SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs531939935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099343 | GCAATCCGCTATTTT[C/T]AAAGCACGATTTATA | 79023 |
rs531950501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102090140 | AAGCCAAAACTTTCT[C/T]TCATTTTCTGACTAA | 79023 |
rs531962844 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104054 | TTGGAATGTTTTTCA[C/T]AGCAGCTGCACCATT | 79023 |
rs532082899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102107720 | GATGAATCTCATATA[C/T]ATAATGTGAAGTGAA | 79023 |
rs532123434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092130 | ATTCTGTTTATTTGT[C/T]CATTCTCCATTTTTA | 79023 |
rs532222880 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102092580 | GGGTAAGTCGTGGTG[-/T]TATTTCCTTAGCAAA | 79023 |
rs532282548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114043 | ACTTATCAAGGAAAG[A/G]AAAACACTGTCAAAT | 79023 |
rs532344706 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102106881 | CTCCTCTGAGTTCCT[G/T]TCTCAGGAAACCGAC | 79023 |
rs532423975 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121544 | TCACCATAGTAATGC[C/T]CTTTTTTTTTTTTTT | 79023 |
rs532488690 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NUP37 | GRCh38.p7 | 12:102114627 | AAGGGCTATTATAAG[C/G]GTTTGAAACTGGCAG | 79023 |
rs532571024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102105387 | ATACAAAAATTAGCC[A/G]GGTGCAGTGGCGTGT | 79023 |
rs532680017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102083960 | GGGATGGGAAAAGAC[A/G]AAATGAAGTTAAAAG | 79023 |
rs532765162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098179 | GCACTCATTTCACTC[A/C]TGACTCCTCAGCTTA | 79023 |
rs532850213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102080353 | CTTGAGCCTGGGAAA[C/T]AGAAACTGCAGTGAA | 79023 |
rs532905408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098649 | CGATTCCCTTGCCTC[A/T]GTCCCCCGAGTAGCT | 79023 |
rs532943752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102087042 | GAGGTGGAGGCTACA[A/G]TGTGCCACGTTTGCA | 79023 |
rs532946568 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098316 | GGTGAGGTAGAAGAA[C/T]ATAATAGTTAAATGT | 79023 |
rs532956786 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116747 | TGGTGGCTCACGCCT[A/G]TAATCCCAGTACTTT | 79023 |
rs532982597 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102087692 | AGTATGAATTTGTCT[G/T]GAAAATTCAGCAAGT | 79023 |
rs533121903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115727 | AAATTCACTATATCT[A/G]CAACGTTTTCTAAAC | 79023 |
rs533168906 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102093933 | ACAGAAAAGAACAAA[G/T]TATCAGCTACTAGAG | 79023 |
rs533190147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102085706 | CCTCTATGTATGTGA[C/T]GTCTTATATCTCTAT | 79023 |
rs533313665 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102095126 | TACTGTTTCTAATAT[A/T]CAAGAACATCTGTTA | 79023 |
rs533508891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102109213 | TCTCTAGCCACTACG[A/C]AAGAAAAGCAAGTAG | 79023 |
rs533636636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078364 | AGATTTGGTAGAATT[C/T]TAAGTGATGATGTGC | 79023 |
rs533869515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092739 | GACAAATCTTTACAG[A/T]GGGTATGGGTAGGTT | 79023 |
rs533889560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116053 | TAGTAATTTGGGCAC[A/G]AGACCTACATTGCTA | 79023 |
rs533907874 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076918 | CTTAAGGTTTAAACA[A/G]TATTTTCTCTTTATA | 79023 |
rs533951763 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105386 | AATACAAAAATTAGC[C/G]GGGTGCAGTGGCGTG | 79023 |
rs534083119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092290 | TAACTGGTAAAGCAA[A/G]AAATATGAACCACAA | 79023 |
rs534120796 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102085300 | GGTGGCATGTGCCTA[C/T]AGTCCCAGCTACTCA | 79023 |
rs534160033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114327 | TCACATATGGAATTA[C/G]TGGGTGGTCATGGGG | 79023 |
rs534300518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107920 | AAGGAAGAAGGCTGA[C/T]TGGAGAGGGGCACAC | 79023 |
rs534467887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114902 | TGTTTCCATGTAAAT[G/T]CTACTCATTATTCCA | 79023 |
rs534509291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121205 | AGCTGGGACTAGACC[A/C]GGGGTTGGCAAACTG | 79023 |
rs534586817 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102105999 | AAGATGATCATCCTG[C/G]ATCTAGGGTGGGCCC | 79023 |
rs534626301 | in-del | -/A | 0.424659 | 0.17887 | intron-variant | NUP37 | GRCh38.p7 | 12:102117441 | GCAAAACTCTGTCTG[-/A]AAAAAAAAAAATAAA | 79023 |
rs534640876 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092038 | GGGATATCCTAGATA[C/T]TCTCAAAGGTCTTTT | 79023 |
rs534672172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102094499 | ATTTTGTGATCTCAA[C/T]TGGGGTGGGGGTGGA | 79023 |
rs534673460 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | NUP37 | GRCh38.p7 | 12:102103098 | TTATAATTTCATATA[A/C]ATTTTTTAATTGATT | 79023 |
rs534692394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111802 | GTTATTTTAAGTTAT[A/G]CTTTCAATAAAGTTG | 79023 |
rs534744477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096863 | GTTTTGGCCTAAGAG[A/G]TTTGGCTTTAATAAC | 79023 |
rs534768848 | in-del | -/ATA | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102095251 | CTTTTGGAGGAGGAG[-/ATA]ATAATTTTTTCTAAA | 79023 |
rs534869217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116737 | CCGCTGGGCATGGTG[A/G]CTCACGCCTGTAATC | 79023 |
rs534879075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098638 | CCAGGTTCAAGCGAT[A/T]CCCTTGCCTCAGTCC | 79023 |
rs535021864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102102331 | AAACAGATCAAAGCC[A/T]CCAGGGAATGATTCT | 79023 |
