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 |