| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs15564 | snp | A/C | 0.496842 | 0.0396107 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627854 | GGCCCGGCTTGTTTC[A/C]GACCAAGATTCCCGG | 57799 |
| rs763011 | snp | C/T | 0.43221 | 0.171171 | intron-variant | RAB40C | GRCh38.p7 | 16:623277 | AAAAGTTACCCCTCT[C/T]CAGCCTTTTAGCATT | 57799 |
| rs763012 | snp | C/T | 0.432357 | 0.171014 | intron-variant | RAB40C | GRCh38.p7 | 16:624024 | GGCCAGCATGCACGC[C/T]TTTACATGCACTGCT | 57799 |
| rs763013 | snp | C/T | 0.432357 | 0.171014 | intron-variant | RAB40C | GRCh38.p7 | 16:624029 | GCATGCACGCTTTTA[C/T]ATGCACTGCTGCTGT | 57799 |
| rs763014 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | RAB40C | GRCh38.p7 | 16:625680 | CTGTGCACACGACAG[C/T]CGGGCGTGGAGCCCA | 57799 |
| rs763015 | snp | C/G | 0.281841 | 0.247964 | intron-variant | RAB40C | GRCh38.p7 | 16:626261 | AGGGGCTCGGCCGGC[C/G]GCAGGTCAGTGACTT | 57799 |
| rs1894675 | snp | C/G | 0.326035 | 0.238157 | | | GRCh38.p7 | 16:596865 | TTGAGCCTAAGGTAG[C/G]GAGGAGGCTTCTGAG | 57799 |
| rs1984395 | snp | C/T | 0.464841 | 0.127841 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628843 | ACGACATGGCCAGCA[C/T]GCAGAAGGAGCCCTC | 57799 |
| rs2269556 | snp | A/G | 0.464629 | 0.128197 | intron-variant | RAB40C | GRCh38.p7 | 16:625215 | GACACCATGGAAGGC[A/G]CCCACCCCCCTGCTG | 57799 |
| rs2269557 | snp | C/T | 0.433463 | 0.169827 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627629 | ATCTCCTAGCGGGGA[C/T]GGGCGGGGCCGCCTG | 57799 |
| rs2384972 | snp | C/T | 0.495891 | 0.0451408 | intron-variant | RAB40C | GRCh38.p7 | 16:624424 | AGGAAGGACACCTCT[C/T]GCTGAGGGAGACCCT | 57799 |
| rs2384973 | snp | A/G | 0.256619 | 0.249912 | intron-variant | RAB40C | GRCh38.p7 | 16:603739 | gctttctgggaggag[A/G]gtggatgtgctcctg | 57799 |
| rs2384974 | snp | C/G | 0.497695 | 0.0338674 | intron-variant | RAB40C | GRCh38.p7 | 16:601279 | AATTCAGAAAGGATG[C/G]ACACTTTCAGAATGA | 57799 |
| rs2384975 | snp | A/C | 0.497695 | 0.0338674 | intron-variant | RAB40C | GRCh38.p7 | 16:601115 | ACACAAGCAGCAGGC[A/C]CATTTACTGAACGGT | 57799 |
| rs2384976 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RAB40C | GRCh38.p7 | 16:601113 | ACAAGCAGCAGGCCC[A/G]TTTACTGAACGGTGA | 57799 |
| rs2891650 | snp | C/T | 0.431473 | 0.171952 | intron-variant | RAB40C | GRCh38.p7 | 16:598547 | TGTGAGACAGAGTCT[C/T]GCTCTGTCACCAAGC | 57799 |
| rs3180836 | snp | A/C | | | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629268 | TAATTCAGCTGTGGT[A/C]CCCACGTTTTGCTGT | 57799 |
| rs3838961 | in-del | -/G | 0.439502 | 0.163061 | intron-variant | RAB40C | GRCh38.p7 | 16:617629 | AGGAGGATCACCTGA[-/G]GTCAGGAGTCCAAGA | 57799 |
| rs3838962 | in-del | -/C | 0.430269 | 0.173214 | intron-variant | RAB40C | GRCh38.p7 | 16:625088 | GACTGGCCGAGAGGA[-/C]ACTTAGCTTCCACAG | 57799 |
| rs4144003 | snp | C/T | 0.498852 | 0.0239341 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595968 | AGGAAACTGTTGAGT[C/T]AGTAGGTAGAATATT | 57799 |