rs535028595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086826 | CCATGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 79023 |
rs535134634 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101233 | CATGCTTTTTATGGA[A/G]GGGGAAAGAAGAATG | 79023 |
rs535183510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108762 | TGCTCATAGGAAACT[C/G]TAGACAAATTTGCCA | 79023 |
rs535533972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102118160 | GCAAAAGTGAAGCCT[C/G]ATACCATTCTTTTTC | 79023 |
rs535541982 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102110500 | GAGATAGAGTGAGAC[C/G]ATGTACCAAAAAAAT | 79023 |
rs535546654 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102102172 | GTAGAAAGAGTATCA[C/T]ACACAAATCTAAATT | 79023 |
rs535553969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111036 | TTCAGCAAAAAATAA[C/T]AACTAAAGCCTAGAA | 79023 |
rs535621612 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080236 | TTTGGAATTACAGTA[C/T]TCTTAATAGAAGAAG | 79023 |
rs535641639 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NUP37 | GRCh38.p7 | 12:102087109 | TCAAAACAACAACAA[A/C]AAAAACCAACAATAA | 79023 |
rs535651070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079321 | CCTAAACACATAAAA[C/T]ATCATTTATTCTATT | 79023 |
rs535687051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115192 | TCTGAATCATAATAT[A/G]CTGCTGAGAACTACA | 79023 |
rs535742521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115939 | GAAAAGCAATAATTT[A/G]TTTTGAAATGGACTT | 79023 |
rs535765251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116881 | GTGGCACGTGCCTGT[A/C]ATTCGAGCTACTCAG | 79023 |
rs535795497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101473 | TTTTAGCCAGGTCAC[A/C]AAGACATATTAAAAA | 79023 |
rs535797077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098344 | TGTATTGTATCTAAA[A/G]AAAACCTTATGCAGA | 79023 |
rs535955742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102089724 | CCCAGACGAGGCGGC[C/T]GGGCAGAGGCGCTCC | 79023 |
rs535984583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086071 | TAATCATGGACAAAA[A/G]AGTCACACACATTTT | 79023 |
rs535992787 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102082420 | TAAATGACTGAAAAC[A/G]TATGGCAGAGCACTG | 79023 |
rs536094332 | snp | A/T | 1.64803e-05 | 0.00287052 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112116 | AACTTACTTGATTAC[A/T]GGAGGCAATGAATCA | 79023 |
rs536203836 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105345 | GCCTGGGTAACATGG[C/T]AAAACCCCATCTCTA | 79023 |
rs536222741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101567 | ATTCCTCCAAATAAA[A/T]CAGATGAAGTAAGAT | 79023 |
rs536252669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081663 | TAGTACAGTCCCTGG[A/G]AAATAGAAAGCATTC | 79023 |
rs536371547 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119244 | GAGTACCAAAATGTG[C/T]GATATAAAAATAATG | 79023 |
rs536394129 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096029 | CTACCTATGTCTTCA[C/T]ATGTAGTTGTTATCT | 79023 |
rs536483603 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119931 | CGAGTTCCTCAAGAC[A/C]CCGCTCCCACCTCCC | 79023 |
rs536570383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102088524 | CACAAAAGGTACCCA[C/T]TATTCTGACTTCAAA | 79023 |
rs536599054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102104999 | GAGATTGATAAAGAC[A/G]TCATTGAATTTGTAG | 79023 |
rs536616303 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102089269 | GCTGTCACTTCACAC[C/T]TGGAAGATTGCACAG | 79023 |
rs536632001 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114439 | CTGAGCCAACTAAAA[C/G]GCCCGTGTGTGTGTG | 79023 |
rs536840481 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102073974 | GTACCTGGCCTTTTT[G/T]TCTCTTTTGATAAAT | 79023 |
rs536852553 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088918 | GGTGATGACTCTTAA[C/G]GAGCATGCTGCCTTC | 79023 |
rs536942805 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119152 | CTTGAAGGAGACCAC[A/T]GTTTAGGGATAGTTA | 79023 |
rs536982544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097440 | TTTTACAAAATGATA[C/G]TGGTAGAAGGCAGTA | 79023 |
rs536990336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116943 | GGAGGCAGAGGTTGC[A/G]GTGAGCAGAGATCGC | 79023 |
rs537144160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105435 | CTTGGGAGACTGAGG[C/T]AGGAAAATCTCTTGA | 79023 |
rs537173236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102089369 | AGACTGGGTGGCGGC[C/T]GGGCAGAGGCACTCC | 79023 |
rs537192468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080740 | CTACAGTGCACACAT[A/G]TTCCCTGCTACAAGG | 79023 |
rs537410625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092180 | GTTTGCTAGGAAATT[A/C]ATCGCAGAAGGGAAT | 79023 |
rs537414224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084615 | CTAGAGTTACTGGAA[A/G]TGAAACTTGGGGCCA | 79023 |
rs537434932 | in-del | -/TTCTT | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102094113 | ATAATTTTTGGAGAG[-/TTCTT]TTAACGACAAAGAAT | 79023 |
rs537452359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077089 | CAATATAAGTCAACA[A/T]TGCACAGATCCAAGA | 79023 |
rs537461459 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NUP37 | GRCh38.p7 | 12:102080052 | ATACATACATACATA[C/T]ACAAAACACTGTATT | 79023 |
rs537590448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077757 | AAATTATTAAAAAAA[A/G]TTATATAAAATTATC | 79023 |
rs537597479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099008 | TTACAACACTCTATA[A/G]AATTTATGTAAAAGT | 79023 |
rs537608420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102102460 | TAAAATATAACTGTT[A/T]TCTTGTGATTGAGTA | 79023 |
rs537609362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110410 | GGAGGCGGAGGTGAG[A/G]GGGAGGGTTGAGGCT | 79023 |
