATCTTTTATATACA	5664
rs529740499	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226878703	CACAGGAGCTTAAGA[A/G]GCATGGGAAGAACAG	5664
rs529798877	snp	C/T	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226885013	AAAGCATGGAGAGAA[C/T]GCAGCCAGCGGTTTG	5664
rs529839710	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226878349	ACAGGCATGAGCACC[A/G]CACCCAGCCCCAGGG	5664
rs529925218	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226879308	TTGTATGGATTTTGC[C/T]GGTTCCCAGAACTTC	5664
rs529960232	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226873193	AAAAAAAAAAAAATG[A/G]TTTCACATCAGTCCT	5664
rs530065304	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891786	GCCTTCATACCCCGA[A/G]GTCTTTGAGCCTCCC	5664
rs530187457	in-del	-/TG			intron-variant	PSEN2	GRCh38.p7	1:226882496	ATATTTGGGCTTCAC[-/TG]TGATCATTCAGCCCC	5664
rs530272850	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226881261	GGTGATGTGTGTCTC[C/T]TTAACATGGTGCCTG	5664
rs530300727	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885203	GTGTGGGTGGGTGGG[A/G]GAATGAGAACTGGAT	5664
rs530383300	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226880271	AGCCCTAGCTACTGA[A/G]GAGGCTGAAGTGGGA	5664
rs530641432	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885889	ATTTTCTTTTTCTTG[A/G]AACATGGTCTCACTC	5664
rs530650914	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226879452	TGGTCAGAAAGCTTC[A/G]GGGGCTCTCCTCTGC	5664
rs530684931	snp	C/T			intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891128	GGACCCCTCCCACAA[C/T]GGCCTCCTAACAATG	5664
rs530708486	snp	C/G	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226874007	CCATATGTGGGCACT[C/G]CCCACCATGGAGCCA	5664
rs530979472	snp	A/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226892808	CTCTAGAGGGTCTAG[A/T]TGCCACTTGTGCTTC	5664
rs531094539	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226881330	GGCCCTCACTGGAAC[A/G]TTGTGCCTTCTGCCC	5664
rs531130450	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226881883	CCTTGTGCTCCTTTT[C/T]CCAGGTGCTTCCAGA	5664
rs531253119	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226895319	CTAGCGCCGTTATCC[G/T]ACTGGTCCTCGAACA	5664
rs531484658	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226889806	CCCCAGCCTGGCCAC[C/T]GCGTCTCGGGTGCAC	5664
rs531490023	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226877937	CCAGGTCACTGTCTA[G/T]ACCAGGTCACTGTCT	5664
rs531521495	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226884216	GGCTTAGAAGAGTGT[C/T]TACTGCACGTGAGTG	5664
rs531693835	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226878403	CTGAATGGAGACGTG[A/G]GAATTGTAAGGAACT	5664
rs531732284	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872465	AGCACCAGGATTTGA[A/G]CATAGCTGGCTACAC	5664
rs531824360	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872035	TGGTGTTGAAGTGCC[C/T]ATGTGCCAAGTCTTG	5664
rs531892696	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226876107	CCACCCCCACCTGCC[C/T]GTGAGTCAGCCTCCG	5664
rs532060308	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226890434	AGCCACCCCTCAGCT[C/T]TCCAGGCTCTTGAGA	5664
rs532249514	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226878030	CAGATGTCAGGGAAC[C/T]TCTGCTCACAGAACT	5664
rs532261426	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226884983	GTGTGTGGGGGATTC[A/G]GCGCAGAACAGGTGA	5664
rs532285087	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872525	AGGTTCCTGTATTCA[A/G]CTCCTACCCGTGTCT	5664
rs532288189	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226878546	GCTATTTGGGAGCCT[A/C]AGAAACACAACATCC	5664
