SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs10070 | snp | A/G | 0.474992 | 0.108989 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808936 | AAAATACAAACAAAC[A/G]TCAACTAATGAATAC | 9063 |
rs17472 | snp | C/T | 0.0836354 | 0.186609 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810573 | TACTGCTCGTAGATT[C/T]GGGTTTGTTTCCCCC | 9063 |
rs476313 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853292 | ttccttttttttttt[A/T]tttaaaaaaaaaaaa | 9063 |
rs477243 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853192 | ccctaaaggctcaag[C/T]gattctcccacctca | 9063 |
rs477826 | snp | A/G | 0.484701 | 0.0861117 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817686 | CTAGATTGTTTACCA[A/G]GCATTACAAGGGTGC | 9063 |
rs478820 | snp | A/G | 0.484701 | 0.0861117 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817819 | TTTCTAACAAAAAAC[A/G]AAACCATCAAAGTCT | 9063 |
rs480008 | snp | A/T | 0.0501905 | 0.150254 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810235 | AAAAGCACAGAGATA[A/T]CAGTTATAAGAACCA | 9063 |
rs501062 | snp | A/G | 0.482159 | 0.0927485 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831172 | ttagtagttctagta[A/G]ctttattatagatta | 9063 |
rs501882 | snp | A/T | 0.455383 | 0.142541 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831103 | agagacagttttact[A/T]cttctttctaacgtg | 9063 |
rs504668 | snp | A/G | 0.485118 | 0.0849685 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830786 | ggtagaattccctag[A/G]gaagacattgggcct | 9063 |
rs512868 | snp | G/T | 0.385741 | 0.209939 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816283 | GAGAATATCAGTGGG[G/T]ACATTTAAAATATCT | 9063 |
rs513775 | snp | C/T | 0.48955 | 0.071525 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816371 | CTCCAAATAAGGGTA[C/T]TACAAAAATGCTTAT | 9063 |
rs514005 | snp | A/C | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858293 | TGGACTTTATGAGGT[A/C]CCATTAGAGTGTGTT | 9063 |
rs541634 | snp | C/G | 0.481703 | 0.0938806 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840308 | CATTAGCCATCAGAG[C/G]AATGACATCATCATC | 9063 |
rs553456 | snp | A/C | 0.499886 | 0.00755962 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832912 | catttggtatggctt[A/C]tcttttttttttttt | 9063 |
rs577200 | snp | A/C | 0.479744 | 0.0985793 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862439 | TCCTTTTCAGATATT[A/C]ATTAGAACACTCTTT | 9063 |
rs578146 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862318 | CCAGCCTGGATGACA[A/G]AGCGAGACTCTGTCT | 9063 |
rs578451 | snp | A/T | 0.470424 | 0.117954 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824562 | ATTTAAAGACTCCGG[A/T]TCGTAAGCAAAGAAA | 9063 |
rs590923 | snp | C/G | 0.486067 | 0.0822953 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824296 | ATGCTCCCACTTTAT[C/G]ATCATAAAAGTATAA | 9063 |
rs593340 | snp | A/G | 0.481932 | 0.0933148 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838383 | TTCTAACTTTGTAAC[A/G]TTAGGTTACTTAGCT | 9063 |
rs605487 | snp | C/G | 0.497881 | 0.0324789 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864815 | AAAATATAACAAAAC[C/G]CTTCAATATTACATT | 9063 |
rs607780 | snp | A/G | 0.497803 | 0.033074 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837493 | GTTCATGTTACACAC[A/G]TGATTTCTTATATAA | 9063 |
rs616900 | snp | A/T | 0.487495 | 0.0780784 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830886 | AAACCAGGCAGGCAT[A/T]GCAACAAAACTAAAT | 9063 |
rs620228 | snp | A/C | 0.482008 | 0.0931261 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832794 | ctactggggaggctg[A/C]ggcaggagaatcact | 9063 |
rs626217 | snp | G/T | 0.498009 | 0.0314867 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849219 | CAAACTCAGAATCAT[G/T]TTAGTCTCACTCAGC | 9063 |
rs630544 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816485 | GAtttttttttttcc[C/T]tttttttgggagaca | 9063 |
rs641366 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850363 | ATTCTATAAACATAA[C/T]CCCTGCCATCTCCAA | 9063 |
rs642897 | snp | G/T | 0.497933 | 0.032082 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816954 | ATAAATCCTCTCCCT[G/T]CTTATGCCAAACAAT | 9063 |
rs643233 | snp | A/G | 0.391397 | 0.206172 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861210 | tgccactgcactcca[A/G]cctgggcgacggagt | 9063 |
rs644731 | snp | C/T | 0.484701 | 0.0861117 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846914 | TCTCCAAGATAGATA[C/T]AGGATCCTGCCCAAT | 9063 |
rs646128 | snp | A/C | 0.454423 | 0.143914 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817728 | AACCTGTTTAATGTA[A/C]ATATTTCTCTCACTG | 9063 |
rs646151 | snp | A/C | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844850 | TAATTCTACAAACAA[A/C]CAAAAAAAACCTGCA | 9063 |
rs649076 | snp | A/G | 0.497933 | 0.032082 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834651 | ACAGAGTCTTTCTCC[A/G]TCACCCAGGTTGGAG | 9063 |
rs658756 | snp | A/G | 0.497933 | 0.032082 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851869 | TGTCTGTGTCCTGGA[A/G]GAAGTCCTTATGTGT | 9063 |
rs669208 | snp | G/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840939 | TGGAAACCACCATTT[G/T]GGGCCTTTTCAACTT | 9063 |
rs669225 | snp | C/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840926 | TTTGGGCCTTTTCAA[C/T]TTAAAAACTCTCTTA | 9063 |
rs680018 | snp | A/T | 0.469247 | 0.120128 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829204 | TTTCCCTACTTAGTG[A/T]GGATGGATGCAGGCA | 9063 |
rs693503 | snp | A/G | 0.484701 | 0.0861117 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840034 | agcatgatggcaggt[A/G]cctgtaatcccaact | 9063 |
rs695001 | snp | A/C | 0.498009 | 0.0314867 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842370 | CATGTAGAATGGCAA[A/C]CTGTATGAAGAAAAA | 9063 |
rs956827 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826284 | ACTGAGGTCATTTCA[A/G]ATTTTGTCGCCCACT | 9063 |
rs1046796 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810740 | GTTTTTTTTTTTTTT[C/T]TTTCACCTTCTCAAG | 9063 |
rs1539881 | snp | C/T | 0.485118 | 0.0849685 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897934 | tggagtgtggcaaca[C/T]gatcttggctctctg | 9063 |
rs1787232 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883027 | cgcttgaacccggga[A/G]gcagaggttgcagtg | 9063 |
rs1787233 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883047 | aggttgcagtgagcc[A/G]agatcacaccactgc | 9063 |
rs1787234 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883055 | gtgagccaagatcac[A/G]ccactgcactgcagc | 9063 |
rs1787235 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885533 | ctcaaaaaaaaaaaa[A/G]gaaaaaaaaGAGCAT | 9063 |
rs1787237 | snp | A/C | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885596 | TGGTTTCAAAATCCC[A/C]AGAGGTTCTGGAATG | 9063 |
rs1787238 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889521 | gcaaatcaaagctac[A/C]ataagataccacctg | 9063 |
rs1789151 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870278 | AGAAGGAATCGGCTT[C/T]GTAAATGCTCCCCCT | 9063 |
rs1789152 | snp | G/T | 0.497803 | 0.033074 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853129 | AAAAAATACAAAAAT[G/T]AGCCAGCCATAGCGG | 9063 |
rs1790378 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46895076 | ttttttttttttttt[C/T]ccgagatggagtttc | 9063 |
rs1790379 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46885644 | caggcgggagtgcag[G/T]ggcgcgaAAAACAGA | 9063 |
rs1790380 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46883030 | gctcactgcaacctc[C/T]gcctcccgggttcaa | 9063 |
rs1893426 | snp | C/T | 0 | 0 | | | GRCh38.p7 | 18:46854961 | CAGCATCCTTGATTT[C/T]TTAAGTAAGATGCTC | 9063 |
rs1893427 | snp | C/T | 0.497933 | 0.032082 | | | GRCh38.p7 | 18:46855024 | GTATTCCCCACTACT[C/T]AGGAGGCTGAGGTAG | 9063 |
rs1893428 | snp | A/T | | | | | GRCh38.p7 | 18:46916404 | TACCTTGATACATTT[A/T]AAAAAAAAAAAAATC | 9063 |
rs1942249 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892628 | aatttaaaaattagc[C/T]agccatggtggtgtg | 9063 |
rs1943673 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816483 | CAGAttttttttttt[C/T]cctttttttgggaga | 9063 |
rs2032215 | snp | A/C | 0.49975 | 0.0111793 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859048 | TTCAGAATTCACTTT[A/C]TACTTAGTATTACTC | 9063 |
rs2051292 | snp | C/G | 0.479984 | 0.0980171 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904409 | GACACAAAAATGTAA[C/G]GGTGAGGAGAAATTT | 9063 |
rs2156049 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875754 | ttaaatattccatcc[A/G]cactctaaacaaaag | 9063 |
rs2156050 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875910 | GTAATGAATTATGCC[A/G]AGCTCTCTCTTGGCT | 9063 |
rs2187090 | snp | A/C | 0.497668 | 0.0340657 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904716 | agatcgcgccactgc[A/C]ctccagcctgggtga | 9063 |
rs2276165 | snp | A/G | 0.178144 | 0.239451 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847000 | ATCAACCCAAAATAG[A/G]AAAATAACCTTTGAA | 9063 |
rs2510016 | snp | A/C | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884899 | tctagcctgggctac[A/C]agagcaaatctgtct | 9063 |
rs2510017 | snp | A/C | 0.00472811 | 0.0483911 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900506 | GACCCAGGTTCTACC[A/C]AAAAAAAAAAATTGT | 9063 |
rs2510440 | snp | A/C | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824921 | AGGAGGATCGCTTCA[A/C]CCCAGGAGGTCAAGA | 9063 |
rs2510441 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824968 | TCACACCACGGCATT[C/T]TAGCCTGGGTCACAA | 9063 |
rs2510442 | snp | A/T | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825008 | CTGTCTCAAAAAATT[A/T]AAAAAAAAAAAAAAT | 9063 |
rs2511021 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884913 | tttttttttttttga[A/G]acagatttgctctgg | 9063 |
rs2956972 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824882 | cctccaagtagctgg[A/G]actaccacccccagc | 9063 |
rs2956973 | snp | C/T | 0.477175 | 0.104362 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870483 | GACTACAGGCGCCCG[C/T]CACCACGTCTGGCTA | 9063 |
rs2956974 | snp | A/C | 0 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816492 | gactcagtgtctccc[A/C]aaaaaaggaaaaaaa | 9063 |
rs2956975 | snp | C/T | 0.454544 | 0.143743 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870406 | ggatggtctcaatct[C/T]ctgacgttgtgatcc | 9063 |
rs2956976 | snp | G/T | 0.0170251 | 0.090679 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808157 | TTGGGGTTTTTCCCC[G/T]CAACCTACAGGCATT | 9063 |
rs2957007 | snp | A/G | 0.497776 | 0.0332724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870387 | ctgggaggccgaggc[A/G]ggtggatcacaacgt | 9063 |
rs3737448 | snp | C/T | 0.0741063 | 0.177655 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815405 | GGGAGACCAGAATTA[C/T]TTCCCTAAATCATCT | 9063 |
rs3786258 | snp | A/G | 0.110872 | 0.20771 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819570 | TATGTTACTGAAACA[A/G]TTGATAATTGGCTCG | 9063 |
rs3819124 | snp | C/G | 0.178144 | 0.239451 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847054 | AGTCCAGAAAGGTAG[C/G]AAAAAAATCCATGTT | 9063 |
rs3826586 | snp | C/T | 0.179425 | 0.239831 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819833 | CTTCCCTCCTTTACT[C/T]TTCTTCCCTCTCCAT | 9063 |
rs3837881 | in-del | -/A | 0.478345 | 0.101778 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834022 | TGGTAAAAAAAAAAA[-/A]GTATATTAAGTGTAA | 9063 |
rs3892820 | snp | A/G | 0.499997 | 0.00119808 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899595 | GCCTCAGCCTCCAGC[A/G]TAACTGGGACTACAA | 9063 |
rs4258717 | snp | C/T | 0.497829 | 0.0328757 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876991 | aggcgtgagccacag[C/T]gcccggcctccttca | 9063 |
rs4442910 | snp | C/T | 0.47709 | 0.104548 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892913 | CAGTGGGATTTTTTT[C/T]ATACTAAGTCTTCAA | 9063 |
rs4531833 | snp | A/C/G/T | 5.31188e-05 | 0.00515335 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855667 | CAATGAGAATTCTCA[A/C/G/T]AACAGTCTCCCCAGG | 9063 |
rs4548968 | snp | A/C | 0.479744 | 0.0985793 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900809 | tgaaaccccatctct[A/C]ctaaaaatacaaaaa | 9063 |
rs4640275 | snp | A/C | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900767 | aatcacgaggtcagg[A/C]gttcaagaccagcct | 9063 |
rs4890340 | snp | A/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857449 | TCACAATTAGTCCAA[A/T]CTAACTAGAAAACAG | 9063 |
rs4890341 | snp | C/G/T | 0.501869 | 0.0433032 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887405 | AAAAGCACACTGATA[C/G/T]GTTTAAGTGTTTTCA | 9063 |
rs4890698 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909762 | acaaatattcacact[A/G]agtgagatcaacaaa | 9063 |
rs4890706 | snp | A/C | 0.455977 | 0.141681 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917629 | GACAGCGCCCGCCCG[A/C]GCCTGCCCCGGCGTG | 9063 |
rs4890707 | snp | C/G | 0.498059 | 0.0310896 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917761 | CCGCGGGCCTGGCCT[C/G]GGGAAGTGGCGGGGA | 9063 |
rs5824641 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887260 | AAAAGCAAAAAATTG[-/A]AAAAAAAAAAAAAAT | 9063 |
rs5824642 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892906 | AAGTGTCAGTGGGAT[-/A]TTTTTTTATACTAAG | 9063 |
rs5824643 | in-del | -/AG | 0.479744 | 0.0985793 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899855 | ACTATATGAAGTAAC[-/AG]TATCAAATTTGTGAG | 9063 |
rs6507709 | snp | A/G | 0.499999 | 0.000798721 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873175 | ACCCCATCAGGTTAG[A/G]ACAATCTTAAAAGGC | 9063 |
rs7229231 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820658 | TAAAGAAACCAAGAA[A/G]AAGTCTCTAAGTACA | 9063 |
rs7231374 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817245 | AAACCTTTTTATAAC[A/G]CTAAGTATTGACAAT | 9063 |
rs7234402 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854661 | CATGCATTTACATTG[A/T]ATACATCCTAGGTGC | 9063 |
rs7234512 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863893 | cacagggtaggtccc[C/T]aatccaatatgacag | 9063 |
rs7234570 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879693 | aatgaataaaacacc[A/G]tgtatacatacaata | 9063 |
rs7235236 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849198 | CATGTAAGAATGAAG[A/T]GTCAGCAAACTCAGA | 9063 |
rs7235496 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823679 | AATTAGTAAATCAAC[A/G]TCTAAAACCTCAGCA | 9063 |
rs7236403 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842698 | ATAATAACCTGAAGA[C/T]ACTGAAAAGAACTCA | 9063 |
rs7237529 | snp | G/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811454 | TGAGAAAATTAAGTT[G/T]TTGGGAAGAAATTAA | 9063 |
rs7238432 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863950 | acggatgcactagca[C/T]agagaaaaggccatc | 9063 |
rs7238877 | snp | C/T | 0.0962929 | 0.197165 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906857 | AAGTTCCTTGAACAA[C/T]TACAAGCCAGGAGGA | 9063 |
rs7240239 | snp | C/T | 0.497776 | 0.0332724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880074 | aatggtcagacagta[C/T]gtattttaccacagt | 9063 |
rs7240843 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903330 | caaaggactactatc[C/T]aggatatacttagaa | 9063 |
rs7240909 | snp | A/G | 0.095934 | 0.196885 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921033 | CCAGGCAATTACCTG[A/G]CTAGGCTACCGTCTT | 9063 |
rs7241061 | snp | A/G | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921103 | GATTAAAGTGTCCTA[A/G]GTTTTTTTGTTTGtt | 9063 |
rs7241306 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859755 | GTGTTGTGCTTGATG[A/C]CCTTGTAGGTCAAAG | 9063 |
rs7241858 | snp | A/T | 0.0973687 | 0.197999 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852164 | ATCTTGTTTTATATT[A/T]AAAAAGACTCCACAT | 9063 |
rs7242143 | snp | C/T | 0.00479614 | 0.0487346 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847063 | AGGTAGGAAAAAAAT[C/T]CATGTTCCAACATTA | 9063 |
rs7242313 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859703 | TAAAAGAACAAAAGA[C/T]AAGCAGGTTTGATGG | 9063 |
rs7243309 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877163 | TTGAAACAGCTCTTA[C/T]TAAAACCTTTTTCAA | 9063 |
rs7243514 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877322 | TGGCTAAGTTCCTCT[C/T]CAAAGGTTTAATTTG | 9063 |
rs7506367 | snp | A/T | 0.0973687 | 0.197999 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859281 | aaaatacaaaaaatt[A/T]gccaggcgtggtggt | 9063 |