rs537622811 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093148 | GTTGATAATAAAGAC[C/T]GCATGTACTTTGAGG | 79023 |
rs537855123 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079480 | TGGGGAAATACACAG[C/T]TAGGTTCCCTGCCAG | 79023 |
rs538008505 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102106966 | TGCACAATGAGGCAC[C/G]AGACCCCTCGTTTGT | 79023 |
rs538136430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099782 | AGAAGTTGCACAGTG[C/G]AGGACTGTGTGAGCA | 79023 |
rs538171743 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NUP37 | GRCh38.p7 | 12:102091446 | CAAAAAACAAAAAAA[A/C]CCCCACAGCCTTCAT | 79023 |
rs538220584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102090439 | GCATGTGTATGAAGA[A/G]GGAATACAGCTTCTT | 79023 |
rs538223172 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102076320 | GTTACTTAAAAAGCA[C/G]AAATAATGGCTTAAG | 79023 |
rs538270312 | snp | A/G/T | 0.000813259 | 0.0201506 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120527 | TGCAGCTTGGAAGAC[A/G/T]GGCCCGTAGAGGCCT | 79023 |
rs538338586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113623 | TGAGACTAAAGAAGG[C/T]CAAATTTTCGCGACA | 79023 |
rs538348863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114223 | GACAAATCAGTCTCC[C/T]AAAAATGAAGTTTTT | 79023 |
rs538350696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106095 | GAAGTGATGCATCAA[A/C]AAGGCAAAGAAAGTC | 79023 |
rs538412087 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUP37 | GRCh38.p7 | 12:102089716 | CCTCACTTCCCAGAC[A/G]AGGCGGCCGGGCAGA | 79023 |
rs538415363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102105678 | CCAGCCTGGTCAACA[C/T]GGCGAAATCCCATCT | 79023 |
rs538450702 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102082499 | AGCAGCTAAAATTGA[C/T]TGAGTGCTTACTATG | 79023 |
rs538583120 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102098964 | TCATGTTTGTGCCAT[A/C]CCTACAGTTCAAATA | 79023 |
rs538775582 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102084486 | CTGTTTCTACAAAAA[A/T]TACAAAAATTAGCCG | 79023 |
rs538794096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113484 | GATAACACATTTTTT[A/G]TAAGCATTAAAATAC | 79023 |
rs539012283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102081810 | GCAATCCTCCCACCT[A/G]AGCCTCCAGAGTAGC | 79023 |
rs539038296 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102100407 | TCTGAGGGTTATTAT[C/T]ATAGTAATAGAAAAC | 79023 |
rs539051073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079287 | GTGACTGTTCTTTAA[G/T]AACGTACTTTTGTAC | 79023 |
rs539051218 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094969 | GATGAGGAGGAGGGA[C/T]GGGATTTACTACTGA | 79023 |
rs539125645 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119990 | TGGGAATAGAGTGGC[A/G]AGGCTGGGCGGCCGG | 79023 |
rs539245743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102089299 | GTGGCCAGGCAGAGG[C/T]GCTCCTCACTTCCCA | 79023 |
rs539275350 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102095945 | GACTGCCTTGCCTCT[-/G]GCCTTACATTTTCAT | 79023 |
rs539526492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102109982 | CAACAGCACACCAGC[C/T]GTTGGCAATGACATT | 79023 |
rs539528601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102108536 | GTGTGAGTCAATACT[C/T]CTTAATAAACTCCCC | 79023 |
rs539594438 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085361 | TGGGAGGCGGAGGCT[A/G]CAATGAGCCAAGATC | 79023 |
rs539614463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092895 | TACTTTCAGTGTGTG[C/T]GTCCAAATATATTTA | 79023 |
rs539630884 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114267 | CATCATCTTGCTACT[C/G]TAACAATATTGTTGA | 79023 |
rs539673331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121305 | GGGAAAAAATGAAAA[G/T]AATAATGTTTTGTGA | 79023 |
rs539899295 | in-del | -/TAT | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102097272 | TGAAAGGAAAGCAAA[-/TAT]TTGTTGAACAATAAT | 79023 |
rs539941693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115447 | ACTTGGATGAGAACA[C/T]TGATTTAGGCAAGCA | 79023 |
rs539953956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108124 | TTTCTGGGTGTATCT[G/T]GGTGTCAAGAGATTA | 79023 |
rs539973064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092394 | TAATACAGAGATGTA[C/G]TTATAAGGATTAGCA | 79023 |
rs540035144 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099335 | TTTCTTAAGCAATCC[A/G]CTATTTTTAAAGCAC | 79023 |
rs540145497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102084664 | TTAAAGGTTGGTTAA[C/T]TGTGCCATTGCACTC | 79023 |
rs540244816 | snp | A/G | 3.60354e-05 | 0.00424457 | intron-variant | NUP37 | GRCh38.p7 | 12:102074519 | GTCCCCAAAATTAAT[A/G]AATAAAAATGACTTT | 79023 |
rs540250513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102114576 | ATTATACAAGGTTTC[A/G]GCATATTTGAGGTTG | 79023 |
rs540257362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102122026 | GGCAGGGAAAGGTGA[C/T]GTAACTTGGCCAAGA | 79023 |
rs540442349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102097509 | ACCCTATGTCAGTCC[C/T]CTAAATTTTTAGAGA | 79023 |
rs540498200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102112514 | TGAAAATGGACTGCT[C/T]GGTCAGGCGTGTTGG | 79023 |
rs540547824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121444 | CTAGAAGGTCAAAGT[A/G]AGTAGTTGTGCATGC | 79023 |
rs540571558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113653 | AAATTTGTCCAAGGA[A/G]TCTTCTGTGCTAACT | 79023 |
rs540594514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098634 | CCTCCCAGGTTCAAG[C/T]GATTCCCTTGCCTCA | 79023 |
rs540634904 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086913 | ATACAGTGAAACTTC[A/G]TCTCTACAAAACACA | 79023 |
