SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs597171 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ABI1 | GRCh38.p7 | 10:26808431 | CATGCATACACACCA[A/G]CCCGCCATCCCACCC | 10006 |
rs666989 | snp | G/T | 0.444444 | 0.157135 | intron-variant | ABI1 | GRCh38.p7 | 10:26791087 | TATTCGCTCTGtttt[G/T]ttttttttttttttt | 10006 |
rs718825 | snp | C/T | 0.452597 | 0.146474 | intron-variant | ABI1 | GRCh38.p7 | 10:26834404 | TTGCAAATATTTTCT[C/T]CCATCTATGGGTTGT | 10006 |
rs718826 | snp | A/G | 0.452597 | 0.146474 | intron-variant | ABI1 | GRCh38.p7 | 10:26834352 | TCCTTTCTTGTGCAG[A/G]AGCTTTTTAGCTTTA | 10006 |
rs718827 | snp | C/T | 0.229136 | 0.249128 | intron-variant | ABI1 | GRCh38.p7 | 10:26834315 | TCCATTTGACTTTGC[C/T]TTGTTGCCTGTGCTT | 10006 |
rs718828 | snp | A/G | 0.452597 | 0.146474 | intron-variant | ABI1 | GRCh38.p7 | 10:26834444 | TTATATATTCTGGTT[A/G]TTGGTCCTGTGTCAG | 10006 |
rs899372 | snp | C/G | 0.140919 | 0.224948 | intron-variant | ABI1 | GRCh38.p7 | 10:26806043 | TAGATGCATTCCAGT[C/G]TGAGGTAATGGCATT | 10006 |
rs899373 | snp | A/G | 0.195214 | 0.243923 | intron-variant | ABI1 | GRCh38.p7 | 10:26805815 | CTTCTTGTATCTGCT[A/G]GGTGCTGGAATTACA | 10006 |
rs1031858 | snp | A/G | 0.453575 | 0.145111 | intron-variant | ABI1 | GRCh38.p7 | 10:26756458 | TTTCAGAACAGTGAT[A/G]AAAAGGTCACTTTTG | 10006 |
rs1046187 | snp | A/C | 0.0573587 | 0.15934 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI1, PDSS1 | GRCh38.p7 | 10:26746630 | AAGTTTTCTGAAAAA[A/C]CTTTTGCAATAAAAA | 10006 |
rs1115707 | snp | C/T | 0.150667 | 0.229419 | intron-variant | ABI1 | GRCh38.p7 | 10:26796214 | GGATCTCTAAACTTA[C/T]TCTGAATATCTGCTA | 10006 |
rs1324636 | snp | C/T | | | intron-variant | ABI1 | GRCh38.p7 | 10:26770680 | GTAAGATCTATAGTT[C/T]GTGTTCATGCACACA | 10006 |
rs1324637 | snp | A/G | 0.448323 | 0.15221 | intron-variant | ABI1 | GRCh38.p7 | 10:26770679 | TAAGATCTATAGTTT[A/G]TGTTCATGCACACAT | 10006 |
rs1408530 | snp | A/G | 0.235564 | 0.249583 | intron-variant | ABI1 | GRCh38.p7 | 10:26757134 | GAAAAGCTATGCTGT[A/G]AAGATACTAATCATT | 10006 |
rs1409127 | snp | C/T | 0.0376037 | 0.131863 | upstream-variant-2KB | ABI1 | GRCh38.p7 | 10:26861308 | ATTCCCCCAGTATCA[C/T]CCTGTGGCGCCACCT | 10006 |
rs1409128 | snp | A/C | 0.494526 | 0.0520291 | upstream-variant-2KB | ABI1 | GRCh38.p7 | 10:26861164 | GCGCTTTGGACGGGC[A/C]GCCTAGCCTAGGAGA | 10006 |
rs1409129 | snp | C/T | 0.44858 | 0.151875 | intron-variant | ABI1 | GRCh38.p7 | 10:26855115 | GTTTCAGATTTTTTT[C/T]TGAATTTTGGAATGT | 10006 |
rs1409130 | snp | C/G | 0.455024 | 0.143057 | intron-variant | ABI1 | GRCh38.p7 | 10:26854943 | GTATAGGAATTACAG[C/G]CTAGCTTTTCACTGA | 10006 |
rs1542553 | snp | A/T | 0.459347 | 0.136653 | intron-variant | ABI1 | GRCh38.p7 | 10:26807139 | TTCTTTATCTTTTTA[A/T]TTTTTCTGCCCTTGA | 10006 |