| rs4247097 | snp | A/G | 0.497586 | 0.0346604 | intron-variant | RAB40C | GRCh38.p7 | 16:604224 | CACACCCGGCTCAGA[A/G]CTAGTTCTTTTAAAT | 57799 |
| rs4984670 | snp | A/G | 0.497329 | 0.0364438 | intron-variant | RAB40C | GRCh38.p7 | 16:591044 | ATCTGGGGTCCGAGG[A/G]AAGGTGTCATAGATC | 57799 |
| rs4984671 | snp | C/T | 0.433236 | 0.170072 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594860 | AGTCTTACTCTCTTG[C/T]GCAGGCTGGAGTGCA | 57799 |
| rs4984672 | snp | A/G | 0.464203 | 0.128908 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596421 | AAGGGGTTGCATCAC[A/G]GCTGAGTCCTCCCCT | 57799 |
| rs4984673 | snp | A/G | 0.428937 | 0.17459 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596571 | CATCCTGGTGCGGAG[A/G]ACGCTGCCGAACCAC | 57799 |
| rs4984674 | snp | A/C | 0.117188 | 0.211804 | intron-variant | RAB40C | GRCh38.p7 | 16:599709 | TCGCAAGGTTTTGTT[A/C]CCTCGTGGCATCAGT | 57799 |
| rs4984675 | snp | C/T | 0.489893 | 0.0703642 | intron-variant | RAB40C | GRCh38.p7 | 16:620117 | AAGAGGAGTTGGGGC[C/T]GGTGCGGTGGTTCAC | 57799 |
| rs4984676 | snp | A/G | 0.497151 | 0.037632 | intron-variant | RAB40C | GRCh38.p7 | 16:620168 | GGGAGGCCAAGGCAG[A/G]CAGATCACGAGGTCA | 57799 |
| rs4984677 | snp | A/G | 0.495818 | 0.0455352 | intron-variant | RAB40C | GRCh38.p7 | 16:621682 | GGGTCACCCAGGTGC[A/G]GGTCCCTTGGTGTGT | 57799 |
| rs4984678 | snp | A/G | 0.432504 | 0.170857 | intron-variant | RAB40C | GRCh38.p7 | 16:624737 | GGACGTTGGGGAGAG[A/G]CGGGCATAGGGGAAT | 57799 |
| rs4984898 | snp | G/T | 0.497091 | 0.0380279 | intron-variant | RAB40C | GRCh38.p7 | 16:591164 | GTGTCATGGGTCTGG[G/T]ATCTCAGGGGAAGGT | 57799 |
| rs4984899 | snp | C/T | 0.427423 | 0.176128 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594048 | CCCCCAGGAACCACC[C/T]GCACAGGGTGCACAC | 57799 |
| rs4984900 | snp | A/G | 0.426813 | 0.17674 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597006 | TAGCGGAGGGACAAG[A/G]GCATTGGCGCTGTGG | 57799 |
| rs4984901 | snp | A/G | 0.497271 | 0.0368399 | intron-variant | RAB40C | GRCh38.p7 | 16:602623 | tttttagtagagatg[A/G]ggtttcaccatgtcg | 57799 |
| rs4984902 | snp | G/T | 0.429388 | 0.174127 | intron-variant | RAB40C | GRCh38.p7 | 16:605262 | agcagccccattgtt[G/T]catagtcccatcagc | 57799 |
| rs5815051 | in-del | -/T | 0.485392 | 0.0842056 | intron-variant | RAB40C | GRCh38.p7 | 16:604239 | GCTAGTTCTTTTAAA[-/T]TTTTTTTTTTTAATT | 57799 |
| rs7185390 | snp | A/G | 0.490231 | 0.0692021 | intron-variant | RAB40C | GRCh38.p7 | 16:616382 | tGAGTActgtcaccc[A/G]ggcaggagtgcagtg | 57799 |
| rs7185527 | snp | C/T | 0.256619 | 0.249912 | intron-variant | RAB40C | GRCh38.p7 | 16:600708 | AGTGAGCCGAGTTTG[C/T]ACCACTACACTCCAG | 57799 |
| rs7189914 | snp | C/T | 0.257732 | 0.24988 | intron-variant | RAB40C | GRCh38.p7 | 16:592222 | GTCCTGTCTGACTGC[C/T]CTGAGCGTCTGCTAT | 57799 |
