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 |
rs9967674 | snp | C/T | 0.084728 | 0.187577 | intron-variant | ABI2 | GRCh38.p7 | 2:203363578 | cttctactctctatt[C/T]ctgtgagttcaattg | 10152 |
rs10167132 | snp | A/G | 0.454784 | 0.1434 | intron-variant | ABI2 | GRCh38.p7 | 2:203354150 | cccgggctcaagcca[A/G]cctcccaccttggcc | 10152 |
rs10172421 | snp | A/C | 0.131038 | 0.219882 | intron-variant | ABI2 | GRCh38.p7 | 2:203373679 | GAAAGTAGTGCTCTT[A/C]CCACCTTCCCAAGGG | 10152 |
rs10172500 | snp | A/G | 0.078151 | 0.181571 | intron-variant | ABI2 | GRCh38.p7 | 2:203336560 | gagatgaggctctct[A/G]ttgtacccttttagg | 10152 |
rs10175337 | snp | C/G | 0.45843 | 0.138046 | intron-variant | ABI2 | GRCh38.p7 | 2:203344043 | GAGGCTGAGGTGGGA[C/G]GATTGCTTGAGCTCA | 10152 |
rs10180372 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203386524 | ACTTAACAAGTTTAA[A/G]AAATTATTAGGGAAG | 10152 |
rs10190316 | snp | C/T | 0.453575 | 0.145111 | intron-variant | ABI2 | GRCh38.p7 | 2:203350303 | gctggcctcgaactc[C/T]tgacctcaggtgatc | 10152 |
rs10191084 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ABI2 | GRCh38.p7 | 2:203377184 | GCTGGGCATGGTGGT[A/G]CATGCCTGTAGTCCT | 10152 |
rs10196646 | snp | A/G | 0.451856 | 0.147493 | intron-variant | ABI2 | GRCh38.p7 | 2:203336845 | ccgtatggtaaatgt[A/G]tgtttagttttatac | 10152 |
rs10197623 | snp | A/T | 0.236434 | 0.249632 | intron-variant | ABI2 | GRCh38.p7 | 2:203379036 | CTTGCAGTTTAAAAA[A/T]TTTTGCTTTAGTGTA | 10152 |
rs10209341 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340322 | ctaatgtactgtgta[A/G]taactatagttaata | 10152 |
rs10221588 | snp | A/G | 0.368003 | 0.236235 | intron-variant | ABI2 | GRCh38.p7 | 2:203378313 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 10152 |
rs10527327 | in-del | -/TTTTTT | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203385139 | ACCCGGCTCAGATTC[-/TTTTTT]TTTTTTTTTTTTTGA | 10152 |
rs10581610 | in-del | -/TTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400104 | TTTTTTTTTTTTTTT[-/TTTT]GAGACAGAGTCTCAC | 10152 |
rs10623184 | in-del | -/TA | 0.454061 | 0.144427 | intron-variant | ABI2 | GRCh38.p7 | 2:203403645 | TGGTGATCATTTTCT[-/TA]TATATCTTATAGGTA | 10152 |
rs10623488 | in-del | -/TTTA/TTTATTTA | 0.497329 | 0.0364438 | intron-variant | ABI2 | GRCh38.p7 | 2:203342552 | TCTCCCTCAAAACCT[-/TTTA/TTTATTTA]TTTATTTATTTATTT | 10152 |
rs10643013 | in-del | -/ACAA | 0.223225 | 0.248562 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432489 | TTTTTAATTCAACAG[-/ACAA]ACAAACACTGAAGAT | 10152 |
rs10686349 | in-del | -/AG | 0.455263 | 0.142713 | intron-variant | ABI2 | GRCh38.p7 | 2:203385157 | TTTTTTTTTTGAGAC[-/AG]AGTCTTGCCGTTGCC | 10152 |
rs10711758 | in-del | -/T | 0.455024 | 0.143057 | intron-variant | ABI2 | GRCh38.p7 | 2:203356849 | TTTGGTTTTACACAA[-/T]TTTTTTTTTTTTAGG | 10152 |
rs10932014 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | ABI2 | GRCh38.p7 | 2:203385966 | TTTGTCTTTTAACCC[G/T]TTTTCTAAAAATCTT | 10152 |
rs11302309 | in-del | -/T | 0.456568 | 0.140818 | intron-variant | ABI2 | GRCh38.p7 | 2:203408166 | TGGCTGCTGGTGGAC[-/T]TTTTTTTTTTTTTGA | 10152 |
rs11325262 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203369914 | CCTCAAGGATTGAAA[-/T]TTTTTTTTTTTACTT | 10152 |
rs11370456 | in-del | -/A | 0.347473 | 0.230215 | intron-variant | ABI2 | GRCh38.p7 | 2:203394400 | CTCTTCTAAGAAGAG[-/A]GTAGGGTCTGGGAAA | 10152 |
rs11376266 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329342 | TTTTTTTTTTTTTTT[-/T]ACCGTGATGGATCGT | 10152 |
rs11390894 | in-del | -/T/TT | 0.492188 | 0.0620098 | intron-variant | ABI2 | GRCh38.p7 | 2:203334668 | ATTTTTTTTTTTTTT[-/T/TT]GAGACAGAGTCTCTG | 10152 |
rs11673977 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203376843 | TGTCCCCAATCCCTA[A/G]ACCAAGTCACATCTC | 10152 |
rs11675251 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | ABI2 | GRCh38.p7 | 2:203384676 | TATGATGTGTTTGTA[A/G]TGAATTTTTCTGTTG | 10152 |
rs11682759 | snp | C/T | 0.452719 | 0.146304 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327478 | TTCAAGGTATTTTCA[C/T]AATAAACGTTGATTT | 10152 |
rs11683496 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370238 | tctctttctgtgtgt[A/G]tgtgtgtgtgtgtac | 10152 |
rs11686036 | snp | A/G | 0.479824 | 0.098392 | intron-variant | ABI2 | GRCh38.p7 | 2:203376916 | TTTTTTAAAGTCTCA[A/G]TTTTTCAAACAAGAA | 10152 |
rs11687758 | snp | A/G | 0.475437 | 0.108066 | intron-variant | ABI2 | GRCh38.p7 | 2:203378258 | GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCC | 10152 |
rs11694861 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370224 | tctctctctctctct[C/T]tctttctgtgtgtat | 10152 |
rs11903155 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365989 | ctttgtttatttttg[G/T]tttttaaattttttt | 10152 |
rs12233048 | snp | A/G | 0.104149 | 0.203046 | intron-variant | ABI2 | GRCh38.p7 | 2:203388186 | AAACATTTTTCACAC[A/G]GGAAAAGCTGCCTTG | 10152 |
rs12466364 | snp | A/G | 0.239326 | 0.249772 | intron-variant | ABI2 | GRCh38.p7 | 2:203361608 | GGAAAACAGAATGAA[A/G]ACTAAAAAAAAGGAG | 10152 |
rs12466863 | snp | G/T | 0.00934559 | 0.067716 | intron-variant | ABI2 | GRCh38.p7 | 2:203424929 | caggctagagtgcag[G/T]gggaaaatcacggct | 10152 |
rs12474416 | snp | G/T | 0.236434 | 0.249632 | intron-variant | ABI2 | GRCh38.p7 | 2:203361280 | GGAGTCAATTCTCGG[G/T]CTTAAATCACCATAT | 10152 |
rs12478920 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425500 | agctaccgcacctgg[C/G]tGGATTTGCATTTCT | 10152 |
rs12617119 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ABI2 | GRCh38.p7 | 2:203340170 | gaggaatctaaaaag[A/T]tgaacccatagaatg | 10152 |
rs12621896 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203398749 | gtaagcccttgatgt[G/T]ttttttttctctaaa | 10152 |
rs12693985 | snp | A/C | 0.454664 | 0.143571 | intron-variant | ABI2 | GRCh38.p7 | 2:203350688 | gggattacgggtgcc[A/C]gccactgtgcgcagc | 10152 |
rs12693986 | snp | A/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203368985 | GCCATGCTTGGCTGA[A/T]TTTTTTTTTTTTTTT | 10152 |
rs12693989 | snp | C/T | 0.237014 | 0.249662 | intron-variant | ABI2 | GRCh38.p7 | 2:203406788 | CCTGCCTCAGCCTCC[C/T]GAGTAGTTGGAACTA | 10152 |
rs12999728 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369014 | ttttttttttttttt[C/T]ttgtagagacagtgt | 10152 |
rs13000591 | snp | C/T | 0.16976 | 0.236773 | intron-variant | ABI2 | GRCh38.p7 | 2:203355703 | aggcatggtggcgca[C/T]gcctgtaatcccagc | 10152 |
rs13011243 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203328743 | CAGCGGAGCCCCCGA[A/T]GGGGGTGGGGAGCTG | 10152 |
rs13012348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332392 | agcactttgggaggc[C/T]gaggcaggcacatca | 10152 |
rs13017614 | snp | G/T | 0.12033 | 0.213742 | intron-variant | ABI2 | GRCh38.p7 | 2:203419707 | ATGTGGTTTGCCTTG[G/T]TTAATATAAGAATGC | 10152 |
rs13018824 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203333297 | TTAAATATTTTTTGT[A/G]TGCACAACTATATAT | 10152 |
rs13030411 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203391160 | TGAGTATATAAGTAG[G/T]AATTGAAAACCATTT | 10152 |
rs13032873 | snp | A/C | 0.020759 | 0.0997424 | intron-variant | ABI2 | GRCh38.p7 | 2:203395485 | cacacacacacacac[A/C]TTTTTTTTTAACCTG | 10152 |
rs13033129 | snp | A/C | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203425697 | TATATTGAGAAATGC[A/C]CACTGATCTCTTCCT | 10152 |
rs13033346 | snp | C/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203425725 | CCTAGCAAGGATCTT[C/G]TAAAGTATTTTCTga | 10152 |
rs13034297 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203328734 | GACACGGCCCAGCGG[A/T]GCCCCCGATGGGGGT | 10152 |
rs13034304 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203328742 | CCAGCGGAGCCCCCG[A/C]TGGGGGTGGGGAGCT | 10152 |
rs13034762 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404044 | aggcgtgagtcaccg[G/T]gcctggccTAAGTTC | 10152 |
rs13034859 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203328735 | ACACGGCCCAGCGGA[A/G]CCCCCGATGGGGGTG | 10152 |
rs13392546 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349023 | ctgcagcctctacct[C/T]gtgggttcaagtgat | 10152 |
rs13394373 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404743 | tttgtatttttagta[A/G]agacagggtttcacc | 10152 |
rs13406479 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328356 | CGCCCCGCCCCCGTC[A/G]CCCCCTCCCCTGTCG | 10152 |
rs13406703 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203328740 | GCCCAGCGGAGCCCC[C/T]GATGGGGGTGGGGAG | 10152 |
rs13410515 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404971 | TTTAAATGCATTTTA[A/T]AATACATACTTCAAT | 10152 |
rs13415818 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203336104 | aatacatttgaaaat[A/C]atcagtgttattgtg | 10152 |
rs13416670 | snp | A/G | 0.227074 | 0.248947 | intron-variant | ABI2 | GRCh38.p7 | 2:203421051 | TAAAAATGACAATGC[A/G]AAGGTGTTGGATTAA | 10152 |
rs13420014 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | ABI2 | GRCh38.p7 | 2:203388687 | ctctgtcttaaaaaa[A/T]aaTAATAATAATAAT | 10152 |
rs13421513 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203410194 | TCCACCACTACTTCC[A/G/T]GGGAATTGCTACAAA | 10152 |
rs13423002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203338093 | tgtagactaatggaa[C/T]agaatggagcccgga | 10152 |
rs13426676 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ABI2 | GRCh38.p7 | 2:203360138 | tgcagggagctaaga[C/T]tgcaccactgcactc | 10152 |
rs13426786 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203369189 | TGCTAATGTGATATA[A/G]AATTTCAAGATCTAT | 10152 |
rs13426796 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203369211 | AAGATCTATTCTTGA[A/G]AATCCTAAAATTTTT | 10152 |
rs13426898 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369293 | AACAAATATAGAAGA[A/G]AAACTAGTATATTTG | 10152 |
rs13430194 | snp | G/T | 0.452103 | 0.147154 | intron-variant | ABI2 | GRCh38.p7 | 2:203330940 | GAAAAGAGAAAAACG[G/T]TACTACTATCAATCT | 10152 |
rs13430972 | snp | A/G | 0.455144 | 0.142885 | intron-variant | ABI2 | GRCh38.p7 | 2:203370753 | TGTAGAGAAGATTGA[A/G]TTGAAGGAATGGAGG | 10152 |
rs13431054 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425044 | ttttttttttttttt[G/T]tattttttttttggt | 10152 |
rs16839728 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203375280 | TGTAGCAAACAATAA[C/T]TATATTAATTGTGTA | 10152 |
rs16839737 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | ABI2 | GRCh38.p7 | 2:203383883 | TTTTCTCTTTCTCAG[A/C]ACTTTTTGAGCTCTG | 10152 |
rs16839748 | snp | C/T | 0.039522 | 0.134904 | intron-variant | ABI2 | GRCh38.p7 | 2:203388885 | TAGCTATCCCATGTA[C/T]AGAATAAAATTCTCT | 10152 |
rs16839765 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | ABI2 | GRCh38.p7 | 2:203406141 | GAAACACATAGGGCT[A/C]ATTATGAGTTAACAG | 10152 |
rs16839772 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | ABI2 | GRCh38.p7 | 2:203408095 | ACTAGCTTTGAAAAA[A/C]GTCTAACTTGTTACC | 10152 |
rs16839780 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | ABI2 | GRCh38.p7 | 2:203410306 | TTAGTTTTATTAGTC[C/T]TAACTGTATTTTGGA | 10152 |
rs16839798 | snp | A/C/T | 0.0130921 | 0.0798413 | intron-variant | ABI2 | GRCh38.p7 | 2:203426516 | TATAGGTATCTGATT[A/C/T]TCTTGTCACTTTTAG | 10152 |
rs17194468 | snp | C/T | 0.108755 | 0.206276 | intron-variant | ABI2 | GRCh38.p7 | 2:203388185 | GAAACATTTTTCACA[C/T]GGGAAAAGCTGCCTT | 10152 |
rs17194601 | snp | A/T | 0.154993 | 0.231244 | intron-variant | ABI2 | GRCh38.p7 | 2:203394018 | ACAGTTCAAAGTAAA[A/T]AATATAGAAAGGCTG | 10152 |
rs17410408 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | ABI2 | GRCh38.p7 | 2:203408635 | AAAGGTCATTTTTTA[C/T]ATTTGGTAGAGAAAC | 10152 |
rs17509508 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ABI2 | GRCh38.p7 | 2:203370165 | TAGGTTTTGTGGGCT[A/G]CGTATGGTGTCATTC | 10152 |
rs17807416 | snp | A/T | 0.479663 | 0.0987666 | intron-variant | ABI2 | GRCh38.p7 | 2:203413985 | GCTCTTTGGATAGAG[A/T]CCAAACTGCTGTAAG | 10152 |
rs28377564 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411276 | TCCACACCTTTTTTG[G/T]TTTTGCAGTATCTCT | 10152 |
rs28398013 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203384301 | TTTTGTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |
rs28516605 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370262 | TGTGTACTTTTTTTT[G/T]TTTGGTTGGGGGATG | 10152 |
rs28550614 | snp | G/T | 0.493568 | 0.0563433 | intron-variant | ABI2 | GRCh38.p7 | 2:203384317 | TTTTTTTTTTTTTTT[G/T]TTTTTTTGAGACAGG | 10152 |
rs28595531 | snp | G/T | 0.469544 | 0.119585 | intron-variant | ABI2 | GRCh38.p7 | 2:203384313 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTGAGA | 10152 |
rs28641947 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402423 | CTGATATAATATCAG[C/G]GAACAATAACTCACC | 10152 |
rs34003485 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358832 | TGACTAACATGGCGA[-/G]AACCCAATCTCTACT | 10152 |
rs34081725 | in-del | -/A | 0.293037 | 0.246268 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431697 | TCTCATATAATTATT[-/A]AAAAAAAAAAACAAT | 10152 |
rs34149664 | in-del | -/AT/TA | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203403646 | GGTGATCATTTTCTT[-/AT/TA]ATATCTTATAGGTAA | 10152 |
rs34182021 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355863 | AAACACCCCACCAAG[-/A]AAACCCCTGGTGTGC | 10152 |
rs34280755 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428167 | GCTAGACACGAAGGT[-/C]CCTAAGGTTCTGAAG | 10152 |
rs34320356 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346934 | ATGTGCTATAGTGCA[-/T]TTTTAAAATTTATTC | 10152 |
rs34342850 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341201 | CTTATCCTTCCATGC[-/T]TTTTTTTACGCCTAC | 10152 |
rs34364876 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408890 | GGTCGGACTGCGGAC[-/T]TGCAGTGGCGCAATC | 10152 |
rs34391928 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392469 | AGTAGGAGACCAAAG[-/T]AATAAAAATAAATTC | 10152 |
rs34442709 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348011 | TTGGGAGGGTGAGGT[-/G]GGGTGGATCACTTGA | 10152 |
rs34459634 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354654 | ATAGCCAGCATATTA[C/G]CATTTTCTTGCACTA | 10152 |
rs34499527 | in-del | -/G | 0.444444 | 0.157135 | intron-variant | ABI2 | GRCh38.p7 | 2:203359846 | AACATGTACATTTTT[-/G]GGGGGGGGACACAAA | 10152 |
rs34530204 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426019 | GAGTGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 10152 |
rs34531531 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203339257 | ATCCTTGTGTGCAGT[A/G]AGAATGTAAATTGGA | 10152 |
rs34691115 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365896 | GCCTCACAAAGAGCT[-/G]GGGATTACAGGCGTG | 10152 |
rs34737067 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203399634 | GATTCTCCTGCCCAG[C/G]CTCCCAAATAGCTGG | 10152 |
rs34772464 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353892 | TTTGAGATTCAGACA[-/T]TTTTACTATGAGATA | 10152 |