rs8083773 | snp | A/T | 0.040671 | 0.13668 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816641 | attattattattatt[A/T]tttttttgtagagag | 9063 |
rs8084833 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862677 | tatatacacacatat[A/G]tatacacacacacat | 9063 |
rs8085090 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862774 | gcagtggtgcgatct[C/T]ggctcactgcaacct | 9063 |
rs8086286 | snp | A/G | 0.482083 | 0.0929373 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887552 | TAACTTCATTAGGCA[A/G]TAAGAATTATAACAC | 9063 |
rs8087259 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875251 | agcatggagccttaa[A/G]aagtccctgtggtga | 9063 |
rs8088346 | snp | C/T | 0.0832709 | 0.186283 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817525 | ATGATTTCATGTGTG[C/T]GGTAAATATAAAGTT | 9063 |
rs8089367 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863370 | tttgttgcccagtct[C/G]gagtgctgcagcatg | 9063 |
rs8089414 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870533 | aggcagaagaatggc[A/G]tgaacccaggaggtg | 9063 |
rs8089938 | snp | C/T | 0.480223 | 0.0974544 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879534 | AATAGAATTACCATA[C/T]GATCCCGCAATTTCA | 9063 |
rs8091984 | snp | G/T | 0.505133 | 0.0571784 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911436 | AGCCAGGCTGGTCTC[G/T]AACTCCTGACCTGAG | 9063 |
rs8092148 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897913 | atctcgttttattgc[C/T]caagctggagtgtgg | 9063 |
rs8092951 | snp | C/T | 0.0213912 | 0.101183 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846693 | TCCTGCTACCCAAAA[C/T]GGAGAGCTTTTACCT | 9063 |
rs8094449 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894496 | CGCTAACTCTCAAAG[A/G]CTCCCAAGTCAGCCC | 9063 |
rs8094938 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910000 | ggtgaaaactaataa[C/T]acaaaaaaattagcc | 9063 |
rs8095217 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889329 | agaaaatatttgcac[A/G]ttcatatatctgata | 9063 |
rs8095524 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852127 | GCTGCAGCATACTCA[C/T]GTAATTCTTAAAAAC | 9063 |
rs8096896 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907058 | AGCCTGCAAAGCTGA[A/G]TCTCTTGATGCCTTC | 9063 |
rs8096909 | snp | A/G | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907077 | CTTGATGCCTTCCCC[A/G]GAGATATCTGCCAAT | 9063 |
rs8098688 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886654 | accagcctggccaac[A/G]taacgaaaccccatc | 9063 |
rs9304336 | snp | C/T | 0.486133 | 0.082104 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881724 | TCTACTTGCTACTTA[C/T]TTCGAATGTGAACAT | 9063 |
rs9304337 | snp | A/G | 0.480223 | 0.0974544 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913131 | CATAGCTATTAGTCT[A/G]TATCCCTGCCCAATA | 9063 |
rs9916891 | snp | C/T | 0.454423 | 0.143914 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913558 | ATACAGAAGGGAGAT[C/T]CTTAAAAAAAAAAAA | 9063 |
rs9945443 | snp | C/T | 0.499997 | 0.00119808 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904682 | cttgaacccacgagg[C/T]ggaggttgcagtgag | 9063 |
rs9948405 | snp | C/G | 0.48498 | 0.0853497 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914564 | AACCAACCCTCCCCC[C/G]CCCAACTCCACCCCC | 9063 |
rs9954336 | snp | A/G | 0.48491 | 0.0855403 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885982 | TGTGATGAACAGAGC[A/G]AAGTAAGAAAATTTC | 9063 |
rs9954637 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916286 | TATACAAAACTGAAC[C/T]TTTTACCGGATTCCT | 9063 |
rs9960888 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829988 | CCCCCTTTTCTTTTG[C/G]TATTGCAATACTTTA | 9063 |
rs9962523 | snp | A/T | 0.499989 | 0.00239614 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906451 | aatctaaagataatt[A/T]atcacaattaggagt | 9063 |
rs9965302 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906996 | AATGCAGGAGGCACT[A/G]CAAAGGCAGTAAGGA | 9063 |
rs10468986 | snp | A/C | 0.347694 | 0.230122 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848970 | AGGTAATTTTGAACA[A/C]AACTTTTGTTTTGCC | 9063 |
rs10502878 | snp | C/T | 0.200801 | 0.245111 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811858 | TCTTTGATGCAATCA[C/T]GAAGAAAAGTGGAAA | 9063 |
rs10502879 | snp | C/T | 0.29789 | 0.24537 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818148 | CATTAGATTTTTTCT[C/T]ATTGATGACAACACA | 9063 |
rs10533549 | in-del | -/TTAT | 0.202035 | 0.245356 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818170 | GACAACACATTTTCC[-/TTAT]TTGAGTCATAAACTT | 9063 |
rs10714256 | in-del | -/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922102 | AAAATTTTTCCTCAC[-/T]TTTTTTTTTTTTTTT | 9063 |
rs10853544 | snp | C/T | 0.497855 | 0.0326773 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894231 | ATGTTGTTTGGCAAA[C/T]CTTACCAGATCCCAC | 9063 |
rs10853545 | snp | A/T | 0.499998 | 0.000998401 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895257 | TGGTAAAGGTCAATA[A/T]GAACTCTGTAGATTC | 9063 |
rs11292180 | in-del | -/T | 0.0325976 | 0.123435 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886843 | ACTCTGTCCCCCCCC[-/T]CCAAAAAAAAACAAA | 9063 |
rs11418545 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46858223 | TAAAAAAAAAAAAAA[-/A]GCAGAGCAAGATGTT | 9063 |
rs11554114 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808965 | CCAAGTTGTCTTTTT[C/T]TTCTGCCAATAAAGT | 9063 |
rs11659693 | snp | C/T | 0.485049 | 0.0851591 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878770 | CTACTCAGGAGACTG[C/T]GGTAGCAGAATCACT | 9063 |
rs11659847 | snp | C/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866089 | GAAACCTCAAAAGGT[C/T]TAAAGTAAGTACAAA | 9063 |
rs11872476 | snp | A/G | 0.0531567 | 0.154119 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901259 | ccatctctaagaaaa[A/G]tacaaaattagccat | 9063 |
rs11874218 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880351 | atctcacaactatac[C/T]ctgcctgggtgagag | 9063 |
rs11874267 | snp | A/G | 0.097727 | 0.198275 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843312 | GGGTAGTCATCAAAT[A/G]CCCACAAAACTACAT | 9063 |
rs11874423 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850865 | ccacatcaacagctg[A/G]tcaccttgaaataAA | 9063 |
rs11874582 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912336 | ttacatcatttctag[C/T]ttacaatacctaata | 9063 |
rs11874634 | snp | G/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912610 | GAACCAAAATGTAAC[G/T]GATAGAAATCAAAGT | 9063 |
rs11875703 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822353 | AACTGATCCATTTAG[A/G]AAGCTTATGACATAT | 9063 |
rs11875918 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845210 | AATCATTCTGCTTTT[A/G]TCGACTTTATGTAAT | 9063 |
rs11876189 | snp | C/T | 0.00947846 | 0.0681864 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853964 | CTTCACTCCCAGGAC[C/T]GTCTCAATGGATTTC | 9063 |
rs11876274 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914438 | AAAGGCAACAAGGTA[C/T]AGAGCTGCCATATTC | 9063 |
rs11876526 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830845 | cttcCAACTCATTGT[A/T]CAAGGTCAGCATTAC | 9063 |
rs11876752 | snp | A/T | 0.0333695 | 0.124785 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811276 | AAATGAAAAAAAAAA[A/T]AAATCTAATGCTGTC | 9063 |
rs11877331 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882029 | ttgaacccaggaggc[A/G]gaggttgcagtgagc | 9063 |
rs11877373 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882230 | TTAACATTAATGTGC[A/G]TATCATTTGAATACT | 9063 |
rs11877429 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850406 | TTTCCCCAATGCTGT[C/T]GTTCTACTGGAGAAA | 9063 |
rs11877721 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891149 | TGATTTTTCCAGCAT[A/T]CTATCAATTGGCATG | 9063 |
rs11877929 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861831 | aaatgtgatttggga[C/T]tgtatctaggaacag | 9063 |
rs11878063 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895446 | gaggccaaagcgggc[A/G]gatcatctgaggtca | 9063 |
rs11878114 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856555 | TTTCATACTGAACCC[C/T]CCAAACTCTtgccac | 9063 |
rs11878135 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856655 | cccatcctagaccta[C/T]agaattagaatctgc | 9063 |
rs12326767 | snp | C/G | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903940 | atttccagaattatg[C/G]tgaatgaaaaagcca | 9063 |
rs12454431 | snp | C/T | 0.102014 | 0.201495 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871681 | gtttgtttcccttta[C/T]ctaatgtcccttgct | 9063 |
rs12454599 | snp | A/C | 0.093777 | 0.195178 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866550 | TTTAAAACATAAATT[A/C]AAAACTGGATCTCTG | 9063 |
rs12454951 | snp | G/T | 0.178144 | 0.239451 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879004 | GATTAAAATGGCTCA[G/T]TCTAGCCAATCTAAC | 9063 |
rs12455289 | snp | G/T | 0.101658 | 0.201233 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830844 | acttcCAACTCATTG[G/T]ACAAGGTCAGCATTA | 9063 |
rs12457353 | snp | C/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870153 | tcctccaggaaggct[C/T]tagtgtgagacagaa | 9063 |
rs12606208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816183 | TTTCTATTCAATTCC[A/G]TGAATTTTTATGCTG | 9063 |
rs12955979 | snp | C/G | | | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917153 | cgtgccctccgccgg[C/G]ccgctcccctccccc | 9063 |
rs16940108 | snp | A/G | 0.00722012 | 0.0596484 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855580 | CTCAACTGAACTTGG[A/G]CTGTATAATCTCTCC | 9063 |
rs16940123 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878415 | ACCTACTTTGTAACA[C/T]TGACTTTATCTTGAT | 9063 |
rs16940131 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885614 | AGGTTCTGGAATGAC[A/G]TTTTTGACCTCATGT | 9063 |
rs16940133 | snp | C/T | 0.093417 | 0.194889 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885638 | CTCATGTCTGTTTTT[C/T]GCGCCACTGCACTCC | 9063 |
rs16940135 | snp | A/G | 0.0402882 | 0.136092 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893614 | GAATTCTGAACAGCA[A/G]ATGGGACAGTCTTTG | 9063 |
rs17182429 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828441 | TACTGCTCATCCTGT[C/T]TCTGCAGGTCAGCAG | 9063 |
rs17708203 | snp | A/G | 0.202035 | 0.245356 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841646 | ACTACTATAGCCCAA[A/G]GAGTAGCATTCATTC | 9063 |
rs17781212 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852073 | TGGCAAGAGCTCACT[A/G]TAACTCCTATAGGGC | 9063 |
rs17781230 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853492 | AGATCTTTGTGCAAA[C/T]TAGCCAAATAAAAGA | 9063 |
rs17781674 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893654 | ATGCTGCAAAGATAA[A/C]GTATTGCTGGACACA | 9063 |
rs28441604 | snp | A/G | 0.0138799 | 0.0821421 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810566 | GTGCAACTACTGCTC[A/G]TAGATTTGGGTTTGT | 9063 |
rs28628455 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919009 | TGTATATATATATAT[A/G]TGTGTGTGTGTGTGT | 9063 |
rs28778279 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832822 | ACTTGAACCTGGGGG[G/T]TGGGGGCTGCAGTGA | 9063 |
rs33932283 | in-del | -/A | 0.477175 | 0.104362 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809774 | AAAAAAAAAAAAAAA[-/A]TTGATTTTAGGAGGC | 9063 |
rs33972989 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810189 | TTCACAGAAAATAGA[-/A]AAAAAAAACAAAAAA | 9063 |
rs33987512 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892907 | AGTGTCAGTGGGATT[-/A]TTTTTTATACTAAGT | 9063 |
rs33989627 | in-del | -/AG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899856 | CTATATGAAGTAACT[-/AG]ATCAAATTTGTGAGG | 9063 |
rs34021972 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46819952 | ATCCAAGATTTTGCG[-/T]TTCTGTGATTGCAGT | 9063 |
rs34052557 | in-del | -/A | 0.45725 | 0.143469 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844142 | AGAGAAAAAAAAAAA[-/A]TTTAAAAAAATTAAG | 9063 |
rs34105496 | in-del | -/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816178 | CCAATTTCTATTCAA[-/T]TTCCGTGAATTTTTA | 9063 |
rs34131713 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884916 | TCAAAAAAAAAAAAA[-/A]CTTAAAAAATTGAAG | 9063 |
rs34137123 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853813 | TGGGAGGGGAGTGGG[-/A]AAAAAAGGATAGCTC | 9063 |
rs34156817 | in-del | -/A | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921705 | TAACAAAAAAAAAAA[-/A]GCACTTCATTAAGAA | 9063 |
rs34171964 | in-del | -/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906311 | CAACATTGTACTGGA[-/G]GATCCTAGCCAGCAC | 9063 |
rs34185543 | in-del | -/A | 0.41408 | 0.188621 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916403 | TACCTTGATACATTT[-/A]AAAAAAAAAAAAAAT | 9063 |
rs34196561 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834172 | CAACTGGAAAAAGGA[-/C]ATCACAAATGTGCCT | 9063 |
rs34206431 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888579 | TCAACAGTCACAACC[-/T]TTTTGGCCAGGACCA | 9063 |
rs34230564 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879385 | CAGGATGGTCACTAT[-/A]AAAAAAAAATAGTAA | 9063 |
rs34296199 | in-del | -/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855998 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 9063 |
rs34371288 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902626 | AAAACTCAACATAGT[-/A]AAAGATGTCAACTTT | 9063 |
rs34424054 | in-del | -/C | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825564 | TCCACTATTCACCTT[-/C]CCCGTTCCCCTGCTC | 9063 |
rs34457697 | in-del | -/A | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823074 | AGACCTTGTATCTAC[-/A]AAAAAAAAAAAAAAG | 9063 |
rs34463734 | snp | A/G | 0.126564 | 0.217402 | intron-variant | PIAS2 | GRCh38.p7 | 18:46881827 | ACAGACACCGGGCAC[A/G]GTGGCTCACGCCTGT | 9063 |
rs34503806 | in-del | -/A | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900676 | CTCATCTGAAAAAAA[-/A]TACAAAATAGAGGCT | 9063 |
rs34520671 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46861117 | AACCCTTTCTCTACT[-/A]AAAAATACAAAAATT | 9063 |
rs34573229 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46891369 | TGCTTTATGACTATA[A/T]AATCTATCACCAATG | 9063 |
rs34618693 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46891371 | TTTATGACTATAAAA[-/A]TCTATCACCAATGAA | 9063 |
rs34633927 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842589 | ATAATAAAAAATCGT[-/C]CAATATCCAACTGTT | 9063 |
rs34684030 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46855073 | TAAATTCAAATCAAG[-/C]CTGGGGAACACAGTA | 9063 |
rs34702120 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902243 | AGCTACAAAACACTG[-/A]AAAAAAAAAAAAAAA | 9063 |
rs34722612 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46904637 | GCACCTGTAGTCCCA[-/G]CTACTCAGGAGGCTG | 9063 |
rs34753952 | in-del | -/A/AA | 0 | 0 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823073 | AGACCTTGTATCTAC[-/A/AA]AAAAAAAAAAAAAAA | 9063 |
rs34755414 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871327 | TCCATTACCTACAGA[-/C]CCCCACACCCCTAAA | 9063 |
rs34756305 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839465 | TTGAATAATCTATAA[-/G]GTACCTATTTGTCAA | 9063 |
rs34958166 | in-del | -/A | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832892 | CAAGCCTCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 9063 |
rs35017213 | in-del | -/G | | | frameshift-variant, downstream-variant-500B, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815313 | TCAGGATACATACCT[-/G]GGGGATCAACTGGAA | 9063 |
rs35046101 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809755 | GCAAGACTCAGCCTC[-/A]AAAAAAAAAAAAAAA | 9063 |
rs35073493 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46896250 | AAACAAACGTATGGT[C/T]TTATAAATGAAAAAA | 9063 |
rs35085118 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853303 | TAAATAAAAAAAAAA[-/A]GGAAAAAATGAAATC | 9063 |
rs35152593 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863092 | TCATCTGCTCTTTAC[-/A]AAATGGGTCTACCAA | 9063 |
rs35222529 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46863488 | TTTCTTGTAGAGACA[-/G]GGGTTTCACCATGTT | 9063 |
rs35256845 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46871259 | AAAGGGAAAAATTAC[-/T]GTTACCCACCTTCCA | 9063 |
rs35369967 | in-del | -/G | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922064 | AAACTAGTATCAAGG[-/G]AAACTGAACAAGGAA | 9063 |