| rs7190358 | snp | A/G | 0.253544 | 0.249975 | intron-variant | RAB40C | GRCh38.p7 | 16:600788 | TTGGTGCCTACGTGC[A/G]TCACACAGACAGTTT | 57799 |
| rs7191397 | snp | G/T | 0.497445 | 0.0356514 | intron-variant | RAB40C | GRCh38.p7 | 16:616517 | ctaattttttgtatt[G/T]ttagtagagacgggg | 57799 |
| rs7191584 | snp | C/T | 0.430136 | 0.173352 | intron-variant | RAB40C | GRCh38.p7 | 16:601517 | TCCCCGCCGCAGCCG[C/T]GTCAGCAGAGCAATG | 57799 |
| rs7197889 | snp | A/G | 0.103438 | 0.202533 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596388 | GTCTGGAGCCCCTGC[A/G]AGCTGGCGTAGAGCA | 57799 |
| rs7198207 | snp | C/T | 0.256061 | 0.249927 | intron-variant | RAB40C | GRCh38.p7 | 16:598515 | gcagagagctgagat[C/T]gtgccactgcactcc | 57799 |
| rs7198877 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | RAB40C | GRCh38.p7 | 16:611439 | TCTCAGGTCAGCCTC[A/G]TGGGGGCTTCAACAG | 57799 |
| rs7198884 | snp | A/G | 0.431916 | 0.171483 | intron-variant | RAB40C | GRCh38.p7 | 16:611451 | CTCATGGGGGCTTCA[A/G]CAGCCAGGACCAAAA | 57799 |
| rs7199115 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | RAB40C | GRCh38.p7 | 16:616320 | GGTCAGTCCAGAGTC[C/T]GGAGAAGCAGCATtt | 57799 |
| rs7203005 | snp | A/G | 0.104504 | 0.2033 | intron-variant | RAB40C | GRCh38.p7 | 16:609852 | GGCTCAGGATGGAGG[A/G]CGGGAGCTGTGTGCC | 57799 |
| rs7203694 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RAB40C | GRCh38.p7 | 16:602941 | TTGTAATCATTGAAA[A/G]TAATCTGAGAGCTAT | 57799 |
| rs7204088 | snp | C/T | 0.432063 | 0.171327 | intron-variant | RAB40C | GRCh38.p7 | 16:611142 | TCCCAGAGCAGCCTC[C/T]GATTCAAGAGCAAGG | 57799 |
| rs7204439 | snp | C/T | 0.492435 | 0.0610346 | intron-variant | RAB40C | GRCh38.p7 | 16:611335 | GGTGTTGCTGGCGCC[C/T]GCCTGCTTGGCCACA | 57799 |
| rs7205409 | snp | C/T | 0.478354 | 0.101757 | intron-variant | RAB40C | GRCh38.p7 | 16:592610 | TGGTGGGCGGCCAAG[C/T]TGATTGTGAAGGTGG | 57799 |
| rs7500178 | snp | A/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:605088 | ttagcctggtgtggt[A/G]acgcacacttgtaat | 57799 |
| rs8047461 | snp | A/G | 0.261884 | 0.249717 | intron-variant | RAB40C | GRCh38.p7 | 16:591260 | CATCTGGGGTCTGAG[A/G]GAAGGTGTCATAGAT | 57799 |
| rs8050792 | snp | C/T | 0.497359 | 0.0362457 | intron-variant | RAB40C | GRCh38.p7 | 16:606033 | ATTTTTAGTTTGGAT[C/T]CAGTTTATTTATAAT | 57799 |
| rs8054842 | snp | C/T | 0.495095 | 0.0492773 | intron-variant | RAB40C | GRCh38.p7 | 16:622799 | GTGAGCCACGGCGCC[C/T]GGCCGAAGTCGCTAG | 57799 |
| rs8055671 | snp | C/T | 0.254664 | 0.249956 | intron-variant | RAB40C | GRCh38.p7 | 16:609469 | TCAGCCCAAAAGAAG[C/T]GGCCACGAGACGCCG | 57799 |
| rs8063979 | snp | A/G | 0.256619 | 0.249912 | intron-variant | RAB40C | GRCh38.p7 | 16:609543 | TAGGGTCTGTCCTTG[A/G]GGGTCACCAGAATGT | 57799 |
| rs9673269 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:613098 | CGCCCTGGCCTGTAG[A/C]ATCAAGAGCAAGGGA | 57799 |