rs34794951 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331198 | ATTTGTTGATTTGTT[-/G]GGGAAAGTTGATAAA | 10152 |
rs34801404 | in-del | -/T | 0.492337 | 0.0614248 | intron-variant | ABI2 | GRCh38.p7 | 2:203392967 | GCTCCTTTTTTTTTT[-/T]AAAAAAAATCTTATT | 10152 |
rs34889407 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417614 | GACTAATCAGCTCAG[-/A]AAAAAAATGTGTGCT | 10152 |
rs34955159 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377519 | GAAGACCCATTTTAT[-/A]AAAAAAGTGTCATAT | 10152 |
rs34981535 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ABI2 | GRCh38.p7 | 2:203329026 | GTTGACGGGTTACCT[C/T]CATCCCCCAAATTCT | 10152 |
rs35021678 | in-del | -/TTT | 0.479744 | 0.0985793 | intron-variant | ABI2 | GRCh38.p7 | 2:203357044 | AAAGCGTTTTTAAAA[-/TTT]TTGTCTGTTTTTAAA | 10152 |
rs35036807 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346909 | GCCCTTGTTTGTGCT[-/G]GCCCGACTTCATGTG | 10152 |
rs35048548 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397072 | GTTGTACTTCGTATT[-/A]AAAAAAAATAAGAAT | 10152 |
rs35048688 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203428091 | CATTGTTGCTAATGG[-/C]CCAGTGTACCCAGAT | 10152 |
rs35071165 | snp | A/T | 0.230603 | 0.249246 | intron-variant | ABI2 | GRCh38.p7 | 2:203378174 | CTGGAGTGCAGTGGC[A/T]CAATCTCGGCTCATT | 10152 |
rs35102540 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376752 | TTTTTTTTTTTTTTT[-/TT]ACTGTTATGGTCTAT | 10152 |
rs35109897 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357456 | AAATACCTAGGTGAC[-/T]TTTATGTTCTGAATC | 10152 |
rs35131904 | snp | A/C | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203348616 | ATGTAATATCACCTC[A/C]CCTGGGTGAAATGAG | 10152 |
rs35175710 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392673 | TTTCCTATGTAAACA[-/T]TTTACATTTATATCA | 10152 |
rs35202752 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333872 | TGAAGAGCTTCCTGG[G/T]TCAAAATTGCTCTTT | 10152 |
rs35302825 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350214 | TTTGAGTAGCTGGGA[-/T]TATGGGTGTGCATTA | 10152 |
rs35331844 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203379291 | CTTGCTCTGTCACCC[A/G]GGCTAGAGTGCAGTG | 10152 |
rs35371788 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355114 | CCCTTTTCCTCTTTG[-/A]ATGTAGATCCTATTT | 10152 |
rs35382487 | in-del | -/T/TT/TTT/TTTT | 0.652814 | 0.132616 | intron-variant | ABI2 | GRCh38.p7 | 2:203351532 | TTTTTTTTTTTTTTT[-/T/TT/TTT/TTTT]CCTTTAGAGATGGGG | 10152 |
rs35399279 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385272 | AGTAGCTGGGACTAC[-/A]AGGCGCCCGCCACCT | 10152 |
rs35433899 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203384314 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTGAGAC | 10152 |
rs35435663 | in-del | -/A | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203421965 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10152 |
rs35485952 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ABI2 | GRCh38.p7 | 2:203348109 | AGCTGGGCATGATGG[C/T]GGGTGTCTGTAATCC | 10152 |
rs35496113 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408471 | CCTGGCTGCTGGTGT[-/A]CTTCTTAAAACCACT | 10152 |
rs35497226 | in-del | -/T | 0.0948562 | 0.196037 | intron-variant | ABI2 | GRCh38.p7 | 2:203387057 | CGCAGGCTCCCTTCC[-/T]TTTTTTTTTTTTTTT | 10152 |
rs35505933 | in-del | -/A | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203330393 | GTGAGACTACATATC[-/A]AAAAAAAAAAAAAAA | 10152 |
rs35533326 | snp | C/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203367212 | CTTTTTGTGGGATGG[C/T]TATCTTCTCTGTGAT | 10152 |
rs35598384 | in-del | -/T | 0.494526 | 0.0520291 | intron-variant | ABI2 | GRCh38.p7 | 2:203367323 | CCTTTTTTTTTTTTT[-/T]AAAACAAATTTCATA | 10152 |
rs35646820 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402153 | ATTCTTACGCCTCAG[-/T]CCTCCCGAGTAGCTG | 10152 |
rs35652563 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395000 | CTCTCTCCTCATGTT[-/A]CTGATTCAACTTTGA | 10152 |
rs35657892 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430320 | TCCAAAATCTGACCA[A/G]TAAAGCAACCATTTT | 10152 |
rs35725229 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342107 | TCATTTCTTAGTGTT[-/C]CAGTAAATTTTTGTT | 10152 |
rs35748117 | in-del | -/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203364749 | TACATATTTTTTTAA[-/T]TTTTTTTTTTTTTTC | 10152 |
rs35757626 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420706 | CCGACAGTCCCTTAT[A/C]TGGTTCATCTTCGTA | 10152 |
rs35773712 | in-del | -/AT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411001 | TATAAAAATGGGATT[-/AT]GTTTTATATATATAA | 10152 |
rs35925477 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398523 | TTTATACAGTACCTG[-/A]AGTTACCAAGCAATT | 10152 |
rs35936869 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351554 | TTTTTTTTTCCTTTA[A/G]AGATGGGGTCTTGGT | 10152 |
rs35984578 | in-del | -/ACAA | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432490 | TTTTAATTCAACAGA[-/ACAA]CAAACACTGAAGATG | 10152 |
rs36029719 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361405 | TGGGAGGCAGAGGCA[-/G]GGAGGATCACTTGAG | 10152 |
rs36077271 | in-del | -/TTTA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342585 | TATTTATTTATTTAT[-/TTTA]TTATTTATTTTTGAG | 10152 |
rs36113671 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404579 | TTGTTTTGTTTTGAG[-/T]ACAAAGTCTTGCTCT | 10152 |
rs55692341 | snp | C/T | 0.479663 | 0.0987666 | intron-variant | ABI2 | GRCh38.p7 | 2:203393203 | GGGATTACAGGTGTG[C/T]GCCACCATTCCCAGC | 10152 |
rs55695294 | in-del | -/TT | 0.412416 | 0.190055 | intron-variant | ABI2 | GRCh38.p7 | 2:203331826 | TTTTTTTTTTTTTTT[-/TT]GACACAGAGTTTCAC | 10152 |
rs55793025 | in-del | -/AT | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203403650 | ATCATTTTCTTATAT[-/AT]CTTATAGGTAAGGAA | 10152 |
rs55860222 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203383167 | TTTAGTGTAGAAAGT[A/G]ATGACAAGATGACTG | 10152 |
rs55944850 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401206 | AAGTGTTTTTTTTTT[C/T]CTTTTCACTTATCTC | 10152 |
rs56102509 | in-del | -/CCCGA | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203330208 | TGTATTTGAGAATGA[-/CCCGA]ACCACTGTATAAACC | 10152 |
rs56123341 | in-del | -/T/TT | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203403764 | TTTTTTTTTTTTTTT[-/T/TT]AAATTGAGATGGAGT | 10152 |
rs56143510 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | ABI2 | GRCh38.p7 | 2:203425935 | CTGAGGCAAGAGAAT[C/T]GCTTGAACCTGGGAC | 10152 |
rs56147729 | in-del | -/AATATATATATATATATATAAATATATATATATA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338963 | ATATATATATATATA[lengthTooLong]TATATATATATAAAG | 10152 |
rs56331960 | in-del | -/GTATATGT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338928 | TGTGTGTGTGTGTGT[-/GTATATGT]ATATATATATATATA | 10152 |
rs56362828 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392310 | ACCACCACCACCACC[A/C]CCACCAACAACAACA | 10152 |
rs56735374 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339612 | AGAAAAAGAAAAAAA[A/G]AAAACCCAGTTCTCC | 10152 |
rs56896436 | in-del | -/GTGTATATGT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338926 | TGTGTGTGTGTGTGT[-/GTGTATATGT]ATATATATATATATA | 10152 |
rs56966940 | in-del | -/G/TTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344568 | TGTTGTTGTTTTTGT[-/G/TTTTT]TTTTTTTTTTTGAGT | 10152 |
rs57525574 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392315 | CACCACCACCACCAC[C/T]AACAACAACAACAAC | 10152 |
rs57591649 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358115 | GTGTGTGTGTGTGTT[-/G]TGTTTGTTTGTTTGT | 10152 |
rs57594422 | in-del | -/ATTT/ATTTATTT | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203342595 | TTTATTTATTTATTT[-/ATTT/ATTTATTT]TTGAGACAAGGTCTC | 10152 |
rs58019010 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358114 | TGTGTGTGTGTGTGT[-/G]TTGTTTGTTTGTTTG | 10152 |
rs58027191 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395452 | ATATATATATATACA[C/T]ACACACACACACACA | 10152 |
rs58382543 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387349 | GGTAGGAGCATTGTA[A/G]AAAAAGTATTAAGTC | 10152 |
rs58478831 | snp | C/G | 0.407845 | 0.193868 | intron-variant | ABI2 | GRCh38.p7 | 2:203397903 | AACAGCTCCAAGGGG[C/G]ATGGTGTTAAACCAT | 10152 |
rs58766130 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344563 | GTTGTTGTTGTTGTT[-/G]TTTGTTTTTTTTTTT | 10152 |
rs58788722 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ABI2 | GRCh38.p7 | 2:203343310 | CGGAGGTTGCAGTTA[C/G]CTGAGATTGCGGCAC | 10152 |
rs58857922 | in-del | -/A | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203360207 | AAAAAAAAAAAAAAA[-/A]GAAGCAGTTGTACCC | 10152 |
rs59111250 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420411 | CTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 10152 |
rs59156204 | in-del | -/CA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395485 | ACACACACACACACA[-/CA]TTTTTTTTTAACCTG | 10152 |
rs59217427 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398693 | AAATTTCCTCCATGC[C/T]CCCTTTATAGTCAGT | 10152 |
rs59583332 | snp | C/T | 0.347253 | 0.230308 | intron-variant | ABI2 | GRCh38.p7 | 2:203364749 | ATTTTTTTTTTTTTT[C/T]CAAGAGACAGGGTCT | 10152 |
rs59683844 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426804 | AAAAAAAAAAAAAAA[-/A]CCACAATATGGTATC | 10152 |
rs60160570 | in-del | -/TTTGTTTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357780 | TTGTTTGTTTGTTTG[-/TTTGTTTG]AGACAGAGTCTCACT | 10152 |
rs60510573 | in-del | -/AATATATATATATATATA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338983 | ATATATATATATATA[-/AATATATATATATATATA]TATATATAAAGGATT | 10152 |
rs60676560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203426538 | CACTTTTAGTCTGTT[A/G]TTATAGTTATATTAA | 10152 |
rs60777028 | in-del | -/TTTTTTTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364105 | CTTTTTTTTTTTTTT[-/TTTTTTTTTT]AAGTTTTATTTTGAG | 10152 |
rs60880097 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344567 | GTTGTTGTTGTTTTT[G/T]TTTTTTTTTTTTGAG | 10152 |
rs60905637 | snp | A/G | 0.482534 | 0.0918038 | intron-variant | ABI2 | GRCh38.p7 | 2:203336342 | CTGTTGTACCCTGGT[A/G]ACAGTGGATGTATCC | 10152 |
rs61021024 | in-del | -/AATATATATATATATATATAAATA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338963 | ATATATATATATATA[-/AATATATATATATATATATAAATA]TATATATATATATAT | 10152 |
rs61124951 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | ABI2 | GRCh38.p7 | 2:203363153 | AAATACTTTTACATT[-/A]AAAAAAAATTTTTCG | 10152 |
rs61207824 | in-del | -/AATATATATATATATATATAAATATATATATA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338963 | ATATATATATATATA[lengthTooLong]TATATATATATATAA | 10152 |
rs61252898 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | ABI2 | GRCh38.p7 | 2:203404764 | GGGTTTCACCATATC[A/G]GCCAAGCTGGTCTTG | 10152 |
rs61515485 | in-del | -/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203344579 | TTTGTTTTTTTTTTT[-/T]GAGTCGGAGGTTTGC | 10152 |
rs61601697 | snp | A/T | 0.475259 | 0.108435 | intron-variant | ABI2 | GRCh38.p7 | 2:203372261 | TAAGGTCACCGATCA[A/T]CAGGATCCCAAGGCA | 10152 |
rs61614046 | in-del | -/A/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426037 | AAAAAAAAAAAAAAA[-/A/AA]TTCTGGTGTTCCTAC | 10152 |
rs61659268 | snp | A/G | 0.00569908 | 0.053076 | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203375980 | GATGGCAAGAATGCA[A/G]ATTATACCGTTGTTA | 10152 |
rs62182770 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387079 | TTTTTTTTTTTTTCC[C/T]CACATGCCTTTACTC | 10152 |
rs62182771 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203392326 | CCACCAACAACAACA[A/C]CAACAACAACAACAA | 10152 |
rs62182774 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203398115 | AAACATATATAAGAT[C/G]TTTACATGTTTTAAA | 10152 |
rs62182775 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400041 | ATATTTTTAAAACCC[C/T]AAATGGTAAATCGAC | 10152 |
rs62182776 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403767 | TTTTTTTTTTTTTAA[A/T]TTGAGATGGAGTCTC | 10152 |
rs62182777 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405563 | TCAAAAAAAAAAAAT[A/T]ATGTAAGTCTCCTGT | 10152 |
rs62182778 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203414122 | TTTTTTTTTTTTTTG[G/T]AGACAGTCTCACTCT | 10152 |
rs62182779 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427483 | ACACTTTTTTTTTTG[G/T]TTTATTCCCCAGTAT | 10152 |
rs62183937 | snp | G/T | 0.347694 | 0.230122 | intron-variant | ABI2 | GRCh38.p7 | 2:203328965 | GAGTGGCATTTTCTG[G/T]TTGACGGAATCCTGC | 10152 |
rs62183938 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203331181 | GATGATAGCTCTTAT[A/G]TGATTTGTTGATTTG | 10152 |
rs62183939 | snp | G/T | 0.347914 | 0.230028 | intron-variant | ABI2 | GRCh38.p7 | 2:203333580 | TTAAGATGACTCAAC[G/T]CATTTGAAATTGATC | 10152 |
rs62183940 | snp | C/T | 0.483418 | 0.0895317 | intron-variant | ABI2 | GRCh38.p7 | 2:203334877 | TATTGGCCAGGCTGG[C/T]CTCGAGATCCTGACC | 10152 |
rs62183942 | snp | C/T | 0.127944 | 0.218179 | intron-variant | ABI2 | GRCh38.p7 | 2:203342704 | TCTGCCTCAGCCTCC[C/T]TAGTACTACTGCTGG | 10152 |
rs62183943 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ABI2 | GRCh38.p7 | 2:203349738 | TTTTACGGCTGAATA[A/G]TATTCTAGTACATGG | 10152 |
rs62183944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350170 | TAACCTCTGTCTCCC[A/G]GATTCAAGCCATTCT | 10152 |
rs62183945 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354500 | TATCAGTAAACTACC[A/G]ATTGTCAAGACCTTC | 10152 |
rs62183946 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203356849 | TTTGGTTTTACACAA[A/T]TTTTTTTTTTTTAGG | 10152 |
rs62183947 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203358122 | GTGTGTGTTTGTTTG[G/T]TTGTTTGTTTTTGAG | 10152 |
rs62183948 | snp | A/G | 0.347473 | 0.230215 | intron-variant | ABI2 | GRCh38.p7 | 2:203367873 | GCCAGGTTTGGTGGT[A/G]CACGCCTGTTGTCCC | 10152 |
rs62183950 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203374092 | TGAGCCCAGGTGGTC[A/G]AGGCTGCAGTGAGCC | 10152 |
rs62183951 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376731 | TACTGTATTGGTCTT[C/T]CCTTTTTTTTTTTTT | 10152 |
rs62183952 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ABI2 | GRCh38.p7 | 2:203377282 | TTGTCCCATTGCACT[C/G]CAGCCTCTGTGACAG | 10152 |
rs62183953 | snp | A/G | 0.346147 | 0.230772 | intron-variant | ABI2 | GRCh38.p7 | 2:203378177 | GAGTGCAGTGGCACA[A/G]TCTCGGCTCATTGCA | 10152 |
rs62183954 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387057 | CGCAGGCTCCCTTCC[C/T]TTTTTTTTTTTTTTT | 10152 |
rs62183955 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387076 | TTTTTTTTTTTTTTT[C/T]CCCCACATGCCTTTA | 10152 |
rs66629152 | in-del | -/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203403743 | TGTTCTTTCTTTCTG[-/T]TTTTTTTTTTTTTTT | 10152 |
rs66727221 | in-del | -/AGA | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203354710 | CATATTGTGATAAGA[-/AGA]GGCCCAGGTGATACT | 10152 |