rs35371145 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848576 | TGTCTACCACAACTT[-/G]GGGAACACCCTTCAC | 9063 |
rs35388072 | snp | A/C | 0.46875 | 0.121031 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822712 | AATAACATGAGACCA[A/C]CTCTCACACACAAGA | 9063 |
rs35397530 | in-del | -/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918969 | GTATTTGTGTAATTG[-/T]TTATTTGATATATAT | 9063 |
rs35407252 | in-del | -/A | | | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823088 | AAAAAAAAAAAAAAA[-/A]GCCACATATGCTGAA | 9063 |
rs35451178 | snp | A/G | 0.0459877 | 0.144496 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828030 | AGGGTCTTCCTCTTC[A/G]TCAGAAGAGCTTTCT | 9063 |
rs35512973 | in-del | -/C | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888571 | GAATAAATCAACAGT[-/C]CACAACCTTTTTGGC | 9063 |
rs35672104 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46867538 | CATTGTCTACAATTT[-/G]GGGAATCAGAAAACC | 9063 |
rs35677026 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46888364 | CAATTTTTTTTTTTT[-/T]ATCAGAAATAGAAAA | 9063 |
rs35724079 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808561 | CCACATTCATGTAGA[-/G]ACTGTAGTAAAAAAG | 9063 |
rs35740498 | in-del | -/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832783 | GTAATCCCAGCTACT[-/G]GGGGAGGCTGAGGCA | 9063 |
rs35776659 | in-del | -/A | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832909 | AAAAAAAAAAAAAAA[-/A]GAGAAGCCATACCAA | 9063 |
rs35783558 | in-del | -/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46822613 | TAAGTTATATTGTAT[-/C]CTAAAGCTCATCTTT | 9063 |
rs35871724 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46828999 | CTTTATTTTTTCCCC[-/T]TTTCTTCTTACTCCA | 9063 |
rs35873943 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824839 | AAACCCCATGTTTAC[-/A]AAAAAAAAAAAAAAC | 9063 |
rs36010442 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834232 | TCTCTACAACTTTCT[A/G]AACACTTTCAAGGAA | 9063 |
rs36061170 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46831265 | ATTAGCCATAATCAC[-/A]AAAATTTTTTAAATA | 9063 |
rs36069574 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46903661 | TTTAGCAAGTTCTTT[-/A]AAAAACTATACATAC | 9063 |
rs36074552 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906762 | TACCAACAAGATGTA[-/TG]TGTGTGTGTGTGGGG | 9063 |
rs55633240 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909728 | CAATTCTATTCCTAG[A/G]ATCTCTACAGTGAAA | 9063 |
rs55650860 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909585 | CAAAAGTAGATGTTA[A/G]CAAGAAAGCTGAGTA | 9063 |
rs55710513 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889857 | AAAATGTGGTATCCT[A/G]TAACACAGAAATATA | 9063 |
rs55752024 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913531 | CAATGCATGAAAAGA[A/C]GGGGATGAAGAATAC | 9063 |
rs55754830 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840222 | TATGTATGTGGGCTA[C/T]AGTTATCAATATTTG | 9063 |
rs55776913 | in-del | -/AA | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859451 | AAAAAAAAAAAAAAA[-/AA]GAATCAATGAAGTGC | 9063 |
rs55779584 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833661 | ATGGCAGAATGTATT[A/G]TGACACTAGTCAAAA | 9063 |
rs55781503 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814449 | TTCACTAGGTACCTT[C/T]GTTATATATACTGCT | 9063 |
rs55821814 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856008 | TTTTGTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 9063 |
rs55849517 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856310 | TGGCCAAAGACTTTT[C/T]TTTTACTATAAAGAC | 9063 |
rs55919369 | snp | A/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907324 | AGCACATTCAAAGGA[A/G]CTTGACATCATTACT | 9063 |
rs55925238 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854569 | GTCCAGTTCTACATT[G/T]ATTATTTTATTTTAT | 9063 |
rs55929919 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905759 | GAAACTTGAAAATAT[G/T]AACAGTCCTACAACC | 9063 |
rs55938990 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841182 | ATTAGATCCTCTTCA[A/G]TAACTACTGTGACAT | 9063 |
rs55990951 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46856003 | TTTTCTTTTGTTTTT[C/T]TTTTTTTTTTTTTTT | 9063 |
rs56009869 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872288 | ACCATCAATGGTTTA[C/G]AGTGATAGACTTAAA | 9063 |
rs56030315 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913535 | GCATGAAAAGAAGGG[G/T]ATGAAGAATACAGAA | 9063 |
rs56064494 | snp | A/G | 0.0832709 | 0.186283 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826475 | TGAATTCAGCCAACT[A/G]CAGTACTTGCAACTC | 9063 |
rs56095591 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831876 | GCTCAGAAAAAATAT[C/T]TGTGACCTTGAGTTA | 9063 |
rs56100943 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811212 | TTAATTCAAACATTT[C/T]TAATTCTCTTTTGTC | 9063 |
rs56104399 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46845327 | CAGAGTTCCAAAGTT[C/T]TAATTCTGGCAGAAG | 9063 |
rs56119924 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887297 | ATTGCCTGCCACTAG[C/T]CAGGCCATACTAACC | 9063 |
rs56142565 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905362 | ACAAGGAGGCAATAC[A/G]CAGACATTTTATGAT | 9063 |
rs56163470 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816794 | TTCATTTCATATGTC[C/T]GTCACTAGCTATATG | 9063 |
rs56169983 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905421 | ATTAATGACAGGCAC[C/T]CAGCTTAAGAAATTA | 9063 |
rs56188847 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853137 | CAAAAATGAGCCAGC[C/T]ATAGCGGTGCATGCC | 9063 |
rs56202233 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811303 | TGTCCCTTTCCCTAA[A/G]TTTGAAAATCACTGC | 9063 |
rs56217029 | snp | A/C | 0.0973687 | 0.197999 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840085 | AGAATTGCTTAAACC[A/C]AGGAGGCGGAAGTTG | 9063 |
rs56277725 | snp | C/G | 0.0876345 | 0.190099 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918084 | CGGTGGGGTTGGGGG[C/G]GGGGAGAAGTGAAAT | 9063 |
rs56318022 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859804 | TGTCTAGAGGGAGGT[A/G]TTGGTAATTTTGCAG | 9063 |
rs56352844 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813892 | CTTCCAAGGAGCTCT[A/G]AAGATGGTTGAATTG | 9063 |
rs56414010 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839793 | TCACTTGAACCTGGG[A/G]GGCAGAGGTTGCAGT | 9063 |
rs56665149 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842294 | AAAAAAAAAAAAAAA[-/A]TTTAAAAAGCCTGAG | 9063 |
rs56745005 | snp | C/T | 0.030665 | 0.119967 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866367 | TCATCCGAAGCAATA[C/T]AGGCCAGAAGGTATC | 9063 |
rs57038700 | snp | A/T | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46809947 | AAAGTCAGGGTCTGG[A/T]TAAGAAACAGTGACC | 9063 |
rs57650764 | in-del | -/TT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46876713 | TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTCTTGC | 9063 |
rs58099640 | in-del | -/AAAA | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870641 | AAAAAAAAAAAAAAA[-/AAAA]GGAACTCGAGTCATT | 9063 |
rs58230183 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880109 | AAAAAAAAAAAAAAA[-/A]TTGGGGATGGGGACA | 9063 |
rs58377160 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816031 | TTCAAGTAATAACAA[A/T]AAATAAAATTTTTAG | 9063 |
rs58401472 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46847923 | CTTAGCTGCAAAAAA[-/A]TCTACATATTGAAAA | 9063 |
rs58444784 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816668 | AGAGAGGGTCTCGCT[A/G]TGTTGCCTAGGTTGG | 9063 |
rs58675073 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902260 | AAAAAAAAAAAAAAT[C/T]TAAGAAAATCTAAAG | 9063 |
rs58855520 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839880 | AAAAAAAAAAAAAAA[-/A]GGCCGGGCACAGTGG | 9063 |
rs58993513 | snp | C/T | 0.485118 | 0.0849685 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894891 | GCCTGACCAACACGG[C/T]GAAACCCCGTCTCTA | 9063 |
rs59066322 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906785 | GTGTGGGGGGGGGGG[-/G]AGGTGTATAACATGA | 9063 |
rs59385589 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46853288 | GCCTTTTTTTTTTTT[-/T]AAATAAAAAAAAAAA | 9063 |
rs59491577 | in-del | -/TA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832913 | AAAAAAAAAAAGAGA[-/TA]AGCCATACCAAATGT | 9063 |
rs59634209 | in-del | -/TA | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826112 | TTTATACAGACTTTT[-/TA]AAAATAAACTTTCAT | 9063 |
rs59693447 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808843 | TTTTTTTTTTTTTTT[-/T]AAACCAACTGAAGGC | 9063 |
rs59760657 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815969 | TCCAATTCGATTTTA[A/G]AAAGAGGAATGTGTA | 9063 |
rs59957336 | in-del | -/A | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855131 | AAAAAAAAAAAAAAA[-/A]TTCCAGGCTTATGTT | 9063 |
rs60059644 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881078 | TTCACTACCACCACC[A/C]TACTGAAAGCCTATT | 9063 |
rs60173105 | snp | A/T | 0.37778 | 0.214877 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892907 | AAGTGTCAGTGGGAT[A/T]TTTTTTATACTAAGT | 9063 |
rs60345708 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46835150 | TCAAATGGTTCAAAA[A/G]AATTCTAAAAATGGT | 9063 |
rs60447275 | in-del | -/A | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908542 | TAAATGAGAAAAGGT[-/A]AAAAAAAAACAAAAA | 9063 |
rs60496589 | in-del | -/TT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46834033 | TACTTTTTTTTTTTT[-/TT]ACCATCTCCCATACT | 9063 |
rs60547242 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811605 | TCAATGGCTGCATAG[-/AG]TTTCTTTTTTGAGAA | 9063 |
rs60590089 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880109 | AAAAAAAAAAAAAAA[-/A]TTGGGGATGGGGACA | 9063 |
rs60707180 | in-del | -/AGAG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46848801 | GTGAGAGAGAGAGAG[-/AGAG]TAGGAAGGTTATGCC | 9063 |
rs60745533 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887274 | GAAAAAAAAAAAAAA[-/A]TAGCCACATTGCCTG | 9063 |
rs60855484 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886121 | TCACTTAGTCCCCCC[C/G]AGTCTTCTGTCCATG | 9063 |
rs61018552 | in-del | -/A | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889569 | ACTATAAAAAAAAAA[-/A]GGAAAATAAAAGTGT | 9063 |
rs61041863 | in-del | -/AGA | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, cds-indel | PIAS2 | GRCh38.p7 | 18:46810064 | TAAGCCCCAATTTCA[-/AGA]TGATAAACTTCAAAG | 9063 |
rs61248600 | in-del | -/A/AA | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864784 | AAAAAAAAAAAAAAA[-/A/AA]TACTAATGCACAGTA | 9063 |
rs61431637 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892913 | AGTGGGATTTTTTTT[-/C]ATACTAAGTCTTCAA | 9063 |
rs61557949 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46854814 | CACTCTCAGCAGCCT[C/T]TGCTTTTCCCCATGC | 9063 |
rs61649386 | in-del | -/C | 0.00128277 | 0.0252931 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891076 | GGAAAGAAAAAAAAA[-/C]ATAAGCCAAGTCACC | 9063 |
rs61749949 | snp | C/T | 0.0178282 | 0.0927161 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855381 | ATTTACTTTTATACA[C/T]AGACTATTTGGATAG | 9063 |
rs61760984 | snp | A/G | 1.65244e-05 | 0.00287436 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812517 | GCTGGATGAACTAAC[A/G]TGAGTACTGCTTTCA | 9063 |
rs61760985 | snp | C/G | 4.9467e-05 | 0.00497303 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890747 | GAGGATGGTGAGTGA[C/G]GTGTAACTGAAGTGG | 9063 |
rs62095374 | snp | A/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809776 | AAAAAAAAAAAAAAT[A/T]GATTTTAGGAGGCTG | 9063 |
rs62095375 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810758 | AAAAAAAAAAAACCC[A/C]AAGCAAGGACAAGTC | 9063 |
rs62095376 | snp | A/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824778 | CAGGCCAAGACAGGT[A/G]GATGGCTTGAGCTCA | 9063 |
rs62095377 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831030 | CAAAAGTCAATCAAC[A/G]TAATTCACCGTATTA | 9063 |
rs62095378 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842353 | TTTGTTTTGGTTGCT[A/C]TCATGTAGAATGGCA | 9063 |
rs62095379 | snp | G/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858618 | GGGAGGATCAATTGA[G/T]CCCGGACATTAAAGG | 9063 |
rs62095380 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859803 | GTGTCTAGAGGGAGG[C/T]GTTGGTAATTTTGCA | 9063 |
rs62095381 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46865410 | CCAGTCATGGTGGCA[C/T]GTGCCTGTAATCCCA | 9063 |
rs62095382 | snp | C/G | 0.203882 | 0.245709 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885456 | AACTTGGGAGGCGGA[C/G]GTTGCAGCTAGCCAA | 9063 |
rs62095383 | snp | A/C | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921371 | GACCTCGTGATCCAC[A/C]TGCCTTGGCCTCCCA | 9063 |
rs62095384 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922095 | TTAAAAAAAAATTTT[A/T]CCTCACTTTTTTTTT | 9063 |
rs63554460 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809774 | AAAAAAAAAAAAAAA[A/T]TTGATTTTAGGAGGC | 9063 |
rs71264811 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906774 | ACCTCCCCCCCCCCC[-/A]CACACACACACATAC | 9063 |
rs71264812 | in-del | ATCT/CTC | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832910 | CATTTGGTATGGCTT[ATCT/CTC]TTTTTTTTTTTTTTT | 9063 |
rs71355036 | snp | A/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884478 | CACCACGCCCGGCTA[A/T]TTTTTGTGTTTTTAG | 9063 |
rs71364568 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888797 | AGCTCAGGCTGTAAT[A/G]CTCGAATTCCTGCTG | 9063 |
rs71364569 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892320 | ATATACACTGTCATA[A/C]CTGTACTTTGTGTAC | 9063 |
rs71364570 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901969 | GTAAGAGTTGAAAGG[A/G]AAAAATAAAACTATA | 9063 |
rs72485572 | in-del | -/AA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46839879 | AAAAAAAAAAAAAAA[-/AA]GGCCGGGCACAGTGG | 9063 |
rs72548219 | in-del | -/GTTAA | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847369 | AATCTTTTAAACCAG[-/GTTAA]GTTAACAAATAAGGA | 9063 |
rs72588440 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892913 | CAGTGGGATTTTTTT[-/T]ATACTAAGTCTTCAA | 9063 |
rs72905292 | snp | C/T | 0.0441095 | 0.141807 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808141 | TTTAATGACATGGAA[C/T]AATGCCTGTAGGTTG | 9063 |
rs72905296 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813753 | CAAGTAAAATTCAGA[C/G]TGCTCTTCAAAAGAA | 9063 |
rs72905301 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813897 | AAGGAGCTCTAAAGA[C/T]GGTTGAATTGTCCAG | 9063 |
rs72907105 | snp | G/T | 0.0832709 | 0.186283 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816041 | AACAATAAATAAAAT[G/T]TTTAGGTCTGAAAAG | 9063 |
rs72907111 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817697 | ACCAAGCATTACAAG[A/G]GTGCTGTCTATATAA | 9063 |
rs72907112 | snp | C/T | 0.0569829 | 0.158885 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818002 | GATATATTTTTATGC[C/T]CTCCGAAGTATTTCA | 9063 |
rs72907114 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818997 | CCAAATTCTGAAATA[A/G]TGTAAATTTCCCCCA | 9063 |
rs72907118 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820721 | ATTTCCTATTCTACT[A/G]TATTTCTTATCACCA | 9063 |
rs72907120 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821637 | GCCACAATCAGAAAC[A/G]AGGATGAGTGTTCAG | 9063 |
rs72907122 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822661 | AGTGGTCCTCCACAG[C/G]GATCAAACGAACAGG | 9063 |
rs72907125 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823776 | TACAAATTCAACTTT[A/G]CATAGAATGGCTTAA | 9063 |
rs72907128 | snp | C/G | 0.0573587 | 0.15934 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824082 | CATTATGCAAGTGAC[C/G]ATTTATATTTTAAAC | 9063 |
rs72907130 | snp | A/G | 0.0433465 | 0.140692 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824098 | ATTTATATTTTAAAC[A/G]TTTGTAACTTTATCC | 9063 |
rs72907132 | snp | A/G | 0.0821764 | 0.185298 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825427 | ATCTGGTAATAAAGA[A/G]CAAACTTAATCCAGC | 9063 |
rs72907134 | snp | C/T | 0.0429648 | 0.14013 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826084 | GCTTCATGGAACGAA[C/T]TAGGTAGCTGCGCTT | 9063 |
rs72907137 | snp | A/G | 0.0085515 | 0.0648276 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828153 | TAAAGAAACAAAAGG[A/G]AAAAAAAATTAAAGG | 9063 |
