SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs146430037 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873489 | GGAGAAGCTCTTGCA[A/G]AAGTAGAGTCAGGAA | 9063 |
rs146430294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814549 | TGCTGTTCATGTAAT[C/T]AGATACAGAGTACTG | 9063 |
rs146442641 | snp | A/G | 0.000680865 | 0.0184382 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821089 | TGTTTTAAATAGCAC[A/G]GGAAATTACAAACAA | 9063 |
rs146492009 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916069 | CTCTGCATAAACTAG[C/T]ATGGGGCATAACATG | 9063 |
rs146543313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891122 | ATCCTATCTAAAATA[C/T]AATGTAAAATGTGAT | 9063 |
rs146554024 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894115 | TGGGCGACAGAGTGA[C/G]ACCCCATCTCAAAAA | 9063 |
rs146562957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871009 | CAACAAAGAAAGGAT[A/G]AAGGACCTATGGAAT | 9063 |
rs146565542 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846355 | ATTTCTCCCCCAAAC[A/G]GATAAAACTTTCTTT | 9063 |
rs146658376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911122 | CTACCAAGACAAGCT[A/G]AATGGCTACAACATG | 9063 |
rs146669175 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863505 | GGTTTCACCATGTTG[C/T]CCAGGCTGGTCTGAA | 9063 |
rs146669635 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914988 | GTTTTTCTTCCTTTA[C/T]TATAATGTCACACAA | 9063 |
rs146681334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868932 | TGGACTCTCAGCAAC[A/G]CAGGTGAAAAGGATC | 9063 |
rs146803114 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889897 | CCAGAAGAAACAGCT[A/C]AAATAATTAAGGTTG | 9063 |
rs146856620 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875365 | AGAAACTCCAACTTA[C/T]GTGGTCCCACCCCAT | 9063 |
rs146944403 | snp | C/T | 1.65002e-05 | 0.00287225 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890692 | CTGCTGCATCTCAAA[C/T]GTGGGCTTAGTATCT | 9063 |
rs146955705 | in-del | -/T | 0.0337553 | 0.125452 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861571 | TCACCAAAAATAAGA[-/T]TATCAATATTATGTT | 9063 |
rs147043181 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871660 | ATTCAAGAGCAGCTC[A/G]TTCCTGTTTGTTTCC | 9063 |
rs147062352 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880462 | TGACACATACCTATA[G/T]TCCCAGCTACTCAGG | 9063 |
rs147062764 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824542 | GACAGGTATTATAAG[A/C]CTGCATTTAAAGACT | 9063 |
rs147098668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830863 | AGGTCAGCATTACTC[C/T]GATAATAAAACCAGG | 9063 |
rs147137573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889066 | GGACACTCACCTAAT[A/G]CCATATACGAAAATT | 9063 |
rs147146786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839477 | ATAAGTACCTATTTG[C/T]CAATTTTTATAATTT | 9063 |
rs147156855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843855 | TCTGAGCCTAAAGCT[A/G]TCTTCCCTCTTCTTT | 9063 |
rs147192730 | in-del | -/GC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887242 | TAAAACATAAATAAA[-/GC]CAAAAAGCAAAAAAT | 9063 |
rs147206849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902869 | GGAAGGGTAGACACA[C/T]AGATCAAGCAAAGAG | 9063 |
rs147243003 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908879 | CCAGGCATGGTGGCG[A/G]GTACCTGTAATCCCA | 9063 |
rs147244453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817595 | TGATACCTCATCCAC[A/G]GAAAATTGAATGTGG | 9063 |
rs147314510 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839813 | GAGGTTGCAGTAAGC[C/T]GAGATCATACCACTG | 9063 |
rs147361449 | in-del | -/ACCCATT | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877482 | TCTTCACTCCTGACC[-/ACCCATT]CTGTAAACTGCCCCT | 9063 |
rs147362060 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848555 | ACAAGCAAAGAGGAA[C/T]ACACCCTGTCTACCA | 9063 |
rs147421189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862501 | CTCTGCTTTTAACAT[A/T]ACAGCCCCCCAAAAA | 9063 |
rs147457050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867135 | CTTAATGTTAGTAGT[C/G]TGTGTCATAACAGAC | 9063 |
rs147466600 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810034 | AGTACTAATGCTCAA[C/G]ACAGATAAACAACGT | 9063 |
rs147474211 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816941 | TTAATAATATTCAAT[A/G]AATCCTCTCCCTTCT | 9063 |
rs147609109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895895 | TCCCTATAATTAAAT[C/T]CACTTTTATTTGAGA | 9063 |
rs147616988 | snp | C/G | 3.29853e-05 | 0.00406098 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890716 | AGTATCTTGAAGCAG[C/G]ACAGAACCAACAGGA | 9063 |
rs147618771 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898697 | TAAAAAACTATAGAA[C/T]AAAAGAAGCTTTGAG | 9063 |
rs147630643 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811524 | GGCTCCAAGATATCA[A/C]TATTTGATAGTGTGA | 9063 |
rs147714199 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916013 | CCACTAAAACCCTTA[A/C]ACTTATCAAGTATGA | 9063 |
rs147724024 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920234 | TATTAGATCACAACT[A/G]GGCATATAAATCTGA | 9063 |
rs147724637 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835490 | TAGAGATGCAACTCA[A/C]TATGTTGCCCAAGCT | 9063 |
rs147916610 | snp | A/G | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921197 | CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC | 9063 |
rs147933822 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880368 | TGCCTGGGTGAGAGA[C/G]AGAGAGACCCTGTCT | 9063 |
rs147976468 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900765 | TGAATCACGAGGTCA[A/G]GCGTTCAAGACCAGC | 9063 |
rs147985658 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852459 | CATGGAGCTGCTGCA[G/T]GCCCCTGGCTCCAGG | 9063 |
rs148025635 | in-del | -/TT | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849242 | ACTCAGCATAAAGTG[-/TT]TTTTCAATCTATTCT | 9063 |
rs148037658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847843 | ATATCCAATTCCCAA[C/T]TACCGCAAGACTTCA | 9063 |
rs148068681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916721 | TAAAACACTAAGAAA[A/G]TATCGAGGTTTAAGG | 9063 |
rs148078925 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871956 | TCCTGATGTATGGGC[A/G]AGAGAAGGAAATCGA | 9063 |
rs148134647 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865308 | ACTCTGGGAGGCCGA[C/G]GCAGGTGGATTACTT | 9063 |
rs148231567 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883668 | ACATAGCAAAATCTC[A/T]TATCTACAAAAAAAT | 9063 |
rs148269545 | snp | C/T | 0.00151632 | 0.027493 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890891 | GTTCGTGGATATCGG[C/T]GTCTATACAATTCTC | 9063 |
rs148283417 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877583 | AAACACGTCTTGTAC[C/T]GTAACAAACAGCCTC | 9063 |
rs148292822 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826170 | ATCTTATACTTACCA[A/G]TGTTAGTTTTTGTTT | 9063 |
rs148347293 | snp | A/G | 0.0263992 | 0.111815 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816715 | TCAAGTGATCCTCCC[A/G]CCTCAGCCTCCCAAA | 9063 |
rs148439765 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839064 | TCCTTTTTAAAAATC[A/T]CATGTTATTCTTTTT | 9063 |
rs148447231 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909803 | TCAGTGCAGGTCAGG[A/G]TTTTTCTGCAAGACA | 9063 |
rs148447528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819135 | ATGCTCATTACCTTT[C/T]TTCAGGATTAATTTT | 9063 |
rs148498708 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46902473 | GTTGAGGTAGGAGAA[C/T]TGCTTGAACCCGGGA | 9063 |
rs148562690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849145 | TAACACTGTCTGACA[C/T]AGTAGAAAAGGGCAA | 9063 |
rs148593381 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919257 | TTTGGGAGGCAGAGG[C/G]GGGCGGATCACCTGA | 9063 |
rs148602954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873841 | GCCAAACAAGCTGCC[A/G]TTTCCTCTGAAACGC | 9063 |
rs148646003 | in-del | -/C | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915527 | GGGGCCATCTTCTAA[-/C]AAATGCAAGAAGTAA | 9063 |
rs148656929 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870613 | AGAGCAAGACTCCGT[C/T]TCAAAAAAAAAAAAA | 9063 |
rs148665109 | snp | A/G | 0.0126979 | 0.078662 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811831 | AAAACCAAGTAACAC[A/G]AATGCCATTTTTCTT | 9063 |
rs148741759 | snp | A/G | 4.99214e-05 | 0.00499582 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828013 | CATTTCCTTTTGGCA[A/G]GAGGGTCTTCCTCTT | 9063 |
rs148742567 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897465 | AGAATAATAACTGCA[C/T]TGGATTCAAACCGAT | 9063 |
rs148771643 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893407 | TTTACAGAAATGACA[A/G]AACAAAGCACAAAGT | 9063 |
rs148806860 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880013 | GGAGATAGATGGCAG[C/T]GATGGTTCCAACAAT | 9063 |
rs148808882 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844596 | ACTCACCAGTAATGT[A/G]TATAAATTAGTATAT | 9063 |
rs148848161 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899667 | AGATGAGATTTCATT[A/G]TGTTTTGCAGGCTGG | 9063 |
rs148849042 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808293 | AGAATCATAGGCAAT[C/T]AATTGTTATACTTTT | 9063 |
rs148910297 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847040 | CAAAATATTTCACAA[A/G]TCCAGAAAGGTAGGA | 9063 |
rs148964835 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841084 | CTGCAGGACAGACTG[A/G]AAATCACTAGCTGAA | 9063 |
rs148968849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911805 | AATCCCACCACTTTG[A/G]GAGGCCAAGGGAGGG | 9063 |
rs149004244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864452 | GTTTCTTTAACGTTA[A/G]GTACGTAACCATTCT | 9063 |
rs149022619 | in-del | -/AG | 0.0905309 | 0.192535 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811603 | ATTCAATGGCTGCAT[-/AG]AGTTTCTTTTTTGAG | 9063 |
rs149058798 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857727 | AAATTAACAAAAACT[A/G]GGAAATACAATGTGC | 9063 |
rs149085712 | in-del | -/TATGTG | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919006 | GCGTGTATATATATA[-/TATGTG]TGTGTGTGTGTGTGT | 9063 |
rs149108487 | in-del | -/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812290 | AGTCTTCTGTGTTCA[-/C]CCCTCAGAAAGCAAA | 9063 |
rs149115492 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921535 | ATTTTTCTAATCTGG[A/G]AAAGAAAAATGACTA | 9063 |
rs149172008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885506 | AGCCCTGGTGACAGT[A/G]CAAGACTCCATCTCA | 9063 |
rs149181545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870956 | GAATTCAGGAATCAG[C/T]ACCTCAGACCCAAGA | 9063 |
rs149217766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816455 | TCTAAAGCCTTTTTG[A/T]AAATTGTTGCTACAG | 9063 |
rs149274941 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888727 | ATGCACAGTTCACAG[C/T]AGGGTTCCTGCACCT | 9063 |
rs149284982 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838688 | TGCCCAAGGCTTTTA[C/T]ATAAATCTCATAAAA | 9063 |
rs149309831 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872365 | TTTGTTTTTGAATGG[C/G]AAGATCCTCATTCTG | 9063 |
rs149338799 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916379 | GTAATTTCAAGTTTA[C/T]ACTCATCTCTACCTT | 9063 |
rs149340328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831723 | ACAAATCTTAACAAA[C/T]GATGGTGCAGCAATC | 9063 |
rs149343588 | in-del | -/T | 0.0425829 | 0.139564 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846484 | ATATAAATATGCATA[-/T]TTCCTTTCCAGGAAA | 9063 |
rs149371199 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901766 | AACAAGAATAGAGGA[C/G]AGCTTCCTCAATTTG | 9063 |
rs149374683 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46809978 | ACATTAAAGGCTGAC[A/G]GATTAATAATCATGA | 9063 |
rs149409766 | in-del | -/TT | 0.494855 | 0.0504572 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876698 | TGATCCCTTTACTAA[-/TT]TTTTTTTTTTTTTTT | 9063 |
rs149427481 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897057 | AATTTTCTATCATTG[A/T]AAATTTAAGAGTGTT | 9063 |
rs149436863 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848723 | AGACAAAGAGAAGAA[C/G]TTCAATAACTTGCAT | 9063 |
rs149520226 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913416 | TTTACCCAGTATCTA[C/T]TGATAAAGTTATCAT | 9063 |
rs149557512 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818441 | ATATCATTTCTTCTT[C/T]GTTCTCCTGCAGATT | 9063 |
rs149644226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893118 | AAAACAAGAAAACTT[C/T]TGGCCTATCTCATAA | 9063 |
rs149657286 | in-del | -/T | 0.0581099 | 0.160244 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856305 | CACCTGGCCAAAGAC[-/T]TTTTCTTTTACTATA | 9063 |
rs149679360 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879931 | CAGGAGCTGGGGGAA[G/T]AGGGAATAGTGAATT | 9063 |
rs149740503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818501 | GGAATGTTAAGAAAT[A/G]TATTAAAACTTTGTT | 9063 |
rs149745769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894759 | GGCAAGCTGAAGGTG[C/T]TACCTCATTAGGTAG | 9063 |
rs149777627 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911214 | ACTTTGTTATATTTC[-/T]CTTTTTTTTTTTTTT | 9063 |
rs149801347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889796 | TCCACAGAATTATTC[A/G]CAATAGCTAAAATGT | 9063 |
rs149889273 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919108 | GTAATCCCAGCACTT[C/T]AGGAAGCCGAGGCAG | 9063 |
rs149890501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833883 | AGTAAATGTGGTTGA[A/G]AATAATCTGGGTGCT | 9063 |
rs149951315 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867503 | TGCAAAGTATGCAGG[C/T]TTTGCAGTTTATTTT | 9063 |
rs149959301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850740 | GCTTCGGCATCCATT[A/G]ATGATAGCTACCTAG | 9063 |
rs150150159 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888145 | TTCAAAATTAACCAC[A/G]AAAATGAAAACCTGT | 9063 |
rs150155457 | in-del | -/AAGG | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870178 | ACAGAACAGTGTAAA[-/AAGG]ATATTCAGAACTCCT | 9063 |
rs150192835 | snp | C/T | 1.68165e-05 | 0.00289965 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46891019 | AAAGCCTAGTAATAC[C/T]TGTAGTTCAGAAACC | 9063 |
rs150261807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911508 | GACGTGAGCCACTGT[A/G]CCCGGCTGACTTTGT | 9063 |
rs150265765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823179 | TAGAGGCTGCAGTGA[A/G]CCATGAATGCTCCAC | 9063 |
rs150268161 | in-del | -/AG | 0.0205511 | 0.0992634 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834638 | GTTTACTTTTGAAAC[-/AG]AGTCTTTCTCCATCA | 9063 |
rs150296365 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896670 | CTTTTAGGCAAAAGC[C/G]TATGAAATGGCGGGC | 9063 |
rs150326279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857457 | AGTCCAATCTAACTA[C/G]AAAACAGGGTTTTTA | 9063 |
rs150348404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891523 | TGAGTAGTAAATCCA[C/T]AAAAATCAAGTCAGA | 9063 |
rs150358849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843214 | AGTTAAATAAAAGAA[C/G]ATACAGTAGAGACTC | 9063 |
rs150409443 | snp | A/C | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921254 | TGCCTCAGCCTCCCA[A/C]GTAGCTGGGATTACA | 9063 |
rs150414258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838116 | GATGTTCTTTTTCTT[C/T]TGGTTCATCTGTAAT | 9063 |
rs150419008 | in-del | -/A | 0.0652144 | 0.168387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910471 | TACAAACCCACTGTT[-/A]AGAGTCACCAATTCA | 9063 |
rs150461992 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887234 | AGTTTTGCTAAAACA[A/T]AAATAAAGCAAAAAG | 9063 |
rs150465357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915754 | GGCCAACAACATTCA[C/T]AAGAGTCTAATAAAA | 9063 |
rs150484159 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853188 | AGAGTGAGATGGGAG[A/T]ATCGCTTGAGCCTCT | 9063 |
rs150525456 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879838 | CACGTAAGTCAAATA[A/G]TAAGACATATAAGTA | 9063 |
rs150632194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865791 | GAAGAGGGAGATGCC[A/G]TTTAAGATGAAGGCC | 9063 |
rs150642438 | snp | C/T | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809721 | GATCGCACCATTGCA[C/T]TCCATCCCGGGCAAC | 9063 |
rs150672493 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889652 | AAATGCAGCTGCCAC[A/G]GAAAACAGTATGGTG | 9063 |
rs150726694 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884486 | CCGGCTAATTTTTTG[C/T]GTTTTTAGTAGAGTC | 9063 |
rs150788000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913109 | TGGAAGATTCTGTTA[C/T]ATCTATCATAGCTAT | 9063 |
rs150789525 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827453 | GGAAATTACCACATG[C/G]CTGACACCGAGGCTT | 9063 |
rs150840375 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907686 | GCAGGTCCACTTATA[C/T]GCATATTTTTTTTTC | 9063 |
rs150872945 | in-del | -/C | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886245 | GCAGGGCTACCCAAG[-/C]CATATCACTAGTCTG | 9063 |
rs150876790 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860756 | CAAAGGAGGGAAGAT[A/C/G]ACTTGAGCACAGGTG | 9063 |
rs150885589 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845032 | AGCTCAATCATTTTA[A/G]AGGTATTTCTTGATC | 9063 |
rs150922992 | in-del | -/G | 0.0520825 | 0.152737 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849186 | GAGAGTAACACTCAT[-/G]TAAGAATGAAGTGTC | 9063 |
rs150969320 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910318 | AAAGTGCATCCTGCT[A/G]AAGTTACACTAATGA | 9063 |
rs150998049 | in-del | -/TA | 0.0607341 | 0.163335 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849582 | ACTCAAAGAATTTTT[-/TA]TGTTTCATGCTCTGA | 9063 |
rs151004543 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902694 | AAATTCCAACAAGAT[-/T]TTTTGTAGATATAGA | 9063 |
rs151075617 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880567 | CACTGCACTCCAGCC[C/T]GGGCAACACAGTGAG | 9063 |
rs151104731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874744 | AGTTACATACTTAGT[C/G]TGTCTTCCACTTTCT | 9063 |
rs151109124 | snp | C/G/T | 0.000891184 | 0.0210905 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836423 | ATCCAGGTGGGCTTT[C/G/T]TCTCATTCATTTGTA | 9063 |
rs151140858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822670 | CCACAGGGATCAAAC[A/G]AACAGGACATCATCA | 9063 |
rs151191654 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903883 | GGAAAACTATTCAGC[A/G]ATAAAAAGGGATGAG | 9063 |
rs151192393 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812104 | TATTTACATAATTTT[A/C]TTGCTCTTTATTTTA | 9063 |
rs151197439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891417 | AACCAACCCCTCCCA[A/C]TATACAATGTAATGT | 9063 |
rs151243326 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897865 | GATAATACAAGGCAA[C/T]ATAATTTTTGGGTTT | 9063 |
rs151252459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886206 | TGTCCTGTGCTTAGC[C/T]ACATTCCTGAGGGGC | 9063 |
rs151262634 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837243 | GTGTATTAACATGCT[C/T]TGTTCCACTCAACCT | 9063 |
rs151313651 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830095 | TACTGAGCATCACCT[C/G]TGTAACTCAATGAGT | 9063 |
rs151338007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915456 | CTGCACCCCTCACTC[A/C]TCTGAAAATTCTCCC | 9063 |
rs180673324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887093 | CGTTCTTTTTACTTG[A/G]TCCAATAATTCTACT | 9063 |
rs180680411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871406 | GCTAAACCATATAAA[A/G]GACATAGAGAGACAA | 9063 |
rs180683786 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903935 | GATGAATTTCCAGAA[A/T]TATGCTGAATGAAAA | 9063 |
rs180758546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832027 | AAGATAAAATGATAG[A/G]AAACATTTAAAAATC | 9063 |
rs180767663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852869 | TGGCACAGTCACACG[A/G]TGATACAGGATAAGC | 9063 |
rs180884134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834501 | AAGATATTATAATGA[C/T]CAATATATGGAATTA | 9063 |
rs180939364 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811638 | CAAGCCTCAAATTTA[C/T]AGAAAACTCTAGAAT | 9063 |
rs180943542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856450 | CTCAGCATCTCCATA[C/G]CATGCAACTTCATAA | 9063 |
rs181014567 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848059 | AAATGAATTAACATA[C/T]TCCCTTTTGTACAGA | 9063 |
rs181014579 | snp | A/G | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890763 | GTGTAACTGAAGTGG[A/G]AGGCAACGAGTGGAT | 9063 |
rs181031677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874425 | AATAGAACCCACTTC[A/G]CTGCACGTCATTAAA | 9063 |
rs181050615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867864 | TATACAGCTCCAAGG[C/G]TGAACCATAAAAATA | 9063 |
rs181054530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900587 | GAGGCTGAGGCAGGA[G/T]GATACCCTGGGCCCA | 9063 |
rs181062387 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883206 | CAATGAATGAGATTA[C/T]GAAGGACTGTCCCTT | 9063 |
rs181087579 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920791 | GAAATCCCTGCACTT[A/C]CTTGAATCCAACTTC | 9063 |
rs181174307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851744 | CAGTCTAGGGACACG[C/T]TGCCATTTTCAAAGT | 9063 |
rs181184189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831090 | AACAAAAGGCATCCA[C/T]GTTAGAAAGAAGAAG | 9063 |
rs181186307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870812 | TGGTAGTCTGGGAAC[A/G]TGAACATCCTCCTGG | 9063 |
rs181201744 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886865 | AAAAACAAATAAAAT[C/T]GAATAAAATAAAATA | 9063 |
rs181204895 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823342 | CTTTTTCCCACTCCC[A/C]CTTCTCTTCCTTTGC | 9063 |
rs181212732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862708 | ATATATACACATATA[C/T]GTATATATTCTTTTG | 9063 |
rs181239646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841268 | CTCACGTCCACTGCA[A/G]ATCACTTTACGAAAA | 9063 |
rs181240911 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880176 | CGAGACGGGAGGATC[C/T]CTTGAGCCCAGGAGT | 9063 |
rs181244655 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903703 | AACCCAGCAACTACA[C/T]TCCTGGGCATTTATC | 9063 |
rs181245305 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914934 | GAATCCAAGATTATT[G/T]CTTCCCCTTTTCTTT | 9063 |
rs181329604 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896527 | AGAATAAAAGCCAGG[A/G]AGTAAAATACATACG | 9063 |
rs181367008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875536 | TCTTCTCTCTGAGTC[A/G]GTTGAAAACAATAAA | 9063 |
rs181368510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857689 | ACAGCTCACTAAGGA[A/G]TTACACTTTATTCTG | 9063 |
rs181375116 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892348 | TACTATATATGTCTC[C/T]ATATTTCATAATGTA | 9063 |
rs181382410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910729 | TTGTAGATTACAATC[G/T]TCTACAGGAGAATAA | 9063 |
rs181432805 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815745 | CACATTTATTTTTCA[G/T]AAATACAGAGGTTCA | 9063 |
rs181443589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835203 | CACAAATGCACACAC[C/T]AAAAATGTGTATATG | 9063 |
rs181486752 | snp | C/T | 0.000648929 | 0.0180012 | utr-variant-5-prime, intron-variant, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920143 | ATGGGTTGGGTAGGT[C/T]TGACTGCAAAGAGTT | 9063 |
rs181536176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847240 | TGGGAAAGAAAAAAA[C/T]CAAACTGGGAAGTGA | 9063 |
rs181567728 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882961 | GCCAGGCCTGGTGGC[A/G]GGTGCCTAGAATCCC | 9063 |
rs181576533 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840161 | GCAAGACTCTATCTC[A/G]AAAAGAAAGAAAAAG | 9063 |
rs181580983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821921 | ATTTTTTTTGCATTC[C/T]TCCTATTTAACCTGC | 9063 |
rs181603021 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900058 | AACATGGTCCAACAT[C/G]GTCTCTACTAAAAAT | 9063 |
rs181664181 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827096 | GCCATTATATACTTA[A/T]GATGGGTACATTTTA | 9063 |
rs181667015 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862326 | GATGACAGAGCGAGA[C/T]TCTGTCTCAAAAAAA | 9063 |
rs181680140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895813 | GCCAGAAAGATACTG[C/T]TTACTCTTTTCAAAG | 9063 |
rs181683205 | snp | A/G | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879567 | TCTGGGTGTATACTC[A/G]TAAGAATTAAAAAAC | 9063 |
rs181705399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867315 | CTCCAGGAACTTACA[A/G]CAACAAAAAATTGTG | 9063 |
rs181709533 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914299 | TCAGGTTTGTGTGCT[C/T]TGACTCTAAGCCCCC | 9063 |
rs181805857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46812875 | ACAAAGGTAAAAGTA[C/T]AATGTCAACAATAAC | 9063 |
rs181822006 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834905 | ATAGCTTACTCCTCC[C/T]GGGAGGCATCTTAAT | 9063 |
rs181888777 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832403 | CCTGGGCGACAGAGC[A/G]AAACTCCATCTCAAA | 9063 |
rs181898712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872199 | GCAAGGCCCCAGAGC[C/T]ATTAACTAAACAGTC | 9063 |
rs181914380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904920 | ATATGGTTTAAAAAT[C/G]GATAGAACTACAAAG | 9063 |
rs181960909 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883672 | AGCAAAATCTCATAT[C/T]TACAAAAAAATACAA | 9063 |
rs181972163 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900758 | AGGCGGGTGAATCAC[A/G]AGGTCAGGCGTTCAA | 9063 |
rs181975562 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921222 | AACCTCTGCCCCCCC[A/G]AATTTAAGCAATTCT | 9063 |
rs182010337 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857334 | TAGGTAACAGAAATA[C/T]AACACCTAAAATAAA | 9063 |
rs182043960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891292 | AATTTTGGTAATCTA[C/T]AGTCTATTGGTTTCT | 9063 |
rs182075843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889107 | AGATCAGGCTTAAAT[A/G]TAAGACCTAAAACTA | 9063 |
rs182096472 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842217 | GGCAACAGAGAGAGA[A/C]CCTGTCTCAAAAAAA | 9063 |
rs182107772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863798 | TGTATCCCCAAAATT[C/T]ATACGTTGAAGTCCT | 9063 |
rs182157916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853881 | ACTAAATGTCCCACC[C/T]GGGGAAACATGTATG | 9063 |
rs182166861 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823910 | ATGCAAAAAATAGAT[A/G]TGAGTAACAGATTCC | 9063 |
rs182173292 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905806 | TCCTCAAAGAAAACA[A/G]TAGTAATAATTTTAT | 9063 |
rs182191458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887477 | AAGCAATCTTCCACA[G/T]CAACTATGAAATGTT | 9063 |
rs182281683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869735 | ATTGTTGTTTCATTT[A/G]GACCACAGAGCTCAT | 9063 |
rs182286316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911621 | ATACTCATGTCAACA[C/T]ACATATTTAAAAGAG | 9063 |
rs182297240 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902207 | AAATGTAACAAACAC[A/G]TACAGGACTTATATG | 9063 |
rs182300273 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885138 | TTTTTCACTTCAAGT[A/G]ATAAAAAAAATTTTA | 9063 |
rs182312597 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875135 | AACCCTTCAGTTTGA[C/T]GCTTGTTCAGTCATC | 9063 |
rs182328138 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910015 | TACAAAAAAATTAGC[A/C]GGGCATGGTGCACAC | 9063 |
rs182345785 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808578 | CTGTAGTAAAAAAGA[C/T]GGTGAATCAGGCTGA | 9063 |
rs182354795 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849506 | GGGCAAATATGCGAG[A/C]TTTCTAAGCAAAGGC | 9063 |
rs182364580 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829109 | AAACTCTAAGTTCAC[A/G]TGTGGGTTTCAATGA | 9063 |
rs182365328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880859 | AACACTTTACAACTG[C/T]ATCTATATAGCAATA | 9063 |
rs182383735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854470 | ACGTGCCATGTTGTA[C/T]TATTTTTTTGATTAT | 9063 |
rs182480274 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832861 | GGTGCCATTGCACTC[C/G]AGCCTGGGCAACAGA | 9063 |
rs182481844 | snp | A/C | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807933 | TGAATCAAGAACTAC[A/C]AAAGTGTTCATATAC | 9063 |
rs182525505 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845797 | AATTCTAGGTCAATT[A/G]ATCATTTTAATTATA | 9063 |
rs182574994 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872530 | GGATGACCTGCTTAT[A/T]TCTGGTGAAGCTATA | 9063 |
rs182579947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854058 | AGGTTCACAAAACAA[C/G]TATTTCTCAGGTCTC | 9063 |
rs182593620 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888054 | CAAAAATCAATTGCA[C/T]TTTTATAAACTAATA | 9063 |
rs182598019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905636 | AGACAAGGGGATATT[A/G]ACTACAAGTAACTGC | 9063 |
rs182617946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833246 | TATATGCAACATAAA[C/T]GTATCTCAAACAAGT | 9063 |
rs182643526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897101 | AGTTTGCTTGAACAG[G/T]GGAAACTGGGTGTGG | 9063 |
rs182651692 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873138 | GGAAGCTAACCTTTG[C/G]GGGAAACTTGGTGGT | 9063 |
rs182733041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837062 | TGTTCCCAATCTTTT[A/G]TCACTACAAACAATG | 9063 |
rs182771294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875752 | GATTAAATATTCCAT[C/T]CGCACTCTAAACAAA | 9063 |
rs182894685 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860354 | CCAGAATGTACAATA[C/T]GCTAGATCAAATAGA | 9063 |
rs182951683 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916393 | ACACTCATCTCTACC[C/T]TGATACATTTAAAAA | 9063 |
rs182956882 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893222 | AAGCAAGTAATACGA[C/T]GCATCTTTCCCTCAA | 9063 |
rs182995645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894302 | TTCACCAAGTTTCAG[A/G]CCCTTCCCCCACAGT | 9063 |
rs182997765 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877443 | ATCTGTAAGTCACAT[C/T]TCTTCCTTATTTGGA | 9063 |
rs183018042 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913116 | TTCTGTTATATCTAT[C/T]ATAGCTATTAGTCTG | 9063 |
rs183020354 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816658 | TTTTTTGTAGAGAGA[C/G]GGTCTCGCTATGTTG | 9063 |
rs183027515 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858352 | GGCTTTAGAAAGATC[A/T]TATGTAGGAGCTTTC | 9063 |
rs183059715 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825837 | ATCCATGAAGATGAC[A/T]ACAAAGTTGTCCTTA | 9063 |
rs183090105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865422 | GCACGTGCCTGTAAT[C/T]CCAGCTACTCCAGAG | 9063 |
rs183095904 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898703 | ACTATAGAATAAAAG[A/C]AGCTTTGAGGCCGGG | 9063 |
rs183133105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880996 | AAAACTGAGTTATTT[A/G]TAGGTGATTTATCTA | 9063 |
rs183139238 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897487 | CAAACCGATTAAATA[C/T]AGTAATGTTTCATTT | 9063 |
rs183142966 | snp | A/G | 0.0287284 | 0.116357 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917261 | GGCCGGCGACGTTGC[A/G]GTTTCCCCACCTCCT | 9063 |
rs183189556 | snp | A/T | 0.0456081 | 0.143958 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844156 | AGAAAAAAAAAAATT[A/T]AAAAAAATTAAGGGT | 9063 |
rs183197387 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864885 | AAATGCTCCCCAGGA[C/G]AACTGTATTCAAGAA | 9063 |
rs183243063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849123 | CTGGAAATTAGAATT[C/T]AAGACATAACACTGT | 9063 |
rs183253739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884169 | GGTAATGTTCCTTTT[C/T]CAGAAAGTAGCAGCT | 9063 |
rs183321210 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818594 | AAAACTCTTCACAGT[A/T]TGACTAACTACATAA | 9063 |
rs183321234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868560 | CAGTGTAGATTGTGC[C/T]GTCTGACTCCAGCCA | 9063 |
rs183337892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845244 | GTTCTCATATTTTCA[C/T]TTAAAAGAGGAATTC | 9063 |
rs183345530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881820 | AGAATACACAGACAC[C/T]GGGCACGGTGGCTCA | 9063 |
rs183377802 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921620 | CTGTAAATTTATAAA[G/T]TGAAAGATGGTAAAT | 9063 |
rs183440307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837633 | AATCAACTGTGTCAA[C/T]TTTTCAACATACTTT | 9063 |
rs183452599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858839 | AAGGGGAGTTTCTAG[A/G]AGGGTATCCAGGTTT | 9063 |
rs183466234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828806 | TCACATTTTCACAGA[A/G]AAGTATGTTATTATC | 9063 |
rs183490851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846364 | CCAAACGGATAAAAC[C/T]TTCTTTGTTCCTCTT | 9063 |
rs183491951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869281 | TAAGCCTCTAGAGAA[C/G]GGAAGGCAAGAAATA | 9063 |
rs183495579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826613 | AAAATTATAACTTCA[C/T]TTTCTGTTTATCATT | 9063 |
rs183506967 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900962 | CTGGGTGATAAGAAC[A/G]AAACTCTGTCTCAAA | 9063 |
rs183573308 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906619 | CTGAAAATAACAAAA[C/T]TTTATTGAAAGATGT | 9063 |
rs183591386 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866222 | GATTTACAAATCAAA[A/C]TCCATGTAAAATAAT | 9063 |
rs183598125 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882171 | TTAACTGAGTTAATA[A/G]AAATAATATATACAG | 9063 |
rs183775010 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909670 | AGATAATCTGACATT[A/G]TCCAATATTGGTGAA | 9063 |
rs183802254 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828676 | GATAAGTTGAAAAAA[A/C]CCCAAACCTCTCAAT | 9063 |
rs183844772 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824861 | AAAAAAAACACAAAA[A/T]AATTAGCTGGGGGTG | 9063 |
rs183917304 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831266 | TTAGCCATAATCACA[A/C]AAATTTTTTAAATAC | 9063 |
rs183924022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871124 | ATTTTGTTATGAACA[C/G]TTGGCCAGATATTGC | 9063 |
rs183927105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851831 | CATGGGTCCATAAAG[A/G]CTGGGTATTACAGTA | 9063 |
rs183967943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893542 | ATGGGCTGTTGTAAA[C/T]AGACAAACAAAAAGT | 9063 |
rs184005028 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848715 | GGAATAAAAGACAAA[A/G]AGAAGAACTTCAATA | 9063 |
rs184028719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886990 | AAAGGCAAAAAGTAA[C/T]GAGATATGACAAGCA | 9063 |
rs184036692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903737 | GAGAAAGATGTGTGC[A/G]TAAGTTTACCAAAAA | 9063 |
rs184114274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876459 | ATTAGAGATGCTAGT[A/G]AAGGAACAGCTAAAC | 9063 |
rs184132467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912635 | CAAAGTCTAGGACAG[C/G]TGGAAAATGACCTAA | 9063 |
rs184177571 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890163 | CAGTGGAAGTAGAAT[A/G]GTAACTGCCAGGGGC | 9063 |
rs184189928 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908680 | AAAAGCCTGATAAAT[A/G]CAATCACATAAAAAT | 9063 |
rs184251938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834409 | TATAATGACTATGTA[C/T]AGGCCAGTAAGAAAA | 9063 |
rs184260350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874194 | ACCACCCATCGGAGG[A/C]AGAACCCTGGAATAG | 9063 |
rs184266952 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856150 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 9063 |
rs184310562 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811889 | TGCAGGACGAAAAGT[A/G]GAATCCAAGCTTTGG | 9063 |
rs184317645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856779 | GAGAAGATCACTAGA[C/G]TGTAGTCCTTTCTTG | 9063 |
rs184336495 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918898 | TTCCCCTGTTATGAC[C/G]TCTCCTAGGACCCTG | 9063 |
rs184343046 | snp | C/T | 4.94409e-05 | 0.00497172 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890843 | CTGAAAACCGATGAT[C/T]TGATTGTGGATAAAT | 9063 |
rs184372146 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838232 | TTTATATAGTTCTAC[A/C]TACGTGCAAGGTACA | 9063 |
rs184379731 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830772 | ACAAAGAAAATCCTA[A/G]GCCCAATGTCTTCTC | 9063 |
rs184422315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834641 | TACTTTTGAAACAGA[C/G]TCTTTCTCCATCACC | 9063 |
rs184443232 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899339 | AGCACTCTATGGATA[C/G/T]CTGAGGAAAAGCATT | 9063 |
rs184451461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866956 | CTGAATGACTGGAGA[C/T]AACCTACCCTGAAAA | 9063 |
rs184458830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874706 | ACATTCCTACGTTTG[A/T]AACTAAAGATCAATT | 9063 |
rs184465472 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882709 | GTACTGGGTAAGTTA[C/T]GGTACATCTATAAGA | 9063 |
rs184477045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839664 | GAGGTCAGGAGTTCG[A/T]CACCAGCCCAGCCAA | 9063 |
rs184479125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877691 | CAGCCAATGGGGACA[C/T]GACACAGAACCAGGG | 9063 |
rs184495683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913842 | GGGTCTCCCTCTGTC[A/G]CTCAGGCTGGAGTGC | 9063 |
rs184565404 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899828 | AGGGAGGTAGTCAAC[G/T]AAACAAACCTTTACT | 9063 |
rs184571384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919757 | CTTGTATTTGTTTAA[C/T]GAATAAAGGAATGAA | 9063 |
rs184586672 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820166 | CAGTAGCCATTTAAG[G/T]TAACAGATTAACTAT | 9063 |
rs184629042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895240 | AATAAGGTTAGAAAT[C/T]ATGGTAAAGGTCAAT | 9063 |
rs184638403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833784 | CAATGGAACAAATAG[C/G]AGTTCAGAAGTTAAC | 9063 |
rs184710142 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902833 | AACTTAGCTAGGACT[A/G]ACAGACTGCATGGTA | 9063 |
rs184714892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878913 | TCCTAGCGGTTACTG[C/T]CAAGGTTAACAGGGG | 9063 |
rs184715146 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862136 | AGGAGTTCAAGACAA[A/C]CCTGGCCAACGTGGT | 9063 |
rs184718591 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810505 | ACCAAAAAACTGCAA[C/G]ATGGTTTGGAAATCT | 9063 |
rs184769200 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820686 | ACAAATTCTTCAAAA[G/T]GAAGAATAAAATCTC | 9063 |
rs184780738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886299 | GTAATAAATTTGCTA[A/G]TCCTTCAACATAGAT | 9063 |
rs184783140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840035 | GCATGATGGCAGGTG[C/T]CTGTAATCCCAACTA | 9063 |
rs184807451 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900384 | AAAAAAAAGATAATA[C/T]AGGCAAGGAACAGTG | 9063 |
rs184922962 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920452 | GAAAAATCACACACA[A/C]ACAAAATCTCAGCAT | 9063 |
rs185010620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819591 | CAGTAACATAAACTT[A/T]CACCAACAGGATAAG | 9063 |
rs185124172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851122 | TTATGTCAGTCCTGA[C/T]TTACTATGAGACAGG | 9063 |
rs185151091 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886807 | AGCGCCACCGCCCTC[C/T]ATCCTGGGCGACAGA | 9063 |
rs185222258 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900610 | TGGGCCCAGGAGTTT[A/G]AGGCTGCAGTGAGCT | 9063 |
rs185226196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883409 | AATACATATAAGAAT[A/G]TAATTATATAGTGCC | 9063 |
rs185258136 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870538 | GAAGAATGGCGTGAA[C/T]CCAGGAGGTGGAGCT | 9063 |
rs185268676 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903236 | TAAAACCTGTGCTAC[A/G/T]CAAAAGACCCCTTTA | 9063 |
rs185283581 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873507 | GTAGAGTCAGGAAGA[C/T]TGCCCAATAATTGGT | 9063 |
rs185289240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848141 | CATGACACTCTCCTA[C/T]GTGCAAGCAGGAATT | 9063 |
rs185297103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828311 | CTGTCTGTAAAATGG[C/T]TGTTCACCTAGGGAG | 9063 |
rs185301271 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867952 | CTATAAAGAAGCCCA[A/C]ATTAGACCACATGAA | 9063 |
rs185303323 | snp | A/G | 5.01995e-05 | 0.00500972 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846850 | CATAGCCCTATAACC[A/G]TAAGAAAGAAAAATT | 9063 |
rs185384560 | snp | A/G | 3.34247e-05 | 0.00408794 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855345 | TAAAAAGCAACTTAC[A/G]GGCAAAGGAAATAGC | 9063 |
rs185403862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826932 | CAGGCATTATAGACA[C/G]AAAAAAACGATTGCC | 9063 |
rs185424039 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889419 | AATTCAAAAATGGGC[A/G]AGAGACTTGGCTATA | 9063 |
rs185487181 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46835818 | TGGTACATGGATGAC[A/G]TGCAATTTTTAAAAA | 9063 |
rs185504311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858049 | GGCATCACAGGGGAC[A/G]TATGAATTGAACTGG | 9063 |
rs185519485 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875546 | GAGTCGGTTGAAAAC[A/G]ATAAAGAAATCCAGA | 9063 |
rs185568368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895398 | ACCTCAGGACGGACA[C/T]GGTGGCTCACACCTG | 9063 |
rs185622227 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830490 | TAAACACTGAAGTAG[C/T]ATTTAAAGGAAAATT | 9063 |
rs185631459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910780 | CTCTGATTAGCACAC[C/G]AAGTATTTTAGATTC | 9063 |
rs185713708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914270 | TCCTTCAATCCATCA[A/G]GATAATCTGCTGATC | 9063 |
rs185768494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850581 | TTTTAGAAACAAAAA[A/C]CTTCACAGAAAATGT | 9063 |
rs185780136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914445 | ACAAGGTATAGAGCT[G/T]CCATATTCTGCTATG | 9063 |
rs185845165 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862630 | GTGTGTATACATATA[C/T]ACATACATATATATA | 9063 |
rs185857297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853890 | CCCACCCGGGGAAAC[A/G]TGTATGGGCCATGTA | 9063 |
rs185861526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895841 | AAGGTCATTGGAGGC[A/C]CCAGTTCCTGGTCCT | 9063 |
rs185865432 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832729 | AACCCCATCTCTACT[A/G]AAGACACAAAAAATT | 9063 |
rs185865585 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879962 | ACTGTTAAATGCATA[C/T]AGAGTTTCAGTTTTG | 9063 |
rs185878055 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920980 | TTTATTACATTTCCA[A/G]TGGTAAAATGTTTTA | 9063 |
rs185888591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893359 | CACTCCTTATACTTA[C/T]TGTCAGATATTCTTC | 9063 |
rs185994719 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813820 | GTTCATCAATAAAAT[A/G]AATGCCACATACAGA | 9063 |
rs186007497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835044 | CAGGGCAATTTTAAA[C/T]TGAAAAAGTAGAAAC | 9063 |
rs186008123 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875817 | AGGCCCAGACTGTCC[C/T]CTTTCCACTCAGATG | 9063 |
rs186016335 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911966 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 9063 |
rs186119747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857391 | AAAAAGTAAGTGCTA[C/T]AGAAAAAGGGAAAAT | 9063 |
rs186210197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841278 | CTGCAAATCACTTTA[C/T]GAAAATACTGTGAAA | 9063 |
rs186218047 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880386 | AGAGACCCTGTCTCA[A/C]AAAAAACAAAACAAA | 9063 |
rs186226116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823545 | CACCTAATAACTGTA[C/T]GTGTCCTGTCACTTA | 9063 |
rs186245503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915124 | GAAAAGCCCAGACTC[C/T]AAAAGCTACATGTCT | 9063 |
rs186287679 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921272 | AGCTGGGATTACAGG[C/T]ACCCGCCACCATGCC | 9063 |
rs186336221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883939 | CTTGAACCTGAGAGG[C/T]AGAGGGTGCAGTGAT | 9063 |
rs186348864 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900800 | CCAAGATGGTGAAAC[C/T]CCATCTCTCCTAAAA | 9063 |
rs186357201 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862709 | TATATACACATATAT[G/T]TATATATTCTTTTGA | 9063 |
rs186367180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867472 | TTTTAACATAACCAT[A/G]AGAAAGAATGCAGGA | 9063 |
rs186403076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896969 | CAAATAATTTGGGGG[A/C]AGTAGGTGGGGACAT | 9063 |
rs186449498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824334 | GCAATTTTGCTACCA[A/G]TTCTTAATGATTATC | 9063 |
rs186460558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842704 | ACCTGAAGATACTGA[A/G]AAGAACTCATGCCTG | 9063 |
rs186463016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827382 | TAGAATGCCATCCTA[A/C]CCACCTATATTTTGC | 9063 |
rs186475210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863888 | AAAGCCACAGGGTAG[C/G]TCCCCAATCCAATAT | 9063 |
rs186475390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904412 | ACAAAAATGTAACGG[C/T]GAGGAGAAATTTTTT | 9063 |
rs186560107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880941 | CCCATTATATACAGC[A/G]AAGTTTTTCTAATTT | 9063 |
rs186561678 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897434 | AGCCTAAGATGAGAA[A/T]ATTTGAGCATCAAAA | 9063 |
rs186565066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847308 | AAATCTGGTGAGTGA[C/T]AAAAATATTTTCCAC | 9063 |
rs186572606 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883039 | GGAAGCAGAGGTTGC[A/C]GTGAGCCAAGATCAC | 9063 |
rs186580327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815871 | CACAAAGCACACACT[C/T]GGGAATTGCTGCGCT | 9063 |
rs186587268 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829144 | GTTAGATAAAAAGAA[A/T]CTCTAAGTTCACCTG | 9063 |
rs186591817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869863 | CAGGAGGAAATAGAT[C/T]ATGCCCTGTATTGGC | 9063 |
rs186605401 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850213 | CTCCCACTCTAGATT[A/G]TTTTAAAGCAAATCT | 9063 |
rs186614255 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885140 | TTTCACTTCAAGTGA[G/T]AAAAAAAATTTTATA | 9063 |
rs186674453 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887785 | AATCAGGATCAATAA[A/G]TAAGATTTGTATCTA | 9063 |
rs186700833 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902292 | CCGGGCACGATGGCT[A/C]ACGCCTGTAATCTCA | 9063 |
rs186725390 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822782 | GAGGAGAGAGAGACT[C/G]GGGTATACGTGAGTG | 9063 |
rs186829342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905746 | CTAAAACAGGTTTGA[A/G]ACTTGAAAATATGAA | 9063 |
rs186870653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872299 | TTTACAGTGATAGAC[C/T]TAAAAGACACCTTCT | 9063 |
rs186885228 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905361 | AACAAGGAGGCAATA[C/T]GCAGACATTTTATGA | 9063 |
rs186885807 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833047 | CACACACCTGGCATG[C/T]GACCAGGCATTCTAC | 9063 |
rs186895122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872625 | CAAAAGGAAAGCTCC[C/G]ATCTGTGGAACCCAA | 9063 |
rs186895288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826019 | TCTTAAGAGTTCTTC[C/T]GTGTATTAATGTGTA | 9063 |
rs186901868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854087 | TCTAAGTCCACAGGC[C/T]GTGTATGCGACAAAT | 9063 |
rs186903288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888077 | AACTAATAATAAATA[A/T]GATGAAAAGGAAATT | 9063 |
rs186933251 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840580 | AGCATACAGAAACGA[A/G]AATATCCAGGACTAT | 9063 |
rs187031415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875136 | ACCCTTCAGTTTGAC[A/G]CTTGTTCAGTCATCT | 9063 |
rs187037973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828979 | TAATTAATAATGGCA[C/T]AAATCCTTTATTTTT | 9063 |
rs187057340 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848829 | GCCCATCTTAAGTTG[C/T]TCAAGTGAAAAAAAA | 9063 |
rs187066789 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910534 | CATCAGAGAAATTCA[A/C]GGTATTTCCCCATAA | 9063 |
rs187185208 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832284 | GCCAGGCGTGGTGGC[A/G]CACACCTGTAGTCCC | 9063 |
rs187211393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871657 | CAGATTCAAGAGCAG[C/G]TCGTTCCTGTTTGTT | 9063 |
rs187237635 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828775 | AAAGACAGTCTCACA[C/G/T]ACCATATTTGTTAAC | 9063 |
rs187245426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868648 | CTCCTTTGTTTGGTG[C/T]GCTCTCGCAGCGGCC | 9063 |
rs187251985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891599 | TAACAAACAAACAAC[A/G]TAATAAAGATATTTT | 9063 |
rs187321683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860518 | ATTAAAGAGCGCTCA[A/C]AGTGGGTTTCAGGGA | 9063 |
rs187333751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894383 | GGTTAGCCTGCTATG[A/G]ACACTACCAAGAATG | 9063 |
rs187338183 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877476 | GCGTCCTCTTCACTC[C/T]TGACCACCCATTCTG | 9063 |
rs187345072 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913617 | CCCATTGAGTGATGA[G/T]AAGTAGGGAAAGTAG | 9063 |
rs187415326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853002 | ATCTTAGCAGCCAGA[C/T]GCAGTGGCTCACACC | 9063 |
rs187420860 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887102 | TACTTGATCCAATAA[C/T]TCTACTCATAGGACT | 9063 |
rs187450222 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810704 | AATCAACATAAAAAG[A/C]ACACACAAAGGCCAT | 9063 |
rs187462279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833823 | TTACAAGAAATGTAT[G/T]AGATAATGCAAGTAG | 9063 |
rs187465725 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881433 | ACTGTATTTGTAAAA[A/C]ACTGAATATTGCTAT | 9063 |
rs187467275 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873534 | TGGTTGGCCCAAACA[A/T]GTTAATGCATGTTTA | 9063 |
rs187470066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897923 | ATTGCCCAAGCTGGA[A/G]TGTGGCAACACGATC | 9063 |
rs187474834 | snp | C/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917731 | CCTAGAGCTGGGTCG[C/G]AACTGAGGCGTTATC | 9063 |
rs187519931 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858439 | GGCTTGAAGCTGGGC[A/G]CAGTGGCTCACGCCT | 9063 |
rs187591316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817029 | TTCAATATTTCTATT[A/G]TTAAGTAAAAAAAGT | 9063 |
rs187756541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818809 | TTTTCAATAATAACA[A/T]CCAGTATCACCATAA | 9063 |
rs187777725 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837289 | ATTAAATTCTTCGGT[A/C]TCTGCCAATCTGGAA | 9063 |
rs187778970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837738 | CAGATTTGATCAGAC[C/T]AGGTTTTCCTACATA | 9063 |
rs187786752 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882054 | GTGAGCCAAGATCCC[A/G]CCACTGCATTCCAGC | 9063 |
rs187786963 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876837 | GAGTAGCTGGGACTA[C/T]AGGTGACTGCCACCA | 9063 |
rs187790954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859155 | AATGAAGGGCCAGAC[A/G]CGGTAGCTCACGCCC | 9063 |
rs187811742 | snp | C/G | 0.0115144 | 0.0749975 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918447 | CCACTCCCCTGCCCC[C/G]GCACCCCGCAAGTTT | 9063 |
rs187856052 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807956 | TCATATACCCTTGAC[C/T]AGAAATTCCACCTCC | 9063 |
rs187867579 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918961 | TTATGTAGGTATTTG[G/T]GTAATTGTTTATTTG | 9063 |
rs187878529 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845591 | TTCATTAGCTATTTA[C/T]AGAGCTATGAACAGA | 9063 |
rs187948654 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899734 | GGCCTCTAAAAGTGC[A/G]TAAGCCACCATGCTG | 9063 |
rs188071977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865628 | ATCCAATGTCAGAGC[A/G]GTTCAACCACAAGTC | 9063 |
rs188088551 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898753 | AATCTCAACACTTTG[C/G/T]GGGGCTGAGGCAGGT | 9063 |
rs188128927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839161 | TTTTTACACAATCAC[G/T]GTGTGGAAACAACTC | 9063 |
rs188138812 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869364 | AGAAATCTCTAATAT[A/G]AGGAGGGACTGAGCC | 9063 |
rs188148719 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901204 | GGGCGGATCACCTGC[A/G]GTCAGGAGTTCGAGG | 9063 |
rs188285908 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825340 | GATTTTGGGACAAAA[G/T]ATTAAATTTCCTAGT | 9063 |
rs188296063 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865071 | TATTGCTTAATGAAG[A/T]CACCCTTATGTATAT | 9063 |
rs188305348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849400 | AGTTGGAATTTTATA[A/G]AATATAAAGTTTAGC | 9063 |
rs188341645 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831973 | CTTCATTCAAAGTAG[A/G]CACTTCTGCTTTTTG | 9063 |
rs188351480 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871377 | AAGCTTACAAAGGAT[C/T]TAAGTCCTCACATGC | 9063 |
rs188357467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852242 | ATGTTTTCCATCAGA[C/T]GCGCATGTGAATTTC | 9063 |
rs188359406 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887054 | ACTAAAATAATTTGG[C/T]AATATGTTATCAAGA | 9063 |
rs188372805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903847 | TGAATGGTTAAACAA[A/C]CTATAGTGAATTCAT | 9063 |
rs188423804 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819738 | ACTAAAAGGGCCTTC[A/G]GAGAGAAGGGAAGTC | 9063 |
rs188434943 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884368 | CCCAGGCCAGAGTGC[A/C]GTGGCTCGATCTAGG | 9063 |
rs188436012 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889804 | ATTATTCGCAATAGC[C/T]AAAATGTGGGAGCAA | 9063 |
rs188492800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827657 | CACACTCCATTACAC[C/T]AGACTTTCTCATCTG | 9063 |
rs188500835 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856389 | TTTTTATAGCTACTA[A/G]GGGGATTCTAATATA | 9063 |
rs188508995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847875 | TCTGATTTTTCAGAG[A/C]CAAAATAATATATTT | 9063 |
rs188513307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874248 | GATTACACTGAAATG[C/T]CCCCAATAGGTCGCC | 9063 |
rs188517454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909154 | GGCAAAAGACATGAA[C/T]AGGAATGTGAGAAAA | 9063 |
rs188584114 | snp | A/G/T | 0.000629983 | 0.0177371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844159 | AAAAAAAAAATTTAA[A/G/T]AAAATTAAGGGTGAC | 9063 |
rs188585235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851001 | GTCTACTATAATCAT[A/T]ATTCTTTCAGATGTC | 9063 |
rs188592036 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912981 | TGAGCCACTGCGCCC[A/C]GCCTATTTCACTTTA | 9063 |
rs188594133 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886300 | TAATAAATTTGCTAG[C/T]CCTTCAACATAGATA | 9063 |
rs188675342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896440 | ACATCTACCCAAACA[A/C]GACAGCTTCATGAAT | 9063 |
rs188727775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908610 | AATGGAAAATATCTT[C/T]GAGAACTCTGTTGAA | 9063 |
rs188813089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833267 | TCAAACAAGTATGTT[A/G]AGTAAAAGAAGTTAG | 9063 |
rs188848926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851241 | TAAGTCTTCTGGCTG[C/G]ACCAAAGGAACTACT | 9063 |
rs188857505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894056 | TCTTCAACCCAGGAG[A/G]TGGAAGTTGCAGTGA | 9063 |
rs188860416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831002 | TCCCACAATACAAGA[C/T]TAGTTTAATATCCAA | 9063 |
rs188878465 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870484 | AGCCAGACGTGGTGA[C/T]GGGCGCCTGTAGTCC | 9063 |
rs188892062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903054 | TCATACCTTATACAA[A/G]AATAACTCCAAATGG | 9063 |
rs188948868 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873330 | CTAAAAGGCCCTGGG[C/T]GTAAATGTTTAGATT | 9063 |
rs188959515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905869 | CCTTTCTAATGTTAC[A/G]TAAACTCTTCCAGAA | 9063 |
rs189013743 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900056 | TCAACATGGTCCAAC[A/T]TCGTCTCTACTAAAA | 9063 |
rs189024029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891875 | ATGAATATTTTTAAC[C/G]CCTTGCAGCCTCAGG | 9063 |
rs189027599 | snp | A/G | 0.00194552 | 0.0311284 | utr-variant-5-prime, intron-variant, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920131 | AGCAGCTCCTGGATG[A/G]GTTGGGTAGGTTTGA | 9063 |
rs189082598 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808696 | GCTCTACATTTTTCT[A/G]TTATGCAAAGAGCTA | 9063 |
rs189103096 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820236 | AACTTAATAATGGCA[A/C]CAAAGTGATGCCAGC | 9063 |
rs189113325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861508 | CAAACAGTAACTTTA[C/T]AGTGCAGATACCTGG | 9063 |
rs189133352 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821726 | GTAGGTGAAATCCTA[A/T]GAGAGTTTATGATTT | 9063 |
rs189151675 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840092 | CTTAAACCAAGGAGG[C/T]GGAAGTTGCAGTGAG | 9063 |
rs189171934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895441 | TTCGGGAGGCCAAAG[C/G]GGGCGGATCATCTGA | 9063 |
rs189175992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878927 | GCCAAGGTTAACAGG[A/G]GCTCATACTATGGCT | 9063 |
rs189240292 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889243 | AACAAATTGGAATTT[C/T]ATGAAAAAATGTTAA | 9063 |
rs189244043 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895298 | ATGATGTATATAATA[C/T]AGGAGAAGACGAGAA | 9063 |
rs189275213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914282 | TCAGGATAATCTGCT[C/G]ATCAGGTTTGTGTGC | 9063 |
rs189402680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839682 | CCAGCCCAGCCAACA[C/T]GGTGAAACCCAATCT | 9063 |
rs189458975 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811530 | AAGATATCAATATTT[C/G]ATAGTGTGAACAAAT | 9063 |
rs189483986 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46846419 | TCTAGTTTATTAAAA[C/T]ACTAAACACAAACAT | 9063 |
rs189494119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826713 | CACTTGAAATACTTC[C/T]TCATTTTGTTCCACA | 9063 |
rs189498452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866752 | AAGGAAATTATCTCC[C/T]CAACAGTTGTGTTTC | 9063 |
rs189507350 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878125 | TATAACAGTCCTATA[A/T]CCTAGCCTTAGCCCT | 9063 |
rs189517067 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882180 | TTAATAAAAATAATA[C/T]ATACAGTAAATTAGA | 9063 |
rs189527158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883092 | GACAGAGGGAGACTC[C/T]GTCTCAAAAGAAAAA | 9063 |
rs189535343 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920521 | TTCTTGAGCCAATGC[C/T]TTTCTTGTAAGGTTT | 9063 |
rs189536636 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914117 | CCTAACAACACAGAT[A/G]CCATAAATAAGCAAC | 9063 |
rs189659634 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834497 | GTAAAAGATATTATA[A/C]TGACCAATATATGGA | 9063 |
rs189697578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903326 | CTGACAAAGGACTAC[C/T]ATCTAGGATATACTT | 9063 |
rs189703628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840713 | ATTGCCTAGTGACTA[C/T]GGCATGTTATTAAAA | 9063 |
rs189716163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880162 | GCACTTTGGAAGGCC[A/G]AGACGGGAGGATCCC | 9063 |
rs189720611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854259 | ACTTGCTTGGCTACT[C/T]GTGAGTACTGCTCAT | 9063 |
rs189726982 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888984 | AGATCATTCAGTGAG[G/T]GAAAGGACAGGCTTT | 9063 |
rs189733908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872680 | AAGTAAAGGCAAGCC[A/C]AGGATAAGGCCCGAA | 9063 |
rs189737619 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905762 | ACTTGAAAATATGAA[C/T]AGTCCTACAACCAAA | 9063 |
rs189791010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870734 | ATACTTGGGCAGAGT[C/T]AATGACCATCCTGGG | 9063 |
rs189806084 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900425 | TTTAATCCCAGCTAT[G/T]TGGGAGGCTGAGGCA | 9063 |
rs189931532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827031 | ATTCTACTACTGAAT[C/T]ATGGTGATGATTGCA | 9063 |
rs189945431 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862668 | ATACACATATATATA[C/T]ACACATATATATACA | 9063 |
rs189953548 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886841 | AGACTCTGTCCCCCC[C/G]CTCCAAAAAAAAACA | 9063 |
rs190039436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823017 | CCAAGGCAGGAGGAT[C/T]GCTTGAGCTGGAAGT | 9063 |
rs190042418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867151 | TGTGTCATAACAGAC[A/T]TATTCTCGGTGTGCC | 9063 |
rs190073469 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893095 | TACAGTGCAGACAAC[A/C]AAGAAGGAAAACAAG | 9063 |
rs190077109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875563 | TAAAGAAATCCAGAC[A/C]CAGAGTCCGGGGAAT | 9063 |
rs190091461 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869479 | AGAAATCTCTAATAT[A/G]AGGAGGGACTGAGCC | 9063 |
rs190091488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910818 | AAAGTTTTCAAAATT[C/G]TGAGGAATTTATAAT | 9063 |
rs190218846 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853914 | CCATGTAAGCAATCC[A/C]CCCTGACCATACCTA | 9063 |
rs190222876 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46807793 | AGTCAGAAAGGCAGA[A/G]GGTCTTAGTGCAGAT | 9063 |
rs190223209 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832819 | ATCACTTGAACCTGG[C/G]GGGTGGGGGCTGCAG | 9063 |
rs190228881 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872405 | AACAATACCAATAGA[A/C/T]AGTCTTGCCCCAAGA | 9063 |
rs190244742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910702 | ACAAATCCCGTAGAT[C/T]GTAGACTACAATTGT | 9063 |
rs190251880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887866 | GTAAGTTCTAGCCAG[A/G]GCAACTAAGCAAGAA | 9063 |
rs190300915 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46846974 | AAAATCATATAGCCC[A/T]TATGATCATTATCAA | 9063 |
rs190301265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882728 | ACATCTATAAGATAA[C/T]AGAACTACTGCAATA | 9063 |
rs190496234 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875002 | AGAGAAAAATGAGCC[A/G]TCACCCCAGGGCCCA | 9063 |
rs190506615 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909824 | CTGCAAGACAAGTTT[G/T]GTGAAACTTTACAGT | 9063 |
rs190509663 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917856 | GCGGTGCCTATGGAC[A/G]GAGAAAGCCGCCGCA | 9063 |
rs190526969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830634 | AACAAACAAATAGAA[A/G]AAAAGAAAAACAGAA | 9063 |
rs190550991 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814606 | GCTTAGCTGACTGAG[A/C]AGCCCATGAAGCAGT | 9063 |
rs190570259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835118 | TAATGTGCAAAGGGG[A/C]ATGACATATGTAACT | 9063 |
rs190580414 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875527 | CCATAAGAATCTTCT[A/C]TCTGAGTCGGTTGAA | 9063 |
rs190584727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857612 | TGGGAAACACGATGT[G/T]AAGAAAGAGAAAAGA | 9063 |
rs190585698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834753 | CCAAAGTGCTGGGAT[A/G]ACAGGTGTGAGCCAC | 9063 |
rs190651592 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912415 | ACTGACAAGGAAAAA[A/T]GTCTGTACATGTTCA | 9063 |
rs190668324 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921548 | GGAAAAGAAAAATGA[C/T]TACACCTATCTCAGG | 9063 |
rs190755573 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46891102 | TCACCCTCAAGCATA[C/T]AAAAATCCTATCTAA | 9063 |
rs190782434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897100 | AAGTTTGCTTGAACA[A/G]GGGAAACTGGGTGTG | 9063 |
rs190817966 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811938 | TTACTTCAATGAAAC[A/G]GAGCAAATCTCCATG | 9063 |
rs190823709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857048 | AAACATGTTAACAAC[A/G]CATGTCAAGTGCCTA | 9063 |
rs190869082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833097 | ATAAATGAAAACAGT[C/T]CACACAAAGACTTGG | 9063 |
rs190874900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862769 | GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 9063 |
rs190896288 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893498 | AGTGATAACATTATT[C/G/T]GGCAAAGGATGTTAA | 9063 |
rs190983892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842817 | CTTTCAGGTCTTACC[C/G]TACTGGAACTGCACA | 9063 |
rs190998184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824462 | AATATGTAAAATTAT[C/G]TTTTAATATGGAAAA | 9063 |
rs191002734 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864863 | ATTATCTAATGAAAG[C/G]AAGTCAAAATGCTCC | 9063 |
rs191019176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897468 | ATAATAACTGCATTG[G/T]ATTCAAACCGATTAA | 9063 |
rs191020945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880977 | GATTTAAATAGAACA[C/T]AGCAAAACTGAGTTA | 9063 |
rs191035187 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916089 | GGCATAACATGTATT[A/C]ATATGTGTTTACTGG | 9063 |
rs191045663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915389 | TAACATGGGTCTGCA[C/T]AGAGCAGTTAAGGCA | 9063 |
rs191113499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841734 | AGTCTCACGAATAGA[C/T]CTGTTGTCACTTCTG | 9063 |
rs191120368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880622 | AAATAATTTTTAAAA[A/T]TTGGGACAAAAAATT | 9063 |
rs191129008 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808442 | TTTTAGGAATTGCAG[A/G]TTCCTAACAAAGTAG | 9063 |
rs191134686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858196 | CAGAGTACAGGTTGT[C/T]AGAAAAGAGTAACAG | 9063 |
rs191135063 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848486 | ACACTTCTGGATTTC[A/G]GCAATGCTAAAATAT | 9063 |
rs191139694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870031 | AATCCCCCACCCCAA[A/G]CAGGTGCACAGGACC | 9063 |
rs191143169 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828667 | TTTCATCTTGATAAG[C/T]TGAAAAAAACCCAAA | 9063 |
rs191144731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850351 | GAAGTCTCCTTTATT[C/T]TATAAACATAACCCC | 9063 |
rs191146885 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886278 | TCTTTCTCAGAATAA[A/T]AGAAAGTAATAAATT | 9063 |
rs191147347 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868359 | TTATTTGGAAAGAGT[C/G]CTCTTTACTCCTGGC | 9063 |
rs191153181 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839958 | ACGAGGTCAAAAGCT[C/T]GAGACCAGCCTGACC | 9063 |
rs191153411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818162 | TCATTGATGACAACA[C/T]ATTTTCCTTATTTGA | 9063 |
rs191159275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46902493 | TGAACCCGGGAGGCA[C/T]AGGTTGCAGCGAGCC | 9063 |
rs191171204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883436 | TGCCAAGCGCAGTGG[C/T]TCATGCCTGTAATCC | 9063 |
rs191177808 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900747 | TTGGGAGACCGAGGC[A/G]GGTGAATCACGAGGT | 9063 |
rs191178538 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885061 | TGTTAACAGTAGAAC[C/T]TTAGCTACAGAGCAC | 9063 |
rs191179829 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921090 | TTATAAGTACTGTGA[C/T]TAAAGTGTCCTAAGT | 9063 |
rs191263279 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46835837 | AATTTTTAAAAAAGT[A/G]TTATTTGAAACAAGA | 9063 |
rs191282827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826444 | GCATCACTAGGCATG[A/G]CCTCTCAACCTGGCA | 9063 |
rs191296252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846289 | AATATCAGTTGTTTA[C/T]AGAAAGGCTAGAACA | 9063 |
rs191316559 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865951 | TTTTCACTATCTGTG[C/G]CTAAGGTCACCAATG | 9063 |
rs191417304 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901697 | TCAAATCAATCAATG[C/T]GAAAAACGCATTTCA | 9063 |
rs191437643 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905410 | AAATGCTGAAAATTA[A/C]TGACAGGCACCCAGC | 9063 |
rs191586545 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869132 | TGGTCACCTCATATG[G/T]CTTATGGCAGATTCC | 9063 |
rs191592789 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900807 | GGTGAAACCCCATCT[C/G]TCCTAAAAATACAAA | 9063 |
rs191595489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909616 | ATGAAAACTTCTGCA[C/T]TGCTGGAGAGAACGA | 9063 |
rs191643517 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849470 | AAAATAAAGTCAAGT[C/T]CATGTGACAGGGAAC | 9063 |
rs191654554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828990 | GGCATAAATCCTTTA[C/T]TTTTTCCCCTTTCTT | 9063 |
rs191665129 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828792 | CCATATTTGTTAACT[C/G]ACATTTTCACAGAAA | 9063 |
rs191709931 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894746 | ATACAAAGATGAAGG[C/G]AAGCTGAAGGTGCTA | 9063 |
rs191710138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913706 | ACAATATTGGAAATA[C/T]GCAACTGGAAGGGTA | 9063 |
rs191826709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853367 | AAAAGGCCATGGGAC[A/C]GGTGCACAGGGTTGT | 9063 |
rs191863370 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884003 | ACCTTATAAAAAGAA[A/C]AAAAACAAAAGGAAT | 9063 |
rs191893415 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810943 | GAGAAAGCTAAACAG[A/C]AAAGTACCAAATCCT | 9063 |
rs191930024 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887207 | TGCAATACTCCACTT[G/T]CTTGGATCACCAGTT | 9063 |
rs191957784 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894159 | ATCCCTTTCCTTTAT[G/T]TAGCACTTACTGATA | 9063 |
rs191976123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849100 | ACTCATGAACTAAAA[G/T]GTGCACTCTGGAAAT | 9063 |
rs192012473 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834366 | ATACATTTGGCACAT[A/G]TGGACAGAGAAATTA | 9063 |
rs192023986 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874147 | GATAATTGTTTAATA[A/T]GCAAAAAAACTAATA | 9063 |
rs192030187 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856063 | CAGGCTGGAGTGCAG[A/T]GGCGCGATCTTGGCT | 9063 |
rs192032332 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890060 | CTAGAACCTTGAGGA[C/T]ATTACATTTAGTGAA | 9063 |
rs192050078 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908656 | GATTCAAAAGCACTA[C/T]CCATAAAGAAAAGCC | 9063 |
rs192072053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837477 | TATTTATAGGCACTC[C/T]TTATATAAGAAATCA | 9063 |
rs192075682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876284 | ACCCTCACGTTTATA[C/T]AGATGCCACTGGAGT | 9063 |
rs192113401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832317 | CTACTTGGGAGGCTG[A/C]GGCAGGAGAATTGCT | 9063 |
rs192138264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914202 | CATTATTGTAACCAT[C/G]TTTGAGCACACAGGC | 9063 |
rs192157759 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837985 | ATGGACTGGAAATGG[A/G]GAAAAGAACAAACAG | 9063 |
rs192179116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859638 | TTTGGTGCCTGGAAT[A/G]TTGTCTGGTCCATAG | 9063 |
rs192181919 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894217 | AAAATTCTACAAATA[C/T]GTTGTTTGGCAAATC | 9063 |
rs192191064 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912995 | CAGCCTATTTCACTT[G/T]AAGTTAAATATATTT | 9063 |
rs192205675 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878273 | AACATGTGAAAGCAT[C/T]CTGAAAACAGTAAGA | 9063 |
rs192248741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819196 | TCAGAATGCTTGCTT[A/G]TAACACATACTGAGA | 9063 |
rs192251050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872107 | CTCATTCAAGATAAG[C/T]GCCTTGAACACTGTA | 9063 |
rs192264186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904899 | TGTGCTAGTAATAAT[A/G]TTAAAATATGGTTTA | 9063 |
rs192369742 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898943 | GAGGTTGCAGTTAGC[A/C]GAGATTGCACCACTG | 9063 |
rs192398323 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866861 | AGCGTGCCACAAGCA[A/G]CAGGTATCTACACCT | 9063 |
rs192417675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882554 | TATATATGTGTACAA[A/G]TATTCAGAAATATAT | 9063 |
rs192425378 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899752 | AGCCACCATGCTGGG[A/C]CCAGAATGAGTATTA | 9063 |
rs192428507 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858650 | TGCAGTGAGCCTTGA[C/G/T]TGCGGCACTGTACTT | 9063 |
rs192481729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846481 | GAAATATAAATATGC[A/G]TATTTCCTTTCCAGG | 9063 |
rs192490600 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826815 | TATATTTGGAAATGT[A/T]AGTATTTTAACAGCA | 9063 |