rs67199066 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394401 | TCTTCTAAGAAGAGG[-/A]TAGGGTCTGGGAAAC | 10152 |
rs67540203 | in-del | -/GACCC | 0.451856 | 0.147493 | intron-variant | ABI2 | GRCh38.p7 | 2:203330206 | TTTGTATTTGAGAAT[-/GACCC]GAACCACTGTATAAA | 10152 |
rs67568159 | in-del | -/ATTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342560 | AAAACCTTTTATTTA[-/ATTT]TTTATTTATTTATTT | 10152 |
rs67984897 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363161 | TTACATTWAAAAAAA[A/T]TTTTTCGTGAGTATA | 10152 |
rs68164287 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | ABI2 | GRCh38.p7 | 2:203344568 | TTGTTGTTGTTTTTG[-/T]TTTTTTTTTTTGAGT | 10152 |
rs71007506 | in-del | -/TGTGTGTGTGTGTGTG | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203358091 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 10152 |
rs71007507 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365647 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 10152 |
rs71007508 | in-del | -/TTT | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203369014 | TTTTTTTTTTTTTTT[-/TTT]GTAAAGACAGTGTCT | 10152 |
rs71007509 | in-del | -/CT | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203370226 | TCTCTCTCTCTCTCT[-/CT]TTCTGTGTGTATGTG | 10152 |
rs71007510 | in-del | -/A | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203374519 | AAAAAAAAAAAAAAA[-/A]GGAATTTCCAATTTT | 10152 |
rs71007511 | in-del | -/TTTTTT | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203385152 | TCTTTTTTTTTTTTT[-/TTTTTT]GAGACAGTCTTGCCG | 10152 |
rs71007512 | in-del | -/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203386456 | TTTTTTTTTTTTTTT[-/T]GGAGAGACGTGGTCT | 10152 |
rs71007514 | in-del | -/ACAC | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203395459 | CACACACACACACAC[-/ACAC]ACACACACACACATT | 10152 |
rs71007515 | in-del | -/AAAAAAA | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203415637 | AAAAAAAAAAAAAAA[-/AAAAAAA]TCCATTTAATTCAAT | 10152 |
rs71007516 | in-del | -/A | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203421984 | AAAAAAAAAAAAAAA[-/A]TCTAGAAAGAGAGCC | 10152 |
rs71007517 | in-del | -/C | 0.359364 | 0.22481 | intron-variant | ABI2 | GRCh38.p7 | 2:203422268 | GCACCACTGCCTGGG[-/C]GACAGTAAGACTCTG | 10152 |
rs71007518 | in-del | -/A/AA | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429770 | AAAAAAAAAAAAAAA[-/A/AA]GTTCCCACAGCTCAC | 10152 |
rs71007519 | in-del | -/AACA | 0 | 0 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432496 | TTCAACAGACAAACA[-/AACA]CTGAAGATGGGTGTT | 10152 |
rs71034236 | in-del | -/AATATATATATATATATA | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203338958 | ATATATATATATATA[-/AATATATATATATATATA]TATAAATATATATAT | 10152 |
rs71034237 | in-del | -/ATATATATATATATATATAAATATATATATATATATATAT | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203338987 | TATATATATAAATAT[lengthTooLong]ATATATATATATATA | 10152 |
rs71408934 | in-del | -/TA | 0.16976 | 0.236773 | intron-variant | ABI2 | GRCh38.p7 | 2:203411000 | ATATAAAAATGGGAT[-/TA]TGTTTTATATATATA | 10152 |
rs71408935 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429148 | TTGCTTTTAGATTTT[C/T]CCCAGCACTTTGTAT | 10152 |
rs71408936 | in-del | -/A/AA | 0.499203 | 0.0199521 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429753 | GAGCGAGACTCCATC[-/A/AA]AAAAAAAAAAAAAAA | 10152 |
rs71425995 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203369153 | ACTTGGTTTTCTGTA[A/G]AAGGAGGGAGGTTGA | 10152 |
rs71425996 | snp | C/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203372573 | CTGACCCCCCCACCT[C/T]CCTCCCGGACGGGGC | 10152 |
rs71425997 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ABI2 | GRCh38.p7 | 2:203374227 | ATTTTGGCCAGGCTC[C/T]GTGGCTCACGCCTGT | 10152 |
rs71689618 | in-del | -/AA | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429769 | AAAAAAAAAAAAAAA[-/AA]AGTTCCCACAGCTCA | 10152 |
rs71906750 | in-del | -/TTGTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384276 | TCCTGTTCCATACTC[-/TTGTTT]TTGTTTTTGTTTTTT | 10152 |
rs72270455 | in-del | -/TTTGTTTG | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203357768 | TGGTTTTTGGGGTTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 10152 |
rs72299086 | in-del | -/TCTC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370187 | GTGTCATTCTCCTAT[-/TCTC]TCTCTCTCTCTCTCT | 10152 |
rs72353757 | in-del | -/A | 0.281841 | 0.247964 | intron-variant | ABI2 | GRCh38.p7 | 2:203426786 | GTAAAGAAAAGCTTT[-/A]AAAAAAAAAAAAAAA | 10152 |
rs72507530 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344885 | ACAGAGGGCTGATTG[G/T]TGTGTTTACAATCCT | 10152 |
rs72926403 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203428030 | CACTCTGAGGGTGGT[A/G]AACGATTGCCACCCG | 10152 |
rs72940129 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203352196 | TGGGGTGCTGCCCCC[A/G]TGCCTATAATCCCAG | 10152 |
rs72940136 | snp | A/C/G/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365572 | AGAAATATTTTTCCT[A/C/G/T]ATCTTGATCCCAGAG | 10152 |
rs72940137 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203369191 | CTAATGTGATATAGA[A/G]TTTCAAGATCTATTC | 10152 |
rs72940139 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ABI2 | GRCh38.p7 | 2:203373710 | CTGAGTAGGACTTAC[C/T]GGGCCAGGTGTTAAA | 10152 |
rs72940141 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ABI2 | GRCh38.p7 | 2:203373714 | GTAGGACTTACTGGG[C/G]CAGGTGTTAAATTAG | 10152 |
rs72940144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375055 | GTATGATTATCTCAA[C/G]GCCATAAGAGGTATC | 10152 |
rs72940154 | snp | C/T | 0.490231 | 0.0692021 | intron-variant | ABI2 | GRCh38.p7 | 2:203387077 | TTTTTTTTTTTTTTT[C/T]CCCACATGCCTTTAC | 10152 |
rs72940155 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | ABI2 | GRCh38.p7 | 2:203387602 | TTCTTTCTTGTACCT[A/G]ATACCTGCTTCACTT | 10152 |
rs72940158 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ABI2 | GRCh38.p7 | 2:203398313 | GCTCCTGCTTTGATA[A/G]AGAATGCATCAGAAA | 10152 |
rs72940179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203417511 | TTTCTTTGCCAAGTA[A/G]TATTGGGCATTTCTT | 10152 |
rs72940182 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203422068 | TAAGAGGCTGAGGCC[A/G]GCGGATTGCTTGAGA | 10152 |
rs73058790 | snp | A/G | 0.0138799 | 0.0821421 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327698 | CCGCAAACCAGGAGA[A/G]AAAGGGGCTAATCTG | 10152 |
rs73060623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371824 | TATTTTGTGTCCTTT[G/T]CTGGTAAGTTTTTTT | 10152 |
rs73060627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392900 | GAGGCCCACTCTGCT[A/G]GTTGATGGCTATAAC | 10152 |
rs73060636 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430937 | TCTTTTAGTAGGTGA[A/C]CTTTCTGCATTAAGA | 10152 |
rs73990632 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366643 | GATAATGGCTTTAGG[G/T]TTTTATTTGCATCTG | 10152 |
rs73990634 | snp | C/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203392312 | CACCACCACCACCAC[C/T]ACCAACAACAACAAC | 10152 |
rs74182359 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203358115 | TGTGTGTGTGTGTGT[G/T]TGTTTGTTTGTTTGT | 10152 |
rs74267862 | snp | C/T | 0.100588 | 0.200439 | intron-variant | ABI2 | GRCh38.p7 | 2:203329695 | CAGTCTTTTTTTTTT[C/T]CCTTTTTTCTTGCTC | 10152 |
rs74281050 | in-del | -/CAG | 0.479744 | 0.0985793 | intron-variant | ABI2 | GRCh38.p7 | 2:203413897 | CCAGTTATAGTGACC[-/CAG]CAGTTATACTGGGGT | 10152 |
rs74513814 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203414120 | TTTTTTTTTTTTTTT[G/T]GGAGACAGTCTCACT | 10152 |
rs74603926 | snp | C/T | 0.457969 | 0.138741 | intron-variant | ABI2 | GRCh38.p7 | 2:203372812 | gcggccgggcagaga[C/T]gctcctcacctccca | 10152 |
rs74662196 | snp | A/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203368988 | ATGCTTGGCTGATTT[A/T]TTTTTTTTTTTTTTT | 10152 |
rs74666046 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ABI2 | GRCh38.p7 | 2:203379235 | AAGCAACTTGGTCTT[C/T]TGGGGTCAAAAAATG | 10152 |
rs74723668 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330208 | TGTATTTGAGAATGA[A/C]CCGAACCACTGTATA | 10152 |
rs74764754 | snp | C/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203418994 | AATGACTGCATGGTT[C/G]TCATCAAAAAGCTGT | 10152 |
rs74778108 | snp | C/G | 0.089084 | 0.191327 | intron-variant | ABI2 | GRCh38.p7 | 2:203329808 | GTGGCGCGATCTCGG[C/G]TCACTGAAACCTCGG | 10152 |
rs74812040 | snp | A/C | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203330395 | GAGACTACATATCAA[A/C]AAAAAAAAAAAAAAA | 10152 |
rs74820665 | snp | A/G | 0.277778 | 0.248452 | intron-variant | ABI2 | GRCh38.p7 | 2:203353690 | TTTAGTAGAGCCAGG[A/G]TTTCACCATGTTGGC | 10152 |
rs75002927 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422267 | TGCACCACTGCCTGG[-/C]GGACAGTAAGACTCT | 10152 |
rs75007410 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203348291 | AAAGGTTAAGCTTAG[C/T]ATTTTAAAGTTTGTT | 10152 |
rs75013800 | snp | A/G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203340383 | TAGATTTTTTTTTTT[A/G/T]TGAGACAGCGTCTTG | 10152 |
rs75069886 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ABI2 | GRCh38.p7 | 2:203414345 | GAGCTCAAATGATCC[C/T]CCTGCCTCAGCCTCC | 10152 |
rs75098343 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203346535 | TTACTGGAGTTGCAC[C/G]TTTTCCCTTGTCATA | 10152 |
rs75141422 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203347893 | CCTGCAGTTTCGATG[C/T]TTTCTAGATATTTAG | 10152 |
rs75194785 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203329342 | AACCTCCTGGTTTAA[A/T]TTTTTTTTTTTTTTT | 10152 |
rs75212257 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329857 | TTCTCATGCTTCAGC[G/T]TCCCGAGTAGCTGGG | 10152 |
rs75257889 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ABI2 | GRCh38.p7 | 2:203341359 | ACTCCGTAAATATTC[A/G]CTAAATGAGCGAATT | 10152 |
rs75287503 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | ABI2 | GRCh38.p7 | 2:203402367 | TAGACATAACTTTCC[A/G]AACTTAATCATATTT | 10152 |
rs75307612 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352909 | TCTATGTTTAGGTAT[G/T]CAAATGCTTACCATT | 10152 |
rs75404969 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | ABI2 | GRCh38.p7 | 2:203371334 | TATCGGGGAGAAATA[A/C]TTCAACAAAACAAAG | 10152 |
rs75432257 | in-del | -/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364103 | CATCTTTTTTTTTTT[-/TTT]AAGTTTTATTTTGAG | 10152 |
rs75471018 | snp | A/G | 0.00636936 | 0.0560724 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432609 | CTAGATTATAAAAGA[A/G]TTTTCTAATGATGTA | 10152 |
rs75472336 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203380608 | AATGAATTATATTTG[A/C]TTGGTTATGATAATA | 10152 |
rs75525921 | snp | C/T | 0.084364 | 0.187256 | intron-variant | ABI2 | GRCh38.p7 | 2:203334982 | AGACTTTTGATAGCT[C/T]ATGGTTGAATTTTTA | 10152 |
rs75537332 | snp | A/T | 0.0850919 | 0.187897 | intron-variant | ABI2 | GRCh38.p7 | 2:203396367 | ATAAAGATTTGTGTT[A/T]TAAAAAAAATTTTTA | 10152 |
rs75611768 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203426786 | GTAAAGAAAAGCTTT[A/T]AAAAAAAAAAAAAAA | 10152 |
rs75629102 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ABI2 | GRCh38.p7 | 2:203396509 | TAAAAATAACAATAC[A/G]AAGGGAACACTTTTC | 10152 |
rs75635810 | snp | C/G | 0.0799831 | 0.183287 | intron-variant | ABI2 | GRCh38.p7 | 2:203345367 | TGAAGGAACAAACTC[C/G]GGACACACCATCTTT | 10152 |
rs75654136 | in-del | -/CCACCA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392311 | CCACCACCACCACCA[-/CCACCA]ACAACAACAACAACA | 10152 |
rs75777536 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429017 | ATATTCCACTTAATG[G/T]TATCTGAGCATTAAA | 10152 |
rs75805346 | snp | C/T | 0.453818 | 0.144769 | intron-variant | ABI2 | GRCh38.p7 | 2:203372842 | agacggggtcgcggc[C/T]gggcgccctcatatc | 10152 |
rs75858505 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382313 | TAAAACCCAATAAAT[A/C]ATTCCTCCTTTTTGT | 10152 |
rs75943779 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | ABI2 | GRCh38.p7 | 2:203334536 | CTTACACCCACCCCA[A/C]ATCCATTTTGCAGCA | 10152 |
rs75950834 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203414117 | TTTTTTTTTTTTTTT[G/T]TTTGGAGACAGTCTC | 10152 |
rs76041163 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ABI2 | GRCh38.p7 | 2:203417564 | TTAGCTAATTATGAT[A/G]TAGCACTTTGGGATA | 10152 |
rs76042865 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ABI2 | GRCh38.p7 | 2:203377608 | TGATTTAGAATGACT[C/T]ACTAAACTTTATTCA | 10152 |
rs76044774 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203340384 | AGATTTTTTTTTTTT[G/T]GAGACAGCGTCTTGT | 10152 |
rs76061088 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203331827 | TTTTTTTTTTTTTTT[G/T]GACACAGAGTTTCAC | 10152 |
rs76098118 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ABI2 | GRCh38.p7 | 2:203369684 | GCCTCAGTCAAAGCT[A/G]TCAGGAATACGTCGA | 10152 |
rs76134837 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | ABI2 | GRCh38.p7 | 2:203356613 | GAGCTCAGGCGATCC[A/T]CCCACCTTGGCCTCC | 10152 |
rs76151469 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427481 | TTACACTTTTTTTTT[G/T]GGTTTATTCCCCAGT | 10152 |
rs76173356 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ABI2 | GRCh38.p7 | 2:203404369 | CCAACTGCCTTAATT[A/G]ATATATACTTCCCTT | 10152 |
rs76197763 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | ABI2 | GRCh38.p7 | 2:203371394 | GTTTTCAAAAACAAG[A/G]TATTAATTGATTAGG | 10152 |
rs76204042 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429020 | TTCCACTTAATGTTA[G/T]CTGAGCATTAAAAAT | 10152 |
rs76216618 | snp | C/G | 0.084364 | 0.187256 | intron-variant | ABI2 | GRCh38.p7 | 2:203336832 | AGTGGGATTATTACC[C/G]TATGGTAAATGTGTG | 10152 |
rs76231334 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | ABI2 | GRCh38.p7 | 2:203340531 | ACCACCACACATGGC[C/T]AATTTTTGTAGTGAC | 10152 |
rs76312664 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203330393 | GTGAGACTACATATC[A/C]AAAAAAAAAAAAAAA | 10152 |
rs76425803 | snp | C/G | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430461 | CGAAAGTCCATGGTG[C/G]TATTAATGAAAGTAC | 10152 |
rs76465572 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203402806 | CTACAAAAAACCCTT[A/G]ATTACAAATAGTGCA | 10152 |
rs76577085 | snp | C/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203373062 | TTCCCAGATGGGGTG[C/G]CGGCCGGGCAGAGGC | 10152 |
rs76646812 | snp | C/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203363217 | GTTACCTGAGATATT[C/T]TGATACAGGCATACA | 10152 |
rs76673409 | snp | A/G | 0.084728 | 0.187577 | intron-variant | ABI2 | GRCh38.p7 | 2:203329470 | CTCCTGGATGAAGCA[A/G]AATATTCTGTGGATT | 10152 |
rs76773271 | snp | A/T | 0.084728 | 0.187577 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365224 | TACACACAGGCACAT[A/T]CAGAATTATGATGAT | 10152 |
rs76788415 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203403616 | TGATTCTTAGAATCA[C/T]GTACAAAATAAGATT | 10152 |
