SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1509671 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095374 | GTGTGTGTTTGTATA[G/T]GCATATGCACAGAAA | 79023 |
rs2136510 | snp | C/T | 0.207559 | 0.246371 | intron-variant | NUP37 | GRCh38.p7 | 12:102111825 | TTACAGATTGTTCAC[C/T]GAATTTACAACTTTA | 79023 |
rs2271266 | snp | A/G | 0.114785 | 0.210278 | intron-variant | NUP37 | GRCh38.p7 | 12:102112266 | ATATTGTTTGTTCTC[A/G]TTACTTATTAAAACA | 79023 |
rs2292303 | snp | C/G | 0.179425 | 0.239831 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119753 | GAGATTCGAGGTCAC[C/G]AAATTGTTCCGTCCC | 79023 |
rs2465233 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105750 | cctcagcctcccgag[C/T]agctgggattatagg | 79023 |
rs2465234 | snp | C/G/T | 3.00314e-05 | 0.00387489 | splice-donor-variant | NUP37 | GRCh38.p7 | 12:102085765 | GAGGAGACTTTTAAG[C/G/T]TTATTATTTATAATT | 79023 |
rs2468269 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086006 | TTACTTAAAAGTGGT[A/G]TTTTAATTTTCTTTA | 79023 |
rs2468270 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086003 | CTTAAAAGTGGTATT[A/T]TAATTTTCTTTAAAA | 79023 |
rs2468271 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085762 | GAGACTTTTAAGCTT[A/G]TTATTTATAATTTAA | 79023 |
rs2888609 | snp | C/T | 0.472147 | 0.114677 | intron-variant | NUP37 | GRCh38.p7 | 12:102113024 | TTCAGTTTATCCTCA[C/T]GGGAAGGTGAGAAAA | 79023 |
rs3028262 | in-del | -/AG | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102111797 | TTTAGTTATTTTAAG[-/AG]TTATACTTTCAATAA | 79023 |
rs3838805 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120848 | TAAATACCGAAGGAC[-/T]ACAGGTCATAAAGGG | 79023 |
rs3841628 | in-del | -/GT | 0.264084 | 0.249603 | intron-variant | NUP37 | GRCh38.p7 | 12:102099456 | TGTGTGTGTGTGTGT[-/GT]TTTTGTAAGAAATGC | 79023 |
rs3905333 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098869 | TCTTTTATCTCTTAT[C/T]TCAGATCCTCACATT | 79023 |
rs4237983 | snp | A/T | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102078322 | CAAGAGCGAAATTCC[A/T]TCTTTAAAAAAAAAA | 79023 |
rs4237984 | snp | A/T | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102078327 | GCGAAATTCCTTCTT[A/T]AAAAAAAAAAAAAAG | 79023 |
rs4611262 | snp | C/T | 0.282369 | 0.247896 | intron-variant | NUP37 | GRCh38.p7 | 12:102108981 | AAAAATGTCAGCAAA[C/T]AGAGGAGTTACAGTA | 79023 |
rs4764863 | snp | A/G | 0.490727 | 0.0674567 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120406 | GTGCCGTGGGACCGA[A/G]GTATTATGGTGCAGT | 79023 |
rs5800497 | in-del | -/C | 0.255782 | 0.249933 | intron-variant | NUP37 | GRCh38.p7 | 12:102114361 | AAGAAATCTCAGGGA[-/C]TGTACAGCCTGGGCT | 79023 |
rs7133417 | snp | C/T | 0.436408 | 0.16659 | intron-variant | NUP37 | GRCh38.p7 | 12:102109423 | AAAGTAAAGAAAGTA[C/T]AGAGAGTTACTATAG | 79023 |
rs7301747 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NUP37 | GRCh38.p7 | 12:102075343 | acgatgcccaggtaa[A/G]ttttaattttttgtt | 79023 |
rs7302337 | snp | A/G | 0.436834 | 0.166111 | intron-variant | NUP37 | GRCh38.p7 | 12:102105850 | ctgggtgacagagcg[A/G]gactccctctcaaaa | 79023 |
rs7314789 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | NUP37 | GRCh38.p7 | 12:102108648 | tatattttataCATG[C/G]AAATAAAGGGTAAGA | 79023 |
rs7342313 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NUP37 | GRCh38.p7 | 12:102083931 | GACTGACTGAGATTA[C/T]GGTGTTAGACCAAGG | 79023 |
rs7956473 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088704 | TTGTTTTTGTTTTAA[A/T]TTttttttttttttt | 79023 |
rs7961439 | snp | A/G | 0.208169 | 0.246476 | intron-variant | NUP37 | GRCh38.p7 | 12:102086250 | AATTACTACTGGGGC[A/G]CTTACAAACACACAC | 79023 |
rs7969562 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088702 | tTTTGTTTTTGTTTT[A/T]ATTTttttttttttt | 79023 |
rs7973378 | snp | A/G | 0.417034 | 0.18601 | intron-variant | NUP37 | GRCh38.p7 | 12:102089495 | cttcccagacggggc[A/G]gccaggcagagacgc | 79023 |
rs7977178 | snp | C/G | 0.256061 | 0.249927 | intron-variant | NUP37 | GRCh38.p7 | 12:102090044 | attcaactttagcag[C/G]tagttatcatcaaat | 79023 |
rs9788185 | snp | C/G | 0.208169 | 0.246476 | intron-variant | NUP37 | GRCh38.p7 | 12:102081074 | ATCTTGGGCAAACGG[C/G]TTACCTTTCTGTGTT | 79023 |
rs10083092 | snp | C/T | 0.438806 | 0.163867 | intron-variant | NUP37 | GRCh38.p7 | 12:102084916 | AATGGCTCCTAACTT[C/T]CCAATGAATCAGCAT | 79023 |
rs10128829 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NUP37 | GRCh38.p7 | 12:102099720 | TAGTTGTTATAAGCC[C/T]ATAGTTATCACCAAC | 79023 |
rs10507140 | snp | C/G | 0.175254 | 0.238565 | intron-variant | NUP37 | GRCh38.p7 | 12:102078982 | GGTATGAGATTGCTA[C/G]GAGTATCTAAGTGCA | 79023 |
rs10507141 | snp | G/T | 0.206336 | 0.246157 | intron-variant | NUP37 | GRCh38.p7 | 12:102097689 | TTGCAGGTTTCATTA[G/T]TCCAAATGCTTGTGA | 79023 |
rs10507142 | snp | G/T | 0.175254 | 0.238565 | intron-variant | NUP37 | GRCh38.p7 | 12:102098235 | ATCTTGTTCTTTATT[G/T]GTGATATTCTCCAGC | 79023 |
rs10673692 | in-del | -/CT | 0.474813 | 0.109357 | intron-variant | NUP37 | GRCh38.p7 | 12:102084470 | GGTAACATGGTGAAA[-/CT]CTGTTTCTACAAAAA | 79023 |
rs10745936 | snp | A/G | 0.490398 | 0.0686206 | intron-variant | NUP37 | GRCh38.p7 | 12:102098812 | GCTGAGATTATAGGC[A/G]TGTGGCACTGTGCCC | 79023 |
rs10778171 | snp | A/T | 0.21725 | 0.247846 | intron-variant | NUP37 | GRCh38.p7 | 12:102083409 | CTGATGAAAGACTCA[A/T]TGGGCCTGGAACAAA | 79023 |
rs11111150 | snp | A/G | 0.209388 | 0.246679 | intron-variant | NUP37 | GRCh38.p7 | 12:102074882 | TTGCAATTTAAGCAG[A/G]TAACAAACGTAAATG | 79023 |
rs11111151 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102079878 | attttaggtgagcaa[C/G]tgcacataagcggac | 79023 |
rs11111152 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | NUP37 | GRCh38.p7 | 12:102081530 | AATCTGTCActgtgt[A/G]accttgggcaaaatg | 79023 |
rs11111153 | snp | A/C | 0.437118 | 0.165792 | intron-variant | NUP37 | GRCh38.p7 | 12:102082309 | TAATCATGAACTCAT[A/C]TCTTTCTTCTCTAGC | 79023 |
rs11111154 | snp | A/G | 0.208169 | 0.246476 | intron-variant | NUP37 | GRCh38.p7 | 12:102082350 | TCATCAAGGCCAAGC[A/G]TAAGAGGCTAACAAT | 79023 |
rs11111155 | snp | C/T | 0.207864 | 0.246424 | intron-variant | NUP37 | GRCh38.p7 | 12:102082651 | AACTGGGATCTGACT[C/T]CAGGCAGTTAATTCA | 79023 |
rs11111156 | snp | C/T | 0.107071 | 0.205113 | intron-variant | NUP37 | GRCh38.p7 | 12:102089799 | GTTTTTTCTTAATGC[C/T]TTATACGGTCTTCAA | 79023 |
rs11111158 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NUP37 | GRCh38.p7 | 12:102090301 | CTAAGTTTTAAAATG[C/T]TGTAAACACAGTGTA | 79023 |
rs11111159 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | NUP37 | GRCh38.p7 | 12:102091956 | GTATCCCTACCATAT[A/G]GTATTTAAATGTTAT | 79023 |
rs11111161 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094050 | TAACACCCTATTTCA[C/G]TGCATTGAATTTAAA | 79023 |
rs11111162 | snp | A/G | 0.380919 | 0.21298 | intron-variant | NUP37 | GRCh38.p7 | 12:102095524 | AATGGTGTAGAATAT[A/G]AGGCTGAATGACTAG | 79023 |
rs11111163 | snp | C/T | 0.261884 | 0.249717 | intron-variant | NUP37 | GRCh38.p7 | 12:102098205 | GCTTATTTCCACCTG[C/T]TATTCTTCCTTTTCA | 79023 |
rs11111164 | snp | C/T | 0.380333 | 0.213338 | intron-variant | NUP37 | GRCh38.p7 | 12:102098780 | CAGGTGATCTGCCCA[C/T]CTTGGTCTCCCAAAG | 79023 |
rs11111165 | snp | A/G | 0.207559 | 0.246371 | intron-variant | NUP37 | GRCh38.p7 | 12:102110263 | CTAACACTTTGGGAG[A/G]TCAAGGTAGGTGAAT | 79023 |
rs11111167 | snp | C/T | 0.255503 | 0.249939 | intron-variant | NUP37 | GRCh38.p7 | 12:102115007 | TAGGTGAAGACACAC[C/T]AAGCAGCAGATTCAG | 79023 |
rs11111168 | snp | A/C | 0.255782 | 0.249933 | intron-variant | NUP37 | GRCh38.p7 | 12:102116153 | TACTAGTTCTTTTTT[A/C]TCATGTTAGTCATTT | 79023 |
rs11111169 | snp | C/T | 0.279991 | 0.248195 | intron-variant | NUP37 | GRCh38.p7 | 12:102116996 | GACAGAGCGAGACTC[C/T]GTCTCAAAACAAAAC | 79023 |
rs11608258 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121161 | AAGGCTTATGGCATA[G/T]GCTCCCACAGCCAGC | 79023 |
rs11609618 | snp | C/T | 0.0729998 | 0.176553 | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074163 | AAATATATATATATA[C/T]ACACACAGAGAACAG | 79023 |
rs11611985 | snp | A/G | 0.00943375 | 0.0680285 | intron-variant | NUP37 | GRCh38.p7 | 12:102078628 | GCCATGTGACTGGCA[A/G]CTTTCTCATTTCTAA | 79023 |
rs11616093 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102096441 | CATACATTTCATGAA[A/C]CTATTCAGGTCACAG | 79023 |
rs12161800 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093554 | GTAATGATTTCATCT[C/T]TAAGGAATTCAGAGT | 79023 |
rs12228159 | snp | A/G | 0.00477324 | 0.0486193 | intron-variant | NUP37 | GRCh38.p7 | 12:102105900 | TCCTCAAaaagataa[A/G]tctatgtgttaaccc | 79023 |
rs12228463 | snp | A/G | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102106139 | taccatcagaatcta[A/G]aaaacaggcatggaa | 79023 |
rs12299508 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089358 | cctcacatcccagac[G/T]gggtggcggccgggc | 79023 |
rs12301640 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | NUP37 | GRCh38.p7 | 12:102090914 | GAGTTTACTGACTTT[C/T]TGTTATCTAAGAAAC | 79023 |
rs12305674 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089349 | agaggcgctcctcac[A/T]tcccagactgggtgg | 79023 |
rs12313916 | snp | A/T | 0.436834 | 0.166111 | intron-variant | NUP37 | GRCh38.p7 | 12:102107984 | ttgacctctgtgatt[A/T]catgaatgtttactt | 79023 |
rs12318787 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | NUP37 | GRCh38.p7 | 12:102094383 | TATGCACTCCCAGAC[A/G]TGGATTACTTTCCAA | 79023 |
rs12319984 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | NUP37 | GRCh38.p7 | 12:102077602 | CGGTAAAATGTAAAC[A/T]TTTGCAATATAcagg | 79023 |
rs12366353 | snp | A/G | 0.00766272 | 0.0614218 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121870 | ACTCAAAACAACTTA[A/G]AAACTCATAATGCAT | 79023 |
rs12368273 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083268 | CTGTGTGTTTTAAGT[A/T]GACTCACTGCTCTCA | 79023 |
rs12423004 | snp | A/G | 0.175254 | 0.238565 | intron-variant | NUP37 | GRCh38.p7 | 12:102116623 | CACACTTCCTCTTAA[A/G]TATGACTATATTCCA | 79023 |
rs12423673 | snp | A/C | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102118040 | GCAGGATGTAGAAAA[A/C]CCGTAATTAATTGGA | 79023 |
rs12425639 | snp | C/T | 0.158302 | 0.232576 | intron-variant | NUP37 | GRCh38.p7 | 12:102086645 | GTCATGGCACCATGT[C/T]GTGAGAATGCTATCC | 79023 |
rs12426078 | snp | A/G | 0.417034 | 0.18601 | intron-variant | NUP37 | GRCh38.p7 | 12:102105254 | CCATggccgggtgca[A/G]tggctcatgcctgta | 79023 |
rs12814672 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NUP37 | GRCh38.p7 | 12:102113323 | GAAAAAACAGACAAA[C/T]AAAAAGAAAATCCTG | 79023 |
rs17032256 | snp | C/T | 0.175254 | 0.238565 | intron-variant | NUP37 | GRCh38.p7 | 12:102095111 | GTTCTTACAGAATGG[C/T]ACTGTTTCTAATATA | 79023 |
rs17032265 | snp | C/T | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102117508 | AGATAGTCCTGAGGG[C/T]TGAACCTTCATTGTT | 79023 |
rs17438178 | snp | C/T | 0.0625605 | 0.165428 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101071 | ATCTGAAGTAAATAA[C/T]CTAATTTTCATATCA | 79023 |
rs17438262 | snp | A/G | 0.16618 | 0.23553 | intron-variant | NUP37 | GRCh38.p7 | 12:102107290 | CACATGGTATGATAG[A/G]TTGCTAATGCCCAAG | 79023 |
rs17528833 | snp | A/C | 0.207864 | 0.246424 | intron-variant | NUP37 | GRCh38.p7 | 12:102096834 | TTTAAAAAAATCTTA[A/C]CTATATTGCTTAGGT | 79023 |
rs17529215 | snp | G/T | 0.255782 | 0.249933 | intron-variant | NUP37 | GRCh38.p7 | 12:102116430 | GTCTTTTTCAAGTAC[G/T]TAACATTGTCTTAAT | 79023 |
rs34065920 | in-del | -/T | 0.409721 | 0.192325 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119358 | CCACCATAGCACACG[-/T]TTTACCTTTGTAATA | 79023 |
rs34145954 | in-del | -/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109960 | TCTTTTAATATAAAA[-/G]GGAAATCAACAGCAC | 79023 |
rs34226089 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099730 | AGCCCATAGTTATCA[-/C]CCAACACAAAAAATC | 79023 |
rs34250518 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080870 | TAAAAATATTTGATA[-/T]TTTTAAGAGTGACTT | 79023 |
rs34394741 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079847 | AAAATAAGAAGCCAG[-/C]AGTTCACCTTGTTCA | 79023 |
rs34407247 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091321 | GAGAACTGCTTGAAT[C/T]TGGGAGGCGGAGGTT | 79023 |
rs34627082 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105234 | TATACATTGCACAAG[-/A]AATGCCATGGCCGGG | 79023 |
rs34643287 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091358 | AGCTGAGATTTTGCC[A/C]CTGTACTCCAGCCCG | 79023 |
rs34727093 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110324 | GGCAACATGGCGAAA[-/C]CCCCATCACTGCAAA | 79023 |
rs34767006 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096173 | CTGTGAGTTTCATTT[-/A]AAAAGGTGTGGTAGG | 79023 |
rs35016757 | snp | A/G | 0.207559 | 0.246371 | intron-variant | NUP37 | GRCh38.p7 | 12:102076396 | ATGTATGTTAATTTA[A/G]GTGAAAAGCAAAAAC | 79023 |
rs35112450 | in-del | -/AG/GA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111796 | ATTTAGTTATTTTAA[-/AG/GA]GTTATACTTTCAATA | 79023 |
rs35193278 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102105396 | TTAGCCGGGTGCAGT[A/G]GCGTGTGCCTGTAGT | 79023 |
rs35286114 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094631 | ATTTGATAAAAATCA[-/T]TTTTTCCTCTTGCAA | 79023 |
rs35312209 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103116 | TTTTAATTGATTTTT[-/C]CTATTTCTGTGAAGA | 79023 |
rs35546007 | in-del | -/CT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084471 | GTAACATGGTGAAAC[-/CT]TGTTTCTACAAAAAA | 79023 |
rs35622775 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090195 | GGTAATAGGTACAGC[-/T]TTTTCAGGTGCTCTT | 79023 |
rs35855638 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121545 | ACCATAGTAATGCTC[-/T]TTTTTTTTTTTTTTT | 79023 |
rs36026997 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104632 | CCCATTTTGAGCTCA[-/T]TTTGTGTAAAGTCCA | 79023 |
rs55747025 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117442 | TCTGAAAAAAAAAAA[-/A]TAAAAATAATAATAA | 79023 |
rs55761511 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102080459 | AAAATGATTCTTTAA[A/G]AACAGGCAAATGTTA | 79023 |
rs55836064 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | NUP37 | GRCh38.p7 | 12:102105682 | CCTGGTCAACACGGC[A/G]AAATCCCATCTCTAC | 79023 |
rs55837493 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | NUP37 | GRCh38.p7 | 12:102103862 | ATAGACAAAATGTTC[C/T]GCATCACAATATAGG | 79023 |
rs56197521 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102087027 | ATTGCTTGAGCACAG[C/G]AGGTGGAGGCTACAA | 79023 |
rs56228030 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NUP37 | GRCh38.p7 | 12:102113752 | ATATTTAATGAAATA[C/T]GTATGTCTATATTGA | 79023 |
rs56951478 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | NUP37 | GRCh38.p7 | 12:102087149 | TGAATTCATTCATTG[C/G]AATTTTTCTTCTAGG | 79023 |
rs57070640 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102086425 | TATACCTTTTGTAAT[C/T]TGGCTTACTTTTCCA | 79023 |
rs57639534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111554 | TGTAGAAGGCAAGGC[C/T]AGTGTTTTGTAACAG | 79023 |
rs57673363 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085887 | CAGTATAATGTTAAT[-/T]GTTCTTGATATATCA | 79023 |
rs57723615 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUP37 | GRCh38.p7 | 12:102082439 | GGCAGAGCACTGAAA[A/G]CCATTAGGCTTGTTA | 79023 |
rs57945278 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121571 | TTTTTTTTTTTTTTT[-/T]AAGACAGAGTCTCAC | 79023 |
rs57973669 | snp | C/G | 0.188 | 0.24219 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119272 | ATGTTCAGGGGGTTG[C/G]GCGGAGGGAGAGCAT | 79023 |
rs58159007 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102097738 | TAAAGAGCTGAAATG[C/T]CATTATTTATTTCCA | 79023 |
rs58224303 | in-del | -/AA | 0.380919 | 0.21298 | intron-variant | NUP37 | GRCh38.p7 | 12:102097460 | GAAGGCAGTAAACTT[-/AA]AAGTCTTATATTCGA | 79023 |
rs58234327 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121574 | TTTTTTTTTTTTTAA[A/G]ACAGAGTCTCACTCT | 79023 |
rs58265217 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102097730 | CTATGTTTTAAAGAG[A/C]TGAAATGCCATTATT | 79023 |
rs58553320 | snp | G/T | 0.0525757 | 0.153374 | intron-variant | NUP37 | GRCh38.p7 | 12:102076854 | TGAGGATAACTAAAA[G/T]ATAATATTTTGCATT | 79023 |
rs58901058 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102102407 | AAAGCATGTCTTCTT[G/T]CAAGAAATGTCTGTC | 79023 |
rs58927483 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102086899 | GACCAGCCTGGCAAA[G/T]ACAGTGAAACTTCGT | 79023 |
rs58978105 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088758 | TGGGTGTTTCTCGGA[A/G]AGGGGGATGTGGCAG | 79023 |