| rs9673273 | snp | A/G | 0.259397 | 0.249823 | intron-variant | RAB40C | GRCh38.p7 | 16:613193 | GGGACAGCCGCCCTC[A/G]CCTGTAGAATCAGCA | 57799 |
| rs9673790 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:613054 | AGGGACAGCCGCCCT[C/G/T]GCCTGTAGCATCAAG | 57799 |
| rs9674305 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:613052 | GCAGGGACAGCCGCC[C/T]TGGCCTGTAGCATCA | 57799 |
| rs9674306 | snp | A/C | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:613063 | CGCCCTGGCCTGTAG[A/C]ATCAAGAGCAAGGGA | 57799 |
| rs9745918 | snp | G/T | 0.496999 | 0.0386216 | intron-variant | RAB40C | GRCh38.p7 | 16:614196 | ACTCTACCGCATCCC[G/T]ATGGTGAACTGCTAA | 57799 |
| rs9923727 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602601 | gcccggctagttttt[G/T]ggtatttttttagta | 57799 |
| rs9929621 | snp | C/T | 0.284995 | 0.247539 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629412 | CGGGCTGACCTGCCG[C/T]GGTTGGCTGGGTTCG | 57799 |
| rs9932481 | snp | A/G | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:606473 | GTGTGGGTTTCCCTG[A/G]GCTGAAGTCAAGGTG | 57799 |
| rs9932507 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | RAB40C | GRCh38.p7 | 16:623200 | CGGGCCTTCTGCTCT[A/C]TTTCTAGAGTTTTCA | 57799 |
| rs9935061 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:606527 | gtcctcagtccagtg[G/T]gggtttccctgggct | 57799 |
| rs10153107 | snp | C/T | 0.0611083 | 0.163768 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628877 | GGACCCAGGACCCCC[C/T]GTGGTGGACTCCGCG | 57799 |
| rs10153225 | snp | A/G | 0.0596104 | 0.162024 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628980 | TGGGAGATGAGGGCC[A/G]TGGCCTGCATGAACT | 57799 |
| rs10656981 | in-del | -/AT/TA | | | intron-variant | RAB40C | GRCh38.p7 | 16:600441 | GTTTAAAACATTGTT[-/AT/TA]GTTGGACTTTTTTAA | 57799 |
| rs11248939 | snp | A/G | 0.167158 | 0.235875 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597094 | GGGTGCTGCACATGT[A/G]GGTAGCAGGGGGAGG | 57799 |
| rs11248940 | snp | C/T | 0.19646 | 0.2442 | intron-variant | RAB40C | GRCh38.p7 | 16:605686 | AAGGCTGCAGTGCAT[C/T]GGCTCCACTCCAGAT | 57799 |
| rs11248941 | snp | G/T | 0.236724 | 0.249647 | intron-variant | RAB40C | GRCh38.p7 | 16:608271 | agaactcactcaccc[G/T]cacaaaaacagcagg | 57799 |
| rs11285441 | in-del | -/C | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611869 | GTAGAATCAAGAGCA[-/C]GGGACAGCCGCCCTG | 57799 |
| rs11340032 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612487 | GTAGAATCAAGAGCA[A/C]GGGACAGCCGCCCTG | 57799 |
| rs11548187 | snp | A/C/T | 3.5092e-05 | 0.00418865 | synonymous-codon, missense | RAB40C | GRCh38.p7 | 16:627599 | CCCCAGAACTGCTCG[A/C/T]GGAGTAACTGCAAGA | 57799 |
| rs11548188 | snp | A/G | 0.278399 | 0.248382 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628020 | TGACTTCATGGCCAC[A/G]CCAGCTGCGGGGACG | 57799 |
| rs11548189 | snp | C/G | 0.0596104 | 0.162024 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628264 | AGGAGGTGCACCTGG[C/G]AGCCCACATTTTTGT | 57799 |