rs76803878 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | ABI2 | GRCh38.p7 | 2:203379649 | ACTAGATTAATTTCG[A/G]GGGCTTTCTTAATCA | 10152 |
rs76807835 | snp | A/C | 0.084728 | 0.187577 | intron-variant | ABI2 | GRCh38.p7 | 2:203346438 | TGTGTATGATACCAT[A/C]TTACTGCCTGAATGA | 10152 |
rs76832567 | snp | A/C | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203391822 | TGAGCCCCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 10152 |
rs76833031 | snp | G/T | 0.0923359 | 0.194016 | intron-variant | ABI2 | GRCh38.p7 | 2:203382417 | CACTGCTCTATCCTT[G/T]TGCCTAGAACAGTAC | 10152 |
rs76844255 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203384277 | CCTGTTCCATACTCT[G/T]GTTTTTGTTTTTGTT | 10152 |
rs76861336 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421572 | CCACTGTGCTTTTTT[C/T]AAGTAGAAGGACAAA | 10152 |
rs76882447 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349936 | AATTGCTGGATCATA[C/T]GGTAACTGTATATTT | 10152 |
rs77022355 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363817 | TTACCCAGGCTGGAG[A/T]GCAATGGTGCGATCT | 10152 |
rs77042496 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203391966 | TAAACTTGACTTACT[C/G]TGATTGAGATTTACG | 10152 |
rs77051645 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203349098 | CCACTGCACCCGAGT[A/T]ATTTTTTTTTTTGTA | 10152 |
rs77058822 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | ABI2 | GRCh38.p7 | 2:203405769 | TGAGGAAGTGAGCTG[A/G]CAATCTTTGGAAGGT | 10152 |
rs77100272 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203373921 | CCCAGCACTTTGGGA[A/G]GCTGAGGCAGGCGGA | 10152 |
rs77245363 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203359416 | ATTTGTAGAATGTAC[A/C]AAGATCCCAAATCTG | 10152 |
rs77287936 | snp | A/G | 0.000668803 | 0.0182744 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328502 | TGAGGAGGAGGAGGA[A/G]GAGGATGTGAAGATG | 10152 |
rs77296156 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ABI2 | GRCh38.p7 | 2:203402330 | ATGAGTCACTGCACC[C/T]GGCCCTAATTAGTAA | 10152 |
rs77354356 | snp | C/T | 0.0014721 | 0.0270903 | intron-variant | ABI2 | GRCh38.p7 | 2:203402540 | TCTGAGATAATTTTC[C/T]TTTAATGACATATGT | 10152 |
rs77371918 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203340385 | GATTTTTTTTTTTTT[G/T]AGACAGCGTCTTGTT | 10152 |
rs77385734 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | ABI2 | GRCh38.p7 | 2:203424079 | ATGATTTTGATACTA[G/T]GCGTGATATACATGC | 10152 |
rs77434733 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387331 | AGAAGGTAGAGCAGG[A/G]TAGGTAGGAGCATTG | 10152 |
rs77504766 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423941 | TTAGAATGTATTTTT[A/G]CTTTAGCAGAAACAT | 10152 |
rs77605666 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203390634 | GAGACTCTGTCTCAG[A/G]AAAAAAAAAAGAAAG | 10152 |
rs77691082 | snp | A/G | 0.120326 | 0.21374 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431688 | TTTTGAGAATCTCAT[A/G]TAATTATTAAAAAAA | 10152 |
rs77760351 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203334682 | GATTTTTTTTTTTTT[G/T]GAGACAGAGTCTCTG | 10152 |
rs77771011 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ABI2 | GRCh38.p7 | 2:203387854 | TCTGTCTCTCTCTCT[C/G]TCGCTGTCGTTAAGT | 10152 |
rs77798518 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | ABI2 | GRCh38.p7 | 2:203424091 | CTATGCGTGATATAC[A/G]TGCATAATTGGAAAA | 10152 |
rs77824896 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203342450 | AACAAAGTTGAATAG[C/G]GGAAGCCAACAAGGG | 10152 |
rs77921554 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203349100 | ACTGCACCCGAGTAA[A/T]TTTTTTTTTTGTATT | 10152 |
rs77924556 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203405561 | TCTCAAAAAAAAAAA[A/T]TTATGTAAGTCTCCT | 10152 |
rs77947140 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | ABI2 | GRCh38.p7 | 2:203426883 | TTGTGTACCTCTTCA[A/G]TGAGGTACTTCCCTG | 10152 |
rs77963649 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203421983 | AAAAAAAAAAAAAAA[A/T]ATCTAGAAAGAGAGC | 10152 |
rs77976487 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ABI2 | GRCh38.p7 | 2:203335040 | GAGGTAGCATGTAGG[A/G]CAACACATTCTATTT | 10152 |
rs78060075 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419557 | GTATTTTTTTTTTTT[-/TT]GGTAGAGACGGGGTT | 10152 |
rs78064386 | snp | C/T | 0.104504 | 0.2033 | intron-variant | ABI2 | GRCh38.p7 | 2:203405045 | TTAAAGTAAAAAGAT[C/T]CCCACTTTATGGAAT | 10152 |
rs78067749 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429021 | TCCACTTAATGTTAT[C/G]TGAGCATTAAAAATC | 10152 |
rs78096969 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203391820 | AGTGAGCCCCTGTCT[A/C]AAAAAAAAAAAAAAA | 10152 |
rs78181293 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203398374 | TTTTAGTAATTAAAT[A/G]TTAATTGAATAACAG | 10152 |
rs78199571 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203331825 | TTTTTTTTTTTTTTT[G/T]TTGACACAGAGTTTC | 10152 |
rs78265856 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ABI2 | GRCh38.p7 | 2:203401335 | TTCCGCTTTCTTCTC[C/T]ACCTGCTTATTTCTC | 10152 |
rs78300893 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203349009 | GTGATCTCGGCTCAC[C/T]GCAGCCTCTACCTCG | 10152 |
rs78312670 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419785 | CCTGAGGTTGGGAGT[G/T]GGAGACCAGCCTGAC | 10152 |
rs78353544 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | ABI2 | GRCh38.p7 | 2:203375000 | GTTCATGAGGGAGAT[C/G]TGGGAGTGGGGCTCA | 10152 |
rs78396853 | snp | A/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203368832 | AATTTTTTTTTTTTT[A/T]AAGAGACAAAGTCTT | 10152 |
rs78444112 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | ABI2 | GRCh38.p7 | 2:203363334 | CAGTTATTTTAAAAT[A/G]TACAATTAAATTATT | 10152 |
rs78464165 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382314 | AAAACCCAATAAATA[A/C]TTCCTCCTTTTTGTT | 10152 |
rs78476860 | snp | C/T | 0.0287284 | 0.116357 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428582 | TGTATCTAATCACAT[C/T]GATAAAAATTAATAT | 10152 |
rs78487596 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365580 | TCAAGATTAGGAAAA[A/T]TATTTCTCTCTCTCA | 10152 |
rs78533587 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203421065 | CGAAGGTGTTGGATT[A/T]AAAAAAAAATCTGGT | 10152 |
rs78578399 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424413 | TCATTTAAAAATTAC[-/T]TATCAGGGTCTCGTT | 10152 |
rs78579510 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ABI2 | GRCh38.p7 | 2:203354839 | GGGATATGCTATCTT[A/T]GTATCTTCTAAGACT | 10152 |
rs78643187 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ABI2 | GRCh38.p7 | 2:203376561 | TTTAAAGAATTTAAT[C/T]CTGGGAAACATTTCA | 10152 |
rs78660217 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | ABI2 | GRCh38.p7 | 2:203335555 | CCTGTCAGCCGCCAT[G/T]CCTGGCCTTGAATTA | 10152 |
rs78732489 | snp | C/T | 0.084728 | 0.187577 | intron-variant | ABI2 | GRCh38.p7 | 2:203409857 | ACAGCCAGGAAATGA[C/T]GGATCAGAGATTTGA | 10152 |
rs78871923 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | ABI2 | GRCh38.p7 | 2:203403475 | ATAAGCCTTGAATTT[C/T]ATGGAGCTGCAGTTT | 10152 |
rs78891853 | snp | G/T | 0.084364 | 0.187256 | intron-variant | ABI2 | GRCh38.p7 | 2:203368585 | AATTTGTCAGACCAA[G/T]TTAGAGAGATTTCTT | 10152 |
rs78999781 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | ABI2 | GRCh38.p7 | 2:203425314 | CTCAAGTGATTCTCT[C/T]GCCTCAGCCTCCCAA | 10152 |
rs79013625 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203390633 | CGAGACTCTGTCTCA[A/G]AAAAAAAAAAAGAAA | 10152 |
rs79064136 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365643 | TTTTTTTTTTTTTTT[G/T]TTTTGAGACGGAGTC | 10152 |
rs79072736 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203397387 | AGCCTCTGTAAGTCT[A/G]TTTTTAACAGAATCT | 10152 |
rs79083473 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ABI2 | GRCh38.p7 | 2:203358322 | TTATTTTTATTTTTT[A/G]TTTTTTGTAGAGACA | 10152 |
rs79110796 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ABI2 | GRCh38.p7 | 2:203377891 | AGCCTGGGCGACAGA[A/G]TGAGATACTGTCTCA | 10152 |
rs79115618 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427787 | CCCAGTGGGTACCCT[A/T]GCCCCTTCTTTTCTT | 10152 |
rs79188986 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203422551 | CTGGCTCCACAGAAG[C/T]GTAGTAATCAGATAA | 10152 |
rs79211709 | snp | C/G/T | 0.0588605 | 0.161139 | intron-variant | ABI2 | GRCh38.p7 | 2:203347558 | AAGGCGTTTATCAAT[C/G/T]TCCACCATGTGCCAA | 10152 |
rs79255871 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203371331 | CTGTATCGGGGAGAA[A/G]TACTTCAACAAAACA | 10152 |
rs79268093 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203375935 | TTCTGCCCACAGGCA[A/G]TACTGCAGTTCAACC | 10152 |
rs79319473 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350540 | CTTTTTCTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 10152 |
rs79371502 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408837 | CCTTCTCCTTTCTTT[C/T]TTTTTTTTTTTTGAG | 10152 |
rs79389212 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422752 | GAAGGAATATGGCTG[G/T]ATTAGTTAAGCAGCA | 10152 |
rs79440665 | snp | C/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203335291 | TGAGACAGGGTCTCA[C/G]TCTGTCACTCAGGCT | 10152 |
rs79444090 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203421966 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 10152 |
rs79501473 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203405549 | AGTGAGACCCTGTCT[A/C]AAAAAAAAAAAATTA | 10152 |
rs79506776 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382317 | ACCCAATAAATAATT[C/G]CTCCTTTTTGTTTTA | 10152 |
rs79508859 | snp | A/C | 0.0581099 | 0.160244 | intron-variant | ABI2 | GRCh38.p7 | 2:203343959 | AAAAGACGAGAGAGA[A/C]CCCGTCTCTACAAAA | 10152 |
rs79646470 | snp | C/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203406681 | GGAAGATTTTTTTTT[C/T]TCCCCAAAGTCTTGC | 10152 |
rs79799505 | snp | A/G | 0.0115144 | 0.0749975 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432428 | CCACTCGCACCTGGG[A/G]TTTTCTTACCACTTT | 10152 |
rs79815922 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365622 | TTCTGGGGCTGTTAT[C/T]TTTTTTTTTTTTTTT | 10152 |
rs79967834 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203408180 | CTTTTTTTTTTTTTT[G/T]AGATGGAGTTTTGCT | 10152 |
rs80027249 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203368834 | TTTTTTTTTTTTTTA[A/G]GAGACAAAGTCTTGC | 10152 |
rs80151132 | snp | C/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203414320 | TTGGCCAGGCTGGGC[C/T]TGAACTCCTGAGCTC | 10152 |
rs80151562 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ABI2 | GRCh38.p7 | 2:203371537 | AACATGGATTATGTT[A/G]TGTATTTTAGGGCTG | 10152 |
rs80168790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359213 | CAAATGTGATCTGCT[A/G]TGACAGATTAAGGTT | 10152 |
rs80174433 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203368222 | CCATTTAAAATAATA[C/T]TGCAGTGAAAAACCA | 10152 |
rs80191566 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203347783 | AGTTATTGGGTGTTG[G/T]TAATGGCTTTTTGGT | 10152 |
rs80309552 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382316 | AACCCAATAAATAAT[C/T]CCTCCTTTTTGTTTT | 10152 |
rs80335184 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203426783 | AAGGTAAAGAAAAGC[A/T]TTAAAAAAAAAAAAA | 10152 |
rs111259503 | snp | C/G | 0.0887219 | 0.191022 | intron-variant | ABI2 | GRCh38.p7 | 2:203425806 | GCAAGTGGATCACCT[C/G]AGGTCAGGAGTTCAA | 10152 |
rs111289662 | snp | C/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203380751 | GTATTTATCAGCAGA[C/G]TTTTGGCATTAGTTT | 10152 |
rs111306314 | snp | C/T | 0.494896 | 0.0502606 | intron-variant | ABI2 | GRCh38.p7 | 2:203350893 | GTGTGTGTGTGTGTG[C/T]GCGCGCGCATACTTT | 10152 |
rs111338287 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203349669 | CTTGGCCTCCCAAAG[C/T]GGTGGGATTACAGGT | 10152 |
rs111398594 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203338934 | TGTGTGTGTGTATAT[A/G]TATATATATATATAT | 10152 |
rs111592781 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203395306 | TGGAATATAAAAAGG[C/T]AATATTTATTGTTTT | 10152 |
rs111593539 | snp | C/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203396121 | ATTAGTAACAAAGGA[C/T]TGGGCAGATATAAAA | 10152 |
rs111615300 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203363787 | CTTTTTTTTTGAGAC[A/G]GAGTTTTGCTTTTGT | 10152 |
rs111654133 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402687 | TTACTTCACAAACAA[A/G]CCTTCAGAATCAGAT | 10152 |
rs111659553 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203368302 | GGTCTGCCTCCCTTT[G/T]TTTGAATAGATCTTT | 10152 |
rs111665039 | snp | C/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203346650 | TAAACTTGTGCTGTT[C/T]TCTTTCTCATTCCAT | 10152 |
rs111703384 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338928 | TGTGTGTGTGTGTGT[A/G]TATATGTATATATAT | 10152 |
rs111708047 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369013 | TTTTTTTTTTTTTTT[A/T]TTTGTAGAGACAGTG | 10152 |
rs111716706 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203395889 | TTTTTTTTCTTTAGG[A/G]ATCATAAATATTGGG | 10152 |
rs111721767 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415348 | ATTCACCGGGCGCGG[C/T]GGCTCACGCCTGTAA | 10152 |
rs111817237 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203426974 | CTCAATTTAGAGCCT[A/G]ACATCCCTAGAAAAT | 10152 |
rs111856379 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203409551 | GTTAGTGACATCTCC[A/G]TCTTCATAGTTACGA | 10152 |
rs111859211 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203361123 | CAATCCTTGCTTGAA[A/G]TAAAATTTTCCATTA | 10152 |
rs111869940 | snp | A/C | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203349161 | TGCGCAAGCTGGTCT[A/C]CAACTCCTGAACTCA | 10152 |
rs111971804 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203416724 | CAAGAGAGGGAGAAC[A/G]TCATACTTGGAGCTC | 10152 |
rs111976057 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ABI2 | GRCh38.p7 | 2:203388955 | ATTGATGTAGTTTTA[A/G]TGTTTGGTTCACTTC | 10152 |
rs112034602 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203350014 | TTTCCATTTCCACCA[G/T]CAGTGTGTGAGCGTT | 10152 |
rs112086124 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331826 | TTTTTTTTTTTTTTT[G/T]TGACACAGAGTTTCA | 10152 |
rs112383847 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203413518 | TCCCTAATTTGACCA[C/G]CCTATCACAGTTGAT | 10152 |
rs112389518 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203384296 | TTTGTTTTTGTTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |
rs112389929 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ABI2 | GRCh38.p7 | 2:203358234 | TCCTGGGCTCAAGTG[A/G]TCCTCCCTTCTCTGC | 10152 |
rs112425394 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428219 | TCTTAGCAGGCATCC[C/T]GAACCCCTGCTTCGG | 10152 |
rs112431378 | snp | A/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203386257 | ACAACCTACACACAC[A/T]TCCCCTCTTCTATTT | 10152 |