rs72907140 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828480 | CAGAAAGACACGCAG[A/G]GTTAGGGAACTGGTC | 9063 |
rs72907142 | snp | A/C | 0.0818113 | 0.184966 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829618 | GGGAAAACTATATAT[A/C]ATCAAAAGACTGAGT | 9063 |
rs72907143 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834005 | CTTACCTTCACAGCA[C/T]TTTACACTTAATATA | 9063 |
rs72907146 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834241 | CTTTCTAAACACTTT[C/G]AAGGAAGACATTCAA | 9063 |
rs72907148 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836645 | AATAGAAATCCAAAT[C/T]AGAATGTATTCCCAA | 9063 |
rs72907151 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837257 | TTTGTTCCACTCAAC[C/T]TTTTCAATATAATGT | 9063 |
rs72907152 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837718 | ACCAAGACGTACACA[A/G]CACTCAGATTTGATC | 9063 |
rs72907154 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838411 | GAAAATGGCAGAGCA[A/G]GTCTGACCTGGGAAG | 9063 |
rs72907155 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838874 | ATGCCAGTTTTATAA[C/T]ATTACAAATGGTGTT | 9063 |
rs72907162 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840389 | AGAACACAAAATGCC[A/G]AAATTGTGTGTCCAT | 9063 |
rs72907164 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840712 | AATTGCCTAGTGACT[A/G]TGGCATGTTATTAAA | 9063 |
rs72907165 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840870 | TAAGCTGGCATTATC[C/T]AAATTCTATTCACTG | 9063 |
rs72907170 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842247 | AATTTAAAATAAATT[A/T]AAAAAAAAAAAAAGG | 9063 |
rs72907174 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844427 | CAGCAGTACCCTGAG[C/T]GTCAAAGCTTTTCCA | 9063 |
rs72907177 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848436 | AGGCAATGATAATAC[A/G]TCACAGCTGACACCT | 9063 |
rs72907179 | snp | A/T | 0.0858192 | 0.188533 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848788 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGTA | 9063 |
rs72907196 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854526 | GGTACCAATTTAGTA[A/T]TGTATCCAAAATGGA | 9063 |
rs72907199 | snp | C/T | 0.097727 | 0.198275 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855084 | CAAGCCTGGGGAACA[C/T]AGTAGGACCTTGTCT | 9063 |
rs72907200 | snp | A/G | 0.00744113 | 0.0605408 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855623 | AAAAATCCCTGTTGG[A/G]AAGAGAAAGAAAATG | 9063 |
rs72909104 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855690 | TCCCCAGGAGGAAAA[A/C]AAGGAAAAGCATTAT | 9063 |
rs72909108 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857410 | AAAAGGGAAAATTTT[C/T]GTCTTGAAAGTTCAA | 9063 |
rs72909109 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858331 | TCAAAGAGAAAAAAC[C/T]GAATGGGCTTTAGAA | 9063 |
rs72909171 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860077 | TCAAGCGTCTAGTCT[A/C]GATCTTACTACCACT | 9063 |
rs72909181 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865196 | AAAAGTTAATATATA[G/T]AGAGGCCTCAAGTCT | 9063 |
rs72909189 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865579 | ACTGTCCAGTTTTCC[C/T]GCTACATGAAGATAA | 9063 |
rs72909190 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865620 | AGTTGGATATCCAAT[A/G]TCAGAGCGGTTCAAC | 9063 |
rs72909191 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865854 | TAATTATGGAGCATC[A/T]AACACAGAAACATAA | 9063 |
rs72909195 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866908 | GACCCTCTGTGAATT[C/T]ACGAATATAAATGCC | 9063 |
rs72909200 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867016 | GAAAAGAGAATGGTT[C/T]CATAGTCATGTTGTA | 9063 |
rs72909201 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867048 | ATGTATGTTCAACAT[A/G]TACTTTTATATCAAA | 9063 |
rs72911104 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868732 | CTTCATTTGGCATTT[C/G]GGTGCTTGTTTTCCT | 9063 |
rs72911106 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869042 | GGTGGTTGGGACAAC[G/T]TGGAGCTTGAATGTG | 9063 |
rs72911111 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870259 | GGGAAGTGCCCCTTG[A/G]AGGAGAAGGAATCGG | 9063 |
rs72911116 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871756 | AAAGCAAGAATCTTA[A/G]AAGACACAGAGGTCA | 9063 |
rs72911118 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872165 | CTGTAAAGAAATTAG[A/G]CGGGTCATGCTGACT | 9063 |
rs72911123 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875507 | AGATGTTATAGGACG[C/G]GACCCCATAAGAATC | 9063 |
rs72911125 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877507 | TAAACTGCCCCTCCC[A/G]CCGAAACAGCTCTTC | 9063 |
rs72911127 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877553 | TTCCTGCCTTTGCCG[C/T]GCCCTGACATGCCCA | 9063 |
rs72913049 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882312 | AAGGATAAAAAGAGA[C/T]TGATTCTTATTAATT | 9063 |
rs72913052 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884231 | ACTTAACATGTTTTA[C/T]ATACATATTCCTTTA | 9063 |
rs72913060 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887361 | ATTTAACCAAGACAG[A/G]CTGCAGTACAATCCT | 9063 |
rs72913063 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887818 | CCCATTCACACGGAA[A/G]CAATCTGATTTCTAC | 9063 |
rs72913066 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888384 | TTTTTTTATCAGAAA[C/T]AGAAAAACTCATTCT | 9063 |
rs72913070 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888726 | CATGCACAGTTCACA[A/G]TAGGGTTCCTGCACC | 9063 |
rs72913075 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888836 | CTGCTGCTCACCTCC[C/T]GCTGTGCGACCTGGT | 9063 |
rs72913076 | snp | A/C | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889328 | GAGAAAATATTTGCA[A/C]ATTCATATATCTGAT | 9063 |
rs72913080 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889366 | TATATCCAGAATATA[C/T]AGAGAACTCCTAAAA | 9063 |
rs72913087 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892571 | TGAGCCCAGGAGTTC[A/G]AGACCACACTGGACA | 9063 |
rs72913089 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894230 | TATGTTGTTTGGCAA[A/T]TCTTACCAGATCCCA | 9063 |
rs72913091 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894345 | TGAGTAGAGAGGGTC[A/G]CCAGAGCCCACATGG | 9063 |
rs72913096 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896541 | GGAGTAAAATACATA[C/T]GTGTTAGAAGACAAA | 9063 |
rs72913098 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897134 | ATGTGGGGACTCTAC[C/T]ACCTTCCCAAGTTTT | 9063 |
rs72915060 | snp | A/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897706 | CTCAATAAACAAGAA[A/T]AGAAAGAAATTCTGT | 9063 |
rs72915064 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900035 | AGAAGTTTGAGATCA[C/G]TCTGGTCAACATGGT | 9063 |
rs72915071 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902691 | ATCCAAATTCCAACA[A/T]GATTTTTGTAGATAT | 9063 |
rs72915074 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903998 | TCTATTTATGTAATA[C/T]TTTTGAAAAGACAAA | 9063 |
rs72915084 | snp | G/T | 0.0429648 | 0.14013 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907828 | CACATGATTTTCCTG[G/T]TGGGAGGGTGGATCC | 9063 |
rs72915093 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910769 | CTGCAATGGACCTCT[C/G]ATTAGCACACCAAGT | 9063 |
rs72915096 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911694 | AGAAAACTTTAGAAG[A/G]GTTATAAAACATTAT | 9063 |
rs72917106 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914335 | TGGATGATTAGAACA[G/T]AAGTAGAGACCTAAA | 9063 |
rs72917111 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915342 | TGTAATGGGATGTAA[A/G]GGCGGGGTACAGTTC | 9063 |
rs72917116 | snp | A/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920988 | ATTTCCAATGGTAAA[A/T]TGTTTTAGTGCTCTT | 9063 |
rs73437121 | snp | A/T | 0.046775 | 0.145601 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830507 | TTTAAAGGAAAATTT[A/T]TAGCATTAATCTTCC | 9063 |
rs73437129 | snp | C/T | 0.046775 | 0.145601 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842539 | GTATGTGGAATAGAG[C/T]TGGCAATTAATGTTT | 9063 |
rs73437134 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848309 | TTTTCAGACAACAGC[C/T]AGGATTCATGCTTCT | 9063 |
rs73437140 | snp | G/T | 0.046775 | 0.145601 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852814 | CAATGCCACAGAGTT[G/T]AGGCACAACCTCACA | 9063 |
rs73437141 | snp | A/G | 0.046775 | 0.145601 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853053 | AGGCCAACATAGGTG[A/G]ATCACTTGAGCCCAG | 9063 |
rs73437146 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867522 | GCAGTTTATTTTCTC[C/T]CCATTGTCTACAATT | 9063 |
rs73437151 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872350 | GACAGCAGGGACATA[G/T]TTGTTTTTGAATGGG | 9063 |
rs73437155 | snp | A/C | 0.046775 | 0.145601 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888390 | TATCAGAAATAGAAA[A/C]ACTCATTCTAAAATT | 9063 |
rs73437166 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913258 | ATGGTGACTCCTGGT[A/T]GGTGTAAGGAAACCA | 9063 |
rs73953892 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46807869 | AGACCACCCTTCCCA[C/T]ACCATCTAGCTGCAG | 9063 |
rs73953893 | snp | A/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46811128 | TCAGAGGTTCCCTGG[A/T]GTGTTTGGGGTAGCA | 9063 |
rs73953894 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842814 | GGGCTTTCAGGTCTT[A/G]CCCTACTGGAACTGC | 9063 |
rs73957803 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851326 | TTTAAAAGAAATATT[C/G]TTGTCAACCCTTCTT | 9063 |
rs73957805 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866989 | TTCCAAAACCCATGA[A/C]CCTTAACATTTGAAA | 9063 |
rs73957806 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46867392 | GATAAGTCAATTTTA[C/T]GACAGAACAGCAGCC | 9063 |
rs73957807 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877919 | TGTTTTGGAAGACTA[C/T]ATTATACAGCAACAG | 9063 |
rs73957808 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896345 | TAAATACAGATAAAA[C/G]TGGTTTCCTAGAAAA | 9063 |
rs73957810 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914314 | TTGACTCTAAGCCCC[C/T]GGCTATGGATGATTA | 9063 |
rs73957811 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46915950 | GTTCAGGGTTCGTTG[C/T]TTGAAAAGCTCCACA | 9063 |
rs74172045 | in-del | -/A | 0.5 | 0 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824853 | CAAAAAAAAAAAAAA[-/A]CACAAAAAAATTAGC | 9063 |
rs74340805 | snp | A/G | 0.178785 | 0.239642 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911788 | CAGCGGCTCATGCCT[A/G]TAATCCCACCACTTT | 9063 |
rs74405718 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818316 | ATAAGGCAGTCATAT[A/T]TTTCCTTGAAATAAG | 9063 |
rs74446041 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880792 | TAGCTCATTTTTGAT[A/G]ACCTGTGTCTTGACA | 9063 |
rs74450953 | snp | A/C | 0.179425 | 0.239831 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857300 | CACAGTATTTGCTTC[A/C]AAGGATTTATATGCT | 9063 |
rs74479262 | snp | A/C | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863260 | ATGCCCCAGTTTGGA[A/C]TGATAAAGCTTATGG | 9063 |
rs74525924 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862466 | AGGAAGTAAACACCT[C/T]TAATTTACTCAATTC | 9063 |
rs74562954 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885000 | TTTAAGGAAAGAAAA[C/T]GGAGATTTTTGCTAG | 9063 |
rs74623791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873323 | CCCAAATCTAAAAGG[C/T]CCTGGGCGTAAATGT | 9063 |
rs74694107 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905700 | CAAGAATGTGGATGA[A/G]ATGAACAACTTTCTA | 9063 |
rs74741090 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872169 | AAAGAAATTAGACGG[G/T]TCATGCTGACTAGTG | 9063 |
rs74743187 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916182 | CAATCTCCGTTTAGA[A/G]CAGAGGATACGTTCT | 9063 |
rs74871789 | snp | C/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844689 | CTCATATGCTCAATC[C/T]TTTTTTTTTTTTTTA | 9063 |
rs74906790 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864256 | GCTTTGAACTGGGAA[A/G]AAAAAAAAAAAGAAA | 9063 |
rs74921470 | snp | A/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892906 | AAAGTGTCAGTGGGA[A/T]TTTTTTTATACTAAG | 9063 |
rs75000203 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833083 | AGTATTTACCCAAGA[C/T]AAATGAAAACAGTCC | 9063 |
rs75034646 | snp | G/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897890 | GGGTTTTTTTTTTTT[G/T]AGACAGGATCTCGTT | 9063 |
rs75049923 | snp | G/T | | | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919283 | CCTGAGGTTGGGAGT[G/T]GGAGGCCAGCCTGAC | 9063 |
rs75172167 | snp | C/T | 0.179105 | 0.239737 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862350 | AAAAAAAAAATTATG[C/T]AATTAAGTACAGAAT | 9063 |
rs75198066 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827603 | AAGTAAGCGATGGTG[A/T]GCCAAAATTGGAATC | 9063 |
rs75241378 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811830 | AAAAACCAAGTAACA[A/C]GAATGCCATTTTTCT | 9063 |
rs75384495 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815851 | GTACATAGTCCAACG[C/T]TCTGCACAAAGCACA | 9063 |
rs75414342 | snp | A/C | 0.178785 | 0.239642 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839365 | GAGAATTAAATCTGG[A/C]AAAATCTATCATGCT | 9063 |
rs75543496 | snp | G/T | 0.102014 | 0.201495 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889621 | GGAACCCTTGTGCAC[G/T]GTTGAAGGGAATGTA | 9063 |
rs75579114 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906773 | ATGTATGTGTGTGTG[G/T]GGGGGGGGGGGGAGG | 9063 |
rs75642401 | snp | C/G | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899855 | TACTATATGAAGTAA[C/G]TATCAAATTTGTGAG | 9063 |
rs75687409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815725 | CTTAAGCTCTTAAGA[C/T]ATTTCACATTTATTT | 9063 |
rs75705976 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46832273 | TACAAAAATTAGCCA[A/G]GCGTGGTGGCGCACA | 9063 |
rs75717202 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838636 | TATTTTTCCTGCCTT[A/T]AAAAACAAATTATTT | 9063 |
rs75747385 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816748 | GCTGGGATTACAGAC[A/C]TAAGCCACCGCACCC | 9063 |
rs75756258 | snp | A/C | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875022 | CCCAGGGCCCACCCC[A/C]ACCAAATTACCTCTA | 9063 |
rs75851356 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860468 | TTGCAGCAGAGAAAA[C/T]ACAAGATAAGCCTTC | 9063 |
rs75861747 | snp | C/T | 0.178465 | 0.239547 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906930 | TCATACCAACCCTCC[C/T]TGTGAGAACTTAACA | 9063 |
rs75903490 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848858 | AAAAAAAGTTGCTCA[A/G]AAAAAAAAAAACAAC | 9063 |
rs75979881 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880540 | TGCACAATGATCATG[C/T]CTGTGAATAACCACT | 9063 |
rs76114348 | snp | G/T | 0.103438 | 0.202533 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816679 | CGCTATGTTGCCTAG[G/T]TTGGTTTTGAACTCC | 9063 |
rs76214465 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46884946 | TAAAAAATTGAAGAG[G/T]AAATCAAGACTGCCT | 9063 |
rs76277993 | snp | A/C | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855778 | AATGAAATCACTGTA[A/C]TGATGATAAACCTGA | 9063 |
rs76316241 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916495 | CCATCTCATTCGTCA[C/G]ACTTAGTTAGGACTT | 9063 |
rs76502664 | snp | A/G | 0.0174175 | 0.0916809 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809648 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 9063 |
rs76519025 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922119 | TTTTTTTTTTTTTTT[G/T]AGACAGGGTCTCACT | 9063 |
rs76525461 | snp | A/C | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885521 | GCAAGACTCCATCTC[A/C]AAAAAAAAAAAAGAA | 9063 |
rs76560693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905896 | AGAAGAGAAAAGGTA[C/T]ATTTTTTAACTATAG | 9063 |
rs76577993 | snp | A/C | 0.0333695 | 0.124785 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810459 | TAGAGCAGCAACATA[A/C]AACTTTATTAGAAAG | 9063 |
rs76660776 | in-del | -/ATTT | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46818172 | CAACACATTTTCCTT[-/ATTT]GAGTCATAAACTTTT | 9063 |
rs76704819 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917082 | GTGTGCGGACCACTG[G/T]CAGCACTCAGGAGCC | 9063 |
rs76750595 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823435 | TTACACGTAACAACA[A/G]TAACAGAGCTCCCTT | 9063 |
rs76752173 | snp | A/G | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839880 | AAAAAAAAAAAAAAA[A/G]GGCCGGGCACAGTGG | 9063 |