rs60678181 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102109321 | TTCTAAATGTAAGAT[A/T]AAAATTAATGATGAT | 79023 |
rs60870810 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097746 | TGAAATGCCATTATT[A/T]ATTTCCAGTGACCGA | 79023 |
rs61008062 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | NUP37 | GRCh38.p7 | 12:102117767 | AGGAGATGCTAAATA[C/T]CTTATTCAAGGTCTC | 79023 |
rs61031763 | snp | A/C | 0.0637235 | 0.166737 | intron-variant | NUP37 | GRCh38.p7 | 12:102107250 | AAGAAAAAAAATAAT[A/C]CCCTCCTATGCTGCA | 79023 |
rs61108535 | snp | G/T | 0.030278 | 0.119257 | intron-variant | NUP37 | GRCh38.p7 | 12:102080140 | TCTAGAAAAGAGAAT[G/T]ATGAAAAAATCAGAC | 79023 |
rs61389942 | in-del | -/A | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102108306 | TCATCTTTCTCCTGT[-/A]GTTGGATGCTTCCTG | 79023 |
rs61439127 | snp | A/G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097747 | GAAATGCCATTATTT[A/G/T]TTTCCAGTGACCGAA | 79023 |
rs61577226 | in-del | -/T | 0.433361 | 0.169938 | intron-variant | NUP37 | GRCh38.p7 | 12:102103044 | CCTCCGGGTTTGTTC[-/T]TTTTTTTGCTCAAAA | 79023 |
rs61936654 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NUP37 | GRCh38.p7 | 12:102116743 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGTA | 79023 |
rs61936655 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120829 | TTATGCTCATTAGAG[A/G/T]TTTTAAATACCGAAG | 79023 |
rs66521551 | snp | C/T | 0.43555 | 0.167544 | intron-variant | NUP37 | GRCh38.p7 | 12:102111375 | GGTTGTACAAATATA[C/T]GTATTTGTCAAAACT | 79023 |
rs71438453 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121571 | TTTTTTTTTTTTTTT[-/T]AAGACAGAGTCTCAC | 79023 |
rs71464302 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NUP37 | GRCh38.p7 | 12:102087050 | GGCTACAATGTGCCA[C/T]GTTTGCACCTCTGCA | 79023 |
rs71466203 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUP37 | GRCh38.p7 | 12:102090876 | AAATAAGGCAGGTAG[A/G]CATTCTTTTAAAATG | 79023 |
rs71466204 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NUP37 | GRCh38.p7 | 12:102105113 | TAATTTCTTTCTGCA[A/G]TGTTTTGTAGCTTTT | 79023 |
rs72004608 | in-del | -/CA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099471 | ACACACACACACACA[-/CA]TTTTTATTGTACCTG | 79023 |
rs72096550 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078325 | GAGCGAAATTCCTTC[-/T]TTAAAAAAAAAAAAA | 79023 |
rs73185907 | snp | A/C | 0.0733688 | 0.176922 | intron-variant | NUP37 | GRCh38.p7 | 12:102076178 | ATGTATCTTAACGAT[A/C]CATGGCATTCTTACA | 79023 |
rs73185908 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | NUP37 | GRCh38.p7 | 12:102078904 | ACAAAATAATAAAAT[A/G]TGAAAAAATTTTTCT | 79023 |
rs73185910 | snp | G/T | 0.0733688 | 0.176922 | intron-variant | NUP37 | GRCh38.p7 | 12:102083369 | AGAACATTTCACTCA[G/T]GCACATATGCAGAGT | 79023 |
rs73185912 | snp | A/C | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102093126 | AAAATAATATGTCAA[A/C]ATCAGAGTTGATAAT | 79023 |
rs73185914 | snp | A/G | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102094515 | TGGGGTGGGGGTGGA[A/G]GAAGAACACTCCATC | 79023 |
rs73185915 | snp | C/T | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102098446 | TTCCACACAAACTTA[C/T]CATACAGCATCTGTA | 79023 |
rs73185916 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | NUP37 | GRCh38.p7 | 12:102098449 | CACACAAACTTATCA[C/T]ACAGCATCTGTAAAG | 79023 |
rs73185920 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NUP37 | GRCh38.p7 | 12:102106640 | TAACCTAACAAATAC[C/T]TATATTTAATTAACA | 79023 |
rs73185922 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | NUP37 | GRCh38.p7 | 12:102108098 | GTACTGGTTCTGGGT[A/G]TATCTGGGTGTTTCT | 79023 |
rs73185927 | snp | A/C | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102110714 | AGGCATGATGATGGG[A/C]GCCTATAGTCCCAGC | 79023 |
rs73185929 | snp | A/G | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102110715 | GGCATGATGATGGGC[A/G]CCTATAGTCCCAGCT | 79023 |
rs73185933 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | NUP37 | GRCh38.p7 | 12:102117373 | GAGAATCAACTGAAC[C/T]CGGGAGATGAAGGTT | 79023 |
rs73382887 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NUP37 | GRCh38.p7 | 12:102085689 | AAATCATTGATCTTC[C/T]TCCTCTATGTATGTG | 79023 |
rs73382891 | snp | C/T | 0.084364 | 0.187256 | intron-variant | NUP37 | GRCh38.p7 | 12:102087274 | TTATTTCAAAGAAAG[C/T]AGAGTATGTATTGGA | 79023 |
rs73382893 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102090937 | TAAGAAACTTTTGGT[C/G]TAGACCACGTCAGAC | 79023 |
rs73382897 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NUP37 | GRCh38.p7 | 12:102092163 | ATTTTTGGCAGCTCA[C/T]TGTTTGCTAGGAAAT | 79023 |
rs73384806 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NUP37 | GRCh38.p7 | 12:102106029 | CAAAATTTAACAATG[A/C]ATGAACACAAAAAAG | 79023 |
rs73384815 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NUP37 | GRCh38.p7 | 12:102110086 | AAAACATGCAACATC[C/T]TCACAACCTATAAGA | 79023 |
rs73384816 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NUP37 | GRCh38.p7 | 12:102115529 | TTATTGCACTGCTTT[A/G]TATGTAAATATTTCC | 79023 |
rs73384817 | snp | A/G | 0.0887219 | 0.191022 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120762 | ACTTGTTTCACTAAC[A/G]TCTCATTCTGTGAGG | 79023 |
rs74241017 | snp | C/G/T | 0.00478085 | 0.0486577 | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074171 | ATATATACACACACA[C/G/T]AGAACAGAGTAGAAA | 79023 |
rs74241019 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107025 | CCTGTCTTTCCACAT[G/T]TAGTTGCATTTCTTC | 79023 |
rs74366186 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | NUP37 | GRCh38.p7 | 12:102112542 | TGGCTCACGTCTATA[A/G]TCCCAACACTTTGCG | 79023 |
rs74366525 | snp | A/G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108306 | TCATCTTTCTCCTGT[A/G/T]GTTGGATGCTTCCTG | 79023 |
rs74405783 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NUP37 | GRCh38.p7 | 12:102112848 | ACATGTGGCATTATA[C/T]GTGTGTAAGATGCTA | 79023 |
rs74410524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102091646 | ATGGGAAAGTTATGT[A/G]CTGACATATTAAGGT | 79023 |
rs74559621 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074224 | ATTTTATTTAATAAA[A/C]GCAACTGAGACATTT | 79023 |
rs74628580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120890 | GTGATATCTGACTCG[A/G]AAGTGTAGTTCTTTC | 79023 |
rs74806450 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | NUP37 | GRCh38.p7 | 12:102086145 | AAATTAAATTATTTA[C/T]ATACTCTTTATTTTG | 79023 |
rs74851314 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | NUP37 | GRCh38.p7 | 12:102103409 | TGTTAGTATATTAGA[A/C]AGGTTACTGATTTTT | 79023 |
rs74959779 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102081834 | GAGTAGCTGGGACTA[C/T]GGTCGAGCACCACAC | 79023 |
rs75077993 | snp | A/T | 0.0696718 | 0.173152 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121456 | AGTGAGTAGTTGTGC[A/T]TGCCTCAAATATTTA | 79023 |
rs75162381 | snp | A/G | 0.25634 | 0.24992 | intron-variant | NUP37 | GRCh38.p7 | 12:102103920 | TCATTCTTAATGGTG[A/G]GAAGATGGTGGTCTC | 79023 |
rs75232693 | snp | C/T | 0.159292 | 0.232964 | intron-variant | NUP37 | GRCh38.p7 | 12:102081071 | AAGATCTTGGGCAAA[C/T]GGCTTACCTTTCTGT | 79023 |
rs75580367 | snp | A/G | 0.0264439 | 0.111905 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120475 | GGCGGAGTTCACAGT[A/G]TCTAGCGATGGAGCT | 79023 |
rs75783996 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121545 | CACCATAGTAATGCT[C/T]TTTTTTTTTTTTTTT | 79023 |
rs75794412 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102108461 | AGGTTTTGGGACTCA[C/G]ACTGGCTGCCTTGCT | 79023 |
rs75821858 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | NUP37 | GRCh38.p7 | 12:102079437 | TATAAAGTTGCTGCA[A/C]ACACTCAACTAGTGA | 79023 |
rs75829921 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | NUP37 | GRCh38.p7 | 12:102107303 | AGGTTGCTAATGCCC[A/C]AGTTTTGATATCAGA | 79023 |
rs75830911 | snp | A/C | 0.0637235 | 0.166737 | intron-variant | NUP37 | GRCh38.p7 | 12:102107678 | ACTACATAGTAATAA[A/C]TAACTAGATCTACAA | 79023 |
rs75928275 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NUP37 | GRCh38.p7 | 12:102098213 | CCACCTGCTATTCTT[C/T]CTTTTCATCTTGTTC | 79023 |
rs75939336 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108305 | TTCATCTTTCTCCTG[-/T]AGTTGGATGCTTCCT | 79023 |
rs76079810 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NUP37 | GRCh38.p7 | 12:102085501 | GATTGTTGGAACACC[A/G]GTTTTTACACTGAAA | 79023 |
rs76085361 | snp | A/C | 0.16911 | 0.236552 | intron-variant | NUP37 | GRCh38.p7 | 12:102110845 | GCCAGACCTTGTCTC[A/C]AAATGAATGAATGAG | 79023 |
rs76114601 | snp | G/T | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102088746 | ATTGAACATTCTTGG[G/T]TGTTTCTCGGAGAGG | 79023 |
rs76248942 | snp | A/C | 0.181659 | 0.240478 | intron-variant | NUP37 | GRCh38.p7 | 12:102096686 | TGTGATAATGTAAGA[A/C]TATATATGTGATATT | 79023 |
rs76279354 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102104516 | TTGTTGCCTGTGCTT[C/T]TGTTATCAAAACTAA | 79023 |
rs76300280 | snp | A/T | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102081716 | TATTTCATTTAGCTA[A/T]TTTTTTTTTTTTGAG | 79023 |
rs76374411 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NUP37 | GRCh38.p7 | 12:102114131 | AAGACAGCAGCCACT[A/G]AACAATTTTAAAATA | 79023 |
rs76465814 | snp | C/T | 0.175254 | 0.238565 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121678 | CCTGTCTCAGCCTCC[C/T]AAGTAGCTGGGGTTA | 79023 |
rs76606581 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | NUP37 | GRCh38.p7 | 12:102079438 | ATAAAGTTGCTGCAA[A/T]CACTCAACTAGTGAA | 79023 |
rs76709069 | snp | A/G | 0.444444 | 0.157135 | intron-variant | NUP37 | GRCh38.p7 | 12:102107487 | CTAAGAAACACTGAA[A/G]AAATACGTGTCGGCT | 79023 |
rs76830567 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102082605 | AAAGTTTAAGTAACT[C/T]GTCAGAGATCACACA | 79023 |
rs76830759 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118246 | CTCTATGGATCTTAT[C/T]TTTTTTTTTTTTAAC | 79023 |
rs76911393 | snp | A/T | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102117456 | GAAAAAAAAAAATAA[A/T]AATAATAATAATACT | 79023 |
rs76924228 | snp | A/G | 0.175576 | 0.238665 | intron-variant | NUP37 | GRCh38.p7 | 12:102097132 | TGACAGAGCACAGGA[A/G]GTCAAGTCAAGCCAG | 79023 |
rs77016373 | snp | G/T | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102104633 | CCCATTTTGAGCTCA[G/T]TTGTGTAAAGTCCAA | 79023 |
rs77210012 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102106643 | CCTAACAAATACCTA[C/T]ATTTAATTAACAATG | 79023 |
rs77236739 | snp | A/G | 0.175254 | 0.238565 | intron-variant | NUP37 | GRCh38.p7 | 12:102083378 | CACTCATGCACATAT[A/G]CAGAGTATAATTCTA | 79023 |
rs77242280 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102077799 | TGTATAAGGTATACA[C/T]GAAACATAAATGAAT | 79023 |
rs77431996 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118258 | TATCTTTTTTTTTTT[A/T]AACATTCAAACTCAA | 79023 |
rs77614510 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | NUP37 | GRCh38.p7 | 12:102098432 | GTCATAGTTCATTAT[A/T]CCACACAAACTTATC | 79023 |
rs77619182 | snp | A/G | 0.132627 | 0.220734 | intron-variant | NUP37 | GRCh38.p7 | 12:102077245 | GTCTCAGGTATAACA[A/G]GATGGATGAGTGGAT | 79023 |
rs77799466 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118247 | TCTATGGATCTTATC[C/T]TTTTTTTTTTTAACA | 79023 |
rs78000058 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NUP37 | GRCh38.p7 | 12:102103450 | TTGTATCATGCAACC[C/T]TACTGAATTCACTAA | 79023 |
rs78040272 | snp | A/C | 0.0168055 | 0.0901129 | intron-variant | NUP37 | GRCh38.p7 | 12:102086538 | TCAATAGTTACAAAT[A/C]CACAGTAACAAGGAC | 79023 |
rs78250265 | snp | A/G | 0.277778 | 0.248452 | intron-variant | NUP37 | GRCh38.p7 | 12:102082896 | TAGTGAAAATGAAGG[A/G]AAAATTAAAAGACCT | 79023 |
rs78299962 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | NUP37 | GRCh38.p7 | 12:102077750 | ATGCACAAAATTATT[A/T]AAAAAAGTTATATAA | 79023 |
rs78462723 | snp | C/T | 0.255782 | 0.249933 | intron-variant | NUP37 | GRCh38.p7 | 12:102107942 | GGGGCACACTGGCAG[C/T]CTCAAGTGTTAGTAA | 79023 |
rs78471714 | snp | C/T | 0.178144 | 0.239451 | intron-variant | NUP37 | GRCh38.p7 | 12:102076656 | AGGCAATGACTTAGT[C/T]GGGAAAGTAAAATAA | 79023 |
rs78694177 | snp | C/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102075680 | CAATCCTTTTTTTCA[C/G]AACCAAAGGGGTAAT | 79023 |
rs78709810 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | NUP37 | GRCh38.p7 | 12:102096848 | ACCTATATTGCTTAG[A/G]TTTTGGCCTAAGAGG | 79023 |
rs79147237 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NUP37 | GRCh38.p7 | 12:102103365 | TTTTGTAAATCATAT[C/T]ACCTTAATTTCTTTT | 79023 |
rs79284171 | snp | C/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102104881 | TTGAAATAAAGAAGT[C/G]TGAGAACTTCAGCTT | 79023 |
rs79292208 | snp | A/C | 0.0491753 | 0.148894 | intron-variant | NUP37 | GRCh38.p7 | 12:102099076 | TTAAAATGGCAATTT[A/C]AAAATGTGGTTATAA | 79023 |
rs79312878 | in-del | -/TT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075890 | CTTACTTTTTTTTTT[-/TT]GTTTAATTGTTCGGC | 79023 |
rs79575592 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | NUP37 | GRCh38.p7 | 12:102117453 | TCTGAAAAAAAAAAA[A/T]AAAAATAATAATAAT | 79023 |
rs79579070 | snp | A/C | 0.0592355 | 0.161582 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120855 | CGAAGGACTACAGGT[A/C]ATAAAGGGGGAGCCT | 79023 |
rs79661040 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | NUP37 | GRCh38.p7 | 12:102111582 | CAGATCTTAAATAAC[C/T]TAACATATTCTTGCC | 79023 |
rs79712085 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NUP37 | GRCh38.p7 | 12:102074831 | AACATCAAAAAAAAA[A/C]CACACAAAAAACAAA | 79023 |
rs79729274 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NUP37 | GRCh38.p7 | 12:102093490 | ACTTCAAAAATTAAA[C/T]TCTCAACTGCAAAGA | 79023 |
rs79850286 | snp | C/T | 0.130694 | 0.219696 | intron-variant | NUP37 | GRCh38.p7 | 12:102077980 | TAAAGGAAGAGGCTA[C/T]GTAAAAATCTCTAGA | 79023 |
rs80024875 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | NUP37 | GRCh38.p7 | 12:102088396 | CAAATCTTAAATGTA[C/T]AATTCAAAGAGAATA | 79023 |
rs80065536 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102109667 | ACTGAATTTGTATAG[C/T]TCCAAAAAGGTCTTG | 79023 |
rs80184009 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NUP37 | GRCh38.p7 | 12:102084741 | TATGAAGACATTAGA[A/G]GACTGTGGGAGCCTA | 79023 |
rs80232263 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NUP37 | GRCh38.p7 | 12:102097739 | AAAGAGCTGAAATGC[A/C]ATTATTTATTTCCAG | 79023 |
rs111343405 | snp | C/T | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102098682 | AATCACAAGTGCGCA[C/T]TACCGTGCCTGGCTA | 79023 |
rs111384318 | snp | C/T | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102117760 | TGTTTACAGGAGATG[C/T]TAAATATCTTATTCA | 79023 |
rs111394995 | snp | A/C | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102085895 | TGTTAATTGTTCTTG[A/C]TATATCATTACTAAA | 79023 |
rs111581346 | snp | G/T | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102100653 | TGTGCTCTTAACCGC[G/T]TTGGAATTCTGCCTG | 79023 |
rs111589903 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102116249 | GACTTTCTCCCTCAA[A/C]ATTTCTTAATCATAA | 79023 |
rs111908125 | snp | C/T | 0.00517822 | 0.0506191 | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102073926 | CACTCCCTTCAGCCT[C/T]CCAAAGTGTTGGGAT | 79023 |
rs111972355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114531 | GGCAGGAAATTAAGA[C/T]ACTTTGGAAAACTTG | 79023 |
rs112120544 | snp | A/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102086007 | AAAGAAAATTATAAC[A/G]CCACTTTTAAGTAAT | 79023 |
rs112491678 | snp | A/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102075382 | GAATGGGGTCTTGCT[A/G]TCTTGCCCAGGCAGG | 79023 |
rs112601662 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120788 | TGAGGTAGGAATTCC[A/C]TTCCTGGTTTTGCAG | 79023 |
rs112620903 | snp | A/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102074872 | CCACCTTTTCTTGCA[A/G]TTTAAGCAGATAACA | 79023 |
rs112649668 | snp | C/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102095208 | AATAAGCTTAACCCA[C/G]TAAATACTTAAATGA | 79023 |
rs112652702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103227 | AATTCATCCAATCCA[C/T]GAACACAGGATATCT | 79023 |
rs112682727 | snp | C/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102075227 | GTCACCCAGGCTGGA[C/G]TGCAGAAGTGCTAAC | 79023 |
rs112714391 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NUP37 | GRCh38.p7 | 12:102117459 | AAAAAAAAATAAAAA[A/T]AATAATAATACTCTG | 79023 |