rs112446218 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203378453 | AATTGTAAGATTACT[A/G]CCATGGTTAGTTTTT | 10152 |
rs112691550 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203379944 | GTTGTTCTTTTCTCC[A/G]AACATTAAAAAATGT | 10152 |
rs112745301 | snp | C/T | | | splice-donor-variant | ABI2 | GRCh38.p7 | 2:203328633 | ACAACTACATACAGG[C/T]GCGAAGCATCCCCAG | 10152 |
rs112825499 | snp | G/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203384295 | TTTTGTTTTTGTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |
rs112826786 | snp | G/T | 0.32 | 0.24 | intron-variant | ABI2 | GRCh38.p7 | 2:203384290 | CTTGTTTTTGTTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |
rs112843162 | snp | C/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203344522 | AGGCAACTGCCGCCA[C/T]ACCCGGCTAATTTTT | 10152 |
rs112884990 | in-del | -/C | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203401207 | AGTGTTTTTTTTTTC[-/C]TTTTCACTTATCTCC | 10152 |
rs112968004 | snp | C/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203329697 | GTCTTTTTTTTTTTC[C/T]TTTTTTCTTGCTCCC | 10152 |
rs113004687 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203404700 | AGTAGCAGGGATTAC[A/G]GGCACCTGCCACTAC | 10152 |
rs113026930 | snp | A/T | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203398408 | CCTGGCTCAGTGTTC[A/T]CTAAATAAACATTTG | 10152 |
rs113074339 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203426951 | AATGTGCTTTTTCCC[C/G]ATTTGTACTCAATTT | 10152 |
rs113090237 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ABI2 | GRCh38.p7 | 2:203355926 | CTAGATGTAGAATTA[C/T]AGATTGGAAATAATT | 10152 |
rs113117670 | snp | A/C | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203375080 | GGTATCCTTAAGGAA[A/C]CTGGGTTTGGCACTG | 10152 |
rs113176700 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203360042 | GTACAGAAATTAGCT[A/G]GGCGTGGTGGTGCAT | 10152 |
rs113217304 | snp | A/G | 0.236724 | 0.249647 | intron-variant | ABI2 | GRCh38.p7 | 2:203416397 | ACCTCCCCGGTTCCA[A/G]CGATTCTTGTGCCTT | 10152 |
rs113272073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409226 | AAGCCTCTGAGTGGG[A/G]AGCAGACACGCAAGT | 10152 |
rs113272649 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203381126 | TTTTTTCTAATATAA[A/G]CATACTTAAAAAACA | 10152 |
rs113273810 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366534 | AAGCAGAAGAAAGTG[A/T]GTCAAAATTTATACG | 10152 |
rs113320543 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384306 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |
rs113416539 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ABI2 | GRCh38.p7 | 2:203340547 | AATTTTTGTAGTGAC[A/G]GGGTTTCGCCCTGTT | 10152 |
rs113436466 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203423979 | AACAATGTGTAAGTC[C/G]TTTTCTGTTTCAGTC | 10152 |
rs113503336 | snp | C/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203377011 | CCTGTTCATTCTCTG[C/G]AGATTTATTAATATT | 10152 |
rs113705942 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203391314 | ACATTTTTATACTTC[A/G]GAAAGATTTGTTTAG | 10152 |
rs113714239 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203409128 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCCAACTA | 10152 |
rs113742464 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203351869 | CTCGTACAGTCATGC[A/G]CAGCATAATGATGTT | 10152 |
rs113772643 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384912 | CGATCTTGGCTCACT[G/T]CAACCTCCGCCTCCC | 10152 |
rs113822483 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427453 | GTAGAATGAAGGATA[C/G]AAATGATAAAAATTA | 10152 |
rs113825438 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203350195 | CATTCTCATGCCTCA[A/C/G]CCTTTTGAGTAGCTG | 10152 |
rs113857824 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ABI2 | GRCh38.p7 | 2:203407857 | TCAAAATTCTGCTTA[A/G]ATTCACTTAAAATGG | 10152 |
rs113863012 | snp | C/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203395486 | ACACACACACACACA[C/T]TTTTTTTTAACCTGT | 10152 |
rs113913246 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394396 | TCCAACTCTTCTAAG[A/G]AGAGGTAGGGTCTGG | 10152 |
rs113917218 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203354616 | CTGGGTCAAAGGCGT[A/G]GGACTTTATTACAGC | 10152 |
rs113951639 | snp | A/G | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203350249 | GCCCGGCTAATTCTC[A/G]TATTTTTAGTAGAGA | 10152 |
rs114028612 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ABI2 | GRCh38.p7 | 2:203378865 | AAAAAATTTTTTTTA[C/T]GTTGTATTCAGCACA | 10152 |
rs114110905 | snp | A/G | 0.000981574 | 0.022132 | intron-variant | ABI2 | GRCh38.p7 | 2:203394875 | CTCAGTGCAAAATGT[A/G]ATGGTCATAGTACCA | 10152 |
rs114221428 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | ABI2 | GRCh38.p7 | 2:203374222 | TTCTAATTTTGGCCA[C/G]GCTCCGTGGCTCACG | 10152 |
rs114275317 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ABI2 | GRCh38.p7 | 2:203336409 | GATCTGAATCTTGGC[C/T]GAGCACTTTGTGATC | 10152 |
rs114388177 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366532 | AAAAGCAGAAGAAAG[C/T]GAGTCAAAATTTATA | 10152 |
rs114448021 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | ABI2 | GRCh38.p7 | 2:203400173 | GCCCACTGCAATCTC[C/T]GCTGCCTGGATTCAA | 10152 |
rs114552719 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203337552 | TTTGATATTGTTAAC[A/C]TGTCCATACTACACA | 10152 |
rs114624846 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203346244 | AATCTTTGAGGAGTT[C/T]ATTGTTGCAGATGTG | 10152 |
rs114649171 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203394957 | TCTTTTCCTCACTCT[A/G]TTCTCCCAAACCTCA | 10152 |
rs114658175 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203389981 | ATGTTACATCTTTCT[C/G]ATGCCTGAATTCACC | 10152 |
rs114683067 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ABI2 | GRCh38.p7 | 2:203421929 | AGATCACTCGCCACC[A/G]CACTCCAGCCTGGCA | 10152 |
rs114688279 | snp | A/T | 0.084728 | 0.187577 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328246 | GCGAGGGTGGGAATC[A/T]TTTTCGGGCTCCCGG | 10152 |
rs114689048 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203356361 | TTTTTTAATTTAATG[A/C]AATTTTATTTTATTT | 10152 |
rs114706783 | snp | A/G | 0.084728 | 0.187577 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430169 | TATTAATCATCTGTG[A/G]GGGTAGTATTTTTTG | 10152 |
rs114730615 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203367682 | ATTTTGGTATATCTC[C/T]TTGTAATCCTTTTTC | 10152 |
rs114758550 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203404547 | GGTACCTGCCACCAC[C/G]CCTGGCTAATTTTTG | 10152 |
rs114933730 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203413150 | TCATTTTGAACAAAA[C/G]TGGTTCTGAGCAGCT | 10152 |
rs114936333 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203356679 | CAGTCCAAATTTTTA[A/C]ATTTTTTGTGGAGAT | 10152 |
rs115014914 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ABI2 | GRCh38.p7 | 2:203425626 | TTTTTGTATTTTCTT[A/G]TATTTAAACTTGTAT | 10152 |
rs115081771 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203420107 | AGTTAAGTGTTAGAA[C/T]TGGGATTTGACTGGG | 10152 |
rs115179064 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ABI2 | GRCh38.p7 | 2:203412579 | TGACTTCATAAGATG[C/T]TTTGTTGAGTTTAAG | 10152 |
rs115222046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203376935 | TTCAAACAAGAAATA[C/T]GTGCTTGTTATAAAA | 10152 |
rs115333251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203401089 | TATCATCTGTTCCTC[C/T]AGTCCCCCCTCCTCT | 10152 |
rs115340749 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ABI2 | GRCh38.p7 | 2:203340393 | TTTTTTTGAGACAGC[A/G]TCTTGTTCTGTTACC | 10152 |
rs115559087 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ABI2 | GRCh38.p7 | 2:203403179 | ATACAATTCTCATAC[C/T]AAACCCATGGTGGAA | 10152 |
rs115608175 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203343256 | GTAGTCCCAGCTACT[C/T]GGGAGGTTGAAGCAG | 10152 |
rs115711798 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | ABI2 | GRCh38.p7 | 2:203404546 | AGGTACCTGCCACCA[C/T]GCCTGGCTAATTTTT | 10152 |
rs115756451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330753 | GTAAGAAATAAAAAA[C/T]AAACAGATTTCTCTC | 10152 |
rs115778704 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ABI2 | GRCh38.p7 | 2:203348584 | AATTTTCCCTCAATT[A/G]AAAACATTCAACAAT | 10152 |
rs116061906 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ABI2 | GRCh38.p7 | 2:203425008 | GGGACCACAGGCACG[C/T]GCTACCATGCCAGGC | 10152 |
rs116063943 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ABI2 | GRCh38.p7 | 2:203375693 | GAATGTTAAAGCTGC[A/G]TGATAGATGTGAGGA | 10152 |
rs116065737 | snp | C/T | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428187 | AGGTTCTGAAGAGAC[C/T]TGAACTGTGGAAATG | 10152 |
rs116096391 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203387557 | GGAGGTTTCTGTCTG[G/T]TAGGGAAAAAGTGGG | 10152 |
rs116104837 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ABI2 | GRCh38.p7 | 2:203416040 | CATAGATGAAGTAAC[C/T]CAAGTTTGTTGATGA | 10152 |
rs116231585 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203339441 | AAAAATTAGCTGGGT[A/G]TGGTTGGCGGGTGTC | 10152 |
rs116286210 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ABI2 | GRCh38.p7 | 2:203347974 | GCTGGGCGCAGGTGG[C/T]TCATGCCTATAATCC | 10152 |
rs116324883 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ABI2 | GRCh38.p7 | 2:203371918 | TTCTTTTTTCTTTTT[A/C]TTTTTATTTTATTTA | 10152 |
rs116337496 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ABI2 | GRCh38.p7 | 2:203358789 | CTGAGGTGGGCAGAT[C/T]ACTTAAATCCATGAG | 10152 |
rs116388309 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | ABI2 | GRCh38.p7 | 2:203404102 | TATTTAAAAAATTTT[G/T]CTCTTATCCTCCCAA | 10152 |
rs116422644 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365089 | TGCCCAAGTTAAAAA[A/G]AAATTAAGCCATACT | 10152 |
rs116426890 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | ABI2 | GRCh38.p7 | 2:203331895 | GCTCACTGCAACCTT[C/T]GTCCCCCGGGTTCAA | 10152 |
rs116474721 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203397021 | ATCTGGCTATTCTCT[C/T]ACTTGCACCTCTGAT | 10152 |
rs116596320 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203344136 | ATATTTCCATTTGGT[G/T]CTTACTCCATAGTAA | 10152 |
rs116769978 | snp | A/C | 0.084728 | 0.187577 | intron-variant | ABI2 | GRCh38.p7 | 2:203426040 | AAAAAAAAAAAAATT[A/C]TGGTGTTCCTACAAT | 10152 |
rs116949532 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203350237 | GTGCATTACTATGCC[C/T]GGCTAATTCTCGTAT | 10152 |
rs117002930 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327678 | AAAAGCTGAGGCCCA[C/T]GGCACCGCAAACCAG | 10152 |
rs117219927 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203350248 | TGCCCGGCTAATTCT[C/T]GTATTTTTAGTAGAG | 10152 |
rs117262164 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428373 | TCACTGGGAGTACAA[A/G]GTTTGCTAATGTGCT | 10152 |
rs117282455 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ABI2 | GRCh38.p7 | 2:203407733 | AAGAGTCTTGTCTTA[C/T]GAGGAATCATTTTAG | 10152 |
rs117338093 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ABI2 | GRCh38.p7 | 2:203389008 | TTGGGTTTTATGTTG[C/T]TTAAGGTTGAGCTTA | 10152 |
rs117587214 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ABI2 | GRCh38.p7 | 2:203407553 | GGACTTTATAAATAA[C/G]CAGGAAGGTTGTACT | 10152 |
rs117831748 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203356638 | GCCTCCGAAAGTGCT[A/G]TGATTGCAGGCGTTA | 10152 |
rs117891741 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203423714 | GCGTGAGCCACCGCG[A/C]CCAGCCCAATCTGGG | 10152 |
rs137877694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203335940 | TTCCTTGTACCCTCT[A/G]TAGTCAGTCCTGTCC | 10152 |
rs137886846 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203424025 | CCAGATGTCTAGCAT[G/T]TTAAGTTTTTTCTTA | 10152 |
rs137904261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203411946 | GGAGGCCTGTATCAA[C/T]ATTCAGTGAGGAATT | 10152 |
rs137954280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203376829 | GGGTAATATGTAAAT[A/G]TCCCCAATCCCTAGA | 10152 |
rs137983445 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203358466 | AATGTAGTTTGAACA[A/C]ACTTAAACAACAAAA | 10152 |
rs138159520 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203406688 | TTTTTTTTCTCCCCA[A/G]AGTCTTGCTTTGTTG | 10152 |
rs138204560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409914 | CTTTCCACTAAGCAC[G/T]CTTCCACCAGGCATA | 10152 |
rs138211429 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203354614 | TTCTGGGTCAAAGGC[A/G]TAGGACTTTATTACA | 10152 |
rs138252101 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203343083 | CAGCCTGCAGATTGG[A/G]AAGTGGAGCCTCCAG | 10152 |
rs138254973 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203388044 | TAGTTTAACTTTAAT[A/T]ATAATATAGATTTTA | 10152 |
rs138321013 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203393940 | TTTTCATCCTCTTTA[C/G]GAGGAAATTTTGGGA | 10152 |
rs138325801 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340371 | TACTAAGTCAGTAGA[-/T]ATTTTTTTTTTTTTG | 10152 |
rs138362686 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203381163 | TGGATGGAAATCAGT[G/T]AAATCTAAATTTAAT | 10152 |
rs138397782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203329900 | CGCCACCACAGCCGG[A/C]TAATTTTTGTATTTT | 10152 |
rs138417140 | in-del | -/TC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331807 | GTTTTTGCTCAGTGT[-/TC]TTTTTTTTTTTTTTT | 10152 |
rs138479169 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203407338 | TAAGCATCTCAACTC[G/T]CATGGGCTATATAAT | 10152 |
rs138509190 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203381999 | TCTTAAATTCATCAG[A/G]GAAACTTCTGTTCAT | 10152 |
rs138521139 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203416750 | AGCTCTAGAACGTTA[C/T]AGTTGGTGGGAAGAC | 10152 |
rs138549982 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203330869 | GATTATTAAAGCTGA[A/G]AGGTTAAAGGCATCA | 10152 |
rs138550062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385717 | TTTGTAGTAACATCA[A/G]CCTTTGAGAGACCCA | 10152 |
rs138552153 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365471 | GTATAATTTAAAGCT[A/G]CAAATGTAGCAGAAC | 10152 |
rs138553024 | snp | A/G | 0.0119135 | 0.0762987 | intron-variant | ABI2 | GRCh38.p7 | 2:203420217 | TTGGCTTTACAGTTT[A/G]TGAGCATTAAGTCCT | 10152 |
rs138599756 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203370654 | ATTATTATTTAAAAT[A/G]TTGTGTGTTTCTAGA | 10152 |
rs138646383 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203402310 | AAAGTGCTGGGATTA[C/T]AGGCATGAGTCACTG | 10152 |
rs138803942 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394349 | CATTCATGAAGTACA[C/G]TTGGGAGACTTTAAT | 10152 |
rs138874981 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203386354 | TTCAGTGGCATGATA[C/G]CTCACTGTATCCTTG | 10152 |
rs138925504 | in-del | -/AC | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203329758 | TCTTTTCTTTTTGAG[-/AC]ACAACCTCGTTCTGT | 10152 |