rs532490879	snp	C/T	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226873061	ACATGCCTGTAATCC[C/T]AGCTACTCAGGAGGC	5664
rs532635035	snp	A/G	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226885964	AGCCTCAACCTCCTG[A/G]GCTCAAGTTCTCCCA	5664
rs532645922	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226874230	CCTGCCTGTGTGACC[A/G]AACCCTGGCCACTGG	5664
rs532695077	in-del	-/C	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226892083	CTGTGCTGGGTGAGG[-/C]CCAGCCCTGGTGGGA	5664
rs532697278	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891690	GTTGTTTCTCTCTCT[C/T]GTTGTCCCCTCCTCA	5664
rs533050660	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226893801	GGTTGTAAGTCACCC[A/C]GTCCACAGGTGTCCC	5664
rs533076166	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869843	AAATATAGAGACAGA[A/T]GTAGACTGGTAATTG	5664
rs533129077	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226870776	TGGCCACGGTCCCTT[C/T]CCCGGCTGTGGGTCT	5664
rs533201718	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226888376	CACATGTTTCTGTCT[C/T]GTTCCTGATTTAAAA	5664
rs533388448	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226894879	ACCACCAGACTGCCT[C/T]ACCTGAGCCCTGCTG	5664
rs533450453	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226883254	CTGCAAATTCCCAGT[A/G]TCTTAGTCACACGCA	5664
rs533539240	snp	A/G			downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896180	TTGTGCTGTGAGCCC[A/G]GGATGGAGGCAGTTT	5664
rs533545630	snp	A/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226887709	TCTATATGTCATCTA[A/T]CACCCCTCACACTGG	5664
rs533598396	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226893278	GGACCAGCCAAATGA[A/G]GAGACAGTGAAGAAG	5664
rs533813519	snp	A/C	0.000329446	0.0128302	missense, nc-transcript-variant	PSEN2	GRCh38.p7	1:226888097	GTTGTCTAGTTCATC[A/C]ATGGCTGGTTGATCA	5664
rs534025859	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876760	AGATTTTTGGTGGTC[C/T]TGTCACAGTCTCCAT	5664
rs534060807	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226882574	GAGCCACTTAGTTGT[A/G]TCCTTTCTCTCCCGA	5664
rs534201499	snp	C/T	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226894531	GAGGACCATGTTTTC[C/T]CCCTCCTCCATGCCA	5664
rs534272310	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226870982	CGCCGAGCCCCGGCT[G/T]GGGGTGGGCGCGGCG	5664
rs534434147	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226883961	GGTGGGGTGAGGGCT[A/G]AGTTGCCAGGGGGTG	5664
rs534447699	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226894950	CCTGGACCACTGCCT[A/G]CATCAGCTGGGTCAG	5664
rs534507840	snp	A/G	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226891980	GAGGCATCTCTGTGA[A/G]AGTAGAAGATGCCTG	5664
rs534511499	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226881108	GGACTCTGCCCTCAC[G/T]TGCATCCATCCTGCT	5664
rs534694170	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226873479	GGAGTGCGATGGTAT[A/G]ATCTCAGCTAACTGC	5664
rs534795975	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226881386	TCCATCAGATAGGCT[C/T]TTCTCTAGAAAACAT	5664
rs535203364	snp	C/T			intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891682	GACCAGCTGTTGTTT[C/T]TCTCTCTTGTTGTCC	5664
rs535312397	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226879003	GCTGAGCCAGAGGAG[A/G]ACCTTACAGTTTTTT	5664
rs535351856	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869368	TACTCAGGAGGCCGA[G/T]GCAAGATAATTGCTC	5664
rs535423166	snp	C/T	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226889516	TCCTGACCTTGTGAT[C/T]GGCCCGCCTCAGCCT	5664