rs112810728 | snp | C/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102114302 | CAAGTCCTTTAATTT[C/G]TTACCCAAATCACAT | 79023 |
rs112852795 | snp | A/T | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102095990 | CTGATATCCAGTCTT[A/T]CTCATTGTAAAGAAG | 79023 |
rs113119845 | snp | C/T | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102101021 | AAAGATTTATATGGT[C/T]GTCAACATACCTTAT | 79023 |
rs113212339 | snp | C/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102086746 | CAGCCGGTGACAGAA[C/G]TCGGTGGGAGGCTGG | 79023 |
rs113225616 | snp | G/T | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102114418 | TCCTGGCAGCACTGT[G/T]TGCCACTGAGCCAAC | 79023 |
rs113230345 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102088504 | CTCATACTTCCTTAC[G/T]GTCTCACAAAAGGTA | 79023 |
rs113305130 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NUP37 | GRCh38.p7 | 12:102075221 | TGCTCTGTCACCCAG[G/T]CTGGAGTGCAGAAGT | 79023 |
rs113326065 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102122013 | ATGAGGAAGCTGAGG[C/T]AGGGAAAGGTGATGT | 79023 |
rs113344992 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NUP37 | GRCh38.p7 | 12:102105737 | ATGGTGATGTGCACC[C/T]ATAATCCCAGCTACT | 79023 |
rs113787560 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NUP37 | GRCh38.p7 | 12:102110149 | ATATACCAAAAAAGC[A/G]TCAGCATTATCACTC | 79023 |
rs113842405 | snp | A/G | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102105093 | TTTCTATTTATTTGT[A/G]TCTTTAATTTCTTTC | 79023 |
rs113857973 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118695 | AGCTCAAAAGAAACA[C/T]TTAAAGTACTTATCA | 79023 |
rs113894791 | snp | C/T | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102089734 | GCGGCCGGGCAGAGG[C/T]GCTCCTCACTTCCCA | 79023 |
rs113927186 | in-del | -/T | 0.5 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102075879 | TTCTTCTCCTCTTAC[-/T]TTTTTTTTTTTTGTT | 79023 |
rs114063469 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | NUP37 | GRCh38.p7 | 12:102092847 | GTGGAGACAACAAAA[G/T]AGCAGGATAGTTGGA | 79023 |
rs114101910 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | NUP37 | GRCh38.p7 | 12:102113402 | CAAAAGAATTGCTAA[G/T]GTTCCTTTTCTTAAA | 79023 |
rs114200876 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NUP37 | GRCh38.p7 | 12:102115462 | TTGATTTAGGCAAGC[A/C]TATATGTTCATGCTC | 79023 |
rs114257847 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121915 | TGCTTTTATACATGC[C/T]AGGCACTGTTCTAAA | 79023 |
rs114258540 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NUP37 | GRCh38.p7 | 12:102087676 | TAACCACTACTGAAA[C/T]AGTATGAATTTGTCT | 79023 |
rs114382045 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | NUP37 | GRCh38.p7 | 12:102117029 | AACAAAAACAGAATT[G/T]CCTTCTCAGTAAAGG | 79023 |
rs114578921 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NUP37 | GRCh38.p7 | 12:102098678 | CTGGAATCACAAGTG[C/T]GCACTACCGTGCCTG | 79023 |
rs115187349 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | NUP37 | GRCh38.p7 | 12:102108065 | AAGTGTCAACTTGCT[G/T]GGATTGAAGGATACA | 79023 |
rs115382987 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | NUP37 | GRCh38.p7 | 12:102110684 | CTGTCCCTACAAAAA[A/C]TACCAAAATTAGCCA | 79023 |
rs115474962 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NUP37 | GRCh38.p7 | 12:102086956 | AGGCATAGTGATGCA[A/C]ACTTGTAGCCCCAGC | 79023 |
rs115536492 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP37 | GRCh38.p7 | 12:102111301 | GGTACAATGATTAAC[C/T]GGGAAGAAGTATGAC | 79023 |
rs115734896 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NUP37 | GRCh38.p7 | 12:102098272 | CACTATTAAAATGTT[A/G]TAGCTACCTCATCTG | 79023 |
rs115805756 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | NUP37 | GRCh38.p7 | 12:102116260 | TCAACATTTCTTAAT[C/G]ATAAATGAGATAAAC | 79023 |
rs115864739 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NUP37 | GRCh38.p7 | 12:102085580 | ATGATGGCTGTCAAA[C/T]AAAAACCTTAACAAT | 79023 |
rs115950538 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NUP37 | GRCh38.p7 | 12:102110434 | TGAGGCTGAGCCAAG[A/G]GAGGTTGAGGCTGCA | 79023 |
rs116086828 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | NUP37 | GRCh38.p7 | 12:102117717 | TAGTATATTTACATA[C/T]ACTAAAATTCAAGCA | 79023 |
rs116088161 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | NUP37 | GRCh38.p7 | 12:102101444 | AAAAGGATGGATTTT[A/T]AAAAGTATCTTCATT | 79023 |
rs116399813 | snp | A/G | 0.030278 | 0.119257 | intron-variant | NUP37 | GRCh38.p7 | 12:102114888 | GTTAAGCCAAAATCT[A/G]TTTCCATGTAAATTC | 79023 |
rs116473986 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NUP37 | GRCh38.p7 | 12:102087678 | ACCACTACTGAAATA[A/G]TATGAATTTGTCTTG | 79023 |
rs116539016 | snp | A/G | 0.0788843 | 0.182262 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119375 | TTACCTTTGTAATAA[A/G]CCTGCACGTCCCGCA | 79023 |
rs116560766 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NUP37 | GRCh38.p7 | 12:102085254 | GCGAAACCTCAGCCC[C/T]ACCAAAAATACAAAA | 79023 |
rs116747556 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUP37 | GRCh38.p7 | 12:102093201 | ACCCTGTTTCATACA[A/G]AACACTAATAAACTA | 79023 |
rs116780432 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NUP37 | GRCh38.p7 | 12:102078583 | AAGAGCACAGACACG[C/T]CGCTTCCTTCACTTA | 79023 |
rs116831441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102107310 | TAATGCCCAAGTTTT[A/G]ATATCAGAACTTTGC | 79023 |
rs116845991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092450 | GGAAAGGGACCCTCA[A/G]CATTCTTAGACAAGA | 79023 |
rs116868345 | snp | C/T | 0.010774 | 0.0726012 | intron-variant | NUP37 | GRCh38.p7 | 12:102077226 | GCTTTCGCTTGACAG[C/T]ATAGTCTCAGGTATA | 79023 |
rs117003991 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102100666 | GCTTTGGAATTCTGC[C/T]TGTGCTATGCTGTAC | 79023 |
rs117012086 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NUP37 | GRCh38.p7 | 12:102086609 | ACCATTGCAGAGGGA[A/G]AGCAAGACTCAGAAA | 79023 |
rs117184799 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NUP37 | GRCh38.p7 | 12:102094436 | TCAGAAGGCTCTCAG[A/T]TTCCTTTTTGCTGTT | 79023 |
rs117189026 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102114444 | CCAACTAAAAGGCCC[A/G]TGTGTGTGTGTGGTA | 79023 |
rs117404833 | snp | A/G | 0.0188252 | 0.0951747 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120444 | CGCTCGAGCCTGGTT[A/G]GGCCTGGGGGCTGTA | 79023 |
rs117414580 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | NUP37 | GRCh38.p7 | 12:102099424 | ACACTATTAGCTTAG[G/T]CTTTCTTTTCTAGTA | 79023 |
rs117435512 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | NUP37 | GRCh38.p7 | 12:102083088 | ACAAATTAAGTTAAA[G/T]CATATGGAAGAAAGA | 79023 |
rs117534677 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NUP37 | GRCh38.p7 | 12:102112534 | AGGCGTGTTGGCTCA[C/T]GTCTATAATCCCAAC | 79023 |
rs117579760 | snp | C/T | 0.030278 | 0.119257 | intron-variant | NUP37 | GRCh38.p7 | 12:102105255 | CATGGCCGGGTGCAA[C/T]GGCTCATGCCTGTAA | 79023 |
rs117754089 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102087886 | TATTAAATAAAAACT[C/G]GTCAGTTAATGAAAT | 79023 |
rs117845658 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | NUP37 | GRCh38.p7 | 12:102108011 | ACTTTATAATAAACA[A/T]GTTAAAATGCACATA | 79023 |
rs117852620 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NUP37 | GRCh38.p7 | 12:102089806 | CTTAATGCCTTATAC[A/G]GTCTTCAATTAATTC | 79023 |
rs117953815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097099 | TAGCTATCTAGGACA[C/T]GCTCATCTCATAGCA | 79023 |
rs117970575 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NUP37 | GRCh38.p7 | 12:102113116 | TCTCCCATTACAACA[C/T]TGCAAAAATTCAAAT | 79023 |
rs118034789 | snp | C/T | 0.067446 | 0.170804 | intron-variant | NUP37 | GRCh38.p7 | 12:102081341 | GGTGATAAGAACAGA[C/T]AGGGTAGAAAAGTTA | 79023 |
rs118084892 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102075330 | ACAGGTGTGTACTAC[A/G]ATGCCCAGGTAAGTT | 79023 |
rs137871787 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NUP37 | GRCh38.p7 | 12:102106970 | CAATGAGGCACCAGA[A/C]CCCTCGTTTGTCATG | 79023 |
rs137892155 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102074604 | AATATGCTCCCTTAC[A/T]GGTGAAATACACATT | 79023 |
rs138013316 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077362 | ACCAATCATTTCCTG[C/T]AACGGCTCCAACTTT | 79023 |
rs138025111 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102116897 | ATTCGAGCTACTCAG[A/G]AGGCTGAGGCAGGAT | 79023 |
rs138088621 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NUP37 | GRCh38.p7 | 12:102112850 | ATGTGGCATTATATG[C/T]GTGTAAGATGCTACA | 79023 |
rs138136174 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102099633 | ACTACTTAACAAACA[C/T]ACACAGGATGGACTT | 79023 |
rs138199237 | in-del | -/TTTTG | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102088693 | GTAATTTGTTTTTGT[-/TTTTG]TTTTAATTTTTTTTT | 79023 |
rs138224911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086862 | GCTGAGACAGAAGGA[C/T]TGCTTGAGCCCAGGA | 79023 |
rs138261252 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102104199 | ATGTGGTTTTGATTT[A/G]TATTTCTTTAATGAT | 79023 |
rs138365807 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102075036 | GAATTTGAAACTGGC[C/T]TGCCATTTTGCCAGG | 79023 |
rs138413267 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NUP37 | GRCh38.p7 | 12:102112614 | CCAGACTGGGCAACA[C/G]AGTGAGACCTGTGTC | 79023 |
rs138612202 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | NUP37 | GRCh38.p7 | 12:102117360 | GAGGCTGAGGCAGGA[G/T]AATCAACTGAACCCG | 79023 |
rs138724101 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102085986 | GTACTTAATGTATAT[A/C]TTTTTAAAGAAAATT | 79023 |
rs138745104 | in-del | -/TATGT | 0.0637235 | 0.166737 | intron-variant | NUP37 | GRCh38.p7 | 12:102108628 | GTGTGTTTAAACACG[-/TATGT]TATATTTTATACATG | 79023 |
rs138765891 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NUP37 | GRCh38.p7 | 12:102080733 | TGTTTAACTACAGTG[C/G]ACACATGTTCCCTGC | 79023 |
rs138987896 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102106681 | AAAATAGGTGCTTTG[A/C]TTTGGGACATTACAG | 79023 |
rs139022639 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NUP37 | GRCh38.p7 | 12:102104830 | TTTATGCCAGTACCA[C/T]ACTGTTTTGATTACT | 79023 |
rs139136839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102105120 | TTTCTGCAATGTTTT[A/G]TAGCTTTTAGTCTTT | 79023 |
rs139155937 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | NUP37 | GRCh38.p7 | 12:102099990 | AATATTAAAAAAAAA[A/C]CAAAAAACAAAAAGA | 79023 |
rs139203126 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102101505 | ATTGTTATACATCTA[C/T]CTTAGTCTTTGCCCT | 79023 |
rs139220175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102094539 | CTCCATCTTAATTAT[A/G]GATCTTAAAGACTTT | 79023 |
rs139236449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102110080 | TAGGAAAAAACATGC[A/G]ACATCTTCACAACCT | 79023 |
rs139236610 | snp | C/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, splice-donor-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118362 | AGTTTTGTAGACTAA[C/T]CTGAAACGTACACGT | 79023 |
rs139377474 | snp | C/T | 0.180064 | 0.240019 | intron-variant | NUP37 | GRCh38.p7 | 12:102078082 | CTTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 79023 |
rs139413412 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102095476 | ATGTGAGTGCATCTG[C/T]ATATGGTAGACATGA | 79023 |
rs139489080 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | NUP37 | GRCh38.p7 | 12:102076603 | GTAAAGAAAATATTT[G/T]GAAAACAAATCAACT | 79023 |
rs139625051 | snp | C/T | 0.000538367 | 0.016398 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118369 | TAGACTAACCTGAAA[C/T]GTACACGTGCCAATG | 79023 |
rs139659916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115611 | AATGAAAATTTGACA[A/C]ATACACGACACCAGT | 79023 |
rs139705253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102109276 | GAATTTAAGGCAACT[A/G]CATGCTAATGATAAG | 79023 |
rs139716924 | snp | C/G/T | 0.00159641 | 0.0282137 | intron-variant | NUP37 | GRCh38.p7 | 12:102081232 | CATTGGCTATTATTA[C/G/T]AGGTTAAAGTCAAAT | 79023 |
rs139799882 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102100784 | GTTTTCTTATTTGTT[G/T]TTCCTACCTAATATT | 79023 |
rs139831841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097157 | AGCCAGGCAAAACAT[C/T]TGAAGCTTCTGCTGT | 79023 |
rs139915870 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119392 | CTGCACGTCCCGCAC[A/C]CGTATCCCGGAACTT | 79023 |
rs140080767 | snp | A/G | 0.000193008 | 0.00982174 | intron-variant | NUP37 | GRCh38.p7 | 12:102076787 | AGCTCCAACAAAAAC[A/G]GTACATTACCTGAAT | 79023 |
rs140127385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102083748 | AAAAGGGAACATATA[C/T]GCAAAGTTGCTCAAG | 79023 |
rs140314899 | in-del | -/ATTTTACACAGTAAA | 0.0170251 | 0.090679 | intron-variant | NUP37 | GRCh38.p7 | 12:102079721 | CTGTGCTTGGGGATG[-/ATTTTACACAGTAAA]ATTTTACACAGTAAA | 79023 |
rs140318358 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099981 | TAGAAATGTAATATT[-/A]AAAAAAAAACAAAAA | 79023 |
rs140323643 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102097864 | CATGTAAATCTTTCA[C/T]ATCTCTGACATGAAA | 79023 |
rs140356713 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102091612 | TGTTTGCAAGGGAAA[G/T]TTAAAAGGAAAAGCT | 79023 |
rs140663520 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NUP37 | GRCh38.p7 | 12:102112498 | TTCATAATAAGTTCA[A/G]TGAAAATGGACTGCT | 79023 |
rs140678531 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111382 | CAAATATACGTATTT[C/G]TCAAAACTGATCAAA | 79023 |
rs140706461 | in-del | -/AG | 0.472241 | 0.114494 | intron-variant | NUP37 | GRCh38.p7 | 12:102111795 | AATTTAGTTATTTTA[-/AG]AGTTATACTTTCAAT | 79023 |
rs140712736 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106779 | GGTGAAACTGGCCCA[A/G]CTTCCCCACAGAACT | 79023 |
rs140777562 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102090111 | CCCCTCTCATATTTA[A/C]TTACCAGTGGAAAAA | 79023 |
rs140882128 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102098966 | ATGTTTGTGCCATAC[C/G]TACAGTTCAAATAAG | 79023 |
rs141023649 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102106038 | ACAATGAATGAACAC[A/G]AAAAAGGATAAACAC | 79023 |
rs141026226 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102082134 | CCTAGCTCCTATTGA[C/G]TCTTATTGGATTTGG | 79023 |
rs141154086 | snp | C/T | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102116786 | GAGGCGGGCGGATCA[C/T]GAGGTCAGTTCAAGA | 79023 |
rs141236719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102075579 | TTCCAGGAAAATATT[C/T]CATAAATATTTTCTC | 79023 |
rs141270823 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121732 | CTAATTTTTAGTAGA[C/T]AGGGTTTCACCATGT | 79023 |
rs141322538 | snp | G/T | 3.29576e-05 | 0.00405928 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118417 | ACCATATGCAATTAG[G/T]TTTCCTGAATCCCCA | 79023 |
rs141386955 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106188 | TAATAAACCAACCCC[-/C]ACTGATAACTTGATT | 79023 |
rs141426767 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | NUP37 | GRCh38.p7 | 12:102086622 | GAGAGCAAGACTCAG[A/T]AATCTCAGTCATGGC | 79023 |
rs141481425 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102104857 | TACTGTATAGCATTG[C/T]GATACGATTTGAAAT | 79023 |
rs141641956 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102103888 | ATAGGCCATCTATGA[C/T]GAGCCCACAGGTAAC | 79023 |
rs141673554 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUP37 | GRCh38.p7 | 12:102105142 | TTAGTCTTTGGCTTC[A/G]TTGGTTGTCTAGTGA | 79023 |
rs141748287 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | NUP37 | GRCh38.p7 | 12:102080317 | GTCCCAGATACTCAG[C/G]AGGCTGAGGCAGGAG | 79023 |
rs141844079 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102086044 | GTAGGATGAAGAATT[C/T]AAATTTTACCATAAT | 79023 |
rs141927127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102078680 | ATGGCTGCAGGATTG[C/T]TGTGATGATTAAATA | 79023 |
rs141971008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102118105 | ATGTTCAGTTAATCA[C/T]AGCCTTCACTTATCA | 79023 |
rs142002021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102100651 | TCTGTGCTCTTAACC[A/G]CTTTGGAATTCTGCC | 79023 |
rs142054565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120787 | GTGAGGTAGGAATTC[C/T]CTTCCTGGTTTTGCA | 79023 |
rs142196240 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081317 | CAATTATGACAAATC[-/T]TTTTTTTGGGTGATA | 79023 |
rs142208212 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NUP37 | GRCh38.p7 | 12:102103289 | TCATCAATGTTTTAT[C/T]GTTTCTGTGTACAGA | 79023 |
rs142245208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113863 | GAAATCCAAGTAGAT[A/G]TACTGATTTTTCCAG | 79023 |