rs138939318 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203362996 | CCACCACGCCCGGCT[A/G]TTTTTCGTATTTTTA | 10152 |
rs138969946 | in-del | -/TT | 0.451359 | 0.148171 | intron-variant | ABI2 | GRCh38.p7 | 2:203420397 | GACTGTGACAGTCCC[-/TT]TTTTTTTTTTTTTGA | 10152 |
rs138996705 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203357542 | AAAGTGCTCCTCTGA[C/T]ACTTTGGTGTGTAGG | 10152 |
rs139009732 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203352252 | ACGGCTTGAGTTCAG[A/G]AGTTCAAGGTTACAG | 10152 |
rs139063422 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350891 | GTGTGTGTGTGTGTG[C/T]GCGCGCGCGCATACT | 10152 |
rs139139272 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203345199 | CACTCCTGAAGCCAG[C/T]GAGACCACAAACTTA | 10152 |
rs139219229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421254 | TAATGGCCTCAACCA[A/G]GGTAGTGGTGCTGAA | 10152 |
rs139245655 | in-del | -/AGCAC | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431568 | TCCAACACTGGCAGG[-/AGCAC]AGCACAGCACAGCAG | 10152 |
rs139278950 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332845 | TTTTCTTTTTGTTAG[A/G]TAAAAGTTACTGATT | 10152 |
rs139291552 | snp | C/T | 0.000121098 | 0.00778038 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391080 | AGATGGGTGGGCTGC[C/T]GCGTACAACACCTCC | 10152 |
rs139293159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203424818 | ACTCTCAGCTCTCTA[C/T]CATTATAAACAGTCT | 10152 |
rs139365963 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203383950 | TTTTCAGACAGTCTC[C/T]AGAGAAAGTCATCAT | 10152 |
rs139380718 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203417235 | AGGTTCATGATTTTG[A/C]AAGTTACACTAGTAA | 10152 |
rs139413002 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365966 | CAGGACTTTATTTGT[A/G]TTTTTATCTTTGTTT | 10152 |
rs139417786 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203404442 | TTTAAATCATTCTGA[A/G]CTTAAATTTTGACAA | 10152 |
rs139430526 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203334045 | TCCTGGGTTCAAGCA[A/G]TTCTCCTGCTTCAGC | 10152 |
rs139430659 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203389058 | TTAAAAAAATCTTCT[A/G]GTTTCAGAAATTAAG | 10152 |
rs139452784 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203399104 | TAAGTAAATTTTTAA[C/T]GTCATAAGAAACTGC | 10152 |
rs139502276 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203383768 | CCTGATGAGCAATAG[C/T]ATTATGGATTCCTTA | 10152 |
rs139519348 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203390447 | GATCAGCCTGGGCAA[C/T]ACGGTGAAACCCTGT | 10152 |
rs139557667 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ABI2 | GRCh38.p7 | 2:203389919 | TTGCATTTTCAGTTG[C/G]GGATAGAATAGTGAG | 10152 |
rs139590401 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203340142 | GACAAATACCGTATG[A/G]TTTCACTTATATGAG | 10152 |
rs139610920 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419815 | CCAACATGGAGAAAC[A/C]CCGTCTCTACTAAAA | 10152 |
rs139649339 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203402939 | ATTTCCACGTAAAGT[C/G]ATACAACTTAGTTTT | 10152 |
rs139664045 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340534 | ACCACACATGGCTAA[-/T]TTTTGTAGTGACGGG | 10152 |
rs139683641 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203425602 | ATTCTAAATTGTATT[G/T]TCTGGGTTTTTTTGT | 10152 |
rs139728489 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203360176 | GGTGACAGAACGAGA[C/T]TCCATCTCAAAAAAA | 10152 |
rs139867075 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203417993 | AAAGAGAAACATAAT[A/G]TTTCTGGAGACGAAA | 10152 |
rs139946139 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ABI2 | GRCh38.p7 | 2:203426329 | ATTCTTCAAGTGGAA[C/T]TGAGGATGTTACAGG | 10152 |
rs139978101 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431659 | AGTTTACTTTGTGCT[C/G]ACCTTTGTTCCTGTT | 10152 |
rs140016257 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203338069 | AGTGTGTTACTGGCA[A/T]AAAAGACATGTAGAC | 10152 |
rs140067087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377832 | AATCATTTCAGCCTG[A/G]GAGGTCGAGGATGCA | 10152 |
rs140151522 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348889 | TAGTACAAAGCCCCC[-/C]TGAACCTTGCTGAAG | 10152 |
rs140156023 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203335550 | TTACACCTGTCAGCC[A/G]CCATGCCTGGCCTTG | 10152 |
rs140193256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413006 | TCCGGTTTAATCACA[A/G]TGATTAATGATGGTA | 10152 |
rs140193425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203355978 | ATTCTTTTAGTTTAT[C/T]GTCTCCTAGCTTTTG | 10152 |
rs140298539 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203376298 | TTTCTATATTCTGCA[A/G]TCCTCAAGACAGCAG | 10152 |
rs140338129 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203379514 | AAAGTGCTTGGATTA[C/T]GGGCCTGAGCCACTG | 10152 |
rs140353783 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203418849 | AAGAAGTTCAATAAA[A/C]CCCAAATAGAAGAAA | 10152 |
rs140372177 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327426 | CTCTGCAAGAGGAAA[A/T]TTATCTGCCTTGAAT | 10152 |
rs140401325 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ABI2 | GRCh38.p7 | 2:203369203 | AGAATTTCAAGATCT[A/G]TTCTTGAGAATCCTA | 10152 |
rs140422559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203351629 | CAGCCTTGAACTCCT[A/G]TGCTCAAGTGATCAT | 10152 |
rs140464703 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409350 | CTGTTCTTTGCATCT[A/G]GATATTCAAGATTAT | 10152 |
rs140477610 | in-del | -/CAG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413898 | CAGTTATAGTGACCC[-/CAG]AGTTATACTGGGGTA | 10152 |
rs140487294 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203354728 | GGCCCAGGTGATACT[C/T]GTATATGCAAGGGTT | 10152 |
rs140507301 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203408288 | CTGGTTCAGCCTCCC[A/G]AGTAGCTGGGGTTAC | 10152 |
rs140544648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393108 | TTGTACAATATTGGC[G/T]CACTGCAACCTCTGC | 10152 |
rs140578031 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203342860 | CACACATCTCATTGT[C/T]TTTGAGAGAAAAGGA | 10152 |
rs140619626 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203353938 | CTTATATTTCTTCCT[A/G]TCTTCTTAACATGTA | 10152 |
rs140652932 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203356112 | TGATGATCCTTCCTA[C/T]GGGTCTTTTTCATTA | 10152 |
rs140750193 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203380533 | CTTGCTACTATAACT[C/G]TTTTACCCTTTTTGC | 10152 |
rs140777044 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203414005 | ACTGCTGTAAGGCCC[C/T]TCCTGCCTCATCCTC | 10152 |
rs140783336 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203422919 | AAAGTATGTTAAATG[-/T]TTTGCTGGCTTAGGA | 10152 |
rs140793695 | snp | A/T | 0.000743808 | 0.0192705 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402690 | CTTCACAAACAAGCC[A/T]TCAGAATCAGATGAA | 10152 |
rs140821537 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326128 | CCTGTGTCGGCCTCC[A/C]AAAGTGCTGGAATTA | 10152 |
rs140830613 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203417393 | CACATTATTATTCCT[A/G]CCTCCATGCTTTAGA | 10152 |
rs140888009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203331649 | ACAGGCGTGAGCCAC[C/T]GCACCTGGCCAATTT | 10152 |
rs140921530 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328622 | TTACTGCGAGAACAA[C/T]TACATACAGGTGCGA | 10152 |
rs140922536 | snp | C/T | 0.00797794 | 0.0626524 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203417035 | GTATAGTGATCCTTA[C/T]GCTGAAGAGGACCCA | 10152 |
rs140942058 | snp | A/C | 0.0850919 | 0.187897 | intron-variant | ABI2 | GRCh38.p7 | 2:203419913 | GAATCACTTGAACTC[A/C]AGAGGCGGAGGTTGG | 10152 |
rs140972186 | in-del | -/AT | 0.495671 | 0.0463237 | intron-variant | ABI2 | GRCh38.p7 | 2:203329315 | TGTTTCTTAGAGAGA[-/AT]TGGGAAGATGAACCT | 10152 |
rs141003437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361705 | CAGTTCCTTATTTCT[A/C]CTTAAAACATGACTG | 10152 |
rs141006173 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ABI2 | GRCh38.p7 | 2:203423710 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCCAATC | 10152 |
rs141056236 | in-del | -/C | 0.132957 | 0.220909 | intron-variant | ABI2 | GRCh38.p7 | 2:203376169 | CCTTCCTCTATAGAT[-/C]TTTGGTTCTCAACCA | 10152 |
rs141094826 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419767 | GCTGAGGCGGGCCGA[A/C]CACCTGAGGTTGGGA | 10152 |
rs141122054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385689 | TATCCGACACAGCAC[C/T]TGGAGGAAAACCTTT | 10152 |
rs141218310 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203410338 | CTAACAGAGGCATTT[C/T]CTCTTTATAAGAAAA | 10152 |
rs141253334 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203358180 | GGAGCGCAGTGGTAG[G/T]TAGTCATAGCTCGCT | 10152 |
rs141263734 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203397218 | TGAATTTCATTTATT[A/G]GAGATTTTTAAGTTT | 10152 |
rs141348252 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203348496 | TTCATATGGTCAGTT[A/T]TATGTTATATGTCGA | 10152 |
rs141384174 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203352780 | CTGTACAGTAATGTC[C/T]TAGGCCCTCCTATTA | 10152 |
rs141392713 | snp | A/G | 0.00104444 | 0.0228282 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380343 | TATATTAGAAAACCT[A/G]TTGACTATACAATTC | 10152 |
rs141407640 | in-del | -/GTGC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350890 | TGTGTGTGTGTGTGT[-/GTGC]GCGCGCGCATACTTT | 10152 |
rs141454592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203383230 | CCACACAACTTTCCC[C/T]TGCCCGTGGTAGGTA | 10152 |
rs141476588 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203406448 | GGTATGCTGTTTCAC[A/G]AAGAGAAAGTGTCAG | 10152 |
rs141488270 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203332493 | AGCTGGCTATGGTGG[C/T]GTGTGCCTGTAGTCC | 10152 |
rs141523547 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365536 | GAGGTGTTGGTATTT[A/T]TTTTATTTTATTTTT | 10152 |
rs141537612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203362732 | GGGTTTCTCCATGTC[A/G]GGCAGGCCGGTCTTG | 10152 |
rs141541786 | in-del | -/C/TC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387076 | TTTTTTTTTTTTTTT[-/C/TC]CCCACATGCCTTTAC | 10152 |
rs141589567 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203371365 | TAATAACCCACTCTT[G/T]CTAAATGTCAAATGT | 10152 |
rs141592086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416802 | TGAAGGAATATTACA[G/T]TTATTTTCAAGTCTA | 10152 |
rs141648538 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340824 | AGCTGAAAAAAAAAA[-/A]CCCAAAGCAAACTGA | 10152 |
rs141657311 | in-del | -/A | 0.350327 | 0.228986 | intron-variant | ABI2 | GRCh38.p7 | 2:203352570 | CAAAAAAAGTTAAAG[-/A]AAAAAAAAATAGAGA | 10152 |
rs141701114 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203364474 | TACCACTGAACCACC[A/G]TTGCGCTGACTTATC | 10152 |
rs141776076 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419810 | CCTGACCAACATGGA[A/G]AAACCCCGTCTCTAC | 10152 |
rs141822026 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428233 | CCGAACCCCTGCTTC[C/G]GTGCTGTTTTGAGGA | 10152 |
rs141839501 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354397 | ATAATTCATTTTTTT[A/G]ACTTGCTTAGTTACC | 10152 |
rs141876329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337541 | GAATTGGTAGATTTG[A/T]TATTGTTAACATGTC | 10152 |
rs141877453 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203425203 | TCTGAATTACTTTTC[A/C]TGGGTTTGCATTTCT | 10152 |
rs141893637 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203381384 | TGGGCTCAGGTGATC[C/T]TCCCTTGTCAGCTTC | 10152 |
rs141941210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341790 | GAAAGTTGGCAAATA[C/T]TTTTTATTTGTCCAG | 10152 |
rs141947637 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ABI2 | GRCh38.p7 | 2:203344637 | GCATGATCTTTAGAG[A/G]TGAAGCCAGCTGGGC | 10152 |
rs141957667 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430551 | CAATGTGTCAAAATC[A/G]ACATCTGAGAGATTC | 10152 |
rs141958154 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427687 | TCTTTCTCAGGAATA[C/T]TGTATACCCTTGGGA | 10152 |
rs141979360 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203420908 | AAGCTGAGGGAATCA[C/T]GTGAGTGAGAGGGCA | 10152 |
rs141986225 | in-del | -/TGTGTATA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338925 | GTGTGTGTGTGTGTG[-/TGTGTATA]TGTATATATATATAT | 10152 |
rs141997118 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203349554 | GAATTACAGGCACAT[A/G]CCACCATGCCTGGCT | 10152 |
rs142003572 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203347178 | GGAGTGATCATATAG[A/G]AAGCAAGGAAGTGAT | 10152 |
rs142022374 | snp | C/T | 0.084364 | 0.187256 | intron-variant | ABI2 | GRCh38.p7 | 2:203372019 | TAGTGGAGGGAAGGT[C/T]AGCAGATAAACAAGT | 10152 |
rs142061228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404368 | ACCAACTGCCTTAAT[G/T]GATATATACTTCCCT | 10152 |
rs142106111 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ABI2 | GRCh38.p7 | 2:203384888 | CACCCAGGCTGGAGT[A/G]CAGTGGCACGATCTT | 10152 |
rs142206187 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203344970 | GGACCAACCAGTGCT[C/G]TGTAAAATGGACCAA | 10152 |
rs142241120 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203418193 | AGGAGATGTGAGAGG[A/C]AAAAGAGTTGAAACA | 10152 |
rs142241591 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ABI2 | GRCh38.p7 | 2:203410162 | TGAGAGGTCATTTCA[C/T]TGTAGCCCTCCTTAC | 10152 |
rs142293268 | in-del | -/CTTGT | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203358397 | AAGTGATTCTTCTGC[-/CTTGT]CTTCCCAAAGTGCCA | 10152 |
rs142306108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203414850 | TATAAAATGAAAAAC[A/G]CCACCTCCCAATATA | 10152 |
rs142306778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357644 | ACATATTTTAAAAGT[G/T]TCATGTTATTGAGAA | 10152 |
rs142342133 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203409117 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 10152 |
rs142362163 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203412766 | ATCCATAGTGTGATC[C/T]TCTGCCAGGCTTGTG | 10152 |
rs142389733 | in-del | -/AAG | 0.226779 | 0.248919 | intron-variant | ABI2 | GRCh38.p7 | 2:203354706 | TTCACATATTGTGAT[-/AAG]AAGAGGCCCAGGTGA | 10152 |
rs142427739 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203416746 | TTGGAGCTCTAGAAC[A/G]TTATAGTTGGTGGGA | 10152 |
rs142493474 | snp | A/G | 0.00054509 | 0.0164999 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402682 | TTCCATTACTTCACA[A/G]ACAAGCCTTCAGAAT | 10152 |
rs142515241 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ABI2 | GRCh38.p7 | 2:203355704 | GGCATGGTGGCGCAC[A/G]CCTGTAATCCCAGCT | 10152 |
rs142583475 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203379532 | GCCTGAGCCACTGTG[C/T]CTGGCTTTATTTTTA | 10152 |
rs142592116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386130 | GTCTCTAGAAAGCCA[A/C]ATAATTATGTACTAG | 10152 |
