SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs723115 | snp | C/T | 0.455024 | 0.143057 | intron-variant | ABI2 | GRCh38.p7 | 2:203415879 | CATACCAATATATAG[C/T]AACATCAAAAAGATT | 10152 |
rs998027 | snp | C/G | 0.454664 | 0.143571 | intron-variant | ABI2 | GRCh38.p7 | 2:203406494 | AATGGTTTTAAAAGC[C/G]ACTAAAAAAATAGGA | 10152 |
rs1058730 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431967 | TACTTTTAGCTCCCA[A/G]AGGGAGAGTTGGTGG | 10152 |
rs1058733 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432066 | GTGTGCCATTAAACC[A/C]CCTCCAGATGAGTGG | 10152 |
rs1058736 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432091 | GAGTGGAGGAACATC[A/C]CTTTTTAATTTTTTA | 10152 |
rs1135718 | snp | C/G | | | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395676 | CTACTTGGGTGGCTC[C/G]CTCCACTACTCCCAC | 10152 |
rs1376877 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | ABI2 | GRCh38.p7 | 2:203407367 | ATATATATATCTCCT[C/T]TAAATGTGATGTTCA | 10152 |
rs1452050 | snp | C/T | 0.453575 | 0.145111 | intron-variant | ABI2 | GRCh38.p7 | 2:203413596 | TTCTCATTTACACAA[C/T]GTATAAAAAAATTGT | 10152 |
rs1470788 | snp | G/T | 0.453453 | 0.145282 | intron-variant | ABI2 | GRCh38.p7 | 2:203414442 | GAGGGTAGGATGGCA[G/T]AGGCATTGATATTTC | 10152 |
rs1470789 | snp | C/G | 0.453818 | 0.144769 | intron-variant | ABI2 | GRCh38.p7 | 2:203412885 | AAGTCCTTCAATTCT[C/G]GTACTGTAATTAAAT | 10152 |
rs1470790 | snp | C/T | 0.454423 | 0.143914 | intron-variant | ABI2 | GRCh38.p7 | 2:203412755 | CAGAGGATCACACTA[C/T]GGATGTGCTTGGCAC | 10152 |
rs1802776 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380310 | ATTGCTCCAGCCAAC[C/T]TTGAACGACCAGTTC | 10152 |
rs1982417 | snp | A/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203406618 | AAACGTCTAGAAGAA[A/T]ACTGATGTGTTGGGG | 10152 |
rs2044946 | snp | G/T | 0.117188 | 0.211804 | intron-variant | ABI2 | GRCh38.p7 | 2:203415191 | TAGGATGAAAGACAT[G/T]CTATTTAATGACTGA | 10152 |
rs2044947 | snp | C/T | 0.453697 | 0.14494 | intron-variant | ABI2 | GRCh38.p7 | 2:203416219 | ATTTCTGATAACTTA[C/T]CCTTGAATACAGTGT | 10152 |
rs2060827 | snp | A/T | 0.496314 | 0.0427728 | intron-variant | ABI2 | GRCh38.p7 | 2:203415929 | TCCATGTGAGATATT[A/T]TAAATTACTCTGATA | 10152 |
rs2123118 | snp | A/G | 0 | 0 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394833 | TCTGTGAATCAAAGA[A/G]ATCGAACTTACAGGT | 10152 |
rs2123119 | snp | A/G | 0.104149 | 0.203046 | intron-variant | ABI2 | GRCh38.p7 | 2:203413068 | TGTTTTTACTATTGT[A/G]ATGAGTGTACACCTT | 10152 |
rs2248015 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ABI2 | GRCh38.p7 | 2:203409772 | AACAAGGTAATGCAA[C/T]CTACTTCCAATAGTG | 10152 |
rs2248848 | snp | A/C | 0.169435 | 0.236663 | intron-variant | ABI2 | GRCh38.p7 | 2:203402831 | AACAAATGGTGCTAA[A/C]CACCTACCATGCACT | 10152 |
rs2252464 | snp | C/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203395450 | ATATATATATATATA[C/T]ACACACACACACACA | 10152 |
rs2252836 | snp | A/T | 0.173586 | 0.238036 | intron-variant | ABI2 | GRCh38.p7 | 2:203392977 | TGCTCCTTTTTTTTT[A/T]AAAAAAAATCTTATT | 10152 |
rs2254175 | snp | C/T | 0.459004 | 0.137176 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429689 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCCA | 10152 |
rs2254878 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ABI2 | GRCh38.p7 | 2:203424146 | TCTAGATTTTATTTA[A/G]TCTGGAAAACTGGTT | 10152 |