rs540769836 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102367 | CAAGGTCTTCTCAGA[A/G]GCAAAATTAAAGTTG | 79023 |
rs540797754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075780 | AGCCTAACTTTGTTC[A/T]GGGCACAGTGTGTCC | 79023 |
rs540897137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116978 | CTGCACTCCAGCCTG[A/G]ATGACAGAGCGAGAC | 79023 |
rs540951277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102105771 | GAGGCTGAGGCAGGG[A/G]GAATCACTTGAACCT | 79023 |
rs540958494 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102110180 | ATCATGGAAATGTCA[C/T]TGTGGCATCAACCAG | 79023 |
rs540965919 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084808 | TTAACTTTAAGAAAG[A/G]TGATTGTAGTAACTT | 79023 |
rs541005279 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084403 | GTAGTCCCAGCAATA[C/T]GGGAGGCCGAGGTGG | 79023 |
rs541039962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086154 | TATTTATATACTCTT[C/T]ATTTTGTGGGCAAAA | 79023 |
rs541077107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078969 | CTGTGGGAGATAAGG[C/T]ATGAGATTGCTACGA | 79023 |
rs541125065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096111 | TATCATAAAATTAAG[A/G]GACGATAATAATTTT | 79023 |
rs541187944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100869 | CTTAATAATATAGTA[A/G]GCTAGTTATTATAAC | 79023 |
rs541320733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102110621 | GCCAAGGCACATGGA[C/T]TGCCTGAGCTCAGGA | 79023 |
rs541323241 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUP37 | GRCh38.p7 | 12:102092459 | CCCTCAACATTCTTA[A/G]ACAAGAAACATATTT | 79023 |
rs541358807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102102751 | CTTAAGTTTAAGTCT[A/T]TAATCCAATTTCAGT | 79023 |
rs541409815 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093819 | TCCACTTACTGTAAC[C/T]ACATGAGGGCCACAT | 79023 |
rs541449251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102075903 | TTTTGTTTAATTGTT[C/T]GGCAAATGGAGTACT | 79023 |
rs541561705 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102079385 | TTATACACACACACA[G/T]GGATAGTCAATTTCA | 79023 |
rs541747224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102085561 | GAATAAATGCCATTT[A/G]TGGATGATGGCTGTC | 79023 |
rs541882862 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102110137 | TAGAAGAAACAAATA[C/T]ACCAAAAAAGCGTCA | 79023 |
rs541886597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101747 | TTTTTTTTCCTTTGA[A/G]ACAGACTTGCTCTGT | 79023 |
rs541923674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102102659 | CTTTTAGGGTCAGAT[C/T]CAAAAAATTCACTGT | 79023 |
rs542013710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102078799 | TACTCTAAGATACCA[C/T]TGAGTTAAGATGTTT | 79023 |
rs542053512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107327 | TATCAGAACTTTGCC[C/T]AATTTAGTTCAACAT | 79023 |
rs542056218 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102115623 | ACAAATACACGACAC[C/G]AGTTAACAGTACTAT | 79023 |
rs542062391 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077827 | AATTTCATGTTTAGA[C/G]TTGGGTCCCATTCCC | 79023 |
rs542081776 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102110705 | AAATTAGCCAGGCAT[A/G]ATGATGGGCGCCTAT | 79023 |
rs542097558 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106078 | ATGAAGGGTAAGAGA[C/T]TGAAGTGATGCATCA | 79023 |
rs542159382 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119703 | GTGACCAGCAAGTGT[C/T]ATGGACACGGAGACA | 79023 |
rs542195731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102084971 | TGTAGTGTATTTTTA[A/G]TATTTTAGAAAGCTC | 79023 |
rs542451074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104330 | CATTTATTTTGTTGT[A/G]GTTGAGTTGTAGAAG | 79023 |
rs542488050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100308 | TTTATCTTTGTTTTA[C/T]AACAATATTCATATT | 79023 |
rs542489719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105073 | ATCCATGAACACAGG[C/T]TGTCTTTCTATTTAT | 79023 |
rs542524989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102091809 | TAAATAGAACTCTTA[A/G]ATTTAGCTGTGATGA | 79023 |
rs542533647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097082 | TCTCATTCTGGGATC[A/G]GTAGCTATCTAGGAC | 79023 |
rs542561968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089453 | CCTCACTTCCCAGAC[A/G]GGGCGGCCGGGCAGA | 79023 |
rs542597993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081245 | TATAGGTTAAAGTCA[A/T]ATTAAAACTCAGTTC | 79023 |
rs542625275 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098960 | AAACTCATGTTTGTG[A/C]CATACCTACAGTTCA | 79023 |
rs542694927 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097183 | GCTGTGTCACACCTG[C/T]TAATGCTACATTGGC | 79023 |
rs542757885 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102100921 | TCTAAATTATATACT[C/T]TAATGATGACCATAA | 79023 |
rs542802156 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NUP37 | GRCh38.p7 | 12:102114643 | GTTTGAAACTGGCAG[C/G]CCCTCCCACCACACC | 79023 |
rs542804232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086929 | TCTCTACAAAACACA[A/T]AAAAATTGGCCAGGC | 79023 |
rs542927049 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112341 | TTATGCTTTTGAAAA[A/G]TTCAAAAGCAAATTA | 79023 |
rs543096050 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118697 | CTCAAAAGAAACATT[C/T]AAAGTACTTATCAAG | 79023 |
rs543158974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102095841 | CCTAAAACTGTAGAT[C/T]TGCTCAGCGCTATGA | 79023 |
rs543331489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103566 | TTTCCTATTTGGATG[C/T]GTTTTAATTCTTTTT | 79023 |
rs543355680 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118710 | TTTAAAGTACTTATC[A/G]AGGGACAGAAACTGC | 79023 |
rs543361804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096960 | TGTTGTGCATCAACC[C/T]GAAAATCTCGGTGGT | 79023 |
