| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs9560 | snp | A/T | 0.177239 | 0.239177 | utr-variant-3-prime, downstream-variant-500B | ASB9 | GRCh38.p7 | X:15244250 | GACTTTTTTCCCTGC[A/T]TGGAGAGTGTCATAA | 140462 |
| rs14252 | snp | G/T | 0.177239 | 0.239177 | utr-variant-3-prime, downstream-variant-500B | ASB9 | GRCh38.p7 | X:15244310 | AACTCAAGCCAGGGT[G/T]GAAAGACACTGCATA | 140462 |
| rs731197 | snp | C/T | 0.460652 | 0.134633 | intron-variant | ASB9 | GRCh38.p7 | X:15249126 | CCTCATGCTGTACAT[C/T]CAATAACATTATCAG | 140462 |
| rs899646 | snp | C/T | 0.459905 | 0.135794 | utr-variant-5-prime, intron-variant | ASB9 | GRCh38.p7 | X:15270071 | GATCAGAGAGAGGCA[C/T]GCGCTCGTGTACACA | 140462 |
| rs899647 | snp | A/G | 0.0204488 | 0.0990265 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon | ASB9 | GRCh38.p7 | X:15270297 | AGGGTGGGGGTGAAG[A/G]AAACAGCTCACTTTC | 140462 |
| rs1073366 | snp | C/G | | | downstream-variant-500B | ASB9 | GRCh38.p7 | X:15243537 | attagccacatttca[C/G]gtataaaatatgcac | 140462 |
| rs1139868 | snp | A/G | 0.338027 | 0.23399 | intron-variant, utr-variant-3-prime | ASB9 | GRCh38.p7 | X:15248697 | TGTTGACATCCCTTG[A/G]GGCTCTAGTAGAAGG | 140462 |
| rs1479926 | snp | A/G | 0.0271702 | 0.113344 | intron-variant | ASB9 | GRCh38.p7 | X:15259268 | CCCATTTAGTTAAGC[A/G]AGAGCTTCACTAATT | 140462 |
| rs1479927 | snp | A/G | 0.460204 | 0.13533 | intron-variant | ASB9 | GRCh38.p7 | X:15264700 | AAAACAGCATTCTGA[A/G]TGTTCCCCATTCCAC | 140462 |
| rs1842302 | snp | A/G | 0.27346 | 0.248897 | intron-variant | ASB9 | GRCh38.p7 | X:15262841 | ttcaccatgttggcc[A/G]ggctggtctccaact | 140462 |
| rs1842303 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | ASB9 | GRCh38.p7 | X:15268201 | gccgggtgtggtggc[A/G]ggcgcttataatccc | 140462 |
| rs1842304 | snp | A/G | 0.461096 | 0.133934 | intron-variant | ASB9 | GRCh38.p7 | X:15268264 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 140462 |
| rs2291122 | snp | A/G | 0.499792 | 0.0101966 | intron-variant | ASB9 | GRCh38.p7 | X:15247335 | GTCACCGTGCAAAAC[A/G]TAAATTCAAAATTAA | 140462 |
| rs2291123 | snp | C/T | 0.457931 | 0.138798 | intron-variant | ASB9 | GRCh38.p7 | X:15248022 | AAAGTCCCAGAATCC[C/T]TAAGACTTCAGAGTC | 140462 |
| rs2291125 | snp | A/G | 4.59765e-05 | 0.00479438 | intron-variant | ASB9 | GRCh38.p7 | X:15254862 | GAAGGAGGGGAAACA[A/G]TCAGAGTAAGGGGTG | 140462 |