rs192611078 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862069 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9063 |
rs192630949 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895393 | AATCTACCTCAGGAC[A/G]GACACGGTGGCTCAC | 9063 |
rs192694780 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819865 | TTAAATTTTGTAATA[C/T]GGCCTTGGTTGCAGA | 9063 |
rs192697892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860915 | CCAGGTGGTCAAGGC[C/T]GCAACAAGCCATGAT | 9063 |
rs192724049 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882128 | GACTACATAGCCATA[A/T]CCAAATTAAGTCCTT | 9063 |
rs192778936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844980 | TCAATCACTGCGAAG[C/G]GGACAAAATTCACCA | 9063 |
rs192791733 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918572 | CGATTCTCCTACCTC[C/T]GCCTCCCGAGTAGCT | 9063 |
rs192829139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881710 | CATGCAAACACCTAT[A/C]TACTTGCTACTTATT | 9063 |
rs192868208 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877584 | AACACGTCTTGTACC[G/T]TAACAAACAGCCTCC | 9063 |
rs192901638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839162 | TTTTACACAATCACT[C/G]TGTGGAAACAACTCA | 9063 |
rs192910664 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830681 | AAACTTATTTACACT[C/T]ACTCCAAAAGAAACA | 9063 |
rs192925517 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870485 | GCCAGACGTGGTGAC[A/G]GGCGCCTGTAGTCCC | 9063 |
rs192978226 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825626 | ATGATCAGCACTGAC[C/T]GAAATGCTCTGAGAG | 9063 |
rs192983250 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865194 | AAAAAAGTTAATATA[G/T]ATAGAGGCCTCAAGT | 9063 |
rs193043235 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898519 | TTAGAAATATAAGAC[A/C]ATCCACTGAAAAATT | 9063 |
rs193091865 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855001 | GCCAGGTACAGTGGT[A/G]CACAACTGTATTCCC | 9063 |
rs193161875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851101 | TTAAAAGAAGAAATG[C/T]TGAGTTTATGTCAGT | 9063 |
rs193165332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886486 | TCTTTAAAAACAAGG[C/G]TAAAGATGAAAGTAA | 9063 |
rs193231136 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906351 | AGAAAAAGAAAGAAA[A/G]AAAAAAAGCATAAGA | 9063 |
rs193250149 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833545 | AAATGCCTACTTCAT[A/T]AGAGGTTTATTTTTC | 9063 |
rs193252812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873424 | TATTCATAGATGGCC[A/C]CTCTAGGGTAATTGG | 9063 |
rs193289393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830356 | AGTTCAAATTAAGTC[C/T]GTACCAGAAAAACCT | 9063 |
rs199507063 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812358 | AAAAAAAAAAAAAAA[C/T]AACGTTTCCACAGAC | 9063 |
rs199626361 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842282 | GTTATGAATGCAAAA[A/C]AAAAAAAAAAAATTT | 9063 |
rs199671767 | snp | A/T | 0.000550399 | 0.01658 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828108 | TACAGTCACTGAACA[A/T]GGCTTACTGAGGACG | 9063 |
rs199683812 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855104 | GGACCTTGTCTCTTT[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAATT | 9063 |
rs199791876 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46818879 | TTGTTTGCTCAATAT[C/T]AGCTTGAAACACATT | 9063 |
rs199985832 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895272 | AGAACTCTGTAGATT[C/T]CCCATCTGCTATGAT | 9063 |
rs200086804 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810984 | AAAATGATTTAGGAA[C/G]TCAAATGAAGCAAAC | 9063 |
rs200089770 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896271 | ATGAAAAAAAAAAAA[-/A]CTAAACAAATTTCTT | 9063 |
rs200201594 | snp | A/G/T | 1.65971e-05 | 0.00288067 | missense, synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890628 | CATCATAAAAGGGCA[A/G/T]ATTTTTTAACTGCAC | 9063 |
rs200227557 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810395 | CCACACAAACCAAGT[G/T]AAGTTTTTTCTATCT | 9063 |
rs200280227 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908552 | AAGGTAAAAAAAAAA[-/C]AAAAACAAAAAACAA | 9063 |
rs200294833 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840986 | TTTTTTTTTTTTTTT[-/T]AAACATACTAGAATC | 9063 |
rs200296874 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837625 | TTTTATATAATCAAC[C/T]GTGTCAATTTTTCAA | 9063 |
rs200316932 | in-del | -/AGAAGTC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820657 | ATAAAGAAACCAAGA[-/AGAAGTC]TCTAAGTACAAATTC | 9063 |
rs200333402 | snp | C/T | 3.29636e-05 | 0.00405964 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890809 | GTCAGGTTCTACAGG[C/T]GATGAGCCACCATCC | 9063 |
rs200359302 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915753 | TGGCCAACAACATTC[A/C]CAAGAGTCTAATAAA | 9063 |
rs200371441 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46903321 | CATATCTGACAAAGG[A/G]CTACTATCTAGGATA | 9063 |
rs200394650 | snp | A/G | 4.94564e-05 | 0.0049725 | synonymous-codon, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812557 | GTGGTGGTGACAGAC[A/G]TACTGCTTGCTGTTA | 9063 |
rs200505883 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890736 | AACCAACAGGAGAGG[A/G]TGGTGAGTGAGGTGT | 9063 |
rs200510017 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878617 | GTCACTCCTGTAATC[C/T]CAGCACTTTGGGAGG | 9063 |
rs200528992 | snp | A/G | 0.00199808 | 0.0315444 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846671 | TCAACCCTCAGTGGG[A/G]TCACTGTCCTGCTAC | 9063 |
rs200570227 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915791 | GAAAGTTTTCATTAA[A/C]AAAAAAAAAAAAAAG | 9063 |
rs200689085 | in-del | -/ACTTT | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921956 | GATGTTTTCCAAGCC[-/ACTTT]ACTTCTTTTGCTAAG | 9063 |
rs200698458 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46827991 | TTGTGTTTCTGACAT[A/G]AAGATGCATTTCCTT | 9063 |
rs200843380 | in-del | -/A | 0.0256215 | 0.110247 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884622 | GGCCTCATGTTTTTT[-/A]AAAAATTATCTTGCC | 9063 |
rs200863981 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899008 | CAAAAAAAAAAAAAA[-/A]GCTTTGAATAAATTA | 9063 |
rs200927393 | snp | A/G | 1.80735e-05 | 0.00300607 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844725 | TTGGTCTTATTAAAC[A/G]TTACTTACTTAGTGC | 9063 |
rs200991593 | in-del | -/AC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899853 | TTACTATATGAAGTA[-/AC]ACTATCAAATTTGTG | 9063 |
rs200999595 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846372 | ATAAAACTTTCTTTG[-/T]TCCTCTTCATAAATA | 9063 |
rs201016046 | snp | C/T | | | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890897 | GGATATCGGCGTCTA[C/T]ACAATTCTCGGATTT | 9063 |
rs201032401 | snp | C/T | 5.0891e-05 | 0.0050441 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844764 | GATCAGGGTTTCTAA[C/T]ACCTTTCATTTTTAA | 9063 |
rs201039542 | snp | C/T | 1.65007e-05 | 0.00287229 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829762 | ACACGGTTGGCTGGA[C/T]ACTTTCATAGCTTCT | 9063 |
rs201082243 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896157 | ATTACAGGATAAAAA[A/G]AAAAAAGCAAAAAAA | 9063 |
rs201169180 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856310 | TGGCCAAAGACTTTT[-/C]TTTTACTATAAAGAC | 9063 |
rs201170691 | snp | C/T | 0.000813879 | 0.0201563 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821088 | CTGTTTTAAATAGCA[C/T]GGGAAATTACAAACA | 9063 |
rs201332652 | snp | C/T | 0.000203634 | 0.0100884 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864130 | GTGAATAAACCAATA[C/T]TCATGAGAAATATAT | 9063 |
rs201346777 | in-del | -/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825005 | CCCTGTCTCAAAAAA[-/T]TTAAAAAAAAAAAAA | 9063 |
rs201349024 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852703 | TGTAGACCTCCTACA[A/G]GAAGGTATCATCCCA | 9063 |
rs201382502 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829808 | GGACACCAAGAACCA[C/T]CTTCTTGGAATTTGA | 9063 |
rs201493846 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810679 | ATTTGTGGAAAACCA[C/T]ATGAATTTAAATCAA | 9063 |
rs201525370 | snp | C/T | 3.30622e-05 | 0.00406571 | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812600 | GACTATCCAAAAACA[C/T]AGGAGGACAGTACTG | 9063 |
rs201532083 | in-del | -/A | 0.0437281 | 0.141251 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904209 | AAGATGTTAACTCTG[-/A]AAAAAAAACTAGAGA | 9063 |
rs201720653 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908551 | AAAGGTAAAAAAAAA[A/C]CAAAAACAAAAAACA | 9063 |
rs201833502 | in-del | -/AAG | 0.0505692 | 0.150756 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820653 | TATAATAAAGAAACC[-/AAG]AAGAAGTCTCTAAGT | 9063 |
rs201927526 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810741 | TTGAGAAGGTGAAAG[-/A]AAAAAAAAAAAAACC | 9063 |
rs201971761 | snp | A/G | 3.32077e-05 | 0.00407465 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855518 | CAGAACTACATGCAC[A/G]TAGTAAGCAAGTATA | 9063 |
rs202042059 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906776 | TATGTGTGTGTGTGG[C/G/T]GGGGGGGGGAGGTGT | 9063 |
rs202103771 | in-del | -/GA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848786 | TGTGTGTGTGTGTGT[-/GA]GTGAGAGAGAGAGAG | 9063 |
rs202138910 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810188 | TGTTCACAGAAAATA[A/C/G]AAAAAAAAACAAAAA | 9063 |
rs202192788 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908541 | TTAAATGAGAAAAGG[-/T]AAAAAAAAAACAAAA | 9063 |
rs202197418 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864522 | ACACCTGTAATCCCA[A/G]CACTTTGGGAAGCCA | 9063 |
rs202206178 | snp | C/T | 9.89315e-05 | 0.00703249 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890770 | TGAAGTGGAAGGCAA[C/T]GAGTGGATTCCAGCC | 9063 |
rs202223268 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871713 | CTCAGAAGAACTTTT[A/T]GTCTTGGGGGTGAAA | 9063 |
rs202223655 | snp | A/G | 0.460589 | 0.13473 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896164 | GATAAAAAGAAAAAA[A/G]CAAAAAAAAAAAAAA | 9063 |
rs202223902 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852011 | TTTCTTTTGTGGCTT[G/T]TTGATGCTTCTTAAA | 9063 |
rs367636994 | snp | C/T | 1.66776e-05 | 0.00288765 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46827985 | GCTGCTTTGTGTTTC[C/T]GACATAAAGATGCAT | 9063 |
rs367730368 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46835716 | ATTTCAGTCTTTTTT[-/T]AATGTCAATAACAAA | 9063 |
rs367808162 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815872 | ACAAAGCACACACTC[A/G]GGAATTGCTGCGCTA | 9063 |
rs367814205 | snp | C/T | 0.000170579 | 0.00923365 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855313 | TTTATATTAAACTTA[C/T]ATGCAAATCTGGTGA | 9063 |
rs367830681 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841873 | GGTAATGTTTGGAAG[A/G]AACTGCTCCCTATTC | 9063 |
rs367836521 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875506 | CAGATGTTATAGGAC[A/G]GGACCCCATAAGAAT | 9063 |
rs367847196 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860860 | TGTACACCTGTAGTC[-/C]TAGCTTCTTGTGGGG | 9063 |
rs367933016 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809463 | AAGAAAGATAAAAAC[A/T]TTTTATTTTGGCCAG | 9063 |
rs367964533 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858016 | GAGACAAATGACACA[A/T]TAAAGCAAATCTGGA | 9063 |
rs367970705 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870400 | GCAGGTGGATCACAA[C/T]GTCAGGAGATTGAGA | 9063 |
rs367978905 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920832 | AGTAATGTGGTATAC[C/T]CTTAAAGGGGAGTGG | 9063 |
rs368014337 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905512 | GAAACAGGAAGGATA[A/C]ACTAAAGAGCATAAA | 9063 |
rs368046700 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46846848 | TGCATAGCCCTATAA[C/T]CGTAAGAAAGAAAAA | 9063 |
rs368057835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902009 | GGAATGATTGTTCAC[A/G]TAGAAAATCTCAACA | 9063 |
rs368078409 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916967 | CACCCCGGTGAAGGT[A/G]CAAGATCAAACGTTG | 9063 |
rs368084725 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863213 | TCTTATCTCAGAATA[A/G]TTATTAGTAATGTTT | 9063 |
rs368085885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875788 | TTGTTATGCTTGTGC[A/G]CACCGCAGGCCAGAG | 9063 |
rs368212974 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827212 | TGAAAGAATGTGTTC[A/G]TAGACAGCCAGGAGA | 9063 |
rs368244139 | snp | G/T | 1.66048e-05 | 0.00288134 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855554 | AAGGTAACAGAAAAT[G/T]TCAAACTCACCTCAA | 9063 |
rs368325377 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875472 | GAACCCTCCATATTC[C/G]AATGGTATGGGTTAG | 9063 |
rs368385382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823436 | TACACGTAACAACAA[C/T]AACAGAGCTCCCTTT | 9063 |
rs368398508 | snp | G/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907996 | GTTAGCCACTGGGGA[G/T]GGGAATATTTAGAGT | 9063 |
rs368503297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897102 | GTTTGCTTGAACAGG[A/G]GAAACTGGGTGTGGG | 9063 |
rs368506273 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46836613 | GAAGATGTCATACAA[C/G]AAGATGATAAAAATG | 9063 |
rs368574347 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884388 | CTCGATCTAGGCTCA[C/T]TGCAAGCTCCGCCTC | 9063 |
rs368610293 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902836 | TTAGCTAGGACTGAC[A/G]GACTGCATGGTATTA | 9063 |
rs368648989 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809233 | ATAAATGCCATATAA[C/T]CTAAATTCACCTCAA | 9063 |
rs368656245 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810812 | CTTAAGTAGGATGTC[A/C]CTATTCTAACGGAAA | 9063 |
rs368667893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870571 | CCGTGAGCCATGATC[A/G]TGCCACTGCACTCCA | 9063 |
rs368674753 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878817 | AGTTTGCAGTGAGCG[A/G]AGATCACACCACTGC | 9063 |
rs368680844 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832774 | GTGGGTGCCTGTAAT[A/C]CCAGCTACTGGGGAG | 9063 |
rs368694933 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920346 | TAGGACATTTATTCA[G/T]TGATTAGAGATAAGA | 9063 |
rs368850815 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834288 | CTTGATAAAAAAAAA[C/T]GTAAACCTTCTGAAT | 9063 |
rs368859632 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894896 | ACCAACACGGTGAAA[A/C]CCCGTCTCTACTAAA | 9063 |
rs368866820 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856067 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 9063 |
rs368882620 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892813 | TACATTAACATAGTT[A/G]TTTAACCCAATATAT | 9063 |
rs369021708 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829789 | TTCTTTCTTCGGTCT[A/C]ATTGGACACCAAGAA | 9063 |
rs369033986 | snp | A/G | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919740 | CCTAACAAATAGTTG[A/G]CCTTGTATTTGTTTA | 9063 |
rs369091258 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855992 | GACTTTTTTCTTTTT[-/C]TTTTGTTTTTTTTTT | 9063 |
rs369141675 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871471 | ACAAAATACATGCTT[C/T]AAATGTGGAGGAGCA | 9063 |
rs369182678 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837773 | TTCAAACCTCCCCAT[A/G]TATTTCCTTTACAGA | 9063 |
rs369188533 | snp | A/G | 0.000132269 | 0.00813123 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864115 | ATGGCAGCCCTACAG[A/G]TGAATAAACCAATAT | 9063 |
rs369218908 | snp | A/G | 8.43547e-05 | 0.00649386 | intron-variant | PIAS2 | GRCh38.p7 | 18:46812646 | GATGCCAATGAGGAA[A/G]AGGCTACTTGATTTT | 9063 |
rs369242442 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909807 | TGCAGGTCAGGGTTT[C/T]TCTGCAAGACAAGTT | 9063 |
rs369250650 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856618 | TTCCTTAGGAGCTTG[C/T]TGGAAATGCAGACTC | 9063 |
rs369257967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831752 | TCACATGGCCATATA[A/C]CAAACAAAAACAAAA | 9063 |
rs369301377 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875391 | CCCATCAAATTGTAA[A/G]TCACTGCAATGTAAC | 9063 |
rs369304572 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864137 | TGAAATCGCTGAAT[A/G] | 9063 |
rs369366751 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46846357 | TTCTCCCCCAAACGG[A/C]TAAAACTTTCTTTGT | 9063 |
rs369379045 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885389 | GCTGGGCGTGGTGGC[A/G]GGTGCCTGTAATCCC | 9063 |
rs369388062 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857059 | CAACACATGTCAAGT[A/G]CCTAAATATAAGATG | 9063 |
rs369487788 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827556 | AAAAAGAGGCTCAAT[C/G]AAATTAAGTATTTCA | 9063 |
rs369491603 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862241 | GAGGCTGAGGCAGGA[A/G]AATCGCCTGAAACCG | 9063 |
rs369493732 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883102 | ACTCCGTCTCAAAAG[-/A]AAAAAAAAAAAAACA | 9063 |
rs369509408 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855158 | TGTTTTCCATCTCCT[C/T]CAGACCTGAAATAAG | 9063 |
rs369555624 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46815130 | TAAAGACAAAAATCA[C/T]AAACTGAAAACAACT | 9063 |
rs369673569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827390 | CATCCTACCCACCTA[C/T]ATTTTGCCCTGGAGA | 9063 |
rs369737848 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829706 | ACGAGTCTCACTGCT[C/T]TACTCTCTGCTGCTA | 9063 |
rs369779815 | in-del | -/AGTCTCCTTTA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850338 | TAGTTAGGTCTCTGA[-/AGTCTCCTTTA]TTCTATAAACATAAC | 9063 |
rs369810132 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905100 | CTTCATGTACAAATA[A/G]AAATTATTAAAATGG | 9063 |
rs369816318 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917630 | ACAGCGCCCGCCCGC[A/G]CCTGCCCCGGCGTGC | 9063 |
rs369820499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880589 | CACAGTGAGACCCCC[A/G]TCTACTAAAAAAGTA | 9063 |
rs369937001 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860260 | TCCTAAATCTCCCCA[C/G]CTGATGCTAATATGC | 9063 |
rs369965972 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827820 | ACAATGTGCTTACTC[A/G]AAAATATTTCAACTC | 9063 |
rs369978102 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870875 | CAGCCCAAGACCCTC[A/G]ATGGGTCAATAACAA | 9063 |
rs369984656 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811406 | AAAATACAAAGTTTC[A/G]TCAAATATTTCACTA | 9063 |
rs370016671 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809376 | ACAGACCTCAGGCAC[A/G]AAACTATTTTCAGCA | 9063 |
rs370047295 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832198 | GAGGCGGGTGGATCA[C/T]GAGGTCGGGAGTTCG | 9063 |
rs370049522 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870382 | GCACTCTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 9063 |
rs370059551 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822261 | TGAGAGTACATACAT[C/T]GTTGAGTTGGCAACT | 9063 |
rs370088438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894900 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 9063 |
rs370155043 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897672 | TTTGATAAAATTCTA[C/T]TCATTCCTGATGAAA | 9063 |
rs370157475 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857867 | AAGCATTTACCATAT[A/G]CTAGGTACTGTAATG | 9063 |
rs370238206 | snp | A/G | 1.68755e-05 | 0.00290473 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844829 | ACAAGATATACAGAC[A/G]TAGAGTAATTCTACA | 9063 |
rs370240164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822819 | AGGGGACTAAAGAAG[A/T]GGTCTGATTATTCTG | 9063 |
rs370286368 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920419 | AGCCAACCTGAGAAC[C/G]AACCCTTCTTGTGAG | 9063 |
rs370359194 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46843013 | ATGTACTTGTAATCA[A/G]GACATGTATATTTCA | 9063 |
rs370434534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875596 | ATGGGATCCAACACT[C/T]TCCCCAAACATATCA | 9063 |
rs370440428 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900961 | CCTGGGTGATAAGAA[C/T]GAAACTCTGTCTCAA | 9063 |
rs370473711 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860113 | CAAAGGGGAGGGAGC[C/T]AGAAACACAGCTGTG | 9063 |
rs370478377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816215 | CATTCAGAGACACCC[C/T]GAATATAACCACCAC | 9063 |
rs370583071 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881928 | ATGGTGAAACCCTGT[C/G]TCTACTAAGAATACA | 9063 |
rs370588193 | snp | C/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823047 | TTTGAGACCAGACTA[C/T]GGAACATAGGGAGAC | 9063 |
rs370637456 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46893833 | ACACCCCCCAAAAAA[A/G]TCCCTCTCCTTGGCC | 9063 |
rs370647963 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840608 | TATAAAAGTTGCTGA[A/C]CCTAAATTTAATTCT | 9063 |
rs370678170 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901203 | CGGGCGGATCACCTG[C/T]GGTCAGGAGTTCGAG | 9063 |
rs370705200 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887260 | AAAAGCAAAAAATTG[A/G]AAAAAAAAAAAAAAT | 9063 |
rs370720297 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867158 | TAACAGACATATTCT[C/T]GGTGTGCCTTTTATT | 9063 |
rs370735791 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842062 | GGCGAAAGATCTCTA[A/C]AAAAGACACCAAAAT | 9063 |
rs370750516 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46893845 | AAAATCCCTCTCCTT[G/T]GCCAGGCACAGTGGC | 9063 |
rs370763113 | in-del | -/AA | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808004 | AAATAATTTATACAC[-/AA]AGACATTCATTGTGG | 9063 |
rs370860673 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853393 | GTTGTGTATTAATCT[A/G]TTTTGCCAGGCTTTC | 9063 |
rs370883274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869865 | GGAGGAAATAGATTA[C/T]GCCCTGTATTGGCAG | 9063 |
rs370897595 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844090 | AAGGCTAGTTGTAGC[A/G]ATTTCACTATCAGGA | 9063 |
rs370997885 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872522 | CAATACGTGGATGAC[C/G]TGCTTATATCTGGTG | 9063 |
rs371059031 | snp | C/T | 1.65496e-05 | 0.00287655 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836479 | CAGATGTGTACAAGT[C/T]ACTGCACGGCATGGG | 9063 |
rs371078724 | in-del | -/CTTT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853408 | GTTTTGCCAGGCTTT[-/CTTT]GTCACACATGCAGTT | 9063 |
rs371089675 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869174 | TTATACCGACACACC[A/G]ATGCTAAGAGGGACT | 9063 |
rs371092346 | snp | A/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921635 | GTGAAAGATGGTAAA[A/T]TTTTTGTATCTAAAC | 9063 |
rs371096554 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900435 | GCTATTTGGGAGGCT[A/G]AGGCAGGAAGATCAC | 9063 |
rs371104300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840677 | AGAAGGAATTTGTTA[A/C]CAGCTAGCAAAATTT | 9063 |
rs371201517 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888837 | TGCTGCTCACCTCCC[A/G]CTGTGCGACCTGGTT | 9063 |
rs371247977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849306 | ATTCTGAGTTATCTG[A/G]TAACTTGTATTCTAC | 9063 |
rs371288462 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814848 | GATGATTGACATATA[G/T]CAACTTTAAACTGGG | 9063 |
rs371409166 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916031 | TTATCAAGTATGAAC[A/G]CCCTTTACCTACACT | 9063 |
rs371435945 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878905 | AGAATGCTTCCTAGC[A/G]GTTACTGCCAAGGTT | 9063 |
rs371498239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877463 | CCTTATTTGGAAAGC[A/G]TCCTCTTCACTCCTG | 9063 |
rs371510941 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897539 | AATCACTGATCTCCT[C/T]TAAAGGATGTTAAGG | 9063 |
rs371550683 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808970 | TTGGCAGAAAAAAAA[-/A]GACAACTTGGCTGGA | 9063 |
rs371607073 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, synonymous-codon | PIAS2 | GRCh38.p7 | 18:46827955 | GAACTATAAATTAAC[A/G]AACCCTTTGGTTGGG | 9063 |
rs371689098 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904533 | AGGTGGGCAGATCAC[C/G]TGAGATCAGGAGTTC | 9063 |
rs371698694 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879425 | GTGCAGATGAGGACA[-/G]GGAGAAACTGGAACC | 9063 |
rs371703092 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905009 | AATAAAGATATGAGA[C/T]TTGAACAACATAATT | 9063 |
rs371721216 | snp | G/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826432 | ACTCATGAGTCAGCA[G/T]CACTAGGCATGACCT | 9063 |
rs371726494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896542 | GAGTAAAATACATAC[A/G]TGTTAGAAGACAAAT | 9063 |
rs371734891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46835863 | CAAGATACTAAAAAT[C/T]AGTTCATGTCATTTT | 9063 |
rs371760004 | snp | A/G | 5.01098e-05 | 0.00500524 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846846 | GGTGCATAGCCCTAT[A/G]ACCGTAAGAAAGAAA | 9063 |
rs371805454 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848657 | ATGTGTAATCTATAA[C/T]TTGCAACAAAATTCT | 9063 |
rs371831508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885334 | CGAACCTGGCCAACA[C/T]AGTGAAACCCCGTCT | 9063 |
rs371836184 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889815 | TAGCTAAAATGTGGG[A/G]GCAACCCAAGTGTCC | 9063 |
rs371848550 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863699 | TATTCTAACACACAG[C/T]ATTTACTAAATATTT | 9063 |
rs371863179 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917625 | CGGCGACAGCGCCCG[C/T]CCGCGCCTGCCCCGG | 9063 |
rs371914466 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902355 | TGAGGCCGGGAGTTC[A/C/G]AAACCAGTCTCACCA | 9063 |
rs371957263 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870273 | GGAGGAGAAGGAATC[A/G]GCTTTGTAAATGCTC | 9063 |
rs372024400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844976 | ATGGTCAATCACTGC[A/G]AAGGGGACAAAATTC | 9063 |
rs372050186 | in-del | -/C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829977 | TGTTAGCTGACCCCC[-/C/T]TTTTCTTTTGGTATT | 9063 |
rs372216088 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853348 | GCAAAGAAAAATGGT[A/T]ATGAAAAGGCCATGG | 9063 |
rs372237273 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909880 | TGGATTTAAGAAATA[C/T]GGATGGCCAGACACA | 9063 |
rs372249131 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856715 | TACACATTACAGTTT[C/T]AAAAAGTATTGCCCT | 9063 |
rs372284726 | in-del | -/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823269 | ATCGTGTTTTTTTTT[-/T]CTCTGCCACTGAAAG | 9063 |
rs372285195 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46811017 | AAAAACTGGATGAAA[A/G]TGTTTCTCTAAGAGT | 9063 |
rs372400091 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883192 | TGACTCTAGCTGAGC[A/G]ATGAATGAGATTACG | 9063 |
rs372451190 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897233 | AAAGCGGTTATGGCA[C/T]AAATACTATTTCCCA | 9063 |
rs372455434 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822558 | GCAATGTTAGAAAAG[C/G]CAGACTCTGGAGGAA | 9063 |
rs372481796 | snp | A/T | 0.0005934 | 0.0172148 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844154 | AGAGAAAAAAAAAAA[A/T]TTAAAAAAATTAAGG | 9063 |
rs372547014 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898496 | TACAAATGACAAGAC[C/T]CTCTCTATTAGAAAT | 9063 |
rs372551667 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858030 | ATTAAAGCAAATCTG[A/G]AAAGGCATCACAGGG | 9063 |
rs372568492 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911818 | TGGGAGGCCAAGGGA[C/G]GGGGAGTGGATCACC | 9063 |
rs372642937 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837799 | ACAGAAAATATCACT[A/G]TTTATAACCAGTCCT | 9063 |
rs372654536 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912051 | GCAAAATCCTGTCTC[-/A]AAAAAAAAAAGGAAA | 9063 |
rs372670353 | snp | A/G | 0.000333472 | 0.0129083 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829872 | CCATAAAAAGCCTAA[A/G]AAACAATTAAGAAGT | 9063 |
rs372716777 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820381 | TAGGGTTCTGTAATA[C/T]CTGTGGTTTCAGACA | 9063 |
rs372727648 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855273 | TCAGCTGTCACTGTT[A/G]CACTGTTTCTAGGCC | 9063 |
rs372729125 | in-del | -/AAG | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907034 | CACCAAGACTCTGAA[-/AAG]AAGGAGAGCCTGCAA | 9063 |
rs372744626 | snp | A/C | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824197 | TATGCTGGATCAGAG[A/C]ATTGCATGAAACTCA | 9063 |
rs372773802 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918939 | TCCTGAGATGTCTCC[A/G]TGGTAATTATGTAGG | 9063 |
rs372812488 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820880 | TCACAGATTAAGATT[-/A]AAAAAAATAAACTTT | 9063 |
rs372868754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847214 | TTCAAAATACATGCA[C/T]ATATTGGAGGTGGGA | 9063 |
rs372880815 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877545 | AACTACCCTTCCTGC[C/T]TTTGCCGCGCCCTGA | 9063 |
rs372886899 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817040 | TATTATTAAGTAAAA[A/G]AAGTTTATTGGAACA | 9063 |
rs372891175 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916417 | TAAAAAAAAAAAAAA[-/A]TCAGGGTTTCTGTCC | 9063 |
rs372906718 | in-del | -/AAAAAAAAAAAA | 0.471673 | 0.115589 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859428 | GCGAGACTCCGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAGA | 9063 |
rs372958025 | in-del | -/TT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834032 | TATACTTTTTTTTTT[-/TT]ACCATCTCCCATACT | 9063 |
rs372979397 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815298 | AATTAGTTGCTTAAA[C/T]TCAGGATACATACCT | 9063 |
rs373009343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885687 | AGACTCCGTCTCAAA[A/G]AAAAAAAACAGTGAT | 9063 |
rs373014428 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828256 | GTGAAGCCACATACT[C/G]CAACCCATGGACAAA | 9063 |
rs373041300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818600 | CTTCACAGTATGACT[A/G]ACTACATAAAAATTA | 9063 |
rs373057048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844528 | AAAGATAAAAATATT[C/T]ATACTTCCTTTGATA | 9063 |
rs373062651 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849424 | GTTTAGCCTTCACAC[A/G]TATTTCTAACAATTT | 9063 |
rs373075885 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910587 | AAAAGAAAGAAAAAT[C/G]AAAGATGATAGAAGA | 9063 |
rs373085801 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911565 | TTTAACAGAAGTGAA[C/G]TTTCTCTATGGCTCC | 9063 |
rs373097024 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871018 | AAGGATGAAGGACCT[A/G]TGGAATTCCTAGAGA | 9063 |
rs373116041 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838849 | CAAATGGTCCTCACA[A/T]CCCAGAGACATGCCA | 9063 |
rs373139810 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827530 | TATTTAGCTCCATTT[A/T]ACAGAACACAAAAAA | 9063 |
rs373235206 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875571 | TCCAGACCCAGAGTC[C/T]GGGGAATATATGGGA | 9063 |
rs373270850 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866934 | ATGCCAGTATTTGAG[G/T]CTCTGTCTGAATGAC | 9063 |
rs373277151 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869915 | ACCCCCTAAAAGCTA[C/T]AGGAAGTAAGCCAGA | 9063 |
rs373288546 | snp | A/G | 3.306e-05 | 0.00406558 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829751 | TCTATTTTTGTACAC[A/G]GTTGGCTGGATACTT | 9063 |
rs373471608 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46812777 | GGAAGATAGCATGAA[G/T]TTAGCTATTTTACAT | 9063 |
rs373522634 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818139 | AATTGACTCATTAGA[-/T]TTTTTTCTCATTGAT | 9063 |
rs373532547 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892193 | TTTTTAAGTCTCAGG[A/G]ACGGCCCAGAAGCAA | 9063 |
rs373534399 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832213 | CGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 9063 |
rs373537803 | snp | C/T | 1.66018e-05 | 0.00288108 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828045 | GTCAGAAGAGCTTTC[C/T]ATTGTAAGATCAATA | 9063 |
rs373557638 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901333 | AGAATCGCTTGAACC[C/T]GGGAGGCGGACGTTG | 9063 |
rs373559249 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820578 | ATCAATATATTCTGA[A/G]GTTCTGATGAGCTAC | 9063 |
rs373571332 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832862 | GTGCCATTGCACTCC[A/C]GCCTGGGCAACAGAG | 9063 |
rs373579456 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851545 | AGATGGGAGATGGTC[C/T]CTGCAGCAGGTTCTT | 9063 |
rs373597662 | snp | C/T | 1.68812e-05 | 0.00290522 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828124 | GGCTTACTGAGGACG[C/T]TTGAACCTGCATGTA | 9063 |
rs373659152 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840329 | CATCATCATCATCTA[C/T]TGGGTAACCCACGTT | 9063 |
rs373662238 | snp | C/G | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915699 | TGCTTTTACTCTGCT[C/G]TATAAGAGCGAGTAA | 9063 |
rs373681766 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900535 | GTTTTTAATTACCAC[A/G]GCTTGGTGGTGCTCA | 9063 |
rs373726976 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881813 | ACAATTAAGAATACA[C/T]AGACACCGGGCACGG | 9063 |
rs373736558 | snp | C/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822953 | ACTTAAGAGTACATT[C/T]AGAGCCAGGCAAGGT | 9063 |
rs373767630 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809395 | CTATTTTCAGCACCA[A/G]TTACACTGTGGGGGG | 9063 |
rs373770548 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46835388 | CAGCAAAGGAAAGTT[A/C]AGAAAGGAACATTAA | 9063 |
rs373811474 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920485 | ACTTTGATACTCACT[C/T]TGCCTCTGTACTGGC | 9063 |
rs373821695 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890377 | ACAATAAAAGAATTG[C/G]AGAAGAAGAAAGATC | 9063 |
rs373883918 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901344 | AACCTGGGAGGCGGA[C/T]GTTGTGGTGAGCCAG | 9063 |
rs373926121 | snp | A/G | 4.17258e-05 | 0.0045674 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864284 | AAAGATAATATTTCA[A/G]TAACAAATCCAACAC | 9063 |
rs373978874 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898732 | GGTGCAGTGGCTCAC[A/G]CCTCTAATCTCAACA | 9063 |
rs374033931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909175 | TGTGAGAAAAGGGAA[G/T]AATGGCTAATCAGTA | 9063 |
rs374041286 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855997 | TTTTCTTTTTCTTTT[-/G]TTTTTTTTTTTTTTT | 9063 |
rs374043050 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864905 | GTATTCAAGAATTAA[A/C/G]TGTTTTTTGTTTATT | 9063 |
rs374083985 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868538 | TTTAAATGGTAGCCA[A/G]TCAGGTCAGTGTAGA | 9063 |
rs374096853 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917668 | CGGCTTGGCCCCGCT[C/T]GGCCCCAGGTCGTGC | 9063 |
rs374097096 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918604 | CGATTGTATTTTTGG[C/T]AGAAACGAGGTTTCT | 9063 |
rs374133338 | snp | G/T | 1.66824e-05 | 0.00288806 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46827981 | TTGGGCTGCTTTGTG[G/T]TTCTGACATAAAGAT | 9063 |
rs374229173 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815962 | GTAATTGTCCAATTC[G/T]ATTTTAGAAAGAGGA | 9063 |
rs374253063 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907880 | ACCAAGGGGCAACTG[C/T]ATATATACTACACAG | 9063 |
rs374262433 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853051 | GGAGGCCAACATAGG[C/T]GGATCACTTGAGCCC | 9063 |
rs374271624 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899837 | GTCAACTAAACAAAC[C/T]TTTACTATATGAAGT | 9063 |
rs374298044 | snp | A/C/T | 4.94999e-05 | 0.00497473 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46821003 | GTCTGTTAATGAAGG[A/C/T]GGAATAGCAGCAGGA | 9063 |
rs374315216 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889219 | CATAGGCAACAACAA[C/T]AAAAAATAAACAAAT | 9063 |
rs374317895 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904699 | GAGGTTGCAGTGAGC[A/C]GAGATCGCGCCACTG | 9063 |
rs374333923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876808 | TTCACACCATTCTCC[C/T]GCCTCAGCCTCCCGA | 9063 |
rs374416443 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906998 | TGCAGGAGGCACTAC[A/G]AAGGCAGTAAGGACC | 9063 |
rs374464401 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809234 | TAAATGCCATATAAC[C/T]TAAATTCACCTCAAT | 9063 |
rs374494405 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842845 | ACACCTCTTCCCTGC[A/G]TTTGCTAAGAGCAGG | 9063 |
rs374622820 | snp | C/T | 3.31301e-05 | 0.00406989 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836496 | CTGCACGGCATGGGA[C/T]TGTCAGCCTCATTTT | 9063 |
rs374687308 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844716 | TTTAAATGCTTGGTC[C/T]TATTAAACATTACTT | 9063 |
rs374723472 | snp | C/T | 2.18936e-05 | 0.00330852 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890565 | TCAGAAGAAACTGAA[C/T]TCTCAAACACTTACC | 9063 |
rs374752728 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833853 | GTATCTCAGATCTGT[A/G]GGAGAGATTATTCAA | 9063 |
rs374766130 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855986 | CTTGAAGACTTTTTT[-/C]TTTTTCTTTTGTTTT | 9063 |
rs374848279 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831211 | AATAACATATGTTGA[C/T]ATGACAGCAATATAC | 9063 |
rs374866355 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863178 | CAGCTCACTTTACCC[A/G]TAACTACCTCAGTTT | 9063 |
rs374918692 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866503 | AGCAGACATGCATTA[A/C]AAGAAATGTAAAACA | 9063 |
rs374944143 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831213 | TAACATATGTTGATA[C/T]GACAGCAATATACAA | 9063 |
rs375004816 | snp | C/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825477 | AAGAACTACAAGGTG[C/G]GTATCAAATAATCTC | 9063 |
rs375081350 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842241 | AAAAAAAATTTAAAA[A/T]AAATTAAAAAAAAAA | 9063 |
rs375111815 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881949 | TAAGAATACAAAAAT[C/T]AGCTGGGCATGGTGA | 9063 |
rs375143947 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870104 | CTGCCCCAATGCCCC[A/G]TGCCCTCCCTAACCA | 9063 |
rs375145663 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896556 | CGTGTTAGAAGACAA[A/G]TATAGAAAAATGCTG | 9063 |
rs375147989 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826683 | AATAAATGATTGGCA[C/T]ACCAGGAAAAAATCC | 9063 |
rs375151355 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904642 | TGTAGTCCCAGCTAC[C/T]CAGGAGGCTGAAACA | 9063 |
rs375158237 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921643 | TGGTAAATTTTTTGT[A/G]TCTAAACAGCTAAGC | 9063 |
rs375166466 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885345 | AACATAGTGAAACCC[C/T]GTCTCTATTAAAAAT | 9063 |
rs375177423 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857642 | ACAAGACATGAGCCT[A/C]GAAAGATGGATGGGG | 9063 |
rs375234392 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863904 | TCCCCAATCCAATAT[A/G]ACAGTGTCTTTACCA | 9063 |
rs375298379 | snp | A/G | | | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46902556 | CAAAAGTAAAACTCT[A/G]TCTCAAAAAAAAAAG | 9063 |
rs375367874 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858608 | GGCTAAGGTGGGAGG[-/G]ATCAATTGAGCCCGG | 9063 |
rs375385479 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920149 | TGGGTAGGTTTGACT[A/G]CAAAGAGTTCTAGGT | 9063 |
rs375469650 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818400 | GCACAGTATCAGAAG[A/G]TGTTCCAAGCTTCAG | 9063 |
rs375503784 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810318 | TGATTAAATTGGGGG[A/G]GTCTCTGACAATCTA | 9063 |
rs375534195 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910133 | TGCACTCCAGCCTGG[A/G]CAAGAAGAGCAAAAC | 9063 |
rs375540517 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819424 | CCAAATTACATGTGG[A/G]GTAACTATATCTAAG | 9063 |
rs375594467 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854864 | GCTAATGCAGACATC[C/T]CACACATGCTGTCCT | 9063 |
rs375634937 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832171 | CCTGTAATCCCAGCA[C/T]TTTGGGATGCTGAGG | 9063 |
rs375682316 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822766 | GGACACAGTGGGTAA[A/G]GAGGAGAGAGAGACT | 9063 |
rs375720561 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830653 | AGAAAAACAGAAAAA[C/T]CAGTTTCTAGTCAAA | 9063 |
rs375729334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913519 | AGAATAAATTCTCAA[C/T]GCATGAAAAGAAGGG | 9063 |
rs375733640 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46821383 | TCACTTTTATTAATA[C/T]GTATGTAATATGTAT | 9063 |
rs375747035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887858 | ATGCTTGAGTAAGTT[C/G]TAGCCAGAGCAACTA | 9063 |
rs375750067 | snp | C/G | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919622 | CCATTGCACTCCAGC[C/G]TGGGCAACAGAGTGA | 9063 |
rs375759891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897299 | CTGACTGCAGGTCTG[C/G]GGCAGGAAATGCACA | 9063 |
rs375842679 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892738 | GTGATCACACCACCA[C/T]ATTCCAGCCTAGGCA | 9063 |
rs375925741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855513 | AAATTCAGAACTACA[C/T]GCACATAGTAAGCAA | 9063 |
rs375937523 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883429 | TATATAGTGCCAAGC[A/G]CAGTGGCTCATGCCT | 9063 |
rs375951083 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908611 | ATGGAAAATATCTTC[A/G]AGAACTCTGTTGAAA | 9063 |
rs375975552 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812567 | CAGACGTACTGCTTG[C/T]TGTTAAGGGTGAGGT | 9063 |
rs376069867 | in-del | -/GC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896164 | GATAAAAAGAAAAAA[-/GC]AAAAAAAAAAAAAAA | 9063 |
rs376088999 | in-del | -/TA | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918995 | ATATGTGTGTGCGTG[-/TA]TATATATATATATGT | 9063 |
rs376221337 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844038 | ATTCCCCAAAATGTT[C/T]TGTTGCTTTACTTAC | 9063 |
rs376234005 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901759 | CCTCAAAAACAAGAA[C/T]AGAGGAGAGCTTCCT | 9063 |
rs376263668 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907397 | TGTCTAAAATTAAAA[-/A]GGGTAGACAAGGATA | 9063 |
rs376282702 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885858 | TCTGGCATTATTTTA[C/T]CTAAGCCAAATGAGA | 9063 |
rs376288813 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828542 | ACAGCTATGTATTCT[C/T]GCACACATGTGGCAC | 9063 |
rs376337404 | snp | C/T | 5.0218e-05 | 0.00501064 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829887 | AAAACAATTAAGAAG[C/T]ACATACATGTGATCA | 9063 |
rs376362320 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885519 | GTGCAAGACTCCATC[A/T]CAAAAAAAAAAAAAG | 9063 |
rs376363807 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840496 | TTGCAAACTGCTGTT[C/T]AGGGATTGTTTTTGT | 9063 |
rs376436858 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881459 | GCTATATAGATGCAA[C/T]TGTATTTTATTCTAT | 9063 |
rs376467957 | in-del | -/CA | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920444 | TGTGAGCAGAAAAAT[-/CA]CACACACACAAAATC | 9063 |
rs376468890 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818415 | ATGTTCCAAGCTTCA[A/G]TTCATTATTAATATC | 9063 |
rs376516880 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872359 | GACATATTTGTTTTT[C/G]AATGGGAAGATCCTC | 9063 |
rs376523955 | snp | A/C/G | 0.0592355 | 0.161582 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847627 | ACTGGGACTACAGGC[A/C/G]CCTGCCACAACATCC | 9063 |
rs376529656 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920830 | ATAGTAATGTGGTAT[A/G]CCCTTAAAGGGGAGT | 9063 |
rs376569557 | snp | A/G | | | utr-variant-5-prime, intron-variant, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46903569 | TAACACCAAATGCTG[A/G]CGAGGATGCTGAGAA | 9063 |
rs376590705 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824837 | TAAAACCCCATGTTT[-/A]ACAAAAAAAAAAAAA | 9063 |
rs376628294 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870847 | AACATTCCTGCAGCC[A/G]ACCAAAAATTTCCAG | 9063 |
rs376646380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839261 | CCAATCTACACATAC[G/T]AATATACTTAAGATA | 9063 |
rs376653252 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871316 | CTGATACTACTCTCC[A/G]TTACCTACAGACCCC | 9063 |
rs376741499 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46812803 | TACATTATTTAGAGA[A/C]TGCAGCATATATTCT | 9063 |
rs376810531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832938 | AAATGTTAATGAGAA[C/T]GAGGAGCAATCAAAA | 9063 |
rs376810863 | in-del | -/C | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918084 | CGGTGGGGTTGGGGG[-/C]GGGGAGAAGTGAAAT | 9063 |
rs376889292 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900300 | CCCAGGAGGCAGAGG[C/T]TGCAGTAAGCAGAGA | 9063 |
rs376973502 | snp | A/C/T | 7.14845e-05 | 0.00597812 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818353 | TCCACTCCATAAATA[A/C/T]AAATTATTTGTTTTA | 9063 |
rs377046012 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847134 | GGTTTTCCTTTTTCA[C/T]AGGACACCAAGCTTT | 9063 |
rs377081727 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912374 | AATGCTATGAAATGG[C/T]TGTTATACTATACTG | 9063 |
rs377105484 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909274 | GTAAAAACTTTTTTT[C/T]TTGAAACAGGGTCTC | 9063 |
rs377132699 | snp | A/G | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822956 | TAAGAGTACATTTAG[A/G]GCCAGGCAAGGTGGT | 9063 |
rs377134112 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833206 | TGGGTTAGAATGCAA[C/T]TCAGCAATAAAAATG | 9063 |
rs377185848 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899193 | ATATAATATGGCAGG[G/T]CATGATGAATAAAAT | 9063 |
rs377282850 | snp | C/T | 1.66134e-05 | 0.00288208 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855532 | CATAGTAAGCAAGTA[C/T]AAAACTAAGGTAACA | 9063 |
rs377301114 | in-del | -/A | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879394 | CACTATAAAAAAAAA[-/A]TAGTAATAATAGTAA | 9063 |
rs377366293 | snp | A/G | 2.64876e-05 | 0.00363911 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812425 | CCCAGAATCAAGTGA[A/G]TCCTCCTTTAGTCCA | 9063 |
rs377389488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905091 | ACATAGTCTCTTCAT[A/G]TACAAATAAAAATTA | 9063 |
rs377391427 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869173 | CTTATACCGACACAC[C/T]GATGCTAAGAGGGAC | 9063 |
rs377397431 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808182 | CCCCAAGATATAAAT[C/T]ACACTGAGAATGATG | 9063 |
rs377430375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827611 | GATGGTGTGCCAAAA[C/T]TGGAATCCATACTTG | 9063 |
rs377492811 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887259 | AAAAAGCAAAAAATT[G/T]AAAAAAAAAAAAAAA | 9063 |
rs377499530 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866977 | ACCCTGAAAAGTTTC[C/T]AAAACCCATGAACCT | 9063 |
rs377506034 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918223 | CGTAATGTGCTGATA[C/T]AGGATGAAGGAAGAT | 9063 |
rs377512907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46893823 | AAAATAACAAACACC[C/T]CCCAAAAAAATCCCT | 9063 |
rs377554947 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899455 | CCACTGCCGAACCAG[A/G]GTAATCTAGAGGAAT | 9063 |
rs377557379 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860556 | ATATCAAAAGGGCAT[A/G]GGAGCCAACCTGAAA | 9063 |
rs377611842 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850116 | AAACATATACAAAAA[C/T]AGAGAAAAAAGTATA | 9063 |
rs377678221 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919059 | ACACAACACACACAC[A/G]TATTGTTTTGGCCAG | 9063 |
rs377729779 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844689 | CTCATATGCTCAATC[-/T]TTTTTTTTTTTTTTA | 9063 |
rs386387588 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884922 | TCTGTCTCAAAAAAA[-/A]AAAAAACTTAAAAAA | 9063 |
rs386802912 | in-del | ATTTTTTC/TTTTTTT | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892907 | AAGTGTCAGTGGGAT[ATTTTTTC/TTTTTTT]ATACTAAGTCTTCAA | 9063 |
rs397732999 | in-del | -/A/T | 0.00012715 | 0.00797237 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844153 | AGAGAAAAAAAAAAA[-/A/T]TTTAAAAAAATTAAG | 9063 |
rs397737403 | in-del | -/A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810197 | AAATAGAAAAAAAAA[-/A/C]CAAAAAAACAAATCA | 9063 |
rs397794255 | in-del | -/T | 0.375 | 0.216506 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865540 | CAAGGACCATTTGCC[-/T]TTTTTTTTTTTTTTT | 9063 |
rs397817996 | in-del | -/AAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879393 | TCACTATAAAAAAAA[-/AAA]ATAGTAATAATAGTA | 9063 |
rs397820405 | in-del | -/T | 0.375 | 0.216506 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834033 | ATACTTTTTTTTTTT[-/T]ACCATCTCCCATACT | 9063 |
rs397858717 | in-del | -/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922118 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC | 9063 |
rs398041371 | in-del | -/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888375 | CAATTTTTTTTTTTT[-/T]ATCAGAAATAGAAAA | 9063 |
rs527300805 | snp | A/C | 0.00010843 | 0.0073623 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917314 | CTCCGCTCTCCACTC[A/C]CGCTTACCCTCAACT | 9063 |
rs527315543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824816 | GAGACCAGCCTGTGC[A/G]ACATGGTAAAACCCC | 9063 |
rs527316452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869305 | AGAAATATCTAATAC[A/G]AGGAGGGACTGAGCC | 9063 |
rs527319282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876902 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 9063 |
rs527334272 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882699 | CATCAAAAAAGTACT[A/G]GGTAAGTTACGGTAC | 9063 |
rs527372992 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876177 | TTGTGCTCTGATCCA[A/G]TTGGCCATCCCTTTC | 9063 |
rs527375360 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847582 | CGCCTCTCGGGTTCA[C/T]GCCAGTCTCCTGTCT | 9063 |
rs527401105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832285 | CCAGGCGTGGTGGCG[C/T]ACACCTGTAGTCCCA | 9063 |
rs527444585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839553 | GTTATCAGTTCTCAT[C/T]TGGTTTCAAAACCCC | 9063 |
rs527454990 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903112 | TGTAAAACTTTTTTT[-/A]TAATAAGCAGGAAAA | 9063 |
rs527566008 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846158 | ATCTCAAAATTGACA[C/T]AATTTATTATAAGAC | 9063 |
rs527626607 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894991 | GGCAGGAGAATCGCT[C/T]GAAACCGGGAGGCGG | 9063 |
rs527627578 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902906 | GAACCCAGAAACAGA[A/C]ATATACATACATACC | 9063 |
rs527655180 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853288 | GCCTTTTTTTTTTTT[A/T]AAATAAAAAAAAAAA | 9063 |
rs527678567 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845736 | CAAGTATTTTAAATA[-/T]TTTTTAATGTTCTTT | 9063 |
rs527708616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909817 | GGTTTTTCTGCAAGA[C/T]AAGTTTGGTGAAACT | 9063 |
rs527713104 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848127 | CATACATTTTTCCAC[A/G]TGACACTCTCCTATG | 9063 |
rs527732783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868309 | CTGTAAACAACTACT[C/T]CTGCCAGTCCCAATC | 9063 |
rs527755869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46815076 | GTAGGAGATGCCAAC[C/T]GATTAAGCTAAATAA | 9063 |
rs527795117 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883816 | ACTCTAACCTGGGCA[A/C]TTAAGTGACCCTCTC | 9063 |
rs527797344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867369 | TGTATTAACATTGAC[A/G]GTTCTTAGATAAGTC | 9063 |
rs527862520 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898609 | TGGCTGAAAAAGAGT[A/G]TTAAAAAAACCGAAG | 9063 |
rs527883372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823136 | GCTACTTGGGAGGCT[A/G]AGGCTGAGACTGCTT | 9063 |
rs527886145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915646 | TTTGGTTTCTATCAC[C/T]TTCCAGTTGCTGGTT | 9063 |
rs527918131 | snp | A/C | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921790 | ACCTGGTTGGACCAA[A/C]CATGTAACCTTGAGT | 9063 |
rs527919993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830436 | GATTTTAAACTGAAT[G/T]AAAATAAAAATGTAA | 9063 |
rs527979689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880550 | TCATGCCTGTGAATA[A/G]CCACTGCACTCCAGC | 9063 |
rs527980775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881398 | AATGGGATTATAATT[C/T]AAAGCAGTGATAAGT | 9063 |
rs527995534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829959 | ACCTTGAAAACATAA[A/G]TAATGTTAGCTGACC | 9063 |
rs528001841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837781 | TCCCCATATATTTCC[C/T]TTACAGAAAATATCA | 9063 |
rs528036970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898823 | ACACGGTGAAATCCC[A/G]TCTCTACTAAAAATA | 9063 |
rs528045297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850055 | TCAGATCTCCCAGGT[A/G]CCTCAAAATTTCTTT | 9063 |
rs528081815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857053 | TGTTAACAACACATG[C/T]CAAGTGCCTAAATAT | 9063 |
rs528130872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865074 | TGCTTAATGAAGTCA[C/T]CCTTATGTATATTAT | 9063 |
rs528165484 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810860 | GGGCACTTCAGTTTG[A/G]GAAATCAATTGGTTG | 9063 |
rs528186256 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909433 | GTTTTGTTTTGGTAG[A/C]GATGGGGTTTCACCA | 9063 |
rs528191583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864627 | AATATAAAATTAGCT[C/G]GGCATGGTGGTGCAT | 9063 |
rs528205619 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810177 | AACATTAAAACTGTT[C/T]ACAGAAAATAGAAAA | 9063 |
rs528206993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871877 | GTATAGGCCTACATG[C/T]CAGTCCAAACGGATT | 9063 |
rs528272662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819417 | CCAACTCCCAAATTA[C/T]ATGTGGAGTAACTAT | 9063 |
rs528279917 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920684 | ATATGTTCAAAGGAA[A/T]GGCTGAGTGGTAAAG | 9063 |
rs528292472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913055 | CTCAGGTGAAGCCTT[C/G]GAAATTTTAGTTGCA | 9063 |
rs528298792 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919997 | GAGCTTACACCCATA[A/T]AGAGGACCAACATAA | 9063 |
rs528307554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871150 | ATTGCTAAGAAATTA[C/G]AAAAGATAGAGAATT | 9063 |
rs528309580 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901885 | AAAGATGCCTACTAT[C/T]ACCCCTCATTCAACA | 9063 |
rs528369929 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813376 | GATCCCAAACAAGTA[-/T]CAAACCTGAATGTAC | 9063 |
rs528371321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909119 | TGAAATAATTTTTTT[A/T]AAAAACTAGTACAAA | 9063 |
rs528394029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834084 | TTTTAGACCTAGTAT[C/G]TGACACATGATAGGT | 9063 |
rs528403817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884773 | ATATAATAAATTAGC[C/T]GGGCGTGGTGGCACA | 9063 |
rs528411378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826494 | TACTTGCAACTCATG[C/T]TTTTCCACTATATTC | 9063 |
rs528426468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841939 | ACTTTCACTATTATT[G/T]AAAGTTTGGCTAGGT | 9063 |
rs528430214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833418 | CATACATGAGAAAAC[G/T]TTAGGTGTGATGGGT | 9063 |
rs528465109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884376 | AGAGTGCAGTGGCTC[A/G]ATCTAGGCTCACTGC | 9063 |
rs528467082 | snp | A/G | 4.94401e-05 | 0.00497168 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890837 | TCCAAACTGAAAACC[A/G]ATGATTTGATTGTGG | 9063 |
rs528514861 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826959 | TGCCTAGATTTGGGG[-/T]GTAAATAGGAATAAA | 9063 |
rs528581960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889826 | TGGGAGCAACCCAAG[C/T]GTCCAATGGATAAGC | 9063 |
rs528639356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904779 | AAAAAAACAGAGATG[A/G]GGGTCTCACTATGGT | 9063 |
rs528644756 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809282 | ACAATTACCTTAGGA[C/G]AGATGCCAAGTTTTT | 9063 |
rs528649436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855699 | GGAAAAAAAGGAAAA[A/G]CATTATTTGTATTTT | 9063 |
rs528655207 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46821162 | CATTCTCAGTCGTTC[A/G]TTCACCAGTTTCAGC | 9063 |
rs528656263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847997 | TTTAATTATGTACTA[C/T]TGAGAAAGAGAAAAT | 9063 |
rs528704154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863410 | GCTCACTGCAGCCTC[A/G]ACCTCCCAGGCTCAA | 9063 |
rs528709522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904157 | TCTTGATTGTGTTCA[C/T]GTCAATATCCTGGTT | 9063 |
rs528726747 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870717 | CTTAGGGCCACAGCT[C/G]TATACTTGGGCAGAG | 9063 |
rs528731601 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808455 | AGGTTCCTAACAAAG[C/T]AGGGGTGAGGGGGGT | 9063 |
rs528790442 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817273 | AATGGTGTTGGAATA[C/T]TGTGTACTGAAGCCA | 9063 |
rs528794860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911461 | CCTGAGGCGATCCGC[C/G]TGCCTGGGCCTCTCA | 9063 |
rs528843410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838669 | TAAACAGAATCTTAC[A/G]GTATGCCCAAGGCTT | 9063 |
rs528868287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881645 | GAATTCTCCATTCAT[C/T]AGGCCAATGCAGTAA | 9063 |
rs528885611 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860304 | AAACATGGGGAGAGA[A/G]GTAGTTAAATGACAC | 9063 |
rs528924210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837874 | CCAAAAAGACGGTCT[A/G]GATCTCTGCTCACCA | 9063 |
rs528996686 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898313 | CCACCACACCTGGCT[-/A]AATTTTGTATTTTAG | 9063 |
rs529006120 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900951 | TGTACTCCAGCCTGG[A/G]TGATAAGAACGAAAC | 9063 |
rs529006613 | in-del | -/CTT | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime, nc-transcript-variant, cds-indel | PIAS2 | GRCh38.p7 | 18:46817101 | TTCTTTTTACAGTAA[-/CTT]CTTATCTTTTCAGTT | 9063 |
rs529045802 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844599 | CACCAGTAATGTATA[C/T]AAATTAGTATATACA | 9063 |
rs529083781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851393 | ATATTTCTCACAAAT[A/T]GTTTAGAAGAAAAAT | 9063 |
rs529096877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900766 | GAATCACGAGGTCAG[A/G]CGTTCAAGACCAGCC | 9063 |
rs529152872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886609 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTCAG | 9063 |
rs529185251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908284 | CAGGCAAGAAGTTTG[A/T]TTATGCTAGCAGCAG | 9063 |
rs529198093 | snp | C/T | 2.22106e-05 | 0.00333239 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812442 | CCTCCTTTAGTCCAA[C/T]GAGATGATGTCAGGA | 9063 |
rs529207705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866666 | ACAGCTAAAGTGATG[A/G]CATTGAAAGGCAGGA | 9063 |
rs529231692 | in-del | -/TAA | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904892 | TCTTTCATGTGCTAG[-/TAA]TAATGTTAAAATATG | 9063 |
rs529246241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914817 | CTACTGCCAAGAAGT[C/T]AGCCAACAAACTAAT | 9063 |
rs529287713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823864 | AATCTTCACAAAGAC[A/C]ACATTCAGAAACAAA | 9063 |
rs529293622 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921995 | TATCTATTTATATCA[C/T]ATTTCCTAACTCCTA | 9063 |
rs529305049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821565 | TTTGCAATCTTTCCT[A/G]GGAATCATCTGAGCA | 9063 |
rs529318535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873903 | CCCTACCGCCATTCC[C/T]ATCTTCTCCCCCGCT | 9063 |
rs529336724 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921281 | TACAGGCACCCGCCA[C/T]CATGCCCAGCTAATT | 9063 |
rs529338435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865761 | ATATTTTTTCAGAAC[A/G]CTTTAAAAAGGAGGG | 9063 |
rs529365347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873038 | CCTGTGGCCTTTGTA[C/T]CAAAAGTTTTTGACC | 9063 |
rs529430981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828874 | ATGGAAAAGCAACAG[A/C]AACTTATCAACTAAA | 9063 |
rs529475844 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893369 | ACTTATTGTCAGATA[C/T]TCTTCATTTTAAGGG | 9063 |
rs529490524 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851335 | AATATTCTTGTCAAC[A/C]CTTCTTCCTTTCTTC | 9063 |
rs529524740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885620 | TGGAATGACATTTTT[G/T]ACCTCATGTCTGTTT | 9063 |
rs529538288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843494 | AGTTGGTTTTATTTT[C/T]CAAACTCAATTATTA | 9063 |
rs529557987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835085 | TATCAAGAATTTAGT[A/G]AACACATCACAAAAT | 9063 |
rs529578330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892053 | TACCTGTGGTTTGGT[G/T]TCCCATCCCATCCTC | 9063 |
rs529591893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891543 | ATCAAGTCAGAACTG[C/T]GATCCAAAATGCAAT | 9063 |
rs529599632 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912229 | GCTGGTACCAGGGTC[C/T]CCTGCAGATACCAAA | 9063 |
rs529601201 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828294 | TCCCTAACTCCAGAC[-/CT]CTGTCTGTAAAATGG | 9063 |
rs529641420 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899786 | TCACAGAATGATGTT[A/C]GTTTTTCACAGAAAA | 9063 |
rs529658911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911573 | AAGTGAAGTTTCTCT[A/G]TGGCTCCACAGTACT | 9063 |
rs529676767 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919060 | CACAACACACACACA[C/T]ATTGTTTTGGCCAGG | 9063 |
rs529680116 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808644 | CATGAACCTAGGACC[A/C]CTAAATCCAATGTCA | 9063 |
rs529691342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870570 | GCCGTGAGCCATGAT[C/T]GTGCCACTGCACTCC | 9063 |
rs529708482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862682 | ACACACATATATATA[C/T]ACACACACATATATA | 9063 |
rs529727048 | in-del | -/TCCTGCTGCTCACC | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888804 | CTGTAATGCTCGAAT[-/TCCTGCTGCTCACC]TCCTGCTGCTCACCT | 9063 |
rs529743331 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900131 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAAATCAC | 9063 |
rs529749583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876980 | ACTGGGATTACAGGC[A/G]TGAGCCACAGTGCCC | 9063 |
rs529806766 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872699 | ATAAGGCCCGAACGG[C/G]TCAAAGGAATCGTGT | 9063 |
rs529814455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883597 | TAATCCCAGCACTTT[A/G]GGAAGCTGAGGCAGG | 9063 |
rs529829181 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918169 | GGAGTCAAACGCCAA[C/G]GCAGAGTAAGTAGAT | 9063 |
rs529864960 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837462 | TAATCTTTTGTTATC[G/T]ATTTATAGGCACTCT | 9063 |
rs529867522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832701 | TTGGAGACCAGCCTG[A/G]CCACTATGGCGAAAC | 9063 |
rs529933402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889361 | GGGATTATATCCAGA[A/C]TATACAGAGAACTCC | 9063 |
rs530040716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854029 | AGTGATGCAGTGTTG[C/T]TCAAGCCCTTTAAAG | 9063 |
rs530052915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888939 | TAAAACCTCACATAC[A/G]TGGTCAAATACTTTT | 9063 |
rs530062771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895485 | AGAACAGCCAGGCCA[A/G]AAAGGCAAAACCCTG | 9063 |
rs530065862 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838846 | ATCCAAATGGTCCTC[A/G]CATCCCAGAGACATG | 9063 |
rs530074001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847030 | AAAAAGGTTACAAAA[C/T]ATTTCACAAGTCCAG | 9063 |
rs530086252 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918668 | CTCAGGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 9063 |
rs530094201 | snp | C/G | | | intron-variant, splice-donor-variant | PIAS2 | GRCh38.p7 | 18:46894810 | GCGCGGTGGCTCATA[C/G]CTGTAATCCCAGCAC | 9063 |
rs530126960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862038 | AAATTACTACAAAAT[A/G]TAAAGTTTTTATGCC | 9063 |
rs530148382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816259 | GACATTATGCTTTTA[C/T]GCAAAATAGAGAATA | 9063 |
rs530162190 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861036 | TGTAATCCCAACACT[C/T]TGGGAGGCCGAGGCA | 9063 |
rs530227612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917136 | CGCCCCCGCGCCGCC[A/C]GCGTGCCCTCCGCCG | 9063 |
rs530303795 | in-del | -/ATATATACACATAT | 0.0134861 | 0.0810011 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862648 | TACATATATATACAC[-/ATATATACACATAT]ATATATACACATATA | 9063 |
rs530311820 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909937 | TTTGGGAGGCCAAGG[A/C]GGGTGGATCACCTGA | 9063 |
rs530315082 | snp | A/T | 8.25321e-05 | 0.00642334 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815330 | GGGATCAACTGGAAT[A/T]AGGGAAAGAAAATCC | 9063 |
rs530323819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916457 | TCATTTATGTCGCCA[C/G]TAATTCAGCGATACA | 9063 |
rs530338613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874748 | ACATACTTAGTCTGT[C/T]TTCCACTTTCTCTTC | 9063 |
rs530348868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831151 | GACTATATAGAAAAT[C/G]CTATGTAATCTATAA | 9063 |
rs530351715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868550 | CCAATCAGGTCAGTG[C/T]AGATTGTGCCGTCTG | 9063 |
rs530389014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843725 | CATTTATCAGGCCCT[A/G]GTCACTTTATTGCTA | 9063 |
rs530389076 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830027 | AACAATTATTACACT[C/T]CCTTTGTCCTATGTT | 9063 |
rs530392673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892077 | CATCCTCATCACTCC[C/T]CCAACCCAGCCCGTG | 9063 |
rs530425067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882164 | ATACTTATTAACTGA[A/G]TTAATAAAAATAATA | 9063 |
rs530427601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850717 | TCTACCATGAAGTTC[C/T]CCGTCAAGCTTCGGC | 9063 |
rs530523728 | snp | A/C/G | 0.00954224 | 0.0684493 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872804 | GATTAATATGCCCTA[A/C/G]AGATGAAACCCTTAT | 9063 |
rs530548040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857262 | TCATATTCTGGGTGC[C/T]GGAGCTTCAAAGACA | 9063 |
rs530600010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899864 | AAGTAACTATCAAAT[C/T]TGTGAGGTTAAGAAA | 9063 |
rs530603529 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863773 | AGGTCAACTGTTATG[A/G]ACTGAATTGTGTATC | 9063 |
rs530607384 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810936 | TTAGAGAGAGAAAGC[G/T]AAACAGAAAAGTACC | 9063 |
rs530617469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857892 | GTAATGGGTTGTGAG[A/G]TGATAAAAATGAGTA | 9063 |
rs530632625 | snp | A/C | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825527 | TCAGTCCTTAAGATC[A/C]ACTCATCCATCTTGC | 9063 |
rs530643660 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831471 | CAAAATCCCAGCAGG[-/T]TTTTTTCCCCTAATT | 9063 |
rs530644083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820491 | CCCCACTCTAGGGAA[A/G]CAGATGGTAGACTCT | 9063 |
rs530653971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865233 | TCCTAACAATTGCAA[A/C]ATCACCCAAGTAAAG | 9063 |
rs530664319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898902 | TGGGAGGCTGAGGCA[A/G]GAAAATTGCTTGAAT | 9063 |
rs530666366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907333 | AAAGGAGCTTGACAT[A/C]ATTACTTATTAGGGA | 9063 |
rs530679717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906607 | GCAATACTTTAACTG[A/G]AAATAACAAAACTTT | 9063 |
rs530727655 | snp | A/C | 1.65927e-05 | 0.00288029 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828068 | GATCAATAACATCTA[A/C]TTTCTTCTTGCTTGC | 9063 |
rs530795538 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833765 | GGCCCAGTAATACTT[C/T]GATCAATGGAACAAA | 9063 |
rs530832478 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46817865 | TTTAAGCAGAATATT[-/A]AAACTCTTATATAAA | 9063 |
rs530835857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879095 | GATCCTGAGCTATCC[A/G]GTTCTCATCACCTAC | 9063 |
rs530953202 | snp | A/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890893 | TCGTGGATATCGGCG[A/T]CTATACAATTCTCGG | 9063 |
rs530955499 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918195 | TAGATAGAAGGAAGC[C/T]TGATGGCCCCCCCGT | 9063 |
rs530957369 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888869 | CTAACAGGCTGTGGA[C/G]TGGTGCTAGTCCACG | 9063 |
rs531011551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884858 | GGAGGCAGAGGTTGC[A/G]GTGAGCTGAGACCGT | 9063 |
rs531029223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905514 | AACAGGAAGGATACA[C/T]TAAAGAGCATAAACA | 9063 |
rs531093065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889901 | AAGAAACAGCTAAAA[C/T]AATTAAGGTTGTTGC | 9063 |
rs531095289 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849056 | CAAATAAAAATAATG[C/T]TACAGGGTCTGTCAG | 9063 |
rs531101361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841321 | TTATTCTATCACCCT[A/G]CACTATCATTTTCTC | 9063 |
rs531101985 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855245 | TCTGGATGCTAAAAC[C/T]GTTCACTGGTATTCA | 9063 |
rs531112309 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809456 | CTAAGTGAAGAAAGA[A/T]AAAAACATTTTATTT | 9063 |
rs531131720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856181 | CGGCTAATTTTATTT[C/T]TATCAGAGATAGGGT | 9063 |
rs531132048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848697 | TAAAAACGTTTGAGC[A/G]GGGGAATAAAAGACA | 9063 |
rs531152085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904911 | AATGTTAAAATATGG[C/T]TTAAAAATCGATAGA | 9063 |
rs531198522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916529 | AGGTTATCAGTCTGG[A/G]GGGAAAAAGTCTCTT | 9063 |
rs531220807 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855814 | TTAACTTCTAGCCAC[C/G]TCTTTATGGCAATTT | 9063 |
rs531259353 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877211 | TCAGATAAGCTCCTA[C/T]TTTTAGAAAACCAGG | 9063 |
rs531259672 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907434 | AACTGGAACTCTACT[A/G]TATCACTAGCAAAAG | 9063 |
rs531358744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875453 | TCCCCAAACAATGGC[C/T]CAAGAACCCTCCATA | 9063 |
rs531368860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887412 | CACTGATATGTTTAA[A/G]TGTTTTCACATGACT | 9063 |
rs531369169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837967 | ATAGGAGAATGAATG[A/G]ACATGGACTGGAAAT | 9063 |
rs531378856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831280 | AAAAATTTTTTAAAT[A/G]CCACAGAGATATGAA | 9063 |
rs531411527 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838811 | CTCACTGAGACACAG[C/G]TGATGGAGCTATATC | 9063 |
rs531425655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882192 | ATATATACAGTAAAT[G/T]AGAATATTATATTTT | 9063 |
rs531437103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888086 | TAAATATGATGAAAA[A/G]GAAATTATGTAGTTT | 9063 |
rs531484313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901833 | TATTATACTCAGGGC[A/G]GAAAGATTGCTTTCC | 9063 |
rs531498925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845941 | AATTCCTGCTATAAA[C/T]AATGCCTCAATTTCT | 9063 |
rs531621770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859226 | GAGGTCAGGAGATCG[A/C]GACCATCCTGGCTAA | 9063 |
rs531624997 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852378 | CTCCCCATTGCCTTC[C/T]ATTTTTGAAAATATG | 9063 |
rs531625750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908458 | TTTATTATTCTTTGA[A/G]GAAAAACCATGCATC | 9063 |
rs531659759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859997 | GCCAAAAAGAGAACT[A/G]AATCCAATGTTCAAT | 9063 |
rs531691010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874609 | ATTGCCTTACTGAGG[G/T]TCTGAACTACCCCTC | 9063 |
rs531702811 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874165 | AAAAAAACTAATAAG[C/T]GAATCCTAAGAAAAC | 9063 |
rs531711835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866727 | GCAAAAAGAATGGAG[C/G]GGGTAGATAAAGGAA | 9063 |
rs531721739 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871699 | AATGTCCCTTGCTCC[G/T]CAGAAGAACTTTTTG | 9063 |
rs531724300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830329 | AAATTTAAAATAAGT[A/G]TATTTGAATTAAGTT | 9063 |
rs531727483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813776 | CAAAAGAACAAGTTA[C/T]TTAATGCTTTGGATA | 9063 |
rs531753595 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840627 | AAATTTAATTCTACT[C/G]TAGTGGTCTTATAAG | 9063 |