rs142323969 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103401 | TAGTTCATTGTTAGT[A/G]TATTAGAAAGGTTAC | 79023 |
rs142357316 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102099637 | CTTAACAAACACACA[C/T]AGGATGGACTTCACC | 79023 |
rs142517698 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NUP37 | GRCh38.p7 | 12:102089848 | ACATATATATTCATT[C/G]TACTCCTGACAGACA | 79023 |
rs142719568 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102080790 | TGAGTGGTCTAGTGT[C/G]CTATAGTATGCAGTG | 79023 |
rs142783955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102076699 | CAATAAGGGAAAAAA[A/G]AAATCCAGTGCAAAG | 79023 |
rs142857083 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102105974 | AAACATGATTAAATT[A/G]AAGGATACTAAGATG | 79023 |
rs142932112 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NUP37 | GRCh38.p7 | 12:102081918 | GCCCAGGCTGGTCTC[C/T]AACTACTGAGCTCAA | 79023 |
rs143097605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120944 | GTGACAATTTTCTGT[C/T]TCACAGTTTTTGCTC | 79023 |
rs143166989 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102100218 | ATTAACCAATCCATA[C/T]AGTACATTAAGCCCA | 79023 |
rs143234883 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094915 | GTCAGTTTTCTTTCA[C/T]CATAAACTTTTATCT | 79023 |
rs143248256 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NUP37 | GRCh38.p7 | 12:102097523 | CCCTAAATTTTTAGA[G/T]AATTTTGCTAGTTTA | 79023 |
rs143315557 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102090217 | GGTGCTCTTATTTTG[G/T]AAGGTACATTTCTCA | 79023 |
rs143377918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104828 | TCTTTATGCCAGTAC[C/T]ATACTGTTTTGATTA | 79023 |
rs143413294 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102116351 | AAAATTAGTTTTACC[C/T]GTAGGAGGCTGCTTT | 79023 |
rs143499305 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091230 | GGTGAAACCCTGACT[C/T]TACTAAAAACACAAA | 79023 |
rs143518890 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NUP37 | GRCh38.p7 | 12:102079929 | TGCTCCCTGCGTATG[C/T]CTGTGACTAAAGAAG | 79023 |
rs143646924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113182 | TTATAAGGGTATCTG[C/T]CTACATGCAATGATT | 79023 |
rs143657656 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102093129 | ATAATATGTCAAAAT[C/T]AGAGTTGATAATAAA | 79023 |
rs143673124 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102115317 | GACCTTATGAAGCAC[A/G]TGAAATGTGGCTAGT | 79023 |
rs143740905 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NUP37 | GRCh38.p7 | 12:102110623 | CAAGGCACATGGATT[A/G]CCTGAGCTCAGGAGT | 79023 |
rs143764675 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102100430 | TAGAAAACACACATA[C/T]GGCGTTTACTATGTA | 79023 |
rs143789006 | snp | A/T | 1.64792e-05 | 0.00287042 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118467 | CTACCACATGCACAT[A/T]ATCTTCACAATCCAC | 79023 |
rs143869875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102096916 | GTTGGTGAACTAAGC[C/T]GTAAATTCTAAAAAT | 79023 |
rs143908180 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102094122 | GGAGAGTTCTTTTAA[C/T]GACAAAGAATCTCTA | 79023 |
rs143926105 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102108442 | GTTGGCTTTCCTACT[C/T]GTGAGGTTTTGGGAC | 79023 |
rs143944545 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102087607 | ATGGCAACTGATCAA[C/G]TATTTCTTCTCTATT | 79023 |
rs143960640 | in-del | -/CT | 0.0126979 | 0.078662 | intron-variant | NUP37 | GRCh38.p7 | 12:102116207 | CTCTCTCATCTTTGC[-/CT]CTCTTTTCCTAATTT | 79023 |
rs144179253 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NUP37 | GRCh38.p7 | 12:102076417 | AAGCAAAAACATGTC[A/G]CAGAGATATACTATC | 79023 |
rs144341460 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119109 | GTGTGGAGAACCAGC[A/G]CTAATGAAGAAAAAA | 79023 |
rs144377635 | in-del | -/CTTTTT | 0.0532157 | 0.154195 | intron-variant | NUP37 | GRCh38.p7 | 12:102075164 | CTTTTCTGAAGCGGG[-/CTTTTT]CTTTTTCTTTTTCTT | 79023 |
rs144409309 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102115617 | AATTTGACAAATACA[C/T]GACACCAGTTAACAG | 79023 |
rs144473944 | snp | A/C/G/T | 6.59091e-05 | 0.00574028 | synonymous-codon, missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077329 | GAAAGTACCTGGACC[A/C/G/T]AGTAATATCCCAAAT | 79023 |
rs144542242 | snp | C/G/T | 0.000197772 | 0.00994217 | synonymous-codon, missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112190 | CATGGTGAAATGTTC[C/G/T]AAGTGTTTTATACTG | 79023 |
rs144639946 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102117675 | ATGGATTACAATGTT[A/G]TCAGATGCCCTCTTG | 79023 |
rs144851525 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102080414 | CCACAGAGTGAGACC[C/T]TGCCTCAAAAACAAA | 79023 |
rs144957606 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102084779 | ACCATGAACTTTAGA[G/T]AACAGATGAAGAGTT | 79023 |
rs144972337 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102082179 | GAGGTCTCTTGACTT[C/T]TGTATATTTTACTAT | 79023 |
rs144996335 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | NUP37 | GRCh38.p7 | 12:102101967 | TGACCTCAGATGATC[C/T]GCCCATCTTGGCCTC | 79023 |
rs145223486 | snp | C/T | 0.000528629 | 0.0162491 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118391 | GTGCCAATGACCACA[C/T]AATTATTGCCACCAT | 79023 |
rs145287177 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109598 | GATTGTGCCTTCAGG[G/T]TGCTCTAAAAATAGT | 79023 |
rs145320551 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NUP37 | GRCh38.p7 | 12:102105760 | CAGCTACTCGGGAGG[C/T]TGAGGCAGGGAGAAT | 79023 |
rs145381637 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NUP37 | GRCh38.p7 | 12:102115679 | TAATCAAAGGGACAA[C/T]ATGAGATTCTGAAAA | 79023 |
rs145601255 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086344 | GTAAATTTAGCAACA[C/T]GGCCATCTTCCATAC | 79023 |
rs145777915 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 12:102079331 | TAAAACATCATTTAT[C/T]CTATTATTCATCTAA | 79023 |
rs145843606 | snp | C/T | 0.0108173 | 0.0727438 | intron-variant | NUP37 | GRCh38.p7 | 12:102074973 | AAAAAAAAAAAAGCA[C/T]GTATGTTACAAAACA | 79023 |
rs145869250 | snp | A/C/G | 0.00835444 | 0.0641245 | intron-variant | NUP37 | GRCh38.p7 | 12:102111459 | TAATTTAAAAAAAAC[A/C/G]AAGTTAGCTTAATAG | 79023 |
rs145874946 | snp | A/C | 0.0655868 | 0.168795 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119774 | GTTCCGTCCCTACAC[A/C]TACTGCTCATTAAAG | 79023 |
rs145914673 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106787 | TGGCCCAACTTCCCC[A/G]CAGAACTAATGTTCA | 79023 |
rs145953226 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102117219 | CAGCACTTGGGAGGC[C/T]GAGGTAGGCAAATGA | 79023 |
rs146059848 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | NUP37 | GRCh38.p7 | 12:102080943 | AGGGCTAAGTCTACC[G/T]GAGCCTGGTCCGAAG | 79023 |
rs146080422 | snp | A/G | 0.00195094 | 0.0311715 | intron-variant | NUP37 | GRCh38.p7 | 12:102076754 | TGGTGGCACAGCAAC[A/G]TCAAAAGATCAAATC | 79023 |
rs146182222 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104862 | TATAGCATTGCGATA[C/T]GATTTGAAATAAAGA | 79023 |
rs146319964 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NUP37 | GRCh38.p7 | 12:102118116 | ATCATAGCCTTCACT[C/T]ATCAGAATATTCCAT | 79023 |
rs146372547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103591 | CTTTTTCATATCTAA[C/T]TGCTCTGGCTAGGAC | 79023 |
rs146378091 | in-del | -/AG | 0.17461 | 0.238362 | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074170 | TATATATACACACAC[-/AG]AGAACAGAGTAGAAA | 79023 |
rs146496562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099969 | CTGCTCACTATGTAG[A/C]AATGTAATATTAAAA | 79023 |
rs146702324 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102097863 | TCATGTAAATCTTTC[A/G]TATCTCTGACATGAA | 79023 |
rs146721931 | snp | A/T | 0.0640965 | 0.167152 | intron-variant | NUP37 | GRCh38.p7 | 12:102091158 | TCCCAACACCTTGGG[A/T]GGCTGAGGCAGGCGG | 79023 |
rs146842889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102111211 | GTATGATCCCACTTA[C/T]ATGAAGTTCTAGAAT | 79023 |
rs146932578 | snp | G/T | 0.00874735 | 0.0655527 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120204 | AGCGGCGACAGCGGC[G/T]ACTGCGGCGGCCGCG | 79023 |
rs146948707 | snp | C/T | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102116806 | TCAGTTCAAGACCAG[C/T]CTGACCAACATGGTG | 79023 |
rs147202652 | snp | C/T | 3.30311e-05 | 0.0040638 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099182 | AACCATTAATGAAAT[C/T]GGTATGGCCCTCTAA | 79023 |
rs147209030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113688 | TTTTCTTTATAAAAG[C/T]GTATGGTATTATAAA | 79023 |
rs147225296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102109978 | AAATCAACAGCACAC[C/T]AGCTGTTGGCAATGA | 79023 |
rs147281270 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094498 | TATTTTGTGATCTCA[A/G]TTGGGGTGGGGGTGG | 79023 |
rs147298033 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088335 | TGAGATAGTCACTTT[C/T]TTTTGGGTAAAATTT | 79023 |
rs147346307 | in-del | -/TTTTATTTAGTATA | 0.417034 | 0.18601 | intron-variant | NUP37 | GRCh38.p7 | 12:102117695 | ATGCCCTCTTGGAAT[-/TTTTATTTAGTATA]TTTACATATACTAAA | 79023 |
rs147364971 | in-del | -/TG | 0.0123036 | 0.0774623 | intron-variant | NUP37 | GRCh38.p7 | 12:102108669 | AAGGGTAAGAAAAAC[-/TG]TAAAACAAAGCTTAT | 79023 |
rs147403270 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102108846 | AATGAAATCATAAAA[C/G]TTTGTTCAAAATGTC | 79023 |
rs147543277 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102088792 | CATAGGATAATAGTG[C/G]AGAGAAGGTCAGCAG | 79023 |
rs147575527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120712 | AATTTTTAAATTGAG[C/T]ACCTACTAAATGCCT | 79023 |
rs147734913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102082074 | CAATTCTTTGATCCC[A/G]TGACATCCTGAATCC | 79023 |
rs147751381 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NUP37 | GRCh38.p7 | 12:102078497 | TCTCAAGAGAGACAG[A/G]CATTTATGTGTTACA | 79023 |
rs147769007 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | NUP37 | GRCh38.p7 | 12:102083277 | TTAAGTAGACTCACT[G/T]CTCTCAGGGAGAAAT | 79023 |
rs147785385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102079701 | CACTAGCCAGCACTA[C/T]ATTACTGTGCTTGGG | 79023 |
rs147838891 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NUP37 | GRCh38.p7 | 12:102105681 | GCCTGGTCAACACGG[C/T]GAAATCCCATCTCTA | 79023 |
rs147855909 | in-del | -/TTTACA | 0.077417 | 0.180873 | intron-variant | NUP37 | GRCh38.p7 | 12:102114766 | ATCTGAAAAAAAGAG[-/TTTACA]TTTACACAACCCCTC | 79023 |
rs147890165 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | NUP37 | GRCh38.p7 | 12:102103672 | TAAAAAGATCATTCA[A/C]CATGATCAAGTGGGA | 79023 |
rs148063047 | in-del | -/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110358 | ACAAAAAATTAGCCG[-/G]GGAGTGGTGGTGCAT | 79023 |
rs148099671 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NUP37 | GRCh38.p7 | 12:102093260 | TCTTCATGAAGCTTT[A/G]GGGAGGATAAAAATT | 79023 |
rs148117644 | in-del | -/AAAC | 0.273318 | 0.24891 | intron-variant | NUP37 | GRCh38.p7 | 12:102097564 | CTCAGAGTCATAAGA[-/AAAC]AAACAAACAAAAACA | 79023 |
rs148171042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102112380 | GATTTAACTAGTTCA[C/T]TGAATTAAAAAAAAA | 79023 |
rs148222645 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102108563 | CCCCTTCATATATAC[A/T]TCTATCCTATTAGTT | 79023 |
rs148293835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086599 | CAATTGCTTTACCAT[C/T]GCAGAGGGAGAGCAA | 79023 |
rs148553020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081585 | TCTCATCTACAAAAT[A/C]CAATACTACTACTGT | 79023 |
rs148673079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102102267 | TGATGTGTTGGTAGA[C/T]CTTTGCTACTACACC | 79023 |
rs148692160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113748 | CTTGATATTTAATGA[A/C]ATACGTATGTCTATA | 79023 |
rs148699564 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091150 | GCCTGTAATCCCAAC[A/C]CCTTGGGAGGCTGAG | 79023 |
rs148709528 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102117984 | ATCTCCTGGAAGATT[A/G]TTTTTTGGGCTCTCA | 79023 |
rs148837922 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | NUP37 | GRCh38.p7 | 12:102107437 | GTGGACAAGACAAGG[-/A]AAAAAAAAGGGGAAA | 79023 |
rs148849647 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102079890 | CAAGTGCACATAAGC[A/G]GACTCAAACTTTTTG | 79023 |
rs148918792 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NUP37 | GRCh38.p7 | 12:102092398 | ACAGAGATGTAGTTA[C/T]AAGGATTAGCAGGCA | 79023 |
rs148936867 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NUP37 | GRCh38.p7 | 12:102105907 | AAAGATAAGTCTATG[C/T]GTTAACCCCTGGTAA | 79023 |
rs148959642 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075509 | TTTTTGTATAAAACC[-/C]AGTGATTTTAATAAT | 79023 |
rs149076157 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102085285 | AAATTAGCCAGGTGT[G/T]GTGGCATGTGCCTAT | 79023 |
rs149164256 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102110215 | GCTAAAATTAAAAAG[A/G]CAGGCTGGGCACAGT | 79023 |
rs149216774 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NUP37 | GRCh38.p7 | 12:102116298 | AGTGTTTGCGAATAC[A/G]ATCCTATGTTGTTAT | 79023 |
rs149248943 | snp | C/G/T | 1.74983e-05 | 0.00295784 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076806 | CATTACCTGAATAAG[C/G/T]AGGCTCGATCCATGT | 79023 |
rs149268372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102112695 | GATATTCTAGGTAAA[C/T]GAATTACCAGAACCG | 79023 |
rs149319972 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117658 | ACAACTAAAACATAC[A/C]TATGGATTACAATGT | 79023 |
rs149373520 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102081337 | TTTGGGTGATAAGAA[C/T]AGATAGGGTAGAAAA | 79023 |
rs149463112 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102107926 | GAAGGCTGATTGGAG[A/G]GGGGCACACTGGCAG | 79023 |
rs149533710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102076347 | TAAGGACCACACTAT[A/G]CAATGGAGTATTATG | 79023 |
rs149620812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102104281 | TTTGGAGAAATGTTC[A/G]TTTAAGTCTTTTTGA | 79023 |
rs149723183 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102105566 | GTCATCTTTAGCAGG[C/T]TGAAAAGTGCCCTCA | 79023 |
rs149845472 | snp | A/G/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119402 | CGCACACGTATCCCG[A/G/T]AACTTAAAAATTAAA | 79023 |
rs149865493 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NUP37 | GRCh38.p7 | 12:102096153 | TATTTGGAAGGCTAC[A/G]TTTTCTGTGAGTTTC | 79023 |
rs149917438 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102101606 | TATAACTATAAAAGC[G/T]GATAATATTTATACC | 79023 |
rs149986411 | snp | A/G | 0.000436461 | 0.0147662 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118370 | AGACTAACCTGAAAC[A/G]TACACGTGCCAATGA | 79023 |
rs149986663 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUP37 | GRCh38.p7 | 12:102110143 | AAACAAATATACCAA[A/G]AAAGCGTCAGCATTA | 79023 |
rs150056317 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102078477 | AGAATAGCTAAGTAT[G/T]TATCTCTCAAGAGAG | 79023 |
rs150083754 | snp | A/C | 0.000157766 | 0.00888021 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074352 | AAGGTACAGAAAACA[A/C]TTTATACTTCAGTCA | 79023 |
rs150087928 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102112569 | TGCGGGGCTGAGGTG[A/G]AAGGATTGCTTGAGC | 79023 |
rs150177462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099018 | CTATAGAATTTATGT[A/G]AAAGTCACATTTTTT | 79023 |
rs150317506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084006 | TCAAACATTTAGAAA[C/T]AAAAGGTGTGATGAA | 79023 |
rs150439449 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102104113 | GTTTCAATTTCTCCA[C/T]ATCCCGGGTCAACAT | 79023 |
rs150543104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105318 | CTACTTGAGCCCAGG[C/T]GTTCCAGACCAGCCT | 79023 |
rs150612630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114081 | CTTCGTAATTTGTGT[A/G]TATAATAGTTGTATA | 79023 |
rs150700617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100693 | GTACTGATCATTTGT[C/T]CCCATGAAGTTCAAC | 79023 |
rs150772316 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102075699 | CAAAGGGGTAATAGT[A/G]TGGTAGAAGAAACAA | 79023 |
rs150804566 | snp | C/T | 0.00036294 | 0.0134662 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112217 | ACTGAATGCCTTCAA[C/T]GTCTGCTTCTTCTTC | 79023 |
rs150842427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086625 | AGCAAGACTCAGAAA[C/T]CTCAGTCATGGCACC | 79023 |
rs150894851 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102095104 | CTGACTTGTTCTTAC[A/C]GAATGGTACTGTTTC | 79023 |