rs543368253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096210 | AAAATGTTTGTTAGA[A/G]AGGCAGTGTTGGAAC | 79023 |
rs543395931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102087817 | CCAAAATATTTTCAT[C/G]ATTTTTTTCTTTCAA | 79023 |
rs543531743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117553 | CATGTAAAACTAGCT[C/T]TCCTCTGGGAAAACA | 79023 |
rs543534392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088963 | CAAAGCACATCTTGC[A/G]CCACCCTTAATCCAT | 79023 |
rs543564973 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102093262 | TTCATGAAGCTTTGG[G/T]GAGGATAAAAATTTT | 79023 |
rs543627064 | snp | G/T | | | splice-acceptor-variant | NUP37 | GRCh38.p7 | 12:102085858 | CCAAGTTCCAAATCC[G/T]AATAAAAGAATAACA | 79023 |
rs543663912 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112036 | GAAAAAAGTATCTAT[A/G]ATCAGACTTCCAATC | 79023 |
rs543739310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086887 | CCAGGAGTTCAAGAC[C/T]AGCCTGGCAAATACA | 79023 |
rs543769401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102076657 | GGCAATGACTTAGTC[A/G]GGAAAGTAAAATAAC | 79023 |
rs543864422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113932 | ATACTACACATCTTT[A/C]TCTGCATAATTCAGA | 79023 |
rs543925509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114543 | AGATACTTTGGAAAA[C/T]TTGCTATAATACAAA | 79023 |
rs543933553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121429 | ATGGCTATTTTCACA[C/T]TAGAAGGTCAAAGTG | 79023 |
rs544056876 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075143 | TATCCTATGGATAAT[A/G]ACAAGCTTTTCTGAA | 79023 |
rs544081082 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087590 | GAATTAGATTATTAA[G/T]TATGGCAACTGATCA | 79023 |
rs544093751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082671 | CAGTTAATTCAAGAG[C/T]CCACACTCTTAACCA | 79023 |
rs544124293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078983 | GTATGAGATTGCTAC[A/G]AGTATCTAAGTGCAT | 79023 |
rs544129843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102083780 | GGACTCAGATAATGC[A/G]GCTTTAAAAATCAAA | 79023 |
rs544173330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102090794 | ACTCATAACCTAAGA[A/C]AAAAAAGCACTGGCC | 79023 |
rs544413621 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107014 | ACCCCACAATTCCTG[C/T]CTTTCCACATGTAGT | 79023 |
rs544475001 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099596 | TAGGCTTTTTACATT[A/G]TATCTGCTGTTCTGC | 79023 |
rs544661714 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120252 | GGATCCTTCCGCACA[A/C]TGAAGAGTACGTCTT | 79023 |
rs544709678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098517 | CCAATATTGAAGAAT[C/T]TGATCCAATATGTTT | 79023 |
rs544720808 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120748 | TAGGTGGGTTATGTA[C/G]TTGTTTCACTAACGT | 79023 |
rs544764635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097835 | TAGTACCTGGGGCCC[C/T]AGAATCTTAATGTCA | 79023 |
rs544782809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102081839 | GCTGGGACTACGGTC[A/G]AGCACCACACCTGGC | 79023 |
rs544867118 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118987 | ACAAATCTAAAGGCA[A/G]GTACTACCTCTGGTC | 79023 |
rs544896336 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102089474 | GCCGGGCAGAGGCGC[C/T]CCTCACTTCCCAGAC | 79023 |
rs544958935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082629 | TCACACAGCTAGTAA[C/G]TGGTGAAACTGGGAT | 79023 |
rs545001758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075914 | TGTTCGGCAAATGGA[A/G]TACTTCTCTTATGCC | 79023 |
rs545102645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111472 | ACGAAGTTAGCTTAA[G/T]AGTTGATAACTTTTA | 79023 |
rs545155526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104607 | TATAGTTTCAGGTCT[C/T]ATGTTTAGGTCCCAT | 79023 |
rs545339061 | snp | C/T | 0.000144335 | 0.00849392 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074308 | AAATTCTTCAAAATA[C/T]GTACTAAAAATACAA | 79023 |
rs545402799 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094480 | ATTTTTAGGTATACT[G/T]CATATTTTGTGATCT | 79023 |
rs545463913 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102078000 | AAATCTCTAGAGAAT[A/G]TAAAAAACCTTAGAG | 79023 |
rs545500284 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106284 | GGTGGTTTGTTATGG[-/C]AACAGTGGGAAATAA | 79023 |
rs545543108 | in-del | -/AT | 0.00358779 | 0.0422022 | intron-variant | NUP37 | GRCh38.p7 | 12:102079384 | GTTATACACACACAC[-/AT]GGATAGTCAATTTCA | 79023 |
rs545558706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088735 | TTTTAGTATTTATTG[A/G]ACATTCTTGGGTGTT | 79023 |
rs545573897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108812 | GAGGGTCTCCTACGG[A/T]TTTCCTCAGTTATAG | 79023 |
rs545598323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101555 | TTAGTTTTTTCTATT[C/T]CTCCAAATAAATCAG | 79023 |
rs545734280 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118816 | AGACAATAACACTGC[A/T]AAGTTCTGTTTAGAT | 79023 |
rs545765443 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109382 | GGTGATAGACTACTA[C/T]TTATTTTAGAATACT | 79023 |
rs545816383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108256 | AAACAGACAGATGGA[A/G]GTGGAAGGAGATGAC | 79023 |
rs545950446 | snp | A/G | 1.7416e-05 | 0.00295088 | intron-variant | NUP37 | GRCh38.p7 | 12:102077255 | TAACAGGATGGATGA[A/G]TGGATCATTTAGCAA | 79023 |
rs545989398 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102085403 | CTCCAACCTGGGTGA[C/T]AGAGTGAGACCCTGT | 79023 |
rs546064680 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121606 | TCACCTAGGCTGGAG[A/T]GCAGTAGTGCTATCT | 79023 |
rs546135135 | in-del | -/CTC | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102109507 | ATAGGTGGCATTCTT[-/CTC]CTTATTTTCTGTGTT | 79023 |