| rs2317328 | snp | G/T | | | intron-variant | ASB9 | GRCh38.p7 | X:15267751 | ttttttttttttttg[G/T]tttttttgaagtgga | 140462 |
| rs3830223 | in-del | -/AC | 0.230204 | 0.249215 | intron-variant | ASB9 | GRCh38.p7 | X:15248175 | AAGCCCTACTTCCAT[-/AC]ACACTGCTCAACCAC | 140462 |
| rs3840971 | in-del | -/T | 0.494581 | 0.0517701 | upstream-variant-2KB | ASB9 | GRCh38.p7 | X:15270502 | CATATAGACACATTT[-/T]CCCATAAGAAACTCC | 140462 |
| rs4363349 | snp | C/T | 0.185696 | 0.241589 | intron-variant | ASB9 | GRCh38.p7 | X:15268714 | TAAACCACCGTGCCC[C/T]GCCTATATATACAGG | 140462 |
| rs4830525 | snp | C/T | 0.481251 | 0.0949886 | intron-variant | ASB9 | GRCh38.p7 | X:15259664 | AGCCCTAATATATAA[C/T]ATACAGGTTGAGCAT | 140462 |
| rs4830526 | snp | G/T | 0.470496 | 0.117819 | intron-variant | ASB9 | GRCh38.p7 | X:15263350 | CCAGAACCTGGAAAG[G/T]ATCTGGGTGCTGTAT | 140462 |
| rs4830527 | snp | C/G | 0.461096 | 0.133934 | intron-variant | ASB9 | GRCh38.p7 | X:15269095 | ACGTGACATCAGCAA[C/G]TTTGCAGACTTGGGG | 140462 |
| rs4830528 | snp | A/G | 0.111166 | 0.207907 | intron-variant | ASB9 | GRCh38.p7 | X:15269390 | TGTTTGAACATCTTT[A/G]TAAACCCTGCCCCAC | 140462 |
| rs4830934 | snp | C/G | 0.402499 | 0.198101 | intron-variant | ASB9 | GRCh38.p7 | X:15263134 | AAGATGCACTAATTG[C/G]TACATGCTGAAAATA | 140462 |
| rs5901553 | in-del | -/C | | | intron-variant | ASB9 | GRCh38.p7 | X:15261081 | ATAGATACTCAATGT[-/C]CTCACGGCATTCTCT | 140462 |
| rs5934228 | snp | A/T | 0.0245906 | 0.108123 | intron-variant | ASB9 | GRCh38.p7 | X:15252525 | TCCTCAGCTATAAAA[A/T]GGAGAAATAACTACG | 140462 |
| rs5935917 | snp | A/G | 0.26482 | 0.24956 | intron-variant | ASB9 | GRCh38.p7 | X:15249260 | TAATGGAACCTAAGT[A/G]TTAGCCAGTACAGCC | 140462 |
| rs5935918 | snp | A/C | 0.410516 | 0.191663 | intron-variant | ASB9 | GRCh38.p7 | X:15251645 | GTCATTACGATGATG[A/C]TAAATATTGGAGAAA | 140462 |
| rs5935919 | snp | G/T | 0.485674 | 0.0834144 | upstream-variant-2KB | ASB9 | GRCh38.p7 | X:15271931 | ctaaagttcatattt[G/T]tgtacatgtggcttt | 140462 |
| rs5978720 | snp | C/G | 0.0358881 | 0.129059 | intron-variant | ASB9 | GRCh38.p7 | X:15245597 | tcaatccaggtagca[C/G]ttcagactcacctgg | 140462 |
| rs5978721 | snp | A/G | 0.187793 | 0.242137 | intron-variant | ASB9 | GRCh38.p7 | X:15245672 | AGGGATGTTGCTTCA[A/G]TTATTGTTGGGTGAA | 140462 |
| rs5978722 | snp | A/G | 0.485852 | 0.0829075 | intron-variant | ASB9 | GRCh38.p7 | X:15257361 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 140462 |