rs76781150 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870963 | GGAATCAGTACCTCA[A/G]ACCCAAGATATTTCC | 9063 |
rs76809492 | in-del | -/AAAAAAAAGAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46859445 | AAAAAAAAAAAAAAA[-/AAAAAAAAGAA]TCAATGAAGTGCAGC | 9063 |
rs76976513 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856569 | CTCCAAACTCTTGCC[A/G]CGCAACATGGAGTCT | 9063 |
rs77002622 | snp | A/G | 4.33135e-05 | 0.00465348 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864257 | CTTTGAACTGGGAAG[A/G]AAAAAAAAAAGAAAG | 9063 |
rs77026283 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903216 | ACACTGGACTTCACA[A/C]AAACTAAAACCTGTG | 9063 |
rs77040088 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843962 | TTCAGCATTCTTCAT[A/G]ATATATCATTCATTC | 9063 |
rs77050695 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907083 | GCCTTCCCCGGAGAT[A/T]TCTGCCAATGGAAAA | 9063 |
rs77190254 | snp | G/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876715 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT | 9063 |
rs77320851 | snp | C/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901155 | GGGTGCGGTGGCTCA[C/G]ACCTGTAATCTCAGC | 9063 |
rs77346689 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842260 | TTAAAAAAAAAAAAA[A/G]GGATATGTTATGAAT | 9063 |
rs77361726 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843504 | ATTTTTCAAACTCAA[G/T]TATTAACATTCTAAG | 9063 |
rs77411090 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46812973 | TGGGTGTCAATTTTG[A/G]AAGAATTGTTGATCT | 9063 |
rs77415171 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816085 | TTCAACATCAGTTCA[C/G]CTAGACCTCCCTGTG | 9063 |
rs77468548 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842765 | AGTCGTGTGTCCTTC[C/T]GCATGCCTCCTAGAA | 9063 |
rs77527049 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811908 | TCCAAGCTTTGGCCA[C/T]GTACTGAAACTTCAT | 9063 |
rs77528543 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872624 | TCAAAAGGAAAGCTC[C/T]GATCTGTGGAACCCA | 9063 |
rs77585986 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922117 | TTTTTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA | 9063 |
rs77596153 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845635 | CACATAAATGTTAAA[A/T]AAAAAAAACCTATCT | 9063 |
rs77653126 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913373 | AATTATGACACAACA[A/G]ATTTACCCAGTTTGG | 9063 |
rs77692045 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824841 | AACCCCATGTTTACA[A/C]AAAAAAAAAAAACAC | 9063 |
rs77762784 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883103 | ACTCCGTCTCAAAAG[A/G]AAAAAAAAAAAACAA | 9063 |
rs77783889 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824874 | AAAAATTAGCTGGGG[G/T]TGGTAGTTCCAGCTA | 9063 |
rs77784138 | snp | A/C | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885520 | TGCAAGACTCCATCT[A/C]AAAAAAAAAAAAAGA | 9063 |
rs77887961 | snp | A/T | | | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892914 | AGTGGGATWTTTTTT[A/T]TACTAAGTCTTCAAT | 9063 |
rs77980291 | snp | A/G | 0.0182019 | 0.0936463 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811234 | TCTTTTGTCGTTTGT[A/G]GTTTCAGGTAAGATA | 9063 |
rs77980651 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860008 | AACTGAATCCAATGT[C/T]CAATCTTCACAAGAT | 9063 |
rs78107599 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46838637 | ATTTTTCCTGCCTTT[A/T]AAAACAAATTATTTC | 9063 |
rs78192124 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848836 | TTAAGTTGCTCAAGT[A/G]AAAAAAAAAAAAAGT | 9063 |
rs78233235 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46880541 | GCACAATGATCATGC[A/C]TGTGAATAACCACTG | 9063 |
rs78236567 | snp | A/C | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898996 | TGAGACTCCATCTCA[A/C]AAAAAAAAAAAAGCT | 9063 |
rs78239693 | snp | C/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844688 | TCTCATATGCTCAAT[C/T]TTTTTTTTTTTTTTT | 9063 |
rs78255841 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817626 | TGACTTATACAACAC[A/C]ATAATAAAATACCTA | 9063 |
rs78296291 | snp | C/G | 0.093777 | 0.195178 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853230 | ACTGCAGAGTGAGCC[C/G]AGACTACACTAATGC | 9063 |
rs78341686 | in-del | -/TA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46894698 | ATTATTAAAAATTTT[-/TA]AAAGCTGGGATATTA | 9063 |
rs78452804 | snp | C/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854803 | CTGTAGTTAGCCACT[C/T]TCAGCAGCCTCTGCT | 9063 |
rs78527086 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910914 | TTTATCACCAGCATA[C/T]CCTTCCAGAAACAAC | 9063 |
rs78686129 | snp | A/C | 0.031825 | 0.122064 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897689 | CATTCCTGATGAAAT[A/C]TCTCAATAAACAAGA | 9063 |
rs78699343 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46835966 | GCATGAATTCCAGTT[C/T]TGAACTTAAGAGCTA | 9063 |
rs78752650 | snp | A/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844706 | TTTTTTTTTTTTTAA[A/T]TGCTTGGTCTTATTA | 9063 |
rs78816790 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922116 | CTTTTTTTTTTTTTT[G/T]TTGAGACAGGGTCTC | 9063 |
rs78823612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889496 | ACAATATCACCATCA[C/T]TACAGACATGCAAAT | 9063 |
rs78876311 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830406 | AAAAGAAACATGAGT[C/G]AAAGATAAAAATAAG | 9063 |
rs78941153 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888972 | ACAAGGGTGCTAAGA[G/T]CATTCAGTGAGGGAA | 9063 |
rs78990204 | snp | G/T | 0.24134 | 0.24985 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906775 | GTATGTGTGTGTGTG[G/T]GGGGGGGGGGAGGTG | 9063 |
rs79032073 | snp | G/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875664 | CTAAGGTAACGGCTG[G/T]GGAGGTGAAAGAATT | 9063 |
rs79074217 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918997 | TATGTGTGTGCGTGT[A/G]TATATATATATGTGT | 9063 |
rs79163746 | snp | C/T | 0.176219 | 0.238865 | intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919939 | TGTGGGAGGAGTTTT[C/T]GGGGAATAGACGAAT | 9063 |
rs79175561 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842262 | AAAAAAAAAAAAAAG[A/G]ATATGTTATGAATGC | 9063 |
rs79190542 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839016 | ATATCCTTTCAATTA[C/T]AAAATGAATAATTTT | 9063 |
rs79199725 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886816 | GCCCTCCATCCTGGG[C/T]GACAGAACAAGACTC | 9063 |
rs79254242 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848861 | AAAAGTTGCTCAGAA[A/G]AAAAAAAACAACTCC | 9063 |
rs79305863 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911119 | AGTCTACCAAGACAA[A/G]CTGAATGGCTACAAC | 9063 |
rs79339430 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46859166 | AGACGCGGTAGCTCA[C/T]GCCCATAATCCCAGC | 9063 |
rs79344667 | snp | G/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898173 | ATAATTTTTTTTTTT[G/T]GAGAGAGAGAATCTC | 9063 |
rs79595846 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897860 | TTCTAGATAATACAA[A/G]GCAATATAATTTTTG | 9063 |
rs79609991 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918202 | AAGGAAGCTTGATGG[C/T]CCCCCCGTAATGTGC | 9063 |
rs79653985 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820532 | GGAGAATAAAATCCA[C/T]AGCTTGTAGGAAAAA | 9063 |
rs79655167 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909584 | ACAAAAGTAGATGTT[A/G]GCAAGAAAGCTGAGT | 9063 |
rs79692714 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875115 | ACTCAAACTAACCAT[C/T]CCTTAACCCTTCAGT | 9063 |
rs79706371 | snp | C/G | 0 | 0 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826551 | CCAGAAACATCACAT[C/G]TAAGCATTCATTCCC | 9063 |
rs79706612 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914091 | TTCACAAACTAATCA[C/G]TCCTTCAGCTCCTAA | 9063 |
rs79716003 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812301 | TTCACCCCTCAGAAA[A/G]CAAAAGAATCCATCT | 9063 |
rs79796823 | snp | C/T | 0.179425 | 0.239831 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837597 | AATATATTTTTCATT[C/T]ATGAAAATTTGTTTT | 9063 |
rs79873463 | snp | A/T | 6.11353e-05 | 0.00552846 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844703 | CTTTTTTTTTTTTTT[A/T]AAATGCTTGGTCTTA | 9063 |
rs80023465 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810754 | AGAAAAAAAAAAAAA[A/C]CCCCAAGCAAGGACA | 9063 |
rs80167037 | in-del | -/AAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899007 | TCAAAAAAAAAAAAA[-/AAA]AGCTTTGAATAAATT | 9063 |
rs80197386 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856978 | TGCCTCAGTTTCTAC[A/T]TCTGTTAAAGATGGA | 9063 |
rs80198277 | snp | C/T | 0.178465 | 0.239547 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46908105 | TACTTCCTATGTGTA[C/T]GCTATATATCAAAAG | 9063 |
rs80241183 | snp | A/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858223 | ACAGGAGATAAGATT[A/T]AAAAAAAAAAAAAGC | 9063 |
rs111261294 | snp | A/G/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855342 | GAATAAAAAGCAACT[A/G/T]ACAGGCAAAGGAAAT | 9063 |
rs111297750 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870390 | GGAGGCCGAGGCAGG[C/T]GGATCACAACGTCAG | 9063 |
rs111327265 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856157 | ACTACAGGCGCCCGC[C/T]ACCACGCCCGGCTAA | 9063 |
rs111549455 | snp | C/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914685 | CAGCACTAGCCAGGA[C/T]ATGAACTGCTCTGGT | 9063 |
rs111562382 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899447 | AAAGCTCACCACTGC[C/T]GAACCAGAGTAATCT | 9063 |
rs111567725 | snp | A/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884500 | GTGTTTTTAGTAGAG[A/T]CGGGGTTTCACCATG | 9063 |
rs111664318 | snp | A/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46836323 | AACAGCTGTTGTATT[A/T]GTCCATATCAGCTGT | 9063 |
rs111688438 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884761 | TCTCTACTAAAAATA[C/T]AATAAATTAGCCGGG | 9063 |
rs111712247 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865267 | AAATGAGGCCGGGCA[C/T]AGTGGCTCACACGTG | 9063 |
rs111750080 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913161 | AAATGGGGAGAGGAG[C/T]GTGATGAGGACCTCT | 9063 |
rs111750347 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849135 | ATTTAAGACATAACA[C/T]TGTCTGACACAGTAG | 9063 |
rs111764132 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870544 | TGGCGTGAACCCAGG[A/G]GGTGGAGCTTGCCGT | 9063 |
rs111800303 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915433 | GATGCTTACTGCATG[G/T]GCCCAGCCTGCACCC | 9063 |
rs111824091 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861137 | ATACAAAAATTAGCC[A/G]GGCATGGTGAAGAAT | 9063 |
rs111909936 | in-del | -/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834021 | TTACACTTAATATAC[-/T]TTTTTTTTTTTTACC | 9063 |
rs111947715 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46877258 | AGAAATGTTAAAAAC[A/G]TTTGAAGAGGAAGAA | 9063 |
rs111973370 | snp | C/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870311 | ACTAGCTCAGAAGTT[C/T]GAAATTTAAAAAAGG | 9063 |
rs112144628 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809696 | GTAGGTGGAGGTTGC[A/G]GTGAGCCAAGATCGC | 9063 |
rs112191574 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817422 | ATTGAAATTAAAAAT[A/T]GAAGCTCTATCACCA | 9063 |
rs112217640 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816087 | CAACATCAGTTCACC[C/T]AGACCTCCCTGTGTG | 9063 |
rs112341033 | snp | A/C/T | 0 | 0 | splice-donor-variant | PIAS2 | GRCh38.p7 | 18:46855343 | AATAAAAAGCAACTT[A/C/T]CAGGCAAAGGAAATA | 9063 |
rs112363277 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920494 | CTCACTCTGCCTCTG[G/T]ACTGGCCAGTTTTCT | 9063 |
rs112384752 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46844823 | TGCCGTACAAGATAT[A/G]CAGACATAGAGTAAT | 9063 |
rs112384907 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839641 | AGGCCGAGGAGGGTG[C/G]ATCACCTGAGGTCAG | 9063 |
rs112427539 | in-del | -/GT | 0.5 | 0 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919031 | TGTGTGTGTGTGTGT[-/GT]TGTGTATATATACAC | 9063 |
rs112534538 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46908132 | AAAGAAGTTTGGTTT[C/T]TTATTATAAAAAATA | 9063 |
rs112551799 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844509 | TATTAAATTTGTAAA[C/T]AGAAAAGATAAAAAT | 9063 |
rs112572892 | snp | C/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46819072 | CAAGTGATTGGTAAA[C/T]TGTGTCTATGCTACT | 9063 |
rs112604286 | snp | A/G | 0.48498 | 0.0853497 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884575 | CTCGGCCTCCCAAAA[A/G]TGTTGGGATTACAGA | 9063 |
rs112618275 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879384 | ATCAGGATGGTCACT[A/G]TAAAAAAAAATAGTA | 9063 |
rs112628118 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46891934 | ATTCTGAACTCAGAG[A/G]CAAATCACACTTGGG | 9063 |
rs112688509 | in-del | -/A/AA | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864769 | AGTGAACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA | 9063 |
rs112743728 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901145 | ACTACAGGCTGGGTG[C/T]GGTGGCTCACACCTG | 9063 |
rs112749646 | snp | A/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814182 | TAATTGTAGCTACAA[A/T]GACAAGAATTAAGGG | 9063 |
rs112771838 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831174 | ATCTATAATAAAGCT[A/G]CTAGAACTACTAAGG | 9063 |
rs112786041 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870216 | CCCTCCACCTCTAAG[A/G]AATCAGCCCCAACTC | 9063 |
rs112788937 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886869 | ACAAATAAAATCGAA[C/T]AAAATAAAATACTTG | 9063 |
rs112892032 | snp | A/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840576 | CCACAGCATACAGAA[A/G]CGAGAATATCCAGGA | 9063 |
rs112912486 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870652 | AAAAAAAAGGAACTC[A/G]AGTCATTATTAGATG | 9063 |
rs112914794 | snp | A/C | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834325 | CAAAGGTCACAATAA[A/C]TACAAATAAAAGGGA | 9063 |
rs112927638 | in-del | -/A | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895076 | GAAACTCCATCTCGG[-/A]AAAAAAAAAAAAAAA | 9063 |
rs113080982 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821283 | TCTCAACAGCAGCTG[C/T]GACATAAGAGCAAGT | 9063 |
rs113107644 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850483 | TATTGCTTCCTCGAA[C/G]TATAAGGTTTGTTGC | 9063 |
rs113119505 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839959 | CGAGGTCAAAAGCTC[A/G]AGACCAGCCTGACCA | 9063 |
rs113153668 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919209 | TACAAAAATTAGGCC[A/G]GGAGCTGTGGCCCAC | 9063 |
rs113187189 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910110 | GCGGTGAGTCAAGAT[C/T]GCGCCACTGCACTCC | 9063 |
rs113210566 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46810677 | GGATTTGTGGAAAAC[C/T]ATATGAATTTAAATC | 9063 |
rs113345428 | snp | A/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837539 | CATTTATGTTATTTA[A/T]AGGCACTCTTTATAT | 9063 |
rs113371808 | snp | A/G/T | 1.71702e-05 | 0.00292998 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846886 | AAATCATCTGCAGGA[A/G/T]GATTAAACATTTTCT | 9063 |
rs113399746 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832440 | AAACAAACAAACAAA[A/C]AAAAAAAAGTGGGCA | 9063 |
rs113417732 | snp | C/G | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866257 | AGAAAACTACCTAGT[C/G]ACATCATAGTCATAC | 9063 |
rs113470028 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904194 | CTGTACTATGGTCTT[A/T]AAGATGTTAACTCTG | 9063 |
rs113500934 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46851408 | TGTTTAGAAGAAAAA[C/T]AATCCAGCTTCTTAA | 9063 |
rs113535584 | snp | C/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821310 | AAGTTGACATTCAAA[C/T]ACAATGTACAGTGCT | 9063 |
rs113556859 | snp | C/T | 0.5 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885452 | CTTGAACTTGGGAGG[C/T]GGAGGTTGCAGCTAG | 9063 |
rs113647154 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880388 | AGACCCTGTCTCAAA[A/C]AAAACAAAACAAAAC | 9063 |
rs113716258 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842270 | AAAAAAGGATATGTT[A/G]TGAATGCAAAAAAAA | 9063 |
rs113747245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895442 | TCGGGAGGCCAAAGC[A/G]GGCGGATCATCTGAG | 9063 |