rs2254889 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ABI2 | GRCh38.p7 | 2:203423825 | TTCTTAGCTTAAATG[A/T]TTCTCTTTTTAATTT | 10152 |
rs2255047 | snp | A/G | 0.281313 | 0.248031 | intron-variant | ABI2 | GRCh38.p7 | 2:203422410 | GGTGCACTAACTGGG[A/G]CGGTGACTATGATGA | 10152 |
rs2443791 | snp | C/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203422347 | GGTACCTGAGATTTT[C/T]TAAGCAGTGTGGGTG | 10152 |
rs2443792 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203403632 | TAAGAAAATGATCAC[C/G]AATCTTATTTTGTAC | 10152 |
rs2443793 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203392317 | TTGTTGTTGTTGTTG[G/T]TGGTGGTGGTGGTGG | 10152 |
rs2469954 | snp | A/G | 0.458545 | 0.137872 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427794 | CAAGTGGAAGAAAAG[A/G]AGGGGCTAGGGTACC | 10152 |
rs2469963 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ABI2 | GRCh38.p7 | 2:203412920 | TTGTATGGAGTATGT[A/T]GAATGGAACCAGCAT | 10152 |
rs2469964 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409133 | GAAGGTAGTTGGGCC[A/G]GGCGCGGTGGCTCAC | 10152 |
rs2469965 | snp | A/G | 0.16911 | 0.236552 | intron-variant | ABI2 | GRCh38.p7 | 2:203408924 | GTGAACCCGGGAAGC[A/G]GAGCTTGCAGTGAGC | 10152 |
rs2469966 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | ABI2 | GRCh38.p7 | 2:203407717 | TAAGACAAGACTCTT[C/T]CCCAATAACCACCAA | 10152 |
rs2600715 | snp | G/T | | | | | GRCh38.p7 | 2:203402452 | CCTTGCATTGTATAT[G/T]TCAGATACCAGTTAA | 10152 |
rs2882829 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | ABI2 | GRCh38.p7 | 2:203412926 | GTTCCATTCTACATA[C/T]TCCATACAAGGTGGA | 10152 |
rs3731651 | snp | C/T | 0.117537 | 0.212022 | intron-variant | ABI2 | GRCh38.p7 | 2:203396712 | TCTAACATTAAATAC[C/T]CTAATACCTTTTCTA | 10152 |
rs3731652 | snp | C/G | 0.318733 | 0.240366 | intron-variant | ABI2 | GRCh38.p7 | 2:203397000 | CATTGGCAGGCAGAT[C/G]CAGTCATCTGGCTAT | 10152 |
rs3769674 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | ABI2 | GRCh38.p7 | 2:203392500 | CAACCAGGAATAGGA[G/T]GACTTTATTAGGAGT | 10152 |
rs3769675 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395448 | ATATATATATATATA[C/T]ACACACACACACACA | 10152 |
rs3769676 | snp | C/T | 0.4087 | 0.193169 | intron-variant | ABI2 | GRCh38.p7 | 2:203401620 | GACTTAGGGATGATA[C/T]TAAAAATAAGATATA | 10152 |
rs3769677 | snp | A/G | 0.453818 | 0.144769 | intron-variant | ABI2 | GRCh38.p7 | 2:203406231 | TACATGTGAGTATGT[A/G]TACATATACTTACAT | 10152 |
rs3769678 | snp | C/T | 0.479824 | 0.098392 | intron-variant | ABI2 | GRCh38.p7 | 2:203411604 | ATAAGAAAAGAAAGA[C/T]CACATCCTACTGAGG | 10152 |
rs3769679 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203411997 | ACATAGACTGTATGA[G/T]GGACAAATCCTCTTC | 10152 |
rs3835893 | in-del | -/T | 0.496279 | 0.0429702 | intron-variant | ABI2 | GRCh38.p7 | 2:203412618 | TCACATATAATTAGG[-/T]TGATTTCATATGTTT | 10152 |
rs3884656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369230 | CCTAAAATTTTTCCA[G/T]GTTTGAAGCATTAGC | 10152 |
rs3950504 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203392329 | ccaacaacaacaaca[A/C]caacaacaacaacaa | 10152 |
rs4234075 | snp | A/G | 0.453818 | 0.144769 | intron-variant | ABI2 | GRCh38.p7 | 2:203386393 | TGATCCTCCTGCCTC[A/G]GCCTCTCAAGTAGCG | 10152 |
rs4261696 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | ABI2 | GRCh38.p7 | 2:203369592 | TGGTCAATTAATGCT[A/G]TCTTTTAAAGCTATC | 10152 |
rs4315500 | snp | G/T | 0.454182 | 0.144256 | intron-variant | ABI2 | GRCh38.p7 | 2:203347163 | GTCCTAACAGGGTAA[G/T]GAGTGATCATATAGA | 10152 |