rs150946077 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102089914 | ATGCTGCTGTAAGCC[A/G]TCTTGCATATGTCTT | 79023 |
rs150998089 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NUP37 | GRCh38.p7 | 12:102098728 | GTAGAAATGGAGTTT[C/T]GCCATGTTGGTCAGG | 79023 |
rs151015661 | in-del | -/AGCATAGAATACAAC | 0.00636936 | 0.0560724 | intron-variant | NUP37 | GRCh38.p7 | 12:102109801 | CTAAGCAACAAGGAA[-/AGCATAGAATACAAC]AGCTGAATATGTAGA | 79023 |
rs151068075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105983 | TAAATTAAAGGATAC[C/T]AAGATGATCATCCTG | 79023 |
rs151086754 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119110 | TGTGGAGAACCAGCG[C/T]TAATGAAGAAAAAAA | 79023 |
rs151298377 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102077970 | AGATCAAATGTAAAG[A/G]AAGAGGCTATGTAAA | 79023 |
rs180675613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100694 | TACTGATCATTTGTT[C/T]CCATGAAGTTCAACT | 79023 |
rs180679076 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121876 | AACAACTTAGAAACT[C/G]ATAATGCATGATAAT | 79023 |
rs180784441 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112403 | AAAAAAAATCCAAAG[A/T]TGTCTAAGCCTCACA | 79023 |
rs180965696 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099457 | CATTTCTTACAAAAA[A/C]ACACACACACACACA | 79023 |
rs181015488 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102110222 | TTAAAAAGACAGGCT[A/G]GGCACAGTGGCTCAT | 79023 |
rs181025100 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079281 | TAAAATGTGACTGTT[A/C]TTTAAGAACGTACTT | 79023 |
rs181065851 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102089566 | TCACTTCCTAGACGG[A/G]GCAGCCGGGCAGAGG | 79023 |
rs181206028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116378 | CTTTACTCTTTTGTA[C/T]ATTGGTGGCTTGCAT | 79023 |
rs181207099 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093189 | AAGGAAGGAGGTACC[C/T]TGTTTCATACAGAAC | 79023 |
rs181214541 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102083869 | TGAAGGAAAAGGCCA[C/T]GGGATGTGTTGAAAA | 79023 |
rs181305764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102076670 | TCGGGAAAGTAAAAT[A/G]ACCACTTATAAAACA | 79023 |
rs181307728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099779 | ATGAGAAGTTGCACA[C/G]TGGAGGACTGTGTGA | 79023 |
rs181319831 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120929 | CACACTGCCTGCCCA[A/G]TGACAATTTTCTGTC | 79023 |
rs181331214 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102089721 | CTTCCCAGACGAGGC[A/G]GCCGGGCAGAGGCGC | 79023 |
rs181455727 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111064 | GAAACTGTATTGGTA[C/T]CTATTTACAGAAGAA | 79023 |
rs181757741 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102094731 | ATTTGGTTACATTCT[A/G]ATATCTTATTCTTTA | 79023 |
rs181760923 | snp | A/G | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102117008 | CTCCGTCTCAAAACA[A/G]AACAAAACAAAAACA | 79023 |
rs181884502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111865 | TTCAGATGAATCTCA[C/T]GTAAAAGGTTTTGTA | 79023 |
rs181908706 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102083497 | CCTCTGTGAAAGCTG[A/C/T]GAGAAGATTTGGTTA | 79023 |
rs181910685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104712 | CAGACTATCCTTTTC[C/T]CCATTGTGTAGCCTT | 79023 |
rs182014345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077609 | ATGTAAACATTTGCA[A/G]TATACAGGTTCAGCA | 79023 |
rs182029965 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121215 | AGACCAGGGGTTGGC[A/C]AACTGGCTGTGCTGC | 79023 |
rs182085423 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102074969 | ATTAAAAAAAAAAAA[A/G]GCACGTATGTTACAA | 79023 |
rs182120552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102081411 | GGGAATTTTTCCTTT[A/G]GGAATTTTCAGAAGT | 79023 |
rs182125007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102102904 | AAATAATCGATTGAC[C/T]ATAAATGCATGAATT | 79023 |
rs182196014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102095470 | ATATGCATGTGAGTG[A/C]ATCTGCATATGGTAG | 79023 |
rs182303621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100392 | GCAATTTTGACCCAA[C/T]CTGAGGGTTATTATT | 79023 |
rs182373700 | snp | A/G | 0.00329924 | 0.0404813 | intron-variant | NUP37 | GRCh38.p7 | 12:102112252 | GCATACACAGTAAAT[A/G]TTTTAATAAGTAATG | 79023 |
rs182445893 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102074691 | CAGACTCCATTTTTG[C/T]AGTCTACACCAACCA | 79023 |
rs182464707 | snp | C/T | 0.00196217 | 0.0312608 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118354 | TTCGGTGCAGTTTTG[C/T]AGACTAACCTGAAAC | 79023 |
rs182477922 | snp | A/G | 0.000183158 | 0.00956793 | intron-variant | NUP37 | GRCh38.p7 | 12:102075108 | ACCTAAGAAATAAGG[A/G]AGCGTAAAATTAAGT | 79023 |
rs182587798 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102080158 | GAAAAAATCAGACAA[C/T]AATTTAAGGCAAAAT | 79023 |
rs182605671 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102101828 | CTCCCAGGTTCAAAC[A/G]ATTCTCCTACCTCAG | 79023 |
rs182619200 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102091047 | CAAAGTCAGTTATAA[C/T]CACAGAAGCACACTT | 79023 |
rs182730203 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102075412 | GTCTCAAACTCCTGG[C/G]CTCAAGTGATCCTCC | 79023 |
rs182734881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102097613 | GATCCTAGGTCTCTC[C/T]GGCTTTCGTTCACTA | 79023 |
rs182745041 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120062 | CACCGCAGAGCGCCA[A/G]GAACCGACCAGAGGC | 79023 |
rs182947340 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119873 | AAGGGAGGGAACAAG[A/G]TAAGTCTCTGCAATG | 79023 |
rs182963341 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NUP37 | GRCh38.p7 | 12:102087936 | CAAAGTTTTACCTAA[C/T]TTTTAACCAGTATTT | 79023 |
rs183102443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102091607 | TTAAATGTTTGCAAG[A/G]GAAATTTAAAAGGAA | 79023 |
rs183243427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105957 | TGAAAATAGGGTTTT[C/G]CAAACATGATTAAAT | 79023 |
rs183250460 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102106976 | GGCACCAGACCCCTC[A/G]TTTGTCATGACTGGT | 79023 |
rs183378481 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102112664 | ACAAAGAAAATGGAA[C/T]GCTCTAAAGAATCAA | 79023 |
rs183406633 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120222 | TGCGGCGGCCGCGGG[A/G]GGGCATCCCGTTGGG | 79023 |
rs183464992 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102086891 | GAGTTCAAGACCAGC[C/G]TGGCAAATACAGTGA | 79023 |
rs183466062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085588 | TGTCAAATAAAAACC[G/T]TAACAATTATAGAGA | 79023 |
rs183478017 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106523 | AATAAAGTAAAGGAG[A/C]CTAGATTAGTTTACT | 79023 |
rs183687461 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117700 | CTCTTGGAATTTTTA[A/T]TTAGTATATTTACAT | 79023 |
rs183762507 | snp | A/C | | | stop-gained, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077431 | GCACTTGTTCTGATT[A/C]AAGAGATAAAATAGC | 79023 |
rs183816992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081003 | GTAAGCAGGTGTGCA[G/T]CCTCTATGGCCAGAC | 79023 |
rs184013858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102102707 | TGAAGCTTTTTCTGT[C/T]TTCTTCTAGCCATTT | 79023 |
rs184149137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102076292 | TGGTTTTAGTCTCTT[A/G]TTTGGTTTTGCTGTT | 79023 |
rs184161296 | snp | C/T | 1.67545e-05 | 0.0028943 | intron-variant | NUP37 | GRCh38.p7 | 12:102099094 | AATGTGGTTATAACA[C/T]AAGCAACATACCTGC | 79023 |
rs184172564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115697 | GAGATTCTGAAAAAT[A/G]CTTTATTGAAATTCA | 79023 |
rs184175754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120698 | ATGATGTTGAGTGCA[A/G]TTTTTAAATTGAGCA | 79023 |
rs184211036 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097566 | CAGAGTCATAAGAAA[A/G]CAAACAAACAAAAAC | 79023 |
rs184281419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102103417 | TATTAGAAAGGTTAC[C/T]GATTTTTGAATGTTG | 79023 |
rs184292130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102093214 | CAGAACACTAATAAA[C/G]TACACCACACAAAAT | 79023 |
rs184305906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102092691 | AGAGGTGGGGAACCA[C/T]GTAACTGAAAGCCCA | 79023 |
rs184406781 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092769 | TAGAGTTGGTAAATA[A/G]AGTTTTGTCAGTTTA | 79023 |
rs184410634 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102100069 | ATCATTCTCCAAAGC[G/T]TCTGTCACAGTCTAC | 79023 |
rs184421474 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121041 | TTTGTATAGTGCAGC[C/G]TGCCATTCAGAGTGC | 79023 |
rs184687526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092425 | GGCACTTTACAATGT[C/T]ACTGGTACAGGAAAG | 79023 |
rs184693968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102113156 | CAAACGACTACCAAG[A/G]TATGCAGCTGTTATA | 79023 |
rs184815450 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NUP37 | GRCh38.p7 | 12:102089454 | CTCACTTCCCAGACG[A/G]GGCGGCCGGGCAGAG | 79023 |
rs184819851 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102108810 | TTGAGGGTCTCCTAC[A/G]GATTTCCTCAGTTAT | 79023 |
rs184952557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102083737 | GAGTATAAAGAAAAA[A/G]GGAACATATACGCAA | 79023 |
rs184964996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104966 | GATGGCTTTTCTGTT[C/T]CTGTAAAAAGTGCCA | 79023 |
rs185001254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082026 | CTTTAACCTCTTTTT[C/T]CTTAGGGTCAGAGAC | 79023 |
rs185025253 | snp | A/C/G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091438 | AAAAAACCCAAAAAA[A/C/G/T]AAAAAAAACCCCACA | 79023 |
rs185028919 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NUP37 | GRCh38.p7 | 12:102116410 | AGAGAAATGGTTTTT[C/T]CTCAGTCTTTTTCAA | 79023 |
rs185034024 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076841 | AGGTCTCTTATTTTG[A/G]GGATAACTAAAAGAT | 79023 |
rs185100680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102079799 | GTGGCACTAAACTGA[C/T]GAGGAAAAGACACAT | 79023 |
rs185104659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102101412 | GAATTTAATTTTAAA[C/T]GTTTTCTTAAAAGCA | 79023 |
rs185117094 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121958 | GTTTATGTCGTTGAC[A/T]TGTCATAAAACCCTA | 79023 |
rs185131951 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102089295 | CACAGTGGCCAGGCA[A/G]AGGCGCTCCTCACTT | 79023 |
rs185290326 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102103875 | TCCGCATCACAATAT[A/G]GGCCATCTATGACGA | 79023 |
rs185544201 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102082944 | GGGAAAGAAGAATTA[A/G]AGATGATTTTAGGAT | 79023 |
rs185659909 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098362 | AACCTTATGCAGAAA[C/T]CTCTGAATTTATCAA | 79023 |
rs185681595 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097283 | CAAATATTTGTTGAA[A/C]AATAATATCAACAAC | 79023 |
rs185792471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075824 | GAGACATAATTAGTT[C/T]AAGGCAGTCATAGCA | 79023 |
rs185802708 | snp | C/G | 0.000798403 | 0.0199641 | splice-donor-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120287 | TCTACCCCTAATCAC[C/G]TAAGTCTCGCGTCTG | 79023 |
rs185847988 | snp | A/G | 5.13914e-05 | 0.00506883 | intron-variant | NUP37 | GRCh38.p7 | 12:102074974 | AAAAAAAAAAAGCAC[A/G]TATGTTACAAAACAT | 79023 |
rs185858061 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119168 | GTTTAGGGATAGTTA[C/T]GACTCAACGTGAAAA | 79023 |
rs185932315 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084063 | GAAAAAGGGAATTTT[A/T]AAGAGCAAGACCTAT | 79023 |
rs185958249 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | NUP37 | GRCh38.p7 | 12:102089621 | GCGGCAGGGCAGAGG[C/T]GCTCCTCACATCCCA | 79023 |
rs185978094 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102090100 | TATTTCCTTTTCCCC[C/T]CTCATATTTAATTAC | 79023 |
rs185979086 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102095590 | AACACATCTATCAGA[C/G/T]GCTTGCTTTTTGTTT | 79023 |
rs186100524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110617 | GGAGGCCAAGGCACA[C/T]GGATTGCCTGAGCTC | 79023 |
rs186104441 | snp | A/C | 4.70113e-05 | 0.00484803 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074318 | AAATATGTACTAAAA[A/C]TACAAAGTTTGTGAA | 79023 |
rs186106530 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102095347 | GGTCATAACTATGAA[A/C/T]GTATTTATATTTTTC | 79023 |
rs186120021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117072 | TTATAATAACTATCA[C/T]TTTAGTGATAGTTAT | 79023 |
rs186470108 | snp | C/G/T | 0.000316739 | 0.0125807 | missense, synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076838 | AACAGGTCTCTTATT[C/G/T]TGAGGATAACTAAAA | 79023 |
rs186509124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105540 | TGTCTCAACAACAAC[A/T]AGAATTCCGTGTCAT | 79023 |
rs186531926 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083065 | TTTAATGATATGTAG[A/G]AGAAAAAACAAATTA | 79023 |
rs186568028 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090929 | TTGTTATCTAAGAAA[C/G]TTTTGGTCTAGACCA | 79023 |
rs186571819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111871 | TGAATCTCACGTAAA[A/T]GGTTTTGTAGTTTGG | 79023 |
rs186584927 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114118 | AGCCAGATATGCCAA[A/G]ACAGCAGCCACTAAA | 79023 |
rs186639392 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NUP37 | GRCh38.p7 | 12:102111182 | AAAAACAAGCCAGAC[A/C]CAAAAGACATTCTGT | 79023 |
rs186701510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102087083 | CCAGCCTGGGTGACA[C/G]AGACCCTGTCTCAAA | 79023 |
rs186718544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102084268 | GACTATAGGCCTGGC[A/G]TATGTAAGCACTACG | 79023 |
rs186721343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102106893 | CCTTTCTCAGGAAAC[C/T]GACCTTCAGGCCTCC | 79023 |
rs186793555 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086248 | ATAATTACTACTGGG[C/G]CGCTTACAAACACAC | 79023 |
rs186850163 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102081757 | ATTCTGTTGCCCAGG[A/C]TGAAGGGCTCACTGC | 79023 |
rs186877562 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102102158 | TTTTCAATTCTTTGG[G/T]AGAAAGAGTATCATA | 79023 |
rs187006319 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102106039 | CAATGAATGAACACA[A/C]AAAAGGATAAACACA | 79023 |
rs187166466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075175 | CGGGCTTTTTCTTTT[C/T]CTTTTTCTTTTTTTT | 79023 |
rs187179333 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096604 | TTAAGTAAGCACTGG[A/G]TCTGCTCTTTACAGT | 79023 |
rs187182685 | snp | C/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119877 | GAGGGAACAAGATAA[C/G]TCTCTGCAATGAGCG | 79023 |
rs187301255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102091668 | TATTAAGGTGCCAAT[A/G]CAGACCAAATCAAAG | 79023 |
rs187310312 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102112895 | ACTATTATTGTTTAT[A/G]AATAGTGAATATGTA | 79023 |
rs187362456 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102100397 | TTTGACCCAATCTGA[A/G]GGTTATTATTATAGT | 79023 |
rs187430771 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102097677 | CATTTTTCCCCTTTG[C/G]AGGTTTCATTATTCC | 79023 |
rs187432483 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120084 | ACCAGAGGCAGGCTG[A/G]TCTTCCTTGGGGGCT | 79023 |
rs187539523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092529 | AGTTCCAATTAATCA[A/G]TTACTAAGTTAATCA | 79023 |
rs187541878 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102076064 | AACAAGCCCTGAGAC[C/T]ACCTCCTCTAGACTT | 79023 |
rs187550324 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113949 | CTGCATAATTCAGAT[A/G]CCCTTTGAAAATAAC | 79023 |
rs187554126 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120319 | CCTACCTGCCCTGTC[G/T]CATTTTTAAGTGGTG | 79023 |
rs187617756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102078065 | GGGTGTGGTGGCTCA[C/T]GCTTGTAATCCCAGC | 79023 |
rs187634353 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121661 | CTGGTTCAAGCGATT[C/T]TCCTGTCTCAGCCTC | 79023 |
rs187634809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102091114 | TTAAAAGCTCACAGC[C/T]GGCCAGGCACTGTGG | 79023 |
rs187680884 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120353 | CAGGCTGTGGCTTTT[G/T]AGGGTGTTTTGCACT | 79023 |
rs187788438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107434 | ACAAGTGGACAAGAC[A/G]AGGAAAAAAAAGGGG | 79023 |
rs187802180 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102098650 | GATTCCCTTGCCTCA[A/G]TCCCCCGAGTAGCTG | 79023 |
rs187922713 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102112342 | TATGCTTTTGAAAAG[C/T]TCAAAAGCAAATTAC | 79023 |