rs546138336 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112950 | TTAGATATTTGATTC[C/T]GGGAATAAATGCTTA | 79023 |
rs546218388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106802 | ACAGAACTAATGTTC[A/G]TGGTTTGGAGATAAT | 79023 |
rs546234912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098781 | AGGTGATCTGCCCAC[C/T]TTGGTCTCCCAAAGA | 79023 |
rs546361177 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087213 | AGGTTAAACCAAACA[A/G]GTTTAACCAATTTGA | 79023 |
rs546361580 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093614 | CCTTAACAAAAGCAA[C/T]AGTAACACTACCCAG | 79023 |
rs546398116 | in-del | -/AC | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115891 | GAATAGTAATGTTTA[-/AC]AGTGTTTAGCTAGAT | 79023 |
rs546495830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099256 | AAAATAACCTACAAT[A/G]TTCCTACATAATATT | 79023 |
rs546498611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086819 | CTGGGTGCCATGGCT[C/G]ATGCCTGTAATCCCA | 79023 |
rs546571773 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092177 | ATTGTTTGCTAGGAA[A/T]TTCATCGCAGAAGGG | 79023 |
rs546595465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113976 | TAACTTCAAATTTCA[G/T]GTGAACTTAAGAGTT | 79023 |
rs546696164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102091175 | GCTGAGGCAGGCGGA[A/T]CACCTGAGGTCAGGA | 79023 |
rs546721558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075566 | ATTAGACCGGGAATT[A/C]CAGGAAAATATTCCA | 79023 |
rs546775665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089921 | TGTAAGCCGTCTTGC[A/G]TATGTCTTTTAGTGA | 79023 |
rs546814386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102083038 | AAGAAAGGAGATGGG[A/G]TAAGGTGGAATTTTA | 79023 |
rs546828189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113355 | CATGCAAAATACCTA[C/T]CATGAGTAAGGGAAG | 79023 |
rs547002474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102089291 | ATTGCACAGTGGCCA[A/G]GCAGAGGCGCTCCTC | 79023 |
rs547170161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079255 | TCAGATTCAAAAACT[G/T]ACTGTATGGCTAAAA | 79023 |
rs547299455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097494 | AATAAAAAGTTAGCA[A/G]CCCTATGTCAGTCCC | 79023 |
rs547339706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098124 | CCCTCACAGTATCGT[C/T]AAAGCAAATGAAGCA | 79023 |
rs547366601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121830 | GTGTGAACCACCATG[C/T]CCAGGCAATGCTCTT | 79023 |
rs547536265 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116719 | CTGTAAGATACAGAA[C/T]TGCCGCTGGGCATGG | 79023 |
rs547598732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102109186 | AGAACTGAAATAACA[C/T]GAACAATGAATTCTC | 79023 |
rs547635656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102091950 | CATTAAGTATCCCTA[C/T]CATATGGTATTTAAA | 79023 |
rs547658525 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NUP37 | GRCh38.p7 | 12:102101353 | TATTCTGGATGTGCT[C/T]CTTCAGTAATAAAAG | 79023 |
rs547697494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101862 | CCCAAGTAGCTGGGA[A/T]TACAGGCGCCCACCA | 79023 |
rs547699277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092814 | GAGAACTTTGAGAGC[C/T]AGGCAAAAGCCTTAA | 79023 |
rs547735699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102093827 | CTGTAACCACATGAG[A/G]GCCACATAAAGCAAG | 79023 |
rs547743102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078259 | TGAATCCGAGAGGCA[C/G]AGGTTGCAGTGAGCC | 79023 |
rs547773433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085064 | TTTTTGTTCACACAG[C/T]AGGGCTCACAAGCGT | 79023 |
rs547813531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114913 | AAATTCTACTCATTA[C/T]TCCACGTTCCATCTC | 79023 |
rs547836003 | in-del | -/AACA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087985 | ACATTTAAGAAAACT[-/AACA]AACAAACAAAAACCT | 79023 |
rs547858714 | snp | C/T | 0.000142414 | 0.00843722 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085793 | CTCAGGATGCCAGCA[C/T]ACACTCATGCCAGGA | 79023 |
rs547868488 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085237 | GCACCCTGGGTAACA[C/T]GGCGAAACCTCAGCC | 79023 |
rs547933255 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084316 | GAAACTTATCTTCTC[A/T]TGCAAACTTGAGGAC | 79023 |
rs548145229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077587 | AGATTCACTGTTGTA[C/T]GGTAAAATGTAAACA | 79023 |
rs548230012 | in-del | -/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100443 | TACGGCGTTTACTAT[-/G]TATCAACATTATTCT | 79023 |
rs548359609 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081728 | CTATTTTTTTTTTTT[C/T]GAGACAGAGTCTCAT | 79023 |
rs548398776 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078442 | TTACTTTTAAGTTAT[A/G]TTAGTTATATTGTCT | 79023 |
rs548430167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107847 | AACTGATAAAACTAT[A/T]AAAAAAAGCAAGGAG | 79023 |
rs548451355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100536 | ACCCACATTTTACAG[A/G]TAAGGATATTAGCAC | 79023 |
rs548457356 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103027 | AATCAGGTAGTGTGA[-/T]GCCTCCGGGTTTGTT | 79023 |
rs548467069 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102108419 | GGCCACAGATTGAAG[A/G]CTGCAATGTTGGCTT | 79023 |
rs548475005 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102097552 | TACAAAAAAAATCTC[-/AG]AGTCATAAGAAAACA | 79023 |
rs548487079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092249 | AATGGATGACATTAA[A/G]TGACACATCTGTATC | 79023 |
rs548539464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099411 | TTGATCATTCAACAC[A/G]CTATTAGCTTAGTCT | 79023 |
rs548604714 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121170 | GGCATAGGCTCCCAC[A/T]GCCAGCTAGCTACAG | 79023 |