rs531856065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822390 | CTTGAGGCAATAACA[C/T]AAGCCTGGTATTTGA | 9063 |
rs531858958 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914559 | CGAATAACCAACCCT[-/C]CCCCCCCCAACTCCA | 9063 |
rs531860554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844423 | AATGCAGCAGTACCC[C/T]GAGCGTCAAAGCTTT | 9063 |
rs531872951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879916 | CAAGATGGTGGTTGC[C/T]AGGAGCTGGGGGAAG | 9063 |
rs531912786 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921791 | CCTGGTTGGACCAAC[C/T]ATGTAACCTTGAGTT | 9063 |
rs531915454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886327 | GATAAGGAAAAAAAA[A/T]TTTTTTAAGTAATAA | 9063 |
rs531953078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903922 | ATACAACAACTTGGA[C/T]GAATTTCCAGAATTA | 9063 |
rs531970361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836774 | TACATTGAAAGTATG[A/G]CTCCTTCTTACCTGG | 9063 |
rs531985402 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828959 | TAGTGTCAATCGCAG[A/G]GGAATAATTAATAAT | 9063 |
rs532030459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871093 | GACCCTCTTGGGCAG[A/G]GAATACTCAAGTTAC | 9063 |
rs532049979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864560 | TGGATCACCTGAGGT[C/T]GCAAGTTCGAGACCA | 9063 |
rs532090274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878116 | AGACCAGAATATAAC[A/C]GTCCTATATCCTAGC | 9063 |
rs532090699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870651 | AAAAAAAAAGGAACT[C/T]GAGTCATTATTAGAT | 9063 |
rs532090908 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898092 | ACTTCTGGGTCCAAG[C/T]GATCCTTCCACCTTG | 9063 |
rs532125618 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900813 | ACCCCATCTCTCCTA[A/T]AAATACAAAAATTAG | 9063 |
rs532136893 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810097 | TGTATTTTTTAAAAT[C/G]CAAGTTGCCTGTATG | 9063 |
rs532148435 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833934 | TTAATGGGATCACCT[A/G]TTCCCTACTGTAAAG | 9063 |
rs532161879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826345 | CTTATCAAACACAGA[C/T]AAAAATGTAGTAAAG | 9063 |
rs532170919 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840376 | TCCTAAGAGAAAAAG[A/G]ACACAAAATGCCAAA | 9063 |
rs532173606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819236 | GACACTCTTCCAACA[A/C]CCCATGTTACAGCCA | 9063 |
rs532175577 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809647 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 9063 |
rs532248782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833320 | GATTCCATTCATATA[A/G]AAGTCTAGAAAATCC | 9063 |
rs532262850 | snp | A/G/T | 3.65283e-05 | 0.0042735 | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818426 | TTCAGTTCATTATTA[A/G/T]TATCATTTCTTCTTT | 9063 |
rs532281474 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919900 | GAATTTAACATTGTT[C/T]AGTAGGCTTTAAGTG | 9063 |
rs532292928 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884321 | ATTTATTTATTTTTT[A/T]TTTTTTTTTGAGACA | 9063 |
rs532302931 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920306 | GTGGACCCGTGCCCT[A/G]AGGTAGGCTAATCAG | 9063 |
rs532337688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848485 | GACACTTCTGGATTT[C/T]GGCAATGCTAAAATA | 9063 |
rs532373029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847940 | CTACATATTGAAAAG[G/T]AGATACCATATTTCA | 9063 |
rs532435915 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874188 | AAGAAAACCACCCAT[C/T]GGAGGAAGAACCCTG | 9063 |
rs532437887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883659 | GCCTGGGCAACATAG[A/C]AAAATCTCATATCTA | 9063 |
rs532460769 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870948 | AATAAAAGGAATTCA[A/G]GAATCAGTACCTCAG | 9063 |
rs532488839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854879 | CCACACATGCTGTCC[G/T]ATACATGAAAGTGCC | 9063 |
rs532500209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889384 | AGAACTCCTAAAACT[C/G]AACAACAATAAAACA | 9063 |
rs532550267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911433 | GTTAGCCAGGCTGGT[C/T]TCTAACTCCTGACCT | 9063 |
rs532566697 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816757 | ACAGACATAAGCCAC[C/T]GCACCCAGCTTGCTG | 9063 |
rs532572757 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862546 | GAAGCCTTAGTTTTA[C/T]CATGCTGAATCTTTT | 9063 |
rs532612988 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917854 | ACGCGGTGCCTATGG[A/C]CGGAGAAAGCCGCCG | 9063 |
rs532683729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824664 | TTTGTAAAATTGTTT[A/G]TAAGAATAATTTTTA | 9063 |
rs532690973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895612 | GGAAGTGGTGGTTGC[A/G]GTGAGCGGAGATCAC | 9063 |
rs532704517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903328 | GACAAAGGACTACTA[C/T]CTAGGATATACTTAG | 9063 |
rs532753090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862104 | TGGGAGGCCGAACAG[A/G]TGGATCACTTGAGGC | 9063 |
rs532755111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910683 | GAAACCTTTCAGAAT[A/G]TAAACAAATCCCGTA | 9063 |
rs532777878 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882965 | GGCCTGGTGGCGGGT[G/T]CCTAGAATCCCAGCT | 9063 |
rs532804825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869288 | CTAGAGAAGGGAAGG[C/T]AAGAAATATCTAATA | 9063 |
rs532813534 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856126 | TTCTCCTGCCTCAGC[A/C]TCCCGAGTAGCTGGG | 9063 |
rs532814489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844518 | TGTAAACAGAAAAGA[C/T]AAAAATATTTATACT | 9063 |
rs532815361 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897426 | CTCCTAGTAGCCTAA[C/G]ATGAGAAAATTTGAG | 9063 |
rs532824315 | in-del | -/AAT | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824684 | AATAATTTTTACTAA[-/AAT]AATAATACCTCTTAA | 9063 |
rs532839615 | snp | C/G/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824948 | AAGACTGCAGTGAGC[C/G/T]GCGATCACACCACGG | 9063 |
rs532847354 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839605 | ACCTAGGCCAGGCAC[A/G]GTGGCTCCCAGCACT | 9063 |
rs532867686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917200 | TTCGTCCGCGGGCCG[A/G]GGCTCAGGGCTCCGC | 9063 |
rs532868949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875958 | ACCCTATGGGTCAGG[A/C]CCTGAGGGCCACGTC | 9063 |
rs532924244 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886834 | CAGAACAAGACTCTG[C/T]CCCCCCCCTCCAAAA | 9063 |
rs532955439 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812307 | CCTCAGAAAGCAAAA[G/T]AATCCATCTGACTTT | 9063 |
rs532956461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850737 | CAAGCTTCGGCATCC[A/G]TTGATGATAGCTACC | 9063 |
rs532973620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914786 | ATGTGGCATCCAGAT[C/T]GGCTGACCAATTTCT | 9063 |
rs532991526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857990 | CAGAAAATAAGTACA[C/T]GGCACAGTGAGAGAC | 9063 |
rs533075421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821399 | GTATGTAATATGTAT[A/G]TGGGTATCAGTAATT | 9063 |
rs533088513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900753 | GACCGAGGCGGGTGA[A/G]TCACGAGGTCAGGCG | 9063 |
rs533098715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908255 | GATGGGATTACAGCC[C/T]TGAGCCACCTCACCA | 9063 |
rs533151278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820647 | AGGTTCTATAATAAA[C/G]AAACCAAGAAGAAGT | 9063 |
rs533155302 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921268 | AAGTAGCTGGGATTA[A/C]AGGCACCCGCCACCA | 9063 |
rs533168800 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908424 | AAGAAAAAAATTTGC[A/C]TGAAAGGTGATGGAA | 9063 |
rs533214880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865692 | AAAATATTCTTTTCT[A/G]TAAGCACAGTTTATT | 9063 |
rs533260687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879207 | CAGGACTTCTAAAAC[C/T]CAACAGCTAAAAACA | 9063 |
rs533288293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834973 | TCTATTTCTAAGAAC[C/T]TGAAGAAAACTCCAC | 9063 |
rs533362598 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817602 | TCATCCACGGAAAAT[G/T]GAATGTGGTGACTTA | 9063 |
rs533382122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876996 | TGAGCCACAGTGCCC[A/G]GCCTCCTTCACTAAT | 9063 |
rs533396255 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820426 | TGGAACTTATCCCCC[A/G]TGGATAAGGGGAAAG | 9063 |
rs533407066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835616 | TTCAAGTTGTACAAG[C/T]ATCTTTAAAACTCTA | 9063 |
rs533416129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848598 | ACCCTTCACTGTCTC[A/G]TAAGAGGCAAGACAG | 9063 |
rs533422641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898715 | AAGAAGCTTTGAGGC[C/T]GGGTGCAGTGGCTCA | 9063 |
rs533422652 | snp | A/G | 1.67251e-05 | 0.00289176 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890997 | GTCCACTTTTATTCC[A/G]TCCAGCAAAGCCTAG | 9063 |
rs533453914 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886119 | CTTCACTTAGTCCCC[C/G]CCAGTCTTCTGTCCA | 9063 |
rs533478320 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892062 | TTTGGTGTCCCATCC[A/C]ATCCTCATCACTCCC | 9063 |
rs533483823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898014 | GTAGCTGGGAGGCCA[A/G]CCCAGTTAATTTTTA | 9063 |
rs533551900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910083 | ATTGCTTGAACCTGG[C/G]AGGAGGAGGTTGCGG | 9063 |
rs533571604 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831282 | AAATTTTTTAAATAC[-/CA]CAGAGATATGAAATA | 9063 |
rs533578023 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815633 | AATATTTCCCCCTTT[C/G]CCGCTTAACAGAATG | 9063 |
rs533579843 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841722 | AGCTCAAAAGACAGT[C/T]TCACGAATAGACCTG | 9063 |
rs533614408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842176 | AGCTGCAGTGAGCTG[C/T]GTTCATGCTACTGCA | 9063 |
rs533616251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849887 | CAAAAATACACATTT[C/T]TTTTTGTCCTTATTT | 9063 |
rs533673720 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824166 | GCTATATAGCAAATA[G/T]TAGTATTCCGGATTA | 9063 |
rs533720621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906460 | ATAATTAATCACAAT[C/T]AGGAGTATAGCAAGG | 9063 |
rs533781782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46902515 | CAGCGAGCCGAGATC[A/G]TGCCATTGCACTCCA | 9063 |
rs533788528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861204 | AGATTGTGCCACTGC[A/G]CTCCAACCTGGGCGA | 9063 |
rs533866808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868745 | TTGGGTGCTTGTTTT[C/T]CTTGTGACTCCAAGC | 9063 |
rs533879788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823951 | GTAAATGGCTATGGA[A/T]GGTGAAATGATGGAT | 9063 |
rs533891528 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887079 | TCAAGAGTCTAAAAC[G/T]TTCTTTTTACTTGAT | 9063 |
rs533936836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831410 | TCAGAAGACTCAATA[C/T]TCTTATGTCACCACA | 9063 |
rs533955613 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893594 | ACTATGAATGCGGAA[C/T]CACAGAATTCTGAAC | 9063 |
rs533959042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875094 | GGTCACCTTGTCATC[C/T]ATGTGACTCAAACTA | 9063 |
rs534152321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845303 | TGGTCTGAATTAACA[C/T]TGCAAATCCAGAGTT | 9063 |
rs534153393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866764 | TCCCCAACAGTTGTG[C/T]TTCCTGCTTTTTTCT | 9063 |
rs534190799 | snp | A/C/T | 0.000588898 | 0.0171496 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844822 | CTGCCGTACAAGATA[A/C/T]ACAGACATAGAGTAA | 9063 |
rs534214730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865965 | GGCTAAGGTCACCAA[A/T]GACCTCTTAACTGCC | 9063 |
rs534282142 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884559 | CTCGTGATCCGCCCA[C/T]CTCGGCCTCCCAAAA | 9063 |
rs534293589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851864 | ATCATACACATAAGG[A/C]CTTCTTCCAGGACAC | 9063 |
rs534297756 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834893 | TAGAAGGGAAAAATA[C/G]CTTACTCCTCCTGGG | 9063 |
rs534334316 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859302 | GCGTGGTGGTGGGTG[C/T]CTGTAGTCCCAGCTA | 9063 |
rs534340651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900836 | AAAATTAGCTGGGCC[C/T]GGTGGCAGGCGCCTA | 9063 |
rs534388461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46812837 | TTCTCTCTAAACTTG[A/T]GGAACTTGTTTGCTG | 9063 |
rs534402047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908604 | TACAATAATGGAAAA[C/T]ATCTTCGAGAACTCT | 9063 |
rs534402910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915021 | AGGATGTTACCAATC[A/T]TTTAATTTAGGAGCA | 9063 |
rs534410533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848759 | TATGGAAATGAAAGA[C/G]AGAGACAGTGTGTGT | 9063 |
rs534427353 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46812060 | AGTGATTACAATTTT[C/T]TTTTTAATTAGAAAA | 9063 |
rs534441155 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855914 | CATGCAAGGAAGCAG[A/C]CTAAGTTCGGAAAGA | 9063 |
rs534474096 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884437 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 9063 |
rs534513242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905113 | TAAAAATTATTAAAA[G/T]GGACCACATTTTTAA | 9063 |
rs534527024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821772 | ATGCTACCAAAAATA[C/T]AAATTAAACATATGT | 9063 |
rs534578395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842218 | GCAACAGAGAGAGAC[C/T]CTGTCTCAAAAAAAA | 9063 |
rs534631765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898169 | CAATATAATTTTTTT[C/T]TTTTGAGAGAGAGAA | 9063 |
rs534670187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826005 | TATGTGAGTCTGTTT[C/T]TTAAGAGTTCTTCCG | 9063 |
rs534680854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877059 | ACTTATGTCCTCAAT[A/C]CTTACTTCTCTTGCC | 9063 |
rs534682994 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909150 | CATGGGCAAAAGACA[C/T]GAATAGGAATGTGAG | 9063 |
rs534706880 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812207 | ATACAGTTATGGTTG[A/C]ATGTATCTGATGCTG | 9063 |
rs534743242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832818 | AATCACTTGAACCTG[G/T]GGGGTGGGGGCTGCA | 9063 |
rs534771414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864670 | AGCTACATGGGAGGC[A/G]GAGGCAGGAGAATCA | 9063 |
rs534776971 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840349 | TAACCCACGTTAAAC[A/G]TCACTTTATGCTCCT | 9063 |
rs534795082 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856843 | TCTAACTGGGCCAGT[C/T]TACTCACCGTTCCCA | 9063 |
rs534827223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904470 | AAAATAACCTAGAAG[A/G]CCGGGTGCGGTGGCT | 9063 |
rs534853504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818592 | CCAAAACTCTTCACA[A/G]TATGACTAACTACAT | 9063 |
rs534887460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911793 | GCTCATGCCTGTAAT[C/T]CCACCACTTTGGGAG | 9063 |
rs534913565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870703 | CAAATTGATCAATTC[C/T]TAGGGCCACAGCTGT | 9063 |
rs534931136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895777 | AAGCTAATGCCATAC[A/G]TAAGAGGAACTATGT | 9063 |
rs534996033 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918434 | CCAGGTCTTCCTTCC[A/T]CTCCCCTGCCCCCGC | 9063 |
rs535001317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854275 | GTGAGTACTGCTCAT[A/G]TATTAGTCCAGAGCC | 9063 |
rs535043238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903428 | TGTCATGGATTGGGA[C/T]ATACAGATGGCAAAT | 9063 |
rs535102152 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876687 | TCAGGAATAAATGAT[C/G]CCTTTACTAATTTTT | 9063 |
rs535119800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830038 | CACTCCCTTTGTCCT[A/G]TGTTTTAAATCTGTA | 9063 |
rs535146000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822028 | CTGTTACTGGTCTTA[C/T]GGTTGATGGTGGGAA | 9063 |
rs535164884 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884470 | GGTGCCCGCCACCAC[A/G]CCGGCTAATTTTTTG | 9063 |
rs535168309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883222 | GAAGGACTGTCCCTT[C/T]CTTATGATTTTTGAT | 9063 |
rs535171283 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921630 | ATAAAGTGAAAGATG[G/T]TAAATTTTTTGTATC | 9063 |
rs535360818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853588 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGCCCA | 9063 |
rs535371932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862239 | AAGAGGCTGAGGCAG[A/G]AGAATCGCCTGAAAC | 9063 |
rs535378463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843261 | TTCTGACACAATTTC[A/T]CCCCATTTAAAAAAC | 9063 |
rs535380907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822708 | TTCAAATAACATGAG[A/G]CCACCTCTCACACAC | 9063 |
rs535403642 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874344 | GCAGCCACCAGTAAT[A/G]TAGTTAAGGCATTAA | 9063 |
rs535451736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907675 | GTTTGAACTGTGCAG[G/T]TCCACTTATACGCAT | 9063 |
rs535463557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906997 | ATGCAGGAGGCACTA[C/G]AAAGGCAGTAAGGAC | 9063 |
rs535477571 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899218 | TAAAATGAACAAAAA[A/C]AAAGGAGGAAGGGAC | 9063 |
rs535526411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913841 | AGGGTCTCCCTCTGT[C/T]GCTCAGGCTGGAGTG | 9063 |
rs535530417 | snp | A/C/T | 0.00239401 | 0.0345304 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880584 | GGCAACACAGTGAGA[A/C/T]CCCCGTCTACTAAAA | 9063 |
rs535621336 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880856 | AGAAACACTTTACAA[A/C]TGCATCTATATAGCA | 9063 |
rs535634936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819872 | TTGTAATATGGCCTT[C/G]GTTGCAGAAGTCCTG | 9063 |
rs535636046 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913323 | TACAGAATTACTTAG[C/G/T]CTTCTTAGCATGAAA | 9063 |
rs535643189 | snp | A/C/T | 0.000445544 | 0.0149191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844026 | ATAAAAAGTCAAATT[A/C/T]CCCAAAATGTTTTGT | 9063 |
rs535756067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878698 | ACATGGCGAAACCCC[A/G]TCTCTAATAAAAATA | 9063 |
rs535773162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900080 | ACTAAAAATACAAAA[A/G]TTGGCTGGGCATGGT | 9063 |
rs535844735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851805 | GTACATGAAGTATAG[C/T]GGTCAACTGCCATGG | 9063 |
rs535880181 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46811148 | TTGGGGTAGCATGGA[C/T]TGAGACAGGAAGTGG | 9063 |
rs535919729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862297 | GATCATGCTACTGCA[C/T]TCACTCCAGCCTGGA | 9063 |
rs535949402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865305 | AGCACTCTGGGAGGC[C/T]GAGGCAGGTGGATTA | 9063 |
rs535975863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869480 | GAAATCTCTAATATA[A/T]GGAGGGACTGAGCCT | 9063 |
rs535988297 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908716 | ACTTCTACTCATCAA[A/G]AAACGCATAAGGCTG | 9063 |
rs536002256 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896450 | AAACAAGACAGCTTC[A/G]TGAATAAATTCCACC | 9063 |
rs536017879 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879349 | AAATCAAAACTATAA[C/T]GCAATGCCACCTCAC | 9063 |
rs536051034 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917428 | CCGCCACCACGGCCG[C/T]CGCCGCCTCCAGCAC | 9063 |
rs536103080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827508 | AATGATCCTGTAATA[C/T]AGGCGTTATTTAGCT | 9063 |
rs536193588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882508 | TTCATATTTTGACCC[A/C]ACAACTTCACATCCG | 9063 |
rs536213246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888408 | TCATTCTAAAATTCA[C/T]GTGGAATCTCAAGGG | 9063 |
rs536219517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839020 | CCTTTCAATTATAAA[A/G]TGAATAATTTTAATA | 9063 |
rs536225205 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862411 | ATTTTTGAAAAACTC[C/T]TACTATCATCTCAAA | 9063 |
rs536245380 | in-del | -/T | 0.0865458 | 0.189163 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853276 | ACAGACCTGAGAGCC[-/T]TTTTTTTTTTTTAAA | 9063 |
rs536255856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846331 | ATCACAACATGTGTA[C/T]ATTTAACCATTTCTC | 9063 |
rs536264940 | in-del | -/GGGTAG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863882 | TTAAATAAAGCCACA[-/GGGTAG]GTCCCCAATCCAATA | 9063 |
rs536268451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854351 | CAATAGTTGCGAAGA[C/G]TGTCAGCTCTGGTGA | 9063 |
rs536268897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887678 | AAATAAAATTAAATA[C/T]AAAAGGTTTATTTCT | 9063 |
rs536270183 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46895058 | AGCCTAGGCAACGAG[A/G]GGGAAACTCCATCTC | 9063 |
rs536392753 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867836 | AACCAACAGTGTACA[A/G]TTTAAGTGATGCTAT | 9063 |
rs536421021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868855 | GAGATGCGTCCCCCT[A/G]CCTCACTGTGGTGGC | 9063 |
rs536451236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916895 | ACTTCAGCTTTCAGA[A/G]AACAGTCCTCCACCA | 9063 |
rs536462562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900871 | CCCAGCTGCTCAGGA[A/G]GCTGAGGCAGAAGAA | 9063 |
rs536478394 | in-del | -/T | 0.242201 | 0.249878 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847483 | TAGTCATCAACCGTA[-/T]TTTTTTTTTTTTTTT | 9063 |
rs536500589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859352 | AGAATGGCGTGAACT[C/T]GGGAGTCAGAGCTTG | 9063 |
rs536513829 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915803 | TAACAAAAAAAAAAA[A/G]AAGAACTTAGAAAAC | 9063 |
rs536526887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831583 | GGAAGAGTCACACTA[C/T]CTGACTTCCAGCAAA | 9063 |
rs536534585 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825041 | TTGCTCACATAATTT[C/T]GGGGCTGTAAATTAG | 9063 |
rs536542079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867457 | TTAGCTAAATGGTTA[C/T]TTTAACATAACCATG | 9063 |
rs536555209 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822178 | CTGGAAAACTATTTC[A/G]TAACCTCAATTTAAA | 9063 |
rs536587141 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887661 | TCCCTGTGCCACTTT[A/G]GAAATAAAATTAAAT | 9063 |
rs536613093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878816 | GAGTTTGCAGTGAGC[A/G]GAGATCACACCACTG | 9063 |
rs536644919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834631 | TTGTTTTGTTTACTT[C/T]TGAAACAGAGTCTTT | 9063 |
rs536723605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885300 | GAAGTGGGCAGACCA[C/T]GAGGTCAGGAGTTCG | 9063 |
rs536738417 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842273 | AAAGGATATGTTATG[A/C]ATGCAAAAAAAAAAA | 9063 |
rs536743577 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845390 | ATCACGCAAATGAAC[A/C]AGGTATCAGCTTTCT | 9063 |
rs536787332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894447 | GTTGGTATCTTTAGT[C/T]TAATTTTTTCCAAGC | 9063 |
rs536788059 | snp | A/G | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919765 | TGTTTAATGAATAAA[A/G]GAATGAATGAACAAT | 9063 |
rs536835102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901428 | AAAAATTAAACTACA[A/C]ACCAATATTCGTCAT | 9063 |
rs536846131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909405 | GTGTGGGCCACTATG[A/C]CCAGCTAATTTTGTT | 9063 |
rs536898305 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855943 | GAGTTTTAATCAGCA[A/T]ATCTATTTGCTTAGA | 9063 |
rs536962361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866874 | CAGCAGGTATCTACA[C/T]CTGTAAAGTTGGGCA | 9063 |
rs536966415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813019 | GCTTAATAACATTTT[A/T]AAAAGTATTTGTTAG | 9063 |
rs536975234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908751 | CAGTTGCTCATGCCT[A/G]TAATCCCAGCACTTT | 9063 |
rs537000628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818616 | ACTACATAAAAATTA[C/T]GCATAAAAATAAAAC | 9063 |
rs537014741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835127 | AAGGGGCATGACATA[A/T]GTAACTCTCAAATGG | 9063 |
rs537015000 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885662 | GCACTCCAGCCTGGG[G/T]GACAGAGCGAGACTC | 9063 |
rs537025609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870766 | ATCCTCTTTTCAGGG[A/G]AAGAAAGAAGCATGA | 9063 |
rs537085580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826587 | AAATACATTTTGAAC[A/G]TAACCATTTCAAAAT | 9063 |
rs537128755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826029 | TCTTCCGTGTATTAA[C/T]GTGTATGTATGTCTA | 9063 |
rs537129856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891623 | ATATTTTAAAATATT[A/G]AAGCTAAAAAATCAC | 9063 |
rs537135662 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914703 | GAACTGCTCTGGTTA[C/T]ACTTGTCCAAAATGA | 9063 |
rs537199834 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898274 | TGCCTCAGCCTCCCA[A/G]ATACTTGGGATTACT | 9063 |
rs537237367 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829162 | CTAAGTTCACCTGTG[C/T]GTTTCAATTACTCCA | 9063 |
rs537258904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905790 | AAAGCAATTGAAGCA[A/T]TCCTCAAAGAAAACA | 9063 |
rs537260772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897549 | CTCCTTTAAAGGATG[C/T]TAAGGGAAAAATTCA | 9063 |
rs537271156 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817061 | TATTGGAACATTTTG[C/T]TCTGCTTCAAATGGT | 9063 |
rs537322908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889560 | TATAATGGCCACTAT[A/T]AAAAAAAAAGGAAAA | 9063 |
rs537351177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864723 | TGCAGTGAGCCAAGA[C/T]TGCACCATTGCACTC | 9063 |
rs537424337 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872935 | CTTAGCCCTTCCTTC[A/C]CTAGAAAAACCATTT | 9063 |
rs537462509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875431 | CCTTGTTGCTAATTA[C/T]AGATAATCCCCAAAC | 9063 |
rs537490645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813129 | CCTTTGTACATAAAC[A/G]TAAAATACTTGTGTC | 9063 |
rs537494491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817838 | CCATCAAAGTCTTCT[C/T]GCATTTTACATTTTA | 9063 |
rs537527192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833540 | GCCAAAAATGCCTAC[C/T]TCATAAGAGGTTTAT | 9063 |
rs537527294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822801 | TATACGTGAGTGCTG[G/T]GGAGGGGACTAAAGA | 9063 |
rs537528091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877694 | CCAATGGGGACACGA[C/T]ACAGAACCAGGGAAT | 9063 |
rs537590611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884438 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 9063 |
rs537600200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885380 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGGGTGCC | 9063 |
rs537656101 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897204 | ACTGTTAGTCTGTTT[A/G]AAGGTGAGGTAAAAA | 9063 |
rs537734393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836278 | ATTTAGAATTTAGTT[C/T]AGTAAGTTGTAGTGA | 9063 |
rs537739335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839929 | GCATTTTGGGAAGCC[A/G]AGGCGGGGGAATCAC | 9063 |
rs537774248 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847574 | GCAAGCTCCGCCTCT[C/T]GGGTTCACGCCAGTC | 9063 |
rs537788519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889091 | AAAATTAACTCAAAA[A/G]AGATCAGGCTTAAAT | 9063 |
rs537860203 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842446 | TCCTTAGGTAAGTTG[G/T]GTAGACTTTCTTCCT | 9063 |
rs537881655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831352 | TGAAAACTACAAAAC[A/T]CTGTTGAGACAAATA | 9063 |
rs537899096 | snp | A/G | | | missense, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812583 | TGTTAAGGGTGAGGT[A/G]AGACTATCCAAAAAC | 9063 |
rs537941444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874417 | ATTCAGATAATAGAA[C/T]CCACTTCGCTGCACG | 9063 |
rs537975825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907738 | ATGGTATTTGCAGGA[C/T]GTGAAACCCACATAT | 9063 |
rs538011248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830074 | CAACATAATAGTTAA[A/G]TAACTTACTGAGCAT | 9063 |
rs538048467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837285 | TGTTATTAAATTCTT[C/T]GGTCTCTGCCAATCT | 9063 |
rs538056574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913992 | GGAGGAGGAAGCAAG[A/G]CAGCAGTGACAGAAG | 9063 |
rs538076163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873206 | AGGAAGATGGCTCAC[C/T]GACTCAAGGATTTTA | 9063 |
rs538129428 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921157 | TTTTGGGACGGAGTC[C/T]CGCTCTGTTGCCCAG | 9063 |
rs538152392 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879401 | AAAAAAAAATAGTAA[C/T]AATAGTAAGTGCAGA | 9063 |
rs538182292 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893438 | CATCCTACCTAAGCT[G/T]GACTCTCAGAGGAAT | 9063 |
rs538199985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897447 | AAAATTTGAGCATCA[A/G]AAAGAATAATAACTG | 9063 |
rs538201800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889623 | AACCCTTGTGCACTG[C/T]TGAAGGGAATGTAAA | 9063 |
rs538215715 | snp | A/T | 0.000593374 | 0.0172144 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844157 | GAAAAAAAAAAATTT[A/T]AAAAAATTAAGGGTG | 9063 |
rs538253354 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899075 | CTCAACACTGAAAAG[A/G]TATCAATTGTTTCCA | 9063 |
rs538254491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850992 | TAGTTTTGAGTCTAC[C/T]ATAATCATTATTCTT | 9063 |
rs538263223 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896900 | ATTTCTATCCTTACA[A/G]TCATAAGATTGAGTA | 9063 |
rs538293174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870401 | CAGGTGGATCACAAC[A/G]TCAGGAGATTGAGAC | 9063 |
rs538397545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821664 | TCAGGATTTAAAATA[C/T]AATATCCAGAAATAA | 9063 |
rs538425154 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914451 | TATAGAGCTGCCATA[C/T]TCTGCTATGACCAGC | 9063 |
rs538443605 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921308 | AATTTTTGTACTTTT[A/G]GTAGAGATGGGGTTT | 9063 |
rs538484872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820724 | TCCTATTCTACTATA[A/T]TTCTTATCACCAGGA | 9063 |
rs538519397 | snp | C/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828463 | GGTCAGCAGTCGTTT[C/T]ACAGAAAGACACGCA | 9063 |
rs538528642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881821 | GAATACACAGACACC[A/G]GGCACGGTGGCTCAC | 9063 |
rs538532868 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827422 | GGTGAAAAGGGAAAG[A/C/G]AATCAATTTTTATTG | 9063 |
rs538536823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869702 | CTAAACATAATAAAA[A/T]ACAACAAATGACAAA | 9063 |
rs538593543 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855259 | CTGTTCACTGGTATT[C/T]AGCTGTCACTGTTGC | 9063 |
rs538623645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883108 | GTCTCAAAAGAAAAA[A/T]AAAAAAACAAAAAGA | 9063 |
rs538629777 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832313 | CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 9063 |
rs538641299 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870461 | TCTACTAAAAATACA[A/G]AAAAATTAGCCAGAC | 9063 |
rs538641424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904931 | AAATCGATAGAACTA[C/T]AAAGAAAAATGAAAA | 9063 |
rs538649377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848231 | TGCAAGTCACTGACA[A/C]CATTAACTGGATGTG | 9063 |
rs538667135 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834840 | GGCTGAGAAGTGGAC[A/G]ATGTTATGCCTGTTG | 9063 |
rs538682953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870289 | GCTTTGTAAATGCTC[C/T]CCCTTCACTAGCTCA | 9063 |
rs538694557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839736 | TGGGTGTGGTGGTGG[C/G]CACCTGTAATCCCAG | 9063 |
rs538733228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847098 | TAAAGATGCTGACAT[C/G]TTGCCACATTGGCTA | 9063 |
rs538757387 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808789 | TAAGAAAATAAAAAT[A/G]TTTACTAAAGAAAGA | 9063 |
rs538788094 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839814 | AGGTTGCAGTAAGCC[A/G]AGATCATACCACTGC | 9063 |
rs538825063 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903736 | CGAGAAAGATGTGTG[C/T]GTAAGTTTACCAAAA | 9063 |
rs538839094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910911 | AAGTTTATCACCAGC[A/G]TATCCTTCCAGAAAC | 9063 |
rs538915104 | in-del | -/CACA | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851069 | ATTGGGGTGAGTGTG[-/CACA]CACACAATTATGTGT | 9063 |
rs538962591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815500 | CATGATCAGTGATAT[C/T]TGAAGTGTTTAAAAC | 9063 |
rs539031751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819483 | TTTTCTATGGATACT[A/G]TAAAATGTCTATTCT | 9063 |
rs539075406 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46908147 | TTTATTATAAAAAAT[A/G]TTATCTTACACAGAG | 9063 |
rs539096585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836104 | TTTCCTGTGGGCTTT[A/G]TAAAATATAATCTTG | 9063 |
rs539103905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882632 | GCCTGATACATGCTA[C/T]ACACAAAAATACTTC | 9063 |
rs539106415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828547 | TATGTATTCTCGCAC[A/G]CATGTGGCACAGTTA | 9063 |
rs539112850 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890281 | CAGTGATGGCTGCAC[A/G]ACATTACCAACATAC | 9063 |
rs539133870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843904 | AATAATACAAAGAAT[C/T]GTGACTTAATCATGA | 9063 |
rs539140513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879504 | AACAGTTTAGTGGTT[C/T]CTCAAATAATTAAAA | 9063 |
rs539165833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888507 | CATATTACATAGCTA[C/T]GGTAATCAAAACTGT | 9063 |
rs539186864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895229 | GGGGAAGTGCTAATA[A/G]GGTTAGAAATCATGG | 9063 |
rs539205433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885723 | GGATTCCTGAAAAAC[A/G]TTGTTTTTAGTTCAA | 9063 |
rs539215960 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843176 | AAAATGAAGACAACT[A/C]CTCCACACAGGTTTG | 9063 |
rs539248158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46902460 | AGCTACTCGGGAGGT[C/T]GAGGTAGGAGAATTG | 9063 |
rs539268037 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877760 | GTTTGGTGTGCTCTC[A/G]CAGTGGCCAAAAGTG | 9063 |
rs539334590 | in-del | -/A | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921693 | TGATAAACACATAAC[-/A]AAAAAAAAAAAAGCA | 9063 |
rs539355223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860415 | TAAAGCCTAATGAGA[C/G]AAACCAGGGCTCCCT | 9063 |
rs539356224 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46811046 | GTAAAACCCAGTTTT[A/C]TCTGTGATTTAAAAT | 9063 |
rs539363680 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864586 | GACCAGCCTGACCAA[C/T]ATGGAGAAACCCCAT | 9063 |
rs539369020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901488 | TATTAGTCAATAAAA[A/T]TCAGCAATATATAAA | 9063 |
rs539372982 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818657 | TCACAAAAGAGCACA[-/T]TTAACAATAAAATCA | 9063 |
rs539384441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856586 | GCAACATGGAGTCTA[C/T]GGGGAAGCAGCACTT | 9063 |
rs539385991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880003 | AGGGTTCTCTGGAGA[C/T]AGATGGCAGCGATGG | 9063 |
rs539418579 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921452 | AAGATTTTAATACAC[A/G]AAGTCAAAAATCTCA | 9063 |
rs539442469 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810396 | CACACAAACCAAGTT[A/G]AGTTTTTTCTATCTG | 9063 |
rs539460269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913238 | CAGCACTTGAAGTTA[A/T]CAGGATGGTGACTCC | 9063 |
rs539498379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886470 | AACCAGATAAATCAA[C/T]TCTTTAAAAACAAGG | 9063 |
rs539581735 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892283 | TAAAATGCAAACAGA[C/T]TTAAATATGCCAAAG | 9063 |
rs539603530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826643 | TTAAATTACAGATGT[A/G]CCAACCAATTTGTCT | 9063 |
rs539604042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891714 | ATGAGAAAAAGACCT[C/T]TGAAGAGCAAGGAAA | 9063 |
rs539627708 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842101 | TGTGGTGGCGTGTGG[C/T]GGTAGTCCCTGCTAC | 9063 |
rs539666289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899079 | ACACTGAAAAGGTAT[C/G]AATTGTTTCCAAGTT | 9063 |
rs539690542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833672 | TATTATGACACTAGT[C/T]AAAAAAATTCTGAAA | 9063 |
rs539757406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906876 | AAGCCAGGAGGACTT[A/G]TGCTACTTCTGTCTC | 9063 |
rs539778492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898452 | CCCAGCAAGGCAATA[C/T]AAATTTTTTAAAAGT | 9063 |
rs539782995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890518 | ATCATTAATCAATAG[C/T]TGAAGGTCTCTCATT | 9063 |
rs539808741 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918369 | CTGTTTAATCAGCCT[C/T]CTACCTACCGCCTCT | 9063 |
rs539830024 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813120 | CATTGGACTCCTTTG[C/T]ACATAAACGTAAAAT | 9063 |
rs539855022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901682 | AACCAAATCATATGA[A/T]CAAATCAATCAATGC | 9063 |
rs539870868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864736 | GATTGCACCATTGCA[C/G]TCCAGCCTGGGCAAC | 9063 |
rs539896027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912681 | AAAAGTTAAGAAATA[C/T]TTTTTTTGAGTTGAA | 9063 |
rs539902718 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833745 | AATTAAAATAGTTTC[A/G]TATTGGCCCAGTAAT | 9063 |
rs539921496 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909657 | CACCTTTTTTGGAAG[A/T]TAATCTGACATTATC | 9063 |
rs539928253 | snp | A/C/T | 0.00239401 | 0.0345304 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878643 | GGAGGCCAAGGTGGG[A/C/T]GGATCACCTGAGGTC | 9063 |
rs539971783 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902187 | AAATTAAAATACATA[C/T]GTAAAAATGTAACAA | 9063 |
rs539980938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834264 | ACATTCAAAAAGGAA[A/G]AGACAAGACTTGATA | 9063 |
rs540009119 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870779 | GGGAAGAAAGAAGCA[C/T]GATCCAAAGGGTTGC | 9063 |
rs540047240 | snp | A/G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873215 | GCTCACCGACTCAAG[A/G/T]ATTTTAAAGTATGAT | 9063 |
rs540086979 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812345 | TACCAAATTATTAAA[A/G]AAAAAAAAAAAAGAA | 9063 |
rs540096452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46815004 | AACTGTATTTGTAAA[A/G]TTTTAACTTCTAGCC | 9063 |
rs540105084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822891 | AACAGGCAGGCTTTT[G/T]AAGACCAAATATATA | 9063 |
rs540123871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841377 | TCACTTCTTATTTAA[C/G]TGCCTGGGATTTATT | 9063 |
rs540139026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874432 | CCCACTTCGCTGCAC[A/G]TCATTAAAAAGCTAG | 9063 |
rs540143171 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830208 | ACAAACATCAGCAGA[A/T]AAAGGTTACTATATA | 9063 |
rs540154041 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921960 | TTTTCCAAGCCACTT[C/T]ACTTCTTTTGCTAAG | 9063 |
rs540207754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880956 | AAAGTTTTTCTAATT[C/T]AATCAGATTTAAATA | 9063 |
rs540228039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894798 | TCATTAGGCTGGGCG[C/T]GGTGGCTCATACCTG | 9063 |
rs540252458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886749 | GGCTGAGAGAGGAGA[A/T]CTGCTTGAACCCGGG | 9063 |
rs540279105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852219 | TGTGGATCAAGTGGT[A/G]GTTTAAGATGTTTTC | 9063 |
rs540293346 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900926 | TTGCGGTGAGCCGAC[A/G]TCGTGCCATTGTACT | 9063 |
rs540404266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851054 | GGAGGTGCCTCTTCA[A/T]ATTGGGGTGAGTGTG | 9063 |
rs540427327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892015 | GCTGACCAAAGCCCT[A/G]TCAGAAACCTACCCA | 9063 |
rs540505988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822198 | CTCAATTTAAATGTC[A/G]AACCACTTAAATATG | 9063 |
rs540506465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829199 | CTCAGTTTCCCTACT[C/T]AGTGTGGATGGATGC | 9063 |
rs540517169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866584 | ATGAAAATCATACAG[C/T]AAATAAGCATAAATG | 9063 |
rs540531934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865507 | ATCACACCAGTGCAC[C/T]ACAGCGATAGTCTTC | 9063 |
rs540567221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873883 | CTCCCTCCTTGCCTT[C/T]CTCCCCCTACCGCCA | 9063 |
rs540584142 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921212 | GGCTCACTGCAACCT[C/G]TGCCCCCCCGAATTT | 9063 |
rs540594932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829566 | AGATGGTATAAACTT[C/T]AGCACATTCCTTCAG | 9063 |
rs540607552 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919000 | GTGTGTGCGTGTATA[C/T]ATATATATGTGTGTG | 9063 |
rs540614201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856990 | TACATCTGTTAAAGA[C/T]GGAAAATTACTGCAC | 9063 |
rs540618983 | in-del | -/A/AA | 0.0292345 | 0.117314 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864257 | TTTGAACTGGGAAGA[-/A/AA]AAAAAAAAAAGAAAG | 9063 |
rs540639616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836596 | GTCAGTTGTAAAAGT[C/T]GGAAGATGTCATACA | 9063 |
rs540649863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884162 | AAGATATGGTAATGT[C/T]CCTTTTTCAGAAAGT | 9063 |
rs540720582 | snp | C/T | | | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894811 | CGCGGTGGCTCATAC[C/T]TGTAATCCCAGCACT | 9063 |
rs540726525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844245 | ATGTATTGACAACAC[A/G]ATCACACTCCCAATA | 9063 |
rs540762504 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883502 | GACCTCAGGAGTTCA[A/G]GACCAGCCTGGACAA | 9063 |
rs540762793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889671 | AACAGTATGGTGATG[C/T]CTCAAAATACTAAAA | 9063 |
rs540808195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836143 | AAACATTGCCCTCAA[C/T]GCAAATCATATTATA | 9063 |
rs540841473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850486 | TGCTTCCTCGAAGTA[C/T]AAGGTTTGTTGCTCT | 9063 |
rs540884030 | in-del | -/CTGCT | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877395 | CTTCTTCTAAGCTAC[-/CTGCT]CTGTAAACAACTTCT | 9063 |
rs540984148 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910012 | TAATACAAAAAAATT[A/T]GCCGGGCATGGTGCA | 9063 |
rs540997816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869810 | ATTGAATTTGTCAAC[A/T]TCTAATAGAGTATGT | 9063 |
rs541005956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861902 | AGTCTGTAGTTAATA[A/G]TACTGTACCAATGTT | 9063 |
rs541030676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833173 | AAAAAACCCATCAAC[A/G]CATGAAATGACAAAC | 9063 |
rs541115818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816212 | TGGCATTCAGAGACA[A/C]CCCGAATATAACCAC | 9063 |
rs541116645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832660 | CTTTGGGAGGCTGAG[A/G]TGGGTGGATCACCTG | 9063 |
rs541118916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840851 | CTTTTTTCCTATAAA[A/G]TGTTAAGCTGGCATT | 9063 |
rs541167229 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832712 | CCTGGCCACTATGGC[A/G]AAACCCCATCTCTAC | 9063 |
rs541234031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839218 | ACTATACCTATTCAA[A/C]AAAATGCCCACAATG | 9063 |
rs541360951 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808151 | TGGAATAATGCCTGT[A/G]GGTTGCGGGGAAAAA | 9063 |
rs541378291 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816884 | TTCTCTATTAAAATG[A/G]TAATAGGTGAGATAT | 9063 |
rs541389323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845679 | AATATATTCATTCAA[C/T]TGATTCTACAATAAA | 9063 |
rs541398994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902910 | CCAGAAACAGACATA[C/T]ACATACATACCCAAA | 9063 |
rs541400522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857800 | TCTGACATTCATTTC[C/T]GCCAATCACTGTTCT | 9063 |
rs541407874 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848318 | AACAGCCAGGATTCA[C/T]GCTTCTTTCTCAAAA | 9063 |
rs541454405 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899803 | TTTTTCACAGAAAAC[A/T]AATGTGGGGAGGGAG | 9063 |
rs541494024 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917093 | ACTGGCAGCACTCAG[A/G]AGCCGGCTCGCCGCG | 9063 |
rs541550595 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907691 | TCCACTTATACGCAT[-/A]TTTTTTTTTCAACCA | 9063 |
rs541553974 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879475 | GAATGTAAAATGGTG[C/T]AGCTGCTGTGGAAAA | 9063 |
rs541578603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823947 | AAATGTAAATGGCTA[A/T]GGATGGTGAAATGAT | 9063 |
rs541585620 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820375 | AGTATATAGGGTTCT[G/T]TAATATCTGTGGTTT | 9063 |
rs541621989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871887 | ACATGTCAGTCCAAA[C/T]GGATTTCTCACCTCA | 9063 |
rs541628853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835305 | GTTACATGGGAGGTT[C/T]TTTGTGCTAGTGTTC | 9063 |
rs541634138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882087 | GGGTGACAGAACAAG[A/G]CTTTGTCTCGGTGGC | 9063 |
rs541663072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888665 | GTTCCACCTCAGATC[A/G]TCAGGCATTAGATTC | 9063 |
rs541705303 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920695 | GGAATGGCTGAGTGG[C/T]AAAGGGTAGAAAGGG | 9063 |
rs541839751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907959 | TTAGGATAGTAGGTC[A/G]CTTTTGGAAGAATGA | 9063 |
rs541850000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907185 | AAACATAACCAGCAA[A/G]AGATGGTTTCCAAGA | 9063 |
rs541852053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914592 | CCCGACACACAAGTC[C/T]GAAAAGCAAAGGCAC | 9063 |
rs541871158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841940 | CTTTCACTATTATTG[A/C]AAGTTTGGCTAGGTG | 9063 |
rs541884295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821223 | CACTCCACTCTACTC[C/T]CCTCTCCCATAATAG | 9063 |
rs541891727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905914 | TTTTTAACTATAGGC[C/T]AGTTTTACTCATTAT | 9063 |
rs541909846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848985 | AAACTTTTGTTTTGC[C/T]TGTTTTGGGCCTGGA | 9063 |
rs541913402 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914195 | TATAACACATTATTG[C/T]AACCATCTTTGAGCA | 9063 |
rs541969727 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46809975 | ACCACATTAAAGGCT[A/G]ACGGATTAATAATCA | 9063 |
rs541999996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847982 | ATGTCAGTGATGTAA[A/T]TTAATTATGTACTAT | 9063 |
rs542012295 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905497 | AGAGCAAAAATTAAT[A/G]AAACAGGAAGGATAC | 9063 |
rs542018236 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895315 | GGAGAAGACGAGAAG[C/T]TGCTGAGGGCAACTG | 9063 |
rs542057505 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809361 | AGTGAGTGAGTGACA[A/G]CAGACCTCAGGCACG | 9063 |
rs542068687 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878956 | CTAACATAGGGAAAA[G/T]ATAAACCAAGAGGTT | 9063 |
rs542068848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885799 | TCTAACTGAAGCTAC[A/G]ACCAAAATGCAGGGA | 9063 |
rs542137645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842579 | ACTAGGGATACATAA[C/T]AAAAAATCGTCAATA | 9063 |
rs542179303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885423 | TACTTGGGAGGCTGA[A/G]GCAAGGAGAATTGCT | 9063 |
rs542203194 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891362 | AGTTATTTGCTTTAT[A/C/G]ACTATAAAATCTATC | 9063 |
rs542211997 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873904 | CCTACCGCCATTCCC[A/G]TCTTCTCCCCCGCTG | 9063 |
rs542215355 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898612 | CTGAAAAAGAGTATT[A/T]AAAAAACCGAAGTAA | 9063 |
rs542224902 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890006 | ATTGTATTATTTAGC[C/T]TTTAAAAGGAAAGAA | 9063 |
rs542249955 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876059 | AGTTTAAGCCATTCC[A/G]AGAGCTGACCTATCA | 9063 |
rs542274042 | snp | A/G | 0.000380062 | 0.0137799 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846828 | ATCCCATTTTTAGGC[A/G]GTGGTGCATAGCCCT | 9063 |
rs542406059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901704 | AATCAATGCGAAAAA[C/T]GCATTTCACAAATTC | 9063 |
rs542413847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864399 | GAAGTACTAAACTGC[A/G]TTCATCTTGGAATCA | 9063 |
rs542477735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909055 | AGCCCAATTGAAAGG[A/G]GAAATTTGCACCACA | 9063 |
rs542478203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919768 | TTAATGAATAAAGGA[A/T]TGAATGAACAATGTC | 9063 |
rs542494541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870939 | GGAAATGGTAATAAA[A/G]GGAATTCAGGAATCA | 9063 |
rs542505739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863504 | GGGTTTCACCATGTT[G/T]CCCAGGCTGGTCTGA | 9063 |
rs542523592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916197 | GCAGAGGATACGTTC[C/T]TTTGCTCACGTCCAC | 9063 |
rs542557866 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919703 | AATTGTAAACCCACT[A/G]GACTATAATGGCTGA | 9063 |
rs542591380 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917752 | AGGCGTTATCCGCGG[C/G]CCTGGCCTCGGGAAG | 9063 |
rs542616473 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863188 | TACCCATAACTACCT[C/T]AGTTTATGTTCTTAT | 9063 |
rs542620617 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889219 | ATAGGCAACAACAAC[-/A]AAAAAATAAACAAAT | 9063 |
rs542660243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845887 | CAATGTCTGTAAAGT[C/T]ACTCCCAGCTCTGCA | 9063 |
rs542694297 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908983 | CACTGCACTCCAGCC[A/C]GGGCTACAGAGTGAG | 9063 |
rs542696094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853709 | CTGGAGAACTGCCTG[A/C]ACCCAGGAGGCAGAG | 9063 |
rs542742751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837617 | AAATTTGTTTTTATA[C/T]AATCAACTGTGTCAA | 9063 |
rs542753809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887109 | TCCAATAATTCTACT[C/T]ATAGGACTTTGTACA | 9063 |
rs542764325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886794 | AGTGAGCCGAGACAG[C/T]GCCACCGCCCTCCAT | 9063 |
rs542778664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882298 | ATGTTCAAGAATTTA[A/T]GGATAAAAAGAGATT | 9063 |
rs542779775 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844922 | CTTATTTAAGAAACT[C/G]TGGTTTCTAAAAATA | 9063 |
rs542782342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853142 | ATGAGCCAGCCATAG[C/T]GGTGCATGCCTGTAG | 9063 |
rs542786186 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832995 | TAAAATAGTACAACC[A/G]CTTTGGAAAACAGTT | 9063 |
rs542862433 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896567 | ACAAATATAGAAAAA[C/T]GCTGAACACAAAACA | 9063 |
rs542887232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813714 | ACAGTCCCAGGTTTA[A/G]GTTGCCAGCCAGAGG | 9063 |
rs542919117 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823620 | GCAACACCAAAAGGT[A/T]GACTGTCAAAACATG | 9063 |
rs542942665 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888574 | ATAAATCAACAGTCA[C/T]AACCTTTTTGGCCAG | 9063 |
rs542971254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874573 | TTAGAGACTCGACTA[C/T]CATGGACCAAATGCC | 9063 |
rs542985650 | snp | G/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826913 | TTTATATAAAATGTC[G/T]AAACAGGCATTATAG | 9063 |
rs543011024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823048 | TTGAGACCAGACTAC[A/G]GAACATAGGGAGACC | 9063 |
rs543027015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912890 | AAAAATATGAGAAAT[A/G]GAAATGAGAGAATAA | 9063 |
rs543049685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830311 | AATAAAAGAAGTCTC[A/C]ATAAATTTAAAATAA | 9063 |
rs543089360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877992 | TTATCAATTCCAAGT[A/C]TTCAGATTCATTTAT | 9063 |
rs543100270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919875 | GTAGACCTTGATTTA[C/T]ACCTCAGTAGAATTT | 9063 |
rs543132880 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836686 | ATATATTTTTATTCA[C/T]TGACTGCCCTATGAT | 9063 |
rs543135467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829665 | AAACGTATAGTTCTA[A/G]GGGCCAAGATTAATG | 9063 |
rs543152121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877510 | ACTGCCCCTCCCGCC[A/G]AAACAGCTCTTCCCA | 9063 |
rs543217727 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825008 | TGTCTCAAAAAATTA[-/A]AAAAAAAAAAAAAAT | 9063 |
rs543223390 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892819 | AACATAGTTATTTAA[C/T]CCAATATATCAAAAC | 9063 |
rs543270361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889778 | GATACGTGTATACCC[A/G]TGTCCACAGAATTAT | 9063 |
rs543306709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856570 | TCCAAACTCTTGCCA[C/T]GCAACATGGAGTCTA | 9063 |
rs543348148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847879 | ATTTTTCAGAGCCAA[A/T]ATAATATATTTTTTA | 9063 |
rs543406071 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886114 | GCATCTTCACTTAGT[-/C]CCCCCCCAGTCTTCT | 9063 |
rs543409258 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866145 | AAATGAGACATTAAA[A/G]AAGAAAACTACTTGC | 9063 |
rs543410308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914970 | TATTCCGTTTTTTAG[G/T]CTGTTTTTCTTCCTT | 9063 |
rs543446927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826940 | ATAGACACAAAAAAA[C/T]GATTGCCTAGATTTG | 9063 |
rs543446981 | in-del | -/T | 0.480144 | 0.097642 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888363 | CTCTCAAAATCCCAA[-/T]TTTTTTTTTTTTATC | 9063 |
rs543495903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833942 | ATCACCTATTCCCTA[C/T]TGTAAAGTTCCTTCC | 9063 |
rs543512994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862486 | TTACTCAATTCCTTG[C/T]TCTGCTTTTAACATT | 9063 |
rs543531073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816997 | TAGCCCTTGTAATAC[C/T]TTCAGAGTTTTGCAT | 9063 |
rs543541112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884682 | GCACTTTGTGAGGCC[A/G]AGGCAGGCAGATCAC | 9063 |
rs543542815 | in-del | -/ACACACATATATATACAC | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862667 | TATACACATATATAT[-/ACACACATATATATACAC]ACACACATATATATA | 9063 |
rs543579028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825144 | ATGATAAACTTACAC[A/G]GCACAGGAAAACCAT | 9063 |
rs543615841 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824600 | GGACTGCCATCAAAA[C/T]GGCAATGATTCTCTC | 9063 |
rs543631087 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917772 | GCCTCGGGAAGTGGC[A/G]GGGAGGAAGAAGAGG | 9063 |
rs543657322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879176 | TGCACTAAAATAAAA[G/T]GGAGTAGGGTAGGAG | 9063 |
rs543753979 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809107 | TTACCTTTCTTCAAA[C/T]TCCTCAAGACTAAGG | 9063 |
rs543778523 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896397 | TCAAGAAGAGGTATA[C/T]TGTCTTGCCCTCCCT | 9063 |
rs543786934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896379 | CAAATTACTCCATCT[A/G]ATTCAAGAAGAGGTA | 9063 |
rs543818812 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839172 | TCACTGTGTGGAAAC[A/G]ACTCAATCACTAAAC | 9063 |
rs543824365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863064 | TCCTTTTCTTTCTTC[C/T]TACATCTCTTAGTTC | 9063 |
rs543841807 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873018 | AACATGGGGGCCACT[-/G]ACAACCTGTGGCCTT | 9063 |
rs543866295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908792 | GGTGGGCAGATCACC[C/T]GAGGTCAGGAGTTCG | 9063 |
rs543884339 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812261 | ATCCTTGCATGTCAT[C/T]TGGTTCTTGTTGCAG | 9063 |
rs543886921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859700 | GAATAAAAGAACAAA[A/C]GATAAGCAGGTTTGA | 9063 |
rs543901302 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911375 | TGCCCACCACCACGT[A/C/T]GGGCTAATTTTTGCA | 9063 |
rs543959523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869233 | AAGGACAAAGCAAAA[A/G]GAGAGTAAAAAAGAC | 9063 |
rs543960601 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822104 | CCTTTCCTGTTATTG[C/T]TGATTATTAAATATC | 9063 |
rs543991392 | snp | C/G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877049 | AATGGAAAGGACTTA[C/G/T]GTCCTCAATCCTTAC | 9063 |
rs543995449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876789 | GCAAGCTCTGCCTCC[C/T]GGGTTCACACCATTC | 9063 |
rs544003680 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863299 | TCTTTGGGCTACTAT[-/A]AATTCTTTTTATATT | 9063 |
rs544033590 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917148 | GCCCGCGTGCCCTCC[C/G]CCGGCCCGCTCCCCT | 9063 |
rs544053229 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921257 | CTCAGCCTCCCAAGT[A/G]GCTGGGATTACAGGC | 9063 |
rs544106992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883374 | GATGCATATAAACAG[C/T]GAACAAAGAGTCACA | 9063 |
rs544124106 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829416 | TACAGATACTCTAAG[A/T]ACAATTCTGAAAAAC | 9063 |
rs544216476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900922 | GAGGTTGCGGTGAGC[C/T]GACGTCGTGCCATTG | 9063 |
rs544228882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900690 | GAAAAAAATACAAAA[C/T]AGAGGCTGGGCACAG | 9063 |
rs544255141 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873094 | TGTTCAATTTATCAC[A/G]GCTACCGCCTTGTTA | 9063 |
rs544297839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885504 | CCAGCCCTGGTGACA[A/G]TGCAAGACTCCATCT | 9063 |
rs544370391 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914737 | GCCTTGAAGGGTAAT[A/G/T]GAAATCCTCTCTGTG | 9063 |
rs544377886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842672 | ATTTTAACATGAGAG[C/T]GAAGAAAAGTATAAT | 9063 |
rs544387407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873840 | AGCCAAACAAGCTGC[C/T]GTTTCCTCTGAAACG | 9063 |
rs544478861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828771 | CCACAAAGACAGTCT[A/C]ACATACCATATTTGT | 9063 |
rs544497694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880241 | TCTCTACAAAAAAAA[A/T]GTAAAAATTAGCTGG | 9063 |
rs544500607 | snp | G/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920509 | TACTGGCCAGTTTTC[G/T]TGAGCCAATGCCTTT | 9063 |
rs544551970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885923 | TAGTAAATTTATAAA[C/G]AGCATACTATTTAAC | 9063 |
rs544557973 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46809994 | GATTAATAATCATGA[C/T]GTTGCCATAAGGCCA | 9063 |
rs544560794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879645 | TCACAATAGCTAAAA[C/T]GTGGAAGCAATCCAA | 9063 |
rs544607479 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891995 | AAAGAGGAAGAACAC[C/T]TGGAGCTGACCAAAG | 9063 |
rs544653657 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868405 | CTCCCCCTCTTGCTG[A/C]GACAGCTCTCCCTGC | 9063 |
rs544731104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896001 | TATTAAGAGAAACAA[C/T]AAAAAAAATGCTACA | 9063 |
rs544755104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849685 | ATTTTCTAATTACCA[A/C]TACTACTTGAATACT | 9063 |
rs544767325 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830760 | AAAAACTTTGCCACA[A/G]AGAAAATCCTAGGCC | 9063 |
rs544772751 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829326 | GAGCAACTAACCTGT[C/G]ACCATCCCCAAACCA | 9063 |
rs544813323 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856932 | ACAGTCCCAAGCTGC[A/G]CAACATTGTGCAAAT | 9063 |
rs544833656 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810589 | GGGTTTGTTTCCCCC[C/G]CAACATCTTTAAAAT | 9063 |
rs544881119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856244 | CTGACCTCGTGATCC[A/G]TCCGCCTTGGCCTCC | 9063 |
rs544895766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853808 | GGGGATGGGAGGGGA[A/G]TGGGAAAAAAAGGAT | 9063 |
rs544906556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868931 | CTGGACTCTCAGCAA[C/T]GCAGGTGAAAAGGAT | 9063 |
rs544909789 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863311 | TATAAATTCTTTTTA[A/T]ATTGCTTTACCCAAT | 9063 |
rs544933875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861678 | GGTAAAACATCAGCC[A/G]TACCCCCAAATCAGA | 9063 |
rs544949333 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897877 | AATATAATTTTTGGG[-/T]TTTTTTTTTTTTGAG | 9063 |
rs544992734 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833718 | AATACTACCACATAA[C/T]AGAAATCTAATAATT | 9063 |
rs545001648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832233 | CAGCCTGACCAACAT[A/G]GTGAAACCCTGTCTC | 9063 |
rs545009963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882999 | GGGGAGGCTGCGGCA[A/G]GAAAAAAAAAATCGC | 9063 |
rs545034868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839965 | CAAAAGCTCGAGACC[A/G]GCCTGACCAACATGG | 9063 |
rs545061490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916980 | GTGCAAGATCAAACG[C/T]TGCTTCCCACATCGG | 9063 |
rs545123282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888839 | CTGCTCACCTCCCGC[A/T]GTGCGACCTGGTTTC | 9063 |
rs545124358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847790 | CCCGGCCAACTGTTC[A/G]TTTTAAATAGCAAGT | 9063 |
rs545140541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874615 | TTACTGAGGGTCTGA[A/G]CTACCCCTCGGAAAG | 9063 |
rs545157074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846913 | TTCTCCAAGATAGAT[A/G]CAGGATCCTGCCCAA | 9063 |
rs545207808 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827752 | ATAAATACCTCACAC[A/C/G]CTCACTTTCCAAAGA | 9063 |
rs545214973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881914 | CCAGCCTGGCCGACA[C/T]GGTGAAACCCTGTCT | 9063 |
rs545278505 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862638 | ACATATATACATACA[C/T]ATATATACACATATA | 9063 |
rs545295796 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844948 | AAATAACATTCAAAA[A/T]AACTTCCATGGAATG | 9063 |
rs545332406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860769 | ATCACTTGAGCACAG[C/G]TGTCTGAGACTAGCC | 9063 |
rs545363555 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864975 | TTACACAAAACACTC[A/T]TATAAGAAAATTTTG | 9063 |
rs545433235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916273 | GGAAAACAATAAATA[C/T]ACAAAACTGAACCTT | 9063 |
rs545439487 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821138 | GGAGAGAAGAGCTGC[A/T]CCACTGGGCATTCTC | 9063 |
rs545475164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871825 | ATCCCTGAGGCAGGA[A/G]CTAACCTATTAGGAA | 9063 |
rs545536598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881207 | CAAAATGCTCACCAA[C/T]GTCCTATCTCTGAAC | 9063 |
rs545557050 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859386 | TGAGCCAAGATCACG[C/T]CACTGCACTCCAGCC | 9063 |
rs545599906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887174 | TTATTTCAAAGTGAA[C/T]GTAATAAAGAGATAA | 9063 |
rs545653626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826997 | AGAACATGAAGAAAG[C/T]TTTTTGGGTGTTGAA | 9063 |
rs545690435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834008 | ACCTTCACAGCACTT[C/T]ACACTTAATATACTT | 9063 |
rs545690925 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896365 | TTCCTAGAAAAATAC[-/A]AATTACTCCATCTGA | 9063 |
rs545741900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816604 | AGCAGGAGCTACAGG[A/T]GTGTGTCACTATGCC | 9063 |
rs545813598 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848505 | ATGCTAAAATATGCA[A/C]CTTAGGACCAATGAA | 9063 |
rs545825971 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809846 | CTGGTTGGCTGACAG[A/G]ATCTAGGTGACAGCT | 9063 |
rs545862229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913505 | TCTGAGACACACACA[C/G]AATAAATTCTCAATG | 9063 |
rs545913897 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809268 | TTCATTTTGCCTTTA[C/T]AATTACCTTAGGACA | 9063 |
rs545949565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818060 | CTAAAAAGCAGGTAG[A/T]GTTAACATTATTTTA | 9063 |
rs545953888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904763 | CCGTCTCAAAAAAAA[A/G]AAAAAAACAGAGATG | 9063 |
rs546015416 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873463 | GGAGTAATGGGTATT[C/T]GGTGGTTGATGGAGA | 9063 |
rs546042497 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891260 | GGTGTTAATTATATT[C/T]TGTTGTACAAGATCT | 9063 |
rs546155492 | snp | A/G | 6.59576e-05 | 0.00574234 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890771 | GAAGTGGAAGGCAAC[A/G]AGTGGATTCCAGCCA | 9063 |
rs546162649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825411 | AGTCCACTGGACCTA[A/C]ATCTGGTAATAAAGA | 9063 |
rs546181776 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871659 | GATTCAAGAGCAGCT[C/T]GTTCCTGTTTGTTTC | 9063 |
rs546182019 | snp | C/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920742 | GTTGTGATCATTTCT[C/G]CTCTGGTCTAGATTT | 9063 |
rs546200132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856068 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 9063 |
rs546205510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837098 | ATGAATATTTCTAAG[A/C]TTTTTATATTTATAA | 9063 |
rs546245070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836116 | TTTATAAAATATAAT[A/C]TTGGAAAGCAAAAAC | 9063 |
rs546278237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864302 | ACAAATCCAACACTA[C/T]AACCACCTGCAATAA | 9063 |
rs546317029 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900286 | GAGAATCGCTTAAAC[C/T]CAGGAGGCAGAGGTT | 9063 |
rs546359315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862569 | AATCTTTTAAGAATG[A/C]AACTTTAAAGAGTCA | 9063 |
rs546418120 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851333 | GAAATATTCTTGTCA[A/C]CCCTTCTTCCTTTCT | 9063 |
rs546459119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832994 | ATAAAATAGTACAAC[C/T]GCTTTGGAAAACAGT | 9063 |
rs546476695 | in-del | -/A | 0.036205 | 0.129583 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864257 | CTTTGAACTGGGAAG[-/A]AAAAAAAAAAGAAAG | 9063 |
rs546500982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870046 | GCAGGTGCACAGGAC[C/T]CCCTTCACTCAATTC | 9063 |
rs546501118 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890208 | GAGAGGAAGGCTATT[C/G]TTTAATGGGTACAGA | 9063 |
rs546522209 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908277 | ACCTCACCAGGCAAG[A/C]AGTTTGTTTATGCTA | 9063 |
rs546562496 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869093 | AAGCACAAAGCAAGC[A/G]TGGAGTCTGGATCTG | 9063 |
rs546575623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880561 | AATAACCACTGCACT[C/T]CAGCCTGGGCAACAC | 9063 |
rs546617726 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887288 | AATAGCCACATTGCC[C/T]GCCACTAGTCAGGCC | 9063 |
rs546621218 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913789 | TCCTGCTCTCCTCCA[A/T]CCCTGTGCTTAGCTC | 9063 |
rs546629765 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886843 | ACTCTGTCCCCCCCC[A/T]CCAAAAAAAAACAAA | 9063 |
rs546645859 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921080 | AGAAGATTCATTATA[A/G]GTACTGTGATTAAAG | 9063 |
rs546689216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893294 | AAAAAGGCAATCACA[C/T]AGATAAAACATAACT | 9063 |
rs546697759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879780 | ACCTTGAGGACATTA[C/T]GTTTAGTGAAATAAG | 9063 |
rs546721429 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869144 | ATGGCTTATGGCAGA[C/T]TCCTGTTGTGGGGCT | 9063 |
rs546796828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859124 | TTTTAAATATTCAGA[A/G]TGACATAAAAGAATC | 9063 |
rs546830397 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907572 | GACCTTTGAATAACA[A/G]TAACATATAGTTGAA | 9063 |
rs546838643 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858025 | GACACATTAAAGCAA[A/T]TCTGGAAAGGCATCA | 9063 |
rs546859794 | snp | C/T | 0.00074129 | 0.0192379 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46891025 | TAGTAATACTTGTAG[C/T]TCAGAAACCCTAAAA | 9063 |
rs546932953 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849934 | CATGCCATTTAACCC[A/T]GATATTTAACATGCA | 9063 |
rs546953730 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807892 | AGCTGCAGTATAAAT[C/T]AACATACCCATGTGG | 9063 |
rs546962574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865754 | ATGGTTCATATTTTT[C/T]CAGAACGCTTTAAAA | 9063 |
rs546974991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865291 | ACACGTGTAATCCCA[C/G]CACTCTGGGAGGCCG | 9063 |
rs547002273 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919007 | CGTGTATATATATAT[A/G]TGTGTGTGTGTGTGT | 9063 |
rs547044257 | snp | C/T | 0.000139169 | 0.00834058 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917386 | CCGCTGCCGCCGCAC[C/T]CACTCCCGCTGCCGC | 9063 |
rs547060443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828216 | AGTATATTCAGTATA[C/G]TATGTTCCTGACAAC | 9063 |
rs547080190 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816638 | CTAATTATTATTATT[A/T]TTTTTTTTTTGTAGA | 9063 |
rs547100773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869450 | CTCAGCAAGCCTCTA[A/G]AGAAGGGAAGGCAAG | 9063 |
rs547107342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879222 | TCAACAGCTAAAAAC[A/C]ACTCAATTCAAAAAT | 9063 |
rs547124718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821218 | CACAGCACTCCACTC[C/T]ACTCTCCTCTCCCAT | 9063 |
rs547163981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824852 | TACAAAAAAAAAAAA[A/C]ACACAAAAAAATTAG | 9063 |
rs547200057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888867 | TTCTAACAGGCTGTG[G/T]ACTGGTGCTAGTCCA | 9063 |
rs547213333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876254 | TAACAAGAGATAGCC[C/T]TCATGGGTCCTTTGA | 9063 |
rs547269372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842186 | AGCTGTGTTCATGCT[A/G]CTGCATTCCAGCATG | 9063 |
rs547314206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849101 | CTCATGAACTAAAAT[A/G]TGCACTCTGGAAATT | 9063 |
rs547331145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870185 | AGTGTAAAAAGGATA[C/T]TCAGAACTCCTTTTC | 9063 |
rs547335096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817291 | TGTACTGAAGCCAAG[A/C]CACTCAAAAATGCTC | 9063 |
rs547357771 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904747 | CACAGCAAGACTCCA[C/T]CCGTCTCAAAAAAAA | 9063 |
rs547369497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825536 | AAGATCCACTCATCC[A/G]TCTTGCTCCAGATTC | 9063 |
rs547404700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862246 | TGAGGCAGGAGAATC[A/G]CCTGAAACCGGGAGG | 9063 |
rs547417390 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846229 | TAGAGAAAATATTAT[A/G]ATTCTAAGTAAATAT | 9063 |
rs547451361 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853289 | CCTTTTTTTTTTTTT[A/T]AATAAAAAAAAAAAG | 9063 |
rs547451971 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860968 | GGGCAACAGAGCAAG[A/T]CCTTCTCTCAAAAAT | 9063 |
rs547459141 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46895005 | TTGAAACCGGGAGGC[A/G]GAGGATGCAGTGAGT | 9063 |
rs547478400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902219 | CACGTACAGGACTTA[C/T]ATGCTGAAAGCTACA | 9063 |
rs547488902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860102 | ACCACTACAGGCAAA[C/G]GGGAGGGAGCTAGAA | 9063 |
rs547526190 | in-del | -/A | 0.361263 | 0.223876 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880090 | GTATTTTACCACAGT[-/A]AAAAAAAAAAAAAAA | 9063 |
rs547551476 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850720 | ACCATGAAGTTCCCC[A/G]TCAAGCTTCGGCATC | 9063 |
rs547607910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866786 | CTTTTTTCTGATAAA[A/C]CTGAAATCTCCCTAA | 9063 |
rs547625726 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846991 | ATGATCATTATCAAC[C/T]CAAAATAGGAAAATA | 9063 |
rs547630735 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839621 | GTGGCTCCCAGCACT[C/T]TGGGAGGCCGAGGAG | 9063 |
rs547671215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838954 | TCTATTAAAAATGAA[A/C]GTTGACTAAATACCT | 9063 |
rs547673077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830473 | TTGTGGACTGTATTA[A/T]TTAAACACTGAAGTA | 9063 |
rs547690427 | snp | G/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46908099 | TCTGTGTACTTCCTA[G/T]GTGTATGCTATATAT | 9063 |