| rs5980142 | snp | C/T | 0.499135 | 0.0207767 | intron-variant | ASB9 | GRCh38.p7 | X:15250239 | cctcctcctcatcct[C/T]GTTACAAATGAGAGA | 140462 |
| rs5980143 | snp | C/T | 0.0209675 | 0.10022 | intron-variant | ASB9 | GRCh38.p7 | X:15253008 | ggaggccgaggcagg[C/T]ggattgcctgagctc | 140462 |
| rs5980144 | snp | A/G | 0.409392 | 0.192599 | intron-variant | ASB9 | GRCh38.p7 | X:15267124 | TTATCggccgggcac[A/G]gtggctcacacctgt | 140462 |
| rs6418672 | snp | A/G | 0.459755 | 0.136026 | intron-variant | ASB9 | GRCh38.p7 | X:15264411 | TACACAATTTAACTC[A/G]TAACAAGCTACTTTC | 140462 |
| rs6527396 | snp | A/C | 0.361195 | 0.22391 | intron-variant | ASB9 | GRCh38.p7 | X:15253849 | GAAGACAACGAATTC[A/C]TTCTCAAACTCTACT | 140462 |
| rs6527407 | snp | C/T | 0.416248 | 0.186712 | intron-variant | ASB9 | GRCh38.p7 | X:15264373 | CACGGGGGTTAAGAA[C/T]TTAACCATATATATT | 140462 |
| rs6527410 | snp | G/T | 0.457314 | 0.139717 | intron-variant | ASB9 | GRCh38.p7 | X:15266107 | tgcacccagtcaaat[G/T]tttgtatttttagta | 140462 |
| rs6628905 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | ASB9 | GRCh38.p7 | X:15243512 | tcaatacagtagcca[C/T]tagccatttgtgcat | 140462 |
| rs6628929 | snp | A/G | | | intron-variant | ASB9 | GRCh38.p7 | X:15268819 | actccgtctcaaaaa[A/G]aaaaaaaaaTTAATA | 140462 |
| rs6632100 | snp | A/G | 0 | 0 | intron-variant | ASB9 | GRCh38.p7 | X:15245119 | TACATCCTGTATTCA[A/G]AGCTATTCCAATGCT | 140462 |
| rs6632102 | snp | A/C | 0.187374 | 0.242029 | intron-variant | ASB9 | GRCh38.p7 | X:15245371 | AAGGATGCTTCTAAA[A/C]ATCCCAGAGTACACA | 140462 |
| rs6632107 | snp | A/C | 0.230982 | 0.249276 | intron-variant | ASB9 | GRCh38.p7 | X:15247097 | CGGAGAAACAGGTGG[A/C]CTGAAGCAAATGAAT | 140462 |
| rs6632147 | snp | A/G | 0.236779 | 0.24965 | intron-variant | ASB9 | GRCh38.p7 | X:15262359 | gtttattttgagact[A/G]ttttccaaagtggct | 140462 |
| rs6632152 | snp | C/T | 0.5 | 0 | intron-variant | ASB9 | GRCh38.p7 | X:15267466 | CTTGTAAAAAGTGGC[C/T]GGGCGTGGTGGCTCA | 140462 |
| rs6632153 | snp | G/T | 0 | 0 | intron-variant | ASB9 | GRCh38.p7 | X:15267548 | aggagattgagacca[G/T]cctggctaacatggt | 140462 |
| rs6632154 | snp | C/T | 0 | 0 | intron-variant | ASB9 | GRCh38.p7 | X:15267555 | tgagaccatcctggc[C/T]aacatggtgaaaccc | 140462 |
| rs6632157 | snp | A/G | | | intron-variant | ASB9 | GRCh38.p7 | X:15267930 | TAAGTGAAATtggat[A/G]aatgaatgaatgaat | 140462 |