rs548638254 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102074787 | ATATGAATACTGGCC[-/A]AAAAAAACCTGTTGT | 79023 |
rs548652446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114257 | TGTAAATACACATCA[C/T]CTTGCTACTGTAACA | 79023 |
rs548689382 | snp | C/T | 0.000182106 | 0.00954042 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077472 | AAAAGATCATAAAAC[C/T]GGATTGTTCCATTCT | 79023 |
rs548715090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114859 | TAGCTCTAATTATTA[G/T]AAGAGTTCTTAACGT | 79023 |
rs548745059 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118243 | TTTCTCTATGGATCT[C/T]ATCTTTTTTTTTTTT | 79023 |
rs548756635 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094633 | TTTGATAAAAATCAT[C/T]TTTCCTCTTGCAACA | 79023 |
rs548757223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111102 | ACAGACTATGGTCTA[C/T]TGATACACTGTAATG | 79023 |
rs548803934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102090200 | ATAGGTACAGCTTTT[C/T]AGGTGCTCTTATTTT | 79023 |
rs548827009 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120182 | CCGCGAGGTTTGAAC[C/T]GTATTCAGCGGCGAC | 79023 |
rs548991517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110357 | ATACAAAAAATTAGC[C/T]GGGAGTGGTGGTGCA | 79023 |
rs549013861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102102195 | TCTAAATTTATTCTT[C/T]AGTTTGAGTACAGTG | 79023 |
rs549052550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103038 | GTGATGCCTCCGGGT[C/T]TGTTCTTTTTTTTGC | 79023 |
rs549077952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111625 | GCTTCAGCAGGCATT[G/T]CTAGGATTTTTTTCT | 79023 |
rs549090902 | snp | A/G | 1.90235e-05 | 0.00308406 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074465 | AGAACCCATGAGGAT[A/G]GGCTATAAAATATGT | 79023 |
rs549117977 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102079129 | TGTAAATAGTAGTGG[C/T]AGATTGGCAAGAATG | 79023 |
rs549123168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102096283 | CTTGCACAGATCATA[A/G]AATAGTAAAATTAGA | 79023 |
rs549234908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102095411 | CATCAGTATTTTTAT[C/T]AACCTGTGTATATAT | 79023 |
rs549281275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102109328 | TGTAAGATAAAAATT[A/G]ATGATGATAAGAGAG | 79023 |
rs549332326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080566 | GTAAGAGCTTTACAT[G/T]TCTGCTTTATTTAAT | 79023 |
rs549368542 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087608 | TGGCAACTGATCAAG[C/T]ATTTCTTCTCTATTG | 79023 |
rs549662980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117055 | AAAGGAGGAAATAAC[A/G]TTTATAATAACTATC | 79023 |
rs549751010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115806 | CACTTAATTTACCTT[C/T]ACTTAGTTTTCTCTC | 79023 |
rs549752109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102094044 | TTTCATTAACACCCT[A/G]TTTCACTGCATTGAA | 79023 |
rs549753534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079886 | TGAGCAAGTGCACAT[A/G]AGCGGACTCAAACTT | 79023 |
rs549822999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102109270 | GAAAGAGAATTTAAG[A/G]CAACTACATGCTAAT | 79023 |
rs549894147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080413 | GCCACAGAGTGAGAC[C/G]CTGCCTCAAAAACAA | 79023 |
rs550027716 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102095186 | GTATTAGTGAGTTTT[A/T]AAAAATAATAAGCTT | 79023 |
rs550071071 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104491 | AGTCTCATTTGTCTA[G/T]TTTTTGCTTTTGTTG | 79023 |
rs550186546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105454 | AAAATCTCTTGAGCC[C/T]GGGAGGCGGAGGTTG | 79023 |
rs550189389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085044 | TTGCCTTATGCGACT[A/G]ATGTTTTTTGTTCAC | 79023 |
rs550198328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078390 | TGTGCCGTCACTAAG[A/G]AGAAGAGATCAATTT | 79023 |
rs550226223 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082367 | AAGAGGCTAACAATT[C/T]TGGGCTTGCAGAGCA | 79023 |
rs550226504 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113131 | TTGCAAAAATTCAAA[C/T]ACAGACAAGCAAACG | 79023 |
rs550459317 | snp | A/G | 0.000107614 | 0.00733452 | intron-variant | NUP37 | GRCh38.p7 | 12:102074970 | TTAAAAAAAAAAAAA[A/G]CACGTATGTTACAAA | 79023 |
rs550636748 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NUP37 | GRCh38.p7 | 12:102089197 | CCGCCATCGTCATCA[C/T]GGCCCGTTCTCGATG | 79023 |
rs550650232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102098687 | CAAGTGCGCACTACC[A/G]TGCCTGGCTAATTTT | 79023 |
rs550751154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106633 | TTTCATTTAACCTAA[C/G]AAATACCTATATTTA | 79023 |
rs550769373 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121196 | TACAGGAAGAGCTGG[A/G]ACTAGACCAGGGGTT | 79023 |
rs550787878 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104892 | AAGTGTGAGAACTTC[A/C]GCTTTCTCAAGATTG | 79023 |
rs550825811 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119908 | CCGACACCTCTCCCC[C/G]GGCCAGGCGAGTTCC | 79023 |
rs550840052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075399 | CTTGCCCAGGCAGGT[C/T]TCAAACTCCTGGCCT | 79023 |
rs550943326 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119140 | ACAGCCTCCTGGCTT[A/G]AAGGAGACCACAGTT | 79023 |
rs550991569 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097413 | TACTTTTTAGAGTAA[A/T]AATGTCCTTTCTTTT | 79023 |
rs550994109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096811 | CTTGTTTTTATATAC[A/G]TTCTGTTTTTAAAAA | 79023 |
rs551120938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089061 | CATCCCAAGGCAGAA[G/T]AATTTTTCTTAGTAC | 79023 |
rs551154028 | snp | C/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120030 | ATCCCGGCCTCTCGG[C/G]CTCCCAGCTCGATAC | 79023 |