rs1543849 | snp | C/T | 0.457853 | 0.138915 | intron-variant | ABI1 | GRCh38.p7 | 10:26810941 | CTTCTCCTTCCTCCT[C/T]TCTCCCTCTTCCCCT | 10006 |
rs1575607 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ABI1 | GRCh38.p7 | 10:26781693 | attctgtagttttcc[A/T]agtggctgactaaat | 10006 |
rs1590445 | snp | C/T | 0.453939 | 0.144598 | intron-variant | ABI1 | GRCh38.p7 | 10:26782321 | ATAAGGCTGTTGCAG[C/T]ACTAAGCGATATAAG | 10006 |
rs1780190 | snp | C/T | | | intron-variant, downstream-variant-500B | ABI1 | GRCh38.p7 | 10:26762046 | gcgctccagcctggg[C/T]gacagagtgagaccc | 10006 |
rs1803070 | snp | A/C | | | utr-variant-3-prime | ABI1 | GRCh38.p7 | 10:26748092 | AAAATTTATGTATTG[A/C]AATATACTTAAAAAT | 10006 |
rs1853685 | snp | C/G | 0 | 0 | intron-variant | ABI1 | GRCh38.p7 | 10:26777803 | GATTTGGTATGTGTA[C/G]AAAGGGAAAGTTGTC | 10006 |
rs1966967 | snp | A/G | | | intron-variant | ABI1 | GRCh38.p7 | 10:26788910 | tttttttttttttga[A/G]acggagtctcgctct | 10006 |
rs1966968 | snp | A/G | | | intron-variant | ABI1 | GRCh38.p7 | 10:26788886 | tcgctctgttgccca[A/G]gctggagtgcagtgg | 10006 |
rs1966969 | snp | A/G | | | intron-variant | ABI1 | GRCh38.p7 | 10:26788836 | aagctctgcctccca[A/G]gttcatgccattctc | 10006 |
rs1966970 | snp | A/G | | | intron-variant | ABI1 | GRCh38.p7 | 10:26788767 | cgccaaccacgccca[A/G]ctaattttttgtatt | 10006 |
rs1998631 | snp | C/T | 0.456332 | 0.141164 | intron-variant | ABI1 | GRCh38.p7 | 10:26758891 | TTTTAAGAGTAATTG[C/T]TTACCACTTTCTCTT | 10006 |
rs1998632 | snp | C/T | 0.437118 | 0.165792 | intron-variant | ABI1 | GRCh38.p7 | 10:26758810 | CTATATTGAGTATAC[C/T]AAAATTTAACTTTAA | 10006 |
rs1998633 | snp | A/G | 0.150333 | 0.229274 | intron-variant | ABI1 | GRCh38.p7 | 10:26758711 | CATGTTTGAGACAGC[A/G]TAGTAATGGTAAAAT | 10006 |
rs1998634 | snp | C/T | 0.456332 | 0.141164 | intron-variant | ABI1 | GRCh38.p7 | 10:26758664 | GTCAAAGTTTTCCTT[C/T]AAATTAATATAATGA | 10006 |
rs2018904 | snp | A/G | 0.261884 | 0.249717 | intron-variant | ABI1 | GRCh38.p7 | 10:26792973 | GTGTTGCTATGTCAT[A/G]CTTCTTTCCTGCCTG | 10006 |
rs2031562 | snp | C/T | 0.455144 | 0.142885 | upstream-variant-2KB | ABI1 | GRCh38.p7 | 10:26861944 | gagggcaacataatt[C/T]gatccctgtcgctat | 10006 |
rs2094150 | snp | A/G | 0.263535 | 0.249633 | intron-variant | ABI1 | GRCh38.p7 | 10:26827060 | caggcatggtggctc[A/G]tgcctgtagtcccag | 10006 |
rs2148110 | snp | A/T | 0.45889 | 0.13735 | intron-variant | ABI1 | GRCh38.p7 | 10:26830216 | TCTACTCAAATATTC[A/T]TAGTAGCCCAGAACT | 10006 |
rs2148111 | snp | C/T | 0.145642 | 0.227177 | intron-variant | ABI1 | GRCh38.p7 | 10:26828949 | GTGAGCCACCGCGCC[C/T]GGCTAAACTGGTGCT | 10006 |
rs2148112 | snp | A/T | 0.495483 | 0.0473088 | intron-variant | ABI1 | GRCh38.p7 | 10:26822610 | atatagtatttacta[A/T]ttttttttttggtct | 10006 |
rs2182293 | snp | G/T | 0.459118 | 0.137002 | intron-variant | ABI1 | GRCh38.p7 | 10:26830153 | TGGAGAAACAAATTA[G/T]GATACATCCATACAA | 10006 |