| rs7053581 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | ASB9 | GRCh38.p7 | X:15247695 | ACAAGTAATTATTAA[A/G]ATGCAGATAGAACTG | 140462 |
| rs7066576 | snp | C/T | 0.357825 | 0.225552 | intron-variant | ASB9 | GRCh38.p7 | X:15254326 | ACAGGTCCATTTTTG[C/T]TGCTCTTGCAATCCC | 140462 |
| rs7887024 | snp | C/T | 0.385181 | 0.2103 | intron-variant | ASB9 | GRCh38.p7 | X:15261502 | CTAATTTGTAACTGT[C/T]CAGATTTCATAAAAA | 140462 |
| rs10126791 | snp | C/T | 0.358107 | 0.225417 | intron-variant | ASB9 | GRCh38.p7 | X:15255640 | GTGTTTAAGTTCTTT[C/T]ATGCTTATGAAATTT | 140462 |
| rs10126800 | snp | C/T | 0.358107 | 0.225417 | intron-variant | ASB9 | GRCh38.p7 | X:15255777 | GAAATTTTCAAACTG[C/T]GAGGGAAAAGAAATA | 140462 |
| rs10578883 | in-del | -/CT | | | intron-variant | ASB9 | GRCh38.p7 | X:15263600 | CTCTCTTCTCTCTCT[-/CT]CTCTCTCTCTCAATA | 140462 |
| rs10716181 | in-del | -/T | 0.343941 | 0.231679 | upstream-variant-2KB | ASB9 | GRCh38.p7 | X:15271433 | GTACCTATATTATTC[-/T]TTTTTTTTTGAGACA | 140462 |
| rs10856268 | snp | A/G | 0.472891 | 0.113224 | intron-variant | ASB9 | GRCh38.p7 | X:15245619 | CTCACCTGGGGTGGG[A/G]GTACATTCAACTACA | 140462 |
| rs11094672 | snp | A/G | 0.181482 | 0.240427 | intron-variant | ASB9 | GRCh38.p7 | X:15246700 | GCCAGGATGGTCTCT[A/G]TCTCCTGAACTCATG | 140462 |
| rs11094673 | snp | C/T | 0.402031 | 0.198461 | intron-variant | ASB9 | GRCh38.p7 | X:15266656 | TAGGAACTTTAGAAA[C/T]CCTGAACAGTTGGCT | 140462 |
| rs11537782 | snp | C/T | | | synonymous-codon, intron-variant | ASB9 | GRCh38.p7 | X:15269821 | CGCGGGGCCAAGGGA[C/T]TTTCCTGGCATCAGG | 140462 |
| rs11797112 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | ASB9 | GRCh38.p7 | X:15267405 | acagagcgagactcc[A/G]tctaaaaaaaaaata | 140462 |
| rs12006909 | snp | A/C | 0.0323082 | 0.122924 | intron-variant | ASB9 | GRCh38.p7 | X:15254253 | TTGCATTTGCTGTTG[A/C]CAGAAGATAGCAAGC | 140462 |
| rs12010592 | snp | G/T | 0 | 0 | upstream-variant-2KB | ASB9 | GRCh38.p7 | X:15270909 | attagctgggcctgg[G/T]ggcaggcgcctgtaa | 140462 |
| rs12391066 | snp | A/C | | | intron-variant | ASB9 | GRCh38.p7 | X:15267242 | gtctctactaaaata[A/C]aaaaaaaaaacaccc | 140462 |
| rs12556121 | snp | C/T | 0.186955 | 0.24192 | intron-variant | ASB9 | GRCh38.p7 | X:15245143 | CAATGCTTCAATTCA[C/T]AAGTGAAAAGTGAAC | 140462 |
| rs12557432 | snp | C/T | 0 | 0 | intron-variant | ASB9 | GRCh38.p7 | X:15266587 | AGCACCATGCCTTTG[C/T]GTATAACACCTGCCC | 140462 |