rs535474711	snp	C/T	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226892035	CCCCATGTAGTTGTC[C/T]GGCATGTATTGAGTA	5664
rs535558431	snp	C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226874991	ACAAACCACCCTTTT[C/T]CCTGGCTGCTTCAGG	5664
rs535571429	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226868965	TGGCCAACAAACACA[C/T]GAAAAGGAGAATGCT	5664
rs535718848	snp	A/G	0.00279162	0.0372561	intron-variant	PSEN2	GRCh38.p7	1:226892561	TGAGAGGTGCCTTAC[A/G]GGAGCAGCCTGGTGA	5664
rs535755290	snp	C/T	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226886827	TGAGTACCAGCTGGG[C/T]ATTGTGGTGCACGCC	5664
rs535780590	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226872943	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	5664
rs535949101	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871742	CCTGAGCCTCCAAGG[C/T]CTTCAGCCAAGACCT	5664
rs535973879	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226878063	TTTCCAGGGATTGTC[C/T]TTTTTTTCTTTTTCT	5664
rs536042887	snp	C/T			upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869961	ACTAGACAGAGGTGG[C/T]GGTTGCACAGCATTG	5664
rs536075387	snp	A/G	0.00199481	0.0315187	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896361	GACTCAGTTGTGCAC[A/G]GTGGCACAGACACTG	5664
rs536116272	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226874662	CATTTCATCTTCTTT[A/G]TAACTACGACTTATT	5664
rs536237320	snp	G/T	0.000139266	0.00834348	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891364	GACCCGGAGATGGGT[G/T]AGTATCTTGGGGAGC	5664
rs536247389	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226876914	CGCAGTGGGCATTGT[G/T]TTGGGCCTTTTTCAG	5664
rs536317786	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890929	AAAGCACATTCCAGG[C/T]GCATTCCGAGGATGA	5664
rs536513631	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226879783	GTCCTTGTCACTACC[C/T]TCCTGGCTTTTAGCT	5664
rs536693717	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226879101	GGTCTTGAACTCCTG[G/T]GCTCAAGCGATCTGT	5664
rs536726339	snp	A/G	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226878846	TGCTGCAGATGGAAT[A/G]TTATGATTTAGCTTG	5664
rs536845657	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226891013	CTCGGGGGATTCACC[C/T]GTGAACTGTGAGGTC	5664
rs536892251	snp	A/G	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226874272	TCACAAGTGCTGACT[A/G]GGCTGAGAAGAGCTC	5664
rs537128144	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872227	CCCCAAGGGGGGTTT[A/G]CCTCTTGCCTACTTT	5664
rs537485568	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876414	TCCTGGCCAATGAGA[A/G]GGGATCTGGGAGGGG	5664
rs537527025	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226891900	CGGGAGCGGAGACAG[A/G]GGGTGGAGGCTCCCT	5664
rs537558441	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226888448	ATAGAAACCCCCCAA[A/G]ATTTACATTCTGATT	5664
rs537735641	snp	A/C/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226895330	ATCCGACTGGTCCTC[A/C/G]AACAAGCTCCTGTGC	5664
rs537764045	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226874837	GTGGTTCAAATCACA[C/T]AGGCAGGCGATCTGA	5664
rs537889666	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226895650	GTATAGTTTTACACT[A/C]TAGTGCCATATATTT	5664
rs537994260	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871597	ATTCCATAGAGACGA[C/T]TGTAGACTAACTTAA	5664
rs538086351	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226873690	CAAAATGCTGGTATT[A/G]CAAGCATAAGCCATT	5664