rs547696705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874729 | GATCAATTTCTCAGG[A/G]GTTACATACTTAGTC | 9063 |
rs547789825 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840124 | TGAGATCGTGCCACT[A/G]CACTTCAGCCTGGAT | 9063 |
rs547812990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881423 | ATAAGTGAAAACTGT[A/T]TTTGTAAAAAACTGA | 9063 |
rs547820257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817267 | ATTGACAATGGTGTT[A/G]GAATATTGTGTACTG | 9063 |
rs547834046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852615 | TGCCCCAGAGGAAGT[A/G]CTCAACTGCCTAAAT | 9063 |
rs547844729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857083 | TAAGATGTGCTCAAC[A/G]CATGGGAGCAGCTGG | 9063 |
rs547845599 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46815178 | ATTGTGAAATATTTG[C/G]ACAGTACTTCCTTTC | 9063 |
rs547877483 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877477 | CGTCCTCTTCACTCC[C/T]GACCACCCATTCTGT | 9063 |
rs547881516 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856472 | ACTTCATAATTATGT[A/G]TCCAATTAAAGATAC | 9063 |
rs547946070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898223 | AGTGCAGTGGCACCA[C/T]CTTGGCTCACTGCAA | 9063 |
rs547954669 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810870 | GTTTGAGAAATCAAT[C/T]GGTTGGACTGGCCAT | 9063 |
rs547989896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909213 | AGATGCTCAAACTCA[C/T]TAGCAAAGCAAATGA | 9063 |
rs547991755 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916392 | TACACTCATCTCTAC[A/C]TTGATACATTTAAAA | 9063 |
rs548052693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915701 | CTTTTACTCTGCTCT[A/G]TAAGAGCGAGTAAAT | 9063 |
rs548059374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822678 | ATCAAACGAACAGGA[C/T]ATCATCAAAAGTTTT | 9063 |
rs548064909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915086 | CCCAAGGTACCAGAA[C/G]AAAGTAGTGTAGCCC | 9063 |
rs548078151 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910048 | GTAATCCCGGCTACT[C/T]GGGAGGCTGAGGCAG | 9063 |
rs548103803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874302 | GATCACCTTCCTCAC[C/T]GGGTAGAAGTTATTC | 9063 |
rs548109584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826548 | AATCCAGAAACATCA[C/T]ATCTAAGCATTCATT | 9063 |
rs548109869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834161 | GGAACAACTGCACAA[C/T]TGGAAAAAGGAATCA | 9063 |
rs548144221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850056 | CAGATCTCCCAGGTG[C/T]CTCAAAATTTCTTTT | 9063 |
rs548145139 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845913 | CTGCAATTACCTTGG[C/T]GGTAAAACAAAAAAT | 9063 |
rs548173825 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898865 | CGGGCGTGATGGGAG[C/G]GTGCCTGTAATCCCA | 9063 |
rs548196416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833475 | GATTTCATAGGTATA[C/T]AATAAGTCAAAATTT | 9063 |
rs548210009 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919330 | CGTCTCCACCAAAAA[C/T]GCAAAATTAGCCAGG | 9063 |
rs548226090 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870707 | TTGATCAATTCTTAG[G/T]GCCACAGCTGTATAC | 9063 |
rs548240098 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877671 | TAGATTGTGCAGTCT[A/G]ACTCCAGCCAATGGG | 9063 |
rs548383242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913532 | AATGCATGAAAAGAA[C/G]GGGATGAAGAATACA | 9063 |
rs548389626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871216 | GCTCAAAAAGTATAT[A/G]TGAGAAGAGATGAAG | 9063 |
rs548424533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920029 | CACAAAACAGTAAGA[A/G]AAGAAAAGCAAAGCC | 9063 |
rs548449558 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808482 | GGGTGTTACAAACCA[C/G]TCACTAGGCAGGAAC | 9063 |
rs548468667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848017 | AAAGAGAAAATACTA[C/T]GTATATATGGCAAAG | 9063 |
rs548588878 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879606 | GAAGAGATGTTTGTA[C/T]ACTCACAGTCATAGC | 9063 |
rs548613351 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841294 | GAAAATACTGTGAAA[C/T]GTAATAAACATTTAT | 9063 |
rs548675094 | snp | C/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921626 | ATTTATAAAGTGAAA[C/G]ATGGTAAATTTTTTG | 9063 |
rs548700754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848653 | GATAATGTGTAATCT[A/G]TAACTTGCAACAAAA | 9063 |
rs548751830 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895503 | AGGCAAAACCCTGTC[G/T]CTACTAAAAATACAA | 9063 |
rs548754184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897319 | GGAAATGCACAAGAT[A/G]AGCCTATAACATTTT | 9063 |
rs548757069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837908 | AATCCTACTGTCCTA[A/G]CACAATACTAGCTGA | 9063 |
rs548770736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901144 | AACTACAGGCTGGGT[A/G]CGGTGGCTCACACCT | 9063 |
rs548778158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855790 | GTAATGATGATAAAC[C/G]TGACTTGCTTAACTT | 9063 |
rs548787139 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871633 | AACATGAAGTTATAA[C/G]CCTTTTAACAGATTC | 9063 |
rs548790708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889533 | TACAATAAGATACCA[C/T]CTGACACCCATTATA | 9063 |
rs548844976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845163 | CCCTGAAAATGTACC[C/T]TCCTATGACTAACCA | 9063 |
rs548865394 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913181 | TGAGGACCTCTAACC[C/T]CAAATCCCCCATTAA | 9063 |
rs548889237 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898159 | TACACCAAGGCAATA[G/T]AATTTTTTTTTTTTG | 9063 |
rs548900891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862666 | ATATACACATATATA[C/T]ACACACATATATATA | 9063 |
rs548932666 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828740 | ATTATCTGCTAATCA[C/T]GTAGGTTCTTTCTAC | 9063 |
rs548934145 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891561 | CCAAAATGCAATGAA[-/T]TTTTTTACCCCAATT | 9063 |
rs548942384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908341 | TTTTTAACAATTTCT[G/T]TAAAAACAGACTAAC | 9063 |
rs548951733 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874871 | GGAAAGAAGGAAAAC[A/G]CGAACCAGCTTGGGA | 9063 |
rs549013140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881662 | GGCCAATGCAGTAAC[C/T]GACCTTTAGATGTAC | 9063 |
rs549041565 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825647 | GCTCTGAGAGTCATA[C/T]AGCCTAAAATGGAAC | 9063 |
rs549049868 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863762 | ATGAGAGAAACAGGT[C/G]AACTGTTATGGACTG | 9063 |
rs549119790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879847 | CAAATAATAAGACAT[A/G]TAAGTATGATTCTAC | 9063 |
rs549132395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851375 | GCTACACAAGATTTA[C/T]AGATATTTCTCACAA | 9063 |
rs549169393 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922054 | AGACTTTACCAAAAC[A/T]AGTATCAAGGAAACT | 9063 |
rs549179177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879366 | CAATGCCACCTCACA[A/C]CCATCAGGATGGTCA | 9063 |
rs549184249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844641 | ATATATACTAATATA[C/T]TGATGTGAGCAATAT | 9063 |
rs549185831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874129 | CTAGCAAAACAAGTT[A/G]CAGATAATTGTTTAA | 9063 |
rs549196326 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908838 | ACATGGTGAAACCCC[-/G]TCTCTATTAAAAATA | 9063 |
rs549240620 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889275 | TTGTACATCAAAAGA[C/T]ACTATCAACAGAGTA | 9063 |
rs549260637 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851407 | TTGTTTAGAAGAAAA[A/C]TAATCCAGCTTCTTA | 9063 |
rs549293267 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856590 | CATGGAGTCTACGGG[A/G]AAGCAGCACTTATTC | 9063 |
rs549298176 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845405 | CAGGTATCAGCTTTC[C/T]TCTGAGGAAAGCTTT | 9063 |
rs549332060 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861027 | GCTCACACCTGTAAT[C/T]CCAACACTTTGGGAG | 9063 |
rs549348262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859156 | ATGAAGGGCCAGACG[C/T]GGTAGCTCACGCCCA | 9063 |
rs549362274 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811881 | AGTGGAAATGCAGGA[C/T]GAAAAGTGGAATCCA | 9063 |
rs549385605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858125 | AAAAAGGCGGCAAAG[C/G]TGCAAAGATGTGAAC | 9063 |
rs549404076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822360 | CCATTTAGGAAGCTT[A/G]TGACATATAATATGC | 9063 |
rs549413933 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904308 | GTTTAATTAAAACTA[C/T]AAGGAGTAAGACTAT | 9063 |
rs549440892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892068 | GTCCCATCCCATCCT[C/G]ATCACTCCCCCAACC | 9063 |
rs549465608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875342 | AAACAAGTTGCAAGG[A/G]CTGAAACAGAAACTC | 9063 |
rs549478971 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921301 | CCCAGCTAATTTTTG[C/T]ACTTTTAGTAGAGAT | 9063 |
rs549529366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828882 | GCAACAGAAACTTAT[C/T]AACTAAATCACTCCC | 9063 |
rs549555520 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808695 | TGCTCTACATTTTTC[A/T]ATTATGCAAAGAGCT | 9063 |
rs549571998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911607 | TTCTATAGTAACTAA[C/T]ACTCATGTCAACATA | 9063 |
rs549581455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876376 | TACTATTCTGGTGGT[C/T]AACTGTAAATAAAAA | 9063 |
rs549583330 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883598 | AATCCCAGCACTTTG[A/G]GAAGCTGAGGCAGGC | 9063 |
rs549695829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883093 | ACAGAGGGAGACTCC[A/G]TCTCAAAAGAAAAAA | 9063 |
rs549752519 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824722 | AGTTGCTCACAGGCC[A/G]GGCGTGGTGGCTTAT | 9063 |
rs549766021 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852449 | CACAACTGCCCATGG[A/G]GCTGCTGCAGGCCCC | 9063 |
rs549803256 | snp | C/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832394 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAAACTC | 9063 |
rs549808176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818321 | GCAGTCATATTTTTC[C/T]TTGAAATAAGCTGTT | 9063 |
rs549849072 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900914 | TAGAGGCGGAGGTTG[C/T]GGTGAGCCGACGTCG | 9063 |
rs549881486 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900215 | ACAGAAAATAAAAAA[G/T]TAGCTGGGTGTGGTG | 9063 |
rs549888896 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849868 | CCCTAAAACACACAC[A/G]CCACAAAAATACACA | 9063 |
rs549899451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888967 | TTTTGACAAGGGTGC[C/T]AAGATCATTCAGTGA | 9063 |
rs549907749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895576 | CTAGGGAGGCTGAGG[C/T]AGGAGAAATGCTTGA | 9063 |
rs549909242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853379 | GACAGGTGCACAGGG[C/T]TGTGTATTAATCTGT | 9063 |
rs549972010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825685 | GCATGGTATGGATCC[G/T]GGACACTATGCTTAT | 9063 |
rs550010242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824936 | ACCCAGGAGGTCAAG[A/C]CTGCAGTGAGCCGCG | 9063 |
rs550053408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824065 | ACACAGATACGTGTA[C/T]ACATTATGCAAGTGA | 9063 |
rs550069134 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46846429 | TAAAATACTAAACAC[A/T]AACATACATACAATT | 9063 |
rs550090520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823343 | TTTTTCCCACTCCCC[C/T]TTCTCTTCCTTTGCT | 9063 |
rs550092125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861045 | AACACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 9063 |
rs550093299 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910142 | GCCTGGGCAAGAAGA[A/G]CAAAACTCCGTCTCA | 9063 |
rs550180561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843815 | TAGCTGTATATTATC[C/T]ACAACATTAATTACA | 9063 |
rs550181494 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919007 | GTGTATATATATATA[-/TG]TGTGTGTGTGTGTGT | 9063 |
rs550213543 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895113 | ATCAAACAGGTATAC[A/C]TGACAGTTACATGTA | 9063 |
rs550217306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843000 | CAGAATAAAAGAGAT[A/G]TACTTGTAATCAGGA | 9063 |
rs550217473 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844905 | TTTGTTTACATGAAA[C/T]ACTTATTTAAGAAAC | 9063 |
rs550298343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862050 | AATATAAAGTTTTTA[C/T]GCCGGGCATGGTGGC | 9063 |
rs550307201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850098 | TTTATTGTTGAAAAT[C/T]TTAAACATATACAAA | 9063 |
rs550314520 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877058 | GACTTATGTCCTCAA[A/T]CCTTACTTCTCTTGC | 9063 |
rs550342060 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910197 | ATTTTACATATGTAT[A/T]TATGTTAAAAGTATA | 9063 |
rs550375059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910576 | GTTGCTATTTAAAAA[A/G]AAAGAAAAATGAAAG | 9063 |
rs550377550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46891674 | AAACTTCTAAAACAA[C/G]TGAAATTCCCAGCTG | 9063 |
rs550399651 | in-del | -/A | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815695 | GGATTTGAACCATCT[-/A]AAAAAAAAAACATAC | 9063 |
rs550418518 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921990 | GCATATATCTATTTA[G/T]ATCACATTTCCTAAC | 9063 |
rs550431626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907815 | CAGGACTTGAGTACA[C/T]ATGATTTTCCTGTTG | 9063 |
rs550434501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909987 | GCCTGGCCAACATGG[G/T]GAAAACTAATAATAC | 9063 |
rs550441571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814372 | TTAAAAGAACTGGTC[A/G]CATAAAAATTAGTAA | 9063 |
rs550449307 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857941 | TAAGAAGGTTGCAAA[G/T]GCAAGCAGTGAAATA | 9063 |
rs550488178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907351 | TACTTATTAGGGAGA[C/T]GCAAATTAAAACCAC | 9063 |
rs550535513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875401 | TGTAAGTCACTGCAA[C/T]GTAACCCCTTATCCC | 9063 |
rs550549127 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869556 | GCATTGAGCCTCACA[A/T]CAAACCTCCAGGATG | 9063 |
rs550560416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892196 | TTAAGTCTCAGGGAC[A/G]GCCCAGAAGCAACTG | 9063 |
rs550584206 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810277 | TAATTTCTATTAATA[A/T]TTTCATTTACTTTAT | 9063 |
rs550643415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864730 | AGCCAAGATTGCACC[A/G]TTGCACTCCAGCCTG | 9063 |
rs550649067 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888888 | TGCTAGTCCACGGCC[A/T]GAGGGTTGGAGACCT | 9063 |
rs550651463 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46915583 | GATGAAGCTGATCCA[C/T]AAACCAAAACAGAGA | 9063 |
rs550668977 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899973 | AAATTGGTAGTAGGG[G/T]GCAAGGGTGCATTTT | 9063 |
rs550685179 | in-del | -/A/AA | 0.482899 | 0.0955064 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900675 | GTAAGACCTCATCTG[-/A/AA]AAAAAAATACAAAAT | 9063 |
rs550735098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857266 | ATTCTGGGTGCTGGA[A/G]CTTCAAAGACAAATA | 9063 |
rs550778978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898939 | GGCGGAGGTTGCAGT[C/T]AGCCGAGATTGCACC | 9063 |
rs550796484 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810975 | GTGAACTCAAAAATG[A/T]TTTAGGAAGTCAAAT | 9063 |
rs550831729 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865262 | AGGCAAAATGAGGCC[A/G]GGCACAGTGGCTCAC | 9063 |
rs550885572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884461 | GGGACTACAGGTGCC[C/T]GCCACCACGCCGGCT | 9063 |
rs550918309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841322 | TATTCTATCACCCTA[C/T]ACTATCATTTTCTCT | 9063 |
rs550949905 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871417 | TAAAGGACATAGAGA[A/G]ACAAGACCAGGTAAC | 9063 |
rs550949977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879125 | CCAGCTACTGTATCA[C/T]CACCAACTAAAGAAT | 9063 |
rs550996230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916533 | TATCAGTCTGGGGGG[A/G]AAAAGTCTCTTCTGT | 9063 |
rs551102116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824149 | TGAATTGCTAGAATG[C/T]TGCTATATAGCAAAT | 9063 |
rs551144469 | snp | A/G | 0.000874436 | 0.0208915 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890908 | TCTATACAATTCTCG[A/G]ATTTTAATCTGAACC | 9063 |
rs551186247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831300 | AGAGATATGAAATAT[C/T]TAGGAATAAACTTGA | 9063 |
rs551220373 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849063 | AAATAATGTTACAGG[G/T]TCTGTCAGAAGGATA | 9063 |
rs551222604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882202 | TAAATTAGAATATTA[C/T]ATTTTAATGGCTTTA | 9063 |
rs551282239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888144 | TTTCAAAATTAACCA[C/T]GAAAATGAAAACCTG | 9063 |
rs551331561 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824775 | TGGCAGGCCAAGACA[A/G]GTGGATGGCTTGAGC | 9063 |
rs551348672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901188 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACCTGC | 9063 |
rs551353281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875972 | GCCCTGAGGGCCACG[C/T]CAATTTTACCTCATG | 9063 |
rs551384077 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863696 | TTTTATTCTAACACA[C/T]AGTATTTACTAAATA | 9063 |
rs551416250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875458 | AAACAATGGCCCAAG[A/G]ACCCTCCATATTCGA | 9063 |
rs551431085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852412 | TTGCCTTTCTCTCAA[C/T]GCTCTATTTCTTCTC | 9063 |
rs551436934 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824962 | CCGCGATCACACCAC[C/G]GCATTCTAGCCTGGG | 9063 |
rs551442387 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867195 | ACATATCTTTGACTT[C/T]ACCTATATTTGCTGT | 9063 |
rs551466761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860005 | GAGAACTGAATCCAA[C/T]GTTCAATCTTCACAA | 9063 |
rs551532795 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824329 | AAGATGCAATTTTGC[C/T]ACCAATTCTTAATGA | 9063 |
rs551534366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838815 | CTGAGACACAGCTGA[C/T]GGAGCTATATCACAA | 9063 |
rs551545051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915618 | GGCAGAAAGGAAGAG[A/G]AAAAAAAGCTTCTTT | 9063 |
rs551548209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881740 | TTCGAATGTGAACAT[C/T]ACCTCCCTAACTGTG | 9063 |
rs551622267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846129 | AATGTAAATTCCTTG[C/T]TGTATTAACTGGTAT | 9063 |
rs551699712 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828923 | AAAGATGAGAGAAAC[C/T]TTGGTCACTGCACTC | 9063 |
rs551712607 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899102 | TCCAAGTTATAAATA[C/T]AAAAAAATTCCAACG | 9063 |
rs551737310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898142 | TTACAGGTGTGAGCT[A/G]CTACACCAAGGCAAT | 9063 |
rs551750762 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896771 | AAACCAATATTAACA[C/T]ATCAATGTTTCCTGT | 9063 |
rs551768114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903982 | TTATCCACTGTGTGA[A/T]TCTATTTATGTAATA | 9063 |
rs551787337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836891 | TTTAAAGAAATATTT[C/T]CCCAGGAATGATAGT | 9063 |
rs551813450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908577 | AAACAAAAAAACTAC[A/G]TCTTATACTTTTACA | 9063 |
rs551821647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859247 | TCCTGGCTAACATGG[G/T]GAAACCCTGTATCTA | 9063 |
rs551837703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864568 | CTGAGGTCGCAAGTT[C/T]GAGACCAGCCTGACC | 9063 |
rs551845463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813789 | TATTTAATGCTTTGG[A/G]TAGATAACTGTTTTG | 9063 |
rs551847893 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900846 | GGGCCCGGTGGCAGG[C/T]GCCTATAATCCCAGC | 9063 |
rs551866490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848734 | AGAACTTCAATAACT[C/T]GCATTATAATATGGA | 9063 |
rs551873929 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914972 | TTCCGTTTTTTAGTC[G/T]GTTTTTCTTCCTTTA | 9063 |
rs551893855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866729 | AAAAAGAATGGAGGG[G/T]GTAGATAAAGGAAAT | 9063 |
rs551942286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905046 | GCTACATAATGAACA[C/T]ATATAAAACTGCACC | 9063 |
rs551952488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855899 | CATCAAACTTGGTAA[C/T]ATGCAAGGAAGCAGC | 9063 |
rs551974401 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822444 | AAAGACAGAAGGAAG[A/T]TATCTTCCAAAAATC | 9063 |
rs552031743 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922145 | TCACTCTGTCGCCCA[A/G]GCTAGAGTGCAGTGG | 9063 |
rs552079967 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881881 | AGGCAGGCAGATCAC[A/G]AGGTCAAGAGTTCCA | 9063 |
rs552084108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836030 | TTGCATAGACCCTAA[C/T]TGCTACTTCAAGAAA | 9063 |
rs552094865 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921320 | TTTAGTAGAGATGGG[C/G]TTTCACCGTCTTGGT | 9063 |
rs552196743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905651 | AACTACAAGTAACTG[A/C]AAAGAAGAGATTAAC | 9063 |
rs552212372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847977 | CTAGGATGTCAGTGA[C/T]GTAATTTAATTATGT | 9063 |
rs552212523 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839738 | GGTGTGGTGGTGGGC[A/G]CCTGTAATCCCAGCT | 9063 |
rs552222306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877011 | GGCCTCCTTCACTAA[G/T]TTAATGGAAAAATGG | 9063 |
rs552224169 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832795 | TACTGGGGAGGCTGA[A/G]GCAGGAGAATCACTT | 9063 |
rs552250472 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810098 | GTATTTTTTAAAATG[C/T]AAGTTGCCTGTATGA | 9063 |
rs552268509 | in-del | -/A | 0.481473 | 0.0944461 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858222 | ACAGGAGATAAGATT[-/A]AAAAAAAAAAAAAAG | 9063 |
rs552286588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819277 | TTGGGAATTAAGAAT[A/C]TCTGAATTTCCATCT | 9063 |
rs552294110 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874931 | AAACCACTATCTGCA[C/T]GGCCAAAAGGGGATG | 9063 |
rs552370879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877554 | TCCTGCCTTTGCCGC[A/G]CCCTGACATGCCCAA | 9063 |
rs552376393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818477 | GATTCATGTTTATGA[C/T]GTTTAAAAGGAATGT | 9063 |
rs552416108 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878947 | ATACTATGGCTAACA[C/T]AGGGAAAAGATAAAC | 9063 |
rs552432099 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919304 | CCAGCCTGACCAACA[C/T]GGAGAAACCCCGTCT | 9063 |
rs552444907 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833361 | ATAGAAACAGAAAGC[A/T]TATCAGTGTTTGCTT | 9063 |
rs552472794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917240 | CCAGAGGCACGAGCA[A/G]GCGGCGGCCGGCGAC | 9063 |
rs552476148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854211 | CTTAGCACTTGGCTC[C/T]GGAGAGCCCAGAGTC | 9063 |
rs552477113 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884343 | TTTGAGACAGAGTCT[C/T]ACTCTGTCACCCAGG | 9063 |
rs552548565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865513 | CCAGTGCACTACAGC[G/T]ATAGTCTTCAAAAAA | 9063 |
rs552668974 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911705 | GAAGAGTTATAAAAC[A/G]TTATATAAATGCAAT | 9063 |
rs552685085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854900 | TGAAAGTGCCCAAGT[A/C]CTCCCCTTCAACTAT | 9063 |
rs552693928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835255 | TGATAAAACAACTGT[A/G]ATAGAATGTTAACAA | 9063 |
rs552694393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873415 | CAGGACATCTATTCA[C/T]AGATGGCCCCTCTAG | 9063 |
rs552724774 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834699 | TGCTCACTGCGGCCT[C/T]AAACTCCTGGTCTCA | 9063 |
rs552739499 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893546 | GCTGTTGTAAATAGA[C/T]AAACAAAAAGTAAGA | 9063 |
rs552760195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840524 | TGTCGTTTTCTTCTA[C/T]GCTGTTTCCATCTCT | 9063 |
rs552786796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895684 | TCAAAAAAGAATAAT[A/C]ATCATCTACATCTTC | 9063 |
rs552812031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842534 | TGACTGTATGTGGAA[C/T]AGAGCTGGCAATTAA | 9063 |
rs552817799 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820371 | GAACAGTATATAGGG[G/T]TCTGTAATATCTGTG | 9063 |
rs552855570 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910032 | GGCATGGTGCACACC[C/T]GTAATCCCGGCTACT | 9063 |
rs552861507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867087 | ACATGTTGCACATAC[A/G]CAATATATATGTACA | 9063 |
rs552897107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892639 | TAGCCAGCCATGGTG[C/G]TGTGTGTGCCTGTGG | 9063 |
rs552932279 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895216 | CGGCCTAGAATTTGG[C/G]GAAGTGCTAATAAGG | 9063 |
rs552946861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821165 | TCTCAGTCGTTCGTT[A/C]ACCAGTTTCAGCACA | 9063 |
rs552949541 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810433 | GAGTCAATAAATATT[C/G]CATCTGTATTTAGAG | 9063 |
rs552950100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899117 | TAAAAAAATTCCAAC[A/G]ACTGGTTAATGAGTT | 9063 |
rs552956145 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822202 | ATTTAAATGTCAAAC[A/C]ACTTAAATATGGATA | 9063 |
rs552959974 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850318 | CTAGAGCCCCACACC[A/G]CACTTAGTTAGGTCT | 9063 |
rs553001260 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920203 | ATTAAGGACTGTTAT[A/G]TCATTCTGGCCACAG | 9063 |
rs553032321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914125 | CACAGATGCCATAAA[C/T]AAGCAACTGGTAAAT | 9063 |
rs553039277 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809880 | ATCACCCCTCTGAAA[C/T]TCCCTTATATTTGGT | 9063 |
rs553045496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832188 | TTGGGATGCTGAGGC[A/G]GGTGGATCACGAGGT | 9063 |
rs553070061 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920267 | AGTACTGAGCATTTA[C/T]AGGCTTTGCCAAGTA | 9063 |
rs553089629 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868095 | AAGTGCACCTCAAGC[A/G]TATGTCTTCTCAGCT | 9063 |
rs553119814 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856134 | CCTCAGCCTCCCGAG[A/T]AGCTGGGACTACAGG | 9063 |
rs553126250 | snp | A/G | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836144 | AACATTGCCCTCAAC[A/G]CAAATCATATTATAG | 9063 |
rs553148192 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905413 | TGCTGAAAATTAATG[A/G]CAGGCACCCAGCTTA | 9063 |
rs553182708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919736 | AATGCCTAACAAATA[C/G]TTGGCCTTGTATTTG | 9063 |
rs553189543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885768 | TAAGCCATGAGGATA[C/T]GTGTATTTCTGGCAT | 9063 |
rs553206244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885344 | CAACATAGTGAAACC[C/T]CGTCTCTATTAAAAA | 9063 |
rs553239504 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859159 | AAGGGCCAGACGCGG[-/T]AGCTCACGCCCATAA | 9063 |
rs553250988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891794 | TGGCTTGTGCTTGGG[C/T]GTAAAACAAAGGTTA | 9063 |
rs553311366 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849527 | AAGCAAAGGCCACTG[A/G]ACAGCACCAGCGGAA | 9063 |
rs553313409 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816383 | GTATTACAAAAATGC[G/T]TATCAAGTGATACAA | 9063 |
rs553340601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826150 | TGGTTTAGTCACAAA[C/T]TTCTATCTTATACTT | 9063 |
rs553343949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841899 | TATTCTTACATAGAA[A/G]GAATCCTAACCTCTC | 9063 |
rs553365465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877454 | ACATCTCTTCCTTAT[G/T]TGGAAAGCGTCCTCT | 9063 |
rs553405431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910091 | AACCTGGGAGGAGGA[C/G]GTTGCGGTGAGTCAA | 9063 |
rs553413789 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919313 | CCAACATGGAGAAAC[C/T]CCGTCTCCACCAAAA | 9063 |
rs553464814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909659 | CCTTTTTTGGAAGAT[A/C]ATCTGACATTATCCA | 9063 |
rs553466613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916851 | AACGGTAGCATCAGC[C/T]ATAAGAAGAGGAGAG | 9063 |
rs553469736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895284 | ATTCCCCATCTGCTA[C/T]GATGTATATAATACA | 9063 |
rs553477871 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853663 | GTGTGGTGGCAGGCA[C/T]CTGTAATCCCAGCTA | 9063 |
rs553518280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864328 | AATAACCAGGCATTT[C/T]TTATAAAGTACCTGC | 9063 |
rs553529204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902586 | GAGAAAAGAAAACCT[A/T]AACAAATAAATTCTT | 9063 |
rs553543745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877722 | AATAACCGCGTTAGG[A/G]ATAAAAACCCCTTCC | 9063 |
rs553579034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916160 | GCAGGCACTGTGCAA[A/C]CTCCAACAATCTCCG | 9063 |
rs553601966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870881 | AAGACCCTCGATGGG[G/T]CAATAACAATGCAGC | 9063 |
rs553614810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814555 | TCATGTAATCAGATA[C/G]AGAGTACTGAAACAG | 9063 |
rs553638397 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873331 | TAAAAGGCCCTGGGC[A/G]TAAATGTTTAGATTT | 9063 |
rs553654352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833775 | TACTTTGATCAATGG[A/G]ACAAATAGCAGTTCA | 9063 |
rs553701721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823572 | CTTAGTAACATGAAA[C/T]TTTAAATGAGTAAAT | 9063 |
rs553709021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903430 | TCATGGATTGGGATA[C/T]ACAGATGGCAAATAA | 9063 |
rs553740821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887565 | CAGTAAGAATTATAA[C/T]ACAGCAATGCAAAAA | 9063 |
rs553744163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841384 | TTATTTAAGTGCCTG[G/T]GATTTATTTTTTTCC | 9063 |
rs553801438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823998 | ATATGTTAATAAAAA[A/G]ATTTAAAGCTTTTAA | 9063 |
rs553858004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824167 | CTATATAGCAAATAT[C/T]AGTATTCCGGATTAT | 9063 |
rs553868491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868777 | CTTGTTTCTAACAAC[C/T]TGGGGGCTCATCCGC | 9063 |
rs553917660 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860538 | GGTTTCAGGGAGAGA[C/G]GTATATCAAAAGGGC | 9063 |
rs553926724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892667 | TGGTCCAAGCCACTC[A/G]GGAGACTGAGGCGAG | 9063 |
rs553935288 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859333 | CTCAGGAGGCTGCGG[C/G]AGGAGAATGGCGTGA | 9063 |
rs553960590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867915 | CTGTGGGGACACTCA[C/T]TCTTGGAACCTAGCT | 9063 |
rs553979609 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901323 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 9063 |
rs553990200 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823016 | GCCAAGGCAGGAGGA[C/T]TGCTTGAGCTGGAAG | 9063 |
rs554050407 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900837 | AAATTAGCTGGGCCC[A/G]GTGGCAGGCGCCTAT | 9063 |
rs554059949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874474 | GAAATAAGATGGGAA[C/T]ACCATACCCCCTGGC | 9063 |
rs554067671 | in-del | -/GT | 0.0561591 | 0.157879 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848766 | TGAAAGAGAGAGACA[-/GT]GTGTGTGTGTGTGTG | 9063 |
rs554080043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866004 | TAACGTGTATTTTGA[C/G]ATTACAAGTAAACAT | 9063 |
rs554112998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845361 | CCACCTGCTACTACA[C/T]GGCCTTTGAGTAAAT | 9063 |
rs554127124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880966 | TAATTTAATCAGATT[G/T]AAATAGAACATAGCA | 9063 |
rs554146359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838141 | TGTAATTTCTAATTC[C/G]TCTAAAATGAACACC | 9063 |
rs554149327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884563 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAAGTGT | 9063 |
rs554193858 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821784 | ATACAAATTAAACAT[A/G]TGTAATAAATACTTC | 9063 |
rs554241084 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46846996 | CATTATCAACCCAAA[A/G]TAGGAAAATAACCTT | 9063 |
rs554242050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844264 | ACACTCCCAATATAA[A/G]TTAAAGAATTATGAA | 9063 |
rs554272884 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835154 | ATGGTTCAAAAGAAT[C/T]CTAAAAATGGTAATA | 9063 |
rs554329288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855915 | ATGCAAGGAAGCAGC[C/T]TAAGTTCGGAAAGAG | 9063 |
rs554363184 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46812779 | AAGATAGCATGAATT[A/T]AGCTATTTTACATTA | 9063 |
rs554369192 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839758 | TAATCCCAGCTACTC[A/G]GGAGACTGAGGCAGG | 9063 |
rs554392472 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897345 | ATTTTATCGCACCAG[A/G]AAACAGAGAAGCTAT | 9063 |
rs554395486 | in-del | -/TTC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820725 | CCTATTCTACTATAT[-/TTC]TTATCACCAGGAATC | 9063 |
rs554409802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832187 | TTTGGGATGCTGAGG[C/T]GGGTGGATCACGAGG | 9063 |
rs554453225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848401 | ACGCCATGCCAATAA[C/G]ATCAAAGTTGCACAG | 9063 |
rs554454040 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862867 | CCCGCCACCATGCTC[A/G]GCTAATTTGTTGTAT | 9063 |
rs554464077 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873024 | GGGGCCACTGACAAC[C/T]TGTGGCCTTTGTATC | 9063 |
rs554471556 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809699 | GGTGGAGGTTGCGGT[A/G]AGCCAAGATCGCACC | 9063 |
rs554495843 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46812066 | TACAATTTTTTTTTT[A/T]ATTAGAAAAAAGGTT | 9063 |
rs554522390 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914566 | CCAACCCTCCCCCCC[A/C]CAACTCCACCCCCGA | 9063 |
rs554532462 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811379 | AAAACACATTTTCTA[G/T]GTAGTGCTACCAAAA | 9063 |
rs554534718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871776 | CACAGAGGTCAAATA[C/T]AAAAATTGATCAGCC | 9063 |
rs554609662 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841683 | TAGAAAGTGCTCTGA[A/G]AAGATTGATGAACCC | 9063 |
rs554611874 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890740 | AACAGGAGAGGATGG[C/T]GAGTGAGGTGTAACT | 9063 |
rs554646817 | in-del | -/GAAA | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861267 | ACAAAATGAATGAAT[-/GAAA]GAAAGAAAAGAAAAG | 9063 |
rs554685001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832462 | AAGTGGGCAAAAGTT[C/T]GGTCACTTCACCAAA | 9063 |
rs554697605 | snp | A/T | 0.0114469 | 0.0747824 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848766 | ATGAAAGAGAGAGAC[A/T]GTGTGTGTGTGTGTG | 9063 |
rs554720362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825056 | CGGGGCTGTAAATTA[C/G]AGTAAGTTTTCCTGA | 9063 |
rs554735054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864814 | AAAAATATAACAAAA[C/T]GCTTCAATATTACAT | 9063 |
rs554756851 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884718 | GTCAGGAGTTTGAGA[A/C]CAGCCTGACCAACAT | 9063 |
rs554793993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876768 | GTGGCGCTATCTCAA[C/T]TCACTGCAAGCTCTG | 9063 |
rs554834745 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899613 | ACTGGGACTACAAGC[A/G]CACACCACCATGCCT | 9063 |
rs554843704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905138 | TTTTAATAGTCTAAA[A/C]ATATTTCAAAGAGTT | 9063 |
rs554857857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912491 | GTTGGTTGAAACCAA[A/C]GATAAGTCATTCACA | 9063 |
rs554877424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817772 | CTCAAGTACTAACAG[C/T]GAAGTTTGATATGGT | 9063 |
rs554896728 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808978 | AAAAAAAAGACAACT[G/T]GGCTGGAAATGCTGA | 9063 |
rs554950572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822736 | CACAAGAGTTTATAT[A/G]AGAAACTGGAGGAAG | 9063 |
rs554955844 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46835549 | CTCCCACCTCACGTT[C/T]CTGTGTAGCTAGGAC | 9063 |
rs554966005 | snp | A/T | 1.65162e-05 | 0.00287365 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846824 | TTCAATCCCATTTTT[A/T]GGCGGTGGTGCATAG | 9063 |
rs555028357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911309 | CAACCTCCACCTCCC[A/G]GGTTCAAGCAATTCT | 9063 |
rs555032971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813104 | ACCAGCTGAATGATG[A/G]CATTGGACTCCTTTG | 9063 |
rs555040191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830040 | CTCCCTTTGTCCTAT[A/G]TTTTAAATCTGTAAC | 9063 |
rs555075819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829280 | ATTCTTCTCCACAAA[C/G]AAATGGAAGGTAACA | 9063 |
rs555084608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874351 | CCAGTAATGTAGTTA[A/C]GGCATTAATCAAAAA | 9063 |
rs555128439 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883747 | CTCAGGAAGCCTAGG[A/T]AGGAGGATTGCTTCA | 9063 |
rs555137415 | in-del | -/AAAC/AAACAAAC | 0.0134861 | 0.0810011 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832416 | CGAAACTCCATCTCA[-/AAAC/AAACAAAC]AAACAAACAAACAAA | 9063 |
rs555159214 | in-del | -/TTAAG | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867581 | ATTCCATGAATGCCT[-/TTAAG]TTAAGAGCAAATGAA | 9063 |
rs555202128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889068 | ACACTCACCTAATAC[C/T]ATATACGAAAATTAA | 9063 |
rs555209587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847543 | CTGGAGTACAGTGGC[A/G]CGAACTTGGCTCACT | 9063 |
rs555229478 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819834 | TGGAGAGGGAAGAAG[A/G]GTAAAGGAGGGAAGT | 9063 |
rs555294625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836266 | AGAGTAGAATTTATT[G/T]AGAATTTAGTTCAGT | 9063 |
rs555337022 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908729 | AAAAAACGCATAAGG[A/C]TGGATGCAGTTGCTC | 9063 |
rs555350493 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812133 | TAACAAAAACTTTTT[C/T]CACTGATTTGTAGAC | 9063 |
rs555358660 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866264 | TACCTAGTCACATCA[C/T]AGTCATACTATTGAT | 9063 |
rs555440515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914601 | CAAGTCTGAAAAGCA[A/G]AGGCACCAGGGTCAC | 9063 |
rs555442429 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921647 | AAATTTTTTGTATCT[A/G]AACAGCTAAGCTGAT | 9063 |
rs555454359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46906137 | GATAAAATTCATTCA[A/T]GATTTTTTAAATTAG | 9063 |
rs555465626 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856248 | CCTCGTGATCCGTCC[A/G]CCTTGGCCTCCCAAA | 9063 |
rs555557187 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853259 | GCACTCCAGCCTGGG[C/G]AACAGACCTGAGAGC | 9063 |
rs555597498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835317 | GTTCTTTGTGCTAGT[A/G]TTCCAACTCCTCTGT | 9063 |
rs555606052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886614 | AGGCCAAGGCGGGTG[G/T]ATCACCTCAGGTCAG | 9063 |
rs555609104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820714 | CTCTAACATTTCCTA[C/T]TCTACTATATTTCTT | 9063 |
rs555633673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872267 | TCCTCAGCAAAATAC[A/C]ATATGACCATCAATG | 9063 |
rs555664501 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919779 | AGGAATGAATGAACA[A/C]TGTCCAGGTTCTAAA | 9063 |
rs555666054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878758 | CTGTAAGCCCAGCTA[C/T]TCAGGAGACTGCGGT | 9063 |
rs555667411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885831 | TTTAGTTACTCTTCT[A/G]AACAAAATATCTCTG | 9063 |
rs555710267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891931 | TCAATTCTGAACTCA[A/G]AGGCAAATCACACTT | 9063 |
rs555725585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896813 | TAAAAGTCCTCAATG[C/T]ACCCAATACAGTGTA | 9063 |
rs555771753 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899301 | TGAAATAGTAACTGA[A/G]TAAGTAACTGAAGCA | 9063 |
rs555853427 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46821893 | TTTTGAAAAAGTTCA[A/C]GCTTAAACAGAGATT | 9063 |
rs555862549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902704 | CAAGATTTTTGTAGA[C/T]ATAGATGAGATTATT | 9063 |
rs555871262 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857559 | GTAATTCCCAGAAAA[A/T]AAGAAAGGACAGAGA | 9063 |
rs555879470 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878644 | GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA | 9063 |
rs555916482 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850384 | CCATCTCCAAACACA[C/T]ACACTTTTTCCCCAA | 9063 |
rs555916510 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881228 | ATCTCTGAACGACCC[C/T]AGGCTCTTTCCTAGC | 9063 |
rs555941850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871702 | GTCCCTTGCTCCTCA[A/G]AAGAACTTTTTGTCT | 9063 |
rs555945805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819879 | ATGGCCTTGGTTGCA[G/T]AAGTCCTGATACTAA | 9063 |
rs555968614 | in-del | -/GTGT | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881375 | ATTAGAAAAACTTTG[-/GTGT]ATGTAATGGGATTAT | 9063 |
rs555977175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910111 | CGGTGAGTCAAGATC[A/G]CGCCACTGCACTCCA | 9063 |
rs556041377 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847717 | TTGATCTCCTGACCT[C/T]GTGATCAGCCTGCCT | 9063 |
rs556070421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875665 | TAAGGTAACGGCTGT[A/G]GAGGTGAAAGAATTA | 9063 |
rs556102863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868874 | CACTGTGGTGGCCTC[A/C]GGGATGAGGGATCAA | 9063 |
rs556109606 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882668 | GAATAAACAGTGAAA[-/G]CCCATTGAAGATGTA | 9063 |
rs556129049 | snp | C/G | 0 | 0 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826848 | GAAGGCAGCTGAAAA[C/G]GTTTAATTCTTAAAA | 9063 |
rs556129913 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882511 | ATATTTTGACCCAAC[A/T]ACTTCACATCCGGGC | 9063 |
rs556142222 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881900 | TCAAGAGTTCCAGAC[A/C]AGCCTGGCCGACATG | 9063 |
rs556182676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916918 | CTCCACCAAGTGAGT[A/G]GCATGCAGACTTGTG | 9063 |
rs556195883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848244 | CACCATTAACTGGAT[A/G]TGTTAATGGGGATAC | 9063 |
rs556213263 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825567 | CACTATTCACCTTCC[C/T]GTTCCCCTGCTCTGG | 9063 |
rs556232534 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862307 | CTGCACTCACTCCAG[A/C]CTGGATGACAGAGCG | 9063 |
rs556249395 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910825 | TCAAAATTCTGAGGA[A/T]TTTATAATTCCACAT | 9063 |
rs556265526 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854428 | CAGTTACAGTAAATA[A/C]ACCTCCAACTTTGTA | 9063 |
rs556278268 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869617 | AGATATAAAGCTAGT[C/G]ATGATAACAACATTC | 9063 |
rs556302307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853737 | GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG | 9063 |
rs556331440 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890467 | TATATTCAAACATTC[C/G]GCATTGATGCCTCAA | 9063 |
rs556349334 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878044 | CTGGTATAATAGTTA[C/T]GACAGCTCTAAATCT | 9063 |
rs556359835 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917434 | CCACGGCCGCCGCCG[C/G]CTCCAGCACCATCCT | 9063 |
rs556410525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852018 | TGTGGCTTGTTGATG[C/T]TTCTTAAAACTGGAA | 9063 |
rs556416990 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849922 | TCAAATTCTAGACAT[A/G]CCATTTAACCCAGAT | 9063 |
rs556430682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845511 | AGAATGATAAAAATT[A/G]AAAAGTCAAGCCAGA | 9063 |
rs556448322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859512 | AGTGGCCTATCACAA[A/G]GAGGCCTCTGTCAAG | 9063 |
rs556525529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888480 | GAGAATTCACTCTTC[C/G]TGATTCCAAGACATA | 9063 |
rs556528728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823657 | GTGAAAATCCAATGG[C/T]GGTACAAATTAGTAA | 9063 |
rs556530498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831590 | TCACACTACCTGACT[G/T]CCAGCAAATGCAGTA | 9063 |
rs556533927 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871789 | TATAAAAATTGATCA[G/T]CCCACTTTCAATTTC | 9063 |
rs556542695 | in-del | -/TTAG | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916498 | TCTCATTCGTCACAC[-/TTAG]TTAGGACTTTAAAGG | 9063 |
rs556548485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878894 | AAACAAAAACAAGAA[C/T]GCTTCCTAGCGGTTA | 9063 |
rs556574586 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847917 | AAATGTCTTAGCTGC[-/A]AAAAAATCTACATAT | 9063 |
rs556690217 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885668 | CAGCCTGGGTGACAG[A/G]GCGAGACTCCGTCTC | 9063 |
rs556701001 | snp | C/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836229 | ATAAGACGGAAAACA[C/T]ACAAACATCTGGATT | 9063 |
rs556703452 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844935 | CTCTGGTTTCTAAAA[A/G]TAACATTCAAAATAA | 9063 |
rs556719112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849240 | CTCACTCAGCATAAA[A/G]TGTTTTCAATCTATT | 9063 |
rs556721089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841872 | TGGTAATGTTTGGAA[C/G]GAACTGCTCCCTATT | 9063 |
rs556728812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917078 | CCAGGTGTGCGGACC[A/G]CTGGCAGCACTCAGG | 9063 |
rs556756526 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893661 | AAAGATAAAGTATTG[C/T]TGGACACATAGCCAA | 9063 |
rs556785087 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880630 | TTTAAAAATTGGGAC[A/C]AAAAATTTAAATTTC | 9063 |
rs556808992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848791 | TGTGTGTGTGTGTGA[C/G]AGAGAGAGAGTAGGA | 9063 |
rs556846996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909437 | TGTTTTGGTAGAGAT[A/G]GGGTTTCACCATTTT | 9063 |
rs556856988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900906 | CTGAACCCTAGAGGC[A/G]GAGGTTGCGGTGAGC | 9063 |
rs556867173 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832555 | ATGCAAATAAACCCA[A/C]AATGGAGTACCACTA | 9063 |
rs556920431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908754 | TTGCTCATGCCTATA[A/C]TCCCAGCACTTTGGG | 9063 |
rs556940553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827604 | AGTAAGCGATGGTGT[G/T]CCAAAATTGGAATCC | 9063 |
rs556963499 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920466 | ACACAAAATCTCAGC[A/T]TTGACTTTGATACTC | 9063 |
rs556989810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885301 | AAGTGGGCAGACCAC[A/G]AGGTCAGGAGTTCGA | 9063 |
rs557030003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826591 | ACATTTTGAACGTAA[A/C]CATTTCAAAATTATA | 9063 |
rs557031631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46817858 | TTTACATTTTAAGCA[A/G]AATATTAAAACTCTT | 9063 |
rs557064747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826037 | GTATTAATGTGTATG[C/T]ATGTCTAGGTTGGGT | 9063 |
rs557071587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885557 | AGAGCATATACTCAT[C/T]ATGGTTTTTTGACAT | 9063 |
rs557086238 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809126 | TCAAGACTAAGGAAA[A/C]CTTGGTTTTATACCA | 9063 |
rs557104908 | snp | G/T | 0.000424809 | 0.0145679 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891223 | TCATAAGACAATCCC[G/T]TAAAAATTACATTCA | 9063 |
rs557114371 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893114 | AAGGAAAACAAGAAA[A/C]CTTTTGGCCTATCTC | 9063 |
rs557172035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911906 | AAATACAAAAATTAG[C/T]CAGGCATGGTTGCAG | 9063 |
rs557178019 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918523 | GCAATGGCACGATCT[C/T]GGCTCACCGCAATGT | 9063 |
rs557193074 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813014 | TTTTTGCTTAATAAC[A/C]TTTTTAAAAGTATTT | 9063 |
rs557209740 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911407 | TTTTAGTAGAGACGG[A/G]GTTTCACCATGTTAG | 9063 |
rs557242776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898327 | TAAATTTTGTATTTT[A/G]GTAGAGACAGGGTTG | 9063 |
rs557255192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897615 | AGATTTTTGGTTTGA[A/G]TAGAAAAGCCATATG | 9063 |
rs557276827 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858339 | AAAAAACTGAATGGG[C/T]TTTAGAAAGATCATA | 9063 |
rs557294790 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809792 | GATTTTAGGAGGCTG[A/G]CAATTACAGTTCATT | 9063 |
rs557318931 | snp | C/T | 6.64352e-05 | 0.00576309 | synonymous-codon, intron-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46864190 | TATCTCTCTAACTTG[C/T]TGAGGTGTCAAAGCA | 9063 |
rs557333711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832483 | CTTCACCAAAGAAAC[A/G]TACAGATGGAGAATA | 9063 |
rs557417615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919603 | GCAGTGAGCTGCGAT[C/T]GCACCATTGCACTCC | 9063 |
rs557419941 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826516 | ACTATATTCTAAAGC[A/G]TATCATTACAGAGTA | 9063 |
rs557430993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823505 | CAAGTGAATGTACCT[A/G]CACACCTGTCTGTCA | 9063 |
rs557458694 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916383 | TTTCAAGTTTACACT[A/C]ATCTCTACCTTGATA | 9063 |
rs557460270 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860465 | CAGTTGCAGCAGAGA[A/C]AATACAAGATAAGCC | 9063 |
rs557518568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877712 | AGAACCAGGGAATAA[C/T]CGCGTTAGGGATAAA | 9063 |
rs557520483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870442 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 9063 |
rs557540187 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883847 | TCAATAAATAATAAA[A/T]AAATTAAAATCAGTC | 9063 |
rs557556261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832908 | AAAAAAAAAAAAAAA[A/G]AGAGAAGCCATACCA | 9063 |
rs557581187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877394 | TCTTCTTCTAAGCTA[C/T]CTGCTCTGTAAACAA | 9063 |
rs557589052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840567 | TTAAAATTTCCACAG[C/T]ATACAGAAACGAGAA | 9063 |
rs557605057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889580 | AAAAAGGAAAATAAA[A/T]GTGTTGTTAAGGATG | 9063 |
rs557658628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883375 | ATGCATATAAACAGC[A/G]AACAAAGAGTCACAG | 9063 |
rs557792047 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900376 | TTTAAAAAAAAAAAA[A/G]GATAATATAGGCAAG | 9063 |
rs557795456 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898294 | TTGGGATTACTGGCA[A/C]ACACCACCACACCTG | 9063 |
rs557806188 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867577 | AGAGATTCCATGAAT[G/T]CCTTTAAGTTAAGAG | 9063 |
rs557827665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908795 | GGGCAGATCACCTGA[C/G]GTCAGGAGTTCGAGA | 9063 |
rs557841798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915239 | ATTGTGAGAATTAAA[G/T]AAGTATAGAAAAAAT | 9063 |
rs557852122 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888164 | ATGAAAACCTGTACA[A/G]TAACAACTATAAAAC | 9063 |
rs557867130 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914736 | AGCCTTGAAGGGTAA[C/T]GGAAATCCTCTCTGT | 9063 |
rs557905996 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916611 | TCAACAATAAAGTTA[C/T]GATCTTGTTTTAAGA | 9063 |
rs557918509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874961 | GGACAGACCACACGC[A/G]AGTGAAAGGAGTGGC | 9063 |
rs557978000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858226 | GGAGATAAGATTAAA[A/G]AAAAAAAAAAGCAGA | 9063 |
rs558001905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880252 | AAAATGTAAAAATTA[G/T]CTGGGCATGGTGGTG | 9063 |
rs558009526 | snp | A/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906808 | TAACATGAAAATATG[A/T]TTCTAAAATTACATG | 9063 |
rs558046298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909197 | TAATCAGTATAGTAA[A/C]AGATGCTCAAACTCA | 9063 |
rs558079790 | snp | C/T | 1.66076e-05 | 0.00288158 | splice-acceptor-variant | PIAS2 | GRCh38.p7 | 18:46836518 | CCTCATTTTTCCTAA[C/T]TACAGGACAGGAAAC | 9063 |
rs558102000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914459 | TGCCATATTCTGCTA[G/T]GACCAGCCAAGATCT | 9063 |
rs558114686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886658 | GCCTGGCCAACGTAA[C/T]GAAACCCCATCTCTA | 9063 |
rs558149384 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895834 | CTTTTCAAAGGTCAT[C/T]GGAGGCCCCAGTTCC | 9063 |
rs558178863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889651 | AAAATGCAGCTGCCA[C/T]GGAAAACAGTATGGT | 9063 |
rs558189045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896923 | ATTGAGTATTTATGT[A/G]TAAAATTATACAATA | 9063 |
rs558222913 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853952 | TCTGCAATTCCCCTT[A/C]ACTCCCAGGACTGTC | 9063 |
rs558253036 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883965 | GTGATGCCACTGTAC[G/T]CCAGCCTGAATGAAA | 9063 |
rs558288833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850480 | GTATATTGCTTCCTC[A/G]AAGTATAAGGTTTGT | 9063 |
rs558320023 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856745 | TTAGCCATTGTCATA[A/C]ATCTTGGACTCTGTC | 9063 |
rs558340688 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830271 | AAAAGGATAATGGGG[A/T]AGGGGAAGGAGGGAA | 9063 |
rs558350180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865454 | CTGAGGCAGAAGAAT[C/T]GCTTGAACCTGGGAG | 9063 |
rs558364337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907076 | TCTTGATGCCTTCCC[C/T]GGAGATATCTGCCAA | 9063 |
rs558367347 | snp | A/C | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920762 | GGTCTAGATTTATAT[A/C]TCCTCATTAAAAAGA | 9063 |
rs558394706 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811292 | AAATCTAATGCTGTC[C/T]CTTTCCCTAAGTTTG | 9063 |
rs558423958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914054 | ACATTAATTCACAAC[C/T]AGTTAATTCAAAATC | 9063 |
rs558441169 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897038 | GTGTACTGGGGACAC[A/G]AAGAATTTTCTATCA | 9063 |
rs558488438 | snp | C/T | 0.000857732 | 0.0206913 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820981 | TATGGTGGAATGGTA[C/T]TGAGTAGTCTGTTAA | 9063 |
rs558493589 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921158 | TTTGGGACGGAGTCT[C/T]GCTCTGTTGCCCAGT | 9063 |
rs558608603 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872696 | AGGATAAGGCCCGAA[C/T]GGGTCAAAGGAATCG | 9063 |
rs558623097 | snp | A/C | 0.00044247 | 0.0148674 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855319 | TTAAACTTATATGCA[A/C]ATCTGGTGAATAAAA | 9063 |
rs558641285 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904418 | ATGTAACGGTGAGGA[A/G]AAATTTTTTAAATTA | 9063 |
rs558645468 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842227 | AGAGACCCTGTCTCA[A/G]AAAAAATTTAAAATA | 9063 |
rs558691453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847801 | GTTCGTTTTAAATAG[C/T]AAGTATACTCATTTC | 9063 |
rs558714292 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809565 | GTTCGAGACCAGCCT[A/G]ACCAAAATGGAGAAA | 9063 |
rs558755991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882684 | CCCATTGAAGATGTA[C/T]ATCAAAAAAGTACTG | 9063 |
rs558759036 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808874 | CAGAGAAATGAAAGG[C/T]ATACCCGTGAATTAA | 9063 |
rs558791475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845627 | TATAATTTCACATAA[A/G]TGTTAAAAAAAAAAA | 9063 |
rs558798168 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808091 | GCACATCCATAACAA[G/T]GGAGTACCATAAAAT | 9063 |
rs558839357 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889559 | TATAATGGCCACTAT[-/A]AAAAAAAAAAGGAAA | 9063 |
rs558847594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825028 | AAAAAAAAAATAGTT[G/T]CTCACATAATTTCGG | 9063 |
rs558847943 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832347 | TTGAACCCAGGAGGT[C/G]GAAGGTTGCGCTGAG | 9063 |
rs558872736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888530 | AAAACTGTGATACTG[A/G]CATAAAGACAGACAT | 9063 |
rs558906657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876579 | GGAACTCAATGTTGT[A/C]CTTTTATACCTAATA | 9063 |
rs558918746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883155 | TTAACATAACACAAG[C/T]GGAGAAAAAATAAAC | 9063 |
rs558933106 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832417 | CGAAACTCCATCTCA[A/C]AACAAACAAACAAAC | 9063 |
rs558935827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864997 | AAAATTTTGAATGTC[A/C]AAACTTTTAAGTTTT | 9063 |
rs558975591 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864636 | TTAGCTGGGCATGGT[A/G]GTGCATGCCTGTAAT | 9063 |
rs558993335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853037 | ATCCCAACACCTTGG[A/G]AGGCCAACATAGGTG | 9063 |
rs559000094 | in-del | -/GTTAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847374 | TTTAAACCAGGTTAA[-/GTTAA]CAAATAAGGATAATC | 9063 |
rs559023120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917059 | GGCGCCCCGACCCCC[C/T]GCGCCAGGTGTGCGG | 9063 |
rs559048210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864573 | GTCGCAAGTTCGAGA[A/C]CAGCCTGACCAACAT | 9063 |
rs559059292 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862648 | ATACATATATATACA[C/T]ATATATACACATATA | 9063 |
rs559111114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871125 | TTTTGTTATGAACAG[C/T]TGGCCAGATATTGCT | 9063 |
rs559172266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853518 | AAAGATAGGCCAGGC[A/G]TGGTGGCTCACGCCT | 9063 |
rs559189485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834061 | ACTAGAAGTGCCCTG[C/T]TCACCATTTTTAGAC | 9063 |
rs559223516 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46906023 | TATACTTGCAACACA[A/G]AGTTTGTTTAAATAT | 9063 |
rs559224452 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841937 | CTACTTTCACTATTA[C/T]TGAAAGTTTGGCTAG | 9063 |
rs559312240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901634 | GTATTTGTTTTGAGA[G/T]CTATAGAATACATCA | 9063 |
rs559329429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906479 | AGTATAGCAAGGTTA[C/T]TATACAAAGTCAAAC | 9063 |
rs559364620 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888683 | AGGCATTAGATTCTC[A/G]TAAGGAGCATGCAAT | 9063 |
rs559407452 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810741 | TTGAGAAGGTGAAAG[A/G]AAAAAAAAAAAAACC | 9063 |
rs559438158 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865403 | AAATTAGCCAGTCAT[A/G]GTGGCACGTGCCTGT | 9063 |
rs559439982 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831067 | TAGTCAATGCAAGGC[A/G]GTGGGAAAACAAAAG | 9063 |
rs559440684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819370 | ACTTTACAATTTGTG[C/T]TAGCTGGGTCTACAA | 9063 |
rs559444258 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810153 | TTTCAGTGTAAAACA[A/C]CAAAACCGAACATTA | 9063 |
rs559476382 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848851 | GAAAAAAAAAAAAAG[G/T]TGCTCAGAAAAAAAA | 9063 |
rs559476753 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833093 | CAAGATAAATGAAAA[C/G]AGTCCACACAAAGAC | 9063 |
rs559479469 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827004 | GAAGAAAGTTTTTTG[G/T]GTGTTGAAAATATTC | 9063 |
rs559501962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878220 | GTAACACTTTTCTCA[C/T]CTGCCTTTTTAAGAT | 9063 |
rs559529416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897729 | AATTCTGTTAACATG[A/G]TAACTGGTATCTGTC | 9063 |
rs559537081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818134 | CTGTGAAATTGACTC[A/C]TTAGATTTTTTCTCA | 9063 |
rs559538922 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886654 | CCAGCCTGGCCAACG[-/T]TAACGAAACCCCATC | 9063 |
rs559562210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919946 | GGAGTTTTCGGGGAA[C/T]AGACGAATAGAGTAC | 9063 |
rs559641402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854904 | AGTGCCCAAGTCCTC[C/T]CCTTCAACTATGCTG | 9063 |
rs559702086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837858 | CACTAGATCTTATGC[C/T]CCAAAAAGACGGTCT | 9063 |
rs559762628 | snp | A/G | 6.59467e-05 | 0.00574187 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890788 | GTGGATTCCAGCCAC[A/G]GCCAAGTCAGGTTCT | 9063 |
rs559828083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889821 | AAATGTGGGAGCAAC[C/T]CAAGTGTCCAATGGA | 9063 |
rs559841650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897222 | GGTGAGGTAAAAAAG[C/T]GGTTATGGCATAAAT | 9063 |
rs559845520 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838582 | AAAAGGTCAGAATAA[A/G]ACCTGGGGCAGCTTC | 9063 |
rs559870154 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878542 | CAAGCACTATATTGA[C/T]ACCTTTTAATAAACT | 9063 |
rs559926460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912088 | AACAAAGGCTAGGAA[C/G]GGAGGAGGGAAAAAC | 9063 |
rs559942148 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894055 | TTCTTCAACCCAGGA[A/G]GTGGAAGTTGCAGTG | 9063 |
rs559964742 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845069 | CACTTTAAAACATTC[A/G]CTGGTATGGGAATAT | 9063 |
rs559973229 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869289 | TAGAGAAGGGAAGGC[A/C]AGAAATATCTAATAC | 9063 |
rs560002743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852228 | AGTGGTGGTTTAAGA[C/T]GTTTTCCATCAGATG | 9063 |
rs560004319 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842884 | ATCCAAGCAATCCTC[A/G]TATCAAAAAATTATA | 9063 |
rs560004562 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908283 | CCAGGCAAGAAGTTT[A/G]TTTATGCTAGCAGCA | 9063 |
rs560017734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914815 | CTCTACTGCCAAGAA[C/G]TTAGCCAACAAACTA | 9063 |
rs560019470 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900209 | GTCTCTACAGAAAAT[-/A]AAAAATTAGCTGGGT | 9063 |
rs560026480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862595 | AGTCATATAAATAAT[A/G]TTTTGTTAACACTAA | 9063 |
rs560033450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825421 | ACCTAAATCTGGTAA[C/T]AAAGAACAAACTTAA | 9063 |
rs560059255 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894409 | GAATGGATTTCAGTT[C/G]TTTTTCTCCACCAAC | 9063 |
rs560079934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845701 | TACAATAAACATCAT[A/C]CTTTTAATAGCTGCC | 9063 |
rs560142653 | snp | A/G/T | 6.60093e-05 | 0.00574466 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812402 | AAAAGCAGTTCTGAT[A/G/T]AATGATTCCCAGAAT | 9063 |
rs560176733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886775 | CCGGGGAAGTGGAGG[C/T]CGCAGTGAGCCGAGA | 9063 |
rs560214911 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883543 | CTCCTCTCCACAAAT[-/A]AAAAAAAATCAAAGC | 9063 |
rs560231652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822252 | CAGTCATCTTGAGAG[C/T]ACATACATTGTTGAG | 9063 |
rs560275120 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873885 | CCCTCCTTGCCTTTC[C/T]CCCCCTACCGCCATT | 9063 |
rs560311965 | in-del | -/A | 0.377582 | 0.214995 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842278 | ATATGTTATGAATGC[-/A]AAAAAAAAAAAAAAA | 9063 |
rs560357517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892032 | CAGAAACCTACCCAG[A/G]AGAACTACCTGTGGT | 9063 |
rs560371508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891540 | AAAATCAAGTCAGAA[A/C]TGTGATCCAAAATGC | 9063 |
rs560388463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859782 | AAAGGAGAGGCACTG[A/T]AAAAGGTGTCTAGAG | 9063 |
rs560402868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867074 | TCAAATTGTACTTAC[A/G]TGTTGCACATACGCA | 9063 |
rs560425365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859139 | ATGACATAAAAGAAT[C/G]AATGAAGGGCCAGAC | 9063 |
rs560426763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857693 | CTCACTAAGGAGTTA[C/T]ACTTTATTCTGGCAA | 9063 |
rs560472195 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866664 | TGACAGCTAAAGTGA[C/T]GGCATTGAAAGGCAG | 9063 |
rs560510493 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843489 | ATGGGAGTTGGTTTT[A/T]TTTTTCAAACTCAAT | 9063 |
rs560517730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821563 | TATTTGCAATCTTTC[C/T]TGGGAATCATCTGAG | 9063 |
rs560538065 | in-del | -/CTGTAATTCCAG | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895546 | TGTGGTGTCTCGCAC[-/CTGTAATTCCAG]CTACTAGGGAGGCTG | 9063 |
rs560597935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879813 | AATCACAAGAAGACA[G/T]ATAATATGACACGTA | 9063 |
rs560602170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828825 | TATGTTATTATCTGT[A/C]ATGTATTTAGTTAAA | 9063 |
rs560614376 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897847 | AGTATTCTAAAAATT[C/T]TAGATAATACAAGGC | 9063 |
rs560622417 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921279 | ATTACAGGCACCCGC[C/T]ACCATGCCCAGCTAA | 9063 |
rs560639311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907093 | GAGATATCTGCCAAT[A/G]GAAAAGGGCAATGGA | 9063 |
rs560649381 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870888 | TCGATGGGTCAATAA[A/C]AATGCAGCTCACCAA | 9063 |
rs560701916 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913339 | CTTCTTAGCATGAAA[A/G]ACCCAAATCTGATCT | 9063 |
rs560730423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883565 | AATCAAAGCCTGGCA[C/G]AATGGCTCATGCATT | 9063 |
rs560788144 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876929 | ATGGTCTCGATCTCC[C/T]GACCTCATGATCCAC | 9063 |
rs560788155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871867 | CTAAAACTAGGTATA[A/G]GCCTACATGTCAGTC | 9063 |
rs560793074 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868935 | ACTCTCAGCAACGCA[C/G]GTGAAAAGGATCCTC | 9063 |
rs560796778 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824726 | GCTCACAGGCCAGGC[A/G]TGGTGGCTTATGCAT | 9063 |
rs560803280 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888928 | GAACCTGGAAATAAA[A/T]CCTCACATACATGGT | 9063 |
rs560807427 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918133 | CATGCTAAAAAGTCG[C/G]GGAAATCTGATAGCT | 9063 |
rs560826000 | in-del | -/AGG | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, cds-indel, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893458 | CTCAGAGGAATTTCT[-/AGG]AGGTCTCATATCTCA | 9063 |
rs560857383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898757 | TCAACACTTTGGGGG[A/G]CTGAGGCAGGTGGAT | 9063 |
rs560887538 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826187 | GTTAGTTTTTGTTTT[C/T]TTTTCAGCCTAAATG | 9063 |
rs560900023 | in-del | -/A | 0.484632 | 0.086302 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810188 | GTTCACAGAAAATAG[-/A]AAAAAAAAACAAAAA | 9063 |
rs560903217 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919028 | GTGTGTGTGTGTGTG[C/T]GTGTTGTGTATATAT | 9063 |
rs560943130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877492 | TGACCACCCATTCTG[C/T]AAACTGCCCCTCCCG | 9063 |
rs560943724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854019 | GAGTCACGTCAGTGA[C/T]GCAGTGTTGCTCAAG | 9063 |
rs560982323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861946 | TGATCATTGTACTAT[A/G]GTGATATAAGATTTA | 9063 |
rs560998750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839631 | GCACTTTGGGAGGCC[A/G]AGGAGGGTGGATCAC | 9063 |
rs561006962 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837460 | ATTAATCTTTTGTTA[C/T]CTATTTATAGGCACT | 9063 |
rs561010222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832672 | GAGGTGGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 9063 |
rs561015760 | snp | G/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892306 | TGCCAAAGTAATCCA[G/T]ATACACTGTCATAAC | 9063 |
rs561068322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861002 | ATAAAATAAAAGGCC[A/G]GGTGTGGTGGCTCAC | 9063 |
rs561186983 | snp | A/C | 0.460589 | 0.13473 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896165 | ATAAAAAGAAAAAAG[A/C]AAAAAAAAAAAAAAA | 9063 |
rs561208693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847857 | ATTACCGCAAGACTT[A/C]ACTCTGATTTTTCAG | 9063 |
rs561251773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903860 | AAACTATAGTGAATT[C/T]ATATCGTGGAAAACT | 9063 |
rs561255739 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840116 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTTCA | 9063 |
rs561267690 | snp | A/C | 0.000165265 | 0.00908873 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815270 | AGTATGACATAACCA[A/C]CAATCAAATACAAAT | 9063 |
rs561314006 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868422 | ACAGCTCTCCCTGCC[G/T]AAACTACCCTTCCCG | 9063 |
rs561320457 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837250 | AACATGCTTTGTTCC[A/C]CTCAACCTTTTCAAT | 9063 |
rs561325729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875376 | CTTACGTGGTCCCAC[C/T]CCATCAAATTGTAAG | 9063 |
rs561343330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850695 | CAGGGGATGTCAGCC[C/T]GATTCCTCTACCATG | 9063 |
rs561368799 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909924 | GTGATCCCAGCACTT[A/C/T]GGGAGGCCAAGGCGG | 9063 |
rs561368808 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917110 | GCCGGCTCGCCGCGG[C/G]CCAGGCCCGCCGCCC | 9063 |
rs561379895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857828 | TCTAGGAAGTTTTAC[A/C]TACTGGTCCATCAGA | 9063 |
rs561429771 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916418 | TAAAAAAAAAAAAAA[A/T]CAGGGTTTCTGTCCG | 9063 |
rs561480276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821232 | CTACTCTCCTCTCCC[A/C]TAATAGTCTTCATTT | 9063 |
rs561607561 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819345 | TAGACTTTGTATATA[-/C]TTTACAAATACTTTA | 9063 |
rs561622727 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811478 | AAATTAAATTTTGTT[A/G]TTACCACCTCCCAAA | 9063 |
rs561660268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865596 | CTACATGAAGATAAA[A/G]AAGATGCCAGTTGGA | 9063 |
rs561696322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834855 | GATGTTATGCCTGTT[G/T]GCATGAGAGTGAAAT | 9063 |
rs561696643 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921238 | AATTTAAGCAATTCT[C/G]TGCCTCAGCCTCCCA | 9063 |
rs561703337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907991 | GTGAGGTTAGCCACT[A/G]GGGAGGGGAATATTT | 9063 |
rs561728945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834163 | AACAACTGCACAACT[C/G]GAAAAAGGAATCACA | 9063 |
rs561757267 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907715 | TCAACCAAATGCAGA[C/T]CAAAAATATGGTATT | 9063 |
rs561766318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907238 | CAGTATGGAAAAGAC[A/G]GATGTCCCAATATAA | 9063 |
rs561855456 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810928 | GATAAAGCTTAGAGA[C/G]AGAAAGCTAAACAGA | 9063 |
rs561871304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879583 | TAAGAATTAAAAAAC[A/G]GAATCTTGAAGAGAT | 9063 |
rs561925363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871891 | GTCAGTCCAAACGGA[G/T]TTCTCACCTCATTAA | 9063 |
rs561938830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820463 | ACATATAAAAGATAT[A/C]CCAAGTATTAAGCCC | 9063 |
rs561971627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905505 | AATTAATGAAACAGG[A/G]AGGATACACTAAAGA | 9063 |
rs561980657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891375 | ATGACTATAAAATCT[A/G]TCACCAATGAATATA | 9063 |
rs561993306 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920743 | TTGTGATCATTTCTG[C/T]TCTGGTCTAGATTTA | 9063 |
rs561993761 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898672 | TTTTAAAATTTTGCA[A/G]GAGGTACATTAAAAA | 9063 |
rs562026358 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814111 | CAACAGGCTCTGTGC[A/G]TTGAATTCTTAGTAG | 9063 |
rs562032959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912771 | AAAAACAAACAAACA[A/G]AAATGGTTAAAAGCA | 9063 |
rs562041863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885440 | CAAGGAGAATTGCTT[C/G]AACTTGGGAGGCGGA | 9063 |
rs562055706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912188 | GGAAGTGAGGAAATA[C/T]AGTTGTCTCTCAGTA | 9063 |
rs562105610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884832 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 9063 |
rs562113757 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876613 | CTGCTCCCGATGGAA[C/T]CATAACAACAAAAGC | 9063 |