rs2182294 | snp | A/C | 0.261332 | 0.249743 | intron-variant | ABI1 | GRCh38.p7 | 10:26830140 | TAGGATACATCCATA[A/C]AATAGAACACTACTT | 10006 |
rs2182295 | snp | G/T | 0.366266 | 0.221319 | intron-variant | ABI1 | GRCh38.p7 | 10:26822698 | CGTAATCCCTCCCTC[G/T]TGTCCCTTGTCCTTA | 10006 |
rs2219796 | snp | G/T | 0.457271 | 0.139781 | intron-variant | ABI1 | GRCh38.p7 | 10:26782371 | agtcgggtttttttt[G/T]ttgttgttgttgagG | 10006 |
rs2225015 | snp | A/G | 0.448836 | 0.15154 | intron-variant | ABI1 | GRCh38.p7 | 10:26855388 | CTGTGCTCTTTTCAT[A/G]TCATACTGTTTTCAC | 10006 |
rs2242232 | snp | C/T | 0.00686019 | 0.0581638 | intron-variant | ABI1 | GRCh38.p7 | 10:26751583 | GGTAAGGTACAGTCA[C/T]TGAGTTGATGTGAAG | 10006 |
rs2279173 | snp | C/G/T | 0.217074 | 0.262149 | intron-variant | ABI1 | GRCh38.p7 | 10:26754950 | GGGATTTTTTTTTGT[C/G/T]GGGGGGGAGAAGTTA | 10006 |
rs2296544 | snp | C/T | 0.142947 | 0.22592 | utr-variant-5-prime, upstream-variant-2KB | ABI1 | GRCh38.p7 | 10:26860979 | GCCGTCCCACAATAC[C/T]AGGCGGGAGGGCGGG | 10006 |
rs2306236 | snp | C/G/T | 0.000378919 | 0.0137594 | missense, intron-variant | ABI1 | GRCh38.p7 | 10:26759148 | GTTCGTCTGTATCCA[C/G/T]CAGAAGATGTCGAAG | 10006 |
rs2368184 | snp | G/T | 0.452597 | 0.146474 | intron-variant | ABI1 | GRCh38.p7 | 10:26750588 | GTCTCAAGAGCTACA[G/T]CTACTAGCTTAAAGT | 10006 |
rs2368185 | snp | C/T | 0.453331 | 0.145452 | intron-variant | ABI1 | GRCh38.p7 | 10:26755120 | GTAATTTACTTATTC[C/T]TGGTCATTCAATCTT | 10006 |
rs2477938 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ABI1 | GRCh38.p7 | 10:26820447 | tatccttgcaaaacc[C/T]gaaaatacttgcaaa | 10006 |
rs2477939 | snp | A/T | 0.021333 | 0.101051 | intron-variant | ABI1 | GRCh38.p7 | 10:26828674 | AGCACAGTAATTCGA[A/T]TGTACATTCTTAATA | 10006 |
rs2477940 | snp | A/T | | | intron-variant | ABI1 | GRCh38.p7 | 10:26843487 | aaaaaaaaaaaaAAa[A/T]atatatatatatata | 10006 |
rs2477941 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ABI1 | GRCh38.p7 | 10:26844370 | TCAACCCACGTCATA[A/T]GTATTTGAAATTTAT | 10006 |
rs2505969 | snp | C/T | 0.444133 | 0.157519 | upstream-variant-2KB | ABI1 | GRCh38.p7 | 10:26862752 | ATTTATCATCATCAT[C/T]ATTATTATTCATTCA | 10006 |
rs2505970 | snp | C/T | 0.492337 | 0.0614248 | intron-variant | ABI1 | GRCh38.p7 | 10:26857862 | tttttttctttcttt[C/T]tttttttttttttga | 10006 |
rs2505971 | snp | C/T | 0.403158 | 0.197592 | intron-variant | ABI1 | GRCh38.p7 | 10:26836612 | AACAGAAATGTTACG[C/T]GGCTATTGTGGATCA | 10006 |
rs2763197 | snp | A/C | | | intron-variant | ABI1 | GRCh38.p7 | 10:26766009 | AATGGGAAAACTGAC[A/C]TGAAAAGGTAATGTA | 10006 |
rs2927920 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ABI1 | GRCh38.p7 | 10:26809036 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 10006 |
rs2927923 | snp | A/G | | | intron-variant | ABI1 | GRCh38.p7 | 10:26758066 | tttttttttttttga[A/G]acagagtttcactct | 10006 |