rs113887072 | snp | A/G | 0.0132679 | 0.0803611 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890743 | AGGAGAGGATGGTGA[A/G]TGAGGTGTAACTGAA | 9063 |
rs113913745 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851904 | CCACCATATTCAGAG[C/G]TCTAATGGGCAATTC | 9063 |
rs113946841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860345 | CATCCGAATCCAGAA[C/T]GTACAATATGCTAGA | 9063 |
rs114029862 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861149 | GCCAGGCATGGTGAA[A/G]AATCGCTTGAACCTG | 9063 |
rs114037070 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888027 | AAAGTAGCAGAATAC[A/G]AAGTCAACACGCAAA | 9063 |
rs114057769 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820014 | ACATGGAAAATTCCA[A/G]AAATAATTCATAAGT | 9063 |
rs114084493 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870319 | AGAAGTTCGAAATTT[A/G]AAAAAGGAACTCAAG | 9063 |
rs114091764 | snp | A/G | 0.0341408 | 0.126114 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46811105 | TTCAAAGTGCACCCA[A/G]TAAAACCTCAGAGGT | 9063 |
rs114091962 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835020 | CCACCTTCAAAAATG[C/T]TAACATCACAGGGCA | 9063 |
rs114095511 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868268 | TTAAGCTCAACTTCC[C/T]TGTCCCTTCTCCTAA | 9063 |
rs114135676 | snp | C/T | 1.65649e-05 | 0.00287788 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846837 | TTAGGCGGTGGTGCA[C/T]AGCCCTATAACCGTA | 9063 |
rs114140692 | snp | C/T | 0.000743365 | 0.0192647 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46846827 | AATCCCATTTTTAGG[C/T]GGTGGTGCATAGCCC | 9063 |
rs114202049 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905519 | GAAGGATACACTAAA[C/G]AGCATAAACAATATC | 9063 |
rs114224145 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853182 | CTAAGGAGAGTGAGA[C/T]GGGAGAATCGCTTGA | 9063 |
rs114237381 | snp | C/T | 0.0248432 | 0.108648 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918456 | TGCCCCCGCACCCCG[C/T]AAGTTTTGTTTTTTT | 9063 |
rs114243916 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912969 | AGATTACAGCCTTGA[A/G]CCACTGCGCCCAGCC | 9063 |
rs114312939 | snp | C/T | 0.0256215 | 0.110247 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827796 | TCCATCAAAATTTGC[C/T]TCCTATAAACAATGT | 9063 |
rs114351839 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901859 | TTTCCCTCTAATATT[A/G]GGACTGAGGCAAAGA | 9063 |
rs114368266 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832513 | AAATACGCAAAAAGA[C/T]GCTCAAAACAATTAG | 9063 |
rs114378248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863261 | TGCCCCAGTTTGGAA[C/T]GATAAAGCTTATGGT | 9063 |
rs114385081 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849967 | TCTAATAAGACTTTA[A/G]AAACCCACAGCATTA | 9063 |
rs114416555 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875909 | GGTAATGAATTATGC[C/T]AAGCTCTCTCTTGGC | 9063 |
rs114464252 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868884 | GCCTCAGGGATGAGG[A/G]ATCAAGACCTCCCCC | 9063 |
rs114467524 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894734 | TTGAAACACTACATA[C/T]AAAGATGAAGGCAAG | 9063 |
rs114552666 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913644 | GTAGATTAACCAGGT[A/T]AAAGTGTAGCAGGGA | 9063 |
rs114554410 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856737 | TATTGCCCTTAGCCA[C/T]TGTCATAAATCTTGG | 9063 |
rs114580282 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875117 | TCAAACTAACCATCC[C/T]TTAACCCTTCAGTTT | 9063 |
rs114592701 | snp | C/T | 0.0418186 | 0.138422 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46908027 | GCTGGTAATGTTCTC[C/T]TTCTTGACCTGCACG | 9063 |
rs114594634 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861698 | CCCAAATCAGAAAGA[A/G]TCTACAAAACACCTG | 9063 |
rs114596483 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829662 | TCCAAACGTATAGTT[C/T]TAGGGGCCAAGATTA | 9063 |
rs114649549 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831064 | GACTAGTCAATGCAA[G/T]GCGGTGGGAAAACAA | 9063 |
rs114702228 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912129 | TTTGGCTTTTAAATC[C/T]CAAAAGGAAAGGGAT | 9063 |
rs114708418 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894594 | TGTGTAAAAAGATAC[A/G]TAATCTAAATTCTAA | 9063 |
rs114732952 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823508 | GTGAATGTACCTACA[C/T]ACCTGTCTGTCACTA | 9063 |
rs114738114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813540 | TTTAAGTTTGTCATT[A/G]GTTCAACTGTATGAA | 9063 |
rs114789758 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856346 | CACTGGATATTCTTA[C/T]TGATCTCAAGTACAG | 9063 |
rs114805229 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843376 | AAGTTCTTCTTAACC[A/G]GAAAGGGTTCCCCTC | 9063 |
rs114814936 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818880 | TGTTTGCTCAATATC[A/C]GCTTGAAACACATTT | 9063 |
rs114819161 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825034 | AAAATAGTTGCTCAC[A/T]TAATTTCGGGGCTGT | 9063 |
rs114819878 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903731 | ATCTCCGAGAAAGAT[A/G]TGTGCGTAAGTTTAC | 9063 |
rs114853608 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817356 | TTTCAATTAAAATAC[A/G]CAAGCTTGATATAAA | 9063 |
rs114877915 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886310 | GCTAGTCCTTCAACA[C/T]AGATAAGGAAAAAAA | 9063 |
rs114914015 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826022 | TAAGAGTTCTTCCGT[A/G]TATTAATGTGTATGT | 9063 |
rs114953859 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914412 | GGCTGGTATTCTGGT[C/T]ACCCGGACTGAAAGG | 9063 |
rs114983808 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834864 | CCTGTTGGCATGAGA[A/G]TGAAATGATTTACTA | 9063 |
rs115001087 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907075 | CTCTTGATGCCTTCC[C/T]CGGAGATATCTGCCA | 9063 |
rs115015056 | snp | A/G | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906474 | TTAGGAGTATAGCAA[A/G]GTTATTATACAAAGT | 9063 |
rs115016655 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870231 | GAATCAGCCCCAACT[A/C]TTTTCCCCTTGAGGG | 9063 |
rs115017073 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814042 | TTTTTGATTGCCTTA[C/T]AGGAAAAAGATACTC | 9063 |
rs115020263 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840207 | ACCTCAAAGACATTT[C/T]ATGTATGTGGGCTAT | 9063 |
rs115074212 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846511 | GAAAATAAAGAGATG[A/T]TATTCAGGAAAGCTC | 9063 |
rs115095049 | snp | C/G/T | 0.000181386 | 0.00952168 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890734 | AGAACCAACAGGAGA[C/G/T]GATGGTGAGTGAGGT | 9063 |
rs115158075 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834865 | CTGTTGGCATGAGAG[G/T]GAAATGATTTACTAG | 9063 |
rs115271233 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902400 | CGTCTCTACTAAAGA[C/T]GCAAAAAAAATTAGC | 9063 |
rs115333970 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908936 | ATCTCTTGAACCTTG[A/G]GGGTGGAGGGTGCAG | 9063 |
rs115351599 | snp | A/G | 0.0046482 | 0.0479843 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829689 | ATTAATGATAATGTT[A/G]CACGAGTCTCACTGC | 9063 |
rs115357197 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | PIAS2 | GRCh38.p7 | 18:46841688 | AGTGCTCTGAAAAGA[C/T]TGATGAACCCCCAGG | 9063 |
rs115379109 | snp | A/T | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907562 | GAATACAGTTGACCT[A/T]TGAATAACAATAACA | 9063 |
rs115424472 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46834239 | AACTTTCTAAACACT[C/T]TCAAGGAAGACATTC | 9063 |
rs115435246 | snp | A/C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886383 | TATATAAATGAACCA[A/C/T]GACATTGTGCATGAT | 9063 |
rs115505402 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914437 | GAAAGGCAACAAGGT[A/G]TAGAGCTGCCATATT | 9063 |
rs115514707 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886947 | TTCATCTAAAAATCA[A/C]AGAGATCTGTTTTCA | 9063 |
rs115523454 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863734 | GACTTTAGTCAAAGT[A/G]TACTACCCTTTCATG | 9063 |
rs115528593 | snp | C/G | | | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823846 | GCAGGCTTTTGTTAT[C/G]AAAATCTTCACAAAG | 9063 |
rs115569866 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876995 | GTGAGCCACAGTGCC[C/T]GGCCTCCTTCACTAA | 9063 |
rs115599755 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895154 | AATAAAAATATTTCC[C/T]TGAGATTGCTCTTCA | 9063 |
rs115604453 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848388 | CAGCTAACCAGTCAC[A/G]CCATGCCAATAACAT | 9063 |
rs115618132 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914812 | TTTCTCTACTGCCAA[C/G]AAGTTAGCCAACAAA | 9063 |
rs115633748 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912735 | TATATTTTTAGACTT[C/T]TGGAACAACAATAAA | 9063 |
rs115659546 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852282 | TTCTATAGGACTTTA[C/T]GGAGCTAGGGTAAAA | 9063 |
rs115691292 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895932 | TGGGTTTCTCCCTTA[C/T]AAGATAATGATTACA | 9063 |
rs115739186 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813448 | AGCATTATATCAGTA[A/T]AGAATATTTTTATGT | 9063 |
rs115782618 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814110 | TCAACAGGCTCTGTG[C/T]GTTGAATTCTTAGTA | 9063 |
rs115785872 | snp | A/T | 0.0509478 | 0.151255 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825009 | TGTCTCAAAAAATTA[A/T]AAAAAAAAAAAAATA | 9063 |
rs115800586 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907761 | CCACATATACAGAGG[A/G]CCAACTTTTCCTATA | 9063 |
rs115805160 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916958 | AGACACGTACACCCC[A/G]GTGAAGGTGCAAGAT | 9063 |
rs115857693 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838709 | TCTCATAAAATCTTC[A/G]TAACTCTATGACTCC | 9063 |
rs115867632 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900214 | TACAGAAAATAAAAA[A/T]TTAGCTGGGTGTGGT | 9063 |
rs115924196 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PIAS2 | GRCh38.p7 | 18:46885769 | AAGCCATGAGGATAC[A/G]TGTATTTCTGGCATT | 9063 |
rs115929032 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871799 | GATCAGCCCACTTTC[A/C]ATTTCTGTTAATCCC | 9063 |
rs115980832 | snp | C/T | 0.000430043 | 0.0146573 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829750 | TTCTATTTTTGTACA[C/T]GGTTGGCTGGATACT | 9063 |
rs115995524 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921877 | ACTTTACTGATTTTA[A/C]TATCTCTCTTTTCCT | 9063 |
rs116005265 | snp | C/T | 0.00392136 | 0.0441056 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890674 | AGGAATTGGGGGAGA[C/T]GGCTGCTGCATCTCA | 9063 |
rs116007544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46822170 | TTTGTACTCTGGAAA[A/G]CTATTTCATAACCTC | 9063 |
rs116047518 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842729 | TGCCTGAAGGTTTGC[A/G]TAGAGCCTGCACTCA | 9063 |
rs116047745 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908406 | ATGGCATCCAAACCA[C/G]TGAAGAAAAAAATTT | 9063 |
rs116049692 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850382 | TGCCATCTCCAAACA[A/C]ACACACTTTTTCCCC | 9063 |
rs116050179 | snp | C/T | 0.0263992 | 0.111815 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826252 | CACAGATGTAAACTA[C/T]CCTTATTCCTCTGCA | 9063 |
rs116091921 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818867 | TGGATATTAGTCTTG[A/T]TTGCTCAATATCAGC | 9063 |
rs116099168 | snp | C/T | 0.0581099 | 0.160244 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824499 | GAGGTTTTCTAAATG[C/T]CTTAAGATTAACATA | 9063 |
rs116102106 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891299 | GTAATCTATAGTCTA[C/T]TGGTTTCTACTAACC | 9063 |
rs116146720 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896477 | CACCAAGCTTTCAAG[C/G]AAAGGATGGAATTCT | 9063 |
rs116182649 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46829819 | ACCATCTTCTTGGAA[C/T]TTGATCTCATCTACA | 9063 |
rs116271713 | snp | A/G | 0.000198046 | 0.00994906 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820965 | ATGCTTGATATTGGC[A/G]TATGGTGGAATGGTA | 9063 |
rs116276854 | snp | C/T | 0.0644693 | 0.167566 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892541 | GCTTTTGGAGGCCAA[C/T]ACAAGAGGATCACTT | 9063 |
rs116295744 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854788 | GGGAATTTTTGATCT[C/T]TGTAGTTAGCCACTC | 9063 |
rs116331138 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851149 | CAGGCCATCAGGGTA[A/T]CTAACACACAACATC | 9063 |
rs116350989 | snp | A/G | 0.000329685 | 0.0128349 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890758 | GTGAGGTGTAACTGA[A/G]GTGGAAGGCAACGAG | 9063 |
rs116364674 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895811 | AAGCCAGAAAGATAC[C/T]GCTTACTCTTTTCAA | 9063 |
rs116391789 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46877713 | GAACCAGGGAATAAC[C/T]GCGTTAGGGATAAAA | 9063 |
rs116400299 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870900 | TAACAATGCAGCTCA[A/C]CAAGAGAATATGAAA | 9063 |
rs116406972 | snp | A/G | 0.00147423 | 0.0271098 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46855608 | TCCTACCACCTGGCA[A/G]AAAATCCCTGTTGGA | 9063 |
rs116424627 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854166 | AGGGTCAGTCTCAGT[C/T]ATGGAATTTCTTCAC | 9063 |
rs116425739 | snp | A/G | 0.0652144 | 0.168387 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916707 | TGCAGATTTCTTACT[A/G]AAACACTAAGAAAAT | 9063 |
rs116426062 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862436 | CTCAAAGAGTGTTCT[A/G]ATTAATATCTGAAAA | 9063 |
rs116451202 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838541 | TCAAGGTATGTGGCA[C/T]GATATAACTCATCAC | 9063 |
rs116455407 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828439 | CCTACTGCTCATCCT[A/G]TCTCTGCAGGTCAGC | 9063 |
rs116464755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855880 | CAAAATTTATTTCAA[C/T]AGACATCAAACTTGG | 9063 |
rs116485430 | snp | A/C | 0.0256215 | 0.110247 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46824408 | TTAGAATACCTTCTT[A/C]TTAAGGCAAAGCAAC | 9063 |
rs116522191 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856903 | GCACAGCAGTGACAA[C/T]CACCTTAAGTTCTAC | 9063 |
rs116522644 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914192 | ATATATAACACATTA[C/T]TGTAACCATCTTTGA | 9063 |
rs116577469 | snp | A/G | 3.29886e-05 | 0.00406118 | missense, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890892 | TTCGTGGATATCGGC[A/G]TCTATACAATTCTCG | 9063 |
rs116583742 | snp | A/T | 0.078151 | 0.181571 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46827300 | AAATACCCAAACCTG[A/T]TTTTTAATGCAGGTC | 9063 |
rs116601180 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46813342 | GTCCCCTTACAATCC[C/T]GGTTACTGATCCCAT | 9063 |
rs116640407 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912146 | AAAAGGAAAGGGATC[A/G]GTGTTATATCTTTTT | 9063 |
rs116771966 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893042 | GGTAGCTCTAAATCA[C/T]ACTCTAATAGAACAC | 9063 |
rs116774824 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882786 | TACTGTTAAGAAAGA[C/T]TGTCACGGTGCAAAA | 9063 |
rs116799177 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875387 | CCACCCCATCAAATT[G/T]TAAGTCACTGCAATG | 9063 |
rs116871366 | snp | C/T | 0.0170251 | 0.090679 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46808042 | GAGATATAATCTAAA[C/T]TGTTCAAAATAAGTA | 9063 |
rs116962257 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864912 | AGAATTAAATGTTTT[C/T]TGTTTATTTTTCTTT | 9063 |
rs116968615 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918049 | TGAAGGTCACGGACT[A/G]CAGAGTTGGGAGAGT | 9063 |
rs116999500 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888734 | GTTCACAGTAGGGTT[A/C]CTGCACCTATGAGAA | 9063 |
rs117042984 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888037 | AATACAAAGTCAACA[C/T]GCAAAAATCAATTGC | 9063 |
rs117053250 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915205 | GGTTAACCTCTCTGT[A/G]CTTCAATTTCTTGAA | 9063 |
rs117089559 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916084 | TATGGGGCATAACAT[C/G]TATTAATATGTGTTT | 9063 |
rs117151539 | snp | C/T | 0.0147112 | 0.0844936 | utr-variant-3-prime, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46812480 | TTCCACTGCTGGTTA[C/T]GACCCCTGTCTCACT | 9063 |
rs117185943 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913356 | CCCAAATCTGATCTT[C/T]GAATTATGACACAAC | 9063 |