rs188097262 | snp | G/T | | | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112144 | TCAAGTCTAGTCTCT[G/T]GGCTCCAAGCTATGC | 79023 |
rs188110076 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102089462 | CCAGACGGGGCGGCC[A/G]GGCAGAGGCGCTCCT | 79023 |
rs188111968 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109234 | AAGCAAGTAGGGATG[G/T]AAAGAGTAGAAAGGC | 79023 |
rs188248221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102083755 | AACATATACGCAAAG[C/T]TGCTCAAGAGGACTC | 79023 |
rs188261447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102105319 | TACTTGAGCCCAGGC[A/G]TTCCAGACCAGCCTG | 79023 |
rs188283645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080750 | CACATGTTCCCTGCT[A/G]CAAGGCTAGGCTGCT | 79023 |
rs188312222 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111798 | TTTAGTTATTTTAAG[A/T]TATACTTTCAATAAA | 79023 |
rs188451951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088625 | TCTTGGTCTGACTTC[C/T]TTTACTCATCATTAG | 79023 |
rs188492595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102076592 | TGTTTTTCTGTGTAA[A/G]GAAAATATTTGGAAA | 79023 |
rs188492744 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102099334 | ATTTCTTAAGCAATC[C/T]GCTATTTTTAAAGCA | 79023 |
rs188507196 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120898 | TGACTCGGAAGTGTA[G/T]TTCTTTCAACCATTT | 79023 |
rs188563542 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117708 | ATTTTTATTTAGTAT[A/T]TTTACATATACTAAA | 79023 |
rs188705513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075558 | TCTTTACAATTAGAC[C/T]GGGAATTCCAGGAAA | 79023 |
rs188718228 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097567 | AGAGTCATAAGAAAA[A/C]AAACAAACAAAAACA | 79023 |
rs188965541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102102792 | TATGGAGTGAAATAA[C/T]GGTTCAATTTCATTC | 79023 |
rs188979703 | snp | G/T | 4.97863e-05 | 0.00498906 | intron-variant | NUP37 | GRCh38.p7 | 12:102074998 | AAAACATTTCCACAT[G/T]ACCTGAGGGTGTCCT | 79023 |
rs189005823 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | NUP37 | GRCh38.p7 | 12:102089337 | TGGCGGCCGGGCAGA[C/G]GCGCTCCTCACATCC | 79023 |
rs189039479 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094374 | GGCATGGTTTATGCA[C/T]TCCCAGACGTGGATT | 79023 |
rs189047260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116450 | ATTGTCTTAATCATA[C/T]GACTTTTTATGATCC | 79023 |
rs189156182 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083400 | ATAATTCTACTGATG[A/G]AAGACTCAATGGGCC | 79023 |
rs189160432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121786 | TAACCTTAGGTGAGC[C/T]TCGGCTTCCCAAAGT | 79023 |
rs189172930 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121042 | TTGTATAGTGCAGCC[G/T]GCCATTCAGAGTGCT | 79023 |
rs189233693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081199 | AACTGTTTTGGCACA[A/T]AGCAGGCACTCAAAA | 79023 |
rs189259119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102093133 | TATGTCAAAATCAGA[C/G]TTGATAATAAAGACT | 79023 |
rs189409788 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102110932 | ACCACTTTAGAAACT[G/T]GCATTTTCTTAAAAT | 79023 |
rs189687328 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | NUP37 | GRCh38.p7 | 12:102089660 | GCGGCTGGGCAGAGG[C/T]GCTCCTCACTTCCCA | 79023 |
rs189836518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102090998 | TCAAAATTTGAAAAT[G/T]CAGGTTTTAATATTT | 79023 |
rs189844570 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107511 | GTCGGCTGTTGGGGG[A/G]AAATGTTTCAAGTAT | 79023 |
rs189929589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082536 | TTAAAGGATTTTACA[C/T]GTTAGCACATTTAAT | 79023 |
rs189956018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079800 | TGGCACTAAACTGAC[A/G]AGGAAAAGACACATA | 79023 |
rs189962335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102101479 | CCAGGTCACCAAGAC[A/G]TATTAAAAATATTGT | 79023 |
rs190087915 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102100290 | GATTGGAAAGGTTTG[C/T]AATTTATCTTTGTTT | 79023 |
rs190107302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096702 | TATATATGTGATATT[A/G]TAAGAATCTTACATT | 79023 |
rs190115634 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119951 | TCCCACCTCCCGGGG[C/T]CCGAAGTGGGAAGGA | 79023 |
rs190187562 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103618 | GGACTTCAAGTACTA[C/T]GTTGACAAAATACTA | 79023 |
rs190211818 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102104052 | CTTTGGAATGTTTTT[A/C]ATAGCAGCTGCACCA | 79023 |
rs190315067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108560 | ACTCCCCTTCATATA[C/T]ACATCTATCCTATTA | 79023 |
rs190320835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102076948 | AGGACAGAATGTCCA[A/G]TGTGTTTAAACTATA | 79023 |
rs190485156 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097502 | GTTAGCAACCCTATG[A/T]CAGTCCCCTAAATTT | 79023 |
rs190494253 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093997 | TTAGAAAATGTTTTC[A/T]TCACTTTACTGACTT | 79023 |
rs190500054 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102075393 | TGCTATCTTGCCCAG[G/T]CAGGTCTCAAACTCC | 79023 |
rs190744171 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090580 | TAAGTCAATGCCAAC[G/T]AACTAAAGGTTAAGT | 79023 |
rs190745722 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078584 | AGAGCACAGACACGC[C/G/T]GCTTCCTTCACTTAT | 79023 |
rs190756218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111543 | GATTTGACATTTGTA[A/G]AAGGCAAGGCTAGTG | 79023 |
rs190883845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117148 | ATAATTTGAGAAATA[C/T]GGTTCTATTAATAAT | 79023 |
rs190894051 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102086772 | GCTGGCAAAGTGCAC[A/G]TATAATTCTGATCCT | 79023 |
rs190898598 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NUP37 | GRCh38.p7 | 12:102106156 | AAACAGGCATGGAAT[A/G]GATTCTCCCTCAGAG | 79023 |
rs190899106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096212 | AATGTTTGTTAGAAA[C/G]GCAGTGTTGGAACTG | 79023 |
rs191008503 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102100577 | GGTTACTTAACCAAG[G/T]TCACACCACGACTAA | 79023 |
rs191013715 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117699 | CCTCTTGGAATTTTT[A/C]TTTAGTATATTTACA | 79023 |
rs191039031 | snp | C/T | 0.000362438 | 0.0134569 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112136 | GCAATGAATCAAGTC[C/T]AGTCTCTGGGCTCCA | 79023 |
rs191060222 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112632 | TGAGACCTGTGTCTA[C/T]GTTATAAAAAAAGAA | 79023 |
rs191144140 | snp | G/T | 5.0804e-05 | 0.00503978 | intron-variant | NUP37 | GRCh38.p7 | 12:102074979 | AAAAAAGCACGTATG[G/T]TACAAAACATTTCCA | 79023 |
rs191158277 | snp | A/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119404 | CACACGTATCCCGGA[A/T]CTTAAAAATTAAAAT | 79023 |
rs191298792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102091515 | TTTCTCAAAGCATAA[A/G]AGTATAGAATAAATG | 79023 |
rs191557532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084369 | AGCATGGAGATGGCC[G/T]GTACGGTGGCTCACA | 79023 |
rs191568011 | snp | C/T | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102087628 | CTTCTCTATTGCTTT[C/T]TGCAAAATAAAGTGT | 79023 |
rs191569797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106959 | TTGCATCTGCACAAT[A/G]AGGCACCAGACCCCT | 79023 |
rs191576873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102076192 | TCCATGGCATTCTTA[C/T]ATTTAGTCGAATGTA | 79023 |
rs191689177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103266 | ATTTGTGCCAAGTTC[A/T]ATGTCTTTCATCAAT | 79023 |
rs191721919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102102612 | TAGTTTAATACAATT[C/T]CACTTGTCTAGTTTT | 79023 |
rs191821230 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102074684 | TACAGTCCAGACTCC[A/G]TTTTTGCAGTCTACA | 79023 |
rs191834740 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105849 | CCTGGGTGACAGAGC[A/G]GGACTCCCTCTCAAA | 79023 |
rs192011753 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080955 | ACCTGAGCCTGGTCC[A/G]AAGGTAGTAGGGGCA | 79023 |
rs192125500 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NUP37 | GRCh38.p7 | 12:102095441 | TGTGTGCATATATTT[C/T]TATATATACATGTAT | 79023 |
rs192251864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092164 | TTTTTGGCAGCTCAT[C/T]GTTTGCTAGGAAATT | 79023 |
rs192261163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102113053 | AAAAAATCAACTTTA[A/G]AAGTCAAGCCATCTG | 79023 |
rs192394536 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102089397 | TCCTCACATCCCAGA[C/T]GGGGCAGCCGGGCAG | 79023 |
rs192406600 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NUP37 | GRCh38.p7 | 12:102108757 | TTATTTGCTCATAGG[A/T]AACTCTAGACAAATT | 79023 |
rs192491064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098996 | GGTATGCTTCTTTTA[A/C]AACACTCTATAGAAT | 79023 |
rs192527319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081364 | AAAAGTTAAGTAAGT[C/T]TGGGAGTAGCTGAAT | 79023 |
rs192719462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089015 | ACGTTTCAGAGAGCA[C/T]GGGGTTGGGGGTAAG | 79023 |
rs192799861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120380 | CACTGTAATACCTCG[A/G]TCGTAGCAAAGTGCC | 79023 |
rs192928170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108080 | TGGATTGAAGGATAC[A/G]AAGTACTGGTTCTGG | 79023 |
rs192991338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103671 | TTAAAAAGATCATTC[A/G]CCATGATCAAGTGGG | 79023 |
rs193036879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075724 | AAACAAATAAGGCAT[C/G]AAATATGACAGCCAT | 79023 |
rs193048666 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120105 | CTTGGGGGCTGCCGC[A/G]ACGCGCTGTGGCTCT | 79023 |
rs193104098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092575 | AAAGAAGGGTAAGTC[A/G]TGGTGTATTTCCTTA | 79023 |
rs193174718 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109612 | GTTGCTCTAAAAATA[G/T]TCTAAAATTAATGGC | 79023 |
rs193195514 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102082799 | GAGCCAAAGACTTTA[G/T]AAACAAGCTAAGGCT | 79023 |
rs193225690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102097679 | TTTTTCCCCTTTGCA[A/G]GTTTCATTATTCCAA | 79023 |
rs193258028 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102102793 | ATGGAGTGAAATAAC[C/G]GTTCAATTTCATTCT | 79023 |
rs193262926 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102114017 | AGTTTTTCCACAAAT[C/G]AAAGAAATACACTTA | 79023 |
rs199516203 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121148 | AGGAACCACGTGTAA[A/G]GCTTATGGCATAGGC | 79023 |
rs199547118 | snp | A/G | 0.000681106 | 0.0184415 | intron-variant | NUP37 | GRCh38.p7 | 12:102077526 | ACAGAAAAATAAAAA[A/G]AAACTCAATCACTTA | 79023 |
rs199559131 | in-del | -/AT | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074149 | TTTGTAAGATTAAAA[-/AT]ATATATATATATACA | 79023 |
rs199693601 | snp | A/T | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074151 | TTGTAAGATTAAAAA[A/T]ATATATATATACACA | 79023 |
rs199776643 | in-del | -/AAG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096595 | TAAATTTTCTTAAGT[-/AAG]CACTGGGTCTGCTCT | 79023 |
rs199849100 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078130 | GTCAGGAGTTCGAGA[C/T]CAGCCTGGCCAACAT | 79023 |
rs199936860 | snp | A/G | 0.174932 | 0.238463 | intron-variant | NUP37 | GRCh38.p7 | 12:102089190 | GACAAAACCGCCATC[A/G]TCATCATGGCCCGTT | 79023 |
rs199999275 | in-del | -/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119357 | ACCACCATAGCACAC[-/G]TTTTACCTTTGTAAT | 79023 |
rs200051982 | snp | A/C/T | 0.000255867 | 0.0113079 | intron-variant | NUP37 | GRCh38.p7 | 12:102100988 | AGCAAAAAACAAACA[A/C/T]GTTTTAAAATAAGCT | 79023 |
rs200229630 | in-del | -/A | 0.0244538 | 0.107838 | intron-variant | NUP37 | GRCh38.p7 | 12:102090604 | TTAAGTTTCTAAAAG[-/A]AAAAAAAACTCACTC | 79023 |
rs200266251 | snp | A/G | 0.00346878 | 0.0415013 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118316 | GTGTAAGTTCTCTTA[A/G]TAGTGAAATATGTTC | 79023 |
rs200272661 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092709 | AACTGAAAGCCCAAA[C/T]CTAGAGATTAGATGG | 79023 |
rs200338826 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117698 | CCCTCTTGGAATTTT[A/T]ATTTAGTATATTTAC | 79023 |
rs200368728 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102079896 | CACATAAGCGGACTC[A/G]AACTTTTTGTTGTTC | 79023 |
rs200377092 | in-del | -/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103052 | TTTGTTCTTTTTTTT[-/G]CTCAAAATTGCTTTG | 79023 |
rs200408754 | in-del | -/GTAT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108627 | TGTGTGTTTAAACAC[-/GTAT]GTTATATTTTATACA | 79023 |
rs200545737 | snp | A/G | | | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074441 | GGACAGTCCAGATCC[A/G]ACGGCTACAGAACCC | 79023 |
rs200608639 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111152 | CTGGTATACATAACA[A/G]TGTGGAAAAATTGCA | 79023 |
rs200637933 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | NUP37 | GRCh38.p7 | 12:102112053 | TCAGACTTCCAATCA[C/T]GTAACACAATCAAAG | 79023 |
rs200673059 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075192 | TTTTTCTTTTTTTTT[A/T]AGAGACAGGGTCTTG | 79023 |
rs200673698 | snp | A/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121571 | TTTTTTTTTTTTTTT[A/T]AAGACAGAGTCTCAC | 79023 |
rs200776224 | in-del | -/A | 0.0441095 | 0.141807 | intron-variant | NUP37 | GRCh38.p7 | 12:102112730 | TCTACTGACAATATT[-/A]AAAAAAATACACTGT | 79023 |
rs200965605 | in-del | -/AC | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074162 | AAAATATATATATAT[-/AC]ACACACAGAGAACAG | 79023 |
rs201191648 | snp | C/T | 0.000140809 | 0.00838955 | intron-variant | NUP37 | GRCh38.p7 | 12:102101029 | ATATGGTTGTCAACA[C/T]ACCTTATATTCATTT | 79023 |
rs201208592 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant | NUP37 | GRCh38.p7 | 12:102082240 | TCCTGATCTTACGGC[-/T]TTTTTTTATGGTTTA | 79023 |
rs201226758 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078206 | TGTGGTGGCATGCGC[A/G]TAATCCTAGCTACTC | 79023 |
rs201252968 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088709 | TTTGTTTTAATTTTT[C/T]TTTTTTTTTTTTTTA | 79023 |
rs201414541 | in-del | -/T | 0.0655868 | 0.168795 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121521 | GAATGAGACTCTTGG[-/T]TTTTCTGTCACCATA | 79023 |
rs201479172 | snp | C/T | 0.00022816 | 0.0106784 | intron-variant | NUP37 | GRCh38.p7 | 12:102076786 | CAGCTCCAACAAAAA[C/T]GGTACATTACCTGAA | 79023 |
rs201547407 | snp | G/T | 0.000563782 | 0.0167801 | intron-variant | NUP37 | GRCh38.p7 | 12:102099203 | GGCCCTCTAAAACCT[G/T]ACAGAAAGAGAAACA | 79023 |
rs201555524 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102099463 | TTACAAAAACACACA[A/C]ACACACACATTTTTA | 79023 |
rs201584832 | in-del | -/A | 0.360421 | 0.224293 | intron-variant | NUP37 | GRCh38.p7 | 12:102110516 | ATGTACCAAAAAAAT[-/A]AAAAAAAAAAAAAGA | 79023 |
rs201599013 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110515 | CATGTACCAAAAAAA[A/T]AAAAAAAAAAAAAAG | 79023 |
rs201634490 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120521 | TTCGTCTGCAGCTTG[-/G]AAGACAGGCCCGTAG | 79023 |
rs201681002 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098679 | TGGAATCACAAGTGC[A/G]CACTACCGTGCCTGG | 79023 |
rs201703332 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102109045 | AATCTTACTGGGATC[G/T]AAATAAAACCAAACA | 79023 |
rs201720150 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088816 | TCAGCAGATTAACAC[A/G]TGAACAAAGGTCTCT | 79023 |
rs202027932 | snp | C/G | 2.72283e-05 | 0.00368964 | intron-variant | NUP37 | GRCh38.p7 | 12:102101004 | GTTTTAAAATAAGCT[C/G]TAAAGATTTATATGG | 79023 |
rs202041445 | snp | C/T | 0.000165556 | 0.00909674 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085832 | AACAAAATGAGCTGT[C/T]TGCACTCCTTCCAAG | 79023 |
rs202189068 | in-del | -/C | 0.113334 | 0.209338 | intron-variant | NUP37 | GRCh38.p7 | 12:102088708 | TTTGTTTTAATTTTT[-/C]TTTTTTTTTTTTTTT | 79023 |
rs267603269 | snp | A/G | | | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102075021 | GGTGTCCTAAATGAT[A/G]AATTTGAAACTGGCT | 79023 |
rs367579941 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078238 | GGAGGCTGAGGCAGA[A/G]CTGCTTGAATCCGAG | 79023 |
rs367593141 | snp | A/G | 1.67652e-05 | 0.00289522 | intron-variant | NUP37 | GRCh38.p7 | 12:102075124 | AGCGTAAAATTAAGT[A/G]TCGTATCCTATGGAT | 79023 |
rs367794237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086661 | GTGAGAATGCTATCC[C/T]TCACCCACTGCTCAT | 79023 |
rs367936706 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081806 | ATGAGCAATCCTCCC[A/G]CCTGAGCCTCCAGAG | 79023 |