rs2985489 | snp | G/T | 0 | 0 | intron-variant | ABI1 | GRCh38.p7 | 10:26758163 | TATTTACATAGGAGG[G/T]TGCTTTAAGTTCTTT | 10006 |
rs2985490 | snp | G/T | 0 | 0 | intron-variant | ABI1 | GRCh38.p7 | 10:26758126 | ATAATGAATGACCTG[G/T]ATATGTATTTTAAAG | 10006 |
rs3004233 | snp | C/T | 0 | 0 | intron-variant | ABI1 | GRCh38.p7 | 10:26758183 | AATACTCAGTGAATT[C/T]TCCATATTTACATAG | 10006 |
rs3004234 | snp | A/T | 0 | 0 | intron-variant | ABI1 | GRCh38.p7 | 10:26757911 | ctagccaatttttgt[A/T]tttttagaagggaca | 10006 |
rs3214920 | in-del | -/A | 0.196149 | 0.244131 | intron-variant, downstream-variant-500B | ABI1 | GRCh38.p7 | 10:26763610 | GGGGGATTAGACTAG[-/A]AAAATCTAAACAAAC | 10006 |
rs3215811 | in-del | -/A | 0.446252 | 0.154871 | upstream-variant-2KB | ABI1 | GRCh38.p7 | 10:26861109 | AAGACAGTGCGAAAG[-/A]AAAAAAAAAATCCCG | 10006 |
rs3221311 | microsatellite | (CA)18/19/20/21/22/23/24/25/26/27 | 0.729286 | 0.184656 | intron-variant | ABI1 | GRCh38.p7 | 10:26834550 | tcaagacatacaaaa[lengthTooLong]aaaagaagacatacg | 10006 |
rs3758439 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ABI1 | GRCh38.p7 | 10:26755534 | TTTCAGTAACATGTC[G/T]GCACCTATTTTCAAG | 10006 |
rs3758440 | snp | A/G | 0.165853 | 0.235413 | intron-variant | ABI1 | GRCh38.p7 | 10:26776715 | AGAAATGAAACGATA[A/G]AAGTATTTATAAATT | 10006 |
rs3802611 | snp | A/T | 0.141258 | 0.225111 | intron-variant | ABI1 | GRCh38.p7 | 10:26748839 | AATATATAGCACAGC[A/T]AAACTATTTTTATGA | 10006 |
rs3802612 | snp | C/G | 0.446249 | 0.154875 | intron-variant | ABI1 | GRCh38.p7 | 10:26748964 | TGATTAGACTGAATA[C/G]ATCAATAGGTTCTGT | 10006 |
rs3802613 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ABI1 | GRCh38.p7 | 10:26753292 | TCTTTGCCCATAACT[C/T]CCTCTATAAAACTTT | 10006 |
rs3802614 | snp | A/T | 0.25912 | 0.249834 | intron-variant | ABI1 | GRCh38.p7 | 10:26756160 | ATAGCTATAACAGGT[A/T]TGTCTAGCTTTAAGG | 10006 |
rs3802615 | snp | A/T | | | intron-variant | ABI1 | GRCh38.p7 | 10:26760082 | CAAAGAATCTGCTTT[A/T]AAAAAAAAAAAAAAA | 10006 |
rs3802616 | snp | A/G | 0.148996 | 0.228688 | intron-variant | ABI1 | GRCh38.p7 | 10:26771881 | TGACTAGCCTACACA[A/G]CATGAAACAATGTGT | 10006 |
rs3818409 | snp | A/G | 0.493748 | 0.0555599 | intron-variant | ABI1 | GRCh38.p7 | 10:26769344 | TAAATTTAGCTTCCT[A/G]TTTAAAGAACAGTGG | 10006 |
rs3839921 | in-del | -/ATAAG | | | utr-variant-3-prime | ABI1 | GRCh38.p7 | 10:26747759 | TTGGGACAGATTAAG[-/ATAAG]GCTAAAATTTTTTTC | 10006 |
rs3839922 | in-del | -/G | 0.258843 | 0.249844 | intron-variant | ABI1 | GRCh38.p7 | 10:26748871 | GATTTCTTAATTTTT[-/G]TATCTATCAATATAA | 10006 |
rs3839923 | in-del | -/A | | | intron-variant | ABI1 | GRCh38.p7 | 10:26752605 | TGTAATTAAAAAAAA[-/A]CAAACAAAAAGGAAC | 10006 |
rs3839924 | in-del | -/TA | | | intron-variant | ABI1 | GRCh38.p7 | 10:26766139 | AGAAAGGTGATAACA[-/TA]GGGAAATTTTCTGGA | 10006 |