rs117218470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835672 | AAAAATCATATGTAT[A/G]TATTAATATAAATCA | 9063 |
rs117219441 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826945 | CACAAAAAAACGATT[A/G]CCTAGATTTGGGGTG | 9063 |
rs117324999 | snp | A/C | 0.0170251 | 0.090679 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46816588 | CCTCAGCTTCGCAAG[A/C]AGCAGGAGCTACAGG | 9063 |
rs117391297 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823097 | AAAAAAAGCCACATA[C/T]GCTGAAGTATGCCTA | 9063 |
rs117478468 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808422 | GGTACAGCTTTATTT[A/C]TTTCTTTTAGGAATT | 9063 |
rs117639644 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883723 | GGTGCATGCCTGTAG[A/T]CACAGCTACTCAGGA | 9063 |
rs117647727 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910215 | TGTTAAAAGTATAAA[A/G]ACAGACCAGGAATGA | 9063 |
rs117727967 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889728 | TCCACTTGTGGGTAT[A/G]CAGCCAGAAGAATTG | 9063 |
rs117738269 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PIAS2 | GRCh38.p7 | 18:46869877 | TTATGCCCTGTATTG[A/G]CAGCAGGGACCCATC | 9063 |
rs117773149 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910907 | CAGAAAGTTTATCAC[C/G]AGCATATCCTTCCAG | 9063 |
rs117774215 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872274 | CAAAATACCATATGA[C/T]CATCAATGGTTTACA | 9063 |
rs117884261 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46895040 | ACCATACCATTGCAC[G/T]CCAGCCTAGGCAACG | 9063 |
rs117891701 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875219 | ATGTCCGTACTGTAG[C/T]GAGTCAACAAAGTAT | 9063 |
rs117891983 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814481 | TAATGAGGTCAACTC[C/T]GAATGATAAGAAATT | 9063 |
rs117910298 | snp | G/T | 0.0165278 | 0.0893908 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921767 | TAATTTTAGCAAAGA[G/T]CATTCCAACCTGGTT | 9063 |
rs117912202 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910377 | ATGTTTGTTTACATA[C/T]GCCTTACCTGTTATA | 9063 |
rs117970394 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874498 | CCCTGGCACTCACCT[C/T]CATCAGGAAGAGTAG | 9063 |
rs118030134 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862721 | TATGTATATATTCTT[C/T]TGAGATAGAGTTTCA | 9063 |
rs118036342 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831991 | CTTCTGCTTTTTGAC[A/T]TACACTGTTAAAAGA | 9063 |
rs118113327 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850845 | TGTTTCCATAAAGAG[A/C]TTGACCACATCAACA | 9063 |
rs118162785 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911943 | GTAATCCCAGCTAAT[C/T]GCGAGGCTGAGGCAG | 9063 |
rs118185482 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | PIAS2 | GRCh38.p7 | 18:46856817 | TGGAGTACACTGAGC[A/C]CCCATGGTGCTCTAA | 9063 |
rs137874196 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808423 | GTACAGCTTTATTTA[C/T]TTCTTTTAGGAATTG | 9063 |
rs137886690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848698 | AAAAACGTTTGAGCA[A/G]GGGAATAAAAGACAA | 9063 |
rs137907483 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888855 | GTGCGACCTGGTTTC[C/T]AACAGGCTGTGGACT | 9063 |
rs138022745 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46843458 | CCTAACTGTAAGTGA[A/C]GTCTGCACCATTTTT | 9063 |
rs138034257 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883076 | GCACTGCAGCCTGGG[A/C/T]GACAGAGGGAGACTC | 9063 |
rs138049425 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874147 | GATAATTGTTTAATA[-/T]GCAAAAAAACTAATA | 9063 |
rs138126106 | snp | C/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921303 | CAGCTAATTTTTGTA[C/T]TTTTAGTAGAGATGG | 9063 |
rs138148883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46907939 | GCAATACTAATCTGT[C/T]AAAGTTAGGATAGTA | 9063 |
rs138151081 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PIAS2 | GRCh38.p7 | 18:46876922 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 9063 |
rs138170007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887954 | GATGGTAGGCTCTTA[C/T]ATACAGTAAACCTTA | 9063 |
rs138170080 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832479 | GTCACTTCACCAAAG[A/C]AACGTACAGATGGAG | 9063 |
rs138199148 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838236 | TATAGTTCTACCTAC[G/T]TGCAAGGTACAGTGT | 9063 |
rs138207310 | in-del | -/TT | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46902751 | AAGGCAAAAGAAATA[-/TT]AATAGAACAGCCAAA | 9063 |
rs138241863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861154 | GCATGGTGAAGAATC[A/G]CTTGAACCTGGGAGG | 9063 |
rs138303939 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46817026 | ATTTTCAATATTTCT[A/G]TTATTAAGTAAAAAA | 9063 |
rs138349069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46853334 | TTAGCACATCTAGGG[C/T]AAAGAAAAATGGTTA | 9063 |
rs138413801 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900923 | AGGTTGCGGTGAGCC[A/G]ACGTCGTGCCATTGT | 9063 |
rs138429232 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809481 | TTATTTTGGCCAGGC[A/G]CGGTGGCTCACGCCT | 9063 |
rs138431998 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912327 | CTACGTACTTTACAT[A/C]ATTTCTAGTTTACAA | 9063 |
rs138436433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825863 | CCTTATGACGAGATC[A/C]ATCTTATCAATGTAT | 9063 |
rs138516896 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46858653 | AGTGAGCCTTGATTG[A/C]GGCACTGTACTTTCA | 9063 |
rs138578149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46888501 | CCAAGACATATTACA[C/T]AGCTACGGTAATCAA | 9063 |
rs138585966 | in-del | -/GGTTT | 0.0569829 | 0.158885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903238 | AACCTGTGCTACGCA[-/GGTTT]AAAGACCCCTTTAAA | 9063 |
rs138627575 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892559 | AAGAGGATCACTTGA[G/T]CCCAGGAGTTCGAGA | 9063 |
rs138641733 | snp | C/G | 0.029116 | 0.117091 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917720 | CCTGCGGACTGCCTA[C/G]AGCTGGGTCGCAACT | 9063 |
rs138668513 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844404 | AATTAGGAGAGGAAG[C/G]TGGAATGCAGCAGTA | 9063 |
rs138688719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838668 | TTAAACAGAATCTTA[C/T]AGTATGCCCAAGGCT | 9063 |
rs138699699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882710 | TACTGGGTAAGTTAC[A/G]GTACATCTATAAGAT | 9063 |
rs138728595 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831542 | CTACAATAGCCAAGA[C/T]AATTTTGAAAAAGAA | 9063 |
rs138773687 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848069 | ACATATTCCCTTTTG[C/T]ACAGAAGAAACTTCT | 9063 |
rs138838652 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46901439 | TACAAACCAATATTC[A/C/G]TCATGAATATAGACG | 9063 |
rs138856787 | in-del | -/TTATT | 0.0376037 | 0.131863 | intron-variant | PIAS2 | GRCh38.p7 | 18:46837345 | TGAACTACATTCCTC[-/TTATT]TTAAGTGGTAGTTGA | 9063 |
rs138904142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46823578 | AACATGAAACTTTAA[A/G]TGAGTAAATAGCTAC | 9063 |
rs138968540 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PIAS2 | GRCh38.p7 | 18:46860335 | AAGAAGCAATCATCC[A/G]AATCCAGAATGTACA | 9063 |
rs138975253 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897037 | TGTGTACTGGGGACA[C/G]GAAGAATTTTCTATC | 9063 |
rs139008659 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912724 | GAAAGGCATGGTATA[C/T]TTTTAGACTTTTGGA | 9063 |
rs139038851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46833364 | GAAACAGAAAGCATA[C/T]CAGTGTTTGCTTGAG | 9063 |
rs139040964 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864403 | TACTAAACTGCATTC[A/C]TCTTGGAATCATGAG | 9063 |
rs139049322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865927 | CTTTTTTTCTTGTTC[A/G]GACTCCACTTTTCAC | 9063 |
rs139050294 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915137 | TCTAAAAGCTACATG[C/T]CTAAGATTAAAAATC | 9063 |
rs139192090 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871082 | TAGACTTAGAAGACC[C/T]TCTTGGGCAGGGAAT | 9063 |
rs139195196 | snp | G/T | 0.0178098 | 0.0926698 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918492 | GGAGTTTTGCTCTTG[G/T]TGCCCAGGCTGGAGT | 9063 |
rs139214642 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898233 | CACCATCTTGGCTCA[C/G]TGCAACCTCTGCCTC | 9063 |
rs139234180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850730 | TCCCCGTCAAGCTTC[A/G]GCATCCATTGATGAT | 9063 |
rs139234937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873207 | GGAAGATGGCTCACC[A/G]ACTCAAGGATTTTAA | 9063 |
rs139277152 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878368 | ACCAAAATTTCAGGA[A/G]AAAACAAGCAGTTCA | 9063 |
rs139315825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828543 | CAGCTATGTATTCTC[A/G]CACACATGTGGCACA | 9063 |
rs139344561 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845134 | ATTTAGCAAAACTGG[C/T]ACCTTAGGGGCCACC | 9063 |
rs139442776 | in-del | -/AA | 0.0146672 | 0.084371 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46810396 | CACACAAACCAAGTT[-/AA]GTTTTTTCTATCTGA | 9063 |
rs139465932 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879880 | ATATGAGAAATCTAG[A/C]GTAGTCAGAATCTTA | 9063 |
rs139565840 | snp | A/C | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887250 | AAATAAAGCAAAAAG[A/C]AAAAAATTGAAAAAA | 9063 |
rs139644913 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46893899 | TGGGAGGCAAGGCGG[G/T]TGGATCATTTGAGGT | 9063 |
rs139656287 | snp | A/C | 0.0018264 | 0.0301639 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46818355 | CACTCCATAAATACA[A/C]ATTATTTGTTTTATT | 9063 |
rs139666531 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897371 | GCTATCAAAGATCAC[A/G]GGGCCTTGTCAGAAG | 9063 |
rs139847349 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889795 | GTCCACAGAATTATT[C/T]GCAATAGCTAAAATG | 9063 |
rs139850490 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46811215 | ATTCAAACATTTCTA[A/T]TTCTCTTTTGTCGTT | 9063 |
rs139859271 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46910684 | AAACCTTTCAGAATG[C/T]AAACAAATCCCGTAG | 9063 |
rs139879672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914198 | AACACATTATTGTAA[A/C]CATCTTTGAGCACAC | 9063 |
rs139907072 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832651 | ATCCCAGCACTTTGG[A/G]AGGCTGAGGTGGGTG | 9063 |
rs139910457 | in-del | -/AAAA | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46870616 | GCAAGACTCCGTCTC[-/AAAA]AAAAAAAAAAAAAAA | 9063 |
rs140095274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850608 | ATGTTGCATACTTCA[C/T]ATGGTGCTACATCAT | 9063 |
rs140107718 | in-del | -/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46842241 | AAAAAAAATTTAAAA[-/T]AAATTAAAAAAAAAA | 9063 |
rs140114935 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854783 | AAGCTGGGAATTTTT[G/T]ATCTCTGTAGTTAGC | 9063 |
rs140183979 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884878 | GCTGAGACCGTGCCA[C/T]TGCACTCTAGCCTGG | 9063 |
rs140212101 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863733 | TGACTTTAGTCAAAG[C/T]ATACTACCCTTTCAT | 9063 |
rs140225692 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835107 | TCACAAAATATTAAT[A/G]TGCAAAGGGGCATGA | 9063 |
rs140226715 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904163 | TTGTGTTCATGTCAA[C/T]ATCCTGGTTGTGATA | 9063 |
rs140227915 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889248 | ATTGGAATTTCATGA[A/G]AAAATGTTAAGTTGT | 9063 |
rs140228777 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46813326 | TGCTCATATTTCACA[A/C]GTCCCCTTACAATCC | 9063 |
rs140249009 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891484 | ATCAGATTTTCACAA[C/T]GTTAGATGTGTAACT | 9063 |
rs140287397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870160 | GGAAGGCTCTAGTGT[A/G]AGACAGAACAGTGTA | 9063 |
rs140387989 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842921 | TAAAGGCAAATTCAT[A/G]TTTTTAAGTTAATGA | 9063 |
rs140468928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46886801 | CGAGACAGCGCCACC[A/G]CCCTCCATCCTGGGC | 9063 |
rs140488916 | snp | A/G | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921214 | CTCACTGCAACCTCT[A/G]CCCCCCCGAATTTAA | 9063 |
rs140498072 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838100 | GAGGCAGGCTTTTTA[G/T]GATGTTCTTTTTCTT | 9063 |
rs140598945 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915480 | TTCTCCCCAGTTAGT[C/T]TCTGTTGGGCACGTC | 9063 |
rs140609002 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46903534 | ATACCTACCAGAATG[C/G]CTAAAATGAAAAACA | 9063 |
rs140609333 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46889904 | AAACAGCTAAAATAA[C/T]TAAGGTTGTTGCCTC | 9063 |
rs140646377 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PIAS2 | GRCh38.p7 | 18:46908966 | GTAAACTGAGATCAC[A/G]CCACTGCACTCCAGC | 9063 |
rs140648151 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855820 | TCTAGCCACGTCTTT[A/C]TGGCAATTTTAAGGT | 9063 |
rs140685129 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862342 | TCTGTCTCAAAAAAA[A/C]AATTATGTAATTAAG | 9063 |
rs140762308 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46812056 | TTACAATTTTTTTTT[-/T]AATTAGAAAAAAGGT | 9063 |
rs140766038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46815527 | AAACCCAAAGATGAA[C/T]ATATTCTCTGATAAA | 9063 |
rs140790897 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862855 | GGATTACAGGCGCCC[A/G]CCACCATGCTCGGCT | 9063 |
rs140806843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821534 | TCTTCAAGTCTAACT[C/T]GAATTGTATTAATTA | 9063 |
rs140807116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847909 | AGAAAATTAAAATGT[C/T]TTAGCTGCAAAAAAT | 9063 |
rs140984714 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46881422 | GATAAGTGAAAACTG[A/T]ATTTGTAAAAAACTG | 9063 |
rs141097874 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874936 | ACTATCTGCACGGCC[A/G]AAAGGGGATGGACAG | 9063 |
rs141106875 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46887956 | TGGTAGGCTCTTATA[C/T]ACAGTAAACCTTAAA | 9063 |
rs141116434 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46823072 | GGAGACCTTGTATCT[A/C]CAAAAAAAAAAAAAA | 9063 |
rs141126785 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896584 | CTGAACACAAAACAT[A/G]AAATTCAAAAAACAT | 9063 |
rs141144978 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46891246 | TACATTCAAGTTACG[A/G]TGTTAATTATATTTT | 9063 |
rs141184769 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842499 | AACATAATGGTGACA[C/T]GAGTTTCCTCCCCAT | 9063 |
rs141196475 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PIAS2 | GRCh38.p7 | 18:46884398 | GCTCACTGCAAGCTC[C/T]GCCTCCCAGATTCAC | 9063 |
rs141216852 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832780 | GCCTGTAATCCCAGC[C/T]ACTGGGGAGGCTGAG | 9063 |
rs141260986 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851974 | AATACACCAGGATCA[C/T]GGGCAAGGACCACCT | 9063 |
rs141296116 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846537 | AGCTCAGAGTTAAAG[C/T]TTTTAACTTTAAGAA | 9063 |
rs141297906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857272 | GGTGCTGGAGCTTCA[A/G]AGACAAATACAACAC | 9063 |
rs141369263 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826267 | TCCTTATTCCTCTGC[A/G]TACTGAGGTCATTTC | 9063 |
rs141476103 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46906505 | CAAACTGTACTTCTG[A/T]GCACCAGCAAAGTAT | 9063 |
rs141493540 | in-del | -/TTGT | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829024 | ACTCCATTCATTACA[-/TTGT]TTGTTAGAACTTCAA | 9063 |
rs141608391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46852894 | ATAAGCCTTCAAGGT[A/G]AGTCCACAGACACCA | 9063 |
rs141647173 | snp | C/G | 0.0178098 | 0.0926698 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46917807 | CGGGACGCGTGACAG[C/G]AGCATTCGGGAAGAT | 9063 |
rs141664295 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862197 | TTAGCCAGGTATGGC[A/G]GCACCTGCCTGTAGT | 9063 |
rs141668621 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PIAS2 | GRCh38.p7 | 18:46875736 | ATGCCTGGCTGAAAC[C/G]GATTAAATATTCCAT | 9063 |
rs141674300 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46839090 | TTTTTAAGTAGTACC[A/T]ACATAAATATTGGCT | 9063 |
rs141740875 | in-del | -/T | 0.0456336 | 0.143994 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857229 | ATATCACTCCACTCA[-/T]TCATATCAAGACACA | 9063 |