rs368013715 | snp | A/C | 9.90933e-05 | 0.00703824 | intron-variant | NUP37 | GRCh38.p7 | 12:102112065 | TCATGTAACACAATC[A/C]AAGTACATTAGTAAG | 79023 |
rs368115832 | in-del | -/CAAA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085121 | AAACAAACAAACAAA[-/CAAA]AAACTGCCTACTGGG | 79023 |
rs368179847 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116548 | CCCAAACAGACAGTA[C/T]GAAATAGGCTAGGAG | 79023 |
rs368211608 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104812 | TTGGTCTACATATTT[A/G]TCTTTATGCCAGTAC | 79023 |
rs368216437 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102100553 | AAGGATATTAGCACA[A/G]AGAGATTAGGTTACT | 79023 |
rs368251282 | snp | C/T | 0.000193981 | 0.00984647 | intron-variant | NUP37 | GRCh38.p7 | 12:102076745 | GTATCCCAGTGGTGG[C/T]ACAGCAACGTCAAAA | 79023 |
rs368255095 | snp | A/G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087317 | TCTGTGCCAAAACAC[A/G/T]TAACTTCAAATATTC | 79023 |
rs368331607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102075755 | TCTGCCCCTTTTCCA[C/T]GCTAAGTGAAGCCTA | 79023 |
rs368398044 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094273 | ATTAGAGTGAGTTTT[A/T]GAAGACAAGCAGGGA | 79023 |
rs368402017 | in-del | -/AGA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086855 | TTGGGAGGCTGAGAC[-/AGA]AGGATTGCTTGAGCC | 79023 |
rs368484020 | snp | G/T | 8.41007e-05 | 0.00648408 | intron-variant | NUP37 | GRCh38.p7 | 12:102112256 | ACACAGTAAATGTTT[G/T]AATAAGTAATGAGAA | 79023 |
rs368511286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110673 | CAGGCAAATCCCTGT[C/T]CCTACAAAAAATACC | 79023 |
rs368596609 | in-del | -/TATTTAGTATATTT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117698 | CCCTCTTGGAATTTT[-/TATTTAGTATATTT]ACATATACTAAAATT | 79023 |
rs368671382 | snp | C/T | 6.76682e-05 | 0.00581631 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074418 | CACAGAGGGAGAGTT[C/T]GATGCCAGGACAGTC | 79023 |
rs368688640 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105227 | TATATATTTATACAT[G/T]GCACAAGAATGCCAT | 79023 |
rs368746356 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113573 | AAATAAGTAAATCAT[C/T]CTTCTGTTATTTAAA | 79023 |
rs368759420 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084386 | TACGGTGGCTCACAA[C/G]TGTAGTCCCAGCAAT | 79023 |
rs369138823 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099964 | TAGTACTGCTCACTA[G/T]GTAGAAATGTAATAT | 79023 |
rs369195992 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089700 | GCCGGGCAGAGGCGC[C/T]CCTCACTTCCCAGAC | 79023 |
rs369203112 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088671 | CCACCATTTGTTGCA[C/T]GTTGTTGTAATTTGT | 79023 |
rs369240438 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102074854 | AAAACAAAAACAAAT[C/G]AACCACCTTTTCTTG | 79023 |
rs369315924 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112830 | TGATTTTCATGTAGT[A/G]TTACATGTGGCATTA | 79023 |
rs369364338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102111710 | GAACTTACAGATTTA[C/T]ATACTGTTGGACAAA | 79023 |
rs369375339 | snp | C/T | 3.30104e-05 | 0.00406252 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118397 | ATGACCACATAATTA[C/T]TGCCACCATATGCAA | 79023 |
rs369378567 | snp | A/G | 4.14259e-05 | 0.00455096 | intron-variant | NUP37 | GRCh38.p7 | 12:102076858 | GATAACTAAAAGATA[A/G]TATTTTGCATTTTAT | 79023 |
rs369384857 | snp | C/T | | | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118427 | ATTAGGTTTCCTGAA[C/T]CCCCATTCTCAAAGG | 79023 |
rs369396415 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089339 | GCGGCCGGGCAGAGG[C/T]GCTCCTCACATCCCA | 79023 |
rs369409112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102106292 | GTTATGGCAACAGTG[A/G]GAAATAAAGACGCCA | 79023 |
rs369438662 | snp | C/T | 8.43192e-05 | 0.00649249 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118542 | TCAAAATTCAAGCAG[C/T]TGTGAAAATTAAATA | 79023 |
rs369493604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077192 | AATCCATAGCTCTGG[C/G]CTTCTATAGGAAAGA | 79023 |
rs369497976 | snp | C/T | 5.17898e-05 | 0.00508844 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118341 | ATGTTCACTGTCATT[C/T]GGTGCAGTTTTGTAG | 79023 |
rs369524001 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119860 | AACGGCAGAGAAGAA[G/T]GGAGGGAACAAGATA | 79023 |
rs369574065 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078125 | TTGAGGTCAGGAGTT[C/T]GAGATCAGCCTGGCC | 79023 |
rs369645104 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111188 | AAGCCAGACACAAAA[C/G]ACATTCTGTATGATC | 79023 |
rs369657917 | in-del | -/AC | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089963 | CACATACGATCACAT[-/AC]ACACACACACACCTG | 79023 |
rs369698332 | snp | A/G | 0.000786821 | 0.019819 | intron-variant | NUP37 | GRCh38.p7 | 12:102085899 | AATTGTTCTTGATAT[A/G]TCATTACTAAAAAAT | 79023 |
rs369715459 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | NUP37 | GRCh38.p7 | 12:102091553 | GTTTAATTACCTTGG[C/G]CAAAACCTAGGATCT | 79023 |
rs369761533 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112984 | AAGTTGGCTTATTTA[A/T]CCAGTTCAGCCCTAC | 79023 |
rs369774741 | snp | A/C/G | 8.23771e-05 | 0.0064173 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118449 | TCTCAAAGGGATTAA[A/C/G]TTCTACCACATGCAC | 79023 |
rs369826982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089676 | GCTCCTCACTTCCCA[C/G]ACGGGGCAGCCGGGC | 79023 |
rs369828256 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083854 | GCTGGAGAATAAGAA[C/T]GAAGGAAAAGGCCAC | 79023 |
rs369970543 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102114339 | TTACTGGGTGGTCAT[A/G]GGGATAAAGAAATCT | 79023 |
rs369976936 | in-del | -/TT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108848 | TGAAATCATAAAACT[-/TT]GTTCAAAATGTCATC | 79023 |
rs370098323 | snp | C/T | 3.58372e-05 | 0.00423288 | intron-variant | NUP37 | GRCh38.p7 | 12:102076753 | GTGGTGGCACAGCAA[C/T]GTCAAAAGATCAAAT | 79023 |
rs370191133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102075329 | TACAGGTGTGTACTA[C/T]GATGCCCAGGTAAGT | 79023 |
rs370214597 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120488 | GTATCTAGCGATGGA[A/G]CTGGTAGGTCCTGAG | 79023 |
rs370254679 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120802 | CCTTCCTGGTTTTGC[A/G]GGTGAAGAAACTTAT | 79023 |
rs370274689 | in-del | -/CAGG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082652 | ACTGGGATCTGACTC[-/CAGG]CAGTTAATTCAAGAG | 79023 |
rs370324486 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101222 | TAACTCATAATCATG[C/T]TTTTTATGGAGGGGG | 79023 |
rs370437147 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092246 | AAGAATGGATGACAT[G/T]AAATGACACATCTGT | 79023 |
rs370470369 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093419 | TTTAACTTATACAGA[C/G]AGATAAATTTTTGAA | 79023 |
rs370472120 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120266 | ACTGAAGAGTACGTC[C/T]TCGGGTCTACCCCTA | 79023 |
rs370498221 | snp | A/G/T | 7.48332e-05 | 0.00611653 | intron-variant | NUP37 | GRCh38.p7 | 12:102101127 | CAAAAAAACAAAAAT[A/G/T]TACCAATTTTTAGCC | 79023 |
rs370526690 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102076261 | TATTGGAATATAGCA[C/T]ATAATAAAATTTCAC | 79023 |
rs370568728 | in-del | -/AGG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112317 | AATGAATTTATCAGG[-/AGG]TTATGCTTATGCTTT | 79023 |
rs370577630 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091025 | ATTTCCAAAATTATT[A/C]CTATTGCAAAGTCAG | 79023 |
rs370611229 | snp | A/G | 1.95364e-05 | 0.00312535 | intron-variant | NUP37 | GRCh38.p7 | 12:102074470 | CCATGAGGATGGGCT[A/G]TAAAATATGTGAAGA | 79023 |
rs370656191 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102081297 | TACTGTCTGTATAAC[-/TG]TGCTCAATTATGACA | 79023 |
rs370751461 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100603 | ACTAAGTAATAACAC[C/T]GGAGTTTAAATGCAA | 79023 |
rs370755921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082158 | GATTTGGGAGCTTAG[G/T]TTTTGGAGGTCTCTT | 79023 |
rs370776383 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085622 | TTCTACAGTACAGGT[G/T]TCTAGACTAATCCAA | 79023 |
rs371141703 | snp | A/G | 3.13259e-05 | 0.00395752 | intron-variant | NUP37 | GRCh38.p7 | 12:102085763 | TAAATTATAAATAAT[A/G]ACCTTAAAAGTCTCC | 79023 |
rs371165221 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080476 | ACAGGCAAATGTTAA[C/G]ATAATACTAATGCTA | 79023 |
rs371168497 | in-del | -/TG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082500 | GCAGCTAAAATTGAC[-/TG]AGTGCTTACTATGTG | 79023 |
rs371251218 | snp | C/T | 1.64996e-05 | 0.0028722 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099150 | AATTTCTTGGCCTTC[C/T]TTGGGATCAAACACC | 79023 |
rs371375086 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076658 | GCAATGACTTAGTCG[A/G]GAAAGTAAAATAACC | 79023 |
rs371434539 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082364 | CATAAGAGGCTAACA[A/G]TTCTGGGCTTGCAGA | 79023 |
rs371488784 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118871 | CTGAAGATGGAATCA[C/T]TTTAACAGCAAATGT | 79023 |
rs371630269 | snp | C/T | 4.94434e-05 | 0.00497184 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112189 | CCATGGTGAAATGTT[C/T]GAAGTGTTTTATACT | 79023 |
rs371712715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088986 | TAATCCATTTAACCC[C/T]GAGTTGACACAGCAC | 79023 |
rs371796204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101508 | GTTATACATCTACCT[C/T]AGTCTTTGCCCTCTT | 79023 |
rs371894000 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111937 | GTATATTTAAATCAC[A/C]AATTCAGATGATAAG | 79023 |
rs371966612 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111291 | CAGGGAGTGGGGTAC[A/G/T]ATGATTAACTGGGAA | 79023 |
rs371968623 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121952 | ACTTGTGTTTATGTC[A/G]TTGACTTGTCATAAA | 79023 |
rs371982779 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116775 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACGAGG | 79023 |
rs372138363 | snp | C/G/T | 5.01704e-05 | 0.00500831 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118525 | TTGCTTCATCTTGTA[C/G/T]GTCAAAATTCAAGCA | 79023 |
rs372304605 | in-del | -/CAAA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097575 | AAGAAAACAAACAAA[-/CAAA]AACATAGACTACTGA | 79023 |
rs372348503 | snp | A/G | 1.74949e-05 | 0.00295756 | intron-variant | NUP37 | GRCh38.p7 | 12:102076792 | CAACAAAAACGGTAC[A/G]TTACCTGAATAAGCA | 79023 |
rs372454647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102087415 | GATGTTTTTCAAAAT[C/G]ATTATCTTAATGATT | 79023 |
rs372497907 | snp | A/C | 1.64795e-05 | 0.00287045 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118415 | CCACCATATGCAATT[A/C]GGTTTCCTGAATCCC | 79023 |
rs372540164 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117413 | CGAGGTTGACCTCCA[A/G]CCTGGGCGACCAAGC | 79023 |
rs372716187 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102006 | CTGGGATTACAGGCA[C/T]GAGCCACTGCGCCTG | 79023 |
rs372795775 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087203 | GGAACCAATGAGGTT[A/G]AACCAAACAGGTTTA | 79023 |
rs372811518 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088697 | TTTGTTTTTGTTTTT[G/T]TTTTAATTTTTTTTT | 79023 |
rs372880042 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100507 | CATAATCCTATAAGG[C/T]AGCTGCTATGATTAC | 79023 |
rs372887424 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081097 | TCTGTGTTTCGGGTT[C/G]TTATCACTAAGAAGG | 79023 |
rs373083793 | in-del | -/AACA | 0.0119091 | 0.0762411 | intron-variant | NUP37 | GRCh38.p7 | 12:102085103 | TAACTTAAAACAAAC[-/AACA]AACAAACAAACAAAC | 79023 |
rs373141402 | snp | A/G | 0.000200466 | 0.0100096 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074325 | TACTAAAAATACAAA[A/G]TTTGTGAATCTAAGG | 79023 |
rs373217367 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077748 | TCATGCACAAAATTA[C/T]TAAAAAAAGTTATAT | 79023 |
rs373306829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089854 | ATATTCATTCTACTC[C/T]TGACAGACATTTAGG | 79023 |
rs373346409 | snp | C/T | 1.66843e-05 | 0.00288823 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118520 | GCATCTTGCTTCATC[C/T]TGTATGTCAAAATTC | 79023 |
rs373368319 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084514 | CCGAGTGTAGTGGTG[C/T]GTGCCTATAGTCCCA | 79023 |
rs373402930 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102075205 | TTAAGAGACAGGGTC[-/T]TGCTCTGTCACCCAG | 79023 |
rs373460025 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119320 | GCATGTGGAGCTTAA[C/T]ACCTAGGTGATGGGT | 79023 |
rs373469689 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113634 | AAGGCCAAATTTTCG[C/T]GACAAATTTGTCCAA | 79023 |
rs373504193 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114916 | TTCTACTCATTATTC[C/T]ACGTTCCATCTCTGG | 79023 |
rs373546900 | snp | A/G | 1.7009e-05 | 0.0029162 | intron-variant | NUP37 | GRCh38.p7 | 12:102077523 | AAGACAGAAAAATAA[A/G]AAGAAACTCAATCAC | 79023 |
rs373589415 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093897 | TTAAGCACTTGTTTT[A/G]TATTTCATCTACAAG | 79023 |
rs373712284 | in-del | -/GGG | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119332 | TAATACCTAGGTGAT[-/GGG]TGTGCAAACCACCAT | 79023 |
rs373756690 | snp | A/C | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119916 | TCTCCCCGGGCCAGG[A/C]GAGTTCCTCAAGACC | 79023 |
rs373806620 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078327 | GCGAAATTCCTTCTT[-/T]AAAAAAAAAAAAAAG | 79023 |
rs373845578 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116828 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAGAT | 79023 |
rs373854790 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086915 | ACAGTGAAACTTCGT[C/T]TCTACAAAACACATA | 79023 |
rs373858779 | snp | A/T | 4.97938e-05 | 0.00498943 | intron-variant | NUP37 | GRCh38.p7 | 12:102099206 | CCTCTAAAACCTGAC[A/T]GAAAGAGAAACAGAA | 79023 |
rs373881817 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUP37 | GRCh38.p7 | 12:102091373 | ACTGTACTCCAGCCC[A/G]GGAAACAGAGTGAGA | 79023 |
rs373924923 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116285 | ATAAACATTTTTCAG[C/T]GTTTGCGAATACAAT | 79023 |
rs373967898 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089889 | TTCCAATTTTTGGTC[A/G]TCACCAAGAATGCTG | 79023 |
rs374140704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105239 | CATTGCACAAGAATG[C/T]CATGGCCGGGTGCAA | 79023 |
rs374190599 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087871 | AAATATGGATAAAAA[C/T]ATTAAATAAAAACTG | 79023 |
rs374199385 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109452 | AGTATAATCACAATT[A/G]TGTACAATTATGTAC | 79023 |
rs374240179 | snp | A/G/T | 5.01199e-05 | 0.00500574 | intron-variant | NUP37 | GRCh38.p7 | 12:102075112 | AAGAAATAAGGAAGC[A/G/T]TAAAATTAAGTATCG | 79023 |
rs374242305 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | NUP37 | GRCh38.p7 | 12:102099064 | ATGTAATTCTCATTA[A/T]AATGGCAATTTAAAA | 79023 |
rs374313951 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102076726 | AAAGAAGAGAACTAC[A/G]AAAGTATCCCAGTGG | 79023 |
rs374320211 | in-del | -/CTT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096660 | CATATGATATACTCT[-/CTT]GTCACATATGTGATA | 79023 |
rs374407725 | in-del | AATT/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088697 | TTTGTTTTTGTTTTT[AATT/G]TTTTAATTTTTTTTT | 79023 |
rs374432059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092505 | AGAGCAAAACTAGGA[G/T]TTTCTCTTAGTTCCA | 79023 |
rs374470945 | snp | G/T | 0.000470122 | 0.0153245 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074387 | AAACAACAGCTTGTG[G/T]TCTCCTCCAATTACA | 79023 |
rs374554481 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114398 | TTTACCAGTGAAACC[C/T]GTTTTCCTGGCAGCA | 79023 |
rs374683270 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089580 | GGGCAGCCGGGCAGA[A/G]GCACTCCTCACCTCC | 79023 |
rs374819634 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084215 | TGCCTATCTCATGTT[C/T]CCATGAGGAATAAAT | 79023 |
rs374828088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078155 | CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 79023 |
rs374976695 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104858 | ACTGTATAGCATTGC[A/G]ATACGATTTGAAATA | 79023 |
rs374990864 | snp | C/T | 1.66114e-05 | 0.00288192 | intron-variant | NUP37 | GRCh38.p7 | 12:102112240 | TCTTCTTCCTAAGCA[C/T]ACACAGTAAATGTTT | 79023 |
rs375036470 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080092 | AGAAGTCAAAGATAA[A/G]GGACATAATCCTTGA | 79023 |
rs375043638 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085110 | AAACAAACAACAAAC[A/T]AACAAACAAACAAAA | 79023 |
rs375054226 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117119 | TTGGACACTTCCAAA[C/T]TACCGTGCTCATTAT | 79023 |