rs3916988 | snp | A/G | 0.454664 | 0.143571 | intron-variant | ABI1 | GRCh38.p7 | 10:26814028 | CCATTCTAGGTACCC[A/G]CCCTACCTCCCCAGT | 10006 |
rs4372343 | snp | A/G | 0.447032 | 0.153878 | intron-variant | ABI1 | GRCh38.p7 | 10:26838927 | ATTCTAAAAATGAAC[A/G]AAGTATAATTCTAAT | 10006 |
rs4376804 | snp | A/G | 0.455024 | 0.143057 | intron-variant | ABI1 | GRCh38.p7 | 10:26842716 | AGATAAAGGCAAGAC[A/G]TTAATATACAGACCA | 10006 |
rs4403701 | snp | A/T | 0 | 0 | intron-variant | ABI1 | GRCh38.p7 | 10:26834516 | aaggaaaatggcaaa[A/T]gatctggacagatac | 10006 |
rs4463751 | snp | C/T | 0.164546 | 0.234942 | intron-variant | ABI1 | GRCh38.p7 | 10:26796317 | aatggaccacatata[C/T]atcacaccacataat | 10006 |
rs4492706 | snp | A/G | 0 | 0 | intron-variant | ABI1 | GRCh38.p7 | 10:26825102 | ttgaaggttggggta[A/G]ctggggcaatttctt | 10006 |
rs4581345 | snp | C/T | 0.490398 | 0.0686206 | intron-variant | ABI1 | GRCh38.p7 | 10:26818115 | AGTGAGCCAAGATGG[C/T]GCCACTGCACTCCAG | 10006 |
rs4628582 | snp | A/G | 0.164873 | 0.23506 | intron-variant | ABI1 | GRCh38.p7 | 10:26806441 | TGTTTACAGGCAACC[A/G]CACTGGAAACAACAG | 10006 |
rs4747575 | snp | C/T | 0.454544 | 0.143743 | intron-variant | ABI1 | GRCh38.p7 | 10:26813593 | AAAGACTCCTGAAGT[C/T]CCCAAGATCCTGTCT | 10006 |
rs4749185 | snp | C/T | 0.454544 | 0.143743 | intron-variant | ABI1 | GRCh38.p7 | 10:26813739 | AACATTTTAAAGACA[C/T]TTTCAGAAATGTAAA | 10006 |
rs4749186 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI1 | GRCh38.p7 | 10:26818248 | TATATTTTCTGATca[A/G/T]aaataataactatgg | 10006 |
rs4749188 | snp | G/T | 0.148996 | 0.228688 | intron-variant | ABI1 | GRCh38.p7 | 10:26818569 | AGGCAGGGGCAAAGG[G/T]TGCAGTGAGGCAAGA | 10006 |
rs4749190 | snp | C/T | 0.14933 | 0.228835 | intron-variant | ABI1 | GRCh38.p7 | 10:26826110 | aaagttttcaattta[C/T]ttttcccaagttcat | 10006 |
rs4749192 | snp | G/T | 0.455263 | 0.142713 | intron-variant | ABI1 | GRCh38.p7 | 10:26841696 | gatcatgcaatattt[G/T]tcttcctgtgtctgg | 10006 |
rs4749193 | snp | C/T | 0.19334 | 0.243495 | intron-variant | ABI1 | GRCh38.p7 | 10:26860493 | GCAGCGGCGGGCTCC[C/T]GGCTCCCTCGCCCAT | 10006 |
rs4749194 | snp | A/G | 0.145978 | 0.227331 | upstream-variant-2KB | ABI1 | GRCh38.p7 | 10:26862376 | CTTCGACCTCTGAAA[A/G]GAAAAACTCAGTTTC | 10006 |
rs5004352 | snp | A/T | 0.448836 | 0.15154 | intron-variant | ABI1 | GRCh38.p7 | 10:26855026 | AACATGACACAAAAA[A/T]AAATGCTCATTAGAC | 10006 |
rs5010875 | snp | A/G | 0.332568 | 0.235971 | intron-variant | ABI1 | GRCh38.p7 | 10:26814960 | TGAATTCTAAATTTT[A/G]AGATTATGTCCTAAT | 10006 |
rs5025734 | snp | A/G | 0.262159 | 0.249704 | intron-variant | ABI1 | GRCh38.p7 | 10:26809276 | cttatctcaaaaaaa[A/G]aaaaaaaaTTACTAG | 10006 |
rs5783989 | in-del | -/T | 0.44638 | 0.154709 | intron-variant | ABI1 | GRCh38.p7 | 10:26855020 | GCATCAACATGACAC[-/T]AAAAATAAATGCTCA | 10006 |