| rs12557528 | snp | C/G | 0.481354 | 0.0947388 | intron-variant | ASB9 | GRCh38.p7 | X:15266923 | CCTGGGCGACAGAGC[C/G]AGACTCCATCTCAAA | 140462 |
| rs12686917 | snp | A/G | 0.471517 | 0.115889 | intron-variant | ASB9 | GRCh38.p7 | X:15246374 | GCAAATATTCAAGGG[A/G]TTTGCTTTGCTCGGT | 140462 |
| rs12687579 | snp | A/G | 0.39608 | 0.202881 | intron-variant | ASB9 | GRCh38.p7 | X:15265458 | TCCTTTGAAATCATC[A/G]CCCTTTCTCTGTCAT | 140462 |
| rs12687599 | snp | A/C | 0.480942 | 0.0957375 | intron-variant | ASB9 | GRCh38.p7 | X:15265781 | AGCTGGGACTACAGG[A/C]ATGTGCCAACACACC | 140462 |
| rs12840423 | snp | A/G | 0.32941 | 0.237053 | intron-variant | ASB9 | GRCh38.p7 | X:15260171 | TGAGAGGCCGAGGTG[A/G]GCAGATCACCTGAGG | 140462 |
| rs12851530 | snp | G/T | 0.484855 | 0.0856918 | intron-variant | ASB9 | GRCh38.p7 | X:15257773 | TCAGTCGTCAACTAC[G/T]CTTAGTTGACAAAAT | 140462 |
| rs12852688 | snp | C/G | 0.270957 | 0.24912 | intron-variant | ASB9 | GRCh38.p7 | X:15252471 | AAATGTGGGGTCCAC[C/G]ACTCTGAAGATGTTA | 140462 |
| rs12853913 | snp | A/C | | | intron-variant | ASB9 | GRCh38.p7 | X:15252915 | ctcattaatgaggga[A/C]ccagtaagatggtaa | 140462 |
| rs12855615 | snp | C/T | 0.190717 | 0.242869 | intron-variant | ASB9 | GRCh38.p7 | X:15245364 | AGAGGCCAAGGATGC[C/T]TCTAAAAATCCCAGA | 140462 |
| rs13328524 | snp | C/T | | | intron-variant | ASB9 | GRCh38.p7 | X:15251755 | CAACATCAAATACTT[C/T]CAAAAATTGAAAGCT | 140462 |
| rs16979800 | snp | A/G | 0.23137 | 0.249305 | intron-variant | ASB9 | GRCh38.p7 | X:15246393 | GCTTTGCTCGGTAAT[A/G]AAACCAGCTAATTGT | 140462 |
| rs16979805 | snp | G/T | 0.0271702 | 0.113344 | intron-variant | ASB9 | GRCh38.p7 | X:15251678 | AAAAACTTGTGATTT[G/T]ATGAGCTAAGACTAT | 140462 |
| rs17216302 | snp | A/T | 0.0157677 | 0.0873799 | utr-variant-3-prime, downstream-variant-500B | ASB9 | GRCh38.p7 | X:15244056 | GAACCAGGACAGTGA[A/T]GCTGGAAAAGCCTGC | 140462 |
| rs17216316 | snp | C/T | 0.00581083 | 0.0535878 | utr-variant-3-prime, downstream-variant-500B | ASB9 | GRCh38.p7 | X:15244180 | AGTGGCTGTGAGGGC[C/T]AAATTAGATGATGCA | 140462 |
| rs28397638 | snp | A/C | 0 | 0 | intron-variant | ASB9 | GRCh38.p7 | X:15267756 | TTCAAAAAAAACAAA[A/C]AAAAAAAAAAAAAAA | 140462 |
| rs28628283 | snp | A/G/T | 0.563886 | 0.173562 | intron-variant | ASB9 | GRCh38.p7 | X:15244692 | AAGACTCCTTTTTTT[A/G/T]AAAAAAAAAAAGCAT | 140462 |