rs562150586 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848122 | TAATGCATACATTTT[C/T]CCACATGACACTCTC | 9063 |
rs562180662 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885520 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAGA | 9063 |
rs562186323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841982 | GCCTGTAATCCCATT[A/G]TTTTGGGAGGCCAAG | 9063 |
rs562199921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819064 | TAACAGGGCAAGTGA[C/T]TGGTAAATTGTGTCT | 9063 |
rs562222995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849013 | GGAAGATAATTCTGT[C/T]TGCTGGTATGTCCAC | 9063 |
rs562234616 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816990 | ATTTGTCTAGCCCTT[G/T]TAATACCTTCAGAGT | 9063 |
rs562253229 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907374 | AAAACCACTACACAT[C/T]CACCAGAGTGTCTAA | 9063 |
rs562264549 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856166 | GCCCGCCACCACGCC[C/T]GGCTAATTTTATTTT | 9063 |
rs562302618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855807 | GACTTGCTTAACTTC[C/T]AGCCACGTCTTTATG | 9063 |
rs562311757 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897091 | ATAACTCAAAAGTTT[A/G]CTTGAACAGGGGAAA | 9063 |
rs562399553 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809380 | ACCTCAGGCACGAAA[C/G]TATTTTCAGCACCAA | 9063 |
rs562436442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818294 | TGACAATATGGCACT[A/C]GCAATAATAAGGCAG | 9063 |
rs562439733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909710 | ATTCTTCTTAAATAC[C/G]AGCAATTCTATTCCT | 9063 |
rs562451607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882793 | AAGAAAGATTGTCAC[A/G]GTGCAAAACTCTAGG | 9063 |
rs562487190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839363 | TAGAGAATTAAATCT[G/T]GAAAAATCTATCATG | 9063 |
rs562548640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874595 | CCAAATGCCTTCCCA[C/T]TGCCTTACTGAGGGT | 9063 |
rs562549604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888822 | CTGCTGCTCACCTCC[C/T]GCTGCTCACCTCCCG | 9063 |
rs562563897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895308 | TAATACAGGAGAAGA[C/T]GAGAAGCTGCTGAGG | 9063 |
rs562579333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845907 | CCAGCTCTGCAATTA[A/C]CTTGGTGGTAAAACA | 9063 |
rs562658666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859924 | CAAGAAGTCAGTGTG[A/G]GGAACTGAGAGCATG | 9063 |
rs562667022 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853172 | GTCCCAGCTACTAAG[G/T]AGAGTGAGATGGGAG | 9063 |
rs562704159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852283 | TCTATAGGACTTTAC[A/G]GAGCTAGGGTAAAAA | 9063 |
rs562735188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860755 | ACAAAGGAGGGAAGA[C/T]CACTTGAGCACAGGT | 9063 |
rs562797628 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814706 | TCTCCCTTCACTTTT[A/C]TCATGCCTTCTCCTC | 9063 |
rs562811845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916201 | AGGATACGTTCTTTT[C/G]CTCACGTCCACTAAG | 9063 |
rs562820483 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840414 | GTCCATATTATTATA[A/G]AAAGTTTTAACTTTG | 9063 |
rs562831979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868160 | ACCCACACACTGCCC[C/T]TCCAAATTCCTGACC | 9063 |
rs562836421 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882783 | AAATACTGTTAAGAA[A/G]GATTGTCACGGTGCA | 9063 |
rs562850287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851182 | GGAACATAAATCCAT[C/G]AACTCAGAAATACAA | 9063 |
rs562890058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823054 | CCAGACTACGGAACA[C/T]AGGGAGACCTTGTAT | 9063 |
rs562910265 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900504 | GAGACCCAGGTTCTA[C/T]CAAAAAAAAAAAATT | 9063 |
rs562921887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836697 | TTCATTGACTGCCCT[A/G]TGATTTTTGAAAAAC | 9063 |
rs562923004 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900847 | GGCCCGGTGGCAGGC[A/G]CCTATAATCCCAGCT | 9063 |
rs562926904 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830327 | ATAAATTTAAAATAA[A/G]TGTATTTGAATTAAG | 9063 |
rs562931038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822384 | AATATGCTTGAGGCA[A/G]TAACATAAGCCTGGT | 9063 |
rs562979394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873487 | ATGGAGAAGCTCTTG[C/T]AGAAGTAGAGTCAGG | 9063 |
rs563010840 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921150 | TTTTGCTTTTTGGGA[C/T]GGAGTCTCGCTCTGT | 9063 |
rs563016574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870598 | TCCAGCCTGGGCAAC[A/G]GAGCAAGACTCCGTC | 9063 |
rs563039840 | snp | A/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922090 | AGGAATTAAAAAAAA[A/T]TTTTTCCTCACTTTT | 9063 |
rs563076067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887113 | ATAATTCTACTCATA[G/T]GACTTTGTACAAACA | 9063 |
rs563111172 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921327 | GAGATGGGGTTTCAC[C/T]GTCTTGGTCAGGCTA | 9063 |
rs563125660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877542 | CAAAACTACCCTTCC[C/T]GCCTTTGCCGCGCCC | 9063 |
rs563199379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900609 | CTGGGCCCAGGAGTT[C/T]GAGGCTGCAGTGAGC | 9063 |
rs563202425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843624 | CTATGTAAGGAGATA[C/T]AAAAGAAAAATTATT | 9063 |
rs563218761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892075 | CCCATCCTCATCACT[C/G]CCCCAACCCAGCCCG | 9063 |
rs563249825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848469 | TCACCAGCAATTTTA[A/C]GACACTTCTGGATTT | 9063 |
rs563287505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833961 | AAAGTTCCTTCCTCA[A/T]CCCCAATTTTCCTCC | 9063 |
rs563290315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864496 | CTAATGCAGGCTGGG[G/T]GCAGTGGCTCACACC | 9063 |
rs563296505 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904827 | ACTCTTGGGCTCAAG[A/T]GATCCTCCCACCTCA | 9063 |
rs563308674 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859554 | TGCCATTAAGGAAAC[A/G]AGTAATGCAGAAGGA | 9063 |
rs563320478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884689 | GTGAGGCCAAGGCAG[A/G]CAGATCACTTGAGGT | 9063 |
rs563352047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919880 | CCTTGATTTACACCT[C/T]AGTAGAATTTAACAT | 9063 |
rs563409762 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912879 | GCTTTCATTTAAAAA[A/G]TATGAGAAATGGAAA | 9063 |
rs563460087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889383 | GAGAACTCCTAAAAC[A/T]CAACAACAATAAAAC | 9063 |
rs563476955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816998 | AGCCCTTGTAATACC[G/T]TCAGAGTTTTGCATT | 9063 |
rs563484008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833316 | TTATGATTCCATTCA[C/T]ATAAAAGTCTAGAAA | 9063 |
rs563511951 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910282 | GTGAAGGTGGACATG[A/G]TTGCAGTGGATGTGA | 9063 |
rs563543192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884320 | TATTTATTTATTTTT[A/T]ATTTTTTTTTGAGAC | 9063 |
rs563564284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825309 | CAGGTGGCAGCCACT[C/G]TAACACAGAAAATAT | 9063 |
rs563569822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841092 | CAGACTGAAAATCAC[C/T]AGCTGAAATCACCAA | 9063 |
rs563583170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886594 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCG | 9063 |
rs563601451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824627 | TCTCTAGGTGAGATA[C/T]TTTTTGCTTTCTTCT | 9063 |
rs563659208 | in-del | -/TA | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820259 | ATGCCAGCATATTGT[-/TA]TAATTGTTCTATTTT | 9063 |
rs563701994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866669 | GCTAAAGTGATGGCA[C/T]TGAAAGGCAGGATTT | 9063 |
rs563702464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910610 | ATAGAAGAACTCTTA[C/T]AAATTAAAGATAACT | 9063 |
rs563705034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896410 | TATTGTCTTGCCCTC[C/T]CTCCACATCCAAAAA | 9063 |
rs563792567 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839254 | AATAAGACCAATCTA[C/T]ACATACTAATATACT | 9063 |
rs563812243 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917168 | CCCGCTCCCCTCCCC[C/G]GCGCCCTCGGCGCCC | 9063 |
rs563837954 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862424 | TCTTACTATCATCTC[-/AA]AGAGTGTTCTAATTA | 9063 |
rs563841493 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850037 | AACACCTTGTCTTTC[A/G]ATTCAGATCTCCCAG | 9063 |
rs563844313 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854651 | AGACAGGCTGCATGC[A/G]TTTACATTGTATACA | 9063 |
rs563900370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869971 | ACCTCTACCCCAAAA[A/C]AATCCACCAATGTAT | 9063 |
rs563953365 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811766 | AATCCCAGAACTTCA[C/T]ACAGCACTCATTAGC | 9063 |
rs563954599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851252 | GCTGCACCAAAGGAA[A/C]TACTTGGAGATTGCT | 9063 |
rs563963414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822130 | ATATCAGTAATGAGA[A/G]ATGATGACAAATTGC | 9063 |
rs563991992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821394 | AATATGTATGTAATA[C/T]GTATATGGGTATCAG | 9063 |
rs564007445 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885815 | ACCAAAATGCAGGGA[A/G]TTTAGTTACTCTTCT | 9063 |
rs564020623 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921723 | ACTTCATTAAGAAAC[A/G]TAATTAAGAACCATA | 9063 |
rs564042225 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858883 | CTGAAGAGATGGCCA[C/T]GCTACTCACCAGGAC | 9063 |
rs564045506 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921263 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCACCCGC | 9063 |
rs564095983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914779 | GCCAAATATGTGGCA[A/T]CCAGATCGGCTGACC | 9063 |
rs564188822 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856084 | GATCTTGGCTCACTG[C/T]AAGCTCCGCCTCCCG | 9063 |
rs564198066 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891996 | AAGAGGAAGAACACC[C/T]GGAGCTGACCAAAGC | 9063 |
rs564259017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857947 | GGTTGCAAATGCAAG[C/T]AGTGAAATAAATGCA | 9063 |
rs564260487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891449 | TGTTACAGAATTATC[A/G]CCAATTAACCAAACA | 9063 |
rs564270046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866392 | GGTATCTTTAAAGTG[C/G]TGAAAGAACAAACTC | 9063 |
rs564282604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865673 | AAATATTAATTCCCT[A/C]GCTAAAATATTCTTT | 9063 |
rs564302235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835608 | AAAACATTTTCAAGT[C/T]GTACAAGTATCTTTA | 9063 |
rs564308736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879692 | AAATGAATAAAACAC[C/T]ATGTATACATACAAT | 9063 |
rs564318618 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891748 | GCAGTCATCAATCTT[A/G]AAGGGCAACATTTCC | 9063 |
rs564336470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907501 | ATGAATCTGGCAAAC[C/G]AAACAGAAAAAAAGG | 9063 |
rs564372033 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910049 | TAATCCCGGCTACTC[A/G]GGAGGCTGAGGCAGT | 9063 |
rs564446097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905610 | AGAAAAAAAGAAGGC[A/G]TTTTAAAAAAAGACA | 9063 |
rs564481913 | snp | C/T | 5.04664e-05 | 0.00502301 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828122 | AAGGCTTACTGAGGA[C/T]GCTTGAACCTGCATG | 9063 |
rs564539315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843399 | TTCCCCTCCAATTCA[C/T]TCACTGCTCCTGACC | 9063 |
rs564554806 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856933 | CAGTCCCAAGCTGCA[C/T]AACATTGTGCAAATC | 9063 |
rs564562063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820378 | ATATAGGGTTCTGTA[A/G]TATCTGTGGTTTCAG | 9063 |
rs564562819 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874755 | TAGTCTGTCTTCCAC[C/T]TTCTCTTCCCTCAGA | 9063 |
rs564574359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842673 | TTTTAACATGAGAGC[A/G]AAGAAAAGTATAATA | 9063 |
rs564633509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913421 | CCAGTATCTATTGAT[A/T]AAGTTATCATCGCTG | 9063 |
rs564659484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864921 | TGTTTTTTGTTTATT[A/T]TTCTTTGTTGTATTT | 9063 |
rs564662813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849812 | ATTATCAACATGTTG[C/T]CATTCTTGTTTCAAA | 9063 |
rs564701269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849075 | AGGGTCTGTCAGAAG[G/T]ATAGAAATAACTCAT | 9063 |
rs564702174 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824787 | ACAGGTGGATGGCTT[C/G]AGCTCAGGAGTTCGA | 9063 |
rs564715459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888850 | CCGCTGTGCGACCTG[G/T]TTTCTAACAGGCTGT | 9063 |
rs564745004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903866 | TAGTGAATTCATATC[A/G]TGGAAAACTATTCAG | 9063 |
rs564768660 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810637 | GGATAATCCATTGAA[C/T]AAGGAGACAATGTAG | 9063 |
rs564776642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876042 | CCTAAAGGGATGCAG[C/T]GAGTTTAAGCCATTC | 9063 |
rs564777869 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891178 | TGTGCTAGTAACAGC[A/T]TTTCACATACCACTT | 9063 |
rs564790626 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894926 | AAATACAAAAAAATT[A/T]GCCAGGCATGGTGGC | 9063 |
rs564793047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883013 | AGGAAAAAAAAAATC[A/G]CTTGAACCCGGGAAG | 9063 |
rs564829420 | in-del | -/A | 0.460813 | 0.134379 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884915 | GAGCAAATCTGTCTC[-/A]AAAAAAAAAAAAACT | 9063 |
rs564863464 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869133 | GGTCACCTCATATGG[C/T]TTATGGCAGATTCCT | 9063 |
rs564872896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832613 | AAAGATTAACTGGCC[A/G]GATGTGGTGACTCAT | 9063 |
rs564884713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876895 | TTAGTAGAGATGGGG[C/T]TTCACCGTGTTAGCC | 9063 |
rs564893045 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872770 | TTTGGGATTAGTTGG[A/G]TATTGCTGACTATGG | 9063 |
rs564942261 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839971 | CTCGAGACCAGCCTG[A/T]CCAACATGGTGAAAC | 9063 |
rs564943476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883465 | CCCAGCACTTTGGGG[G/T]GCCGGGGCAGAAGGA | 9063 |
rs564948564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868276 | AACTTCCTTGTCCCT[C/T]CTCCTAAGCTATCTG | 9063 |
rs564973674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839507 | TTTTCTTTAAAATAA[C/T]GTTCTAACTCAGCCT | 9063 |
rs565011909 | snp | A/G | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875293 | TTTGGTGGACCACCC[A/G]ATATGGAGGATGGAC | 9063 |
rs565023979 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912940 | TCCACCCGCCCCAGG[C/T]TCCCAAAATGCTGAG | 9063 |
rs565038769 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918103 | GAGAAGTGAAATAAG[A/G]GCGCTCAGAAGGGCC | 9063 |
rs565051500 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833751 | AATAGTTTCGTATTG[G/T]CCCAGTAATACTTTG | 9063 |
rs565086141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860836 | ATAAAAATTAGCCAG[C/G]TGTGGTGTTGTACAC | 9063 |
rs565103379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846157 | TATCTCAAAATTGAC[A/G]TAATTTATTATAAGA | 9063 |
rs565124217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874674 | ATACGGGTTGCCTTA[C/T]TTACACTCCACTGCT | 9063 |
rs565141910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902875 | GTAGACACATAGATC[A/G]AGCAAAGAGAATACA | 9063 |
rs565204141 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868607 | GAACCAGAGATTAAC[C/T]GTGTTAGGGATAAAA | 9063 |
rs565225972 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830241 | AAAATAATTTATAAA[A/C]TTTAACTTCGAGAAA | 9063 |
rs565243526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836971 | CTACTGCACACAAAT[C/T]GGTATATAAAAAGCT | 9063 |
rs565273745 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823105 | CCACATATGCTGAAG[C/T]ATGCCTAAGGTCCTA | 9063 |
rs565293462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46815031 | AGCCACCCAGCACTG[C/T]TTCTATTCATTCTAA | 9063 |
rs565331255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858827 | GCAGGATAAGGGAAG[A/G]GGAGTTTCTAGGAGG | 9063 |
rs565332263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823779 | AAATTCAACTTTACA[C/T]AGAATGGCTTAAAGT | 9063 |
rs565383486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915630 | GAGAAAAAAAAGCTT[C/T]TTTGGTTTCTATCAC | 9063 |
rs565386234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881224 | TCCTATCTCTGAACG[A/T]CCCCAGGCTCTTTCC | 9063 |
rs565400401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887191 | TAATAAAGAGATAAA[A/G]TGCAATACTCCACTT | 9063 |
rs565417301 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831083 | GTGGGAAAACAAAAG[C/G]CATCCACGTTAGAAA | 9063 |
rs565539574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870676 | TTAGATGACCCATGT[C/G]GGGTAGCAGATCAAA | 9063 |
rs565594180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886817 | CCCTCCATCCTGGGC[A/G]ACAGAACAAGACTCT | 9063 |
rs565594826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906526 | AGCAAAGTATAATTA[C/T]AAAAAGTTAATATTT | 9063 |
rs565602980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870338 | AAGGAACTCAAGACC[A/G]GGTGCAGTGGCTCAA | 9063 |
rs565659486 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882899 | TTTTAAGAGACCAGC[A/C]TGGACAACATGGTGA | 9063 |
rs565677538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841492 | AACTGATAATAGGAC[G/T]TACTCTTTCTCAAAC | 9063 |
rs565697658 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819868 | AATTTTGTAATATGG[A/C]CTTGGTTGCAGAAGT | 9063 |
rs565727735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832817 | GAATCACTTGAACCT[G/T]GGGGGTGGGGGCTGC | 9063 |
rs565758940 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901277 | CAAAATTAGCCATGG[A/C]ACATGCCTGTACTCC | 9063 |
rs565766157 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832436 | AAACAAACAAACAAA[A/C]AAACAAAAAAAAGTG | 9063 |
rs565772942 | in-del | -/TCCTGAGGGGCC | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886211 | TGTGCTTAGCCACAT[-/TCCTGAGGGGCC]TCATGAAGCAGGGCT | 9063 |
rs565792484 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855901 | TCAAACTTGGTAACA[C/T]GCAAGGAAGCAGCCT | 9063 |
rs565822102 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809691 | ACCCTGTAGGTGGAG[G/T]TTGCGGTGAGCCAAG | 9063 |
rs565844495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912417 | TGACAAGGAAAAAAG[A/T]CTGTACATGTTCAGT | 9063 |
rs565853005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839746 | GGTGGGCACCTGTAA[G/T]CCCAGCTACTCGGGA | 9063 |
rs565862200 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808934 | TTAAAATACAAACAA[A/G]CGTCAACTAATGAAT | 9063 |
rs565890311 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850447 | TGACCTGAAGAATGA[A/C]TTCGCATTCTAGATT | 9063 |
rs565933566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817699 | CAAGCATTACAAGGG[C/T]GCTGTCTATATAAAA | 9063 |
rs565956172 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861037 | GTAATCCCAACACTT[C/T]GGGAGGCCGAGGCAG | 9063 |
rs565967796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825915 | TGGGATAAACTCTAG[C/T]TGGTCACAGATGTCA | 9063 |
rs565994162 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828750 | AATCACGTAGGTTCT[C/T]TCTACCCACAAAGAC | 9063 |
rs566043601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877050 | ATGGAAAGGACTTAT[A/G]TCCTCAATCCTTACT | 9063 |
rs566095061 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909138 | AACTAGTACAAACAT[A/G]GGCAAAAGACATGAA | 9063 |
rs566114758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830004 | TATTGCAATACTTTA[C/T]ACTTTACAACAATTA | 9063 |
rs566129526 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881580 | CAATCCAAAGTAGGC[A/G]CATTCATCCTTCAAA | 9063 |
rs566191493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889050 | ACAAAAGAACAAAGC[C/T]GGACACTCACCTAAT | 9063 |
rs566195637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896532 | AAAAGCCAGGGAGTA[A/C]AATACATACGTGTTA | 9063 |
rs566204153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837113 | ATTTTTATATTTATA[A/G]TATTTATAATTCCTA | 9063 |
rs566264320 | in-del | -/T/TT | 0.259287 | 0.270905 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834022 | TACACTTAATATACT[-/T/TT]TTTTTTTTTTTACCA | 9063 |
rs566267359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853587 | ACGAGGTCAGGAGTT[C/T]GAGACCAGCCTGCCC | 9063 |
rs566322828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874333 | CCTTTTCAAGTGCAG[C/G]CACCAGTAATGTAGT | 9063 |
rs566325788 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841258 | ACTTTTCAGACTCAC[A/G]TCCACTGCAAATCAC | 9063 |
rs566355208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903422 | GAGACATGTCATGGA[G/T]TGGGATATACAGATG | 9063 |
rs566461779 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826652 | AGATGTACCAACCAA[C/T]TTGTCTCAAAGGAGC | 9063 |
rs566472146 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873690 | ATAGCAAAGGCCAAG[A/T]CCTTGTCCACAAAGA | 9063 |
rs566473913 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811839 | GTAACACGAATGCCA[G/T]TTTTCTTTGATGCAA | 9063 |
rs566509150 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46811133 | GGTTCCCTGGAGTGT[C/T]TGGGGTAGCATGGAT | 9063 |
rs566515117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880041 | AATATTAATATACTT[C/T]ATGCCACTGGATTTT | 9063 |
rs566528333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886859 | CCAAAAAAAAACAAA[C/T]AAAATCGAATAAAAT | 9063 |
rs566548319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843997 | ACTTACTTTTATAGG[A/C]AAGTTAATCATTTAT | 9063 |
rs566565596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832209 | ATCACGAGGTCGGGA[G/T]TTCGAGACCAGCCTG | 9063 |
rs566576373 | in-del | -/AA | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812356 | TAAAAAAAAAAAAAA[-/AA]GAACGTTTCCACAGA | 9063 |
rs566601843 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913819 | CTTCTACAGACTAGT[A/T]TGAGACAGGGTCTCC | 9063 |
rs566655357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907590 | ACATATAGTTGAATA[C/T]TGAATAACAATAACA | 9063 |
rs566699527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892340 | ACTTTGTGTACTATA[C/T]ATGTCTCTATATTTC | 9063 |
rs566759992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899189 | AAACATATAATATGG[C/T]AGGTCATGATGAATA | 9063 |
rs566778907 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885062 | GTTAACAGTAGAACC[A/T]TAGCTACAGAGCACT | 9063 |
rs566795658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858029 | CATTAAAGCAAATCT[A/G]GAAAGGCATCACAGG | 9063 |
rs566817001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872185 | TCATGCTGACTAGTG[C/T]AAGGCCCCAGAGCTA | 9063 |
rs566819074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820665 | ACCAAGAAGAAGTCT[C/G]TAAGTACAAATTCTT | 9063 |
rs566822460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906947 | GTGAGAACTTAACAA[C/G]TGAATATAATATTAA | 9063 |
rs566823777 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864398 | GGAAGTACTAAACTG[A/C]ATTCATCTTGGAATC | 9063 |
rs566836082 | snp | C/T | 1.80837e-05 | 0.00300691 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891083 | AAAAAAAACATAAGC[C/T]AAGTCACCCTCAAGC | 9063 |
rs566861147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865760 | CATATTTTTTCAGAA[C/T]GCTTTAAAAAGGAGG | 9063 |
rs566875118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865297 | GTAATCCCAGCACTC[G/T]GGGAGGCCGAGGCAG | 9063 |
rs566896761 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867033 | ATAGTCATGTTGTAC[A/G]TGTATGTTCAACATG | 9063 |
rs566898016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911511 | GTGAGCCACTGTGCC[C/T]GGCTGACTTTGTTAT | 9063 |
rs566898093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903515 | CTCACTGAGATATCA[C/T]TAGATACCTACCAGA | 9063 |
rs566928322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879225 | ACAGCTAAAAACAAC[A/T]CAATTCAAAAATGGA | 9063 |
rs566983587 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916180 | AACAATCTCCGTTTA[A/G]AGCAGAGGATACGTT | 9063 |
rs567033723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871676 | TTCCTGTTTGTTTCC[C/G]TTTACCTAATGTCCC | 9063 |
rs567037822 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827498 | AAAACCTGAAAATGA[C/T]CCTGTAATATAGGCG | 9063 |
rs567096465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878690 | CCTGGCCAACATGGC[A/G]AAACCCCGTCTCTAA | 9063 |
rs567141875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834315 | GAATGGAGAACAAAG[A/G]TCACAATAAATACAA | 9063 |
rs567159718 | in-del | -/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892496 | AACTAATTTAGGCCA[-/G]GAACAGTGGCTCACA | 9063 |
rs567164938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883077 | CACTGCAGCCTGGGC[A/G]ACAGAGGGAGACTCC | 9063 |
rs567168816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817303 | AAGCCACTCAAAAAT[A/G]CTCATTTTCTAAATG | 9063 |
rs567170832 | snp | A/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920110 | TCTGCCCCTTCCTCA[A/G]TGTGTAGCAGCTCCT | 9063 |
rs567193296 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824362 | ATCAATCTGGAGACA[C/T]ATAGATTTATCCTTA | 9063 |
rs567228690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854338 | TTCCCCATTTCCTCA[A/G]TAGTTGCGAAGAGTG | 9063 |
rs567231636 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851299 | CACATATCCTCTCTA[C/G]TCTTTGGGATCTTTA | 9063 |
rs567238812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888404 | AAACTCATTCTAAAA[C/T]TCACGTGGAATCTCA | 9063 |
rs567274480 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807898 | AGTATAAATTAACAT[A/G]CCCATGTGGAAAAGT | 9063 |
rs567309045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916884 | TCCTAAACGCAACTT[C/T]AGCTTTCAGAAAACA | 9063 |
rs567313659 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922074 | TCAAGGAAACTGAAC[A/G]AGGAATTAAAAAAAA | 9063 |
rs567314865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862255 | AGAATCGCCTGAAAC[C/T]GGGAGGTGGAGGTTG | 9063 |
rs567322043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869466 | AGAAGGGAAGGCAAG[A/C]AATCTCTAATATAAG | 9063 |
rs567328694 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893175 | CTCATGCATTAAACA[A/G]AAGACAACAGCTTCT | 9063 |
rs567329683 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868791 | CTTGGGGGCTCATCC[A/G]CGATTGCCTTTCTCA | 9063 |
rs567331578 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824169 | ATATAGCAAATATTA[A/C/G]TATTCCGGATTATAT | 9063 |
rs567353802 | snp | A/G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888961 | AATACTTTTTGACAA[A/G/T]GGTGCTAAGATCATT | 9063 |
rs567355817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887652 | ATGTCAAACTCCCTG[C/T]GCCACTTTAGAAATA | 9063 |
rs567396597 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863849 | TTGGAGACAAGGCCT[C/T]TAAGGAGGAAATTAA | 9063 |
rs567403431 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917387 | CGCTGCCGCCGCACC[C/T]ACTCCCGCTGCCGCC | 9063 |
rs567414136 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824858 | AAAAAAAAAAACACA[A/C]AAAAATTAGCTGGGG | 9063 |
rs567436178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876283 | GACCCTCACGTTTAT[A/T]TAGATGCCACTGGAG | 9063 |
rs567451194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832319 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATTGCTTG | 9063 |
rs567479684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860179 | ACTTTAAAAACCACT[C/T]ATGTTTGGGTTCAAT | 9063 |
rs567537279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831562 | TTGAAAAAGAAGAAC[A/G]AAGTTGGAAGAGTCA | 9063 |
rs567566512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859345 | CGGCAGGAGAATGGC[A/G]TGAACTCGGGAGTCA | 9063 |
rs567585949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845379 | CCTTTGAGTAAATCA[C/T]GCAAATGAACCAGGT | 9063 |
rs567644831 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915788 | CTGGAAAGTTTTCAT[C/T]AACAAAAAAAAAAAA | 9063 |
rs567658240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838142 | GTAATTTCTAATTCC[C/T]CTAAAATGAACACCT | 9063 |
rs567664960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901339 | GCTTGAACCTGGGAG[G/T]CGGACGTTGTGGTGA | 9063 |
rs567675012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852786 | ACATCTGTAGCCACC[A/G]TATTTTCCATAGCAA | 9063 |
rs567686794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885583 | GACATACAGCTACTG[A/G]TTTCAAAATCCCAAG | 9063 |
rs567749587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850084 | TTTCCTGTTATCCTT[G/T]TATTGTTGAAAATTT | 9063 |
rs567751422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885205 | AAAACAATATACTAA[C/T]GTATCTTCTTAAATA | 9063 |
rs567820523 | snp | C/G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914199 | ACACATTATTGTAAC[C/G/T]ATCTTTGAGCACACA | 9063 |
rs567833580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909390 | TAGCTGGGACTACAG[C/G]TGTGGGCCACTATGC | 9063 |
rs567834128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857243 | ATTCATATCAAGACA[C/T]ATTTCATATTCTGGG | 9063 |
rs567870349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856526 | GAGAATCTAATGGTC[C/T]CATGTAAAATATATT | 9063 |
rs567907840 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823256 | GTACATTTAACCTAT[A/C/T]GTGTTTTTTTTTTCT | 9063 |
rs567911309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822683 | ACGAACAGGACATCA[G/T]CAAAAGTTTTTCAAA | 9063 |
rs567958203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855923 | AAGCAGCCTAAGTTC[A/G]GAAAGAGTTTTAATC | 9063 |
rs568000438 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891609 | ACAACATAATAAAGA[C/T]ATTTTAAAATATTAA | 9063 |
rs568008294 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915102 | AAAGTAGTGTAGCCC[A/C/G]GGCTCTGAAAAGCCC | 9063 |
rs568017186 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875694 | TAAGGCAGACTATAG[C/T]TCTAGAGACAGGATA | 9063 |
rs568059156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827144 | CTCAGTAAAGCCATT[A/G]GAAAACCAAGTGGAC | 9063 |
rs568100256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826586 | AAAATACATTTTGAA[C/T]GTAACCATTTCAAAA | 9063 |
rs568147076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891174 | GGCATGTGCTAGTAA[C/T]AGCATTTCACATACC | 9063 |
rs568166776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864706 | ACCCAGAAGGTGGAG[G/T]TTGCAGTGAGCCAAG | 9063 |
rs568170329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906579 | TGTTAGAAATAAATC[C/T]AACAAAATATTTGCA | 9063 |
rs568183527 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810197 | AAAATAGAAAAAAAA[A/C]CAAAAAAACAAATCA | 9063 |
rs568190968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833510 | AATTGTACATTTTAC[A/G]TGAGTAGTTCTTATG | 9063 |
rs568222410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819552 | CAAGTGGCAAAATTA[C/T]ACCGAGCCAATTATC | 9063 |
rs568227237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832834 | GGGGTGGGGGCTGCA[A/G]TGAGCCAAGATGGTG | 9063 |
rs568287353 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911239 | TTTTTTTCCTGAGAC[A/G]AAGCCTTGCTTTGTC | 9063 |
rs568303980 | snp | C/G | 0.00372559 | 0.042999 | utr-variant-5-prime, intron-variant, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920108 | ATTCTGCCCCTTCCT[C/G]AATGTGTAGCAGCTC | 9063 |
rs568304975 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809706 | GTTGCGGTGAGCCAA[G/T]ATCGCACCATTGCAC | 9063 |
rs568311087 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901183 | AGCACTTTGGGAGGC[C/G]AAGGCGGGCGGATCA | 9063 |
rs568325626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863959 | CTAGCACAGAGAAAA[C/G]GCCATCTGAGACGTG | 9063 |
rs568348029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905139 | TTTAATAGTCTAAAC[A/G]TATTTCAAAGAGTTG | 9063 |
rs568395964 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919347 | CAAAATTAGCCAGGC[A/C/G]TGGTGGCGCATTCCT | 9063 |
rs568411137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912556 | TAGGTCAATAAACAG[A/G]AATTTATAATAAAAA | 9063 |
rs568424114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904183 | TGGTTGTGATACTGT[A/G]CTATGGTCTTTAAGA | 9063 |
rs568469331 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841306 | AAATGTAATAAACAT[G/T]TATTCTATCACCCTA | 9063 |
rs568523823 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877195 | CTCCCCACCACCTTA[C/T]TCAGATAAGCTCCTA | 9063 |
rs568545208 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872901 | AGGAGCTAAAACACC[C/T]ACTCATCACTGCCCC | 9063 |
rs568556740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848692 | ATCATTAAAAACGTT[A/T]GAGCAGGGGAATAAA | 9063 |
rs568581617 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875334 | CCTTCTTCAAACAAG[G/T]TGCAAGGACTGAAAC | 9063 |
rs568590280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883798 | AGTGAGCCAAGATTG[C/T]ACACTCTAACCTGGG | 9063 |
rs568634972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840512 | AGGGATTGTTTTTGT[A/C]GTTTTCTTCTATGCT | 9063 |
rs568635121 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895739 | ACTGCCAGATTAACA[A/T]AATCCCTCAAAAAAG | 9063 |
rs568669909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848021 | AGAAAATACTATGTA[C/T]ATATGGCAAAGAAAT | 9063 |
rs568671846 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889543 | TACCACCTGACACCC[A/G]TTATAATGGCCACTA | 9063 |
rs568680858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847544 | TGGAGTACAGTGGCG[C/T]GAACTTGGCTCACTG | 9063 |
rs568738487 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823718 | AAAGCTAAACTACTT[-/A]AGTGTTGGTTAATTC | 9063 |
rs568819048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900768 | ATCACGAGGTCAGGC[A/G]TTCAAGACCAGCCTG | 9063 |
rs568882767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900161 | CTTGAGGTTAGGAGT[G/T]CATGACCAGCCTGGC | 9063 |
rs568919524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874872 | GAAAGAAGGAAAACG[C/T]GAACCAGCTTGGGAA | 9063 |
rs568941882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837966 | GATAGGAGAATGAAT[A/G]GACATGGACTGGAAA | 9063 |
rs568987032 | snp | C/T | 0.000372377 | 0.01364 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844693 | TATGCTCAATCTTTT[C/T]TTTTTTTTTTAAATG | 9063 |
rs568989186 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886946 | TTTCATCTAAAAATC[A/C]CAGAGATCTGTTTTC | 9063 |
rs568992332 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807998 | CTAAGAAAATAATTT[A/G]TACACAAAGACATTC | 9063 |
rs568994253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907726 | CAGATCAAAAATATG[G/T]TATTTGCAGGACGTG | 9063 |
rs569050703 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, splice-donor-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893430 | CACAAAGTCATCCTA[C/T]CTAAGCTTGACTCTC | 9063 |
rs569068124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845197 | TCTTGCTAACCAAAA[C/T]CATTCTGCTTTTATC | 9063 |
rs569091679 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834146 | GAAGCAATGTATGAC[A/G]GAACAACTGCACAAC | 9063 |
rs569165356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879367 | AATGCCACCTCACAC[A/C]CATCAGGATGGTCAC | 9063 |
rs569192595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851632 | CTTGCACCAAGGGAA[C/T]CTGGAAAATGAATGC | 9063 |
rs569195360 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875074 | CCCTTTTCTTTCCAA[C/G]AGAAGGTCACCTTGT | 9063 |
rs569228596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885654 | GCGCCACTGCACTCC[A/T]GCCTGGGTGACAGAG | 9063 |
rs569230102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850935 | TTAGTGCAACCTCCA[A/G]TGGCTTTAGTATAAT | 9063 |
rs569279226 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904925 | GTTTAAAAATCGATA[G/T]AACTACAAAGAAAAA | 9063 |
rs569281186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896837 | CAGTGTAATCTACCA[A/T]TATAAGAATGGTTTA | 9063 |
rs569315507 | snp | A/C | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858158 | CATAGTTAACCTAGG[A/C]AACACAAATGGGAAA | 9063 |
rs569419714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867439 | TTCCATAAAGTGAAT[C/T]TGTTAGCTAAATGGT | 9063 |
rs569451193 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921151 | TTTGCTTTTTGGGAC[A/G]GAGTCTCGCTCTGTT | 9063 |
rs569458558 | in-del | -/AATA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834921 | GGGAGGCATCTTAAT[-/AATA]AATAGTAAAAGTCTT | 9063 |
rs569459954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828955 | GGTTTAGTGTCAATC[A/G]CAGAGGAATAATTAA | 9063 |
rs569502987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46835930 | GCTTAAAGTTTGGAC[C/T]CCAGAGTCAGAAATA | 9063 |
rs569505362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855836 | TGGCAATTTTAAGGT[A/G]CCTTCAATGCACAGG | 9063 |
rs569507882 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892676 | CCACTCAGGAGACTG[A/G]GGCGAGAGGATCACT | 9063 |
rs569541866 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870119 | GTGCCCTCCCTAACC[A/G]CACGTCTGAGTCTAT | 9063 |
rs569544681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828458 | CTGCAGGTCAGCAGT[C/T]GTTTTACAGAAAGAC | 9063 |
rs569561628 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869657 | GTCCCTTAGGTCTCA[A/C/T]GTTAACATACTGGAG | 9063 |
rs569574057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876430 | ATTACAACCAGCAAC[A/G]ATTTGTTAACTATAT | 9063 |
rs569574980 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809554 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 9063 |
rs569672099 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880411 | AACAAAACAAAACAA[C/T]TGGGCAGGGCAAGGT | 9063 |
rs569674229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855220 | TACCCTAGTGGAAAA[C/T]AGTATTTAATCTGGA | 9063 |
rs569802041 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918215 | GGCCCCCCCGTAATG[G/T]GCTGATATAGGATGA | 9063 |
rs569811406 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855199 | TTTATCCAAGAAGCC[A/T]TGGGTTACCCTAGTG | 9063 |
rs569813255 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883631 | CTCTCTTGACCCCAG[A/G]AGTTCAAGACCAGCC | 9063 |
rs569860500 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908655 | AGATTCAAAAGCACT[A/G]TCCATAAAGAAAAGC | 9063 |
rs569871206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853461 | CTCCAAGTAGGGCTG[C/T]TTCTTCCCTTGGTTC | 9063 |
rs569936044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832401 | AGCCTGGGCGACAGA[A/G]CGAAACTCCATCTCA | 9063 |
rs569940452 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822032 | TACTGGTCTTATGGT[C/T]GATGGTGGGAACCAT | 9063 |
rs569957127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883098 | GGGAGACTCCGTCTC[A/G]AAAGAAAAAAAAAAA | 9063 |
rs569976642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815446 | TCACAAAACATTTGT[C/G]GTAAGTGCTTACCAC | 9063 |
rs570068624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888969 | TTGACAAGGGTGCTA[A/G]GATCATTCAGTGAGG | 9063 |
rs570158099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895588 | AGGCAGGAGAAATGC[C/T]TGAACCCGGGAAGTG | 9063 |
rs570191989 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821619 | CCAACTTGATGGCAA[C/T]AGGCCACAATCAGAA | 9063 |
rs570201658 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848767 | TGAAAGAGAGAGACA[A/G]TGTGTGTGTGTGTGT | 9063 |
rs570207472 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811682 | TTACTAAAAACATAA[C/T]AACACACTTTATGTC | 9063 |
rs570226744 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843175 | CAAAATGAAGACAAC[A/T]CCTCCACACAGGTTT | 9063 |
rs570232576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860389 | TTTTTTTGGAAAGTA[C/G]TGTTACAAAATAAAG | 9063 |
rs570263894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850178 | CTTACCCATGAACAA[C/T]CTTTACCTACTCTAC | 9063 |
rs570272757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861132 | TAAAAATACAAAAAT[C/T]AGCCAGGCATGGTGA | 9063 |
rs570300835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868561 | AGTGTAGATTGTGCC[A/G]TCTGACTCCAGCCAA | 9063 |
rs570302618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814436 | ATACATAGACACTTT[C/T]ACTAGGTACCTTCGT | 9063 |
rs570347255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836053 | TCAAGAAATTCTAGG[C/T]AAGCAAAATGACATC | 9063 |
rs570365282 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46811019 | AAACTGGATGAAAAT[A/G]TTTCTCTAAGAGTAA | 9063 |
rs570372956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916523 | CTTTAAAGGTTATCA[C/G]TCTGGGGGGAAAAAG | 9063 |
rs570387069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886448 | AAACAAATTAGGGAA[A/G]TACGTTAACCAGATA | 9063 |
rs570406353 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909537 | ACAGGCGTGAGCTAC[C/G]ATGCCCAACCGATAA | 9063 |
rs570451762 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810298 | TTTACTTTATAAAAC[C/T]TTGTTGATTAAATTG | 9063 |
rs570488399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819611 | AACAGGATAAGCATT[A/G]TGCTTAAAATAAAGA | 9063 |
rs570559024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892279 | TTACTAAAATGCAAA[C/T]AGATTTAAATATGCC | 9063 |
rs570577656 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46891694 | ATTCCCAGCTGGGTA[G/T]CCAAATGAGAAAAAG | 9063 |
rs570579286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899994 | GGTGCATTTTGGGAG[G/T]CCAAGTGGGCAGATC | 9063 |
rs570594774 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920215 | TATGTCATTCTGGCC[A/G]CAGTATTAGATCACA | 9063 |
rs570627141 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865263 | GGCAAAATGAGGCCG[C/G]GCACAGTGGCTCACA | 9063 |
rs570651806 | in-del | -/TG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901618 | ACTGTGTCTTATCTC[-/TG]TATTTGTTTTGAGAT | 9063 |
rs570660659 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880292 | GGTCCCAGCTACTTA[C/G]GAGGATCACTTAAGC | 9063 |
rs570660910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913645 | TAGATTAACCAGGTT[A/T]AAGTGTAGCAGGGAC | 9063 |
rs570686478 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904766 | TCTCAAAAAAAAAAA[A/C]AAAACAGAGATGGGG | 9063 |
rs570688529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899023 | AGCTTTGAATAAATT[A/G]AACAGACTGTATCAT | 9063 |
rs570693778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877714 | AACCAGGGAATAACC[A/G]CGTTAGGGATAAAAA | 9063 |
rs570728287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849539 | CTGGACAGCACCAGC[A/G]GAACACTTTGTGGTA | 9063 |
rs570729875 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905820 | AATAGTAATAATTTT[A/T]TAAGCAAGTTCTACT | 9063 |
rs570793435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913213 | TTCCCATTCTCCTGC[C/T]GCATCCTAACAGCAC | 9063 |
rs570810170 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864731 | GCCAAGATTGCACCA[C/T]TGCACTCCAGCCTGG | 9063 |
rs570878637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884985 | ACATCAGGATGGTTA[C/T]TTAAGGAAAGAAAAT | 9063 |
rs570890186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815566 | AAAAACTAGCTCCCA[A/G]AGACTCAAATGCAGA | 9063 |
rs570920450 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878588 | AAAAATGCTTCCTAG[A/G]CTAGGTGCAGTGGGT | 9063 |
rs570981857 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917728 | CTGCCTAGAGCTGGG[C/T]CGCAACTGAGGCGTT | 9063 |
rs571050920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842158 | TTGAACCCAGGAGGT[G/T]GAAGCTGCAGTGAGC | 9063 |
rs571061296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884469 | AGGTGCCCGCCACCA[C/G]GCCGGCTAATTTTTT | 9063 |
rs571086711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841368 | ACCCAGGGTTCACTT[C/T]TTATTTAAGTGCCTG | 9063 |
rs571099487 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841955 | AAAGTTTGGCTAGGT[G/T]AGATGGCTCATGCCT | 9063 |
rs571119807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890502 | ACTATATTAACAGCA[C/T]ATCATTAATCAATAG | 9063 |
rs571138210 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46812069 | AATTTTTTTTTTAAT[C/T]AGAAAAAAGGTTACT | 9063 |
rs571161278 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887550 | AATAACTTCATTAGG[A/C]AGTAAGAATTATAAC | 9063 |
rs571249953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869296 | GGGAAGGCAAGAAAT[A/G]TCTAATACGAGGAGG | 9063 |
rs571289208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824156 | CTAGAATGCTGCTAT[A/G]TAGCAAATATTAGTA | 9063 |
rs571304713 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911100 | GCAGGCCAAGACTCC[C/G]GAAAGTCTACCAAGA | 9063 |
rs571320140 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46821785 | TACAAATTAAACATA[C/T]GTAATAAATACTTCA | 9063 |
rs571327431 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916685 | ACAAACCTCACAACA[C/T]AGACTTTGCAGATTT | 9063 |
rs571397111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882225 | TGGCTTTAACATTAA[C/T]GTGCATATCATTTGA | 9063 |
rs571443423 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864492 | AATACTAATGCAGGC[C/T]GGGTGCAGTGGCTCA | 9063 |
rs571455312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838819 | GACACAGCTGATGGA[C/G]CTATATCACAAATCC | 9063 |
rs571544786 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831254 | ATTTCTATATATTAG[-/C]CCATAATCACAAAAA | 9063 |
rs571569932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852418 | TTCTCTCAATGCTCT[A/G]TTTCTTCTCCTCCTT | 9063 |
rs571578382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845292 | CCAAAGGCCAGTGGT[C/T]TGAATTAACACTGCA | 9063 |
rs571621066 | snp | A/G/T | 0.000655363 | 0.0180903 | missense, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844788 | TTTTTAATCTCTGTA[A/G/T]TAACATGGCTGATGT | 9063 |
rs571644185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901192 | GGAGGCCAAGGCGGG[C/T]GGATCACCTGCGGTC | 9063 |
rs571654040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908588 | CTACGTCTTATACTT[C/T]TACAATAATGGAAAA | 9063 |
rs571707086 | in-del | -/A | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919486 | GCGAAACTCCATCTC[-/A]AAAAAAAAAAAAATT | 9063 |
rs571810430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46812807 | TTATTTAGAGAATGC[A/G]GCATATATTCTTGAT | 9063 |
rs571847167 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811991 | TTAAGTTCTTTCCAT[A/G]TATTTTTTTTCCTTC | 9063 |
rs571870185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880511 | CACTTGAGGCCAAGA[A/G]TTCAAGGATGCAGTG | 9063 |
rs571870718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879981 | GTTTCAGTTTTGCAA[A/G]ATGAAAAGGGTTCTC | 9063 |
rs571888625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914563 | TAACCAACCCTCCCC[C/T]CCCCAACTCCACCCC | 9063 |
rs571943537 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860640 | CTGGAATATAACTCA[C/T]AGAGCACCCATGAGT | 9063 |
rs571994365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862406 | ATCTTATTTTTGAAA[A/G]ACTCTTACTATCATC | 9063 |
rs572018235 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921328 | AGATGGGGTTTCACC[A/G]TCTTGGTCAGGCTAG | 9063 |
rs572021329 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909854 | TTTTTTTCTCTTCAT[C/T]TTCAAACATTTGGAT | 9063 |
rs572086016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869805 | TGAGGATTGAATTTG[A/T]CAACTTCTAATAGAG | 9063 |
rs572112426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904463 | AAAAAGAAAAATAAC[A/C]TAGAAGGCCGGGTGC | 9063 |
rs572146968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869023 | GGTGACAAAGTATTT[C/T]CTTGGTGGTTGGGAC | 9063 |
rs572168087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847840 | AGTATATCCAATTCC[A/C]AATTACCGCAAGACT | 9063 |
rs572203912 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831566 | AAAAGAAGAACAAAG[C/T]TGGAAGAGTCACACT | 9063 |
rs572228892 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852852 | GATGCAGCTCCCATC[A/G]CTGGCACAGTCACAC | 9063 |
rs572301507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910269 | GCTACTGTCATTGGT[A/G]AAGGTGGACATGGTT | 9063 |
rs572302673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839215 | TACACTATACCTATT[C/T]AACAAAATGCCCACA | 9063 |
rs572311057 | snp | A/G | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822812 | GCTGGGGAGGGGACT[A/G]AAGAAGTGGTCTGAT | 9063 |
rs572341229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838466 | CTCACTGCTATACTG[C/T]CTCTATCTAAGTGTC | 9063 |
rs572341851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825029 | AAAAAAAAATAGTTG[C/T]TCACATAATTTCGGG | 9063 |
rs572343787 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906557 | ATGATTTGCTATAAA[A/G]ATAATTTGTTAGAAA | 9063 |
rs572352625 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46891245 | TTACATTCAAGTTAC[A/G]GTGTTAATTATATTT | 9063 |
rs572388411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876661 | CTTTATCCAATGAAC[C/T]AGCTAAAAATTCAGG | 9063 |
rs572414958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848753 | TTATAATATGGAAAT[A/G]AAAGAGAGAGACAGT | 9063 |
rs572421426 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917715 | AGGCCCCTGCGGACT[A/G]CCTAGAGCTGGGTCG | 9063 |
rs572459801 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876660 | GCTTTATCCAATGAA[C/G]TAGCTAAAAATTCAG | 9063 |
rs572511972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831957 | AACTTGGTAAACCAG[C/G]CTTCATTCAAAGTAG | 9063 |
rs572548126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865567 | CTTGTATATAACACT[A/G]TCCAGTTTTCCTGCT | 9063 |
rs572572075 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853434 | ATGCAGTTACCCATT[A/G]GTATCTTTCAGCTCC | 9063 |
rs572573996 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820247 | GGCACCAAAGTGATG[C/T]CAGCATATTGTTATA | 9063 |
rs572627631 | in-del | -/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823260 | ATTTAACCTATCGTG[-/T]TTTTTTTTTCTCTGC | 9063 |
rs572650013 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46903385 | AAAAGAATTCAATTA[A/G]AAAAAGGACAAAAGA | 9063 |
rs572700989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835292 | CATCTGGGTCATAGT[C/T]ACATGGGAGGTTCTT | 9063 |
rs572709625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888599 | GGCCAGGACCAGTTT[C/T]ATGGCAGACAATTTT | 9063 |
rs572717264 | snp | A/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917936 | TGTTGGGTAAGCTAT[A/T]GTTCCCATCTAATGG | 9063 |
rs572734813 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811390 | TCTATGTAGTGCTAC[C/T]AAAATACAAAGTTTC | 9063 |
rs572738104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834723 | GGTCTCAGACAATCA[A/T]CCTGCCTTGGCCTTC | 9063 |
rs572804445 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824610 | CAAAATGGCAATGAT[-/TC]TCTCTAGGTGAGATA | 9063 |
rs572807046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872599 | TTTACAAGAGAAGGG[A/G]TTACGAGTTTCAAAA | 9063 |
rs572824957 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868179 | AAATTCCTGACCTAA[A/G]GAATCCATGAGCATG | 9063 |
rs572836243 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907097 | TATCTGCCAATGGAA[A/G]AGGGCAATGGAGAGG | 9063 |
rs572837897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914579 | CCCCAACTCCACCCC[C/T]GACACACAAGTCTGA | 9063 |
rs572858845 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865911 | TATTCACTCCTCAAC[A/C]CTTTTTTTCTTGTTC | 9063 |
rs572868174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879540 | ATTACCATACGATCC[A/C]GCAATTTCACTTCTG | 9063 |
rs572878570 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921219 | TGCAACCTCTGCCCC[C/T]CCGAATTTAAGCAAT | 9063 |
rs573022305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878933 | GTTAACAGGGGCTCA[C/T]ACTATGGCTAACATA | 9063 |
rs573050230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913315 | CCTTCTGTTACAGAA[C/T]TACTTAGGCTTCTTA | 9063 |
rs573064285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912728 | GGCATGGTATATTTT[G/T]AGACTTTTGGAACAA | 9063 |
rs573077573 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900518 | ACCAAAAAAAAAAAA[-/T]TGTTTTTAATTACCA | 9063 |
rs573128690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898561 | TATTAAGGCAAAACA[C/T]TGAATTTTCCGTATA | 9063 |
rs573165111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891856 | ATTTTTTCAGCAAAA[C/G]TTAATGAATATTTTT | 9063 |
rs573167589 | snp | C/G/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827749 | GAAATAAATACCTCA[C/G/T]ACGCTCACTTTCCAA | 9063 |
rs573218710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884552 | TCCTGACCTCGTGAT[C/T]CGCCCACCTCGGCCT | 9063 |
rs573242038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905909 | TATATTTTTTAACTA[C/T]AGGCTAGTTTTACTC | 9063 |
rs573273155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897743 | GATAACTGGTATCTG[C/T]CAGAAAGCAATAGCT | 9063 |
rs573409898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887849 | ACCATAAGAATGCTT[C/G]AGTAAGTTCTAGCCA | 9063 |
rs573414304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877724 | TAACCGCGTTAGGGA[C/T]AAAAACCCCTTCCCT | 9063 |
rs573430660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826801 | ATATATGTGTAAATT[A/G]TATTTGGAAATGTAA | 9063 |
rs573446241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864392 | AAATCAGGAAGTACT[A/G]AACTGCATTCATCTT | 9063 |
rs573449590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910096 | GGGAGGAGGAGGTTG[C/T]GGTGAGTCAAGATCG | 9063 |
rs573497189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877462 | TCCTTATTTGGAAAG[C/T]GTCCTCTTCACTCCT | 9063 |
rs573531959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870489 | GACGTGGTGACGGGC[A/G]CCTGTAGTCCCAGCT | 9063 |
rs573531965 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919315 | AACATGGAGAAACCC[C/T]GTCTCCACCAAAAAT | 9063 |
rs573555333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895289 | CCATCTGCTATGATG[A/T]ATATAATACAGGAGA | 9063 |
rs573558538 | in-del | -/AA | 0.499 | 0.0223418 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870615 | GCAAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 9063 |
rs573577674 | in-del | -/A | 0.0509478 | 0.151255 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825008 | CTGTCTCAAAAAATT[-/A]AAAAAAAAAAAAAAT | 9063 |
rs573596186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894813 | CGGTGGCTCATACCT[G/T]TAATCCCAGCACTTT | 9063 |
rs573600137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845775 | TAAATACCCAACTTA[C/T]GGTGTAAATTCTAGG | 9063 |
rs573619796 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881826 | CACAGACACCGGGCA[A/C]GGTGGCTCACGCCTG | 9063 |
rs573632119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915404 | CAGAGCAGTTAAGGC[A/G]AAGAAAAGCAGATGA | 9063 |
rs573642179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894823 | TACCTGTAATCCCAG[A/C]ACTTTGGGAGGCTGA | 9063 |
rs573694284 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859017 | TGTCTAGGGGCATAC[A/G]GACCTAAGTGGTTGG | 9063 |
rs573703565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901698 | CAAATCAATCAATGC[A/G]AAAAACGCATTTCAC | 9063 |
rs573704694 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865524 | CAGCGATAGTCTTCA[-/A]AAAAAAAAAAAAAAA | 9063 |
rs573723631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853707 | GGCTGGAGAACTGCC[C/T]GAACCCAGGAGGCAG | 9063 |
rs573730836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880969 | TTTAATCAGATTTAA[A/G]TAGAACATAGCAAAA | 9063 |
rs573762804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861226 | CCTGGGCGACGGAGT[A/G]AGACTTTGTCTCAAA | 9063 |
rs573763879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814602 | TTGTGCTTAGCTGAC[C/T]GAGCAGCCCATGAAG | 9063 |
rs573804144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886777 | GGGGAAGTGGAGGCC[A/G]CAGTGAGCCGAGACA | 9063 |
rs573811362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867086 | TACATGTTGCACATA[C/T]GCAATATATATGTAC | 9063 |
rs573827740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813612 | ATTATGCAGCTTATC[A/C]TTAGAGACACTGGAT | 9063 |
rs573832042 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813183 | AAAACACAGACTACA[C/T]GGTAGCTAGCTATCA | 9063 |
rs573849417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860587 | GAACTTCTAATAGCC[A/G]AAGATAGAACAATTT | 9063 |
rs573918817 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882245 | ATATCATTTGAATAC[C/T]GTTTAATCATATCCA | 9063 |
rs573955411 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884777 | AATAAATTAGCCGGG[C/T]GTGGTGGCACATGCC | 9063 |
rs573977848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858574 | TGGTGGCACATGCCT[A/G]TAGTCCCAGCTAGTC | 9063 |
rs573988170 | snp | A/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826557 | ACATCACATCTAAGC[A/T]TTCATTCCCCTTCAA | 9063 |
rs574052150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829446 | CTGTCCATATAAATT[A/C]ATTTGTGACTTTTTG | 9063 |
rs574083197 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830251 | ATAAACTTTAACTTC[A/G]AGAAAAAAGGATAAT | 9063 |
rs574089109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893631 | TGGGACAGTCTTTGC[A/G]TTACAAAATGCTGCA | 9063 |
rs574099376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844907 | TGTTTACATGAAATA[C/T]TTATTTAAGAAACTC | 9063 |
rs574107153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844393 | AACAAAACAACAATT[A/G]GGAGAGGAAGCTGGA | 9063 |
rs574126087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892775 | AGACTGTCTCAAAAA[C/T]AATAATAATAATAAT | 9063 |
rs574127504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877944 | CAACAGTAAATGAAA[G/T]AATGCCACAATTTCA | 9063 |
rs574177158 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877826 | GCTGAGAAATCCTTC[A/G]TTTGAGTACTCATTT | 9063 |
rs574201685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836666 | GTATTCCCAAGAAGA[C/T]TACAATATATTTTTA | 9063 |
rs574205707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884170 | GTAATGTTCCTTTTT[C/G]AGAAAGTAGCAGCTT | 9063 |
rs574235840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900444 | GAGGCTGAGGCAGGA[A/G]GATCACTTGGGCCAG | 9063 |
rs574251023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848776 | GAGACAGTGTGTGTG[C/T]GTGTGTGTGTGTGAG | 9063 |
rs574319141 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46812089 | AAAAGGTTACTTGAA[C/T]ATTTACATAATTTTA | 9063 |
rs574343572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837851 | TTTCTCCCACTAGAT[C/T]TTATGCTCCAAAAAG | 9063 |
rs574367212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919861 | TTGATTTATTCTCCG[C/T]AGACCTTGATTTACA | 9063 |
rs574383901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833926 | TCCCTACCTTAATGG[C/G]ATCACCTATTCCCTA | 9063 |
rs574460220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854765 | AATGCATCATCAAGG[C/T]CCAAGCTGGGAATTT | 9063 |
rs574520852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897511 | TTCATTTTATTCATA[A/G]TAATACTTTAAAAAT | 9063 |
rs574528532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840897 | ACTGTAGACTAATTA[C/T]TACCAATCTAAATTA | 9063 |
rs574549149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889768 | GTCTCAAAGAGATAC[A/G]TGTATACCCGTGTCC | 9063 |
rs574575810 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899674 | ATTTCATTATGTTTT[A/G]CAGGCTGGTCTCAAA | 9063 |
rs574600203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833260 | ATGTATCTCAAACAA[A/G]TATGTTGAGTAAAAG | 9063 |
rs574605011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825100 | GTTCTTTCTCATTTG[C/T]TTACTATCTTTGATG | 9063 |
rs574616525 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848419 | CAAAGTTGCACAGGT[A/G]CAGGCAATGATAATA | 9063 |
rs574689033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824565 | TAAAGACTCCGGTTC[A/G]TAAGCAAAGAAAGGG | 9063 |
rs574709988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862902 | AGTAGAGATGGGTTT[C/T]GCCATGTTGGCCAGG | 9063 |
rs574727190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832145 | CAAAAGGCCAGGCAC[C/G]GTGGCTCATGCCTGT | 9063 |
rs574758741 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921081 | GAAGATTCATTATAA[A/G]TACTGTGATTAAAGT | 9063 |
rs574761520 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808170 | TGCGGGGAAAAACCC[A/C]AAGATATAAATTACA | 9063 |
rs574791579 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884789 | GGGCGTGGTGGCACA[C/T]GCCTGTAATCCCAGC | 9063 |
rs574830734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904705 | GCAGTGAGCCGAGAT[A/C]GCGCCACTGCCCTCC | 9063 |
rs574844775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911814 | ACTTTGGGAGGCCAA[A/G]GGAGGGGGAGTGGAT | 9063 |
rs574856405 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828999 | CCTTTATTTTTTCCC[C/G]TTTCTTCTTACTCCA | 9063 |
rs574889217 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865944 | ACTCCACTTTTCACT[A/G]TCTGTGGCTAAGGTC | 9063 |
rs574895345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876770 | GGCGCTATCTCAACT[C/T]ACTGCAAGCTCTGCC | 9063 |
rs574908086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911370 | ACAGGTGCCCACCAC[C/T]ACGTCGGGCTAATTT | 9063 |
rs574965904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839871 | ACTCTGTCAAAAAAA[A/C]AAAAAAAAAGGCCGG | 9063 |
rs574967015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822790 | AGAGACTGGGGTATA[C/T]GTGAGTGCTGGGGAG | 9063 |
rs574967765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875818 | GGCCCAGACTGTCCC[C/T]TTTCCACTCAGATGG | 9063 |
rs574996312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822076 | GACTGGGATAACCTC[C/T]GGGCATCCTTTCCCT | 9063 |
rs574997938 | snp | G/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916340 | CTAATATCATAAGTG[G/T]TACACAAACGAGTTG | 9063 |
rs575012745 | snp | C/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836025 | GGTTTTTGCATAGAC[C/T]CTAATTGCTACTTCA | 9063 |
rs575026966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889074 | ACCTAATACCATATA[C/T]GAAAATTAACTCAAA | 9063 |
rs575079149 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920863 | AGAAGGAGGGAGGTG[C/T]AGTAATCTTATCACT | 9063 |
rs575083139 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867814 | AATGGCCTTTTGTAA[C/T]AGCATCAACCAACAG | 9063 |
rs575085585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821253 | GTCTTCATTTTAACA[C/T]GAACATATCTTGGCT | 9063 |
rs575085634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829364 | CATTAACCAATGATG[C/T]AGCCTCTCTAACCTC | 9063 |
rs575097638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839259 | GACCAATCTACACAT[A/G]CTAATATACTTAAGA | 9063 |
rs575119314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883277 | TCTGAAAAGAACAAT[A/G]AAGAAATTAAGGAAT | 9063 |
rs575122885 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828734 | TTATGAATTATCTGC[A/T]AATCACGTAGGTTCT | 9063 |
rs575163327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813128 | TCCTTTGTACATAAA[C/T]GTAAAATACTTGTGT | 9063 |
rs575209638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866285 | TACTATTGATTATGT[C/T]TGATTAATCTTGAAA | 9063 |
rs575213685 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812230 | TGATGCTGAGAGTAC[A/G]GCATAATTAAGAAAA | 9063 |
rs575228436 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840043 | GCAGGTGCCTGTAAT[A/C]CCAACTACTTGGGAG | 9063 |
rs575268425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908778 | CTTTGGGAGACCAAG[A/G]TGGGCAGATCACCTG | 9063 |
rs575302216 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921657 | TATCTAAACAGCTAA[A/G]CTGATTTTGAATCTA | 9063 |
rs575369472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874370 | ATTAATCAAAAATAT[A/C]ATACCTAGGTTTGGA | 9063 |
rs575380248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898680 | TTTTGCAAGAGGTAC[A/C]TTAAAAAACTATAGA | 9063 |
rs575380311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907048 | AAAGAAGGAGAGCCT[A/G]CAAAGCTGAGTCTCT | 9063 |
rs575390514 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906302 | AGCTTCTATTCAACA[C/T]TGTACTGGAGATCCT | 9063 |
rs575411390 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868686 | TGACCAGCACCCTTC[A/T]GCAGAAGTAAATTTG | 9063 |
rs575421045 | snp | C/T | 4.94597e-05 | 0.00497266 | missense, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812556 | GGTGGTGGTGACAGA[C/T]GTACTGCTTGCTGTT | 9063 |
rs575424316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836271 | AGAATTTATTTAGAA[C/T]TTAGTTCAGTAAGTT | 9063 |
rs575466516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835344 | CTGTAGGTTTAAAAT[G/T]TTTTCAAAATAAGCT | 9063 |
rs575494681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886633 | ACCTCAGGTCAGAAG[G/T]TCAAGACCAGCCTGG | 9063 |
rs575502674 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843317 | GTCATCAAATACCCA[A/C]AAAACTACATTATAA | 9063 |
rs575544794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872642 | TCTGTGGAACCCAAG[A/G]TTAAGTATTTAGGAC | 9063 |
rs575610112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879636 | CAGCATCATTCACAA[G/T]AGCTAAAATGTGGAA | 9063 |
rs575638252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842612 | CAACTGTTTTTTAAC[C/T]AACAAAAAGGCAATT | 9063 |
rs575698508 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826312 | CTGTGTATGTGCCAT[-/C]CCCTCCTGTTTCATG | 9063 |
rs575736987 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895392 | TAATCTACCTCAGGA[A/C]GGACACGGTGGCTCA | 9063 |
rs575743828 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862650 | ACATATATATACACA[C/T]ATATACACATATATA | 9063 |
rs575758850 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908609 | TAATGGAAAATATCT[C/T]CGAGAACTCTGTTGA | 9063 |
rs575770047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913357 | CCAAATCTGATCTTC[A/G]AATTATGACACAACA | 9063 |
rs575780037 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830580 | AGAAAAAAAAGCAAA[A/T]TATAGTAAAAGCAAG | 9063 |
rs575787125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849677 | TCCTCCAAATTTTCT[A/G]ATTACCACTACTACT | 9063 |
rs575789152 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857607 | TTAGATGGGAAACAC[A/G/T]ATGTGAAGAAAGAGA | 9063 |
rs575822634 | snp | A/C | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920397 | TCGCCATTTTGCTAC[A/C]GTGAAGAGCCAACCT | 9063 |
rs575869740 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46809993 | GGATTAATAATCATG[A/T]TGTTGCCATAAGGCC | 9063 |
rs575879415 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920449 | GCAGAAAAATCACAC[A/G]CACACAAAATCTCAG | 9063 |
rs575905984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819123 | TAATGAACAGAAATG[C/T]TCATTACCTTTTTTC | 9063 |
rs575907240 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889607 | GATGTGGAGAAACTG[A/G]AACCCTTGTGCACTG | 9063 |
rs575914408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870994 | TGAGCATTCCATATA[A/C]AACAAAGAAAGGATG | 9063 |
rs575924275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912862 | CTGTCTGCACAAATA[C/T]TGCTTTCATTTAAAA | 9063 |
rs575982826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819976 | TTGCAGTTACCTGTG[A/G]TCAACTGCAGTCAGA | 9063 |
rs576016794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889170 | CTTCACAGCATGAAG[G/T]TTAGCAATGATTTCT | 9063 |
rs576032929 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848398 | GTCACGCCATGCCAA[G/T]AACATCAAAGTTGCA | 9063 |
rs576093857 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807981 | ACCTCCAGTATTTTA[C/T]CCTAAGAAAATAATT | 9063 |
rs576126657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881909 | CCAGACCAGCCTGGC[C/T]GACATGGTGAAACCC | 9063 |
rs576139155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881176 | ACCTTATTACTTTCA[A/G]CCCCCTTCCTCTGCT | 9063 |
rs576183064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854464 | TGACAAACGTGCCAT[A/G]TTGTACTATTTTTTT | 9063 |
rs576184860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845530 | AGTCAAGCCAGAAAA[C/G]AACAGCGTCCAATCC | 9063 |
rs576188176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861643 | TTCTTGCCAAAAATG[C/T]ACAACCTCCATCTAA | 9063 |
rs576230149 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819818 | GCAAAAGCAATAGCT[A/G]TGGAGAGGGAAGAAG | 9063 |
rs576267467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910141 | AGCCTGGGCAAGAAG[A/C]GCAAAACTCCGTCTC | 9063 |
rs576270055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853770 | CTCCAGCCTGGGTGA[C/T]ACAGCAAGACTCTAT | 9063 |
rs576270715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844947 | AAAATAACATTCAAA[A/G]TAACTTCCATGGAAT | 9063 |
rs576283096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868214 | ACACAGTAAGTTCCT[C/T]TTCAAAGGTTTAATT | 9063 |
rs576303355 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878157 | CTGGTTACTATCCAA[C/G]TTATTTAGGAAATTT | 9063 |
rs576308241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826954 | ACGATTGCCTAGATT[A/T]GGGGTGTAAATAGGA | 9063 |
rs576313753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916239 | CCAGCCAACATCCTT[A/C]CCCCATCCCATCTCT | 9063 |
rs576367206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815889 | GAATTGCTGCGCTAA[A/C]AGGGTTATCAAGGGT | 9063 |
rs576406340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864954 | CTTTTGGTGCTCTGT[A/G]TTTAATTACACAAAA | 9063 |
rs576407335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824372 | AGACATATAGATTTA[C/T]CCTTATTATGTTTCC | 9063 |
rs576407353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814768 | TGCAATCCAGGCTCA[A/C]TGCAAGGTCTTCATG | 9063 |
rs576517060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837706 | TGGTCCACTGGCACC[A/C]AGACGTACACAACAC | 9063 |
rs576524589 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46903235 | CTAAAACCTGTGCTA[C/T]GCAAAAGACCCCTTT | 9063 |
rs576533088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887169 | AATCCTTATTTCAAA[C/G]TGAACGTAATAAAGA | 9063 |
rs576566075 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875920 | ATGCCAAGCTCTCTC[-/TT]GGCTATTCCCTGAAG | 9063 |
rs576579831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842460 | GTGTAGACTTTCTTC[C/T]TGATACAATAGTTTG | 9063 |
rs576637402 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881366 | TCTGATTAAATTAGA[A/G]AAACTTTGGTGTATG | 9063 |
rs576645817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46893804 | GGTCATCAATTTCTA[C/T]TTTAAAATAACAAAC | 9063 |
rs576656809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843239 | AGACTCAACAAATCA[C/T]TCTCTTTTCTGACAC | 9063 |
rs576667015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841893 | GCTCCCTATTCTTAC[A/T]TAGAAGGAATCCTAA | 9063 |
rs576704023 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848793 | TGTGTGTGTGTGAGA[C/G]AGAGAGAGTAGGAAG | 9063 |
rs576723997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913432 | TGATAAAGTTATCAT[C/T]GCTGGCTCTCTCAGG | 9063 |
rs576792477 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901483 | CAAAATATTAGTCAA[C/T]AAAATTCAGCAATAT | 9063 |
rs576803884 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809825 | CTAAGATATTCCAGA[A/C]AATCACTGGTTGGCT | 9063 |
rs576811721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879473 | GGGAATGTAAAATGG[A/T]GCAGCTGCTGTGGAA | 9063 |
rs576850333 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885913 | AGTTTTATTTTAGTA[A/T]ATTTATAAAGAGCAT | 9063 |
rs576879369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834650 | AACAGAGTCTTTCTC[C/T]ATCACCCAGGTTGGA | 9063 |
rs576879606 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885315 | CGAGGTCAGGAGTTC[A/C/G]AGACGAACCTGGCCA | 9063 |
rs576892642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818850 | TGGCTAAATATCAGC[C/T]TTGGATATTAGTCTT | 9063 |
rs576899466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820207 | AGTGCTTCTGTTCAA[A/G]TAACCGTTATTTTAA | 9063 |
rs576959388 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873383 | CAAGGCTGATTTAAG[A/G]GAGACCCTTTTCAAA | 9063 |
rs576970028 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919676 | TTATTATTTTAAAAT[G/T]TTATGTTAAAAAATT | 9063 |
rs576993323 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875843 | AGATGGTCCTCCAGC[C/T]GACCAGGCATGAACT | 9063 |
rs576994094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884712 | CTTGAGGTCAGGAGT[C/T]TGAGACCAGCCTGAC | 9063 |
rs577011182 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826081 | TCAGCTTCATGGAAC[A/G/T]AACTAGGTAGCTGCG | 9063 |
rs577139481 | snp | C/T | 0.00021889 | 0.0104593 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891244 | ATTACATTCAAGTTA[C/T]GGTGTTAATTATATT | 9063 |