rs4433982 | snp | A/G | 0.454302 | 0.144085 | intron-variant | ABI2 | GRCh38.p7 | 2:203347033 | GGACTTTGTGTTCTT[A/G]CATGAGTTTCATATA | 10152 |
rs4496323 | snp | G/T | 0.0112482 | 0.0741458 | intron-variant | ABI2 | GRCh38.p7 | 2:203421433 | tttgttgaaagcaaa[G/T]gaataagagccacct | 10152 |
rs4505504 | snp | C/G | 0.451359 | 0.148171 | intron-variant | ABI2 | GRCh38.p7 | 2:203335471 | CTCACTATGTTGCTC[C/G]GGCTGGTCTTGGAAC | 10152 |
rs4507085 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ABI2 | GRCh38.p7 | 2:203361940 | ATTACTTCCCTTGTG[A/G]TCCTTCATGAATCCT | 10152 |
rs4588167 | snp | A/T | 0.16976 | 0.236773 | intron-variant | ABI2 | GRCh38.p7 | 2:203371941 | tttatttatttattt[A/T]tttttaattgatcat | 10152 |
rs4599086 | snp | G/T | 0.350327 | 0.228986 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326982 | CTAATTTTTTTATTT[G/T]TATTTTTAGTAGAGA | 10152 |
rs4673255 | snp | A/G | 0.453939 | 0.144598 | intron-variant | ABI2 | GRCh38.p7 | 2:203353737 | tttttacctcaagtg[A/G]tctgtccaccttggc | 10152 |
rs4675332 | snp | C/T | 0.229429 | 0.249152 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326184 | TCACCCTTTGATTTC[C/T]TGATAAGGAAACTAG | 10152 |
rs4675333 | snp | C/T | 0.00162074 | 0.0284209 | intron-variant | ABI2 | GRCh38.p7 | 2:203342254 | CTCATGGACCAAGTC[C/T]AGTTCTGTTACCATT | 10152 |
rs4675334 | snp | A/G | 0.454784 | 0.1434 | intron-variant | ABI2 | GRCh38.p7 | 2:203347768 | TGTAGGTGCTTGTTT[A/G]GTTATTGGGTGTTGT | 10152 |
rs4675335 | snp | C/T | 0.454784 | 0.1434 | intron-variant | ABI2 | GRCh38.p7 | 2:203348184 | TGGCGAAGGTTGCAG[C/T]GAGCAGAGATCGCGC | 10152 |
rs4675336 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | ABI2 | GRCh38.p7 | 2:203351836 | ctaccgcacccagcc[A/G]gttttcagtgtttca | 10152 |
rs4675337 | snp | C/T | 0.16846 | 0.236329 | intron-variant | ABI2 | GRCh38.p7 | 2:203373198 | gagtgaaccagactc[C/T]gtctgcaatcccggc | 10152 |
rs4675338 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | ABI2 | GRCh38.p7 | 2:203402171 | TCCCGAGTAGCTGGA[A/G]TTACAGGCGCACGCC | 10152 |
rs5028343 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203392320 | CCACCACCACCAACA[A/C]CAACAACAACAACAA | 10152 |
rs5028344 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203392323 | CCACCACCAACAACA[A/C]CAACAACAACAACAA | 10152 |
rs5741596 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392325 | accaccaacaacaac[-/AA]caacaacaacaacaa | 10152 |
rs5837850 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369489 | AAGGTGAATACTCAG[-/C]CCACCCTAGATTTTG | 10152 |
rs5837854 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403743 | TGTTCTTTCTTTCTG[G/T]TTTTTTTTTTTTTTT | 10152 |
rs6435184 | snp | C/G | 0.451608 | 0.147832 | intron-variant | ABI2 | GRCh38.p7 | 2:203338115 | gagcccggaaatgta[C/G]ccacatctgtgcagt | 10152 |
rs6435185 | snp | C/T | 0.16976 | 0.236773 | intron-variant | ABI2 | GRCh38.p7 | 2:203348780 | tccattattaatatc[C/T]gtctccagagtggta | 10152 |
rs6712670 | snp | C/T | 0.453818 | 0.144769 | intron-variant | ABI2 | GRCh38.p7 | 2:203401207 | AGTGTTTTTTTTTTC[C/T]TTTTCACTTATCTCC | 10152 |
rs6712824 | snp | A/G | 0.453818 | 0.144769 | intron-variant | ABI2 | GRCh38.p7 | 2:203401150 | CCATGAAATGTTTCA[A/G]TGGATTCTTTTGCCC | 10152 |
rs6721546 | snp | C/T | 0.479663 | 0.0987666 | intron-variant | ABI2 | GRCh38.p7 | 2:203403782 | ATTGAGATGGAGTCT[C/T]GCTCTGTTGCCCAGG | 10152 |