rs538122490	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876837	ATTCTTACTCCTTTC[A/C]GTTAAGGCCAGTGCA	5664
rs538285636	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226877436	CGGCTAAGGGCTCAG[C/T]AGGTGCTGGTCCATC	5664
rs538329197	snp	A/G	0.00438332	0.0466095	intron-variant	PSEN2	GRCh38.p7	1:226889190	ATCCCTCCTGAGAGA[A/G]TCGCCTTTGTAAAAC	5664
rs538359198	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226876898	TTTCCACACTCTCCT[C/T]CGCAGTGGGCATTGT	5664
rs538472488	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226878154	GTGCGATCTCAGCTC[A/G]CTGCAGCCTCCGCCT	5664
rs538487258	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226885079	AGTGAATTGCTTCCT[A/G]TGTCTGCTTCCTGAG	5664
rs538511268	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226884053	GCAGGGATGAAGAAC[C/T]GCCCAGGTTCATGGC	5664
rs538637821	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896284	AAGGAGTTAGGAGAG[C/T]AGGGTGGCCTGACAT	5664
rs538682723	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890878	TTGAGGATTCGAGCC[C/T]GTAGAGGAGAATCGC	5664
rs538900224	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871699	AGTAAGGAAGCCTCT[A/G]ATGCCTCTGTAGCCA	5664
rs538926736	snp	C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226885138	TCAGCGGATGGGGGT[C/T]GGGTAGTAGCAGGTG	5664
rs539061345	snp	A/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226892631	GCAAGCTAGGGAAAG[A/T]TCACTCTGCGGTGGG	5664
rs539253335	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226882925	GACTCTCTCTGCAGA[A/G]AACCGGTACTGAAGC	5664
rs539288524	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226872793	CAGCTGCGGAAAGGC[A/G]GGGGTGAGGCTGAGA	5664
rs539352597	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226878930	CCCCATTGCCAGAGT[A/G]GATAGTGAGGGAAAC	5664
rs539453707	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226893106	CCTGGCTCATTTATA[G/T]TTTTAGTAGAGACAA	5664
rs539477280	snp	C/T	0.00199481	0.0315187	intron-variant	PSEN2	GRCh38.p7	1:226886932	TGTAAGACCCTGTCT[C/T]TAAAAAAATAATAAT	5664
rs539565595	snp	C/T	0.0142736	0.0832652	intron-variant	PSEN2	GRCh38.p7	1:226886559	GGGTTGAACCCCTAA[C/T]GATGGAAAGGAAATT	5664
rs539693192	snp	G/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226882527	CCAGGGGAGGAGATT[G/T]TAACGTTAGAAAGAG	5664
rs539696910	snp	A/G	1.65436e-05	0.00287602	synonymous-codon, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226894062	TGTGCTGGTGGGCAA[A/G]GCGGCTGCCACGGGC	5664
rs539755915	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226882115	TACCTTACAGATGAA[A/C]ACCAGACATTCATTC	5664
rs539852939	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226873401	AGTAATTCATGTTTA[C/T]TCTAGAAAATTAGGG	5664
rs539899828	snp	C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226876143	AGTTCATCGCGTCAC[C/T]GGCACTCTAATGTGG	5664
rs539937828	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870311	CCGGGAGGAGGAGGG[A/G]ATGTGGACCCAAAAC	5664
rs540141552	in-del	-/GGCCC	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant	PSEN2, LOC105373119	GRCh38.p7	1:226870510	CGGGACTCCAGGTGG[-/GGCCC]CAGTGGACGAGGGAA	5664
rs540173557	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226895271	CTTAACACCTCAAGA[A/G]CTGTTGCAGGACCAG	5664
rs540263371	snp	A/G	0.0023933	0.0345097	intron-variant	PSEN2	GRCh38.p7	1:226887855	GGAGACCGCAAGGCT[A/G]TGCCGGCAGACCTGA	5664
rs540264416	snp	A/G	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226875217	CCATCCCCAAGTGGT[A/G]TGTGTTACTATATGA	5664
rs540300471	snp	G/T			intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871190	GGGCTCTGCCCGCAC[G/T]TGAGGGGCAGGGCCG	5664