rs142654534 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ABI2 | GRCh38.p7 | 2:203389077 | TCAGAAATTAAGATA[C/T]GCAGTTTTAAAAGCT | 10152 |
rs142741195 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203375014 | TGTGGGAGTGGGGCT[C/T]AGGCTTGCAAAGGAG | 10152 |
rs142765468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203354807 | GGTCTGTAAACATGC[C/T]TGCCCTTTGCTCCAG | 10152 |
rs142830930 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203394116 | GATCAAGGTGAAAGT[C/T]GAGGGAGAAAGTGAG | 10152 |
rs142897031 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203413606 | CACAACGTATAAAAA[A/G]ATTGTGTATGAGGTG | 10152 |
rs143004569 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203377223 | AGGAGGCTGAGGTAA[C/G]AGGATGCTTGAGCCT | 10152 |
rs143156016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421366 | CCAAAAATCAAATAA[C/T]GTATCTTCAAAAATC | 10152 |
rs143215682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203424827 | TCTCTACCATTATAA[A/G]CAGTCTCTGGAATCA | 10152 |
rs143221506 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203373695 | CCACCTTCCCAAGGG[C/T]TGAGTAGGACTTACT | 10152 |
rs143240543 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203357444 | CCACAAATGTAGCAA[A/T]TACCTAGGTGACTTT | 10152 |
rs143284329 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429389 | AAATTAGATGTTCCC[A/G]TTATTTATTTAAACA | 10152 |
rs143287894 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203377401 | AGGTTTACACTCTTA[C/T]AGTTTCATTTCTGAA | 10152 |
rs143313907 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ABI2 | GRCh38.p7 | 2:203423753 | TGCTGGCATGGTACC[A/G]TTATTCTTTGCTTAT | 10152 |
rs143383469 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203426412 | GATTATCTGGTTGAA[A/G]TAAGATAACAGTTGA | 10152 |
rs143387366 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203392726 | GTTGGGTTTTAAGTC[A/C]AGATTGTTAGTAAGA | 10152 |
rs143425694 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203420718 | TATCTGGTTCATCTT[C/T]GTACCTCTAAAAGTC | 10152 |
rs143449792 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ABI2 | GRCh38.p7 | 2:203378401 | TAGGCGTGAGCCACC[A/G]TGCCTGGCTGAGATT | 10152 |
rs143529120 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | ABI2 | GRCh38.p7 | 2:203416239 | GAATACAGTGTAAAG[C/G]TCAGCTGTATTGTAC | 10152 |
rs143557717 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403415 | GAAGCCAGTAAGCCT[A/G]TGTGTGAACACCTCT | 10152 |
rs143562294 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203363525 | CCTGTCCTACCTCCC[C/T]ACTTTCCCCCTACCC | 10152 |
rs143620519 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203351351 | TATAAATTTTAGGAT[C/T]ATTTGTTAATTTCTG | 10152 |
rs143622224 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203406820 | AGGTGTGTGCCACCA[C/T]GCCTGGCTCTTTTTT | 10152 |
rs143668027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406130 | AGGGGGTCATAGAAA[C/T]ACATAGGGCTAATTA | 10152 |
rs143686059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354642 | ACAGCAACAATAATA[A/G]CCAGCATATTAGCAT | 10152 |
rs143701304 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203354125 | TCTCAGTTCACTGCA[A/G]CCTCCACCTCCCGGG | 10152 |
rs143800002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203398538 | GAGTTACCAAGCAAT[C/T]GTTTTTCTTTTTACC | 10152 |
rs143801422 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203408251 | CACTGCAGCCTCTAC[C/T]TCCTGGGTTCAAGCG | 10152 |
rs143841114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330554 | TATACTCTGTAGTGC[A/C]CTGCTGGTACCAAGG | 10152 |
rs143868888 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203356052 | TTTGTATATAGTTTT[C/T]TTTCTCTCTCTCTGA | 10152 |
rs143874517 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203379519 | CTTGGATTACGGGCC[-/T]TGAGCCACTGTGCCT | 10152 |
rs143930258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203359872 | ACAAAAATTCAGACT[A/G]TAGCAATGAATATTT | 10152 |
rs143985111 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203382007 | TCATCAGAGAAACTT[C/T]TGTTCATGACACATT | 10152 |
rs144049635 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203331044 | TAATTTAATAGAAAT[G/T]AACTTAGATTTTAAA | 10152 |
rs144113751 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203335966 | TGTCCCTCCACTACT[A/T]GCCTTTGGTAAACAC | 10152 |
rs144129848 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203334223 | TGGGATTACAGGTGT[A/G]AGCCATCGTGCCCAG | 10152 |
rs144140292 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203395543 | TATTTTGAAGTGGTA[C/T]GCTTTTGAATTACCT | 10152 |
rs144141861 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ABI2 | GRCh38.p7 | 2:203423307 | CCTTGTGTTAGGCGC[C/T]AGGGATACACAGAGA | 10152 |
rs144164319 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203338315 | AAAACTCTTTGGTAT[C/G]GGTCAGATGTTTGTT | 10152 |
rs144213876 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203347209 | GGGTTTGGTCTCTGG[A/T]CAAACCATAGAAGTG | 10152 |
rs144218999 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203422308 | AAAGAAAAAAAATAT[C/G]GAGAGTCCCTATAAA | 10152 |
rs144269076 | snp | C/T | 0.000552792 | 0.016616 | intron-variant | ABI2 | GRCh38.p7 | 2:203351657 | CATCCTGCCTCAGTC[C/T]CTCAGTAGTCTGGGA | 10152 |
rs144317327 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203382189 | CATTTATGCATTAAG[C/T]GGTTGCTTAGATTTA | 10152 |
rs144354847 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366149 | GTGTCAACTTAATTT[A/G]TTTTAAAAATTACTT | 10152 |
rs144489019 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203404522 | ATTTGTTCAGGAGCA[C/T]GGGATTACAGGTACC | 10152 |
rs144491878 | in-del | -/AT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403649 | GATCATTTTCTTATA[-/AT]TCTTATAGGTAAGGA | 10152 |
rs144493776 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203355607 | GGCTGAGGTGGGCGG[A/T]TCACCTGAGGTCTGG | 10152 |
rs144557298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203407923 | TTCTGGCTCACAGAC[A/G]TTCTTGTCAGATGAA | 10152 |
rs144591463 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ABI2 | GRCh38.p7 | 2:203350959 | GAGTCTTTGAAGATT[G/T]TCTCCTAGGAGTTTT | 10152 |
rs144592112 | in-del | -/A | 0.084728 | 0.187577 | intron-variant | ABI2 | GRCh38.p7 | 2:203342847 | TGTCTATACACACAC[-/A]ACATCTCATTGTTTT | 10152 |
rs144653441 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203419968 | ACTCCAGCCTGGGCA[A/G]CAAGAGCGAAACTCC | 10152 |
rs144715060 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203370320 | CTTGAACTCCTGGTC[G/T]CAAGTGATCCTCCCA | 10152 |
rs144722786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386542 | ATTATTAGGGAAGTT[G/T]CATAGAGAAAAACCA | 10152 |
rs144763791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336546 | CTCCTAGTTCCCATG[A/C]GATGAGGCTCTCTAT | 10152 |
rs144783753 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203375927 | ATGTTTTCTTCTGCC[C/T]ACAGGCAATACTGCA | 10152 |
rs144887679 | in-del | -/TTG | 0.0581099 | 0.160244 | intron-variant | ABI2 | GRCh38.p7 | 2:203370123 | TAACTATTTTAGGTT[-/TTG]TGGGCCATGTGTTGA | 10152 |
rs144970407 | snp | A/G | 0.000197837 | 0.00994381 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394782 | AGCCCAACCCGTAAT[A/G]TGGCTCCCTCGCAGC | 10152 |
rs144985351 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203384508 | AGAGATGGGGTCTCA[C/T]TGTGTTGGCCTGGCT | 10152 |
rs145002198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203394163 | AAAGTGTGTATTTTT[A/G]TATATAGATATACTT | 10152 |
rs145019261 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203369790 | TTAAGTTTATACAGA[A/G]TATAAATTATTATGT | 10152 |
rs145031879 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203391540 | AGCTTCAGGCCAGGT[A/G]TGTTGGCTCATGCCT | 10152 |
rs145042404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401492 | AAAGTTTAGGGAGTG[A/G]ATTATATTATTAGGA | 10152 |
rs145076943 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203348591 | CCTCAATTAAAAACA[A/T]TCAACAATAATGTAA | 10152 |
rs145095166 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203340943 | TTCTTTGTTCACTCA[A/G]CTTCAGCCACTTTGG | 10152 |
rs145097266 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203398632 | AAGGTGTACTGACAT[A/G]TAATTGCCACCACAA | 10152 |
rs145109912 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203353087 | CAGAATTGTCTAATG[A/G]CGCATTTCTCAGAAT | 10152 |
rs145244517 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203356514 | GCTGGGACTACAGGC[A/G]CGTGCTGCCACGCCC | 10152 |
rs145270259 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371497 | CATTCATCATATCTA[C/G/T]AAGGCAGTATTAGGG | 10152 |
rs145322815 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203376685 | TTATAACAATGACCC[C/T]TTATTTTAGGCTTAT | 10152 |
rs145351959 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203368725 | TAAGTTAAAAAAAAA[A/T]TGGTGCGTTTTAATG | 10152 |
rs145402424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352664 | GTCAAAAGTTTATGA[C/G]GTAAAAATTACAGTA | 10152 |
rs145412373 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203374168 | TGTCTCAACAACCCA[A/G]AACACAAAAACTTTA | 10152 |
rs145444579 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203347338 | GCACTGGTTTTCACT[C/T]ATCTTTTGTGTGAAA | 10152 |
rs145453275 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327458 | TTTGTAGCACTTAAT[A/G]TTTTTTCAAGGTATT | 10152 |
rs145541325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203340328 | TACTGTGTAGTAACT[A/G]TAGTTAATAATATTG | 10152 |
rs145564884 | snp | A/G | 1.64852e-05 | 0.00287094 | intron-variant, missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411311 | CCTCCTCCTCCCTCC[A/G]TCCTACAGGTAACTC | 10152 |
rs145588832 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203415542 | GATTGGCATGAACCC[A/G]GGAGGCAGAGCTTGC | 10152 |
rs145682580 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ABI2 | GRCh38.p7 | 2:203378322 | TTCACCGTGTTAGCC[A/G]GGATGGTCTCGATCT | 10152 |
rs145718929 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326737 | CATACATTCTGCTAA[G/T]GTATGTATCATGAAG | 10152 |
rs145720267 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427774 | GTTAACCTCATGGCC[C/T]AGTGGGTACCCTAGC | 10152 |
rs145766207 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203405460 | GAGGCTGAGGCAGAA[C/G]GATTGGTTGAACCTA | 10152 |
rs145869685 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203399370 | TATCTGTTCAAATGT[A/T]TTGTTCCTTCTCACC | 10152 |
rs145923886 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203412807 | TGGGATACAGGGTCA[A/C]TGTTGCCAGGTTTTA | 10152 |
rs145944651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203359413 | CTCATTTGTAGAATG[C/T]ACAAAGATCCCAAAT | 10152 |
rs145962993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364491 | TGCGCTGACTTATCC[A/G]TAGAGCAGATAAACG | 10152 |
rs146029501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339912 | CACCCTTGTGGAACG[C/T]GTGTATATGAAAAGT | 10152 |
rs146063995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203337746 | CTATATTACAAAGCT[A/G]TAGGCCTGGCATGGT | 10152 |
rs146085015 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | ABI2 | GRCh38.p7 | 2:203344192 | ACAGTCTTATTGAGC[A/T]GCATAAGTTGTACCA | 10152 |
rs146150364 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203407963 | GGTCCGAAAAGAAAA[G/T]GATGTGGTATCTGAA | 10152 |
rs146171736 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365601 | CTCTCTCTCAGGCTA[C/T]GTGTTTTCTGGGGCT | 10152 |
rs146209531 | in-del | -/TTTGTTTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357760 | TGGTTTTTGGGGTTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 10152 |
rs146243304 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203362744 | GTCGGGCAGGCCGGT[C/G]TTGAACTCCTGACCT | 10152 |
rs146253179 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203347556 | ACAAGGCGTTTATCA[A/G]TCTCCACCATGTGCC | 10152 |
rs146269176 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203383949 | CTTTTCAGACAGTCT[C/G]CAGAGAAAGTCATCA | 10152 |
rs146289944 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430727 | AAAGTTACTGGGTGT[A/G]AGACATTTTCATCCC | 10152 |
rs146290290 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ABI2 | GRCh38.p7 | 2:203344815 | CTAAAGGTTTGCAAG[C/T]GCACCAATCTGCACT | 10152 |
rs146476968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203419727 | TATAAGAATGCTTTG[A/G]GCTGTAATCCCAGCA | 10152 |
rs146477680 | snp | A/C | 0.0418186 | 0.138422 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203327909 | ACAGAGGAGGGTCCC[A/C]AGAGTGGAGGCTGTG | 10152 |
rs146494559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203423340 | AGTGATGGGCCCTTA[C/T]CTCCAGGAGTTTATA | 10152 |
rs146496300 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203334372 | CTTATGTGTAAAATA[C/T]GTAGTAGAGATATTT | 10152 |
rs146532874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203333746 | CCTTGCTCTTTTAAA[C/T]ATTTTGTCATTTGTA | 10152 |
rs146595891 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203400462 | TGTTTTTAACTTGAT[C/T]GTAGGTTTGTATTAG | 10152 |
rs146698450 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203423890 | TCTAGAATGTATTCA[A/G]TTGAAATGCTAAATA | 10152 |
rs146717749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203376279 | AGTTATCTACCTGGA[A/T]GCTTTTCTATATTCT | 10152 |
rs146737091 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | ABI2 | GRCh38.p7 | 2:203379128 | AATACATTCTTACTC[A/G]TATGTCTTATGTGAG | 10152 |
rs146738727 | snp | A/G | 0.00034064 | 0.0130462 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402733 | TTATAGCCAGAATCC[A/G]GGTTAGTTTTTTTGT | 10152 |
rs146753406 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327131 | TTTTTTTTTGAAAGT[A/G]TAAGTTTCCTCATCA | 10152 |
rs146839116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203353813 | CAGAGGTACTTTAAA[C/T]TCTTATCTGTTTCTT | 10152 |
rs146858127 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203356058 | TATAGTTTTTTTTCT[C/G]TCTCTCTGAAAGCTT | 10152 |
rs146900645 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203336050 | GGCATTATGTAGTAT[A/G]TAGCCTTTTGTGTTT | 10152 |
rs146903047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424777 | ATACTAATTTTGGCA[A/G]AAGAAAAAGCTGAAC | 10152 |
rs147004865 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203406625 | TAGAAGAATACTGAT[A/G]TGTTGGGGCTTTAGC | 10152 |
rs147021547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203409595 | AAGAATGACCTTCAG[C/T]TTGTTGCTGTCCTTG | 10152 |
rs147093955 | snp | G/T | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428422 | GCCAGTATTAGTTGC[G/T]GCTGTATTACTGACT | 10152 |
rs147108770 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203381649 | TGTGTAATTGGATGG[C/T]TAGTTAATAACTGAA | 10152 |
rs147124713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385710 | GAAAACCTTTGTAGT[A/C]ACATCAACCTTTGAG | 10152 |
rs147137000 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403000 | GGTTATTTGCTTTTT[-/A]AAATAACATTGTGGT | 10152 |