| rs28710836 | snp | G/T | | | intron-variant | ASB9 | GRCh38.p7 | X:15262724 | GCAACCTCCACCTCC[G/T]GGGTTCAAGTGGTTC | 140462 |
| rs34050715 | in-del | -/G | | | intron-variant | ASB9 | GRCh38.p7 | X:15249097 | TCCATTTAATAATGT[-/G]GGGAAAATCCCACCT | 140462 |
| rs34454817 | in-del | -/AA | 0.454162 | 0.144284 | intron-variant | ASB9 | GRCh38.p7 | X:15266936 | GCGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 140462 |
| rs34610229 | in-del | -/A | | | upstream-variant-2KB | ASB9 | GRCh38.p7 | X:15272259 | AAATTGCACTTTTTG[-/A]AAAGAGGCTGCTCAT | 140462 |
| rs34654544 | in-del | -/TC | 0.400382 | 0.199713 | intron-variant | ASB9 | GRCh38.p7 | X:15263589 | TGTCTCCCTCTCTCT[-/TC]TCTCTCTCTCTCTCT | 140462 |
| rs34885578 | in-del | -/G | | | intron-variant | ASB9 | GRCh38.p7 | X:15267153 | TAATCCTAGCACTTT[-/G]GGGAGGCCGAGGCGG | 140462 |
| rs34929781 | in-del | -/G | | | intron-variant | ASB9 | GRCh38.p7 | X:15249028 | AAAATTTCCTAACAA[-/G]GAGGGGATCCATATT | 140462 |
| rs34955369 | in-del | -/T | 0.436828 | 0.166119 | intron-variant | ASB9 | GRCh38.p7 | X:15265653 | GCTGCATCATCTGCA[-/T]TTTTTTTTTTTGAGA | 140462 |
| rs34974581 | in-del | -/G | | | frameshift-variant, utr-variant-3-prime | ASB9 | GRCh38.p7 | X:15244539 | TGTTTCAGATCCTCT[-/G]GGGAGGACGAGTTTG | 140462 |
| rs35084172 | in-del | -/C | | | intron-variant | ASB9 | GRCh38.p7 | X:15263866 | TTCAGGCAAAACCCC[-/C]AAAAGATAGACACTA | 140462 |
| rs35118279 | in-del | -/G | | | upstream-variant-2KB | ASB9 | GRCh38.p7 | X:15270605 | CACCCCTCCTCCACT[-/G]CATTTTAACTTCTAA | 140462 |
| rs35126991 | in-del | -/C | | | intron-variant | ASB9 | GRCh38.p7 | X:15251225 | TATGGAGGAACAGGA[-/C]CTGAAGGTGGAACTG | 140462 |
| rs35149491 | in-del | -/A | | | intron-variant | ASB9 | GRCh38.p7 | X:15254985 | TTAAAAAAAAAAAAA[-/A]TGCCACACTACTGGT | 140462 |
| rs35170760 | in-del | -/C | | | intron-variant | ASB9 | GRCh38.p7 | X:15256764 | CCTGGGCGACAGCAA[-/C]GACTCCGTCTCAAAA | 140462 |
| rs35176116 | in-del | -/A | | | intron-variant | ASB9 | GRCh38.p7 | X:15261909 | CATTTTCATCACCCC[-/A]AAAAGAAACTCTGTG | 140462 |
| rs35286849 | snp | A/G | 0.5 | 0 | intron-variant | ASB9 | GRCh38.p7 | X:15245358 | AATGGGAGAGGCCAA[A/G]GATGCTTCTAAACAT | 140462 |
| rs35575825 | in-del | -/G | | | intron-variant | ASB9 | GRCh38.p7 | X:15263185 | ACCCCAGTGAATGCT[-/G]GGGCGGTAGCATAAA | 140462 |
| rs35732224 | in-del | -/A | | | intron-variant | ASB9 | GRCh38.p7 | X:15244703 | TTTTAAAAAAAAAAA[-/A]GCATCCAAGATAGAA | 140462 |