rs577201436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898431 | TTACAGGCATGAGCC[A/T]CCATGCCCAGCAAGG | 9063 |
rs577245657 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912636 | AAAGTCTAGGACAGG[G/T]GGAAAATGACCTAAA | 9063 |
rs577256611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863282 | AGCTTATGGTCACCC[C/T]GTCTTTGGGCTACTA | 9063 |
rs577324251 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813377 | GATCCCAAACAAGTA[A/C]AAACCTGAATGTACT | 9063 |
rs577347722 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889149 | AAGGAAAACACAGGG[C/T]AAAACCTTCACAGCA | 9063 |
rs577368324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915273 | TAGACCAGAACCAGG[C/G]ATGGAATAACCACTA | 9063 |
rs577373597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870820 | TGGGAACGTGAACAT[A/C]CTCCTGGCCAAAACA | 9063 |
rs577465395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883892 | ACACCTGTGGGTCCC[A/T]GCAACTTGGAAGGCC | 9063 |
rs577528903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853046 | CCTTGGGAGGCCAAC[A/T]TAGGTGGATCACTTG | 9063 |
rs577529096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901651 | TATAGAATACATCAT[A/G]TTAACAGTTACAAAA | 9063 |
rs577549234 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877419 | AAACAACTTCTCCTG[A/C/T]GAGTCCCAATCTGTA | 9063 |
rs577554902 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809326 | AGAAAATCCTCAAGT[A/G]GCTCACCTAATTGTC | 9063 |
rs577565229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876809 | TCACACCATTCTCCC[A/G]CCTCAGCCTCCCGAG | 9063 |
rs577568701 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886835 | AGAACAAGACTCTGT[-/C]CCCCCCCTCCAAAAA | 9063 |
rs577611236 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866732 | AAGAATGGAGGGGGT[A/G]GATAAAGGAAATTAT | 9063 |
rs577616290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852188 | TCCACATTTCATTAT[C/G]CCAATCAATAGCAAC | 9063 |
rs577629925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840635 | TTCTACTCTAGTGGT[C/T]TTATAAGAACTAATG | 9063 |
rs577650549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859712 | AAAAGATAAGCAGGT[C/T]TGATGGAAGGCAAGC | 9063 |
rs577658352 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829355 | CACCAAGGCCATTAA[C/T]CAATGATGCAGCCTC | 9063 |
rs577701947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908876 | TAGCCAGGCATGGTG[G/T]CGGGTACCTGTAATC | 9063 |
rs577716888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892002 | AAGAACACCTGGAGC[G/T]GACCAAAGCCCTGTC | 9063 |
rs577759503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822862 | TATTAATATCTTATT[C/G]TTTTAAAAATGTTAA | 9063 |
rs577773956 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888305 | ACTTAATATTGCTAA[C/G]ATATCAATACTACCC | 9063 |
rs577776111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867691 | CATAATGTAGATTCT[A/G]TTTTCCAAATATAAC | 9063 |
rs577797660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830104 | TCACCTGTGTAACTC[A/G]ATGAGTATAAATGGC | 9063 |
rs577872735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880263 | ATTAGCTGGGCATGG[G/T]GGTGCACACCTGTGG | 9063 |
rs577879171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865475 | AACCTGGGAGGTGGA[A/G]GTTGCAGTGCGCTGA | 9063 |
rs577888474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867022 | AGAATGGTTCCATAG[G/T]CATGTTGTACATGTA | 9063 |
rs577952972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874431 | ACCCACTTCGCTGCA[A/C]GTCATTAAAAAGCTA | 9063 |
rs577962991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873844 | AAACAAGCTGCCGTT[A/T]CCTCTGAAACGCCCG | 9063 |
rs577979245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886694 | AATACAAAATTAGCC[C/T]GGTGTGGTGGCACAT | 9063 |
rs577985196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854501 | GGCTTTGCTGGCCTT[C/T]TTACAGAATGGTACC | 9063 |
rs578009145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837358 | TCTTATTTTAAGTGG[C/T]AGTTGAGCCTCTTCT | 9063 |
rs578027888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851006 | CTATAATCATTATTC[C/T]TTCAGATGTCAAAAT | 9063 |
rs578095217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858246 | AAAAAAGCAGAGCAA[G/T]ATGTTGAAAACAACT | 9063 |
rs578098260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907791 | ACATGGGTTCTGCAG[A/G]GCCAACTTCAGGACT | 9063 |
rs578098854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844211 | TATATAGCATCTTAA[A/G]ACAAAATGTTACATA | 9063 |
rs578146436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857672 | GGCATAAAGGGTTTT[C/G]AACAGCTCACTAAGG | 9063 |
rs578148968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826226 | TAACATTTATCTCTA[C/T]AGTAGCTGATCACAG | 9063 |
rs578159555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843404 | CTCCAATTCATTCAC[C/T]GCTCCTGACCCTCCC | 9063 |
rs578165798 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879096 | ATCCTGAGCTATCCG[A/G]TTCTCATCACCTACC | 9063 |
rs578241599 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811300 | TGCTGTCCCTTTCCC[C/T]AAGTTTGAAAATCAC | 9063 |
rs578251255 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810682 | TGTGGAAAACCATAT[G/T]AATTTAAATCAACAT | 9063 |
rs745314518 | snp | C/G | 1.74482e-05 | 0.00295361 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844745 | TTACTTAGTGCTCTG[C/G]AATGATCAGGGTTTC | 9063 |
rs745323394 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861612 | GTACCCTGAGAAGGG[A/C]ACATAACTTGAGGTA | 9063 |
rs745365210 | in-del | -/TTAAATAAAGAGA | 1.71097e-05 | 0.00292481 | intron-variant | PIAS2 | GRCh38.p7 | 18:46812660 | AGAGGCTACTTGATT[-/TTAAATAAAGAGA]CTAGAAATTATTAGA | 9063 |
rs745452049 | snp | G/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826702 | AGGAAAAAATCCACT[G/T]GAAATACTTCCTCAT | 9063 |
rs745511143 | snp | A/G | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890748 | AGGATGGTGAGTGAG[A/G]TGTAACTGAAGTGGA | 9063 |
rs745511718 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887473 | AAGAAAGCAATCTTC[C/T]ACATCAACTATGAAA | 9063 |
rs745515758 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874412 | TATTGATTCAGATAA[C/T]AGAACCCACTTCGCT | 9063 |
rs745529433 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890810 | TCAGGTTCTACAGGT[A/G]ATGAGCCACCATCCA | 9063 |
rs745539505 | snp | C/T | 1.65061e-05 | 0.00287277 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844106 | ATTTCACTATCAGGA[C/T]CTGCAGTAAGTTTTT | 9063 |
rs745550219 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854626 | AGTCAAAAGCCATCT[A/G]TTAGGCCAGAGACAG | 9063 |
rs745608104 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899124 | ATTCCAACGACTGGT[C/T]AATGAGTTGGAGAGC | 9063 |
rs745684694 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897870 | TACAAGGCAATATAA[C/T]TTTTGGGTTTTTTTT | 9063 |
rs745703736 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813316 | CCTTTCCTAGTGCTC[A/G]TATTTCACAAGTCCC | 9063 |
rs745716663 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819951 | TTATCCAAGATTTTG[C/T]GTTCTGTGATTGCAG | 9063 |
rs745744706 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831788 | GTTCTTTATCTTACA[A/C]CATACATAAAAATTA | 9063 |
rs745800398 | in-del | -/AAC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868299 | GCTATCTGCTCTGTA[-/AAC]AACTACTTCTGCCAG | 9063 |
rs745803853 | snp | A/T | 1.65026e-05 | 0.00287246 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46821054 | CACCCTTACAGAAGA[A/T]GGCTGATACATGAGA | 9063 |
rs745815319 | snp | C/G | 1.68454e-05 | 0.00290214 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855337 | CTGGTGAATAAAAAG[C/G]AACTTACAGGCAAAG | 9063 |
rs745820167 | snp | A/G | 1.67273e-05 | 0.00289195 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46827965 | TTAACAAACCCTTTG[A/G]TTGGGCTGCTTTGTG | 9063 |
rs745821739 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865860 | TGGAGCATCAAACAC[A/G]GAAACATAAGTAAGC | 9063 |
rs745830514 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813725 | TTTAAGTTGCCAGCC[-/A]GAGGGACAGCAACAA | 9063 |
rs745834576 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830464 | TAATAAAATTTGTGG[A/G]CTGTATTATTTAAAC | 9063 |
rs745859587 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46818564 | TTATTATAAATTATT[-/A]AGTTTATCAATACCA | 9063 |
rs745917292 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904426 | GTGAGGAGAAATTTT[C/T]TAAATTAGGCAAAAC | 9063 |
rs745938010 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810543 | AAGAAGGTAAAACTG[C/G]CAACTATGTGCAACT | 9063 |
rs745951356 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902632 | TCAACATAGTAAAGA[C/T]GTCAACTTTCCCCAA | 9063 |
rs745994125 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809410 | ATTACACTGTGGGGG[C/G]TTACCAGAACAAGAA | 9063 |
rs746000843 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894281 | ATTTTTTCTTAACTT[-/A]AGTCTTTCACCAAGT | 9063 |
rs746003446 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858516 | AGGCTGGGCAACACA[A/G]CAAGACCCCATCTAT | 9063 |
rs746045439 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870929 | AAGATCTCAGGGAAA[C/T]GGTAATAAAAGGAAT | 9063 |
rs746101994 | snp | C/T | 1.67857e-05 | 0.00289699 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829893 | ATTAAGAAGTACATA[C/T]ATGTGATCAACAGCT | 9063 |
rs746219769 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914263 | CTTCCTTTCCTTCAA[C/T]CCATCAGGATAATCT | 9063 |
rs746306541 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814677 | CTCTCAAAGTCTTTT[A/G]TTCTATGTCATTTTC | 9063 |
rs746329573 | snp | A/C | 1.65086e-05 | 0.00287298 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815307 | CTTAAATTCAGGATA[A/C]ATACCTGGGGATCAA | 9063 |
rs746349948 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849035 | TATGTCCACTGGTAG[A/G]TTAACCAAATAAAAA | 9063 |
rs746360762 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894358 | TCACCAGAGCCCACA[C/T]GGGGGTTAAGGTTAG | 9063 |
rs746371809 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847346 | TCTCTGGGTGGAACA[G/T]AAATGGTAATCTTTT | 9063 |
rs746384718 | snp | C/T | 1.66888e-05 | 0.00288862 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855592 | TGGACTGTATAATCT[C/T]TCCTACCACCTGGCA | 9063 |
rs746394782 | in-del | -/TAT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832706 | GACCAGCCTGGCCAC[-/TAT]GGCGAAACCCCATCT | 9063 |
rs746395820 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46903162 | GGCAGAGTTCTTAGA[G/T]TTGACACTAAAAGCA | 9063 |
rs746406546 | in-del | -/A | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917083 | GTGCGGACCACTGGC[-/A]AGCACTCAGGAGCCG | 9063 |
rs746419970 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893574 | AGAAAGAGATAAGAG[C/T]TTAGACTATGAATGC | 9063 |
rs746439825 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886452 | AAATTAGGGAAATAC[A/G]TTAACCAGATAAATC | 9063 |
rs746461697 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872636 | CTCCGATCTGTGGAA[C/T]CCAAGGTTAAGTATT | 9063 |
rs746493520 | snp | C/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918580 | CTACCTCCGCCTCCC[C/G]AGTAGCTGCGATTGT | 9063 |
rs746545617 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811565 | ACAAACATTCCAGTC[-/A]ACACCGTACCCCAAA | 9063 |
rs746575626 | snp | G/T | 1.65778e-05 | 0.002879 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836505 | ATGGGATTGTCAGCC[G/T]CATTTTTCCTAACTA | 9063 |
rs746643210 | snp | C/T | 1.71085e-05 | 0.00292471 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827936 | AAGGGTAATGAACAA[C/T]AGTGAACTATAAATT | 9063 |
rs746651959 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837721 | AAGACGTACACAACA[C/T]TCAGATTTGATCAGA | 9063 |
rs746661600 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853388 | ACAGGGTTGTGTATT[A/C]ATCTGTTTTGCCAGG | 9063 |
rs746669351 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865455 | TGAGGCAGAAGAATC[A/G]CTTGAACCTGGGAGG | 9063 |
rs746689402 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866757 | AATTATCTCCCCAAC[A/G]GTTGTGTTTCCTGCT | 9063 |
rs746723671 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865601 | TGAAGATAAAAAAGA[C/T]GCCAGTTGGATATCC | 9063 |
rs746730119 | snp | A/G | 1.64996e-05 | 0.0028722 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46821012 | TGAAGGCGGAATAGC[A/G]GCAGGATCAACCGAA | 9063 |
rs746754181 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911520 | TGTGCCCGGCTGACT[C/T]TGTTATATTTCCTTT | 9063 |
rs746758609 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817661 | TTTTTCTAAAATATT[A/G]GTTGGAATTCTAGAT | 9063 |
rs746760312 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896405 | AGGTATATTGTCTTG[C/T]CCTCCCTCCACATCC | 9063 |
rs746850441 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830211 | AACATCAGCAGATAA[A/C]GGTTACTATATAGTA | 9063 |
rs746860891 | in-del | -/TT | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816114 | TGTGACTAAACTCTC[-/TT]TAATTATTTCAAAAC | 9063 |
rs746892306 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816664 | GTAGAGAGAGGGTCT[C/T]GCTATGTTGCCTAGG | 9063 |
rs746910945 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829025 | CTCCATTCATTACAT[C/T]GTTTGTTAGAACTTC | 9063 |
rs746982211 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46843529 | TCTAAGCAAGCCTCA[A/G]TATTTTCTCCCACAA | 9063 |
rs747033530 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870048 | AGGTGCACAGGACCC[C/T]CTTCACTCAATTCCT | 9063 |
rs747128356 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46821342 | GAGTGAGATATAACA[C/G]TTCCATCCACAAATA | 9063 |
rs747142844 | in-del | -/AT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814542 | TTTCTGCTGCTGTTC[-/AT]GTAATCAGATACAGA | 9063 |
rs747143089 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833497 | TCAAAATTTATCAAA[C/T]TGTACATTTTACATG | 9063 |
rs747152658 | in-del | -/TAAC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820175 | TTTAAGTTAACAGAT[-/TAAC]TATCTCAGTACACAG | 9063 |
rs747152758 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838390 | TAACCTAACGTTACA[A/T]AGTTAGAAAATGGCA | 9063 |
rs747193241 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46807775 | GTTAACCCCGTTCCA[C/T]AGAGTCAGAAAGGCA | 9063 |
rs747199555 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820338 | TCAACTTTATCATGA[G/T]TATATCTGTATAGAA | 9063 |
rs747201056 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898994 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 9063 |
rs747218781 | snp | A/G | 1.66117e-05 | 0.00288194 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855531 | ACATAGTAAGCAAGT[A/G]TAAAACTAAGGTAAC | 9063 |
rs747235279 | snp | A/G | 1.80231e-05 | 0.00300187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828140 | TTGAACCTGCATGTA[A/G]AGAAACAAAAGGAAA | 9063 |
rs747266004 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848726 | CAAAGAGAAGAACTT[C/T]AATAACTTGCATTAT | 9063 |
rs747289342 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832156 | GCACGGTGGCTCATG[C/T]CTGTAATCCCAGCAC | 9063 |
rs747313945 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912854 | TTTCAGTACTGTCTG[C/T]ACAAATATTGCTTTC | 9063 |
rs747349121 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892275 | TAGTTTACTAAAATG[C/T]AAACAGATTTAAATA | 9063 |
rs747425646 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847723 | TCCTGACCTCGTGAT[C/G]AGCCTGCCTCGGCCT | 9063 |
rs747450414 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826422 | GATCACAACAACTCA[C/T]GAGTCAGCATCACTA | 9063 |
rs747464016 | snp | A/G | 1.64944e-05 | 0.00287175 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844074 | ACATCAAGGATACCC[A/G]AAGGCTAGTTGTAGC | 9063 |
rs747488624 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861304 | ACAGCTCCTCCTTGT[A/G]AAAATAAAATAATCT | 9063 |
rs747494311 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874192 | AAACCACCCATCGGA[A/G]GAAGAACCCTGGAAT | 9063 |
rs747510195 | snp | A/G | 2.67226e-05 | 0.00365521 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812424 | TCCCAGAATCAAGTG[A/G]GTCCTCCTTTAGTCC | 9063 |
rs747526829 | snp | A/T | 1.65097e-05 | 0.00287308 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812525 | AACTAACATGAGTAC[A/T]GCTTTCATGGGAGCT | 9063 |
rs747534121 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852159 | GCAGAATCTTGTTTT[A/G]TATTTAAAAAGACTC | 9063 |
rs747540763 | snp | C/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825534 | TTAAGATCCACTCAT[C/G]CATCTTGCTCCAGAT | 9063 |
rs747541966 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860243 | ACCTGAGTATGAGAA[G/T]TTCCTAAATCTCCCC | 9063 |
rs747554924 | in-del | -/ACTA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879320 | TCAACATCACTAATC[-/ACTA]ATTAAAGAAATGCAA | 9063 |
rs747555041 | in-del | -/TAGCT | 1.74485e-05 | 0.00295363 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828135 | ACGCTTGAACCTGCA[-/TAGCT]TGTAAAGAAACAAAA | 9063 |
rs747573919 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897316 | GCAGGAAATGCACAA[C/G]ATAAGCCTATAACAT | 9063 |
rs747582803 | snp | C/T | 0.000162245 | 0.00900535 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920054 | AAAGCCCCACTGAAA[C/T]TTACGTGCAGTGTTC | 9063 |
rs747656760 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883643 | CAGGAGTTCAAGACC[A/T]GCCTGGGCAACATAG | 9063 |
rs747704012 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851802 | TTTGTACATGAAGTA[C/T]AGTGGTCAACTGCCA | 9063 |
rs747781863 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864405 | CTAAACTGCATTCAT[C/T]TTGGAATCATGAGTA | 9063 |
rs747794705 | snp | A/G | 1.83179e-05 | 0.00302632 | intron-variant, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818428 | CAGTTCATTATTAAT[A/G]TCATTTCTTCTTTGT | 9063 |
rs747821494 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46815119 | AATTTAGATATTAAA[A/G]ACAAAAATCATAAAC | 9063 |
rs747830148 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846801 | AAGGGGCGTCCAGGG[C/T]GCTTCTGTTCAATCC | 9063 |
rs747835216 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876485 | TAAACAATTAGGACC[C/T]ACCAGCCAAATGGCT | 9063 |
rs747862588 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910717 | CGTAGACTACAATTG[C/T]AGATTACAATCTTCT | 9063 |
rs747935677 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46843428 | CCCTCCCATCTCCTC[C/T]TGGTAGTAAAACAGC | 9063 |
rs747938227 | snp | A/G | 1.68852e-05 | 0.00290557 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846666 | GAAAGTCAACCCTCA[A/G]TGGGGTCACTGTCCT | 9063 |
rs747943476 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921489 | GCTTTTCCATTTACT[A/G]GCTGTGTAACTTTAG | 9063 |
rs747984542 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862256 | GAATCGCCTGAAACC[A/G]GGAGGTGGAGGTTGC | 9063 |
rs747993753 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828241 | GACAACATATAGCCA[A/G]TGAAGCCACATACTC | 9063 |
rs748015863 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904230 | AAACTAGAGAGAGTA[C/T]ACAGAATGTCTCTGT | 9063 |
rs748055462 | snp | C/T | 3.29598e-05 | 0.00405941 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890839 | CAAACTGAAAACCGA[C/T]GATTTGATTGTGGAT | 9063 |
rs748062531 | snp | A/G | 8.30144e-05 | 0.00644207 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890957 | TTCAATAAATGCAGC[A/G]CCCTCATCAGGAGGT | 9063 |
rs748072554 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859698 | ATGAATAAAAGAACA[A/G]AAGATAAGCAGGTTT | 9063 |
rs748085664 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888908 | GTTGGAGACCTTGGA[A/G]CAGAGAACCTGGAAA | 9063 |
rs748090524 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885639 | TCATGTCTGTTTTTC[A/G]CGCCACTGCACTCCA | 9063 |
rs748102325 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842189 | TGTGTTCATGCTACT[A/G]CATTCCAGCATGGGC | 9063 |
rs748130134 | snp | A/G | 1.66735e-05 | 0.00288729 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46827989 | CTTTGTGTTTCTGAC[A/G]TAAAGATGCATTTCC | 9063 |
rs748138755 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902373 | ACCAGTCTCACCAAA[A/C]TGGAGAAACCCCGTC | 9063 |
rs748143630 | snp | G/T | 1.68442e-05 | 0.00290204 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844780 | ACCTTTCATTTTTAA[G/T]CTCTGTAATAACATG | 9063 |
rs748191746 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912651 | TGGAAAATGACCTAA[A/G]TTTCTTATCTAGCAA | 9063 |
rs748214822 | snp | A/G | 1.66128e-05 | 0.00288204 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855525 | ACATGCACATAGTAA[A/G]CAAGTATAAAACTAA | 9063 |
rs748216075 | snp | A/C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831895 | GACCTTGAGTTAGGG[A/C/G]AAATGTCTTAAAATA | 9063 |
rs748303778 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847254 | ACCAAACTGGGAAGT[A/G]AGGGGAAAGAAAGAA | 9063 |
rs748318781 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830126 | TAAATGGCTAGAGAG[-/A]AAGTAGATACCTGGA | 9063 |
rs748326398 | snp | A/G | 1.66164e-05 | 0.00288235 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855353 | AACTTACAGGCAAAG[A/G]AAATAGCTTCCCATT | 9063 |
rs748351261 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879528 | ATTAAAAATAGAATT[A/G]CCATACGATCCCGCA | 9063 |
rs748384680 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830629 | AACAAAACAAACAAA[C/T]AGAAAAAAAGAAAAA | 9063 |
rs748414581 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861142 | AAAATTAGCCAGGCA[C/T]GGTGAAGAATCGCTT | 9063 |
rs748468067 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859975 | AAATGGAAGGAGCAG[C/T]GCTAAAGCCAAAAAG | 9063 |
rs748468417 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919004 | TGCGTGTATATATAT[-/GT]ATATGTGTGTGTGTG | 9063 |
rs748495120 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868755 | GTTTTCCTTGTGACT[C/G]CAAGCTCTTGTTTCT | 9063 |
rs748519481 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811802 | ACGTCAAAGTGTAAA[C/T]GATAAGCAGGAAAAA | 9063 |
rs748522225 | in-del | -/TTTCTATTTTTGTACACGGTTGG/TTTCTATTTTTGTACACGGTTGGCTGGATACTTTCATAG | 3.41357e-05 | 0.00413121 | splice-acceptor-variant | PIAS2 | GRCh38.p7 | 18:46828130 | TGAGGACGCTTGAAC[lengthTooLong]CTGCATGTAAAGAAA | 9063 |
rs748543004 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824200 | GCTGGATCAGAGAAT[C/T]GCATGAAACTCACAT | 9063 |
rs748560342 | snp | G/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918303 | TTTCCTTGAAGAATT[G/T]GGTGGAACCCACACA | 9063 |
rs748560608 | in-del | -/A | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921694 | TGATAAACACATAAC[-/A]AAAAAAAAAAAGCAC | 9063 |
rs748568085 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902642 | AAAGATGTCAACTTT[-/C]CCCAAACCGATATAT | 9063 |
rs748569827 | snp | C/T | 0.000616333 | 0.0175438 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46906219 | CTACAGCAAGCATCA[C/T]ACTTAACTGTGAAAC | 9063 |
rs748609597 | snp | C/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825189 | CTGAACTACAAGAAA[C/G]GATATGAAAAGGACA | 9063 |
rs748653091 | snp | G/T | 1.67936e-05 | 0.00289767 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836321 | CCAACAGCTGTTGTA[G/T]TAGTCCATATCAGCT | 9063 |
rs748654784 | snp | C/T | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890631 | CATAAAAGGGCAGAT[C/T]TTTTAACTGCACATC | 9063 |
rs748655013 | snp | C/T | 1.65348e-05 | 0.00287526 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836461 | GGCAGCATCAAAACA[C/T]TGCAGATGTGTACAA | 9063 |
rs748664321 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872529 | TGGATGACCTGCTTA[C/T]ATCTGGTGAAGCTAT | 9063 |
rs748717095 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871590 | GAATTCTACCAAGAG[C/T]CCTTGATAAACTTAG | 9063 |
rs748742824 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863876 | TTAAGGTTAAATAAA[G/T]CCACAGGGTAGGTCC | 9063 |
rs748766334 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894542 | GTTATTCCTACAGAC[A/G]AATTTCCCTACAGAG | 9063 |
rs748770222 | snp | A/T | 1.81358e-05 | 0.00301124 | intron-variant, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818404 | AGTATCAGAAGATGT[A/T]CCAAGCTTCAGTTCA | 9063 |
rs748784372 | in-del | -/ATAT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862637 | TACATATATACATAC[-/ATAT]ATATACACATATATA | 9063 |
rs748791546 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887946 | TGTTCACAGATGGTA[A/G]GCTCTTATATACAGT | 9063 |
rs748833085 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813963 | AACTTTCCACTAAAA[C/G]TGGGGGGTAAATCTA | 9063 |
rs748846475 | in-del | -/A | 0.000298649 | 0.0122162 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844851 | ATTCTACAAACAAAC[-/A]AAAAAAAACCTGCAT | 9063 |
rs748849819 | in-del | -/AAG | 1.67094e-05 | 0.0028904 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829881 | GCCTAAAAAACAATT[-/AAG]AAGTACATACATGTG | 9063 |
rs748881463 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849245 | TCAGCATAAAGTGTT[C/T]TCAATCTATTCTGTA | 9063 |
rs748891140 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828152 | GTAAAGAAACAAAAG[C/G]AAAAAAAAATTAAAG | 9063 |
rs748893326 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814865 | AACTTTAAACTGGGG[A/C]CTCCCCAAAGTCCAA | 9063 |
rs748904248 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862801 | ACCTCTGCCTCCTGG[A/G]TTAATGTGATTCTCC | 9063 |
rs748925936 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914865 | GTCCTATAATTTACT[C/T]GAGCATCACTCTGAC | 9063 |
rs748938824 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876303 | TGCCACTGGAGTCCC[G/T]AGAGGAGTGCCAGAT | 9063 |
rs748948051 | snp | A/G | 1.71616e-05 | 0.00292925 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844755 | CTCTGGAATGATCAG[A/G]GTTTCTAATACCTTT | 9063 |
rs748957812 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908660 | CAAAAGCACTATCCA[A/T]AAAGAAAAGCCTGAT | 9063 |
rs748966599 | snp | A/G | 1.65072e-05 | 0.00287286 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815333 | ATCAACTGGAATAAG[A/G]GAAAGAAAATCCAAA | 9063 |
rs748996572 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904039 | ATGAAAAAGATGAGC[A/G]GGCCCCAGAGAGTGA | 9063 |
rs749007391 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913252 | ATCAGGATGGTGACT[C/T]CTGGTAGGTGTAAGG | 9063 |
rs749017120 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920377 | CTTTCTGGCATGTGG[A/G]ACACTCGCCATTTTG | 9063 |
rs749056169 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878220 | GTAACACTTTTCTCA[-/C]CTGCCTTTTTAAGAT | 9063 |
rs749076244 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890828 | GAGCCACCATCCAAA[C/T]TGAAAACCGATGATT | 9063 |
rs749134237 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837315 | TGGAAGGTGACAAAT[A/G]TCCCATTACAGTTGT | 9063 |
rs749139493 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840628 | AATTTAATTCTACTC[C/T]AGTGGTCTTATAAGA | 9063 |
rs749242409 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820225 | ACCGTTATTTTAACT[G/T]AATAATGGCACCAAA | 9063 |
rs749247052 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853716 | ACTGCCTGAACCCAG[C/G]AGGCAGAGGTTGCAG | 9063 |
rs749260243 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877686 | GACTCCAGCCAATGG[A/G]GACACGACACAGAAC | 9063 |
rs749263900 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862378 | AATTTCCCAAACTTA[C/T]TTAACTGCAACAATC | 9063 |
rs749268187 | snp | A/G/T | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890759 | TGAGGTGTAACTGAA[A/G/T]TGGAAGGCAACGAGT | 9063 |
rs749274337 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868527 | CCATATTCAATTTTA[A/C]ATGGTAGCCAATCAG | 9063 |
rs749279699 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913953 | AGGTGTGAGCTACCA[A/G]GCCCTGCCCTCCAGA | 9063 |
rs749367210 | snp | C/T | | | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836503 | GCATGGGATTGTCAG[C/T]CTCATTTTTCCTAAC | 9063 |
rs749419957 | snp | C/T | 3.3106e-05 | 0.0040684 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846835 | TTTTAGGCGGTGGTG[C/T]ATAGCCCTATAACCG | 9063 |
rs749424338 | snp | A/C | 0.000221263 | 0.0105158 | utr-variant-5-prime, intron-variant, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920096 | TTCCCAGCATTCATT[A/C]TGCCCCTTCCTCAAT | 9063 |
rs749443156 | snp | A/C/T | 3.30476e-05 | 0.00406484 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836448 | TTTGTAGATAGAGGG[A/C/T]AGCATCAAAACACTG | 9063 |
rs749453843 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890162 | ACAGTGGAAGTAGAA[C/T]GGTAACTGCCAGGGG | 9063 |
rs749453952 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810588 | TGGGTTTGTTTCCCC[C/T]CCAACATCTTTAAAA | 9063 |
rs749460675 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46818920 | AGCCAGTTCAGACAT[A/G]TTTTACTGCATTTTT | 9063 |
rs749494391 | snp | C/T | 0.00135962 | 0.0260377 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901215 | CTGCGGTCAGGAGTT[C/T]GAGGCCAGCCTGACC | 9063 |
rs749496601 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842615 | CTGTTTTTTAACCAA[-/C]AAAAAGGCAATTTCA | 9063 |
rs749500503 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872381 | AAGATCCTCATTCTG[A/G]GCGAAAGCAACAATA | 9063 |
rs749517525 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856091 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 9063 |
rs749542192 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809592 | GAAACCCCGTATCTA[C/T]TAAAAATACAAAATT | 9063 |
rs749542876 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882425 | CACAAATGGACTACA[A/G]ATTGGTGCAATGCTG | 9063 |
rs749550486 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904681 | ACTTGAACCCACGAG[A/G]TGGAGGTTGCAGTGA | 9063 |
rs749553026 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858654 | GTGAGCCTTGATTGC[A/G]GCACTGTACTTTCAG | 9063 |
rs749601844 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902969 | TCAGTGGAAGAAAGA[C/T]AGCCTTTCAATATAT | 9063 |
rs749606047 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874329 | ATTCCCTTTTCAAGT[A/G]CAGCCACCAGTAATG | 9063 |
rs749606400 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871372 | GGCCAAAGCTTACAA[A/C]GGATTTAAGTCCTCA | 9063 |
rs749607980 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916292 | AAACTGAACCTTTTA[C/T]CGGATTCCTCTTCCT | 9063 |
rs749619136 | snp | A/G | 1.70093e-05 | 0.00291622 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829919 | CAGCTTTGCCTAAAG[A/G]TGAAATAAGAAAGTA | 9063 |
rs749661258 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46915265 | AAAATGCTTAGACCA[C/G]AACCAGGCATGGAAT | 9063 |
rs749708531 | snp | C/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823276 | TTTTTTTTTCTCTGC[C/T]ACTGAAAGAAACTAA | 9063 |
rs749751900 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870271 | TTGGAGGAGAAGGAA[A/T]CGGCTTTGTAAATGC | 9063 |
rs749765460 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900279 | GAGACAGGAGAATCG[C/T]TTAAACCCAGGAGGC | 9063 |
rs749789856 | snp | C/T | 1.69006e-05 | 0.00290689 | splice-donor-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46864163 | CAAATATTCCTCTTA[C/T]CTGGATATGCATATC | 9063 |
rs749806346 | snp | A/G | 2.00652e-05 | 0.00316737 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864278 | AAAAAGAAAGATAAT[A/G]TTTCAATAACAAATC | 9063 |
rs749806846 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883459 | TGTAATCCCAGCACT[C/T]TGGGGGGCCGGGGCA | 9063 |
rs749856149 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882613 | GTAAAACTGCAAGAA[C/T]AGTGCCTGATACATG | 9063 |
rs749877100 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888680 | ATCAGGCATTAGATT[C/T]TCGTAAGGAGCATGC | 9063 |
rs749906965 | snp | C/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893660 | CAAAGATAAAGTATT[C/G]CTGGACACATAGCCA | 9063 |
rs749912278 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808479 | GGGGGGTGTTACAAA[A/C]CAGTCACTAGGCAGG | 9063 |
rs749938954 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841559 | CAAATCTAATCAAAA[C/T]ACCTGTGTCTGGTAT | 9063 |
rs749990533 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857969 | ATAAATGCAATGATG[A/C]CTTAACAGAAAATAA | 9063 |
rs750059267 | snp | A/G | 1.71029e-05 | 0.00292424 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829693 | ATGATAATGTTGCAC[A/G]AGTCTCACTGCTTTA | 9063 |
rs750081351 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839863 | GAGCAAAACTCTGTC[-/A]AAAAAAAAAAAAAAA | 9063 |
rs750135621 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869808 | GGATTGAATTTGTCA[A/G]CTTCTAATAGAGTAT | 9063 |
rs750177128 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881223 | GTCCTATCTCTGAAC[A/G]ACCCCAGGCTCTTTC | 9063 |
rs750181074 | snp | A/G | 1.72175e-05 | 0.00293402 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855646 | AGAAAATGGGTTAAA[A/G]AAGTACAATGAGAAT | 9063 |
rs750182425 | snp | A/G | 1.66863e-05 | 0.0028884 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828110 | CAGTCACTGAACAAG[A/G]CTTACTGAGGACGCT | 9063 |
rs750270967 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842113 | TGGCGGTAGTCCCTG[A/C]TACTCAGGAGGCTGA | 9063 |
rs750294162 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879826 | CAGATAATATGACAC[A/G]TAAGTCAAATAATAA | 9063 |
rs750335231 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861961 | GGTGATATAAGATTT[A/G]ATATTAAAGGAAACA | 9063 |
rs750342656 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46893920 | CATTTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 9063 |
rs750386849 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847103 | ATGCTGACATCTTGC[C/T]ACATTGGCTATGAAT | 9063 |
rs750444219 | in-del | -/G | 0.000653762 | 0.018068 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818469 | ATTCAGAAGATTCAT[-/G]TTTATGATGTTTAAA | 9063 |
rs750478628 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892228 | TAAAACCCTATATGG[-/TT]TTTTTAAATACTTGT | 9063 |
rs750513018 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896260 | ATGGTCTTATAAATG[-/A]AAAAAAAAAAACTAA | 9063 |
rs750591351 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824060 | AACACACACAGATAC[A/G]TGTATACATTATGCA | 9063 |
rs750593986 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861960 | TGGTGATATAAGATT[C/T]AATATTAAAGGAAAC | 9063 |
rs750595708 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838155 | CCTCTAAAATGAACA[C/G]CTGGTAATGTGGTAA | 9063 |
rs750596416 | snp | A/G | 3.68331e-05 | 0.00429129 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864261 | GAACTGGGAAGAAAA[A/G]AAAAAAGAAAGATAA | 9063 |
rs750597241 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852590 | GAAATCAGCAGTAAC[G/T]AAGTAACAATGCCCC | 9063 |
rs750628904 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883235 | TTTCTTATGATTTTT[G/T]ATTCCAAATATTAAC | 9063 |
rs750629428 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889304 | TAAAAAAGGCAAACC[A/T]CAGAGTGGGAGAAAA | 9063 |
rs750637007 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851342 | TTGTCAACCCTTCTT[C/G]CTTTCTTCAACCTTA | 9063 |
rs750660291 | snp | C/T | 1.67433e-05 | 0.00289333 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890613 | TGAGAACATCAAGGA[C/T]ATCATAAAAGGGCAG | 9063 |
rs750665655 | in-del | -/AGAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861691 | CCGTACCCCCAAATC[-/AGAA]AGAGTCTACAAAACA | 9063 |
rs750691272 | snp | C/T | 1.65081e-05 | 0.00287293 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820964 | CATGCTTGATATTGG[C/T]GTATGGTGGAATGGT | 9063 |
rs750695748 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896738 | GACCATAAGAAGTCT[A/T]TGTGTAACACAATTT | 9063 |
rs750751638 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816935 | TTCATATTAATAATA[C/T]TCAATAAATCCTCTC | 9063 |
rs750752861 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911369 | TACAGGTGCCCACCA[C/G]CACGTCGGGCTAATT | 9063 |
rs750793863 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856044 | AGAGTCTTGCCCTGT[C/T]GCCCAGGCTGGAGTG | 9063 |
rs750826150 | in-del | -/TTA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839188 | ACTCAATCACTAAAC[-/TTA]TTATTAAATTACACT | 9063 |
rs750843418 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816091 | ATCAGTTCACCTAGA[C/T]CTCCCTGTGTGACTA | 9063 |
rs750874718 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828510 | CTCAGGTCATGGGAC[A/G]AGAATGGGTGAGTTC | 9063 |
rs750890215 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809729 | CATTGCACTCCATCC[C/T]GGGCAACAAGAGCAA | 9063 |
rs750904971 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877010 | CGGCCTCCTTCACTA[A/G]TTTAATGGAAAAATG | 9063 |
rs750914153 | snp | A/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827902 | ACATTTATAAATCTA[A/T]CCAAGAGCAATTAGT | 9063 |
rs750917478 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863780 | CTGTTATGGACTGAA[C/T]TGTGTATCCCCAAAA | 9063 |
rs750930980 | snp | A/G | 1.75332e-05 | 0.0029608 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844857 | ACAAACAAACAAAAA[A/G]AACCTGCATTAAAGA | 9063 |
rs750940668 | snp | A/G | 3.47222e-05 | 0.00416652 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891062 | ACCATATTCTAAAAG[A/G]AAAGAAAAAAAAACA | 9063 |
rs750955814 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876277 | TCCTTTGACCCTCAC[A/G]TTTATATAGATGCCA | 9063 |
rs750959341 | in-del | -/C | 0.000162324 | 0.00900755 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920043 | AAAAGAAAAGCAAAG[-/C]CCCACTGAAACTTAC | 9063 |
rs751000534 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899920 | AGGAAAAATATAAAA[A/G]TAAGACAGAATGAAA | 9063 |
rs751017042 | snp | A/C | 1.71164e-05 | 0.00292539 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829684 | CCAAGATTAATGATA[A/C]TGTTGCACGAGTCTC | 9063 |
rs751031716 | snp | A/G | 6.59228e-05 | 0.00574083 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846767 | AGCTGAAGATAACCT[A/G]ACTAAAGATGTAATA | 9063 |
rs751147019 | in-del | -/TACT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890294 | ACAACATTACCAACA[-/TACT]TAACACCACTCAACT | 9063 |
rs751158793 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830378 | GAAAAACCTGAAAAC[C/T]TGGAAACTAAACAAA | 9063 |
rs751162030 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913486 | CAGGCACATTCTCTC[G/T]CATTCTGAGACACAC | 9063 |
rs751178801 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869689 | GACAGTGAAAGGACT[A/G]AACATAATAAAAAAC | 9063 |
rs751183245 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855476 | TCTTAAATAGTGTGC[G/T]CAAACATTCTTATAT | 9063 |
rs751230537 | snp | A/C | | | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46827999 | CTGACATAAAGATGC[A/C]TTTCCTTTTGGCAGG | 9063 |
rs751231140 | snp | C/T | 1.66341e-05 | 0.00288388 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828099 | CTCACTGGCTACAGT[C/T]ACTGAACAAGGCTTA | 9063 |
rs751233776 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867954 | ATAAAGAAGCCCAAA[G/T]TAGACCACATGAAGA | 9063 |
rs751287257 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879748 | AAAAAAAATCTGACA[C/T]GTTATAACATGGACA | 9063 |
rs751309924 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914248 | CAGAGAACTTCCCCA[A/C]TTCCTTTCCTTCAAT | 9063 |
rs751411463 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811549 | GTGTGAACAAATTTC[C/T]AACAAACATTCCAGT | 9063 |
rs751426607 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847026 | TTGAAAAAAGGTTAC[A/G]AAATATTTCACAAGT | 9063 |
rs751433429 | in-del | -/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46817920 | AAATTTTACTGCCTT[-/G]TTTCGTAAGTTTAGC | 9063 |
rs751433523 | snp | C/T | 5.04164e-05 | 0.00502052 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836562 | TTTCAGAAAGGAGAA[C/T]GAGCTCAGAGGGAAC | 9063 |
rs751443659 | in-del | -/TAT | 0.000235195 | 0.0108417 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836318 | TGCCAACAGCTGTTG[-/TAT]TATTAGTCCATATCA | 9063 |
rs751464812 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848217 | GTCTCAGATTTCTCT[A/G]CAAGTCACTGACACC | 9063 |
rs751560964 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914886 | CACTCTGACCACCAC[-/A]AATATATTCTGATCC | 9063 |
rs751618497 | snp | C/T | 1.76213e-05 | 0.00296822 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812470 | GGAATGTTACTTCCA[C/T]TGCTGGTTATGACCC | 9063 |
rs751640197 | snp | A/G | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822852 | TGTCTCAAAGTATTA[A/G]TATCTTATTGTTTTA | 9063 |
rs751651329 | snp | G/T | 3.33156e-05 | 0.00408126 | synonymous-codon, intron-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46864231 | ACTTCTCTTGAAATC[G/T]CTGAATACTGCTTTG | 9063 |
rs751671403 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837001 | TACCATTATATGAAG[G/T]TATCATAATTTATTT | 9063 |
rs751671660 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837021 | ATAATTTATTTAATC[A/T]GTACACTAATGACTG | 9063 |
rs751680608 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839508 | TTTCTTTAAAATAAC[A/G]TTCTAACTCAGCCTA | 9063 |
rs751728186 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834949 | AGTCTTACATTCCCT[C/T]TGAGTATTTCTATTT | 9063 |
rs751728920 | in-del | -/GG/GTG | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906773 | TGTATGTGTGTGTGT[-/GG/GTG]GGGGGGGGGGGGAGG | 9063 |
rs751733459 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816012 | GTAATATACTTTTGA[C/T]ATATTCAAGTAATAA | 9063 |
rs751734468 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863630 | AAATTATTGCCAAAT[A/G]TAACAAAAAGTAATC | 9063 |
rs751757932 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851170 | ACACAACATCAGGGA[A/G]CATAAATCCATGAAC | 9063 |
rs751760189 | snp | A/G | 2.5493e-05 | 0.00357013 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818330 | TTTTTCCTTGAAATA[A/G]GCTGTTTTCCACTCC | 9063 |
rs751768474 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866799 | AACCTGAAATCTCCC[G/T]AAAGACCCTGATAAA | 9063 |
rs751776080 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849981 | AAAAACCCACAGCAT[G/T]ACAACCCCACAAAAA | 9063 |
rs751805719 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895174 | ATTGCTCTTCAATTC[G/T]AAAACATGAGACAGA | 9063 |
rs751809231 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864387 | CTCCAAAATCAGGAA[A/G]TACTAAACTGCATTC | 9063 |
rs751846257 | snp | A/C | 3.30786e-05 | 0.00406672 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820938 | CTCCACATACCTGGC[A/C]AATCTGATGACATGC | 9063 |
rs751852805 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910112 | GGTGAGTCAAGATCG[C/T]GCCACTGCACTCCAG | 9063 |
rs751892925 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828476 | TTTACAGAAAGACAC[A/G]CAGAGTTAGGGAACT | 9063 |
rs751892956 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814542 | TTTCTGCTGCTGTTC[A/G]TGTAATCAGATACAG | 9063 |
rs751927169 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876092 | CTGCCCTGATCCATC[C/T]GCAAGTGGATGTATG | 9063 |
rs751956832 | in-del | -/A | 0.000499034 | 0.0157882 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891067 | ATTCTAAAAGGAAAG[-/A]AAAAAAAACATAAGC | 9063 |
rs751983184 | in-del | -/TT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867192 | TGACATATCTTTGAC[-/TT]TTTACCTATATTTGC | 9063 |
rs751984000 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921196 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAACCT | 9063 |
rs752005933 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884659 | GTGGCTCACGCCTGT[-/A]AATCCCAGCACTTTG | 9063 |
rs752012436 | in-del | -/TTT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844689 | CTCATATGCTCAATC[-/TTT]TTTTTTTTTTTTAAA | 9063 |
rs752026539 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888519 | CTACGGTAATCAAAA[C/T]TGTGATACTGGCATA | 9063 |
rs752027111 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862360 | TTATGTAATTAAGTA[C/T]AGAATTTCCCAAACT | 9063 |
rs752033408 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840288 | GAGTACACAAGCACA[C/T]ATTCCATTAGCCATC | 9063 |
rs752093416 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890801 | ACGGCCAAGTCAGGT[C/T]CTACAGGTGATGAGC | 9063 |
rs752109028 | snp | A/T | 1.76163e-05 | 0.0029678 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827901 | GACATTTATAAATCT[A/T]TCCAAGAGCAATTAG | 9063 |
rs752120187 | snp | C/G | 1.88984e-05 | 0.0030739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844709 | TTTTTTTTTTAAATG[C/G]TTGGTCTTATTAAAC | 9063 |
rs752134139 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812367 | AAAAAAGAACGTTTC[C/T]ACAGACTAGAGATCC | 9063 |
rs752161296 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912208 | GTCTCTCAGTATCCG[A/T]AGGGGGCTGGTACCA | 9063 |
rs752199056 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876350 | ATCAGATAGTGCAGG[G/T]TTTGAGTCCATACTA | 9063 |
rs752210103 | snp | C/T | 1.65627e-05 | 0.00287769 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855458 | AATAAAAGAAAAAAG[C/T]ATTCTTAAATAGTGT | 9063 |
rs752227333 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819425 | CAAATTACATGTGGA[C/G]TAACTATATCTAAGA | 9063 |
rs752307904 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879572 | GTGTATACTCATAAG[A/T]ATTAAAAAACAGAAT | 9063 |
rs752335076 | snp | C/G | 0.000147591 | 0.00858915 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917370 | CCCGCGGGCGCCGCC[C/G]CCGCTGCCGCCGCAC | 9063 |
rs752391747 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874083 | TGTGATGCAGTTCTT[-/G]GGAGTCTCCAGATGT | 9063 |
rs752416489 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845065 | TTATCACTTTAAAAC[A/C]TTCGCTGGTATGGGA | 9063 |
rs752418240 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877264 | GTTAAAAACGTTTGA[A/G]GAGGAAGAATTATAA | 9063 |
rs752423352 | snp | C/T | 3.29739e-05 | 0.00406028 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890787 | AGTGGATTCCAGCCA[C/T]GGCCAAGTCAGGTTC | 9063 |
rs752478572 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889814 | ATAGCTAAAATGTGG[A/G]AGCAACCCAAGTGTC | 9063 |
rs752531462 | snp | C/T | 1.83528e-05 | 0.0030292 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891090 | ACATAAGCCAAGTCA[C/T]CCTCAAGCATACAAA | 9063 |
rs752532875 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811423 | CAAATATTTCACTAC[C/T]ATTCTGTAAAATAAA | 9063 |
rs752551296 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824655 | TCTTGGTGCTTTGTA[A/G]AATTGTTTATAAGAA | 9063 |
rs752573723 | in-del | -/TTGC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885433 | CTGAGGCAAGGAGAA[-/TTGC]TTGCTTGAACTTGGG | 9063 |
rs752604177 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859194 | AGCACTTTGGGAGGC[C/T]GAAGCGGGTGGATCA | 9063 |
rs752650415 | snp | A/G | 1.67259e-05 | 0.00289183 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829885 | AAAAAACAATTAAGA[A/G]GTACATACATGTGAT | 9063 |
rs752660384 | snp | C/T | 1.99866e-05 | 0.00316116 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890573 | AACTGAATTCTCAAA[C/T]ACTTACCTAAACTCG | 9063 |
rs752661943 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870765 | CATCCTCTTTTCAGG[A/G]GAAGAAAGAAGCATG | 9063 |
rs752675932 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916241 | AGCCAACATCCTTCC[A/C]CCATCCCATCTCTTG | 9063 |
rs752707095 | snp | G/T | 1.65356e-05 | 0.00287533 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815388 | TAGTTGTCTCATATT[G/T]TGGGAGACCAGAATT | 9063 |
rs752707321 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894088 | CCAAGACTGAGCCAC[G/T]GCACTCCAACCTGGG | 9063 |
rs752740096 | snp | A/G | 1.65206e-05 | 0.00287403 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836380 | TATTAGACTTTCATA[A/G]GCAGCTTTTTTGTCA | 9063 |
rs752752099 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817570 | TTAAGAGATTTACTT[A/C]TCTGTATATTGATAC | 9063 |
rs752777235 | in-del | -/TGAG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882270 | TATCCAAAAGCTTAA[-/TGAG]TGTGTCCTAATGTTC | 9063 |
rs752805982 | in-del | -/ATT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848616 | AGAGGCAAGACAGTA[-/ATT]ATTAAATGGTAGTCC | 9063 |
rs752826719 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813172 | ACATTCATTCTAAAA[C/T]ACAGACTACACGGTA | 9063 |
rs752842017 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814627 | ATGAAGCAGTGACCC[A/G]TGGTTCTTCCTCTAT | 9063 |
rs752882814 | snp | C/T | 0.00199501 | 0.0315202 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844690 | TCATATGCTCAATCT[C/T]TTTTTTTTTTTTTAA | 9063 |
rs752891763 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863471 | GTGACACTAATTTCT[A/G]TATTTCTTGTAGAGA | 9063 |
rs752898096 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870237 | GCCCCAACTCTTTTC[C/T]CCTTGAGGGAAGTGC | 9063 |
rs752946579 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862101 | CTTTGGGAGGCCGAA[C/G]AGGTGGATCACTTGA | 9063 |
rs752951155 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887061 | TAATTTGGCAATATG[C/T]TATCAAGAGTCTAAA | 9063 |
rs752951997 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909064 | GAAAGGAGAAATTTG[C/T]ACCACATGCATCCAA | 9063 |
rs752974722 | snp | C/G | 1.66153e-05 | 0.00288225 | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812615 | TAGGAGGACAGTACT[C/G]CTTGAAACAAACAAT | 9063 |
rs752999826 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875209 | ATAAGTATCTATGTC[C/T]GTACTGTAGTGAGTC | 9063 |
rs753002751 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921044 | CCTGACTAGGCTACC[A/G]TCTTAAAATGGCTCC | 9063 |
rs753007764 | snp | C/T | 4.95029e-05 | 0.00497484 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844036 | AAATTCCCCAAAATG[C/T]TTTGTTGCTTTACTT | 9063 |
rs753038204 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841196 | AGTAACTACTGTGAC[A/T]TTACCTTCCTTTAGT | 9063 |
rs753053337 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874023 | TCTCATGAGGGAGGT[G/T]TTATCTCAGTTGCAT | 9063 |
rs753081329 | in-del | -/AAAAAAAAAAAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832893 | CAAGCCTCTGTCTCC[-/AAAAAAAAAAAA]AAAAAGAGAAGCCAT | 9063 |
rs753144781 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854330 | TACACAGCTTCCCCA[C/T]TTCCTCAATAGTTGC | 9063 |
rs753157140 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860672 | CACACTGTTATAAAC[A/G]AATAAACGGGCTGGG | 9063 |
rs753219928 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890731 | CACAGAACCAACAGG[A/G]GAGGATGGTGAGTGA | 9063 |
rs753223816 | snp | C/G | 3.31928e-05 | 0.00407373 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828075 | AACATCTACTTTCTT[C/G]TTGCTTGCCTCACTG | 9063 |
rs753247166 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858250 | AAGCAGAGCAAGATG[C/T]TGAAAACAACTGCCA | 9063 |
rs753248101 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886115 | GCATCTTCACTTAGT[C/T]CCCCCCAGTCTTCTG | 9063 |
rs753252239 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867586 | ATGAATGCCTTTAAG[C/T]TAAGAGCAAATGAAA | 9063 |
rs753297490 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898744 | CACGCCTCTAATCTC[A/T]ACACTTTGGGGGGCT | 9063 |
rs753346672 | snp | C/G | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846792 | GTAATATTCAAGGGG[C/G]GTCCAGGGCGCTTCT | 9063 |
rs753375333 | snp | C/T | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829820 | CCATCTTCTTGGAAT[C/T]TGATCTCATCTACAT | 9063 |
rs753450073 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46891075 | AGGAAAGAAAAAAAA[A/C]CATAAGCCAAGTCAC | 9063 |
rs753461526 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828698 | CCTCTCAATTAAGTT[A/C]CTAAGACATTTAAAC | 9063 |
rs753465319 | snp | A/C/T | 1.8659e-05 | 0.00305436 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844883 | AAAGATGAGAGATAA[A/C/T]ATTCTCTTTGTTTAC | 9063 |
rs753478270 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878869 | CAAGACTCCGTCTAT[-/A]AAAAAACAAAAACAA | 9063 |
rs753496788 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905058 | ACATATATAAAACTG[C/T]ACCAAAAACCAGGCA | 9063 |
rs753511847 | snp | A/G | 1.65553e-05 | 0.00287705 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890932 | CTGAACCGCAGGGCT[A/G]CAGCCGCTCTTCAAT | 9063 |
rs753594335 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46903835 | TCCCTCAACAGGTGA[A/C]TGGTTAAACAAACTA | 9063 |
rs753601556 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823751 | ATTACCTGAATGTTG[C/T]AACCATTAATACAAA | 9063 |
rs753603435 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808994 | GGCTGGAAATGCTGA[A/G]TGTCTTGGACTGGTC | 9063 |
rs753609813 | in-del | -/AAT | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, cds-indel, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818297 | CAATATGGCACTAGC[-/AAT]AATAAGGCAGTCATA | 9063 |
rs753625619 | snp | A/G | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829832 | AATTTGATCTCATCT[A/G]CATCAGAACAGTCAT | 9063 |
rs753628342 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895641 | ACACTACTGCACTCC[A/G]GCCTGGGTGACAGAG | 9063 |
rs753646190 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915832 | ACTTGTATACATCTG[C/T]TACTACACAAAAATT | 9063 |
rs753646384 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902015 | ATTGTTCACATAGAA[A/G]ATCTCAACAAATCTA | 9063 |
rs753649872 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834839 | GGGCTGAGAAGTGGA[A/C]GATGTTATGCCTGTT | 9063 |
rs753699329 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914832 | TAGCCAACAAACTAA[C/T]GCCCAAAATTTTTCC | 9063 |
rs753709344 | snp | A/T | 1.74677e-05 | 0.00295526 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855659 | AAAAAGTACAATGAG[A/T]ATTCTCAGAACAGTC | 9063 |
rs753727824 | snp | G/T | 1.69286e-05 | 0.0029093 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829712 | CTCACTGCTTTACTC[G/T]CTGCTGCTATTCTAC | 9063 |
rs753735905 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857792 | AGGCATCTTCTGACA[C/T]TCATTTCTGCCAATC | 9063 |
rs753741696 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849820 | CATGTTGCCATTCTT[A/G]TTTCAAATGCTTTTG | 9063 |
rs753798600 | snp | C/T | | | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894902 | ACGGTGAAACCCCGT[C/T]TCTACTAAAAATACA | 9063 |
rs753798808 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881796 | ATACTTCTGGCTTCT[C/T]CACAATTAAGAATAC | 9063 |
rs753813319 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893260 | AAATACTTCAATTGA[C/T]TGTGGAACACTAATA | 9063 |
rs753891118 | snp | G/T | 1.67402e-05 | 0.00289306 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812491 | GTTATGACCCCTGTC[G/T]CACTCCTGCTGCTGG | 9063 |
rs753934853 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813086 | TTATGAATGTTAAGG[C/T]TGACCAGCTGAATGA | 9063 |
rs754002501 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887235 | GTTTTGCTAAAACAT[A/T]AATAAAGCAAAAAGC | 9063 |
rs754006962 | in-del | -/AGATTTTTGCT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885003 | AAGGAAAGAAAATGG[-/AGATTTTTGCT]AGTTTGTTTTTAGAT | 9063 |
rs754024971 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840060 | CAACTACTTGGGAGG[A/C]TGAGGCAGGAGAATT | 9063 |
rs754032820 | snp | A/C | 3.2987e-05 | 0.00406108 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890711 | GGCTTAGTATCTTGA[A/C]GCAGCACAGAACCAA | 9063 |
rs754034082 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875001 | CAGAGAAAAATGAGC[C/T]GTCACCCCAGGGCCC | 9063 |
rs754046858 | snp | C/G | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919784 | TGAATGAACAATGTC[C/G]AGGTTCTAAATCTGT | 9063 |
rs754155531 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902114 | CCACATCTTTATACA[C/T]TAAAAATGAACATGT | 9063 |
rs754159317 | snp | C/T | 1.66765e-05 | 0.00288756 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890618 | ACATCAAGGACATCA[C/T]AAAAGGGCAGATTTT | 9063 |
rs754210307 | in-del | -/TGTG | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919008 | GTGTATATATATATA[-/TGTG]TGTGTGTGTGTGTGT | 9063 |
rs754312805 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895092 | AAAAAAAAAAAAAAA[-/T]ACCTCATCAAACAGG | 9063 |
rs754326980 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851676 | GTAAAACTCAGCATC[C/T]TGATGTAGGTTAAAA | 9063 |
rs754338551 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833111 | TCCACACAAAGACTT[A/G]GGCATGAATGTTCAC | 9063 |
rs754363241 | snp | A/G | 1.65023e-05 | 0.00287244 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820969 | TTGATATTGGCGTAT[A/G]GTGGAATGGTACTGA | 9063 |
rs754404963 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878188 | ACAAGTCTCTCTACA[C/T]CTCATTTCAAATGGA | 9063 |
rs754417593 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911397 | ATTTTTGCATTTTTA[A/G]TAGAGACGGGGTTTC | 9063 |
rs754424799 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861220 | CTCCAACCTGGGCGA[C/T]GGAGTGAGACTTTGT | 9063 |
rs754441989 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873511 | AGTCAGGAAGATTGC[C/T]CAATAATTGGTTGGC | 9063 |
rs754442341 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911405 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 9063 |
rs754451346 | snp | C/T | 5.01433e-05 | 0.00500691 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821114 | AAACAATCTGGCTGT[C/T]AGTTCACAGGAGAGA | 9063 |
rs754478935 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895528 | ATACAAAAATTAGCC[A/G]GGTGTGGTGTCTCGC | 9063 |
rs754485101 | snp | A/G | 6.59522e-05 | 0.0057421 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846793 | TAATATTCAAGGGGC[A/G]TCCAGGGCGCTTCTG | 9063 |
rs754525273 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877193 | ATCTCCCCACCACCT[C/T]ATTCAGATAAGCTCC | 9063 |
rs754537715 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899698 | TCTCAAACTCCTGGG[C/T]TCAAGTGATGCTCCT | 9063 |
rs754539601 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910696 | ATGTAAACAAATCCC[A/G]TAGATCGTAGACTAC | 9063 |
rs754614849 | snp | C/T | 1.90018e-05 | 0.0030823 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844885 | AGATGAGAGATAATA[C/T]TCTCTTTGTTTACAT | 9063 |
rs754626254 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897065 | ATCATTGTAAATTTA[A/T]GAGTGTTTCAATAAC | 9063 |
rs754643314 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828741 | TTATCTGCTAATCAC[A/G]TAGGTTCTTTCTACC | 9063 |
rs754647093 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876322 | GGAGTGCCAGATGAA[C/T]TTAAGGTGCAAAATC | 9063 |
rs754649021 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830483 | TATTATTTAAACACT[A/G]AAGTAGTATTTAAAG | 9063 |
rs754660532 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810231 | TTATAAAAGCACAGA[C/G]ATATCAGTTATAAGA | 9063 |
rs754661157 | in-del | -/TTT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876698 | TGATCCCTTTACTAA[-/TTT]TTTTTTTTTTTTTTG | 9063 |
rs754661342 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858118 | ACAGAGAAAAAAGGC[A/G]GCAAAGGTGCAAAGA | 9063 |
rs754719250 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889688 | TCAAAATACTAAAAA[C/T]AGAATGACTATGTGA | 9063 |
rs754733319 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46843275 | CTCCCCATTTAAAAA[A/C]CTGCACATTTCTCAA | 9063 |
rs754753468 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841780 | ACATTTCAGAAACTT[A/T]AAACAAGATTTCAAA | 9063 |
rs754792172 | snp | A/C | 1.65553e-05 | 0.00287705 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890937 | CCGCAGGGCTGCAGC[A/C]GCTCTTCAATAAATG | 9063 |
rs754820113 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809078 | CAATCCTACTTTGCT[C/T]AAAATCCAACATTTT | 9063 |
rs754843596 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902294 | GGGCACGATGGCTCA[C/T]GCCTGTAATCTCAGC | 9063 |
rs754874977 | snp | C/T | 1.681e-05 | 0.00289909 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829723 | ACTCTCTGCTGCTAT[C/T]CTACACATACTTTCT | 9063 |
rs754907177 | snp | A/C/T | 3.32736e-05 | 0.00407871 | missense, intron-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46864230 | AACTTCTCTTGAAAT[A/C/T]GCTGAATACTGCTTT | 9063 |
rs754919807 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46821257 | TCATTTTAACATGAA[C/T]ATATCTTGGCTCTCA | 9063 |
rs754941240 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822669 | TCCACAGGGATCAAA[C/T]GAACAGGACATCATC | 9063 |
rs754944225 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847107 | TGACATCTTGCCACA[C/T]TGGCTATGAATGGTT | 9063 |
rs754976778 | snp | C/G | | | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812436 | GTGAGTCCTCCTTTA[C/G]TCCAATGAGATGATG | 9063 |
rs755000016 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842247 | AATTTAAAATAAATT[-/A]AAAAAAAAAAAAAGG | 9063 |
rs755020410 | snp | A/G | | | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846831 | CCATTTTTAGGCGGT[A/G]GTGCATAGCCCTATA | 9063 |
rs755080817 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46891437 | CAATGTAATGTTTGT[A/T]ACAGAATTATCGCCA | 9063 |
rs755080828 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907981 | GAAGAATGAGGTGAG[A/G]TTAGCCACTGGGGAG | 9063 |
rs755085371 | snp | C/T | 1.65034e-05 | 0.00287253 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844028 | AAAAAGTCAAATTCC[C/T]CAAAATGTTTTGTTG | 9063 |
rs755097828 | snp | C/T | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919833 | GTGATCTTCGCTTGG[C/T]TTATTCTTACTCTTG | 9063 |
rs755121245 | snp | A/G | 4.97673e-05 | 0.00498811 | intron-variant, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812610 | AAACATAGGAGGACA[A/G]TACTGCTTGAAACAA | 9063 |
rs755155181 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813112 | AATGATGGCATTGGA[C/G]TCCTTTGTACATAAA | 9063 |
rs755174861 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839567 | TTTGGTTTCAAAACC[C/G]CTTTAAACTCTTAAA | 9063 |
rs755175339 | snp | G/T | 1.65718e-05 | 0.00287848 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812504 | TCTCACTCCTGCTGC[G/T]GGATGAACTAACATG | 9063 |
rs755178471 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906764 | CCAACAAGATGTATG[-/TG]TGTGTGTGTGGGGGG | 9063 |
rs755234410 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857757 | CTAAATATCTTCACA[A/G]ACATTATGAGTAATG | 9063 |
rs755237745 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825129 | TGGCCAAGAAATCCT[A/G]TGATAAACTTACACA | 9063 |
rs755245036 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811743 | TAATCACCAATGAAG[A/C]GTAGCCAAATCCCAG | 9063 |
rs755253821 | in-del | -/TTTTGAAATTTT | 1.64974e-05 | 0.00287201 | cds-indel, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46821010 | ATGAAGGCGGAATAG[-/TTTTGAAATTTT]CAGCAGGATCAACCG | 9063 |
rs755298860 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859722 | CAGGTTTGATGGAAG[A/G]CAAGCTCAATTTTAG | 9063 |
rs755301501 | snp | C/G | 1.66181e-05 | 0.00288249 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890625 | GGACATCATAAAAGG[C/G]CAGATTTTTTAACTG | 9063 |
rs755318608 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902612 | TTCTTCACGGATTGG[-/A]AAACTCAACATAGTA | 9063 |
rs755322921 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873890 | CTTGCCTTTCTCCCC[C/T]TACCGCCATTCCCAT | 9063 |
rs755368290 | snp | C/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918226 | AATGTGCTGATATAG[C/G]ATGAAGGAAGATGCT | 9063 |
rs755373796 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886072 | CATGTCTCCCTCTTG[G/T]AGTACCACTGAGCAA | 9063 |
rs755414319 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837562 | CTTTATATAAGAAAT[C/T]GTGTGTAATATGAAC | 9063 |
rs755447368 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817427 | AATTAAAAATTGAAG[A/C]TCTATCACCAGAGAA | 9063 |
rs755454700 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853102 | GGCAACACGGCGAAG[C/G]CCTGTCTCTACAAAA | 9063 |
rs755480562 | snp | C/G | 1.6734e-05 | 0.00289253 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821116 | ACAATCTGGCTGTTA[C/G]TTCACAGGAGAGAAG | 9063 |
rs755492333 | in-del | -/ATAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862586 | ACTTTAAAGAGTCAT[-/ATAA]ATAATGTTTTGTTAA | 9063 |
rs755519902 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866446 | AAAGCAGAGTGGAAG[A/G]ATAACTTTTCAGATA | 9063 |
rs755544022 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851742 | AACAGTCTAGGGACA[C/T]GTTGCCATTTTCAAA | 9063 |
rs755570608 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876281 | TTGACCCTCACGTTT[A/G]TATAGATGCCACTGG | 9063 |
rs755636935 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914745 | GGGTAATGGAAATCC[C/T]CTCTGTGGCATATCA | 9063 |
rs755651941 | snp | A/G | 4.96069e-05 | 0.00498006 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890924 | ATTTTAATCTGAACC[A/G]CAGGGCTGCAGCCGC | 9063 |
rs755673426 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876531 | GCATTAGACATGATA[C/T]TAGCAGAGAAAGGTG | 9063 |
rs755754343 | snp | C/T | 1.77121e-05 | 0.00297586 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844860 | AACAAACAAAAAAAA[C/T]CTGCATTAAAGATGA | 9063 |
rs755765104 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822514 | CCTCCAGTGCTACTC[A/G]AAGACCTAAAACCAC | 9063 |
rs755776783 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890814 | GTTCTACAGGTGATG[A/G]GCCACCATCCAAACT | 9063 |
rs755803449 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841638 | TTAACACTACTACTA[C/T]AGCCCAAAGAGTAGC | 9063 |
rs755821021 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869843 | ATGACAAGAGTCCCA[A/T]CTCCCAGGAGGAAAT | 9063 |
rs755847217 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864554 | GGTGGGTGGATCACC[G/T]GAGGTCGCAAGTTCG | 9063 |
rs755851244 | snp | C/T | | | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46821065 | AAGATGGCTGATACA[C/T]GAGAACCCTGTTTTA | 9063 |
rs755868376 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881477 | TATTTTATTCTATTT[A/C]TTTCTAAAATAAACC | 9063 |
rs755892898 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889587 | AAAATAAAAGTGTTG[C/T]TAAGGATGTGGAGAA | 9063 |
rs755910197 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854643 | TAGGCCAGAGACAGG[C/G]TGCATGCATTTACAT | 9063 |
rs755947330 | snp | A/G | 1.70883e-05 | 0.00292299 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829695 | GATAATGTTGCACGA[A/G]TCTCACTGCTTTACT | 9063 |
rs756013021 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819961 | TTTTGCGTTCTGTGA[C/T]TGCAGTTACCTGTGG | 9063 |
rs756015315 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912539 | ATACTGTCTAAAAGT[C/G]ATAGGTCAATAAACA | 9063 |
rs756015517 | snp | C/T | 1.66037e-05 | 0.00288125 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855519 | AGAACTACATGCACA[C/T]AGTAAGCAAGTATAA | 9063 |
rs756032415 | snp | G/T | 3.45471e-05 | 0.004156 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855649 | AAATGGGTTAAAAAA[G/T]TACAATGAGAATTCT | 9063 |
rs756097928 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810565 | TGTGCAACTACTGCT[A/C]GTAGATTTGGGTTTG | 9063 |
rs756114438 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890127 | ACGACATGAGGTACT[G/T]GGAATAGTCAAAATC | 9063 |
rs756132574 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848306 | AAGTTTTCAGACAAC[A/G]GCCAGGATTCATGCT | 9063 |
rs756143570 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859533 | CTCTGTCAAGGCAGA[G/T]TCCAATGCCATTAAG | 9063 |
rs756167457 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904472 | AATAACCTAGAAGGC[C/T]GGGTGCGGTGGCTCA | 9063 |
rs756207626 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884810 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 9063 |
rs756209310 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855544 | GTATAAAACTAAGGT[A/G]ACAGAAAATTTCAAA | 9063 |
rs756231085 | snp | C/T | 1.67158e-05 | 0.00289096 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890615 | AGAACATCAAGGACA[C/T]CATAAAAGGGCAGAT | 9063 |
rs756262611 | in-del | -/ATG | 6.13303e-05 | 0.00553727 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818473 | AGAAGATTCATGTTT[-/ATG]ATGTTTAAAAGGAAT | 9063 |
rs756295696 | snp | C/G | 1.67877e-05 | 0.00289716 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829896 | AAGAAGTACATACAT[C/G]TGATCAACAGCTTTG | 9063 |
rs756298713 | snp | A/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815624 | GTCAAAACAAATATT[A/T]CCCCCTTTGCCGCTT | 9063 |
rs756371128 | snp | A/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824070 | GATACGTGTATACAT[A/T]ATGCAAGTGACCATT | 9063 |
rs756377055 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839579 | CCCCTTTAAACTCTT[-/A]AAAGATTAAGACCTA | 9063 |
rs756387051 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813102 | TGACCAGCTGAATGA[C/T]GGCATTGGACTCCTT | 9063 |
rs756414231 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837469 | TTGTTATCTATTTAT[A/C]GGCACTCTTTATATA | 9063 |
rs756422516 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870943 | ATGGTAATAAAAGGA[A/T]TTCAGGAATCAGTAC | 9063 |
rs756430948 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907414 | GGTAGACAAGGATAT[-/G]GAGCAACTGGAACTC | 9063 |
rs756458342 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900136 | TTGGGAGGCCGAGGC[A/G]GGCAAATCACTTGAG | 9063 |
rs756523488 | snp | C/T | 8.0707e-05 | 0.00635193 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818374 | ATTTGTTTTATTTTG[C/T]ATTCACTGTTGCACA | 9063 |
rs756524084 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896944 | TTATACAATATATGG[A/C]GTTTCCTTTCAAATA | 9063 |
rs756560109 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850140 | AAGTATAATATGTAT[A/G]TATCTACCAGTTCAG | 9063 |
rs756567703 | snp | A/T | 1.90907e-05 | 0.0030895 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864267 | GGAAGAAAAAAAAAA[A/T]GAAAGATAATATTTC | 9063 |
rs756634820 | snp | C/T | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846769 | CTGAAGATAACCTAA[C/T]TAAAGATGTAATATT | 9063 |
rs756656088 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814720 | TCTCATGCCTTCTCC[C/T]CCTCTGCTCTGCCTC | 9063 |
rs756686136 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856202 | GAGATAGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 9063 |
rs756788999 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886564 | TCTTGTTGGCCAGGT[A/G]CAGTGGATCACACCT | 9063 |
rs756809608 | in-del | -/AGG | | | intron-variant, cds-indel, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812601 | ACTATCCAAAAACAT[-/AGG]AGGACAGTACTGCTT | 9063 |
rs756810707 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920670 | AATAATCATTCAATA[C/T]ATGTTCAAAGGAATG | 9063 |
rs756846092 | snp | A/C | 1.66549e-05 | 0.00288568 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828105 | GGCTACAGTCACTGA[A/C]CAAGGCTTACTGAGG | 9063 |
rs756866084 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819759 | AAGGGAAGTCATGAA[C/T]GTACTGGTTCTAACT | 9063 |
rs756894501 | snp | C/G | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890802 | CGGCCAAGTCAGGTT[C/G]TACAGGTGATGAGCC | 9063 |
rs756928313 | snp | A/C/T | | | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820951 | GCAAATCTGATGACA[A/C/T]GCTTGATATTGGCGT | 9063 |
rs756956043 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831430 | ATGTCACCACAGACT[A/T]ATCTACAGAGTCAAT | 9063 |
rs756994747 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912373 | AAATGCTATGAAATG[G/T]TTGTTATACTATACT | 9063 |
rs757006870 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868187 | GACCTAAGGAATCCA[C/T]GAGCATGTCAGACAC | 9063 |
rs757024207 | snp | A/G | 1.69441e-05 | 0.00291063 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855327 | ATATGCAAATCTGGT[A/G]AATAAAAAGCAACTT | 9063 |
rs757065482 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879776 | ACAAACCTTGAGGAC[A/T]TTACGTTTAGTGAAA | 9063 |
rs757067649 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866877 | CAGGTATCTACACCT[A/G]TAAAGTTGGGCACAA | 9063 |
rs757112029 | snp | A/C | 1.66048e-05 | 0.00288134 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855515 | ATTCAGAACTACATG[A/C]ACATAGTAAGCAAGT | 9063 |
rs757112134 | snp | A/T | 1.68997e-05 | 0.00290682 | intron-variant, missense | PIAS2 | GRCh38.p7 | 18:46827948 | CAATAGTGAACTATA[A/T]ATTAACAAACCCTTT | 9063 |
rs757120893 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878740 | AGATATGGTGGCCCA[C/T]GCCTGTAAGCCCAGC | 9063 |
rs757122833 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46807754 | CTGCCAATGATCTCC[A/G]TATCAGTTAACCCCG | 9063 |
rs757156669 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900171 | GGAGTTCATGACCAG[-/C]CTGGCCAACATGGTA | 9063 |
rs757158849 | in-del | -/AA | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812342 | AAATACCAAATTATT[-/AA]AAAAAAAAAAAAAAG | 9063 |
rs757168364 | snp | A/G | 0.000162245 | 0.00900535 | synonymous-codon, intron-variant, missense, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920059 | CCCACTGAAACTTAC[A/G]TGCAGTGTTCTTTGT | 9063 |