rs147182547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203351465 | TCTGATCCATGAACA[C/T]GGATGTCTTTTCATT | 10152 |
rs147196182 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203354665 | ATTAGCATTTTCTTG[A/C]ACTATACTGGTTCCC | 10152 |
rs147290778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203417364 | TTCCTTTGGCCTCAG[A/G]AAGATTATTTTTCCA | 10152 |
rs147305038 | snp | G/T | 0.0640965 | 0.167152 | intron-variant | ABI2 | GRCh38.p7 | 2:203331560 | GACGGGATTTCCCCA[G/T]TTTGGCCAGGCTGGT | 10152 |
rs147307505 | snp | A/C | 6.93926e-05 | 0.00588995 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391096 | GCGTACAACACCTCC[A/C]ACTCAGAAGCCCCCT | 10152 |
rs147480700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203421831 | TAGCTGGGTGTGGTG[A/G]TGCACGCCTGTAGTC | 10152 |
rs147497158 | snp | A/C/G | 0.0209421 | 0.100162 | intron-variant | ABI2 | GRCh38.p7 | 2:203374045 | ACACTTGTAGTCCCA[A/C/G]CTACTCAGGAGGCTG | 10152 |
rs147499049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203424843 | CAGTCTCTGGAATCA[C/T]GTTAAGTGTAAATTC | 10152 |
rs147540732 | snp | C/T | 0.000236674 | 0.0108757 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427343 | GTCTATCATGCATTA[C/T]TCTGAGTAAAGCTCA | 10152 |
rs147555518 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | ABI2 | GRCh38.p7 | 2:203391714 | TAGTCCCAGCTACTT[A/G]CGAGGCTGAGACAGG | 10152 |
rs147572001 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203398854 | ATGCATTTGAGAATT[A/G]CCCATGTTGTTGCAT | 10152 |
rs147572213 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203341211 | CCATGCTTTTTTTAC[A/G]CCTACATATTTTCTC | 10152 |
rs147588584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345996 | ACTAGCCAGGACAAC[A/G]TGGTGAAACCCTGTC | 10152 |
rs147596774 | in-del | -/CA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346033 | AAAAATACACACGCG[-/CA]CACACACACACAAAC | 10152 |
rs147795481 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203390443 | TTGAGATCAGCCTGG[A/G]CAACACGGTGAAACC | 10152 |
rs147866919 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203414393 | AGGCGTGAGCCTCCC[C/T]GCCTGGCCTTGTTTT | 10152 |
rs147883791 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203361877 | GTTTGCAGGAATCGA[A/C]ATTTTGAGTGATTGT | 10152 |
rs147900287 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ABI2 | GRCh38.p7 | 2:203367876 | AGGTTTGGTGGTGCA[C/T]GCCTGTTGTCCCAGC | 10152 |
rs147959652 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427933 | CTTGAGTGCACCAAA[C/T]GAGTGAATGCTGAAC | 10152 |
rs148025289 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203363908 | TAGCTGGGATTACAG[A/G]CATGTGCCACCATGC | 10152 |
rs148078130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406409 | TCTATATATAGTTCT[A/G]TGAGATATAGGAGTT | 10152 |
rs148094512 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203354137 | GCAACCTCCACCTCC[C/T]GGGCTCAAGCCAACC | 10152 |
rs148113824 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203336551 | AGTTCCCATGAGATG[A/G]GGCTCTCTATTGTAC | 10152 |
rs148117749 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203425172 | CATCTCTGTTACAAC[A/T]GGCTTCATATTCTCT | 10152 |
rs148147605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203348355 | ATGAAGAGTTTTTCA[A/G]AACTCAGTGATCATT | 10152 |
rs148168573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203420900 | GGCCTTCCAAGCTGA[A/G]GGAATCACGTGAGTG | 10152 |
rs148242054 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203410208 | CAGGGAATTGCTACA[A/G]ATATTGTTGGGTTAA | 10152 |
rs148310998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203402159 | TACGCCTCAGCCTCC[C/T]GAGTAGCTGGAATTA | 10152 |
rs148326389 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203382280 | GGGAGTTAAAGAGAT[A/T]GTTAACTCTTGGCCT | 10152 |
rs148374743 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342582 | TATTTATTTATTTAT[G/T]TATTTATTTATTTTT | 10152 |
rs148377400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377306 | GTGACAGAGTGAGAA[C/T]CTGTTGCAAAAAAAT | 10152 |
rs148396629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203407916 | CAGTATATTCTGGCT[C/T]ACAGACGTTCTTGTC | 10152 |
rs148399160 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353202 | ATTTGTAATTTTTTT[-/T]CAGATTACAATTATC | 10152 |
rs148405849 | snp | A/C/G | 6.597e-05 | 0.00574293 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394801 | CTCCCTCGCAGCAGA[A/C/G]CCCTGTGAGGACAGC | 10152 |
rs148468519 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ABI2 | GRCh38.p7 | 2:203351201 | GAATTCCATTGATCT[A/G]TATGTCTATCTGTAT | 10152 |
rs148486007 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203422853 | AACTCTTCATTGATA[A/G]TGTCCAGGTTAACTT | 10152 |
rs148504571 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326887 | TCCGCTCACTGCAAG[C/T]TCTTCTCCCAGGATG | 10152 |
rs148554784 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203413527 | TGACCACCCTATCAC[A/G]GTTGATTGCCTTTTG | 10152 |
rs148675229 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203395563 | TTGAATTACCTTTAT[C/T]GTAGCTACATTCATC | 10152 |
rs148691855 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203344852 | AAACGCACCAGTCAG[C/T]GCTCTGTGTCTTGCT | 10152 |
rs148711782 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ABI2 | GRCh38.p7 | 2:203374943 | CAAAATATTTTATAC[A/G]GTACCTTCCTGTCAT | 10152 |
rs148764108 | snp | C/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366229 | GAGGCTGAGGCAGGC[C/G]AATGAATCACTTGAG | 10152 |
rs148766477 | in-del | -/TG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338909 | TAAGGGGTTTATATC[-/TG]TGTGTGTGTGTGTGT | 10152 |
rs148856287 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ABI2 | GRCh38.p7 | 2:203340745 | GTGATAACCATTTTA[C/T]AGTTTATGTGTGTAT | 10152 |
rs148858534 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203426890 | CCTCTTCAATGAGGT[A/G]CTTCCCTGTAGGCTC | 10152 |
rs148873987 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203415689 | AAAAAATACTAAATA[A/C]ATTGGATTGCTCAGA | 10152 |
rs148890452 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363503 | CCTATCTTTCCCTCT[A/G]CCTCCTCCTGTCCTA | 10152 |
rs148994207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399914 | ATGAATCGTGCTTTG[A/T]TGGCATATCTAAGAA | 10152 |
rs149063023 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203384820 | ACATCGCCCAAGCAG[A/G]TTCTTTTTTTTTTTT | 10152 |
rs149079721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203334475 | GTGTGTAAGGTAATC[C/T]TTTGGTGGATGAAAT | 10152 |
rs149082538 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352223 | CCAGCTTTTTGGGAG[-/C]CCGAGATGGAAGGAC | 10152 |
rs149085022 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ABI2 | GRCh38.p7 | 2:203369937 | TTTTACTTGTGTTTA[C/T]AGGTAGAATTCTTTA | 10152 |
rs149223046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392012 | GTATAGCCCAGAAGC[C/T]AGGTGATTAAAATTC | 10152 |
rs149225356 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424042 | TAAGTTTTTTCTTAC[A/G]TGTGCTTTATCAGTT | 10152 |
rs149243173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203420692 | GCCACCACGCCCAGC[C/T]GACAGTCCCTTATCT | 10152 |
rs149243900 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203329959 | CCAGACTGGTCTCGA[A/G]CTCCTGACTTCAAGT | 10152 |
rs149261611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203407738 | TCTTGTCTTATGAGG[A/T]ATCATTTTAGCTAAA | 10152 |
rs149333221 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ABI2 | GRCh38.p7 | 2:203350790 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 10152 |
rs149356092 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant, missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411347 | TTACCTTTAATGGGA[A/T]TTGTGGCCAGAGTCC | 10152 |
rs149387073 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ABI2 | GRCh38.p7 | 2:203386366 | ATAGCTCACTGTATC[C/T]TTGGGCTCAAATGAT | 10152 |
rs149403644 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ABI2 | GRCh38.p7 | 2:203336250 | GCAGTGGTGAATATG[A/G]CTGTAAACATTTGTA | 10152 |
rs149421843 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203413274 | TAGCAAAAAATGAGA[C/G]TTGAAAGTTGAATAG | 10152 |
rs149476295 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203358482 | ACTTAAACAACAAAA[C/T]GTAAATTTATTAGTT | 10152 |
rs149596923 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203344062 | TGCTTGAGCTCAGGG[C/T]TGGAGGCTGCAGTGA | 10152 |
rs149597447 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429341 | AGTTAAGCTCTTCTT[C/T]GTGTACTGGTCTATA | 10152 |
rs149617854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203417311 | TGTTCCTATTGGACA[C/T]GCTTTTTATGAATGG | 10152 |
rs149705386 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203390093 | GGATACCTCAGCCCT[A/C]ACTTTCTGGTTCAGA | 10152 |
rs149722115 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203340189 | ACCCATAGAATGAAG[C/G]AGATAATAGAATCTG | 10152 |
rs149790997 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326164 | GAGAGCCACCGTGCC[C/T]GGCCTCACCCTTTGA | 10152 |
rs149793782 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203361874 | TAAGTTTGCAGGAAT[C/G]GAAATTTTGAGTGAT | 10152 |
rs149865036 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203399204 | CCTTGTCAGCCCTTG[A/G]TGTTGCCTTTTTTAG | 10152 |
rs149931275 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203384451 | AGTTGGTACTACATG[C/T]GTGCACCACCATGCC | 10152 |
rs149984118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422084 | GCGGATTGCTTGAGA[C/T]GAGGAGTTCAAGACC | 10152 |
rs149985399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203333270 | TTGAATATATATCTG[A/G]TACTCATACTTTTAA | 10152 |
rs150054908 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366055 | GTTCATATGTAAACT[A/G]TCATAGTATTTCTTA | 10152 |
rs150073787 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203352389 | AGGCAGTCCTTCAGG[A/T]GGATTCCAGATGAAG | 10152 |
rs150093261 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203380921 | ACATATTTTGGCTGT[C/G]TTTTAAGATGTATTT | 10152 |
rs150160734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203415272 | AAGAATACTGATAAG[A/G]CAGCATGGTGTTGAT | 10152 |
rs150251415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203386234 | TCCTCACTATTTCAC[A/G]TACAGACACAACCTA | 10152 |
rs150298234 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ABI2 | GRCh38.p7 | 2:203335644 | TTTTTTGGTGACATT[C/T]ATGTTCTGTAAAGTT | 10152 |
rs150300446 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203423999 | CTGTTTCAGTCATAA[C/T]TGCACAAAAACCAGA | 10152 |
rs150331183 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425046 | TTTTTTTTTTTTTGT[A/T]TTTTTTTTTTGGTAG | 10152 |
rs150355781 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203419358 | CCGCCTAGGCCTCCT[A/G]AAGTGCTGGGATTAC | 10152 |
rs150372467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369670 | TGGAAATTACAGAGG[C/G]CTCAGTCAAAGCTGT | 10152 |
rs150387734 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203354509 | ACTACCAATTGTCAA[C/G]ACCTTCGAAGGGACT | 10152 |
rs150392003 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ABI2 | GRCh38.p7 | 2:203402240 | GGGTTTCACCACGTT[A/G]GCCAGGCTGGTCTGA | 10152 |
rs150408753 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203350044 | TCCAGTTTCTCCACA[C/T]TGTTGTCAGCATTTG | 10152 |
rs150442479 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203356473 | TCTCAGGTTTGAGCA[A/G]TTCTCCTGCCTCAGC | 10152 |
rs150461489 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203342991 | CATGTGTAAATAATA[A/C/T]AGTCTATACCGTTAA | 10152 |
rs150571570 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203389847 | GCTTTCTGTATAAGT[A/G]CTAACATACTCCTTT | 10152 |
rs150622219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425303 | ATCTCAGCTCACTCA[A/G]GTGATTCTCTTGCCT | 10152 |
rs150744052 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203411588 | ATAAAATAAGGCACA[C/T]ATAAGAAAAGAAAGA | 10152 |
rs150775950 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203344987 | GTAAAATGGACCAAT[A/C]AGTAGGACGTGGGCA | 10152 |
rs150781330 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432665 | TTCACAATACCCAAA[A/G]TGATGTTTCAGCTTT | 10152 |
rs150829615 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ABI2 | GRCh38.p7 | 2:203383689 | TCTAATGAAGAATCA[C/G]ACTTAGATAAGATCC | 10152 |
rs150845904 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203332809 | CTGAAATCTGAAAAG[C/T]CAACTTGTTGATATG | 10152 |
rs150870167 | in-del | -/CAACAACAACAACAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392315 | CACCACCACCACCAC[-/CAACAACAACAACAA]CAACAACAACAACAA | 10152 |
rs150904485 | snp | C/G | 0.00204102 | 0.0318801 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203417014 | GGAGGAAGCTGCTGT[C/G]GTTGAGTATAGTGAT | 10152 |
rs150942495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203426963 | CCCCATTTGTACTCA[A/G]TTTAGAGCCTAACAT | 10152 |
rs150959503 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203379922 | TTTCACGTGAAGGTT[G/T]TTTTTGGTTGTTCTT | 10152 |
rs151007755 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203375200 | AACTGTGGGAGAATA[A/G]TTGTTTATTAAGTCC | 10152 |
rs151061321 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203413651 | TTACAGACGTGGCAG[A/G]ACTTAAACATTAGTC | 10152 |
rs151077804 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361615 | AGAATGAAAACTAAA[A/C]AAAAGGAGAAAGGCA | 10152 |
rs151151616 | snp | A/G/T | 0.00637159 | 0.0561118 | intron-variant | ABI2 | GRCh38.p7 | 2:203351972 | AGTGACATGGTAGCC[A/G/T]TCCTAATGTTGTAGC | 10152 |
rs151166547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335549 | ATTACACCTGTCAGC[C/T]GCCATGCCTGGCCTT | 10152 |
rs151293320 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ABI2 | GRCh38.p7 | 2:203408265 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGGTTCA | 10152 |
rs151308128 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203392784 | TAGAAGAATGAAACT[G/T]TGTGTTGTTTTCAAG | 10152 |
rs180677150 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203334527 | TGTGATTTGCTTACA[A/C]CCACCCCAAATCCAT | 10152 |
rs180805182 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203412370 | CTGTAGCTGACCAAA[C/T]GCCCCCCTTTTATCA | 10152 |
rs180837635 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431404 | CGTGAAAAGACATGC[C/T]ATGTTTTGGTAAATA | 10152 |
rs180841848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203402350 | CTAATTAGTAAACTA[G/T]TTAGACATAACTTTC | 10152 |
rs180848861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203349368 | CACTGTCTAATCCTG[A/G]AGTCTCCATTAACAT | 10152 |
rs180853415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421735 | ACTTTGGGAGGCCAA[A/G]GCCGGCAGATGACAA | 10152 |
rs180868597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203368129 | TTGATGTTGTAAGTT[C/T]TTCATAAACATTCTC | 10152 |
rs180875115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384421 | AAGTGGTTCTCCTGC[C/T]TCAGCTTCCTGAGTA | 10152 |