rs540458381	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226870656	GCAGAGCAGGTGAGC[C/G]GGCGGTGCCGGGGGG	5664
rs540463755	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226883594	AGACTGCTCCTTATA[C/T]CTGGAAAGCAACATT	5664
rs540505114	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PSEN2, LOC105373119	GRCh38.p7	1:226869121	TGTACATTGCTGGTA[C/G]GAATATAAAATGGTT	5664
rs540572061	snp	C/G	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226887975	CCCTTCCAGCGTAGG[C/G]ATGAAGTAGCCTAAT	5664
rs540689339	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891141	AACGGCCTCCTAACA[A/G]TGGAGCATGAGCAGA	5664
rs540788825	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226875859	TCCCATTCAGCTGAT[C/T]AATGGGAATGTGCAG	5664
rs540823786	snp	A/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226879288	GATGTGAAGCTGTGC[A/T]CTATTTGTATGGATT	5664
rs540854872	snp	A/C	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226880057	TGGCTGACTTGGTGG[A/C]AGGAACCTGCCTGCT	5664
rs540860628	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226873107	GCTTGAACCCAGGAG[A/G]CGGAGGTTGCAGTGA	5664
rs540877930	snp	A/G	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226883035	ACTTGCCACAGTTCC[A/G]AAACACAAATTCTTA	5664
rs540921564	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226885402	CATGGGGATGGTGCC[C/T]GCACTCCATCAGGGC	5664
rs541000538	snp	A/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226890465	AGGGACTTTGGAGAG[A/G]GATTCTTCAGGGCAG	5664
rs541006636	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	PSEN2	GRCh38.p7	1:226896557	CAATCATGGGTTGCA[A/G]AGAGAATCTCAGAAG	5664
rs541168117	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226896048	ACGGCAGTCACACTG[C/T]TGGGAAGTGGCTTAA	5664
rs541242045	snp	C/T	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226892724	CCAACTGGTGTGCTG[C/T]AGACCAGGAGTTAGC	5664
rs541250526	in-del	-/T			intron-variant	PSEN2	GRCh38.p7	1:226878062	TTTCCAGGGATTGTC[-/T]TTTTTTTTCTTTTTC	5664
rs541495335	snp	C/G/T	0.00159617	0.0282053	intron-variant	PSEN2	GRCh38.p7	1:226885747	CATGGCGGCAGGGCC[C/G/T]GTGAAACAGCCGCCT	5664
rs541667242	snp	C/G			intron-variant	PSEN2	GRCh38.p7	1:226875286	GGTACCCAGGGCCAG[C/G]GGGAGGAAGGTGAGC	5664
rs541779300	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226891000	GAGTGTCCCAGGGCT[C/T]GGGGGATTCACCCGT	5664
rs541841648	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891586	GCTGGGCGTGGGTGG[A/G]TGGAGTGGGGGAAGC	5664
rs541845163	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226892183	GGGGTTGGGGAGGGG[C/T]GGCAGGAGAGCATGC	5664
rs541905012	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891201	CTTTCTGGGACGCAG[A/G]CTGGCCACCTCCCCC	5664
rs542016786	snp	A/G	0.000798403	0.0199641	intron-variant	PSEN2	GRCh38.p7	1:226887019	CTGGGAGGTTGGCAG[A/G]TGGTGGGAAGCAGGG	5664
rs542050023	snp	A/G	0.00119737	0.0244387	intron-variant	PSEN2	GRCh38.p7	1:226874508	GCCATAGTGCCTGGG[A/G]CTGGGCCGGGAATGG	5664
rs542079957	snp	C/G	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226892786	CCCTCCAGACACCAG[C/G]CACAAGCTCTAGAGG	5664
rs542091913	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226881807	TCCAAGTCTCCAGGT[C/T]GCCTCCAGCCACCCC	5664
rs542115191	snp	C/T	0.000399281	0.0141238	intron-variant	PSEN2	GRCh38.p7	1:226880793	TTTAGGGGGCAGGCT[C/T]CCCTCCTGTCCCCTT	5664
rs542283623	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871283	CCAGCAGTGAGGAGA[C/G]AGCCAGAAGCAAGCT	5664

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