rs6725575 | snp | C/T | 0.453331 | 0.145452 | intron-variant | ABI2 | GRCh38.p7 | 2:203404763 | AGGGTTTCACCATAT[C/T]GGCCAAGCTGGTCTT | 10152 |
rs6735597 | snp | C/T | 0.454544 | 0.143743 | intron-variant | ABI2 | GRCh38.p7 | 2:203408878 | GCTCTGTCGCCCAGG[C/T]CGGACTGCGGACTGC | 10152 |
rs6739662 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338959 | atatatatatatata[A/T]ataaatatatatata | 10152 |
rs6744342 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203414501 | TTCCTTCAGGTTTCA[G/T]GAAGCCTTTCCTGAC | 10152 |
rs6747611 | snp | A/T | 0.108402 | 0.206034 | intron-variant | ABI2 | GRCh38.p7 | 2:203381821 | GTAATCCCATTTTTT[A/T]AAAATATATAATTCA | 10152 |
rs6750075 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203338936 | tgtgtgtgtatatgt[A/G]tatatatatatatat | 10152 |
rs6753045 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338963 | atatatatatatata[A/T]atatatatatatata | 10152 |
rs6754063 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ABI2 | GRCh38.p7 | 2:203339749 | gcattattcatggta[A/G]ctaagatatggaaac | 10152 |
rs6759306 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203384300 | TTTTTGTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |
rs7355645 | snp | C/G | 0.453575 | 0.145111 | intron-variant | ABI2 | GRCh38.p7 | 2:203350509 | tagacactaccacat[C/G]tggttactatttttT | 10152 |
rs7563751 | snp | A/G | 0.455024 | 0.143057 | intron-variant | ABI2 | GRCh38.p7 | 2:203343381 | AACATAAAAAAATTT[A/G]ATGTTAGCAGGTTAG | 10152 |
rs7563826 | snp | A/T | 0.454904 | 0.143228 | intron-variant | ABI2 | GRCh38.p7 | 2:203357100 | TTACCACACTCAATT[A/T]TTTCCTAATATAAAA | 10152 |
rs7569951 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ABI2 | GRCh38.p7 | 2:203385094 | cgcctcggcctccca[A/G]agtgttgggattaca | 10152 |
rs7571768 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203338430 | ctcatgaatgatgta[A/G]caccatccctttagt | 10152 |
rs7588790 | snp | A/T | 0.455144 | 0.142885 | intron-variant | ABI2 | GRCh38.p7 | 2:203379706 | AGGGAAAAATTAGCA[A/T]GCTTTAACCcagggg | 10152 |
rs7590031 | snp | C/T | 0.453697 | 0.14494 | intron-variant | ABI2 | GRCh38.p7 | 2:203333947 | CTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTGAGA | 10152 |
rs7590439 | snp | A/C | 0.0777841 | 0.181223 | intron-variant | ABI2 | GRCh38.p7 | 2:203336319 | gtaaatTtaagggaa[A/C]agatcaactgttgta | 10152 |
rs7593791 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203377767 | agaaattaggccagc[A/T]tggtggaacacgcct | 10152 |
rs7593851 | snp | A/G | 0.4582 | 0.138394 | intron-variant | ABI2 | GRCh38.p7 | 2:203374065 | tcaggaggctgaggc[A/G]ggagtatcacttgag | 10152 |
rs7597005 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203415486 | gctgggtgtggtggc[A/G]ggcgcctgtagtccc | 10152 |
rs7598891 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203333149 | ATGATACAAAGattt[A/G]aaatttttatttaat | 10152 |
rs7603053 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392314 | ccaccaccaccacca[A/C]caacaacaacaacaa | 10152 |
rs9678024 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338983 | atatatatatatata[A/T]atatatatatatata | 10152 |
rs9711744 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415471 | aaatacaaaaaatta[A/G]ctgggtgtggtggcg | 10152 |
rs9917202 | snp | C/G | 0.453818 | 0.144769 | intron-variant | ABI2 | GRCh38.p7 | 2:203380777 | AGTTTTCAAAAACAA[C/G]ATATATTAATAGACA | 10152 |
rs9917228 | snp | C/T | 0.089084 | 0.191327 | intron-variant | ABI2 | GRCh38.p7 | 2:203378386 | aaagtgctgggatta[C/T]aggcgtgagccacca | 10152 |