rs375085362 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105256 | ATGGCCGGGTGCAAT[A/G]GCTCATGCCTGTAAT | 79023 |
rs375098950 | snp | C/G/T | 3.62109e-05 | 0.0042549 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076830 | TCCATGTGAACAGGT[C/G/T]TCTTATTTTGAGGAT | 79023 |
rs375104453 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108558 | AAACTCCCCTTCATA[A/T]ATACATCTATCCTAT | 79023 |
rs375176193 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104275 | ACCTTCTTTGGAGAA[A/G]TGTTCATTTAAGTCT | 79023 |
rs375251202 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117978 | TATAAAATCTCCTGG[A/C]AGATTGTTTTTTGGG | 79023 |
rs375362259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082389 | TGCAGAGCACTGAAA[C/T]GACTGTAGAGCACTG | 79023 |
rs375479938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081828 | CCTCCAGAGTAGCTG[A/G]GACTACGGTCGAGCA | 79023 |
rs375603537 | snp | C/T | 9.9167e-05 | 0.00704086 | intron-variant | NUP37 | GRCh38.p7 | 12:102101020 | TAAAGATTTATATGG[C/T]TGTCAACATACCTTA | 79023 |
rs375743860 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120726 | GCACCTACTAAATGC[C/T]TGGCACTAGGTGGGT | 79023 |
rs375771289 | in-del | -/TTACACAGTAAAATT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079739 | TTACACAGTAAAATT[-/TTACACAGTAAAATT]ACCCACAAAAAGTAC | 79023 |
rs375828920 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097046 | ATAATGCCATATGGG[C/T]CCATATCTGCTCCAC | 79023 |
rs375871848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102117951 | AATAGGAAAGCTGAA[C/T]ATTATAAAAGCTATA | 79023 |
rs375880991 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102076679 | TAAAATAACCACTTA[C/T]AAAACAATAAGGGAA | 79023 |
rs375942713 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119995 | ATAGAGTGGCAAGGC[C/T]GGGCGGCCGGCAGAA | 79023 |
rs376061843 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100947 | CATAAAAAGCCATTT[C/T]AAATTGGAATAAATC | 79023 |
rs376067500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102091828 | TAGCTGTGATGATGG[A/G]ATAGAGAGCTATTCA | 79023 |
rs376157583 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094735 | GGTTACATTCTAATA[C/T]CTTATTCTTTATTTT | 79023 |
rs376248372 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113417 | TGTTCCTTTTCTTAA[A/C]CTAAGCAGCAGGTAT | 79023 |
rs376396442 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110869 | GAATGAGTGTTGGAG[A/T]GTAGGAAGACCACCC | 79023 |
rs376432062 | snp | C/T | 1.6543e-05 | 0.00287597 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077466 | TGGGCCAAAAGATCA[C/T]AAAACCGGATTGTTC | 79023 |
rs376507994 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082999 | GGGACTTTCAAACAT[C/T]CTGAAGTCATGGAAA | 79023 |
rs376585055 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089564 | CCTCACTTCCTAGAC[A/G]GGGCAGCCGGGCAGA | 79023 |
rs376591548 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118919 | TTTTATGAACCACTA[A/T]TTGTAGGTACCATAT | 79023 |
rs376665293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084690 | CACTCCAGCCTGGGT[A/G]ACAGCCAGGCTGTGT | 79023 |
rs376727019 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098686 | ACAAGTGCGCACTAC[C/T]GTGCCTGGCTAATTT | 79023 |
rs376783003 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | NUP37 | GRCh38.p7 | 12:102089216 | CCGTTCTCGATGGTC[A/G]CTGTCTCTTCGGAGC | 79023 |
rs376932820 | snp | C/T | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102073957 | TACAAGTGTGAGCCA[C/T]TGTACCTGGCCTTTT | 79023 |
rs376982615 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080434 | TCAAAAACAAAACAA[A/T]CAGAAAACAAAAATG | 79023 |
rs377021872 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098024 | TTTCATAGTTTTATA[C/T]GTACATAAGTACTAA | 79023 |
rs377111538 | snp | C/T | 0.000398098 | 0.0141029 | intron-variant | NUP37 | GRCh38.p7 | 12:102085896 | GTTAATTGTTCTTGA[C/T]ATATCATTACTAAAA | 79023 |
rs377163126 | snp | A/G | 3.37308e-05 | 0.00410661 | intron-variant | NUP37 | GRCh38.p7 | 12:102075136 | AGTATCGTATCCTAT[A/G]GATAATGACAAGCTT | 79023 |
rs377256498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104261 | TTGGCCATTCATATA[A/C]CTTCTTTGGAGAAAT | 79023 |
rs377285779 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114095 | TGTATAATAGTTGTA[C/T]AGCTAACAGCCAGAT | 79023 |
rs377372903 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102085712 | TGTATGTGATGTCTT[A/G]TATCTCTATAAGTCT | 79023 |
rs377481982 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102583 | TCTGTTGTTTCCTTT[A/G]CTGTGCAGCTCTTTA | 79023 |
rs377500463 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089954 | ATAGATACCCACATA[C/T]GATCACATACACACA | 79023 |
rs377512601 | snp | C/G/T | 1.6701e-05 | 0.00288968 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118522 | ATCTTGCTTCATCTT[C/G/T]TATGTCAAAATTCAA | 79023 |
rs377547772 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085194 | TGAGGCTGAGATGAG[C/T]GGATCATCTGAGCTC | 79023 |
rs377677106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102090967 | CAACAGGATTTCTAC[C/T]ATAAAAGAAAAAAAT | 79023 |
rs377750597 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108413 | GCCTTAGGCCACAGA[C/T]TGAAGGCTGCAATGT | 79023 |
rs386377576 | in-del | -/AA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097461 | AAGGCAGTAAACTTA[-/AA]AGTCTTATATTCGAC | 79023 |
rs386765830 | multinucleotide-polymorphism | AA/CG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110714 | AGGCATGATGATGGG[AA/CG]CCTATAGTCCCAGCT | 79023 |
rs386765831 | multinucleotide-polymorphism | CG/TC | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111375 | GGTTGTACAAATATA[CG/TC]TATTTGTCAAAACTG | 79023 |
rs397706779 | in-del | -/AA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097462 | AGGCAGTAAACTTAA[-/AA]GTCTTATATTCGACA | 79023 |
rs397935867 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117452 | TCTGAAAAAAAAAAA[-/A]TAAAAATAATAATAA | 79023 |
rs398116809 | in-del | -/CT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084472 | TAACATGGTGAAACT[-/CT]GTTTCTACAAAAAAT | 79023 |
rs527245576 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076069 | GCCCTGAGACTACCT[C/T]CTCTAGACTTATAAG | 79023 |
rs527245699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102093637 | CTACCCAGGAAATAT[C/T]AGCATTTCATTTTTT | 79023 |
rs527291153 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104420 | CCCCCATTCTATGGG[C/T]TGCCTTTTGACTCTG | 79023 |
rs527419143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102079201 | CTGTTGAGTGACCTG[A/G]AGTTATCTTTCATAT | 79023 |
rs527420986 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100586 | ACCAAGGTCACACCA[C/T]GACTAAGTAATAACA | 79023 |
rs527432945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086953 | GCCAGGCATAGTGAT[A/G]CACACTTGTAGCCCC | 79023 |
rs527573012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101210 | AAGCTTTTATCATAA[C/T]TCATAATCATGCTTT | 79023 |
rs527667162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085558 | TTTGAATAAATGCCA[C/T]TTATGGATGATGGCT | 79023 |
rs527668028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077559 | TCACTAACTATACCT[A/G]AAGTGTAAGCAGAGA | 79023 |
rs527704934 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102078240 | AGGCTGAGGCAGAAC[G/T]GCTTGAATCCGAGAG | 79023 |
rs527720076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121789 | CCTTAGGTGAGCCTC[A/G]GCTTCCCAAAGTGCT | 79023 |
rs527846178 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084749 | CATTAGAGGACTGTG[A/G]GAGCCTAAGGAACTA | 79023 |
rs527865919 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102117456 | AAAAAAAAAAATAAA[-/T]AATAATAATAATACT | 79023 |
rs527891448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102091941 | TCAGCAGAACATTAA[A/G]TATCCCTACCATATG | 79023 |
rs528031054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085053 | GCGACTAATGTTTTT[C/T]GTTCACACAGTAGGG | 79023 |
rs528043647 | snp | A/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119119 | CCAGCGCTAATGAAG[A/G/T]AAAAAACAGCCTCCT | 79023 |
rs528065325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082112 | TGTTATTAGTATGCA[C/T]TGAAATCCTAGCTCC | 79023 |
rs528072458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102074699 | ATTTTTGCAGTCTAC[A/C]CCAACCAAACAAGCA | 79023 |
rs528109998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075342 | TACGATGCCCAGGTA[A/G]GTTTTAATTTTTTGT | 79023 |
rs528150537 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119850 | GTAAAACTACAACGG[C/T]AGAGAAGAAGGGAGG | 79023 |
rs528254700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088199 | GCACAATTTAAGTTG[C/T]TAAGTCTTATTTTCC | 79023 |
rs528273171 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095044 | GTATCCCCCAAAGTA[A/C]TGAATATTGGGTATA | 79023 |
rs528276877 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102089040 | GGTAAGGTTATAGAT[G/T]AACAGCATCCCAAGG | 79023 |
rs528292130 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093536 | TTTTCAAACAGACCA[A/T]GTGTAATGATTTCAT | 79023 |
rs528484765 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102089720 | ACTTCCCAGACGAGG[C/T]GGCCGGGCAGAGGCG | 79023 |
rs528513379 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117504 | AACCAGATAGTCCTG[A/C]GGGTTGAACCTTCAT | 79023 |
rs528552793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103714 | GATGCAACAATGTTC[A/G]ACATATGCAAATAAA | 79023 |
rs528746580 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081034 | TGCCTGGATGGGGCC[C/T]AGCTCTGCCTTCAGG | 79023 |
rs528758717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117081 | CTATCACTTTAGTGA[C/T]AGTTATTTTAAATCT | 79023 |
rs528819930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110374 | GGAGTGGTGGTGCAT[A/G]CCTGTAGTTCCAGCT | 79023 |
rs528955685 | snp | A/G | 0.000356659 | 0.0133492 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074450 | AGATCCAACGGCTAC[A/G]GAACCCATGAGGATG | 79023 |
rs529083822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096275 | CTTATAAACTTGCAC[A/G]GATCATAGAATAGTA | 79023 |
rs529183511 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094186 | TCAACACAAAGTGTC[C/T]ATTTTACCCCATTCT | 79023 |
rs529215054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102087920 | TTCCTGTCCAATGAA[C/T]CAAAGTTTTACCTAA | 79023 |
rs529242868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102117047 | TTCTCAGTAAAGGAG[A/G]AAATAACATTTATAA | 79023 |
rs529300243 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081196 | TAGAACTGTTTTGGC[A/T]CAAAGCAGGCACTCA | 79023 |
rs529306573 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102085088 | CAAGCGTGGATGATG[A/T]AACTTAAAACAAACA | 79023 |
rs529330074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110318 | CAGCCTGGGCAACAT[G/T]GCGAAACCCCATCAC | 79023 |
rs529376223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102103029 | TCAGGTAGTGTGATG[C/T]CTCCGGGTTTGTTCT | 79023 |
rs529377177 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102087388 | TATCATAGTTACATA[A/C]AAATGAACACAGATG | 79023 |
rs529392303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110696 | AAAATACCAAAATTA[A/G]CCAGGCATGATGATG | 79023 |
rs529430471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086412 | GCTACTTCCTATTTA[C/T]ACCTTTTGTAATTTG | 79023 |
rs529466144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079025 | GCCTGAATAAAATGC[C/T]TTTCCACTCTCTACA | 79023 |
rs529503097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079629 | ATGCCTAAACAAAGC[C/T]TACCTAACACATTTA | 79023 |
rs529600660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102116610 | GAAACTTTCAATTCA[C/T]ACTTCCTCTTAAATA | 79023 |
rs529634005 | in-del | -/TCCTAGGCAGAGG | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102088836 | AAAGGTCTCTGGTTT[-/TCCTAGGCAGAGG]TCCTAGGCAGAGGTC | 79023 |
rs529643887 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089935 | CATATGTCTTTTAGT[A/G]AATATAGATACCCAC | 79023 |
rs529665756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113960 | AGATACCCTTTGAAA[A/G]TAACTTCAAATTTCA | 79023 |
rs529785877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107394 | CTGTCAGTCTATCTC[C/T]CCAACCATTCTTCAC | 79023 |
rs529852968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102076174 | CAGGATGTATCTTAA[C/T]GATCCATGGCATTCT | 79023 |
rs530008425 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075219 | CTTGCTCTGTCACCC[A/C]GGCTGGAGTGCAGAA | 79023 |
rs530009438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097926 | CCTATGACTCTATCA[C/T]TTTAAAAAGATGAGC | 79023 |
rs530109518 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102098539 | AATATGTTTGTGTTT[G/T]TTTTTTTTTTGAGAT | 79023 |
rs530175376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082332 | TCTCTAGCTGCCTTA[C/T]TTTCATCAAGGCCAA | 79023 |
rs530200649 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110686 | GTCCCTACAAAAAAT[A/G]CCAAAATTAGCCAGG | 79023 |
rs530253659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089917 | CTGCTGTAAGCCGTC[C/T]TGCATATGTCTTTTA | 79023 |
rs530286026 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119590 | TAACAAACATATCAA[A/G]CACCTTAAGAGTATG | 79023 |
rs530288561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111597 | CTAACATATTCTTGC[C/T]CCTGTAAAGAGGGCT | 79023 |
rs530393316 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120260 | CCGCACACTGAAGAG[A/T]ACGTCTTCGGGTCTA | 79023 |
rs530393376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102112575 | GCTGAGGTGGAAGGA[C/T]TGCTTGAGCTCTGGA | 79023 |
rs530408246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104800 | CACTCTGTTCCATTG[G/T]TCTACATATTTATCT | 79023 |
rs530503288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113218 | CTTCAGTTTGCAAGA[C/G]AGAAGAGACAAATCC | 79023 |
rs530508779 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102089773 | GGCCGGGCAGAGGCG[-/C]CCCTCAATTTGTTTT | 79023 |
rs530521180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102076038 | CTCTTGATGACATTG[A/G]TGAGCTGCTCAACAA | 79023 |
rs530586414 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091058 | ATAACCACAGAAGCA[C/T]ACTTTTCAGGACAGT | 79023 |
rs530601139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102089489 | TCCTCACTTCCCAGA[C/T]GGGGCAGCCAGGCAG | 79023 |
rs530624822 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120102 | TTCCTTGGGGGCTGC[C/T]GCGACGCGCTGTGGC | 79023 |
rs530679049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075397 | ATCTTGCCCAGGCAG[G/T]TCTCAAACTCCTGGC | 79023 |
rs530730204 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081590 | TCTACAAAATACAAT[A/C]CTACTACTGTCTCTG | 79023 |
rs530820035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097398 | TAGTTATTCCTTTCC[C/T]ACTTTTTAGAGTAAT | 79023 |
rs531065833 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119965 | GCCCGAAGTGGGAAG[A/G]AAGAACTCCTGGGAA | 79023 |
rs531211837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102110854 | TGTCTCAAAATGAAT[A/G]AATGAGTGTTGGAGA | 79023 |
rs531268701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103863 | TAGACAAAATGTTCC[A/G]CATCACAATATAGGC | 79023 |
rs531338050 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106503 | CAGGGCTCAGTTTCC[C/T]CCTCAATAAAGTAAA | 79023 |
rs531344844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102092644 | AAAGAATTCAGTGCT[A/G]AAATATCTGGTTTTA | 79023 |
rs531351440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102093437 | ATAAATTTTTGAAGG[A/C]TGGAAATTGTGAGAA | 79023 |
rs531504699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114822 | CTAGCTATTTCTTTG[C/G]GAAGTTTATTCAATT | 79023 |
rs531538798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100484 | TATGAATTTGCTCAG[C/T]CAATGCTCATAATCC | 79023 |
rs531585214 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099980 | TAGAAATGTAATATT[-/A]AAAAAAAAAACAAAA | 79023 |
rs531591711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102091751 | CATCCAATTTGAACG[A/G]TAATTATAATTAACA | 79023 |
rs531618863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107794 | AGAAAGTTCATAAGC[A/G]GGCAAAATTAAGCTA | 79023 |
rs531632081 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076828 | GATCCATGTGAACAG[C/G]TCTCTTATTTTGAGG | 79023 |
rs531682031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108374 | CTCTTAGGCTTACAC[C/T]AGTGGTTTGTCAGGG | 79023 |
rs531709529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121088 | TCATTGACTTCTCAC[A/G]AGGGACTGGAAGGCA | 79023 |
rs531718275 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102088749 | GAACATTCTTGGGTG[-/T]TTCTCGGAGAGGGGG | 79023 |
rs531721460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084157 | ATTTATTTAATTTCT[C/T]TGCGCCTTGGTTTCC | 79023 |