| rs11639703 | snp | A/G | 0.187369 | 0.242028 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594393 | ATCACGGTTTGCTGT[A/G]GATGTTGGGGCCTGG | 57799 |
| rs11639717 | snp | C/T | 0.308908 | 0.242961 | intron-variant | RAB40C | GRCh38.p7 | 16:626989 | ATGAGTCAGGACGCG[C/T]GCTCCCCCGCTCTAG | 57799 |
| rs11639978 | snp | A/G | 0.190833 | 0.242898 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589042 | GACGAGGGCTCGGCG[A/G]CGCCCCCGGGAAGAG | 57799 |
| rs11641903 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RAB40C | GRCh38.p7 | 16:605648 | CTCCCTCCTTCCCCG[C/T]GCCGAGTGGTCTCCC | 57799 |
| rs11642273 | snp | A/G | 0.255224 | 0.249945 | intron-variant | RAB40C | GRCh38.p7 | 16:601538 | CAGAGCAATGTGATC[A/G]TTGCTGGGACTGTTC | 57799 |
| rs11643412 | snp | A/G | 0.261056 | 0.249755 | intron-variant | RAB40C | GRCh38.p7 | 16:615323 | AGGCAGAGAGACCGC[A/G]TGGCTGGCTTGCAGG | 57799 |
| rs11645708 | snp | C/T | 0.259674 | 0.249813 | intron-variant | RAB40C | GRCh38.p7 | 16:611080 | GTGGGCAACCGGGTG[C/T]GGAGCCTGCAGGATG | 57799 |
| rs11647220 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594825 | TCGTCTTCCtttttt[C/T]tttttttttttttag | 57799 |
| rs11648607 | snp | A/G | 0.256897 | 0.249905 | intron-variant | RAB40C | GRCh38.p7 | 16:621245 | CACCCCGGGAGCCCA[A/G]CCCTGTCCTGTGTCT | 57799 |
| rs11649661 | snp | C/T | 0.169435 | 0.236663 | intron-variant | RAB40C | GRCh38.p7 | 16:591486 | TAGGCACGCTGTTCC[C/T]CTGAGGTATTTGCTT | 57799 |
| rs11861429 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RAB40C | GRCh38.p7 | 16:621502 | ACTCCCCGCTGCCGT[C/T]ACCTGTCACACAGCA | 57799 |
| rs11861544 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596503 | GGGCCACGTCAGCCA[C/G]GGTGTCATCCGCCGG | 57799 |
| rs11863012 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:621369 | AGACACAGACTAGCA[A/G]GGACTGTCTGTCCCA | 57799 |
| rs12149200 | snp | C/T | 0.0383715 | 0.133092 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628430 | ATACTTGATGGGCAG[C/T]GGTGCAGACCCCGGG | 57799 |
| rs12149324 | snp | C/G | 0.261608 | 0.24973 | intron-variant | RAB40C | GRCh38.p7 | 16:606997 | GCCGGCCCAGACAGA[C/G]AGACTACCACCTGAG | 57799 |
| rs12149951 | snp | G/T | 0.261608 | 0.24973 | intron-variant | RAB40C | GRCh38.p7 | 16:606842 | cttatgtagttaatt[G/T]gccccacccagataa | 57799 |
| rs12149958 | snp | A/G | 0.258843 | 0.249844 | intron-variant | RAB40C | GRCh38.p7 | 16:606985 | TGCTGGTGGCAGGCC[A/G]GCCCAGACAGACAGA | 57799 |
| rs12444525 | snp | A/G | 0.407158 | 0.194426 | intron-variant | RAB40C | GRCh38.p7 | 16:623430 | cgaggtgggcagatc[A/G]ggaggtcaggagatc | 57799 |
| rs12446884 | snp | A/C | 0.167484 | 0.23599 | intron-variant | RAB40C | GRCh38.p7 | 16:623577 | gagaatggcgtgaac[A/C]cggaagcggagatcg | 57799 |
| rs12447387 | snp | A/G | 0.26818 | 0.249338 | intron-variant | RAB40C | GRCh38.p7 | 16:617490 | CCTCCTGCCCCGGAA[A/G]ACCTGATTCCGTGGT | 57799 |