rs757190717 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830310 | AAATAAAAGAAGTCT[A/C]AATAAATTTAAAATA | 9063 |
rs757230566 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860943 | GATCACCACCACTGC[A/C]CTCCAGCCTGGGCAA | 9063 |
rs757247076 | in-del | -/CTTA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894192 | ATAATCTCAAAGCAG[-/CTTA]CTAAGTAAAATTCTA | 9063 |
rs757247089 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845412 | CAGCTTTCTTCTGAG[C/G]AAAGCTTTGATAAAT | 9063 |
rs757251312 | snp | A/G | 8.63595e-05 | 0.00657056 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812475 | GTTACTTCCACTGCT[A/G]GTTATGACCCCTGTC | 9063 |
rs757259938 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865099 | TATTATTACCTGAAA[C/T]GTATTTATGACTTCA | 9063 |
rs757263610 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811575 | CCAGTCACACCGTAC[A/C]CCAAAGACATTTCAT | 9063 |
rs757302668 | snp | G/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893557 | TAGACAAACAAAAAG[G/T]AAGAAAGAGATAAGA | 9063 |
rs757327097 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46915016 | CAAGAAGGATGTTAC[C/T]AATCATTTAATTTAG | 9063 |
rs757381785 | snp | A/G | 1.72883e-05 | 0.00294004 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864253 | ACTGCTTTGAACTGG[A/G]AAGAAAAAAAAAAAG | 9063 |
rs757410556 | snp | C/T | | | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46902503 | AGGCACAGGTTGCAG[C/T]GAGCCGAGATCGTGC | 9063 |
rs757474437 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895201 | CAGAAGCTGCAATAA[C/T]GGCCTAGAATTTGGG | 9063 |
rs757525483 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46835069 | AGAAACAAATATGGA[A/C]TATCAAGAATTTAGT | 9063 |
rs757559163 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882097 | ACAAGACTTTGTCTC[A/G]GTGGCGGTGGGGGAA | 9063 |
rs757574799 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862383 | CCCAAACTTACTTAA[C/G]TGCAACAATCTTATT | 9063 |
rs757599990 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863706 | ACACACAGTATTTAC[C/T]AAATATTTGGCTGAC | 9063 |
rs757613083 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850005 | ACAAAAATAATCACA[A/G]TTTTAAAAAATCACC | 9063 |
rs757645837 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809441 | AAGGCCTTCATAGTT[C/G]TAAGTGAAGAAAGAT | 9063 |
rs757653188 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876093 | TGCCCTGATCCATCC[A/G]CAAGTGGATGTATGG | 9063 |
rs757670272 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910123 | ATCGCGCCACTGCAC[C/T]CCAGCCTGGGCAAGA | 9063 |
rs757675538 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902425 | ATTAGCCATGCATGG[G/T]GGCACATGCCTGTAA | 9063 |
rs757721837 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841346 | TTTCTCTTGTTTTTG[C/T]CAAATAACCCAGGGT | 9063 |
rs757723420 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909334 | CATGATCACAGCTCA[C/T]TTCCTAGCTTCAGGT | 9063 |
rs757756626 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900576 | TGATTACTTAGGAGG[C/G]TGAGGCAGGAGGATA | 9063 |
rs757771067 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875468 | CCAAGAACCCTCCAT[A/G]TTCGAATGGTATGGG | 9063 |
rs757806268 | snp | C/T | 5.06624e-05 | 0.00503276 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844830 | CAAGATATACAGACA[C/T]AGAGTAATTCTACAA | 9063 |
rs757812582 | in-del | -/TTTT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844689 | CTCATATGCTCAATC[-/TTTT]TTTTTTTTTTTAAAT | 9063 |
rs757818114 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898799 | AGAAGTTAGAGACCA[C/G]CATGGACGACACGGT | 9063 |
rs757859411 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853170 | TAGTCCCAGCTACTA[A/G]GGAGAGTGAGATGGG | 9063 |
rs757895287 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833396 | ACTGAGAGGGAGAGA[C/T]TGAAAACATACATGA | 9063 |
rs757919840 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896602 | ATTCAAAAAACATGC[A/C]AATTATTGGTTTTCA | 9063 |
rs757920479 | snp | C/G/T | 0.000148479 | 0.00861518 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46821008 | TTAATGAAGGCGGAA[C/G/T]AGCAGCAGGATCAAC | 9063 |
rs757923477 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912316 | TACACATCCTCCTAC[A/G]TACTTTACATCATTT | 9063 |
rs757939163 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866670 | CTAAAGTGATGGCAT[C/T]GAAAGGCAGGATTTC | 9063 |
rs757949595 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897457 | CATCAAAAAGAATAA[C/T]AACTGCATTGGATTC | 9063 |
rs757976818 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911450 | CTAACTCCTGACCTG[A/T]GGCGATCCGCCTGCC | 9063 |
rs758000271 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830067 | TAACAGGCAACATAA[C/T]AGTTAAGTAACTTAC | 9063 |
rs758000688 | snp | A/C | 1.70627e-05 | 0.00292079 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855317 | TATTAAACTTATATG[A/C]AAATCTGGTGAATAA | 9063 |
rs758011515 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827461 | CCACATGCCTGACAC[C/T]GAGGCTTTCTTTCAT | 9063 |
rs758032196 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819458 | CAAAGAATAACTTTA[A/G]AAGCCATTTTTTTCT | 9063 |
rs758039078 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921052 | GGCTACCGTCTTAAA[A/G]TGGCTCCAAATTAGA | 9063 |
rs758053365 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865438 | CCAGCTACTCCAGAG[G/T]CTGAGGCAGAAGAAT | 9063 |
rs758069857 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831112 | AAGAAGAAGTAAAAC[C/T]GTCTCTATTTAAAAA | 9063 |
rs758090331 | snp | A/G | 1.73504e-05 | 0.00294532 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827925 | CAATTAGTTGCAAGG[A/G]TAATGAACAATAGTG | 9063 |
rs758136856 | in-del | -/AAAAAAAAAAAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859429 | CGAGACTCCGTCTCA[-/AAAAAAAAAAAA]AAAAAAAAAAAAGAA | 9063 |
rs758142791 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853293 | TTTTTTTTTTTAAAT[-/A]AAAAAAAAAAGGAAA | 9063 |
rs758168669 | snp | C/T | 2.10104e-05 | 0.0032411 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891186 | TAACAGCATTTCACA[C/T]ACCACTTAGAATCAT | 9063 |
rs758172654 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912281 | TTACATGAAATGGCA[C/T]AGTATTTGCATATAA | 9063 |
rs758183914 | snp | C/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846803 | GGGGCGTCCAGGGCG[C/G]TTCTGTTCAATCCCA | 9063 |
rs758193693 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878422 | TTGTAACATTGACTT[C/T]ATCTTGATAAGACAT | 9063 |
rs758197257 | in-del | -/AATACAAAAATTAGTATGG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910428 | AACTTAAATATTTAA[-/AATACAAAAATTAGTATGG]AATACCTAAATACAA | 9063 |
rs758246910 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877446 | TGTAAGTCACATCTC[C/T]TCCTTATTTGGAAAG | 9063 |
rs758259608 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913168 | GAGAGGAGCGTGATG[A/C]GGACCTCTAACCTCA | 9063 |
rs758301009 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904241 | AGTATACAGAATGTC[C/T]CTGTATTATTTCCTA | 9063 |
rs758317689 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859240 | GAGACCATCCTGGCT[A/G]ACATGGTGAAACCCT | 9063 |
rs758335854 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46843513 | ACTCAATTATTAACA[C/T]TCTAAGCAAGCCTCA | 9063 |
rs758343878 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810441 | AAATATTGCATCTGT[A/G]TTTAGAGCAGCAACA | 9063 |
rs758355012 | snp | A/T | 1.65187e-05 | 0.00287386 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836383 | TAGACTTTCATAGGC[A/T]GCTTTTTTGTCACAC | 9063 |
rs758360572 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823968 | GTGAAATGATGGATG[C/T]AAAAATGTGATGCTA | 9063 |
rs758370340 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819530 | TTCACATAATCTAAA[-/C]AAATTTCAAGTGGCA | 9063 |
rs758371159 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858366 | CATATGTAGGAGCTT[C/T]CTAATGGAAAGATCT | 9063 |
rs758371228 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872271 | CAGCAAAATACCATA[A/T]GACCATCAATGGTTT | 9063 |
rs758472428 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870423 | GATTGAGACCATCCT[C/G]GCTAACATGGTGAAA | 9063 |
rs758493340 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909082 | CACATGCATCCAACT[A/G]TGAAACTATTAAAAA | 9063 |
rs758508360 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894105 | CACTCCAACCTGGGC[A/G]ACAGAGTGAGACCCC | 9063 |
rs758508478 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880265 | TAGCTGGGCATGGTG[A/G]TGCACACCTGTGGTC | 9063 |
rs758512713 | in-del | -/AAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913561 | AGAAGGGAGATCCTT[-/AAA]AAAAAAAAAAAAAAA | 9063 |
rs758513278 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849908 | GTCCTTATTTAAACT[C/T]AAATTCTAGACATGC | 9063 |
rs758517292 | snp | A/G | 1.66167e-05 | 0.00288237 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855529 | GCACATAGTAAGCAA[A/G]TATAAAACTAAGGTA | 9063 |
rs758538345 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814519 | CTGCACATTACCTTG[A/G]GCCCAAATTTCTGCT | 9063 |
rs758547971 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913963 | TACCAAGCCCTGCCC[G/T]CCAGACCATTTTTGG | 9063 |
rs758559388 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893216 | TTACCCAAGCAAGTA[A/G]TACGATGCATCTTTC | 9063 |
rs758620620 | snp | G/T | 1.75068e-05 | 0.00295857 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855661 | AAAGTACAATGAGAA[G/T]TCTCAGAACAGTCTC | 9063 |
rs758620954 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833969 | TTCCTCATCCCCAAT[C/T]TTCCTCCCACAGTGT | 9063 |
rs758695437 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851965 | TCATGGTTCAATACA[A/C]CAGGATCACGGGCAA | 9063 |
rs758715747 | in-del | -/CAAA | 0.000232159 | 0.0107715 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855477 | CTTAAATAGTGTGCT[-/CAAA]CATTCTTATATGTTT | 9063 |
rs758717834 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826274 | TCCTCTGCATACTGA[A/G]GTCATTTCAGATTTT | 9063 |
rs758728093 | in-del | -/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844688 | CTCATATGCTCAATC[-/T]TTTTTTTTTTTTTTT | 9063 |
rs758786595 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908302 | ATGCTAGCAGCAGCA[G/T]CATCTTGTTTTAGTT | 9063 |
rs758826108 | snp | C/G/T | 0.000198172 | 0.00995233 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812522 | ATGAACTAACATGAG[C/G/T]ACTGCTTTCATGGGA | 9063 |
rs758843866 | snp | A/G | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919983 | GCCCTGCCACAGAGG[A/G]GCTTACACCCATAAA | 9063 |
rs758866744 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877018 | TTCACTAATTTAATG[G/T]AAAAATGGTTTGGCA | 9063 |
rs758873541 | snp | A/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825259 | ATCACAGAGATGATA[A/T]AACTATAGCATGAGC | 9063 |
rs758887359 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854345 | TTTCCTCAATAGTTG[C/T]GAAGAGTGTCAGCTC | 9063 |
rs758921102 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878225 | ACTTTTCTCACCTGC[C/T]TTTTTAAGATGGTTT | 9063 |
rs758941621 | snp | C/T | 0.000230176 | 0.0107254 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917350 | AAATCCGCCATTTTA[C/T]ACCACCCGCGGGCGC | 9063 |
rs758982022 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905608 | CAAGAAAAAAAGAAG[G/T]CATTTTAAAAAAAGA | 9063 |
rs758983468 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810110 | ATGCAAGTTGCCTGT[A/T]TGAAATAAATTAAAA | 9063 |
rs759031889 | snp | G/T | 3.44133e-05 | 0.00414795 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846887 | AATCATCTGCAGGAA[G/T]ATTAAACATTTTCTC | 9063 |
rs759033463 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898594 | AAATACATTTTCAAA[-/T]GGCTGAAAAAGAGTA | 9063 |
rs759039616 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892349 | ACTATATATGTCTCT[A/G]TATTTCATAATGTAC | 9063 |
rs759065176 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809122 | TCCTCAAGACTAAGG[-/A]AAAACTTGGTTTTAT | 9063 |
rs759097046 | snp | A/G | 0.000133041 | 0.00815491 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836524 | TTTTCCTAACTACAG[A/G]ACAGGAAACACAAGG | 9063 |
rs759105421 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860568 | CATAGGAGCCAACCT[A/G]AAAGAACTTCTAATA | 9063 |
rs759231674 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844896 | AATATTCTCTTTGTT[C/T]ACATGAAATACTTAT | 9063 |
rs759233295 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873146 | ACCTTTGGGGGAAAC[G/T]TGGTGGTGACCACAC | 9063 |
rs759266716 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909663 | TTTTGGAAGATAATC[C/T]GACATTATCCAATAT | 9063 |
rs759291506 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860352 | ATCCAGAATGTACAA[C/T]ATGCTAGATCAAATA | 9063 |
rs759336576 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872024 | AACCCCCAGGGGAAA[C/T]AGTAAGAAGAAAGCA | 9063 |
rs759341679 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883863 | AAATTAAAATCAGTC[A/C]GGTGTGGTGGTATAC | 9063 |
rs759413877 | snp | A/T | 1.65985e-05 | 0.00288079 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836351 | TGTTAAAAGGGATAT[A/T]CTTACCCATCTAATA | 9063 |
rs759414599 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816686 | TTGCCTAGGTTGGTT[C/T]TGAACTCCAGAGCTC | 9063 |
rs759425538 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915838 | ATACATCTGTTACTA[C/T]ACAAAAATTAAAAAT | 9063 |
rs759428312 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837962 | ACCAGATAGGAGAAT[C/G]AATGGACATGGACTG | 9063 |
rs759454296 | snp | C/G | 6.6036e-05 | 0.00574575 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890670 | CAGGAGGAATTGGGG[C/G]AGATGGCTGCTGCAT | 9063 |
rs759456567 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859204 | GAGGCCGAAGCGGGT[-/G]GATCATGAGGTCAGG | 9063 |
rs759526154 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848373 | AAAAGCCAGGGAGTA[C/T]AGCTAACCAGTCACG | 9063 |
rs759538192 | in-del | -/GAAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847259 | ACTGGGAAGTGAGGG[-/GAAA]GAAAGAACAAACTAA | 9063 |
rs759560858 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851078 | GAGTGTGCACACAAT[G/T]ATGTGTTTTAAAAGA | 9063 |
rs759579018 | snp | A/G | 2.21168e-05 | 0.00332534 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890564 | TTCAGAAGAAACTGA[A/G]TTCTCAAACACTTAC | 9063 |
rs759582411 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909029 | ATAAAAATAAAAATG[A/G]TTTAAAAGTGAGCCC | 9063 |
rs759585850 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904299 | TCATTAAAAGTTTAA[C/T]TAAAACTACAAGGAG | 9063 |
rs759646306 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46915468 | TCCTCTGAAAATTCT[-/C]CCCCAGTTAGTCTCT | 9063 |
rs759650098 | snp | G/T | 1.67866e-05 | 0.00289707 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844803 | ATAACATGGCTGATG[G/T]AAGCTGCCGTACAAG | 9063 |
rs759688535 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840067 | TTGGGAGGCTGAGGC[A/G]GGAGAATTGCTTAAA | 9063 |
rs759714227 | snp | A/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827497 | TAAAACCTGAAAATG[A/T]TCCTGTAATATAGGC | 9063 |
rs759733646 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870123 | CCTCCCTAACCACAC[A/G]TCTGAGTCTATGCCT | 9063 |
rs759738504 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807886 | CCATCTAGCTGCAGT[A/G]TAAATTAACATACCC | 9063 |
rs759767583 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871777 | ACAGAGGTCAAATAT[-/A]AAAATTGATCAGCCC | 9063 |
rs759772708 | snp | A/T | 2.28569e-05 | 0.00338052 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844164 | AAAAATTTAAAAAAA[A/T]TAAGGGTGACAAAGA | 9063 |
rs759788975 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890847 | AAACCGATGATTTGA[C/T]TGTGGATAAATCAGA | 9063 |
rs759852617 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854096 | ACAGGCTGTGTATGC[A/G]ACAAATGAGACTCCT | 9063 |
rs759873207 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900916 | GAGGCGGAGGTTGCG[A/G]TGAGCCGACGTCGTG | 9063 |
rs759904669 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886952 | CTAAAAATCACAGAG[A/G]TCTGTTTTCAATAGC | 9063 |
rs759914901 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886451 | CAAATTAGGGAAATA[C/T]GTTAACCAGATAAAT | 9063 |
rs759977482 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898620 | GAGTATTAAAAAAAC[C/T]GAAGTAACACAAAAA | 9063 |
rs760028709 | snp | A/G | 1.65274e-05 | 0.00287462 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855440 | CCAGGCAAAGTCTGC[A/G]TTAATAAAAGAAAAA | 9063 |
rs760030595 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912152 | AAAGGGATCGGTGTT[A/G]TATCTTTTTCTGAAA | 9063 |
rs760050527 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844568 | TACTATGTGGTAATG[C/T]GTCTACAATTTTACT | 9063 |
rs760077689 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819246 | CAACAACCCATGTTA[C/T]AGCCATAAAAGGCAG | 9063 |
rs760094396 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847848 | CAATTCCCAATTACC[A/G]CAAGACTTCACTCTG | 9063 |
rs760104239 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814525 | ATTACCTTGGGCCCA[A/G]ATTTCTGCTGCTGTT | 9063 |
rs760107061 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832275 | CAAAAATTAGCCAGG[C/T]GTGGTGGCGCACACC | 9063 |
rs760130844 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879477 | ATGTAAAATGGTGCA[C/G]CTGCTGTGGAAAACA | 9063 |
rs760150094 | snp | C/T | 1.65935e-05 | 0.00288036 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828064 | GTAAGATCAATAACA[C/T]CTACTTTCTTCTTGC | 9063 |
rs760181272 | snp | C/T | 2.59656e-05 | 0.00360307 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890544 | TCATTTCATTTACTA[C/T]CTTGTTCAGAAGAAA | 9063 |
rs760203822 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904529 | GCCCAGGTGGGCAGA[A/T]CACCTGAGATCAGGA | 9063 |
rs760210854 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905333 | AAAATAACGGAAATA[C/T]CACACACATCAAAAC | 9063 |
rs760222241 | snp | A/C | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824350 | TTCTTAATGATTATC[A/C]ATCTGGAGACATATA | 9063 |
rs760274846 | snp | A/C | 1.66707e-05 | 0.00288705 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836340 | TCCATATCAGCTGTT[A/C]AAAGGGATATACTTA | 9063 |
rs760315403 | snp | A/G | 1.7412e-05 | 0.00295055 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891065 | ATATTCTAAAAGGAA[A/G]GAAAAAAAAACATAA | 9063 |
rs760322694 | snp | A/G | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836200 | TTAAAAAATAAGATT[A/G]AGTATAATTAGGTAT | 9063 |
rs760378804 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857999 | AGTACATGGCACAGT[A/G]AGAGACAAATGACAC | 9063 |
rs760417825 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46835028 | AAAAATGCTAACATC[A/T]CAGGGCAATTTTAAA | 9063 |
rs760429754 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888235 | CACAGCTCATGTTCA[G/T]GTACTGGAAGACTTA | 9063 |
rs760462661 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915677 | GCACTCCAATCTGAG[A/C]ACTGACTGCTTTTAC | 9063 |
rs760470323 | snp | A/C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882994 | CTATTGGGGAGGCTG[A/C/T]GGCAGGAAAAAAAAA | 9063 |
rs760493513 | in-del | -/ATG | 1.73216e-05 | 0.00294287 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855654 | GGTTAAAAAAGTACA[-/ATG]AGAATTCTCAGAACA | 9063 |
rs760497518 | snp | C/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826686 | AAATGATTGGCACAC[C/G]AGGAAAAAATCCACT | 9063 |
rs760512344 | snp | C/T | 3.30568e-05 | 0.00406538 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815377 | TGCTTTGTTAATAGT[C/T]GTCTCATATTTTGGG | 9063 |
rs760515769 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914755 | AATCCTCTCTGTGGC[A/G]TATCAGCAGCCAAAT | 9063 |
rs760517531 | in-del | -/TTAT | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818169 | GACAACACATTTTCC[-/TTAT]TTATTTGAGTCATAA | 9063 |
rs760565063 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828426 | GATTTGTGCAGCTCC[C/T]ACTGCTCATCCTGTC | 9063 |
rs760634333 | snp | C/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815560 | AACTGGAAAAACTAG[C/T]TCCCAGAGACTCAAA | 9063 |
rs760658248 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864698 | TCACTTGAACCCAGA[A/T]GGTGGAGGTTGCAGT | 9063 |
rs760666338 | snp | G/T | 2.33326e-05 | 0.00341552 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818493 | GTTTAAAAGGAATGT[G/T]AAGAAATGTATTAAA | 9063 |
rs760716743 | snp | G/T | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919604 | CAGTGAGCTGCGATC[G/T]CACCATTGCACTCCA | 9063 |
rs760747222 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913614 | CTCCCCATTGAGTGA[C/T]GAGAAGTAGGGAAAG | 9063 |
rs760765565 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873678 | AAGGTCTCATTAATA[C/G]CAAAGGCCAAGACCT | 9063 |
rs760842673 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899444 | CAAAAAGCTCACCAC[C/T]GCCGAACCAGAGTAA | 9063 |
rs760848915 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885798 | TTCTAACTGAAGCTA[C/T]GACCAAAATGCAGGG | 9063 |
rs760851504 | snp | G/T | 1.6504e-05 | 0.00287258 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844024 | TTATAAAAAGTCAAA[G/T]TCCCCAAAATGTTTT | 9063 |
rs760860822 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872692 | GCCAAGGATAAGGCC[C/T]GAACGGGTCAAAGGA | 9063 |
rs760860833 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852599 | AGTAACTAAGTAACA[A/G]TGCCCCAGAGGAAGT | 9063 |
rs760917023 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853867 | CGGAAACCTGACAAA[C/T]TAAATGTCCCACCCG | 9063 |
rs760926212 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912072 | AAAAAGGAAAAAAGA[A/T]AACAAAGGCTAGGAA | 9063 |
rs760939859 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867341 | TTGTGCATATGCTAA[A/T]AAAAATCTAATTTGT | 9063 |
rs760985298 | snp | G/T | 1.64991e-05 | 0.00287215 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890694 | GCTGCATCTCAAATG[G/T]GGGCTTAGTATCTTG | 9063 |
rs760989324 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808156 | AATGCCTGTAGGTTG[-/A]CGGGGAAAAACCCCA | 9063 |
rs760991172 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879403 | AAAAAAATAGTAATA[A/G]TAGTAAGTGCAGATG | 9063 |
rs760997928 | snp | A/C | 3.32613e-05 | 0.00407793 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821094 | TAAATAGCACGGGAA[A/C]TTACAAACAATCTGG | 9063 |
rs761044131 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878077 | GGATCCCTTTTTCCT[C/G]TTTATAAATTTTTAA | 9063 |
rs761154052 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911373 | GGTGCCCACCACCAC[A/G]TCGGGCTAATTTTTG | 9063 |
rs761172984 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820064 | TGAATAGTCTGATGA[A/G]ATCTCATGCTGTCCT | 9063 |
rs761194657 | snp | A/C | 0.000108832 | 0.00737591 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917289 | CCTCTCCCATCCCCT[A/C]CCCCGCGGCCTCCGC | 9063 |
rs761226194 | in-del | -/AAAC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832420 | ACTCCATCTCAAAAC[-/AAAC]AAACAAACAAACAAA | 9063 |
rs761238993 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829596 | GGAAAGAATAAAAAT[C/T]ATTTGGGGGAAAACT | 9063 |
rs761260067 | snp | C/T | | | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846817 | GCTTCTGTTCAATCC[C/T]ATTTTTAGGCGGTGG | 9063 |
rs761262011 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914611 | AAGCAAAGGCACCAG[C/G]GTCACCAAACCACAC | 9063 |
rs761271189 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854314 | TGTTCAGCAGGGATA[G/T]TACACAGCTTCCCCA | 9063 |
rs761271455 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46811077 | CAAACAAACACACTA[C/T]AGAAGAGAAATTTTC | 9063 |
rs761276444 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844580 | ATGTGTCTACAATTT[A/T]ACTCACCAGTAATGT | 9063 |
rs761299300 | snp | C/T | 1.70017e-05 | 0.00291558 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846877 | AATTATTTCAAATCA[C/T]CTGCAGGAAGATTAA | 9063 |
rs761364808 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829806 | TTGGACACCAAGAAC[C/T]ATCTTCTTGGAATTT | 9063 |
rs761385649 | snp | C/G | 1.69801e-05 | 0.00291372 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855626 | AATCCCTGTTGGAAA[C/G]AGAAAGAAAATGGGT | 9063 |
rs761411148 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894782 | TTAGGTAGAAAATAC[C/T]TCATTAGGCTGGGCG | 9063 |
rs761430002 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881151 | TCTCCCACCAGTGTG[G/T]AGTTAGTCCACCTTA | 9063 |
rs761446474 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834157 | TGACGGAACAACTGC[A/C]CAACTGGAAAAAGGA | 9063 |
rs761460709 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826206 | TCAGCCTAAATGAGG[-/A]ACCTTAACATTTATC | 9063 |
rs761464760 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832700 | GTTGGAGACCAGCCT[A/G]GCCACTATGGCGAAA | 9063 |
rs761466495 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849496 | GGAACCAGTGGGGCA[A/C]ATATGCGAGCTTTCT | 9063 |
rs761474697 | snp | A/C/T | 0.000150043 | 0.00866037 | synonymous-codon, missense, intron-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46864178 | CCTGGATATGCATAT[A/C/T]TCTCTAACTTGTTGA | 9063 |
rs761487709 | snp | C/T | 1.71111e-05 | 0.00292494 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829688 | GATTAATGATAATGT[C/T]GCACGAGTCTCACTG | 9063 |
rs761595347 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881042 | TTTATTAATAATCAC[A/C]AGTGATGCTTCCTCT | 9063 |
rs761604815 | snp | C/G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862981 | AAAGTGCTGGGATTA[C/G/T]AAGCATGAGCCACCA | 9063 |
rs761620821 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46893897 | TCTGGGAGGCAAGGC[A/G]GGTGGATCATTTGAG | 9063 |
rs761647881 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861871 | ATTGACCAAAAAACT[C/G]GTGAAATCTGAATAA | 9063 |
rs761660338 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840914 | ACCAATCTAAATTAA[C/G]AGAGTTTTTAAGTTG | 9063 |
rs761672018 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908723 | CTCATCAAAAAACGC[A/G]TAAGGCTGGATGCAG | 9063 |
rs761687658 | in-del | -/ATGT | 1.65023e-05 | 0.00287244 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844033 | GTCAAATTCCCCAAA[-/ATGT]TTTGTTGCTTTACTT | 9063 |
rs761699339 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874775 | CTTCCCTCAGAACTA[A/G]AGGCCTTTTAGCAGA | 9063 |
rs761711721 | snp | C/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907856 | TCCTAGAACCAATCC[C/G]CCAGGTACACCAAGG | 9063 |
rs761738458 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814321 | TACAAAACAGAGCTA[C/T]GAAATAAAAACCTCT | 9063 |
rs761746592 | snp | A/T | 1.6513e-05 | 0.00287336 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815348 | GGAAAGAAAATCCAA[A/T]CCTAAAACAAAAATG | 9063 |
rs761775128 | in-del | -/TA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849581 | ACTCAAAGAATTTTT[-/TA]TATGTTTCATGCTCT | 9063 |
rs761777306 | in-del | -/TAA | 1.82382e-05 | 0.00301973 | intron-variant, cds-indel, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818424 | GCTTCAGTTCATTAT[-/TAA]TATCATTTCTTCTTT | 9063 |
rs761826230 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827353 | CTTACAGAGAATCCA[C/T]GCTAAAATTCAGGTA | 9063 |
rs761826328 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46812972 | TTGGGTGTCAATTTT[C/G]AAAGAATTGTTGATC | 9063 |
rs761846782 | snp | C/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826077 | TACATCAGCTTCATG[C/G]AACGAACTAGGTAGC | 9063 |
rs761850734 | snp | A/G | 1.64955e-05 | 0.00287184 | synonymous-codon, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812581 | GCTGTTAAGGGTGAG[A/G]TGAGACTATCCAAAA | 9063 |
rs761882896 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889004 | GGACAGGCTTTTCAA[C/T]AAATGGTGGGGAAAA | 9063 |
rs761900906 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884237 | CATGTTTTATATACA[C/T]ATTCCTTTATACAGA | 9063 |
rs761920874 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818003 | ATATATTTTTATGCC[A/C]TCCGAAGTATTTCAT | 9063 |
rs761928299 | snp | C/T | 8.26166e-05 | 0.00642662 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820946 | ACCTGGCAAATCTGA[C/T]GACATGCTTGATATT | 9063 |
rs761938892 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852468 | GCTGCAGGCCCCTGG[C/T]TCCAGGGATGCCAGA | 9063 |
rs762008999 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816803 | TATGTCTGTCACTAG[C/T]TATATGACACAGTGG | 9063 |
rs762030385 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844290 | ATGAACATGCAAATT[G/T]CTTTGTTTAAATTCT | 9063 |
rs762086452 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866123 | AGAACTAAAAGAAGA[A/G]AGTGCAAAATGAGAC | 9063 |
rs762086715 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850108 | AAAATTTTAAACATA[C/T]ACAAAAATAGAGAAA | 9063 |
rs762102970 | snp | A/C | 1.65943e-05 | 0.00288043 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821084 | AACCCTGTTTTAAAT[A/C]GCACGGGAAATTACA | 9063 |
rs762115994 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856029 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCCCTGTC | 9063 |
rs762126526 | snp | C/T | 6.59381e-05 | 0.00574149 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846740 | CCAAGAAATGGAAAT[C/T]TGGTTTGGCACAGCT | 9063 |
rs762141567 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877716 | CCAGGGAATAACCGC[A/G]TTAGGGATAAAAACC | 9063 |
rs762178826 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889547 | ACCTGACACCCATTA[A/T]AATGGCCACTATAAA | 9063 |
rs762216616 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838780 | TGCTGAGGCTACAAG[A/G]GGTTAAAACCACACA | 9063 |
rs762257003 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808394 | CCAGGCAAGCATTAA[A/T]GAATGGACATTGGGT | 9063 |
rs762316826 | in-del | -/TAA | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, cds-indel | PIAS2 | GRCh38.p7 | 18:46816927 | ATTTTGTCTTCATAT[-/TAA]TAATATTCAATAAAT | 9063 |
rs762321467 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809684 | CGCTTGAACCCTGTA[C/G]GTGGAGGTTGCGGTG | 9063 |
rs762330582 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867670 | TTTCCTTTTTCAACA[A/G]CCCTTCATAATGTAG | 9063 |
rs762347944 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842790 | CTAGAACCTCTGCCA[A/G]CACCCTCAGGGCTTT | 9063 |
rs762351876 | snp | C/T | 1.65045e-05 | 0.00287263 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890906 | CGTCTATACAATTCT[C/T]GGATTTTAATCTGAA | 9063 |
rs762369323 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888529 | CAAAACTGTGATACT[G/T]GCATAAAGACAGACA | 9063 |
rs762408603 | snp | C/G | 1.66043e-05 | 0.00288129 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828084 | TTTCTTCTTGCTTGC[C/G]TCACTGGCTACAGTC | 9063 |
rs762409026 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858762 | ATACCACTGAGTGAT[A/C]TTCACACATAAAAAA | 9063 |
rs762409683 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823425 | TGAAATAGACTTACA[C/T]GTAACAACAATAACA | 9063 |
rs762421349 | in-del | -/AG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890221 | TTGTTTAATGGGTAC[-/AG]AGTTTCAGCTTCAGA | 9063 |
rs762422665 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832393 | TGCACTCCAGCCTGG[A/G]CGACAGAGCGAAACT | 9063 |
rs762511394 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880704 | AAATACACACACAAA[A/G]AGAACATTCTCATAC | 9063 |
rs762535158 | snp | A/T | 3.31323e-05 | 0.00407002 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855463 | AAGAAAAAAGTATTC[A/T]TAAATAGTGTGCTCA | 9063 |
rs762572955 | snp | C/T | 1.68207e-05 | 0.00290001 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855614 | CACCTGGCAAAAAAT[C/T]CCTGTTGGAAAGAGA | 9063 |
rs762606393 | in-del | -/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920871 | GGAGGTGCAGTAATC[-/T]TATCACTCACAAAAG | 9063 |
rs762613394 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861737 | TCTTCAAAGTGTCAC[G/T]CTGTGAAAGACAAAA | 9063 |
rs762666277 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874701 | TGCTGACATTCCTAC[A/G]TTTGAAACTAAAGAT | 9063 |
rs762690648 | snp | C/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812569 | GACGTACTGCTTGCT[C/G]TTAAGGGTGAGGTGA | 9063 |
rs762692019 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905953 | AAAATCCTAAATTAA[A/G]TATCTCCAAACTGAG | 9063 |
rs762714068 | in-del | -/TT | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818360 | CATAAATACAAATTA[-/TT]TGTTTTATTTTGTAT | 9063 |
rs762731116 | snp | C/T | 1.65029e-05 | 0.00287248 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890686 | AGATGGCTGCTGCAT[C/T]TCAAATGTGGGCTTA | 9063 |
rs762737289 | snp | C/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918018 | TTGCCGAGTTTTTCT[C/G]ACCTTGAAGGGCACC | 9063 |
rs762758114 | snp | C/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892494 | AAAACTAATTTAGGC[C/G]AGGAACAGTGGCTCA | 9063 |
rs762783492 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907690 | GTCCACTTATACGCA[C/T]ATTTTTTTTTCAACC | 9063 |
rs762788195 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824737 | AGGCGTGGTGGCTTA[C/T]GCATTTTGTAATCCT | 9063 |
rs762854135 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906763 | TACCAACAAGATGTA[-/TG]TGTGTGTGTGGGGGG | 9063 |
rs762861154 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873377 | AAAGGTCAAGGCTGA[C/T]TTAAGAGAGACCCTT | 9063 |
rs762891257 | snp | C/T | 1.80837e-05 | 0.00300691 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812465 | TGTCAGGAATGTTAC[C/T]TCCACTGCTGGTTAT | 9063 |
rs762891501 | snp | A/T | 2.11938e-05 | 0.00325522 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844153 | AAGAGAAAAAAAAAA[A/T]TTTAAAAAAATTAAG | 9063 |
rs762916691 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914309 | TGCTTTGACTCTAAG[-/C]CCCCCGGCTATGGAT | 9063 |
rs762955146 | snp | C/T | | | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894888 | CCAGCCTGACCAACA[C/T]GGTGAAACCCCGTCT | 9063 |
rs762958709 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873272 | AACATTAACCACTGA[A/T]AATTCACTTAACCCA | 9063 |
rs762977913 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865993 | GCCAAATGTAATAAC[A/G]TGTATTTTGAGATTA | 9063 |
rs762992818 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838014 | AGGAAACGAAGAAGA[C/T]GGACCTATTTTTATG | 9063 |
rs763017558 | snp | C/T | 1.67228e-05 | 0.00289156 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836547 | ACACAAGGAAAACTA[C/T]TTCAGAAAGGAGAAT | 9063 |
rs763048326 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899302 | GAAATAGTAACTGAA[A/T]AAGTAACTGAAGCAG | 9063 |
rs763071609 | snp | A/G | 1.69243e-05 | 0.00290893 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820907 | CTTTCATTAAAAAAC[A/G]AAAGAAACAAAAACA | 9063 |
rs763121051 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910069 | GCTGAGGCAGTAAAA[C/T]TGCTTGAACCTGGGA | 9063 |
rs763124141 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875956 | GCACCCTATGGGTCA[A/G]GCCCTGAGGGCCACG | 9063 |
rs763135164 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815877 | GCACACACTCGGGAA[C/T]TGCTGCGCTAACAGG | 9063 |
rs763149774 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828459 | TGCAGGTCAGCAGTC[A/G]TTTTACAGAAAGACA | 9063 |
rs763152876 | snp | A/C | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919599 | GGTTGCAGTGAGCTG[A/C]GATCGCACCATTGCA | 9063 |
rs763159368 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881916 | AGCCTGGCCGACATG[A/G]TGAAACCCTGTCTCT | 9063 |
rs763169778 | snp | C/T | 3.36084e-05 | 0.00409915 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46891016 | AGCAAAGCCTAGTAA[C/T]ACTTGTAGTTCAGAA | 9063 |
rs763170608 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827698 | CCAAATTTCCTTACA[A/G]ACAGGTTCAAGAAAA | 9063 |
rs763181505 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857285 | CAAAGACAAATACAA[C/T]ACAGTATTTGCTTCA | 9063 |
rs763184623 | in-del | -/AAAG | 3.71437e-05 | 0.00430934 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864265 | TGGGAAGAAAAAAAA[-/AAAG]AAAGATAATATTTCA | 9063 |
rs763191032 | snp | C/G | 1.65433e-05 | 0.002876 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815392 | TGTCTCATATTTTGG[C/G]AGACCAGAATTATTT | 9063 |
rs763194678 | snp | G/T | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846729 | ATTTCTGATGCCCAA[G/T]AAATGGAAATTTGGT | 9063 |
rs763221648 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876846 | GGACTACAGGTGACT[A/G]CCACCAAGCCCAGCT | 9063 |
rs763221839 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921055 | TACCGTCTTAAAATG[A/G]CTCCAAATTAGAAGA | 9063 |
rs763255353 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841248 | ATTTGCTCCCACTTT[G/T]CAGACTCACGTCCAC | 9063 |
rs763266133 | snp | A/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826350 | CAAACACAGATAAAA[A/T]TGTAGTAAAGGACAG | 9063 |
rs763285403 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890888 | AGAGTTCGTGGATAT[C/T]GGCGTCTATACAATT | 9063 |
rs763351924 | in-del | -/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823327 | AAGCTAATGAATGTC[-/T]TTTTTCCCACTCCCC | 9063 |
rs763376302 | snp | C/T | 6.59228e-05 | 0.00574083 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829791 | CTTTCTTCGGTCTCA[C/T]TGGACACCAAGAACC | 9063 |
rs763434840 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853927 | CCCCCCTGACCATAC[C/G]TACTCAGCCTCTGCA | 9063 |
rs763497890 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46821862 | TAATTTCAAGAAGCA[A/G]TATAATTAAACATAC | 9063 |
rs763504394 | snp | A/G | 4.63134e-05 | 0.00481192 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828170 | AAAAAAATTAAAGGT[A/G]TAACACAAATAAACT | 9063 |
rs763505520 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914389 | CCAGAAGAACTGGAA[C/G]AGAGGTGGGCTGGTA | 9063 |
rs763513806 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899705 | CTCCTGGGCTCAAGT[A/G]ATGCTCCTGCCTTGG | 9063 |
rs763527569 | snp | C/T | 7.77918e-05 | 0.00623617 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828180 | AAGGTATAACACAAA[C/T]AAACTCTAGTGGTAG | 9063 |
rs763549577 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833814 | CACTAGTATTTACAA[C/G]AAATGTATTAGATAA | 9063 |
rs763563676 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869530 | AGAAGGCAAGAAATC[C/T]CTAACATGTGGCATT | 9063 |
rs763580543 | snp | C/T | 1.68963e-05 | 0.00290652 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855620 | GCAAAAAATCCCTGT[C/T]GGAAAGAGAAAGAAA | 9063 |
rs763587523 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820669 | AGAAGAAGTCTCTAA[C/G]TACAAATTCTTCAAA | 9063 |
rs763592934 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880902 | CAAATACAGTTTTCA[-/C]TGAACACTGCTTTAA | 9063 |
rs763656347 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913473 | AACCAGATTCTCACA[C/G]GCACATTCTCTCTCA | 9063 |
rs763657713 | snp | A/G | 1.66211e-05 | 0.00288275 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828096 | TGCCTCACTGGCTAC[A/G]GTCACTGAACAAGGC | 9063 |
rs763657729 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854472 | GTGCCATGTTGTACT[A/G]TTTTTTTGATTATGG | 9063 |
rs763680450 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867832 | CATCAACCAACAGTG[C/T]ACAGTTTAAGTGATG | 9063 |
rs763684550 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832412 | CAGAGCGAAACTCCA[A/T]CTCAAAACAAACAAA | 9063 |
rs763699333 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904673 | GGAGAATCACTTGAA[C/T]CCACGAGGTGGAGGT | 9063 |
rs763699497 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876738 | GTCTTGCTCTGTCAC[C/G]CAGGCTGGAGTGCAG | 9063 |
rs763720000 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880752 | TACATAAAGTCAATA[C/T]AGGCTCTCTTCTATA | 9063 |
rs763727087 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46812842 | TCTAAACTTGTGGAA[A/C]TTGTTTGCTGACCAC | 9063 |
rs763745302 | in-del | -/TTTGT | 2.28778e-05 | 0.00338207 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818360 | CATAAATACAAATTA[-/TTTGT]TTTATTTTGTATTCA | 9063 |
rs763771459 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879747 | GAAAAAAAATCTGAC[A/G]TGTTATAACATGGAC | 9063 |
rs763780864 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904405 | AAGGACACAAAAATG[-/T]TAACGGTGAGGAGAA | 9063 |
rs763785189 | snp | C/T | 1.65715e-05 | 0.00287845 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855468 | AAAAGTATTCTTAAA[C/T]AGTGTGCTCAAACAT | 9063 |
rs763791032 | snp | C/G | | | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890889 | GAGTTCGTGGATATC[C/G]GCGTCTATACAATTC | 9063 |
rs763810230 | snp | A/C | 0.000486973 | 0.0155965 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920038 | GTAAGAAAAGAAAAG[A/C]AAAGCCCCACTGAAA | 9063 |
rs763827541 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826726 | TCCTCATTTTGTTCC[A/G]CACACACAAAAACCC | 9063 |
rs763850693 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861798 | CAGATTGAAGCAGAG[C/T]AGGATGACTCAACAA | 9063 |
rs763883435 | in-del | -/ATTT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894037 | GGCTGAGGCAGGAGA[-/ATTT]ATTTCTTCAACCCAG | 9063 |
rs763893073 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919387 | GCTACTCCGGAGACT[A/G]AGGCAGGAGAATCGC | 9063 |
rs763905508 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860828 | TAAAAAACATAAAAA[C/T]TAGCCAGGTGTGGTG | 9063 |
rs763920772 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895619 | GTGGTTGCGGTGAGC[A/G]GAGATCACACTACTG | 9063 |
rs763949862 | snp | C/T | 1.79922e-05 | 0.0029993 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812466 | GTCAGGAATGTTACT[C/T]CCACTGCTGGTTATG | 9063 |
rs763963904 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892533 | ATCCCAGTGCTTTTG[A/G]AGGCCAACACAAGAG | 9063 |
rs764002551 | snp | A/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826031 | TTCCGTGTATTAATG[A/T]GTATGTATGTCTAGG | 9063 |
rs764017257 | snp | C/T | | | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46891048 | CCCTAAAACTAGAAA[C/T]CATATTCTAAAAGGA | 9063 |
rs764039123 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46906008 | GATCAGGGTTGAATT[C/T]ATACTTGCAACACAA | 9063 |
rs764043468 | snp | A/G | 1.64925e-05 | 0.00287158 | synonymous-codon, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812575 | CTGCTTGCTGTTAAG[A/G]GTGAGGTGAGACTAT | 9063 |
rs764076237 | snp | A/G | 5.03694e-05 | 0.00501818 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836559 | CTATTTCAGAAAGGA[A/G]AATGAGCTCAGAGGG | 9063 |
rs764100582 | snp | C/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918024 | AGTTTTTCTGACCTT[C/G]AAGGGCACCTGAAGG | 9063 |
rs764114085 | in-del | -/GT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848767 | TGAAAGAGAGAGACA[-/GT]GTGTGTGTGTGTGTG | 9063 |
rs764130832 | snp | C/T | 3.3274e-05 | 0.00407871 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820923 | AAAGAAACAAAAACA[C/T]TCCACATACCTGGCA | 9063 |
rs764134576 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913860 | CAGGCTGGAGTGCAG[C/T]GTCAAGATCAGAGCT | 9063 |
rs764148587 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911215 | ACTTTGTTATATTTC[-/T]TTTTTTTTTTTTTTT | 9063 |
rs764149247 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883185 | CTTGATATGACTCTA[G/T]CTGAGCAATGAATGA | 9063 |
rs764166110 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824915 | TGAGGCAGGAGGATC[A/G]CTTCAACCCAGGAGG | 9063 |
rs764173718 | snp | A/G | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846738 | GCCCAAGAAATGGAA[A/G]TTTGGTTTGGCACAG | 9063 |
rs764177276 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859428 | GCGAGACTCCGTCTC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAGAA | 9063 |
rs764200171 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815921 | ACTGGGTTCTGAGCT[A/C]ATGTAATTTTCTGAA | 9063 |
rs764217793 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896583 | GCTGAACACAAAACA[C/T]GAAATTCAAAAAACA | 9063 |
rs764249787 | snp | A/T | 5.09853e-05 | 0.00504877 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818326 | CATATTTTTCCTTGA[A/T]ATAAGCTGTTTTCCA | 9063 |
rs764258270 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851103 | AAAAGAAGAAATGTT[C/G]AGTTTATGTCAGTCC | 9063 |
rs764274634 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849950 | GATATTTAACATGCA[A/T]CTCTAATAAGACTTT | 9063 |
rs764352533 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863535 | ACTCCTGGGCTCAAG[G/T]GATACTGCCACCTCC | 9063 |
rs764368185 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828475 | TTTTACAGAAAGACA[C/T]GCAGAGTTAGGGAAC | 9063 |
rs764384664 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827732 | CAAAAAGTCTCAGGT[A/G]GGAAATAAATACCTC | 9063 |
rs764400674 | in-del | -/A | 0.000499034 | 0.0157882 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891066 | ATTCTAAAAGGAAAG[-/A]AAAAAAAAACATAAG | 9063 |
rs764421295 | in-del | -/CTCA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857678 | AAGGGTTTTGAACAG[-/CTCA]CTAAGGAGTTACACT | 9063 |
rs764423179 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901958 | AAATAAAAGCAGTAA[C/G]AGTTGAAAGGAAAAA | 9063 |
rs764444937 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814534 | GGCCCAAATTTCTGC[C/T]GCTGTTCATGTAATC | 9063 |
rs764512485 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876081 | GACCTATCAGTCTGC[C/T]CTGATCCATCCGCAA | 9063 |
rs764524299 | snp | A/G | 1.68479e-05 | 0.00290236 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844825 | CCGTACAAGATATAC[A/G]GACATAGAGTAATTC | 9063 |
rs764540011 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901146 | CTACAGGCTGGGTGC[A/G]GTGGCTCACACCTGT | 9063 |
rs764558969 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833096 | GATAAATGAAAACAG[C/T]CCACACAAAGACTTG | 9063 |
rs764559857 | snp | A/C | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890793 | TTCCAGCCACGGCCA[A/C]GTCAGGTTCTACAGG | 9063 |
rs764559982 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855810 | TTGCTTAACTTCTAG[C/G]CACGTCTTTATGGCA | 9063 |
rs764565465 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888470 | ATTAAAGCTGGAGAA[C/T]TCACTCTTCCTGATT | 9063 |
rs764574205 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822030 | GTTACTGGTCTTATG[A/G]TTGATGGTGGGAACC | 9063 |
rs764610138 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888788 | AGGAGGTGGAGCTCA[A/G]GCTGTAATGCTCGAA | 9063 |
rs764656048 | snp | A/G | 1.65392e-05 | 0.00287564 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855444 | GCAAAGTCTGCATTA[A/G]TAAAAGAAAAAAGTA | 9063 |
rs764788741 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827421 | GGGTGAAAAGGGAAA[A/G]GAATCAATTTTTATT | 9063 |
rs764816587 | in-del | -/AAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859440 | TCAAAAAAAAAAAAA[-/AAA]AAAAAAAAAAAAGAA | 9063 |
rs764817591 | in-del | -/TT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881371 | TTAAATTAGAAAAAC[-/TT]TGGTGTATGTAATGG | 9063 |
rs764843013 | snp | A/G | 1.67967e-05 | 0.00289794 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821123 | GGCTGTTAGTTCACA[A/G]GAGAGAAGAGCTGCA | 9063 |
rs764847495 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844975 | AATGGTCAATCACTG[C/T]GAAGGGGACAAAATT | 9063 |
rs764852128 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878242 | TTTTAAGATGGTTTT[A/G]TGGACTAAATGCAGG | 9063 |
rs764875837 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824653 | CTTCTTGGTGCTTTG[C/T]AAAATTGTTTATAAG | 9063 |
rs764891992 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892463 | ACACATTAAACCTCC[C/T]AGTAGTCACATTAAA | 9063 |
rs764905231 | snp | A/C | 1.88745e-05 | 0.00307195 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812458 | GAGATGATGTCAGGA[A/C]TGTTACTTCCACTGC | 9063 |
rs764908994 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859055 | TTCACTTTATACTTA[A/G]TATTACTCTAAAGAC | 9063 |
rs764930048 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811348 | CATTGGTGAGAAATA[C/T]GATCATCATAAATCT | 9063 |
rs764935338 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842050 | CCTGGGCAACATGGC[A/G]AAAGATCTCTACAAA | 9063 |
rs764935615 | snp | A/C | 1.65304e-05 | 0.00287488 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836372 | CCATCTAATATTAGA[A/C]TTTCATAGGCAGCTT | 9063 |
rs764973316 | in-del | -/AAG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905602 | AATTATCAAGAAAAA[-/AAG]AAGGCATTTTAAAAA | 9063 |
rs764993407 | snp | A/C | 0.000251762 | 0.0112169 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917354 | CCGCCATTTTATACC[A/C]CCCGCGGGCGCCGCC | 9063 |
rs764997528 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46860715 | CATCTGTAAAGCCAT[A/G]CCTGTAAACCCAATA | 9063 |
rs765037544 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872098 | GTCGAAGGTCTCATT[C/G]AAGATAAGCGCCTTG | 9063 |
rs765073506 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873102 | TTATCACGGCTACCG[C/T]CTTGTTAACTAACAA | 9063 |
rs765090539 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884077 | ACAAATACACATATA[C/T]GATGAAATAAGCAAA | 9063 |
rs765106188 | snp | A/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823809 | TAGTCATTAGTTAGG[A/T]TTATCAAATTACATA | 9063 |
rs765196744 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829572 | TATAAACTTTAGCAC[A/C]TTCCTTCAGGAAAGA | 9063 |
rs765197853 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915951 | TTCAGGGTTCGTTGT[C/T]TGAAAAGCTCCACAG | 9063 |
rs765222274 | snp | A/G | 1.66037e-05 | 0.00288125 | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812612 | ACATAGGAGGACAGT[A/G]CTGCTTGAAACAAAC | 9063 |
rs765258648 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827513 | TCCTGTAATATAGGC[A/G]TTATTTAGCTCCATT | 9063 |
rs765259573 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837005 | ATTATATGAAGGTAT[C/T]ATAATTTATTTAATC | 9063 |
rs765267362 | snp | A/G | 1.67075e-05 | 0.00289023 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829878 | AAAGCCTAAAAAACA[A/G]TTAAGAAGTACATAC | 9063 |
rs765295036 | snp | C/T | 1.68323e-05 | 0.00290101 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844820 | AGCTGCCGTACAAGA[C/T]ATACAGACATAGAGT | 9063 |
rs765311490 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889145 | CTTAAAGGAAAACAC[A/G]GGGCAAAACCTTCAC | 9063 |
rs765368766 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909040 | AATGATTTAAAAGTG[A/G]GCCCAATTGAAAGGA | 9063 |
rs765371731 | snp | C/T | 0.000132258 | 0.00813089 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815382 | TGTTAATAGTTGTCT[C/T]ATATTTTGGGAGACC | 9063 |
rs765378258 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863413 | CACTGCAGCCTCGAC[C/T]TCCCAGGCTCAAGTG | 9063 |
rs765388066 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865334 | ACTTGAGGTCAAGTG[-/A]TTCAAGACCAGCCTG | 9063 |
rs765405733 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915671 | CTGGTTGCACTCCAA[C/T]CTGAGCACTGACTGC | 9063 |
rs765431088 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862084 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 9063 |
rs765481971 | in-del | -/C | 2.09059e-05 | 0.00323303 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844688 | TCTCATATGCTCAAT[-/C]TTTTTTTTTTTTTTT | 9063 |
rs765485608 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841194 | TCAGTAACTACTGTG[A/G]CATTACCTTCCTTTA | 9063 |
rs765489869 | snp | G/T | 4.76349e-05 | 0.00488008 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844170 | TTAAAAAAATTAAGG[G/T]TGACAAAGAAATGGA | 9063 |
rs765522498 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890719 | ATCTTGAAGCAGCAC[A/G]GAACCAACAGGAGAG | 9063 |
rs765527010 | snp | A/C | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919843 | CTTGGCTTATTCTTA[A/C]TCTTGATTTATTCTC | 9063 |
rs765551367 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879020 | TCTAGCCAATCTAAC[A/G]GTAAAATAATTCATA | 9063 |
rs765573589 | snp | C/T | 1.66128e-05 | 0.00288204 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855530 | CACATAGTAAGCAAG[C/T]ATAAAACTAAGGTAA | 9063 |
rs765606621 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867553 | TGGGAATCAGAAAAC[C/T]AATTCTGCAGAGATT | 9063 |
rs765616307 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890785 | CGAGTGGATTCCAGC[C/T]ACGGCCAAGTCAGGT | 9063 |
rs765625752 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887034 | CTTGTGGAATTTAAA[C/T]TGGCACTAAAATAAT | 9063 |
rs765676882 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899649 | TCTTTTTAATTTTAG[C/T]AAAGATGAGATTTCA | 9063 |
rs765737000 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912161 | GGTGTTATATCTTTT[C/T]CTGAAAGACCAGGAA | 9063 |
rs765737562 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886082 | TCTTGGAGTACCACT[A/G]AGCAAAAGCCTACTA | 9063 |
rs765793801 | snp | C/T | 0.000125265 | 0.00791308 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890587 | ACACTTACCTAAACT[C/T]GTGGGCTTGATGAGA | 9063 |
rs765821777 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865870 | AACACAGAAACATAA[A/G]TAAGCCTCTCCATTT | 9063 |
rs765832714 | snp | C/T | 0.000108867 | 0.00737711 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917293 | TCCCATCCCCTCCCC[C/T]GCGGCCTCCGCTCTC | 9063 |
rs765864209 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877127 | TCATACCCTGTGCCA[C/G]AAGCCTAGCACAAAG | 9063 |
rs765901312 | snp | C/T | | | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829830 | GGAATTTGATCTCAT[C/T]TACATCAGAACAGTC | 9063 |
rs765905604 | snp | A/G | 1.86e-05 | 0.00304953 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891067 | ATTCTAAAAGGAAAG[A/G]AAAAAAAACATAAGC | 9063 |
rs765915183 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819339 | TGGCATTAGACTTTG[A/T]ATATACTTTACAAAT | 9063 |
rs765960993 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901842 | CAGGGCGGAAAGATT[A/G]CTTTCCCTCTAATAT | 9063 |
rs765972198 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844587 | TACAATTTTACTCAC[C/T]AGTAATGTATATAAA | 9063 |
rs765990722 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46843106 | ATCCTTGTTCTACCA[A/G]TAACTGTGTAATTTG | 9063 |
rs765993778 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857491 | CAGTGGTTCTGCCTA[C/T]TTCTGCTTAGTGGCT | 9063 |
rs765996619 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846779 | CCTAACTAAAGATGT[A/G]ATATTCAAGGGGCGT | 9063 |
rs766000066 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871869 | AAAACTAGGTATAGG[C/G]CTACATGTCAGTCCA | 9063 |
rs766004500 | snp | A/G | 1.66421e-05 | 0.00288458 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836343 | ATATCAGCTGTTAAA[A/G]GGGATATACTTACCC | 9063 |
rs766020010 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859002 | TGAGGTTTAGTCACC[C/T]GTCTAGGGGCATACG | 9063 |
rs766082973 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808957 | TAATGAATACTTTAT[C/T]GGCAGAAAAAAAAGA | 9063 |
rs766086218 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870532 | GAGGCAGAAGAATGG[C/T]GTGAACCCAGGAGGT | 9063 |
rs766086235 | snp | A/C | 4.97789e-05 | 0.00498868 | missense, intron-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46864208 | AGGTGTCAAAGCAAA[A/C]ATAAAAAACTTCTCT | 9063 |
rs766088096 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829826 | TCTTGGAATTTGATC[C/T]CATCTACATCAGAAC | 9063 |
rs766091002 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823680 | ATTAGTAAATCAACA[C/T]CTAAAACCTCAGCAA | 9063 |
rs766101565 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822541 | CCACAAGCAGTATGT[A/G]AGCAATGTTAGAAAA | 9063 |
rs766132815 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915726 | GTAAATTCTTCGCTT[C/T]ACATTAAGCTTTGGC | 9063 |
rs766226347 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834768 | GACAGGTGTGAGCCA[C/G]CACACCCAAGAGTAG | 9063 |
rs766316349 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909938 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTGAA | 9063 |
rs766323213 | in-del | -/A | 0.00860308 | 0.0650194 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844143 | CTTTAAAAAGAAGAG[-/A]AAAAAAAAAATTTAA | 9063 |
rs766368139 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839450 | TACTTTTTGGTTCTA[C/T]TTGAATAATCTATAA | 9063 |
rs766387786 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826979 | ATAGGAATAAACTAC[-/A]AAAGAACATGAAGAA | 9063 |
rs766387880 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849785 | GCAGGGACCCACCAA[C/T]CAGGTTCAATAATTA | 9063 |
rs766393572 | snp | A/G | 1.74272e-05 | 0.00295183 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855656 | TTAAAAAAGTACAAT[A/G]AGAATTCTCAGAACA | 9063 |
rs766421425 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873776 | CATGTCCCAGGACAC[A/C]AGAAAAATCCTTCTT | 9063 |
rs766429065 | snp | A/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890772 | AAGTGGAAGGCAACG[A/T]GTGGATTCCAGCCAC | 9063 |
rs766443540 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870117 | CCGTGCCCTCCCTAA[A/C]CACACGTCTGAGTCT | 9063 |
rs766513501 | snp | C/G | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919701 | AAAATTGTAAACCCA[C/G]TAGACTATAATGGCT | 9063 |
rs766524492 | in-del | -/T | 1.73942e-05 | 0.00294903 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820888 | TAAGATTAAAAAAAA[-/T]AAACTTTCATTAAAA | 9063 |
rs766556795 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853975 | GGACTGTCTCAATGG[A/G]TTTCAGTCTCAGATG | 9063 |
rs766596868 | snp | C/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824973 | CCACGGCATTCTAGC[C/G]TGGGTCACAAACTGA | 9063 |
rs766616980 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886829 | GGCGACAGAACAAGA[C/T]TCTGTCCCCCCCCTC | 9063 |
rs766623773 | in-del | -/TAGAAGACAC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871754 | TTAAAGCAAGAATCT[-/TAGAAGACAC]AGAGGTCAAATATAA | 9063 |
rs766623913 | snp | C/T | 3.29881e-05 | 0.00406115 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890705 | AATGTGGGCTTAGTA[C/T]CTTGAAGCAGCACAG | 9063 |
rs766669650 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838266 | TTGACTACTACTTCA[A/C]ATTACTCTCAAAAAC | 9063 |
rs766670344 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885862 | GCATTATTTTATCTA[A/C]GCCAAATGAGATAGT | 9063 |
rs766696358 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46818904 | CACATTTTTACCAAA[C/T]AGCCAGTTCAGACAT | 9063 |
rs766713525 | in-del | -/AA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865523 | ACAGCGATAGTCTTC[-/AA]AAAAAAAAAAAAAAA | 9063 |
rs766754605 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866361 | AACTTCTCATCCGAA[C/G]CAATATAGGCCAGAA | 9063 |
rs766780016 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881917 | GCCTGGCCGACATGG[A/T]GAAACCCTGTCTCTA | 9063 |
rs766806849 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912083 | AAGAAAACAAAGGCT[A/G]GGAAGGGAGGAGGGA | 9063 |
rs766809613 | snp | A/G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865270 | TGAGGCCGGGCACAG[A/G/T]GGCTCACACGTGTAA | 9063 |
rs766842926 | snp | A/T | 1.66302e-05 | 0.00288355 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821095 | AAATAGCACGGGAAA[A/T]TACAAACAATCTGGC | 9063 |
rs766859358 | snp | A/G | 1.66128e-05 | 0.00288204 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828036 | TTCCTCTTCGTCAGA[A/G]GAGCTTTCTATTGTA | 9063 |
rs766871319 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830874 | ACTCTGATAATAAAA[A/C]CAGGCAGGCATTGCA | 9063 |
rs766876440 | in-del | -/TATC | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817203 | CTTTAATATTTGCTG[-/TATC]TATCTCTCAGTTCAT | 9063 |
rs766890096 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897001 | TATGACAAAAGACTG[C/G]AGTTGATTAACTTCT | 9063 |
rs766921759 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46903456 | AATAAGCACATAAAA[A/G]TATGTTCAGCATCAT | 9063 |
rs766947208 | snp | A/G | 1.65056e-05 | 0.00287272 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820967 | GCTTGATATTGGCGT[A/G]TGGTGGAATGGTACT | 9063 |
rs766961896 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840799 | TGCTTTTTTGAAATT[C/T]ATTATTTTTATGAAT | 9063 |
rs766996610 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808281 | TTTTCTGGTGACAGA[A/C]TCATAGGCAATTAAT | 9063 |
rs767029961 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904754 | GACTCCATCCGTCTC[-/A]AAAAAAAAAAAAAAA | 9063 |
rs767038904 | snp | C/T | 3.42208e-05 | 0.00413633 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846881 | ATTTCAAATCATCTG[C/T]AGGAAGATTAAACAT | 9063 |
rs767043851 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841380 | CTTCTTATTTAAGTG[C/T]CTGGGATTTATTTTT | 9063 |
rs767072510 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822182 | AAAACTATTTCATAA[C/T]CTCAATTTAAATGTC | 9063 |
rs767092930 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901325 | GAGGCAGGAGAATCG[A/C]TTGAACCTGGGAGGC | 9063 |
rs767127125 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857499 | CTGCCTACTTCTGCT[C/T]AGTGGCTCCACTAGG | 9063 |
rs767133705 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882812 | CAAAACTCTAGGGAA[C/T]ACTATTCACAGATAT | 9063 |
rs767209735 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881118 | TTCAAATGAAACAGC[A/G]GCCCCAACTCCTGCC | 9063 |
rs767217105 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869740 | TGTTTCATTTGGACC[A/G]CAGAGCTCATCCTCA | 9063 |
rs767302172 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848151 | TCCTATGTGCAAGCA[C/G]GAATTTTAGAGAGAA | 9063 |
rs767310503 | snp | G/T | 5.14558e-05 | 0.00507201 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855638 | AAAGAGAAAGAAAAT[G/T]GGTTAAAAAAGTACA | 9063 |
rs767313459 | in-del | -/ATT | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919660 | TCTCAAAAAATAAAA[-/ATT]ATTATTTTAAAATTT | 9063 |
rs767391278 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879825 | ACAGATAATATGACA[C/T]GTAAGTCAAATAATA | 9063 |
rs767402279 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908724 | TCATCAAAAAACGCA[C/T]AAGGCTGGATGCAGT | 9063 |
rs767452440 | snp | C/T | 0.000115553 | 0.00760019 | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812590 | GGTGAGGTGAGACTA[C/T]CCAAAAACATAGGAG | 9063 |
rs767455406 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907889 | CAACTGTATATATAC[C/T]ACACAGGTTCCATTT | 9063 |
rs767489767 | snp | A/G | 1.67643e-05 | 0.00289515 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890612 | ATGAGAACATCAAGG[A/G]CATCATAAAAGGGCA | 9063 |
rs767495845 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852514 | CTGCTTTATGTAGTA[G/T]TCAATATGTTCACAA | 9063 |
rs767535881 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814345 | AACCTCTAGGTTCCA[A/G]GATAATTTTTTTTAA | 9063 |
rs767572280 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814581 | AACAGGAGGCTGATA[C/G]AGGACTTGTGCTTAG | 9063 |
rs767573974 | in-del | -/GGTACCTTAGG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845132 | TTATTTAGCAAAACT[-/GGTACCTTAGG]GGCCACCCTGAAAAT | 9063 |
rs767592005 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896720 | TTCTCATTTATCAAC[A/G]TGGACCATAAGAAGT | 9063 |
rs767627668 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813032 | TTTAAAAGTATTTGT[C/T]AGCCTTTCCCGGTAT | 9063 |
rs767646925 | snp | A/T | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890690 | GGCTGCTGCATCTCA[A/T]ATGTGGGCTTAGTAT | 9063 |
rs767687214 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837626 | TTATATAATCAACTG[-/T]TGTCAATTTTTCAAC | 9063 |
rs767689141 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838015 | GGAAACGAAGAAGAC[A/G]GACCTATTTTTATGC | 9063 |
rs767709785 | snp | C/T | 1.65143e-05 | 0.00287348 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836391 | CATAGGCAGCTTTTT[C/T]GTCACACACAGGACA | 9063 |
rs767752677 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897970 | TCAACCTCCCAGGCT[C/T]AAGTGATCCTCCCAC | 9063 |
rs767793041 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816911 | ATATCTCAATAAGCA[G/T]ATTTTGTCTTCATAT | 9063 |
rs767802541 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828493 | AGAGTTAGGGAACTG[A/G]TCTCAGGTCATGGGA | 9063 |
rs767861717 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829479 | TTGTAACAAACATCA[C/T]ATTTTAAAATGATTT | 9063 |
rs767863131 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808822 | GGTCCGGCTAAGTGC[-/T]TTTTTTTTTTTTTTT | 9063 |
rs767923001 | snp | C/T | 0.000247192 | 0.0111146 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846761 | TGGCACAGCTGAAGA[C/T]AACCTAACTAAAGAT | 9063 |
rs767941640 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857830 | TAGGAAGTTTTACAT[A/G]CTGGTCCATCAGATA | 9063 |
rs767942401 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876251 | GTATAACAAGAGATA[C/G]CCCTCATGGGTCCTT | 9063 |
rs767944760 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889551 | GACACCCATTATAAT[G/T]GCCACTATAAAAAAA | 9063 |
rs767953769 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844400 | CAACAATTAGGAGAG[A/G]AAGCTGGAATGCAGC | 9063 |
rs767956249 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842844 | CACACCTCTTCCCTG[C/T]GTTTGCTAAGAGCAG | 9063 |
rs767960289 | snp | A/C | 1.72296e-05 | 0.00293505 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844847 | GAGTAATTCTACAAA[A/C]AAACAAAAAAAACCT | 9063 |
rs767991082 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833908 | GGTGCTAGGGTGACA[A/T]GATCCCTACCTTAAT | 9063 |
rs768109669 | in-del | -/A | 0.000298649 | 0.0122162 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844852 | ATTCTACAAACAAAC[-/A]AAAAAAACCTGCATT | 9063 |
rs768128211 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909737 | TCCTAGAATCTCTAC[A/G]GTGAAACATACAAAT | 9063 |
rs768157213 | snp | C/T | 1.67534e-05 | 0.0028942 | missense, intron-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46864171 | CCTCTTACCTGGATA[C/T]GCATATCTCTCTAAC | 9063 |
rs768160592 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814872 | AACTGGGGCCTCCCC[A/G]AAGTCCAAATCTGAA | 9063 |
rs768171753 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46908193 | GTTGCCCAGGCTGGT[A/C]TTGAACTCCTGGCTC | 9063 |
rs768177979 | snp | A/G | 1.73153e-05 | 0.00294233 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891057 | TAGAAACCATATTCT[A/G]AAAGGAAAGAAAAAA | 9063 |
rs768181958 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849480 | CAAGTTCATGTGACA[A/G]GGAACCAGTGGGGCA | 9063 |
rs768247451 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882616 | AAACTGCAAGAATAG[C/T]GCCTGATACATGCTA | 9063 |
rs768275084 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859384 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 9063 |
rs768353861 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893670 | GTATTGCTGGACACA[C/T]AGCCAAAGGTAATTA | 9063 |
rs768359527 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862830 | CCTGCCTCAGCTTTC[C/T]GAGTAGCAGGGATTA | 9063 |
rs768359921 | snp | A/T | 1.65083e-05 | 0.00287296 | missense, downstream-variant-500B, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815335 | CAACTGGAATAAGGG[A/T]AAGAAAATCCAAACC | 9063 |
rs768418394 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886793 | CAGTGAGCCGAGACA[A/G]CGCCACCGCCCTCCA | 9063 |
rs768448081 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818423 | AGCTTCAGTTCATTA[C/T]TAATATCATTTCTTC | 9063 |
rs768460034 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868660 | GTGTGCTCTCGCAGC[A/G]GCCAGAAGTGTGACC | 9063 |
rs768471207 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890836 | ATCCAAACTGAAAAC[C/T]GATGATTTGATTGTG | 9063 |
rs768482370 | snp | C/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920423 | AACCTGAGAACCAAC[C/G]CTTCTTGTGAGCAGA | 9063 |
rs768482988 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908690 | TAAATGCAATCACAT[A/T]AAAATTAAGAACTTC | 9063 |
rs768498946 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827211 | TTGAAAGAATGTGTT[C/T]GTAGACAGCCAGGAG | 9063 |
rs768593925 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878935 | TAACAGGGGCTCATA[C/T]TATGGCTAACATAGG | 9063 |
rs768608593 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911880 | ACATGGTGAAACCCT[G/T]TCTCTATTACAAATA | 9063 |
rs768623248 | in-del | -/ATTGCCT | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826941 | AGACACAAAAAAACG[-/ATTGCCT]ATTGCCTAGATTTGG | 9063 |
rs768678155 | snp | A/G | 1.68094e-05 | 0.00289904 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855338 | TGGTGAATAAAAAGC[A/G]ACTTACAGGCAAAGG | 9063 |
rs768683145 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816758 | CAGACATAAGCCACC[A/G]CACCCAGCTTGCTGT | 9063 |
rs768751894 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839966 | AAAAGCTCGAGACCA[A/G]CCTGACCAACATGGT | 9063 |
rs768783000 | snp | C/T | 4.95479e-05 | 0.0049771 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46821063 | AGAAGATGGCTGATA[C/T]ATGAGAACCCTGTTT | 9063 |
rs768799954 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845835 | GTATTATCCCCATTA[C/G]ATGGCAAAAGTTTTC | 9063 |
rs768808150 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877698 | TGGGGACACGACACA[A/G]AACCAGGGAATAACC | 9063 |
rs768814763 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807929 | GGTATGAATCAAGAA[C/T]TACAAAAGTGTTCAT | 9063 |
rs768831637 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865983 | CCTCTTAACTGCCAA[A/G]TGTAATAACGTGTAT | 9063 |
rs768849646 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858681 | TCAGCCTGGGTGACA[C/G]AGCAAGACCCTGGCT | 9063 |
rs768859614 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824138 | CAGCACAAAAGTGAA[C/T]TGCTAGAATGCTGCT | 9063 |
rs768865267 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890259 | AAAGAGTTCTGGAGA[C/T]GGATGGCAGTGATGG | 9063 |
rs768867707 | snp | A/C/G/T | 6.31777e-05 | 0.00562011 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812408 | AGTTCTGATGAATGA[A/C/G/T]TCCCAGAATCAAGTG | 9063 |
rs768882556 | snp | C/T | 1.68032e-05 | 0.0028985 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836316 | CATTGCCAACAGCTG[C/T]TGTATTAGTCCATAT | 9063 |
rs768887058 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877222 | CCTACTTTTAGAAAA[A/C]CAGGCAGAATAACAG | 9063 |
rs768902772 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46891628 | TAAAATATTAAAGCT[-/A]AAAAAATCACATACA | 9063 |
rs768953873 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916420 | AAAAAAAAAAAAATC[A/C]GGGTTTCTGTCCGTA | 9063 |
rs768998953 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918685 | CCTCGGCCTCCCAAA[A/G]TACTGAGATTACAGG | 9063 |
rs769009758 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810591 | GTTTGTTTCCCCCCC[A/T]ACATCTTTAAAATAA | 9063 |
rs769054950 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46903119 | ACTTTTTTTTAATAA[G/T]CAGGAAAATATTTGG | 9063 |
rs769099886 | snp | A/T | 2.01884e-05 | 0.00317707 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864279 | AAAAGAAAGATAATA[A/T]TTCAATAACAAATCC | 9063 |
rs769101413 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809613 | ATACAAAATTAGCTG[G/T]GCGTGGTGATACATG | 9063 |
rs769129663 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847957 | GATACCATATTTCAC[C/T]GATGCTAGGATGTCA | 9063 |
rs769144445 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871392 | TTAAGTCCTCACATG[A/C]TAAACCATATAAAGG | 9063 |
rs769164314 | in-del | -/A | 0.000989874 | 0.0222251 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828152 | TAAAGAAACAAAAGG[-/A]AAAAAAAAATTAAAG | 9063 |
rs769166886 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890148 | GTCAAAATCATAGAC[-/A]AGTGGAAGTAGAATG | 9063 |
rs769167970 | snp | C/G | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829794 | TCTTCGGTCTCATTG[C/G]ACACCAAGAACCATC | 9063 |
rs769172390 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885640 | CATGTCTGTTTTTCG[C/T]GCCACTGCACTCCAG | 9063 |
rs769184237 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823316 | TGGTACAAGAAAAAG[C/T]TAATGAATGTCTTTT | 9063 |
rs769190747 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861615 | CCCTGAGAAGGGCAC[A/G]TAACTTGAGGTATTC | 9063 |
rs769193110 | in-del | -/AAAC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912758 | ACAATAAAACCCTAA[-/AAAC]AAACAAACAAAAATG | 9063 |
rs769214659 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822420 | AAAATACATTTTCCC[A/G]AGGTAGATAAAGACA | 9063 |
rs769307327 | snp | A/C | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826894 | ATGTTGCAAAACAAG[A/C]CATTTTATATAAAAT | 9063 |
rs769370854 | in-del | -/TATATG | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919004 | GTGCGTGTATATATA[-/TATATG]TGTGTGTGTGTGTGT | 9063 |
rs769406607 | snp | A/C | 3.30606e-05 | 0.00406561 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812514 | GCTGCTGGATGAACT[A/C]ACATGAGTACTGCTT | 9063 |