rs141794270 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872086 | CTAAAACCTGTAGTC[A/G]AAGGTCTCATTCAAG | 9063 |
rs141796051 | snp | C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46922135 | AGACAGGGTCTCACT[C/G]TGTCGCCCAGGCTAG | 9063 |
rs141833333 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878011 | AGATTCATTTATAAT[C/T]ACTAAATGAGTAGGC | 9063 |
rs141855097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830515 | AAAATTTATAGCATT[A/G]ATCTTCCCTAATTAG | 9063 |
rs141862934 | snp | C/T | 0.000512375 | 0.0159977 | synonymous-codon, nc-transcript-variant, intron-variant | PIAS2 | GRCh38.p7 | 18:46890923 | GATTTTAATCTGAAC[C/T]GCAGGGCTGCAGCCG | 9063 |
rs141903503 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46865414 | TCATGGTGGCACGTG[C/T]CTGTAATCCCAGCTA | 9063 |
rs142053638 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855058 | GATTGCTTGAGCCTA[C/T]AAATTCAAATCAAGC | 9063 |
rs142086311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896072 | ATTATACAACAGAGA[C/T]TTAAAATAAAGTAGT | 9063 |
rs142117463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868655 | GTTTGGTGTGCTCTC[A/G]CAGCGGCCAGAAGTG | 9063 |
rs142127031 | snp | C/G/T | 0.0111196 | 0.0737302 | intron-variant | PIAS2 | GRCh38.p7 | 18:46898886 | TGTAATCCCAGCTAC[C/G/T]TGGGAGGCTGAGGCA | 9063 |
rs142272256 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809024 | CTGAAGGAAGAACAT[C/G]TGAAAGGTCTGAATG | 9063 |
rs142273225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46851202 | CAGAAATACAATTTA[G/T]AAGGAGAAGGGGGCC | 9063 |
rs142371664 | in-del | -/A | 0.0146672 | 0.084371 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808963 | ATACTTTATTGGCAG[-/A]AAAAAAAGACAACTT | 9063 |
rs142458227 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916029 | ACTTATCAAGTATGA[A/C]CACCCTTTACCTACA | 9063 |
rs142458823 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | PIAS2 | GRCh38.p7 | 18:46915213 | TCTCTGTGCTTCAAT[G/T]TCTTGAAAAAATTGT | 9063 |
rs142460419 | snp | C/T | 0 | 0 | intron-variant | PIAS2 | GRCh38.p7 | 18:46831120 | GTAAAACTGTCTCTA[C/T]TTAAAAAACATTACT | 9063 |
rs142461842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46830073 | GCAACATAATAGTTA[A/G]GTAACTTACTGAGCA | 9063 |
rs142473593 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879453 | ACCCCTGTGCACTGC[G/T]GGTGGGGAATGTAAA | 9063 |
rs142497339 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920511 | CTGGCCAGTTTTCTT[A/G]AGCCAATGCCTTTCT | 9063 |
rs142500683 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46836124 | ATATAATCTTGGAAA[A/G]CAAAAACATTGCCCT | 9063 |
rs142511881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883227 | ACTGTCCCTTTCTTA[A/T]GATTTTTGATTCCAA | 9063 |
rs142642684 | snp | C/T | 0.039522 | 0.134904 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862734 | TTTTGAGATAGAGTT[C/T]CACTCTTGTTGCCCA | 9063 |
rs142657517 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832482 | ACTTCACCAAAGAAA[C/T]GTACAGATGGAGAAT | 9063 |
rs142672816 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46844412 | GAGGAAGCTGGAATG[C/T]AGCAGTACCCTGAGC | 9063 |
rs142691829 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46838305 | AATTACATAACAATT[A/C]TACTAAAAGGATGGT | 9063 |
rs142693220 | in-del | -/TA | 0.0418186 | 0.138422 | intron-variant | PIAS2 | GRCh38.p7 | 18:46873720 | AATTAATCACCCAGG[-/TA]TTAGATAACCTTCAG | 9063 |
rs142698868 | snp | A/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46887238 | TTGCTAAAACATAAA[A/T]AAAGCAAAAAGCAAA | 9063 |
rs142836945 | in-del | -/AC | 0.0441095 | 0.141807 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848793 | GTGTGTGTGTGAGAG[-/AC]AGAGAGAGTAGGAAG | 9063 |
rs142840449 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855488 | TGCTCAAACATTCTT[A/C]TATGTTTTAAAATTC | 9063 |
rs142859803 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842124 | CCTGCTACTCAGGAG[G/T]CTGAGATGGGAAGAT | 9063 |
rs142870881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897438 | TAAGATGAGAAAATT[G/T]GAGCATCAAAAAGAA | 9063 |
rs142909787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46849589 | GAATTTTTTATGTTT[C/G]ATGCTCTGATGACAC | 9063 |
rs142910995 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912976 | AGCCTTGAGCCACTG[A/C/T]GCCCAGCCTATTTCA | 9063 |
rs142947294 | in-del | -/ATT | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46894684 | GAAAATAAACACAAA[-/ATT]ATTAAAAATTTTAAA | 9063 |
rs142952800 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PIAS2 | GRCh38.p7 | 18:46866679 | TGGCATTGAAAGGCA[C/G]GATTTCTAACACAGG | 9063 |
rs142960808 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46919418 | TTGAACCCTGGAGGC[A/G]GAGGTTCCAGGGAGC | 9063 |
rs142963417 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PIAS2 | GRCh38.p7 | 18:46889426 | AAATGGGCAAGAGAC[A/T]TGGCTATACATTTCT | 9063 |
rs142980071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46874275 | CGCCTAAAGTATCTA[C/T]AAGTAATACTGGATC | 9063 |
rs143003490 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900925 | GTTGCGGTGAGCCGA[C/T]GTCGTGCCATTGTAC | 9063 |
rs143042987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46854279 | GTACTGCTCATATAT[C/T]AGTCCAGAGCCCAGT | 9063 |
rs143045254 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857760 | AATATCTTCACAAAC[A/T]TTATGAGTAATGACC | 9063 |
rs143102980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46871357 | ACAAGGGCTACAGGG[A/G]GCCAAAGCTTACAAA | 9063 |
rs143171853 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46891379 | CTATAAAATCTATCA[C/T]CAATGAATATACTCC | 9063 |
rs143218384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46821732 | GAAATCCTAAGAGAG[C/T]TTATGATTTTAAAAT | 9063 |
rs143237975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46914924 | ATCATTTTGAGAATC[A/C]AAGATTATTTCTTCC | 9063 |
rs143252546 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46829478 | TTTGTAACAAACATC[A/G]TATTTTAAAATGATT | 9063 |
rs143295734 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46836589 | GAACATGGTCAGTTG[C/T]AAAAGTCGGAAGATG | 9063 |
rs143355610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905782 | CTACAACCAAAGCAA[C/T]TGAAGCATTCCTCAA | 9063 |
rs143363597 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PIAS2 | GRCh38.p7 | 18:46816467 | TTGAAAATTGTTGCT[A/G]CAGATTTTTTTTTTT | 9063 |
rs143394128 | in-del | -/CC | 0.095934 | 0.196885 | intron-variant | PIAS2 | GRCh38.p7 | 18:46870288 | GGCTTTGTAAATGCT[-/CC]CCCTTCACTAGCTCA | 9063 |
rs143465287 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900135 | TTTGGGAGGCCGAGG[C/T]GGGCAAATCACTTGA | 9063 |
rs143562892 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | PIAS2 | GRCh38.p7 | 18:46906043 | TGTTTAAATATTGGG[-/A]AAAAAATTAATATAA | 9063 |
rs143568767 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46895419 | CTCACACCTGTAACC[C/G]CAGCACTTCGGGAGG | 9063 |
rs143587448 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PIAS2 | GRCh38.p7 | 18:46847686 | ACAGGGTTTCACCAT[A/G]TTAGCCAGGATGGTC | 9063 |
rs143605522 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832357 | GAGGTGGAAGGTTGC[A/G]CTGAGCTGAGATCAT | 9063 |
rs143649527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PIAS2, KATNAL2 | GRCh38.p7 | 18:46916491 | AAATCCATCTCATTC[A/G]TCACACTTAGTTAGG | 9063 |
rs143671116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850665 | TTTCAGTGGTGTCAA[C/G]ATTGATCAGGAGTTC | 9063 |
rs143721331 | in-del | -/GGGGGGGGGG | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46875662 | ACTAAGGTAACGGCT[-/GGGGGGGGGG]GTGGAGGTGAAAGAA | 9063 |
rs143762590 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911853 | GTCAGGAGTTCAAGA[C/T]CAGCCTGACCAACAT | 9063 |
rs143783503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46864456 | CTTTAACGTTAAGTA[C/T]GTAACCATTCTTTAT | 9063 |
rs143906168 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912383 | AAATGGTTGTTATAC[C/T]ATACTGTTTAGGAAA | 9063 |
rs143907783 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46825877 | CCATCTTATCAATGT[A/G]TTTCCTAATATTAAA | 9063 |
rs144019673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46913908 | CCTGGCTTCAAGCGA[C/T]CCTCTTGCCTCTCAA | 9063 |
rs144029498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46814470 | ATATACTGCTGTAAT[C/G]AGGTCAACTCCGAAT | 9063 |
rs144038349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46883481 | GCCGGGGCAGAAGGA[C/T]AGCTTGACCTCAGGA | 9063 |
rs144051868 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46820589 | CTGAAGTTCTGATGA[A/G]CTACCAAGAAGAGTA | 9063 |
rs144058730 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PIAS2 | GRCh38.p7 | 18:46868021 | AGTCCAAGTCATCAG[A/G]TGGCATAGCTGCCAA | 9063 |
rs144073749 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828578 | GCTCAGAACCAGATA[C/T]TTCCATTCTAGCAAT | 9063 |
rs144233257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46890365 | TATGTGTATTTTACA[A/G]TAAAAGAATTGGAGA | 9063 |
rs144249270 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46861240 | TGAGACTTTGTCTCA[A/G]AAAATAAACAAACAA | 9063 |
rs144250418 | snp | C/T | 0.021333 | 0.101051 | intron-variant, utr-variant-3-prime | PIAS2 | GRCh38.p7 | 18:46826167 | TCTATCTTATACTTA[C/T]CAATGTTAGTTTTTG | 9063 |
rs144272228 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PIAS2 | GRCh38.p7 | 18:46893955 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAATTA | 9063 |
rs144305160 | snp | C/T | 9.90475e-05 | 0.00703661 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46820960 | ATGACATGCTTGATA[C/T]TGGCGTATGGTGGAA | 9063 |
rs144309846 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46899376 | CATTCCATAGCAAAT[A/G]CAAAAGTCCTGAAGA | 9063 |
rs144312671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46845536 | GCCAGAAAACAACAG[C/T]GTCCAATCCCATACC | 9063 |
rs144369352 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46893355 | GCTTCACTCCTTATA[C/G]TTATTGTCAGATATT | 9063 |
rs144455637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46903851 | TGGTTAAACAAACTA[C/T]AGTGAATTCATATCG | 9063 |
rs144494274 | snp | C/T | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46909644 | CGAAGACTGACACCA[C/T]CTTTTTTGGAAGATA | 9063 |
rs144496272 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855944 | AGTTTTAATCAGCAA[A/C]TCTATTTGCTTAGAG | 9063 |
rs144524317 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46836364 | ATACTTACCCATCTA[A/T]TATTAGACTTTCATA | 9063 |
rs144560864 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46909669 | AAGATAATCTGACAT[G/T]ATCCAATATTGGTGA | 9063 |
rs144562081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46818942 | TGCATTTTTCTCAAG[C/T]TTGCACATTTCTAAA | 9063 |
rs144601944 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | PIAS2 | GRCh38.p7 | 18:46905334 | AAATAACGGAAATAT[C/T]ACACACATCAAAACA | 9063 |
rs144690299 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902393 | GAAACCCCGTCTCTA[A/C]TAAAGATGCAAAAAA | 9063 |
rs144709333 | snp | C/T | 0.0048818 | 0.0491637 | intron-variant | PIAS2 | GRCh38.p7 | 18:46855315 | TATATTAAACTTATA[C/T]GCAAATCTGGTGAAT | 9063 |
rs144727482 | snp | A/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46920594 | AATTCTGAAATAGGG[A/T]GCTACTTTGTCTCAC | 9063 |
rs144840901 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46921696 | ATAAACACATAACAA[A/C]AAAAAAAAAGCACTT | 9063 |
rs144893416 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PIAS2 | GRCh38.p7 | 18:46842594 | TAAAAAATCGTCAAT[A/T]TCCAACTGTTTTTTA | 9063 |
rs144896248 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46880268 | CTGGGCATGGTGGTG[C/T]ACACCTGTGGTCCCA | 9063 |
rs144902003 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PIAS2 | GRCh38.p7 | 18:46904708 | GTGAGCCGAGATCGC[A/G]CCACTGCCCTCCAGC | 9063 |
rs144923486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46857634 | GAGAAAAGACAAGAC[A/G]TGAGCCTAGAAAGAT | 9063 |
rs145040815 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850765 | ACCTAGACCCATTAT[A/T]TGATTATGAATTGTG | 9063 |
rs145163953 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46863938 | AAGAAAGACACCACG[A/G]ATGCACTAGCACAGA | 9063 |
rs145281824 | snp | A/G | | | intron-variant | PIAS2 | GRCh38.p7 | 18:46898396 | TGATCCACCCACCTC[A/G]GTTTCCCAAAGTGCT | 9063 |
rs145284704 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46808404 | ATTAAAGAATGGACA[C/T]TGGGTACAGCTTTAT | 9063 |
rs145301176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46902598 | CCTAAACAAATAAAT[C/T]CTTCACGGATTGGAA | 9063 |
rs145408945 | in-del | -/AAG | 0.0256215 | 0.110247 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, cds-indel | PIAS2 | GRCh38.p7 | 18:46810063 | GTAAGCCCCAATTTC[-/AAG]ATGATAAACTTCAAA | 9063 |
rs145457230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46879949 | GGAATAGTGAATTAC[C/T]GTTAAATGCATATAG | 9063 |
rs145525181 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PIAS2 | GRCh38.p7 | 18:46882792 | TAAGAAAGATTGTCA[C/T]GGTGCAAAACTCTAG | 9063 |
rs145538212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PIAS2 | GRCh38.p7 | 18:46899527 | GCCCAGAGTGCAGTG[A/G]TGCAAACACTGCTCA | 9063 |
rs145635204 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PIAS2 | GRCh38.p7 | 18:46835244 | AAGGGAGAAAGTGAT[A/G]AAACAACTGTGATAG | 9063 |
rs145670447 | snp | A/C | 0.0146672 | 0.084371 | intron-variant, utr-variant-5-prime | PIAS2 | GRCh38.p7 | 18:46894864 | TCACTTGAGGTCAGG[A/C]GTTTGAGACCAGCCT | 9063 |
rs145700718 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46846939 | CCCAATTTCAGTTAC[A/G]CTATTTTTATTTTAG | 9063 |
rs145797931 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | PIAS2 | GRCh38.p7 | 18:46892484 | TCACATTAAAAAAAC[C/T]AATTTAGGCCAGGAA | 9063 |
rs145809853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46840199 | AAATTAAGACCTCAA[A/G]GACATTTTATGTATG | 9063 |
rs145818113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46911673 | TAGATTTTCCTGCAG[A/C]AGCACAGAAAACTTT | 9063 |
rs145833666 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PIAS2 | GRCh38.p7 | 18:46896143 | AGGGCTGGGGAAGCA[C/T]TACAGGATAAAAAGA | 9063 |
rs145873064 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PIAS2 | GRCh38.p7 | 18:46848067 | TAACATATTCCCTTT[C/T]GTACAGAAGAAACTT | 9063 |
rs145874238 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46809279 | TTTACAATTACCTTA[A/G]GACAGATGCCAAGTT | 9063 |
rs145902098 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46815788 | TTCTTAAACAGATGT[A/C]TATTTCAATGACAGC | 9063 |
rs145999972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46828598 | ATTCTAGCAATTATG[A/C]TTATATCAAAGAAAG | 9063 |
rs146010470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46832503 | GATGGAGAATAAATA[C/T]GCAAAAAGATGCTCA | 9063 |
rs146069491 | in-del | -/A | 0.0505692 | 0.150756 | intron-variant | PIAS2 | GRCh38.p7 | 18:46862075 | GTGGCTCACGCCTGT[-/A]AATCCCAGCACTTTG | 9063 |
rs146077307 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897451 | TTTGAGCATCAAAAA[G/T]AATAATAACTGCATT | 9063 |
rs146118703 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PIAS2 | GRCh38.p7 | 18:46900929 | CGGTGAGCCGACGTC[A/G]TGCCATTGTACTCCA | 9063 |
rs146119686 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PIAS2 | GRCh38.p7 | 18:46850086 | TCCTGTTATCCTTTT[A/G]TTGTTGAAAATTTTA | 9063 |
rs146174831 | snp | A/C/T | 3.31923e-05 | 0.0040737 | PIAS2 | 18 | allele_origin=T(germline)/A(somatic) | 18:46864210 | GTGTCAAAGCAAAAA[A/C/T]AAAAAACTTCTCTTG | 9063 |
rs146199188 | snp | A/C | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | PIAS2, KATNAL2 | GRCh38.p7 | 18:46918318 | GGGTGGAACCCACAC[A/C]CGAGAGGTCTTTAAA | 9063 |
rs146240156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46872866 | TCTCCTATGGACTTC[A/T]GATGAAATCCACCAG | 9063 |
rs146251035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PIAS2 | GRCh38.p7 | 18:46878342 | CATCAAAAGTCTATG[A/C]TTTTTAAGATACCAA | 9063 |
rs146365816 | snp | A/G | 0.000135051 | 0.00821627 | synonymous-codon, nc-transcript-variant | PIAS2 | GRCh38.p7 | 18:46828123 | AGGCTTACTGAGGAC[A/G]CTTGAACCTGCATGT | 9063 |
rs146373928 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PIAS2 | GRCh38.p7 | 18:46897339 | TATAACATTTTATCG[C/T]ACCAGAAAACAGAGA | 9063 |
rs146427027 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PIAS2 | GRCh38.p7 | 18:46912429 | AAGTCTGTACATGTT[C/T]AGTACAGATGTAACC | 9063 |