rs769408270 | snp | C/T | 1.72516e-05 | 0.00293692 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844752 | GTGCTCTGGAATGAT[C/T]AGGGTTTCTAATACC | 9063 |
rs769413069 | in-del | -/AATT | 4.96627e-05 | 0.00498286 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815400 | ATTTTGGGAGACCAG[-/AATT]ATTTCCCTAAATCAT | 9063 |
rs769473635 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908603 | TTACAATAATGGAAA[A/G]TATCTTCGAGAACTC | 9063 |
rs769496866 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919161 | TTGCAGACCAGCCAG[A/G]CCAACATGGTGAAAC | 9063 |
rs769532588 | snp | C/G | 1.65154e-05 | 0.00287358 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844112 | CTATCAGGATCTGCA[C/G]TAAGTTTTTCTTTAA | 9063 |
rs769534898 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907531 | GCAGAAACAACAGAA[C/T]ACATATACAGAAACA | 9063 |
rs769543335 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886711 | GTGTGGTGGCACATG[C/T]CTGTAGCCTCAGCTA | 9063 |
rs769550035 | snp | G/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825843 | GAAGATGACTACAAA[G/T]TTGTCCTTATGACGA | 9063 |
rs769568395 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839724 | ACAAAAATTAGCTGG[G/T]TGTGGTGGTGGGCAC | 9063 |
rs769650312 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899255 | AGTGAAGAAGTAGAG[A/G]ATTTGCCATTTTAAA | 9063 |
rs769699804 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849997 | ACAACCCCACAAAAA[A/T]AATCACAATTTTAAA | 9063 |
rs769714917 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890750 | GATGGTGAGTGAGGT[A/G]TAACTGAAGTGGAAG | 9063 |
rs769726305 | snp | A/C | 3.33517e-05 | 0.00408347 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836534 | TACAGGACAGGAAAC[A/C]CAAGGAAAACTATTT | 9063 |
rs769738535 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853529 | AGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9063 |
rs769768487 | snp | A/G | 0.000108507 | 0.0073649 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891255 | GTTACGGTGTTAATT[A/G]TATTTTGTTGTACAA | 9063 |
rs769844092 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888175 | TACAATAACAACTAT[A/G]AAACATTGCTGAAAG | 9063 |
rs769849626 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828431 | GTGCAGCTCCTACTG[C/T]TCATCCTGTCTCTGC | 9063 |
rs769852816 | snp | C/T | 1.67248e-05 | 0.00289173 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890998 | TCCACTTTTATTCCG[C/T]CCAGCAAAGCCTAGT | 9063 |
rs769873286 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858609 | GGCTAAGGTGGGAGG[A/C]TCAATTGAGCCCGGA | 9063 |
rs769875041 | snp | A/G | 5.00354e-05 | 0.00500152 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846694 | CCTGCTACCCAAAAC[A/G]GAGAGCTTTTACCTT | 9063 |
rs769914674 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867019 | AAGAGAATGGTTCCA[C/T]AGTCATGTTGTACAT | 9063 |
rs769921954 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807940 | AGAACTACAAAAGTG[C/T]TCATATACCCTTGAC | 9063 |
rs769965511 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876783 | CTCACTGCAAGCTCT[A/G]CCTCCCGGGTTCACA | 9063 |
rs769996626 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902659 | CCAAACCGATATATA[A/G]GTTTAACATAATTCC | 9063 |
rs770027216 | in-del | -/CAG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852579 | CTTTGGGACAGAAAT[-/CAG]CAGCAGTAACTAAGT | 9063 |
rs770030583 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870228 | AAGGAATCAGCCCCA[A/G]CTCTTTTCCCCTTGA | 9063 |
rs770032606 | snp | A/G | 1.82794e-05 | 0.00302314 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864135 | TAAACCAATATTCAT[A/G]AGAAATATATTCCAA | 9063 |
rs770044508 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857062 | CACATGTCAAGTGCC[C/T]AAATATAAGATGTGC | 9063 |
rs770044512 | snp | C/T | 6.59228e-05 | 0.00574083 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890848 | AACCGATGATTTGAT[C/T]GTGGATAAATCAGAA | 9063 |
rs770051816 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809483 | ATTTTGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 9063 |
rs770073882 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902734 | TCTAAAATGTATATG[-/A]AAAGGCAAAAGAAAT | 9063 |
rs770114950 | snp | A/G | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829784 | ATAGCTTCTTTCTTC[A/G]GTCTCATTGGACACC | 9063 |
rs770149104 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897223 | GTGAGGTAAAAAAGC[A/G]GTTATGGCATAAATA | 9063 |
rs770154834 | snp | C/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823126 | TAAGGTCCTAGCTAC[C/T]TGGGAGGCTGAGGCT | 9063 |
rs770182958 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871187 | ACTGGACTATTGAAG[A/T]GCTTTTAAGAGAAGC | 9063 |
rs770250795 | snp | A/G | 2.02854e-05 | 0.0031847 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828154 | AAAGAAACAAAAGGA[A/G]AAAAAAATTAAAGGT | 9063 |
rs770295461 | snp | C/G | 1.67368e-05 | 0.00289277 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855604 | TCTCTCCTACCACCT[C/G]GCAAAAAATCCCTGT | 9063 |
rs770315131 | snp | C/T | 1.65979e-05 | 0.00288074 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836515 | CAGCCTCATTTTTCC[C/T]AACTACAGGACAGGA | 9063 |
rs770321376 | in-del | -/C | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918201 | AAGGAAGCTTGATGG[-/C]CCCCCCCGTAATGTG | 9063 |
rs770336105 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900505 | GACCCAGGTTCTACC[-/A]AAAAAAAAAAAATTG | 9063 |
rs770372839 | in-del | -/CT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898495 | TTACAAATGACAAGA[-/CT]CTCTCTATTAGAAAT | 9063 |
rs770401467 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849052 | TAACCAAATAAAAAT[A/C]ATGTTACAGGGTCTG | 9063 |
rs770406157 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833744 | TAATTAAAATAGTTT[C/T]GTATTGGCCCAGTAA | 9063 |
rs770452141 | snp | A/G | 1.65124e-05 | 0.00287331 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890666 | TGGACAGGAGGAATT[A/G]GGGGAGATGGCTGCT | 9063 |
rs770463013 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907218 | TATAATGAACTCCTA[C/T]GAATCAGTATGGAAA | 9063 |
rs770468509 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839432 | ATTTAAAATGATCAT[C/T]TTTACTTTTTGGTTC | 9063 |
rs770494077 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832283 | AGCCAGGCGTGGTGG[C/T]GCACACCTGTAGTCC | 9063 |
rs770532328 | snp | A/G | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844096 | AGTTGTAGCAATTTC[A/G]CTATCAGGATCTGCA | 9063 |
rs770569188 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886102 | AAAGCCTACTACAGC[A/T]TCTTCACTTAGTCCC | 9063 |
rs770683789 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837794 | CCTTTACAGAAAATA[A/T]CACTGTTTATAACCA | 9063 |
rs770698159 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46846885 | CAAATCATCTGCAGG[-/A]AGATTAAACATTTTC | 9063 |
rs770702091 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852007 | CAAATTTCTTTTGTG[A/G]CTTGTTGATGCTTCT | 9063 |
rs770732103 | snp | A/G | 2.32897e-05 | 0.00341237 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818494 | TTTAAAAGGAATGTT[A/G]AGAAATGTATTAAAA | 9063 |
rs770735780 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837350 | ACATTCCTCTTATTT[-/G]TAAGTGGTAGTTGAG | 9063 |
rs770736563 | snp | C/T | 6.59946e-05 | 0.00574395 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46821024 | AGCAGCAGGATCAAC[C/T]GAAGTCACACTGGGC | 9063 |
rs770764447 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896422 | CTCCCTCCACATCCA[A/G]AAACATCTACCCAAA | 9063 |
rs770765198 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904184 | GGTTGTGATACTGTA[A/C]TATGGTCTTTAAGAT | 9063 |
rs770775711 | snp | G/T | 5.16262e-05 | 0.0050804 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890546 | ATTTCATTTACTATC[G/T]TGTTCAGAAGAAACT | 9063 |
rs770805995 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911690 | GCACAGAAAACTTTA[A/G]AAGAGTTATAAAACA | 9063 |
rs770812633 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823843 | GGAGCAGGCTTTTGT[C/T]ATCAAAATCTTCACA | 9063 |
rs770832203 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829114 | CTAAGTTCACGTGTG[G/T]GTTTCAATGAGACTG | 9063 |
rs770876353 | in-del | -/AT | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921689 | ACAGCTGATAAACAC[-/AT]AACAAAAAAAAAAAA | 9063 |
rs770912313 | in-del | -/G | 3.78838e-05 | 0.00435206 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864114 | TATGGCAGCCCTACA[-/G]GTGAATAAACCAATA | 9063 |
rs770934062 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887022 | TCTCTCACTTTGCTT[-/G]TGGAATTTAAACTGG | 9063 |
rs770983891 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46841028 | AATCAAACCTAGCTT[G/T]CTTTCTTTCTTTTTC | 9063 |
rs770995558 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897808 | TAAGACTTCTAAAAT[A/G]TATACTATGTTCTGT | 9063 |
rs770996565 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46807772 | TCAGTTAACCCCGTT[C/T]CATAGAGTCAGAAAG | 9063 |
rs771017884 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878760 | TAAGCCCAGCTACTC[-/A]AGGAGACTGCGGTAG | 9063 |
rs771071309 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912910 | TGAGAGAATAAAAAA[C/T]GTGACATCAGGTGAT | 9063 |
rs771129903 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888034 | CAGAATACAAAGTCA[A/T]CACGCAAAAATCAAT | 9063 |
rs771145152 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817244 | GAAACCTTTTTATAA[C/T]GCTAAGTATTGACAA | 9063 |
rs771169690 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880355 | CACAACTATACCCTG[C/T]CTGGGTGAGAGACAG | 9063 |
rs771201984 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868792 | TTGGGGGCTCATCCG[C/T]GATTGCCTTTCTCAT | 9063 |
rs771226799 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893353 | TTGCTTCACTCCTTA[C/T]ACTTATTGTCAGATA | 9063 |
rs771234961 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844263 | CACACTCCCAATATA[A/G]GTTAAAGAATTATGA | 9063 |
rs771237830 | snp | A/G | 1.88988e-05 | 0.00307393 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828147 | TGCATGTAAAGAAAC[A/G]AAAGGAAAAAAAAAT | 9063 |
rs771238138 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899454 | ACCACTGCCGAACCA[A/G]AGTAATCTAGAGGAA | 9063 |
rs771256725 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867364 | TAATTTGTATTAACA[C/T]TGACAGTTCTTAGAT | 9063 |
rs771307905 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879405 | AAAAATAGTAATAAT[A/G]GTAAGTGCAGATGAG | 9063 |
rs771322855 | in-del | -/AAAC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832417 | CGAAACTCCATCTCA[-/AAAC]AAACAAACAAACAAA | 9063 |
rs771359312 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812540 | TGCTTTCATGGGAGC[C/T]GGTGGTGGTGACAGA | 9063 |
rs771391295 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913255 | AGGATGGTGACTCCT[A/G]GTAGGTGTAAGGAAA | 9063 |
rs771410859 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908951 | GGGTGGAGGGTGCAG[-/T]TAAACTGAGATCACG | 9063 |
rs771414043 | snp | C/T | 1.6498e-05 | 0.00287206 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855405 | TGGATAGTTATCTTC[C/T]TGAGGGCAACTTGTC | 9063 |
rs771426420 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813636 | ACTGGATTATGGAAC[A/G]GGAATTTAAGTCAAG | 9063 |
rs771444710 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847777 | GTGAGCCACAGTGCC[C/T]GGCCAACTGTTCGTT | 9063 |
rs771444875 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812161 | GACTCCATCCATTAA[C/T]GTATGAAAGTGAAAT | 9063 |
rs771474104 | snp | C/T | 2.33462e-05 | 0.00341651 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864299 | ATAACAAATCCAACA[C/T]TACAACCACCTGCAA | 9063 |
rs771501578 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908469 | TTGAGGAAAAACCAT[C/G]CATCTTGGTCACCAC | 9063 |
rs771502035 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837643 | GTCAATTTTTCAACA[C/T]ACTTTTGATTAACTT | 9063 |
rs771523430 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46915590 | CTGATCCACAAACCA[A/C]AACAGAGAGGAAGGC | 9063 |
rs771535744 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861394 | AAAGCCAAGATTCAC[A/G]AGTGAACACTGAATT | 9063 |
rs771557947 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895833 | TCTTTTCAAAGGTCA[C/T]TGGAGGCCCCAGTTC | 9063 |
rs771580087 | snp | A/G | 1.67595e-05 | 0.00289473 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836328 | CTGTTGTATTAGTCC[A/G]TATCAGCTGTTAAAA | 9063 |
rs771580731 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885314 | ACGAGGTCAGGAGTT[C/T]GAGACGAACCTGGCC | 9063 |
rs771592099 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851858 | AGTAAGATCATACAC[A/G]TAAGGACTTCTTCCA | 9063 |
rs771599210 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916634 | TTTTAAGACTGAGAA[A/G]AAAAAAATATTTTTC | 9063 |
rs771619826 | snp | A/C | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890637 | AGGGCAGATTTTTTA[A/C]CTGCACATCAGGATG | 9063 |
rs771731419 | snp | A/G | 1.65176e-05 | 0.00287376 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815358 | TCCAAACCTAAAACA[A/G]AAATGCTTTGTTAAT | 9063 |
rs771749709 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850679 | AGATTGATCAGGAGT[C/T]CAGGGGATGTCAGCC | 9063 |
rs771755938 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882591 | GTTGTTCATAGCTGC[A/G]ATGTCTGTAAAACTG | 9063 |
rs771850247 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875760 | ATTCCATCCGCACTC[C/T]AAACAAAAGAGATTG | 9063 |
rs771863142 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828846 | TTTAGTTAAAAATGA[A/G]TGACAGTTGATAATG | 9063 |
rs771866933 | snp | G/T | 3.37701e-05 | 0.004109 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846667 | AAAGTCAACCCTCAG[G/T]GGGGTCACTGTCCTG | 9063 |
rs771879395 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864416 | TCATCTTGGAATCAT[A/G]AGTAAAGTCACTACA | 9063 |
rs771884811 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828266 | ATACTCCAACCCATG[C/G]ACAAATACCAACTCC | 9063 |
rs771932566 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876549 | GCAGAGAAAGGTGGA[C/G]TTTGTGTCATCATTG | 9063 |
rs771947632 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921600 | ATCAGGTGTATGAGT[A/G]TACTCTGTAAATTTA | 9063 |
rs771948138 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814825 | TCATCTTTGACAGAG[A/G]AAACGGGGATGATTG | 9063 |
rs771950107 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907816 | AGGACTTGAGTACAC[A/G]TGATTTTCCTGTTGG | 9063 |
rs771956917 | snp | C/G | 1.96647e-05 | 0.0031356 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818453 | CTTTGTTCTCCTGCA[C/G]ATTCAGAAGATTCAT | 9063 |
rs771959981 | snp | C/T | 1.6604e-05 | 0.00288127 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890959 | CAATAAATGCAGCGC[C/T]CTCATCAGGAGGTCA | 9063 |
rs771974121 | in-del | -/A | 3.44196e-05 | 0.00414832 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855643 | GAAAGAAAATGGGTT[-/A]AAAAAGTACAATGAG | 9063 |
rs772007468 | in-del | -/ATG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814484 | TGAGGTCAACTCCGA[-/ATG]ATAAGAAATTCCTCA | 9063 |
rs772059748 | in-del | -/G | 0.000251477 | 0.0112105 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844141 | ACTTTAAAAAGAAGA[-/G]GAAAAAAAAAAATTT | 9063 |
rs772099394 | snp | C/T | 1.68823e-05 | 0.00290532 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828125 | GCTTACTGAGGACGC[C/T]TGAACCTGCATGTAA | 9063 |
rs772175531 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853760 | CACCACTGCACTCCA[A/G]CCTGGGTGACACAGC | 9063 |
rs772227746 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879050 | AAAGTAACAATGAAT[A/G]AATCAGTTTAATTAC | 9063 |
rs772228944 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867120 | TTATAGAACTGGCAG[C/G]TTAATGTTAGTAGTC | 9063 |
rs772248940 | in-del | -/ATAT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831656 | GTTCAGAGATCACAC[-/ATAT]AGTCAATTAATTTTT | 9063 |
rs772265352 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845985 | AGGAATATTATTCTG[C/T]TTAGGAACATGTAAT | 9063 |
rs772318554 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807915 | CATGTGGAAAAGTGG[-/T]TATGAATCAAGAACT | 9063 |
rs772327645 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912705 | AGTTGAAAAAATATA[C/G]AGAGAAAGGCATGGT | 9063 |
rs772371572 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906974 | TTAAAAAACAAAAAT[A/C]TGTGTGAATGCAGGA | 9063 |
rs772386276 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911951 | AGCTAATCGCGAGGC[G/T]GAGGCAGGAGAATCG | 9063 |
rs772388225 | snp | A/T | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855372 | TAGCTTCCCATTTAC[A/T]TTTATACATAGACTA | 9063 |
rs772392741 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877985 | CATAATCTTATCAAT[G/T]CCAAGTATTCAGATT | 9063 |
rs772400828 | snp | C/G | 2.98699e-05 | 0.00386446 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812414 | GATGAATGATTCCCA[C/G]AATCAAGTGAGTCCT | 9063 |
rs772423460 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892000 | GGAAGAACACCTGGA[A/G]CTGACCAAAGCCCTG | 9063 |
rs772447853 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890439 | TCAGTCATGGTTGCC[A/G]AATTTTTATCCGTAT | 9063 |
rs772447978 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819751 | TCGGAGAGAAGGGAA[A/G]TCATGAATGTACTGG | 9063 |
rs772476218 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845632 | TTTCACATAAATGTT[-/A]AAAAAAAAAAACCTA | 9063 |
rs772548836 | snp | A/G | 0.00031294 | 0.0125049 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916855 | GTAGCATCAGCCATA[A/G]GAAGAGGAGAGATTC | 9063 |
rs772563641 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904994 | GCTCTCTTAATAAAA[A/G]ATAAAGATATGAGAT | 9063 |
rs772596482 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810930 | TAAAGCTTAGAGAGA[A/G]AAAGCTAAACAGAAA | 9063 |
rs772605204 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847373 | TTTTAAACCAGGTTA[A/C]GTTAACAAATAAGGA | 9063 |
rs772625438 | in-del | -/TTAT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844908 | GTTTACATGAAATAC[-/TTAT]TTAAGAAACTCTGGT | 9063 |
rs772639504 | snp | C/T | 1.67427e-05 | 0.00289328 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836331 | TTGTATTAGTCCATA[C/T]CAGCTGTTAAAAGGG | 9063 |
rs772686475 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859765 | TGATGCCCTTGTAGG[C/T]CAAAGGAGAGGCACT | 9063 |
rs772690510 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824229 | ATTTGCTCAGACTTG[A/G]ATGTCTGAAAATAGG | 9063 |
rs772705403 | snp | C/T | 1.66172e-05 | 0.00288242 | missense, intron-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46864186 | TGCATATCTCTCTAA[C/T]TTGTTGAGGTGTCAA | 9063 |
rs772719074 | snp | G/T | | | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46903529 | ACTAGATACCTACCA[G/T]AATGGCTAAAATGAA | 9063 |
rs772719535 | snp | C/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823495 | TAAAAGGAGTCAAGT[C/G]AATGTACCTACACAC | 9063 |
rs772767344 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858763 | TACCACTGAGTGATA[G/T]TCACACATAAAAAAT | 9063 |
rs772767520 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872595 | ACCATTTACAAGAGA[A/G]GGGGTTACGAGTTTC | 9063 |
rs772769061 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911256 | AGCCTTGCTTTGTCA[C/T]CCAGCCTGGAGTGCA | 9063 |
rs772771825 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809927 | CTAGCAAAATAAACT[A/G]CTAGAAAGTCAGGGT | 9063 |
rs772824278 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46818468 | GATTCAGAAGATTCA[C/T]GTTTATGATGTTTAA | 9063 |
rs772860844 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850719 | TACCATGAAGTTCCC[C/T]GTCAAGCTTCGGCAT | 9063 |
rs772884889 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895956 | GATTACAATAACTCC[C/T]AGGTTAAAGAAATCA | 9063 |
rs772898913 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883706 | AATTAGCCAAGCATG[A/G]TGGTGCATGCCTGTA | 9063 |
rs772914021 | snp | A/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915642 | CTTCTTTGGTTTCTA[A/T]CACTTTCCAGTTGCT | 9063 |
rs772921647 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864653 | TGCATGCCTGTAATG[C/T]CAGCTACATGGGAGG | 9063 |
rs772933259 | snp | C/T | | | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894882 | TTGAGACCAGCCTGA[C/T]CAACACGGTGAAACC | 9063 |
rs772946206 | in-del | -/AAGAGGT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913746 | CTGCTCTGGTTAAAG[-/AAGAGGT]AAGTGATTCCAGAAA | 9063 |
rs772987824 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890535 | GAAGGTCTCTCATTT[C/T]ATTTACTATCTTGTT | 9063 |
rs773032749 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46807946 | ACAAAAGTGTTCATA[C/T]ACCCTTGACTAGAAA | 9063 |
rs773051747 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834525 | GGAATTAAAGAAATA[C/T]CTGATAACTCCTATA | 9063 |
rs773087451 | snp | C/T | 1.6768e-05 | 0.00289546 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846687 | TCACTGTCCTGCTAC[C/T]CAAAACGGAGAGCTT | 9063 |
rs773129096 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909808 | GCAGGTCAGGGTTTT[C/T]CTGCAAGACAAGTTT | 9063 |
rs773140233 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904948 | AAGAAAAATGAAAAA[C/T]GAAACAAAATTCTAG | 9063 |
rs773149972 | snp | G/T | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815387 | ATAGTTGTCTCATAT[G/T]TTGGGAGACCAGAAT | 9063 |
rs773155172 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863328 | TTGCTTTACCCAATA[C/T]ATATATTTTTTCAGA | 9063 |
rs773155351 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828318 | TAAAATGGTTGTTCA[A/C]CTAGGGAGACAGGTG | 9063 |
rs773155717 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908878 | GCCAGGCATGGTGGC[A/G]GGTACCTGTAATCCC | 9063 |
rs773166434 | in-del | -/A | 3.44196e-05 | 0.00414832 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855642 | GAAAGAAAATGGGTT[-/A]AAAAAAGTACAATGA | 9063 |
rs773167020 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820310 | CATCTCTTACTATGC[C/T]TAATTTAAAAATTCA | 9063 |
rs773192980 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895526 | AAATACAAAAATTAG[A/C]CGGGTGTGGTGTCTC | 9063 |
rs773222186 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885778 | GGATACGTGTATTTC[C/T]GGCATTCTAACTGAA | 9063 |
rs773228398 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853852 | CTTGTTGCTAGTAGC[C/T]GGAAACCTGACAAAC | 9063 |
rs773231866 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814427 | CCTAGAAAAATACAT[A/G]GACACTTTCACTAGG | 9063 |
rs773235998 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876606 | AATAATACTGCTCCC[A/G]ATGGAACCATAACAA | 9063 |
rs773262788 | snp | G/T | 3.30551e-05 | 0.00406528 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815375 | AATGCTTTGTTAATA[G/T]TTGTCTCATATTTTG | 9063 |
rs773287719 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875787 | ATTGTTATGCTTGTG[C/T]GCACCGCAGGCCAGA | 9063 |
rs773317410 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854906 | TGCCCAAGTCCTCCC[C/T]TTCAACTATGCTGTT | 9063 |
rs773338024 | in-del | -/AAG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871526 | AATGGGAGAAGGAGA[-/AAG]AAGTCATTCCATTTA | 9063 |
rs773370037 | snp | C/T | 4.98699e-05 | 0.00499324 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828028 | GGAGGGTCTTCCTCT[C/T]CGTCAGAAGAGCTTT | 9063 |
rs773399986 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840017 | AATATAAAAATTAGC[C/T]GAGCATGATGGCAGG | 9063 |
rs773421472 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823479 | CTTTGACTTACATCT[A/G]TAAAAGGAGTCAAGT | 9063 |
rs773431555 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818226 | TGATTAAATATGTAA[A/C]TGTTTAGCACTTTCA | 9063 |
rs773502808 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829516 | AATGTTTCCTTTATT[C/T]TACACAGGAAAAATA | 9063 |
rs773504428 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853035 | TAATCCCAACACCTT[A/G]GGAGGCCAACATAGG | 9063 |
rs773534959 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898053 | ACAGACAGAGTCTCC[C/T]TGTGTTGTCCGGGTT | 9063 |
rs773541220 | snp | C/T | 1.6513e-05 | 0.00287336 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855375 | CTTCCCATTTACTTT[C/T]ATACATAGACTATTT | 9063 |
rs773592274 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46912007 | AGTGAGCCAAGATGG[C/T]GCCATTGCTCTCCAG | 9063 |
rs773595071 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830796 | TCTTCTCTAGGGAAT[C/T]CTACCAAATATTTGA | 9063 |
rs773615169 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905296 | TAAAGAATTCACAAC[A/G]GAAAATAGAAAAATA | 9063 |
rs773624519 | snp | A/C | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892209 | ACGGCCCAGAAGCAA[A/C]TGTTTAAAACCCTAT | 9063 |
rs773626548 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877988 | AATCTTATCAATTCC[A/T]AGTATTCAGATTCAT | 9063 |
rs773649274 | snp | C/G | 1.67725e-05 | 0.00289585 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846854 | GCCCTATAACCGTAA[C/G]AAAGAAAAATTATTT | 9063 |
rs773665438 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916198 | CAGAGGATACGTTCT[C/T]TTGCTCACGTCCACT | 9063 |
rs773681181 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840409 | TGTGTGTCCATATTA[C/T]TATAAAAAGTTTTAA | 9063 |
rs773699039 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46835730 | TTAATGTCAATAACA[A/T]AGTCATCACCATAGG | 9063 |
rs773744888 | snp | A/G | 8.12821e-05 | 0.00637451 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812423 | TTCCCAGAATCAAGT[A/G]AGTCCTCCTTTAGTC | 9063 |
rs773790093 | snp | A/G | 1.67427e-05 | 0.00289328 | synonymous-codon, intron-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46864172 | CTCTTACCTGGATAT[A/G]CATATCTCTCTAACT | 9063 |
rs773812732 | in-del | -/TCTTA | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817103 | CTTTTTACAGTAACT[-/TCTTA]TCTTTTCAGTTTTTC | 9063 |
rs773848765 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914482 | CAAGATCTCTGGTAC[C/T]GGCTCACGCAGCAGT | 9063 |
rs773872115 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858867 | TTTTGGAATGCTGCA[A/G]CTGAAGAGATGGCCA | 9063 |
rs773875912 | snp | A/C | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829797 | TCGGTCTCATTGGAC[A/C]CCAAGAACCATCTTC | 9063 |
rs773879317 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822064 | GTCACAAAGCTAGAC[A/T]GGGATAACCTCTGGG | 9063 |
rs773906261 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850512 | GCTCTACCTCCCATA[G/T]ATTTTTAAAGCCAGT | 9063 |
rs773919177 | snp | A/C | 0.000217604 | 0.0104286 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917284 | CACCTCCTCTCCCAT[A/C]CCCTCCCCCGCGGCC | 9063 |
rs773922774 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849481 | AAGTTCATGTGACAG[C/G]GAACCAGTGGGGCAA | 9063 |
rs773958388 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908720 | CTACTCATCAAAAAA[C/T]GCATAAGGCTGGATG | 9063 |
rs773964504 | snp | A/T | 1.68755e-05 | 0.00290473 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844773 | TTCTAATACCTTTCA[A/T]TTTTAATCTCTGTAA | 9063 |
rs773979350 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862455 | AATATCTGAAAAGGA[A/C]GTAAACACCTCTAAT | 9063 |
rs774009997 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862891 | GTTGTATTTTTAGTA[C/G]AGATGGGTTTCGCCA | 9063 |
rs774068142 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882750 | ACTGCAATAAATCTG[C/T]TGTAATAAATTTCCA | 9063 |
rs774084934 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909758 | ACATACAAATATTCA[C/G]ACTAAGTGAGATCAA | 9063 |
rs774090520 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888038 | ATACAAAGTCAACAC[A/G]CAAAAATCAATTGCA | 9063 |
rs774121108 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880951 | ACAGCAAAGTTTTTC[A/T]AATTTAATCAGATTT | 9063 |
rs774231960 | in-del | -/A | 0.000151093 | 0.00869043 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836559 | TATTTCAGAAAGGAG[-/A]AATGAGCTCAGAGGG | 9063 |
rs774234057 | snp | A/G | 3.29875e-05 | 0.00406112 | synonymous-codon, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812578 | CTTGCTGTTAAGGGT[A/G]AGGTGAGACTATCCA | 9063 |
rs774252563 | in-del | -/AAGGT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883313 | GTTCATAAAACTTTG[-/AAGGT]ATTTCACATAACACC | 9063 |
rs774269604 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920483 | TGACTTTGATACTCA[C/T]TCTGCCTCTGTACTG | 9063 |
rs774292863 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874773 | CTCTTCCCTCAGAAC[C/T]AAAGGCCTTTTAGCA | 9063 |
rs774297354 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827280 | CTGAAAAAGCAACTA[C/T]TGTTAAATACCCAAA | 9063 |
rs774320110 | in-del | -/CA | 1.88113e-05 | 0.00306681 | intron-variant, frameshift-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818386 | TTGTATTCACTGTTG[-/CA]CAGTATCAGAAGATG | 9063 |
rs774321975 | snp | A/G | 1.65094e-05 | 0.00287305 | missense, downstream-variant-500B, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815338 | CTGGAATAAGGGAAA[A/G]AAAATCCAAACCTAA | 9063 |
rs774332474 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866121 | GGAGAACTAAAAGAA[G/T]AGAGTGCAAAATGAG | 9063 |
rs774336928 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897912 | GATCTCGTTTTATTG[A/C]CCAAGCTGGAGTGTG | 9063 |
rs774354160 | in-del | -/AAAAAAAAAAAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859431 | GAGACTCCGTCTCAA[-/AAAAAAAAAAAA]AAAAAAAAAAAGAAT | 9063 |
rs774357769 | snp | A/G | 3.31697e-05 | 0.00407231 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821082 | AGAACCCTGTTTTAA[A/G]TAGCACGGGAAATTA | 9063 |
rs774376499 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901177 | AATCTCAGCACTTTG[A/G]GAGGCCAAGGCGGGC | 9063 |
rs774389536 | snp | C/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826061 | GTTGGGTGTTAAGGG[C/G]TACATCAGCTTCATG | 9063 |
rs774404069 | snp | A/G | 0.000134944 | 0.00821302 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901298 | CCTGTACTCCCAGCT[A/G]CTCAGGAGGCTGAGG | 9063 |
rs774424923 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830547 | AATAAAGTCTCAAAT[C/T]AGTAACTTTATGAAA | 9063 |
rs774433256 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814450 | TCACTAGGTACCTTC[A/G]TTATATATACTGCTG | 9063 |
rs774505529 | snp | C/T | 3.33261e-05 | 0.0040819 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846845 | TGGTGCATAGCCCTA[C/T]AACCGTAAGAAAGAA | 9063 |
rs774518063 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911930 | GTTGCAGGTGCCTGT[A/G]ATCCCAGCTAATCGC | 9063 |
rs774548400 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819567 | TACCGAGCCAATTAT[C/G]AATTGTTTCAGTAAC | 9063 |
rs774561336 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890355 | CATTTTATATTATGT[A/G]TATTTTACAATAAAA | 9063 |
rs774580632 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865164 | AATAATGTTCTAGTG[A/T]CCATTAAAACAAACA | 9063 |
rs774611398 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846739 | CCCAAGAAATGGAAA[C/T]TTGGTTTGGCACAGC | 9063 |
rs774714395 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46911021 | TAACCCAGGAGAACA[A/G]TGTGAAGTAATCCCA | 9063 |
rs774727874 | snp | C/T | 1.68318e-05 | 0.00290096 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46891022 | GCCTAGTAATACTTG[C/T]AGTTCAGAAACCCTA | 9063 |
rs774751695 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889453 | TTCTTGAAAGATACA[A/T]AAATGGCCAAAAAGC | 9063 |
rs774752167 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844244 | AATGTATTGACAACA[C/T]GATCACACTCCCAAT | 9063 |
rs774823638 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858689 | GGTGACAGAGCAAGA[A/C]CCTGGCTCAAAAAAT | 9063 |
rs774836294 | in-del | -/AAT | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823434 | CTTACACGTAACAAC[-/AAT]AACAGAGCTCCCTTT | 9063 |
rs774841052 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810595 | GTTTCCCCCCCAACA[C/T]CTTTAAAATAAGCAG | 9063 |
rs774859315 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809615 | ACAAAATTAGCTGGG[C/T]GTGGTGATACATGCC | 9063 |
rs774882745 | snp | C/T | 1.68015e-05 | 0.00289836 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836319 | TGCCAACAGCTGTTG[C/T]ATTAGTCCATATCAG | 9063 |
rs774922223 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808757 | CATGAAAATGAAGAA[A/G]ATCTTTCAGGAAAAA | 9063 |
rs774940735 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834922 | GGAGGCATCTTAATA[A/T]TAAATAGTAAAAGTC | 9063 |
rs774949256 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808382 | AACATTATTCAACCA[G/T]GCAAGCATTAAAGAA | 9063 |
rs774953447 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871562 | GAGTCAGGGGCTCTA[C/T]TCTTTTTATCTTGAA | 9063 |
rs774956853 | snp | A/C/G | 0.000150897 | 0.008685 | intron-variant | PIAS2 | GRCh38.p7 | 18:46812638 | CAAACAATGATGCCA[A/C/G]TGAGGAAGAGGCTAC | 9063 |
rs774973547 | in-del | -/TTAT | 4.65929e-05 | 0.00482641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818357 | CTCCATAAATACAAA[-/TTAT]TTGTTTTATTTTGTA | 9063 |
rs775031899 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904445 | TTAGGCAAAACTGAC[-/A]AAAAAAAGAAAAATA | 9063 |
rs775054193 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899555 | TCACTGCAGCCTCAA[-/C]CTCCTGAGCTCAAGT | 9063 |
rs775080949 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861666 | CCATCTAATCATGGT[A/G]AAACATCAGCCGTAC | 9063 |
rs775087180 | in-del | -/A | 0.000989874 | 0.0222251 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828153 | TAAAGAAACAAAAGG[-/A]AAAAAAAATTAAAGG | 9063 |
rs775133864 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874603 | CTTCCCATTGCCTTA[A/C]TGAGGGTCTGAACTA | 9063 |
rs775159561 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820959 | GATGACATGCTTGAT[-/A]TTGGCGTATGGTGGA | 9063 |
rs775171766 | snp | C/T | 1.82191e-05 | 0.00301815 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812464 | ATGTCAGGAATGTTA[C/T]TTCCACTGCTGGTTA | 9063 |
rs775194863 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893632 | GGGACAGTCTTTGCA[C/T]TACAAAATGCTGCAA | 9063 |
rs775213219 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865283 | AGTGGCTCACACGTG[A/T]AATCCCAGCACTCTG | 9063 |
rs775214717 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886764 | ACTGCTTGAACCCGG[A/G]GAAGTGGAGGCCGCA | 9063 |
rs775234649 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920245 | AACTGGGCATATAAA[C/T]CTGATTAGTACTGAG | 9063 |
rs775241243 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813495 | GACTTTAGTAAAACA[A/G]GAGGTCTAGTGATAT | 9063 |
rs775249042 | snp | C/T | 3.2975e-05 | 0.00406035 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812564 | TGACAGACGTACTGC[C/T]TGCTGTTAAGGGTGA | 9063 |
rs775307676 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863049 | TAAATGCTACAGATT[C/T]CCTTTTCTTTCTTCT | 9063 |
rs775335222 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856310 | GGCCAAAGACTTTTC[-/T]TTTTACTATAAAGAC | 9063 |
rs775358669 | snp | A/T | 1.67111e-05 | 0.00289055 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836543 | GGAAACACAAGGAAA[A/T]CTATTTCAGAAAGGA | 9063 |
rs775450548 | snp | C/T | 1.65179e-05 | 0.00287379 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844113 | TATCAGGATCTGCAG[C/T]AAGTTTTTCTTTAAC | 9063 |
rs775472239 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885605 | AATCCCAAGAGGTTC[C/T]GGAATGACATTTTTG | 9063 |
rs775480086 | snp | C/T | 1.66263e-05 | 0.00288321 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846700 | ACCCAAAACGGAGAG[C/T]TTTTACCTTCCCAAT | 9063 |
rs775480495 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917997 | AATGTCCTGCAAGTA[C/T]CAACCTTGCCGAGTT | 9063 |
rs775524739 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847521 | GAGTCTGGCTCTGTC[A/G]CCCAGGCTGGAGTAC | 9063 |
rs775530615 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859243 | ACCATCCTGGCTAAC[-/A]TGGTGAAACCCTGTA | 9063 |
rs775530650 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838000 | GGAAAAGAACAAACA[C/G]GAAACGAAGAAGACG | 9063 |
rs775550192 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889336 | ATTTGCACATTCATA[C/T]ATCTGATAAGGGATT | 9063 |
rs775563541 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46843638 | ATAAAAGAAAAATTA[C/T]TGTGCAATTTAAAAG | 9063 |
rs775567846 | snp | A/G | 1.73628e-05 | 0.00294637 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820891 | GATTAAAAAAAATAA[A/G]CTTTCATTAAAAAAC | 9063 |
rs775630990 | in-del | -/GT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877653 | TAGCCAGTTGGGTCA[-/GT]GTAGATTGTGCAGTC | 9063 |
rs775634914 | snp | A/G | 3.30131e-05 | 0.00406269 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890676 | GAATTGGGGGAGATG[A/G]CTGCTGCATCTCAAA | 9063 |
rs775642164 | snp | C/G | 1.67908e-05 | 0.00289743 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46891012 | GTCCAGCAAAGCCTA[C/G]TAATACTTGTAGTTC | 9063 |
rs775653551 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842605 | CAATATCCAACTGTT[C/T]TTTAACCAACAAAAA | 9063 |
rs775727499 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872676 | TAATAAGTAAAGGCA[A/G]GCCAAGGATAAGGCC | 9063 |
rs775760594 | snp | C/T | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890879 | AGTCCTTCAAGAGTT[C/T]GTGGATATCGGCGTC | 9063 |
rs775814297 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833789 | GAACAAATAGCAGTT[C/T]AGAAGTTAACACTAG | 9063 |
rs775866696 | snp | C/T | 3.2963e-05 | 0.00405961 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829787 | GCTTCTTTCTTCGGT[C/T]TCATTGGACACCAAG | 9063 |
rs775903491 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46857114 | CTGCTGTGACTGTTT[C/T]CACTGCTCCCACTGT | 9063 |
rs775928695 | snp | G/T | 0.000104575 | 0.00723026 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828163 | AAAGGAAAAAAAAAT[G/T]AAAGGTATAACACAA | 9063 |
rs775968392 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914355 | AGAGACCTAAACTCA[A/G]CCAATCAGATTCTCT | 9063 |
rs775990013 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861558 | GATCAAGGTTAACAT[C/T]ACCAAAAATAAGATA | 9063 |
rs776004454 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46821804 | ATAAATACTTCACAA[C/T]TGGTATTATATAAAA | 9063 |
rs776034701 | snp | A/G | 3.29734e-05 | 0.00406025 | synonymous-codon, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812548 | TGGGAGCTGGTGGTG[A/G]TGACAGACGTACTGC | 9063 |
rs776058390 | in-del | -/C | 1.65075e-05 | 0.00287289 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812527 | CTAACATGAGTACTG[-/C]TTTCATGGGAGCTGG | 9063 |
rs776115483 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845822 | ATTATAAGGAAGAGT[-/A]TTATCCCCATTACAT | 9063 |
rs776122129 | snp | C/T | 1.7703e-05 | 0.0029751 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864146 | TCATGAGAAATATAT[C/T]CCAAATATTCCTCTT | 9063 |
rs776123684 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825615 | TACCATTCTTGATGA[C/T]CAGCACTGACTGAAA | 9063 |
rs776124636 | snp | C/G | 1.66363e-05 | 0.00288407 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836344 | TATCAGCTGTTAAAA[C/G]GGATATACTTACCCA | 9063 |
rs776125865 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811252 | TTCAGGTAAGATATC[A/G]TTTTAAAAAAATGAA | 9063 |
rs776129586 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886653 | GACCAGCCTGGCCAA[C/T]GTAACGAAACCCCAT | 9063 |
rs776130776 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908498 | ACTTCACACTGTATA[C/T]AAAATCAACTCCAGG | 9063 |
rs776146952 | snp | C/T | 0.000139522 | 0.00835114 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812438 | GAGTCCTCCTTTAGT[C/T]CAATGAGATGATGTC | 9063 |
rs776156284 | in-del | -/GT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848768 | AAAGAGAGAGACAGT[-/GT]GTGTGTGTGTGTGTG | 9063 |
rs776225911 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907287 | GCAAGCCACTTTACA[A/G]AAGAAACCCAAATGG | 9063 |
rs776260551 | snp | A/G | 4.96471e-05 | 0.00498208 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846834 | TTTTTAGGCGGTGGT[A/G]CATAGCCCTATAACC | 9063 |
rs776299867 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872965 | TCACCTTTTCATTAA[C/T]GCAAACAAGGGGGTA | 9063 |
rs776345139 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46829474 | TTGTTTTGTAACAAA[C/T]ATCATATTTTAAAAT | 9063 |
rs776380049 | in-del | -/AA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840271 | ATATTTTTAAAAGAC[-/AA]GAGTACACAAGCACA | 9063 |
rs776392716 | snp | C/G | 1.65111e-05 | 0.0028732 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890667 | GGACAGGAGGAATTG[C/G]GGGAGATGGCTGCTG | 9063 |
rs776416809 | snp | C/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918968 | GGTATTTGTGTAATT[C/G]TTTATTTGATATATA | 9063 |
rs776454433 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831685 | TTTTTGTAAAAGGTG[A/C]AAAAGCAATTCAATG | 9063 |
rs776487218 | in-del | -/A | 0.146092 | 0.228072 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864256 | CTTTGAACTGGGAAG[-/A]AAAAAAAAAAAGAAA | 9063 |
rs776521125 | snp | A/C | 2.23571e-05 | 0.00334336 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890563 | GTTCAGAAGAAACTG[A/C]ATTCTCAAACACTTA | 9063 |
rs776540537 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827446 | TTTATTGGGAAATTA[C/T]CACATGCCTGACACC | 9063 |
rs776549164 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46836591 | ACATGGTCAGTTGTA[A/G]AAGTCGGAAGATGTC | 9063 |
rs776570614 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883256 | AAATATTAACTACTT[C/T]TGTAATCTGAAAAGA | 9063 |
rs776591371 | snp | C/T | 4.94841e-05 | 0.00497389 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46821039 | CGAAGTCACACTGGG[C/T]ACCCTTACAGAAGAT | 9063 |
rs776608088 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46807810 | GTCTTAGTGCAGATG[C/T]CTGCATAAAGATAAA | 9063 |
rs776626109 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920725 | GCATGTTTCTCTTCA[C/T]TGTTGTGATCATTTC | 9063 |
rs776646287 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890845 | GAAAACCGATGATTT[A/G]ATTGTGGATAAATCA | 9063 |
rs776649603 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910906 | TCAGAAAGTTTATCA[A/C]CAGCATATCCTTCCA | 9063 |
rs776651473 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854095 | CACAGGCTGTGTATG[C/T]GACAAATGAGACTCC | 9063 |
rs776687924 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900915 | AGAGGCGGAGGTTGC[A/G]GTGAGCCGACGTCGT | 9063 |
rs776738963 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914146 | ACTGGTAAATTGAGT[A/G]ATTTCTTCTCTGGCA | 9063 |
rs776744592 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46915492 | AGTCTCTGTTGGGCA[C/T]GTCATATGAATTGTG | 9063 |
rs776771464 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46821624 | TTGATGGCAATAGGC[C/T]ACAATCAGAAACGAG | 9063 |
rs776842543 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847968 | TCACTGATGCTAGGA[C/T]GTCAGTGATGTAATT | 9063 |
rs776847321 | snp | C/G/T | 0.00016489 | 0.00907852 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890774 | GTGGAAGGCAACGAG[C/G/T]GGATTCCAGCCACGG | 9063 |
rs776936593 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899491 | ATTTGTTGCTATTTG[A/G]GACAGGGTCTTGGCT | 9063 |
rs776962891 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886842 | GACTCTGTCCCCCCC[A/C]TCCAAAAAAAAACAA | 9063 |
rs777004248 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856036 | TTTGAGACAGAGTCT[C/T]GCCCTGTCGCCCAGG | 9063 |
rs777049578 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867474 | TTAACATAACCATGA[A/G]AAAGAATGCAGGATG | 9063 |
rs777093027 | snp | C/G/T | 0.00018165 | 0.00952859 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890664 | GATGGACAGGAGGAA[C/G/T]TGGGGGAGATGGCTG | 9063 |
rs777110653 | in-del | -/TA | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808794 | AATAAAAATGTTTAC[-/TA]TAAAGAAAGAATGGT | 9063 |
rs777144348 | in-del | -/AGT | 0.000230981 | 0.0107442 | cds-indel, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820983 | GGTGGAATGGTACTG[-/AGT]AGTAGTCTGTTAATG | 9063 |
rs777157786 | snp | A/C | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918827 | TCAGGTTTCACTTTA[A/C]GTGTCACTTCCTCAG | 9063 |
rs777191695 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897394 | GTCAGAAGGGCAAAG[-/A]AAACATCCAGAATGG | 9063 |
rs777219688 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885319 | GTCAGGAGTTCGAGA[C/T]GAACCTGGCCAACAT | 9063 |
rs777223954 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866739 | GAGGGGGTAGATAAA[A/G]GAAATTATCTCCCCA | 9063 |
rs777262401 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839223 | ACCTATTCAACAAAA[C/T]GCCCACAATGATTAA | 9063 |
rs777332805 | snp | C/T | 1.64993e-05 | 0.00287218 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855412 | TTATCTTCTTGAGGG[C/T]AACTTGTCTCTGCCA | 9063 |
rs777335739 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898807 | GAGACCAGCATGGAC[A/G]ACACGGTGAAATCCC | 9063 |
rs777338387 | snp | A/G | 3.45716e-05 | 0.00415747 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827928 | TTAGTTGCAAGGGTA[A/G]TGAACAATAGTGAAC | 9063 |
rs777359321 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818390 | ATTCACTGTTGCACA[A/G]TATCAGAAGATGTTC | 9063 |
rs777484600 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910803 | TTAGATTCCCACAGC[A/G]AAGTTTTCAAAATTC | 9063 |
rs777523704 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46843528 | TTCTAAGCAAGCCTC[A/C]ATATTTTCTCCCACA | 9063 |
rs777574590 | snp | A/C | 5.10851e-05 | 0.00505371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855318 | ATTAAACTTATATGC[A/C]AATCTGGTGAATAAA | 9063 |
rs777610513 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817603 | CATCCACGGAAAATT[C/G]AATGTGGTGACTTAT | 9063 |
rs777660032 | snp | C/G | 3.3432e-05 | 0.00408838 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890995 | GCGTCCACTTTTATT[C/G]CGTCCAGCAAAGCCT | 9063 |
rs777696378 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878611 | CAGTGGGTCACTCCT[A/G]TAATCCCAGCACTTT | 9063 |
rs777742734 | snp | G/T | 1.66651e-05 | 0.00288657 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829734 | CTATTCTACACATAC[G/T]TTCTATTTTTGTACA | 9063 |
rs777787933 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916582 | CTATTCCAGACCTCT[A/G]CTATACAAGGGTATC | 9063 |
rs777807114 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889989 | CTTTAAAAATGTATA[C/G]TATTGTATTATTTAG | 9063 |
rs777807936 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832144 | GCAAAAGGCCAGGCA[C/G]GGTGGCTCATGCCTG | 9063 |
rs777849355 | snp | G/T | 5.17232e-05 | 0.00508517 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828133 | AGGACGCTTGAACCT[G/T]CATGTAAAGAAACAA | 9063 |
rs777863235 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893219 | CCCAAGCAAGTAATA[C/T]GATGCATCTTTCCCT | 9063 |
rs777926748 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880329 | GGTTAGGCTGCAGTG[A/G]GCTGTGATCTCACAA | 9063 |
rs777941876 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913965 | CCAAGCCCTGCCCTC[C/G]AGACCATTTTTGGAG | 9063 |
rs777945433 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813286 | CTAATCTTCTCGTGA[C/T]GCCTGCTTAACACCC | 9063 |
rs777970364 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858847 | TTTCTAGGAGGGTAT[C/T]CAGGTTTTGGAATGC | 9063 |
rs778058536 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908357 | TAAAAACAGACTAAC[A/G]GCCCAGAGTCCAGAA | 9063 |
rs778074259 | in-del | -/TATG | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919005 | GCGTGTATATATATA[-/TATG]TATGTGTGTGTGTGT | 9063 |
rs778145870 | snp | A/C | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826375 | GGACAGAGGGTAGAC[A/C]CTTGTGGCATGCCAC | 9063 |
rs778160006 | in-del | -/TT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46844689 | CTCATATGCTCAATC[-/TT]TTTTTTTTTTTTTAA | 9063 |
rs778178458 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900189 | GGCCAACATGGTAAA[A/G]CACAGTCTCTACAGA | 9063 |
rs778198061 | in-del | -/CTTC | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916302 | TTTTACCGGATTCCT[-/CTTC]CTTATTTGAAAAAGA | 9063 |
rs778243963 | in-del | -/GATACTTT | 1.72417e-05 | 0.00293608 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828133 | GGACGCTTGAACCTG[-/GATACTTT]CATGTAAAGAAACAA | 9063 |
rs778282137 | in-del | -/CT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831996 | GCTTTTTGACATACA[-/CT]GTTAAAAGACTGAAA | 9063 |
rs778290919 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844073 | CACATCAAGGATACC[C/T]GAAGGCTAGTTGTAG | 9063 |
rs778291289 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824624 | TTCTCTCTAGGTGAG[A/G]TATTTTTTGCTTTCT | 9063 |
rs778302927 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840231 | GGGCTATAGTTATCA[A/G]TATTTGTATATTAGA | 9063 |
rs778304318 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874166 | AAAAAACTAATAAGC[A/G]AATCCTAAGAAAACC | 9063 |
rs778312493 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907008 | ACTACAAAGGCAGTA[A/G]GGACCTGAGACACCA | 9063 |
rs778331343 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861290 | GAAAAGAAAAGGAGA[C/T]AGCTCCTCCTTGTAA | 9063 |
rs778359580 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46886412 | ATACTGTCCAAATGC[A/C]ATGATAAAGGAGGAA | 9063 |
rs778362154 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851799 | TACTTTGTACATGAA[A/G]TATAGTGGTCAACTG | 9063 |
rs778385274 | in-del | -/TTC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863058 | CAGATTTCCTTTTCT[-/TTC]TTCTTACATCTCTTA | 9063 |
rs778392383 | snp | A/C | | | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920048 | AAAAGCAAAGCCCCA[A/C]TGAAACTTACGTGCA | 9063 |
rs778407961 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910703 | CAAATCCCGTAGATC[G/T]TAGACTACAATTGTA | 9063 |
rs778421885 | snp | C/T | 2.06665e-05 | 0.00321447 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864282 | AGAAAGATAATATTT[C/T]AATAACAAATCCAAC | 9063 |
rs778445931 | snp | A/C | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918336 | AGAGGTCTTTAAAAC[A/C]ATGTAACTTTTAAGG | 9063 |
rs778467260 | snp | G/T | 4.9467e-05 | 0.00497303 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846798 | TTCAAGGGGCGTCCA[G/T]GGCGCTTCTGTTCAA | 9063 |
rs778501210 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864337 | GCATTTTTTATAAAG[G/T]ACCTGCCAAATTCTG | 9063 |
rs778511137 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817522 | TTGATGATTTCATGT[G/T]TGTGGTAAATATAAA | 9063 |
rs778574598 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868554 | TCAGGTCAGTGTAGA[-/T]TGTGCCGTCTGACTC | 9063 |
rs778585851 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842133 | CAGGAGGCTGAGATG[C/G]GAAGATCACTTGAAC | 9063 |
rs778606295 | snp | A/C | 1.83404e-05 | 0.00302818 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891088 | AAACATAAGCCAAGT[A/C]ACCCTCAAGCATACA | 9063 |
rs778621915 | snp | G/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921441 | TAAAGTGTCATAAGA[G/T]TTTAATACACGAAGT | 9063 |
rs778645502 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876454 | ACTATATTAGAGATG[C/T]TAGTAAAGGAACAGC | 9063 |
rs778675377 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813122 | TTGGACTCCTTTGTA[C/T]ATAAACGTAAAATAC | 9063 |
rs778705190 | in-del | -/TGAATAAAAAGCAAC | 3.39374e-05 | 0.00411917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855325 | TATATGCAAATCTGG[-/TGAATAAAAAGCAAC]TGAATAAAAAGCAAC | 9063 |
rs778705638 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809090 | GCTTAAAATCCAACA[C/T]TTTACCTTTCTTCAA | 9063 |
rs778712077 | in-del | -/AT | 0.00122028 | 0.0246708 | | | GRCh38.p7 | 18:46818426 | TTCAGTTCATTATTA[-/AT]ATCATTTCTTCTTTG | 9063 |
rs778715085 | snp | C/T | 1.65608e-05 | 0.00287752 | | | GRCh38.p7 | 18:46890941 | AGGGCTGCAGCCGCT[C/T]TTCAATAAATGCAGC | 9063 |
rs778754464 | snp | A/G | | | | | GRCh38.p7 | 18:46828744 | TCTGCTAATCACGTA[A/G]GTTCTTTCTACCCAC | 9063 |
rs778786660 | snp | A/C | 1.69258e-05 | 0.00290905 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846660 | AACACAGAAAGTCAA[A/C]CCTCAGTGGGGTCAC | 9063 |
rs778844135 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828235 | GTTCCTGACAACATA[C/T]AGCCAGTGAAGCCAC | 9063 |
rs778894419 | snp | A/G | 1.66106e-05 | 0.00288184 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855523 | CTACATGCACATAGT[A/G]AGCAAGTATAAAACT | 9063 |
rs778955274 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831884 | AAAATATTTGTGACC[C/T]TGAGTTAGGGAAAAT | 9063 |
rs778959927 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859154 | CAATGAAGGGCCAGA[C/T]GCGGTAGCTCACGCC | 9063 |
rs778973178 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902347 | AGATCACCTGAGGCC[A/G]GGAGTTCGAAACCAG | 9063 |
rs779039483 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811788 | CTCATTAGCAAACAA[C/T]GTCAAAGTGTAAATG | 9063 |
rs779078174 | in-del | -/ACAA | 1.66305e-05 | 0.00288357 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821097 | ATAGCACGGGAAATT[-/ACAA]ACAATCTGGCTGTTA | 9063 |
rs779085786 | snp | C/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46908035 | TGTTCTCTTTCTTGA[C/G]CTGCACGATTATTAT | 9063 |
rs779087157 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46878977 | CCAAGAGGTTTTTTA[A/G]GGAGTTTTGTGGATT | 9063 |
rs779127635 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861105 | ACCAACATGGTGAAA[C/T]CCTTTCTCTACTAAA | 9063 |
rs779130719 | snp | G/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825185 | GATGCTGAACTACAA[G/T]AAAGGATATGAAAAG | 9063 |
rs779203643 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918283 | GGACGGTGTCCAGGG[C/T]TCAATTTCCTTGAAG | 9063 |
rs779219465 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849485 | TCATGTGACAGGGAA[-/C]CAGTGGGGCAAATAT | 9063 |
rs779239776 | snp | A/G | 1.65244e-05 | 0.00287436 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836449 | TTGTAGATAGAGGGC[A/G]GCATCAAAACACTGC | 9063 |
rs779252103 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838563 | ACTCATCACTTAGAA[C/T]AGAAAAAGGTCAGAA | 9063 |
rs779276572 | snp | A/T | 1.65029e-05 | 0.00287248 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844031 | AAGTCAAATTCCCCA[A/T]AATGTTTTGTTGCTT | 9063 |
rs779329712 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874534 | ATGAACTAAACCCTA[A/C]AAAGCCACCACACCA | 9063 |
rs779332840 | snp | C/G | 0.000162272 | 0.00900608 | utr-variant-5-prime, intron-variant, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920118 | TTCCTCAATGTGTAG[C/G]AGCTCCTGGATGGGT | 9063 |
rs779343985 | in-del | -/TCC | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916648 | AGAAAAAAATATTTT[-/TCC]TCAAGAGTAAAAGGG | 9063 |
rs779366837 | in-del | -/C | 0.000106829 | 0.00730774 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844691 | ATATGCTCAATCTTT[-/C]TTTTTTTTTTTTAAA | 9063 |
rs779410661 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873949 | ATAAAAATAGGAGCC[A/G]AGGAAAACTCAGAAG | 9063 |
rs779415255 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814793 | TTCATGTTGGGACAC[C/T]GAGCTACTAGGGTTT | 9063 |
rs779420631 | snp | C/G | 1.65064e-05 | 0.00287279 | missense, downstream-variant-500B, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815332 | GATCAACTGGAATAA[C/G]GGAAAGAAAATCCAA | 9063 |
rs779426245 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837563 | TTTATATAAGAAATC[A/G]TGTGTAATATGAACT | 9063 |
rs779446665 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916422 | AAAAAAAAAAATCAG[A/G/T]GTTTCTGTCCGTAAA | 9063 |
rs779462682 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872450 | CTAACCTCTTTGGTC[A/C]AATCCTAGAACAGAT | 9063 |
rs779479504 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897268 | AGGAACCCAGACTCC[C/T]TGGGGAAATAAATGG | 9063 |
rs779485945 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909706 | ACACATTCTTCTTAA[A/T]TACCAGCAATTCTAT | 9063 |
rs779511310 | in-del | -/CAGG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909523 | AAAGTGCTAGGATTA[-/CAGG]CGTGAGCTACCATGC | 9063 |
rs779515501 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885257 | CAGGCAGTGGGTCAT[A/G]CCAGTAATCCCAGCA | 9063 |
rs779531473 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863817 | CGTTGAAGTCCTAAC[A/C]CCCAATGTGACTGTA | 9063 |
rs779545485 | snp | C/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921286 | GCACCCGCCACCATG[C/G]CCAGCTAATTTTTGT | 9063 |
rs779568999 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883524 | CCTGGACAACATAGA[A/G]AGACCTCCTCTCCAC | 9063 |
rs779584931 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876297 | TATAGATGCCACTGG[A/T]GTCCCGAGAGGAGTG | 9063 |
rs779598150 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828638 | TTCACCATAAGCCAG[A/C]ACTTGATAAAAACTT | 9063 |
rs779619080 | snp | A/G | 3.30682e-05 | 0.00406608 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890926 | TTTAATCTGAACCGC[A/G]GGGCTGCAGCCGCTC | 9063 |
rs779624625 | snp | C/T | 1.88799e-05 | 0.00307239 | intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818384 | TTTTGTATTCACTGT[C/T]GCACAGTATCAGAAG | 9063 |
rs779639827 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875535 | ATCTTCTCTCTGAGT[C/T]GGTTGAAAACAATAA | 9063 |
rs779700349 | snp | C/T | 1.82227e-05 | 0.00301845 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844873 | AACCTGCATTAAAGA[C/T]GAGAGATAATATTCT | 9063 |
rs779728340 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827500 | AACCTGAAAATGATC[C/T]TGTAATATAGGCGTT | 9063 |
rs779765631 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868449 | CCCGCCTTTGCCGCA[A/C]CCTGACATGCCCAAA | 9063 |
rs779819693 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868446 | CTTCCCGCCTTTGCC[A/G]CACCCTGACATGCCC | 9063 |
rs779832126 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899300 | CTGAAATAGTAACTG[A/G]ATAAGTAACTGAAGC | 9063 |
rs779872665 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880028 | CGATGGTTCCAACAA[C/T]ATTAATATACTTCAT | 9063 |
rs779882513 | snp | A/T | 3.39801e-05 | 0.00412176 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829708 | GAGTCTCACTGCTTT[A/T]CTCTCTGCTGCTATT | 9063 |
rs779896219 | snp | C/G | 3.4379e-05 | 0.00414588 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844754 | GCTCTGGAATGATCA[C/G]GGTTTCTAATACCTT | 9063 |
rs779950237 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46869858 | TCTCCCAGGAGGAAA[C/T]AGATTATGCCCTGTA | 9063 |
rs779961712 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840453 | TTCAAAGAGTGTCAG[A/G]GACCTTCAGGTATCC | 9063 |
rs779964391 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900569 | GTAGTCTTGATTACT[C/T]AGGAGGCTGAGGCAG | 9063 |
rs779970134 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840971 | TCTTTTCAGCAGGAC[-/T]TTTTTTTTTTTTTTT | 9063 |
rs779990677 | in-del | -/CT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868973 | ATGGCAACCAGGTAA[-/CT]CTGTACACAAACCAA | 9063 |
rs780012396 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46820068 | TAGTCTGATGAAATC[C/T]CATGCTGTCCTGGCT | 9063 |
rs780025087 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890826 | ATGAGCCACCATCCA[A/G]ACTGAAAACCGATGA | 9063 |
rs780028343 | snp | A/G | 0.000162272 | 0.00900608 | stop-gained, intron-variant, synonymous-codon, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920073 | CGTGCAGTGTTCTTT[A/G]TAGTTGCTTCCCAGC | 9063 |
rs780071085 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858613 | AAGGTGGGAGGATCA[A/G]TTGAGCCCGGACATT | 9063 |
rs780107786 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845475 | ACAAGCAGCAGCTAC[C/T]ATAGTATGTAAGACA | 9063 |
rs780119610 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46913738 | AGAAAAAGCTGCTCT[C/G]GTTAAAGAAGAGGTA | 9063 |
rs780122821 | snp | A/T | 0.000283487 | 0.0119022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900991 | AATAATATTAAAAAA[A/T]AAAAATAAGGAAGAA | 9063 |
rs780155557 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877087 | GCCTTTGTAACAGGT[A/G]TGCTTATTCTTGTAG | 9063 |
rs780171513 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906482 | ATAGCAAGGTTATTA[C/T]ACAAAGTCAAACTGT | 9063 |
rs780199365 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864038 | GATCTTGGACAGAAG[C/G]CTCCAGCATTTTGAA | 9063 |
rs780200651 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859618 | CTGTTTTTCAACTTC[A/G]CATCTTTGGTGCCTG | 9063 |
rs780214396 | snp | G/T | 1.94759e-05 | 0.00312051 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864272 | AAAAAAAAAAAGAAA[G/T]ATAATATTTCAATAA | 9063 |
rs780223547 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811613 | CTGCATAGTTTCTTT[C/T]TTGAGAAGGCAAGCC | 9063 |
rs780224061 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904475 | AACCTAGAAGGCCGG[A/G]TGCGGTGGCTCAGGC | 9063 |
rs780243330 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46890144 | GAATAGTCAAAATCA[C/T]AGACAGTGGAAGTAG | 9063 |
rs780252471 | in-del | -/TT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876699 | GATCCCTTTACTAAT[-/TT]TTTTTTTTTTTTTTG | 9063 |
rs780253505 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46872373 | TGAATGGGAAGATCC[C/T]CATTCTGAGCGAAAG | 9063 |
rs780256738 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46905731 | TAAAAGTATGAACTA[C/T]TAAAACAGGTTTGAA | 9063 |
rs780265206 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871161 | ATTACAAAAGATAGA[A/G]AATTGGAAAGACTGG | 9063 |
rs780275458 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46837472 | TTATCTATTTATAGG[C/T]ACTCTTTATATAAGA | 9063 |
rs780276078 | in-del | -/ATT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896882 | AATTGCTTGGTTAAG[-/ATT]ATTTCTATCCTTACA | 9063 |
rs780291979 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851500 | TCTCATCTGGCTGTC[A/C]GTCTGTACACTGGCA | 9063 |
rs780314632 | snp | C/T | 1.69189e-05 | 0.00290846 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829910 | TGTGATCAACAGCTT[C/T]GCCTAAAGGTGAAAT | 9063 |
rs780318575 | snp | C/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918312 | AGAATTGGGTGGAAC[C/T]CACACACGAGAGGTC | 9063 |
rs780376135 | snp | A/G | 1.65116e-05 | 0.00287324 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836428 | GGTGGGCTTTTTCTC[A/G]TTCATTTGTAGATAG | 9063 |
rs780384082 | in-del | -/AATTA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46879316 | ATGCTCAACATCACT[-/AATTA]AATCATTAAAGAAAT | 9063 |
rs780399454 | in-del | -/AG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861976 | AATATTAAAGGAAAC[-/AG]GGATAAAGAATATAT | 9063 |
rs780411027 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46807776 | TTAACCCCGTTCCAT[-/AG]AGTCAGAAAGGCAGA | 9063 |
rs780478321 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46835296 | TGGGTCATAGTTACA[C/T]GGGAGGTTCTTTGTG | 9063 |
rs780486820 | snp | A/G | 1.66902e-05 | 0.00288874 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890617 | AACATCAAGGACATC[A/G]TAAAAGGGCAGATTT | 9063 |
rs780510403 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844105 | AATTTCACTATCAGG[A/G]TCTGCAGTAAGTTTT | 9063 |
rs780551062 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884742 | CCAACATGAAGAAAC[C/T]CTGTCTCTACTAAAA | 9063 |
rs780568604 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46849781 | AATAGCAGGGACCCA[C/T]CAACCAGGTTCAATA | 9063 |
rs780580013 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46873607 | AGGGAATATTTATAC[C/T]GATTCTAAATATGTC | 9063 |
rs780606493 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874255 | CTGAAATGCCCCCAA[C/T]AGGTCGCCTAAAGTA | 9063 |
rs780617401 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46910391 | ACGCCTTACCTGTTA[G/T]AATCTTTTGTACTTA | 9063 |
rs780648065 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816216 | ATTCAGAGACACCCC[A/G]AATATAACCACCACA | 9063 |
rs780657266 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895488 | ACAGCCAGGCCAAAA[A/G]GGCAAAACCCTGTCT | 9063 |
rs780695745 | in-del | -/A | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918221 | CCGTAATGTGCTGAT[-/A]ATAGGATGAAGGAAG | 9063 |
rs780717963 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887415 | TGATATGTTTAAGTG[C/T]TTTCACATGACTGAA | 9063 |
rs780739912 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875505 | GCAGATGTTATAGGA[C/T]GGGACCCCATAAGAA | 9063 |
rs780771420 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46900424 | TTTTAATCCCAGCTA[G/T]TTGGGAGGCTGAGGC | 9063 |
rs780786955 | snp | C/T | 1.80198e-05 | 0.0030016 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844727 | GGTCTTATTAAACAT[C/T]ACTTACTTAGTGCTC | 9063 |
rs780852415 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839638 | GGGAGGCCGAGGAGG[A/G]TGGATCACCTGAGGT | 9063 |
rs780856450 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870673 | TTATTAGATGACCCA[C/T]GTGGGGTAGCAGATC | 9063 |
rs780945760 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854595 | TTTATTAAGACTTGA[C/G]TATCAGGATTTGAAG | 9063 |
rs780952961 | snp | A/T | 5.04104e-05 | 0.00502023 | intron-variant, missense | PIAS2 | GRCh38.p7 | 18:46827956 | AACTATAAATTAACA[A/T]ACCCTTTGGTTGGGC | 9063 |
rs780953395 | snp | C/G | 1.6607e-05 | 0.00288153 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855517 | TCAGAACTACATGCA[C/G]ATAGTAAGCAAGTAT | 9063 |
rs781020773 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887406 | AAAGCACACTGATAT[A/G]TTTAAGTGTTTTCAC | 9063 |
rs781106735 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853439 | GTTACCCATTGGTAT[A/C]TTTCAGCTCCAAGTA | 9063 |
rs781127528 | snp | A/C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46868396 | TTCTGTAAGCTCCCC[A/C/T]TCTTGCTGAGACAGC | 9063 |
rs781149306 | snp | C/T | 1.69166e-05 | 0.00290827 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855330 | TGCAAATCTGGTGAA[C/T]AAAAAGCAACTTACA | 9063 |
rs781159038 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46830328 | TAAATTTAAAATAAG[G/T]GTATTTGAATTAAGT | 9063 |
rs781230295 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818099 | GATAAAATTTTAATT[A/T]AAAAATTTTAAGTGC | 9063 |
rs781243819 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858490 | GGCTGAGGTAGGTGG[A/T]GTTCAGGACCAGGCT | 9063 |
rs781276326 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809246 | AACCTAAATTCACCT[C/T]AATGCTTTCATTTTG | 9063 |
rs781281884 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46882142 | ATCCAAATTAAGTCC[G/T]TATTATATACTTATT | 9063 |
rs781297808 | in-del | -/CTC | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46852425 | AATGCTCTATTTCTT[-/CTC]CTCCTTCACAACTGC | 9063 |
rs781298081 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870788 | GAAGCATGATCCAAA[A/G]GGTTGCTATGGTAGT | 9063 |
rs781308125 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856908 | GCAGTGACAACCACC[G/T]TAAGTTCTACAGTCC | 9063 |
rs781351251 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870122 | CCCTCCCTAACCACA[C/T]GTCTGAGTCTATGCC | 9063 |
rs781364804 | snp | A/G | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46822970 | GAGCCAGGCAAGGTG[A/G]TTCACACCTGTAATC | 9063 |
rs781393742 | snp | A/G | | | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46902504 | GGCACAGGTTGCAGC[A/G]AGCCGAGATCGTGCC | 9063 |
rs781409380 | snp | C/T | 6.70252e-05 | 0.00578862 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829891 | CAATTAAGAAGTACA[C/T]ACATGTGATCAACAG | 9063 |
rs781441905 | snp | A/G | 1.89009e-05 | 0.0030741 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864117 | GGCAGCCCTACAGGT[A/G]AATAAACCAATATTC | 9063 |
rs781442681 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46915093 | TACCAGAACAAAGTA[A/G]TGTAGCCCGGGCTCT | 9063 |
rs781474556 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894470 | TTCCAAGCGGTTTTT[C/T]CACTCCACTGCGCTA | 9063 |
rs781515031 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855258 | ACTGTTCACTGGTAT[C/T]CAGCTGTCACTGTTG | 9063 |
rs781567721 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46814663 | CCTATACTCAACTCC[A/T]CTCAAAGTCTTTTGT | 9063 |
rs781596196 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46897110 | GAACAGGGGAAACTG[C/G]GTGTGGGCATGTGGG | 9063 |
rs781605548 | snp | C/G | 1.65146e-05 | 0.0028735 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829756 | TTTTGTACACGGTTG[C/G]CTGGATACTTTCATA | 9063 |
rs781617913 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46835115 | TATTAATGTGCAAAG[A/G]GGCATGACATATGTA | 9063 |
rs781622301 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921277 | GGATTACAGGCACCC[A/G]CCACCATGCCCAGCT | 9063 |
rs781687117 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46833696 | TCTGAAAAGAAATGG[C/T]CTAAGAAATACTACC | 9063 |
rs781689871 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46850036 | TAACACCTTGTCTTT[C/T]GATTCAGATCTCCCA | 9063 |
rs781716599 | in-del | -/CCGCGGGCG | 0.000121855 | 0.00780464 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917355 | GCCATTTTATACCAC[-/CCGCGGGCG]CCGCGGGCGCCGCCG | 9063 |
rs781743965 | snp | C/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827854 | AAAGGCAAATTAAAA[C/T]AGCCTTCTACAGTTA | 9063 |
rs781748066 | snp | C/T | 1.65258e-05 | 0.00287448 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815281 | ACCAACAATCAAATA[C/T]AAATTAGTTGCTTAA | 9063 |
rs781773286 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908508 | GTATACAAAATCAAC[G/T]CCAGGTGGATTAAAA | 9063 |
rs796203010 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822725 | CACCTCTCACACACA[A/G]GAGTTTATATGAGAA | 9063 |
rs796243013 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46914449 | GGTATAGAGCTGCCA[C/T]ATTCTGCTATGACCA | 9063 |
rs796302926 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839604 | GACCTAGGCCAGGCA[C/T]GGTGGCTCCCAGCAC | 9063 |
rs796326040 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46818897 | CTTGAAACACATTTT[A/T]ACCAAATAGCCAGTT | 9063 |
rs796326712 | multinucleotide-polymorphism | CT/TC | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891995 | AAGAGGAAGAACACC[CT/TC]GAGCTGACCAAAGCC | 9063 |
rs796342265 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839182 | GAAACAACTCAATCA[A/C]TAAACTTATTATTAA | 9063 |
rs796360561 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811909 | CCAAGCTTTGGCCAC[A/G]TACTGAAACTTCATT | 9063 |
rs796424943 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880670 | AAATAGGGGCTGACC[C/T]TCAAACATGTAGAAA | 9063 |
rs796426620 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888169 | AACCTGTACAATAAC[A/T]ACTATAAAACATTGC | 9063 |
rs796431941 | in-del | -/AAAG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46812666 | TACTTGATTTTAAAT[-/AAAG]AGACTAGAAATTATT | 9063 |
rs796477821 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865907 | TTCCTATTCACTCCT[C/T]AACCCTTTTTTTCTT | 9063 |
rs796493836 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46901570 | CAGTATGCAAGACTG[C/G]TTCATTATATGCCAC | 9063 |
rs796499520 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46840776 | ATTCTAATTTAATCA[A/G]ATGATGATGCTTTTT | 9063 |
rs796514831 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46908551 | AAAGGTAAAAAAAAA[-/A]CAAAAACAAAAAACA | 9063 |
rs796538789 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864306 | ATCCAACACTACAAC[C/T]ACCTGCAATAACCAG | 9063 |
rs796559542 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832030 | ATAAAATGATAGAAA[A/G]CATTTAAAAATCATA | 9063 |
rs796568525 | snp | C/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813498 | TTTAGTAAAACAAGA[C/G]GTCTAGTGATATCCT | 9063 |
rs796574543 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46874254 | ACTGAAATGCCCCCA[A/G]TAGGTCGCCTAAAGT | 9063 |
rs796608548 | in-del | -/AA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46864257 | CTTTGAACTGGGAAG[-/AA]AAAAAAAAAGAAAGA | 9063 |
rs796610070 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46866903 | CACAAGACCCTCTGT[A/G]AATTCACGAATATAA | 9063 |
rs796612194 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834650 | ACAGAGTCTTTCTCC[CA/TG]CACCCAGGTTGGAGT | 9063 |
rs796691654 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46862054 | TAAAGTTTTTATGCC[A/G]GGCATGGTGGCTCAC | 9063 |
rs796701164 | snp | A/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921362 | TGAACTCCTGACCTC[A/G]TGATCCACCTGCCTT | 9063 |
rs796989629 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916404 | TACCTTGATACATTT[-/A]AAAAAAAAAAAAATC | 9063 |
rs797003011 | snp | C/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907137 | CAGCAGAACTCTGAA[C/T]AGACTCAGGGGAAAC | 9063 |
rs797008860 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855997 | TTTTCTTTTTCTTTT[G/T]TTTTTTTTTTTTTTT | 9063 |