rs551245350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080713 | CCTGAATTTGAATCC[A/G]GGTCTGTTTAACTAC | 79023 |
rs551258267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104728 | CCATTGTGTAGCCTT[A/G]GAACCTTTGTCAAAG | 79023 |
rs551442656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102096509 | TAGCTGATTATAATA[C/T]AGTGTCTTTCTTGGA | 79023 |
rs551481696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088338 | GATAGTCACTTTTTT[C/T]TGGGTAAAATTTTTG | 79023 |
rs551546322 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088615 | TTACGTATTTTCTTG[A/G]TCTGACTTCTTTTAC | 79023 |
rs551569390 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086255 | CTACTGGGGCGCTTA[C/G]AAACACACACACGCA | 79023 |
rs551690313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102074768 | AACAGAATAAAAAGC[G/T]TCTTATATGAATACT | 79023 |
rs551719579 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117633 | AGTGTTACCACTGCT[C/T]GTATCAATGACAACT | 79023 |
rs551744287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110394 | TAGTTCCAGCTACTT[C/G]GGAGGCGGAGGTGAG | 79023 |
rs551793639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103154 | TGGAGTTTTGATAGA[C/T]AGGCATTGCATTGAA | 79023 |
rs551797084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102103807 | GAAAAAGAATGTGAC[C/T]AAATACAACATTTCT | 79023 |
rs551816135 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102090230 | TGTAAGGTACATTTC[C/T]CAACTCTTTTTTTTT | 79023 |
rs551871116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085102 | GTAACTTAAAACAAA[C/G]AACAAACAAACAAAC | 79023 |
rs551872576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092574 | CAAAGAAGGGTAAGT[C/T]GTGGTGTATTTCCTT | 79023 |
rs552046114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117109 | TCTTTGAAAATTGGA[C/T]ACTTCCAAATTACCG | 79023 |
rs552058415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117784 | TTATTCAAGGTCTCA[C/T]AGCTAGTAAGAAGTA | 79023 |
rs552069567 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102110768 | GAAGACGGCTTGAGC[A/C]TGGGAAGCAGAGATT | 79023 |
rs552172045 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076090 | GACTTATAAGTACCA[C/T]AGCTCATTGATTTTA | 79023 |
rs552382808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120984 | TTGGAATCCAATTTT[G/T]TAAAAACAAGTGTTA | 79023 |
rs552450550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102099737 | TAGTTATCACCAACA[C/T]AAAAAATCTCGACAC | 79023 |
rs552503721 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102083285 | ACTCACTGCTCTCAG[C/G]GAGAAATGTAGGCAT | 79023 |
rs552534765 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110979 | CCCTGTGACTCAGCA[A/G]TTCTACTCCTAAATT | 79023 |
rs552638125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102076289 | CACTGGTTTTAGTCT[A/C]TTATTTGGTTTTGCT | 79023 |
rs552674404 | snp | C/T | 0.00421665 | 0.0457225 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120447 | TCGAGCCTGGTTGGG[C/T]CTGGGGGCTGTAGGC | 79023 |
rs552729051 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089531 | ACCTCCCAGACGGGG[C/T]GGCCAGGCAGAGGCG | 79023 |
rs552776011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102090299 | GCCTAAGTTTTAAAA[C/T]GTTGTAAACACAGTG | 79023 |
rs552790130 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082157 | GGATTTGGGAGCTTA[C/G]TTTTTGGAGGTCTCT | 79023 |
rs552812836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102083506 | AAGCTGCGAGAAGAT[C/T]TGGTTAATCCTTCTT | 79023 |
rs552818320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102105548 | CAACAACAAGAATTC[C/T]GTGTCATCTTTAGCA | 79023 |
rs552857162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098403 | TTTCCATCAATCTTA[C/T]GTAGCAGATGAGAGT | 79023 |
rs552900145 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078885 | TAATATAAATTCCAA[C/T]TTTACAAAATAATAA | 79023 |
rs552933676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102112742 | TATTAAAAAAATACA[C/G]TGTACATTCTCACTA | 79023 |
rs552977430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089752 | TCCTCACTTCCCAGA[C/G]GAGGTGGCCGGGCAG | 79023 |
rs553054086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081667 | ACAGTCCCTGGAAAA[C/T]AGAAAGCATTCAACA | 79023 |
rs553357115 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096693 | ATGTAAGAATATATA[A/T]GTGATATTGTAAGAA | 79023 |
rs553560158 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098657 | TTGCCTCAGTCCCCC[C/G]AGTAGCTGGAATCAC | 79023 |
rs553716006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111857 | GACCTTGATTCAGAT[C/G]AATCTCACGTAAAAG | 79023 |
rs553737677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115460 | CATTGATTTAGGCAA[C/G]CATATATGTTCATGC | 79023 |
rs553767003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085310 | GCCTATAGTCCCAGC[C/T]ACTCAGGAGGCTGAG | 79023 |
rs553797172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102122103 | TCCCAAGTGAGTCTT[C/G]ATTCATAGCAATCAA | 79023 |
rs553913022 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100462 | CAACATTATTCTAAG[C/T]GTTTTATATGAATTT | 79023 |
rs553921494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107173 | TAGTCACTGGCTTTC[C/T]GTGTGGTATGCAACA | 79023 |
rs554042618 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080548 | AACAAGTATAACACT[A/G]GGGTAAGAGCTTTAC | 79023 |
rs554052918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092378 | AAAGAAAAGAACAAA[A/G]TAATACAGAGATGTA | 79023 |
rs554104282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077118 | GATTTCCTCTTTTGC[A/C]CTGTCCTTTCTGGGT | 79023 |
rs554104358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085283 | AAAAATTAGCCAGGT[A/G]TGGTGGCATGTGCCT | 79023 |
rs554117347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106300 | AACAGTGGGAAATAA[A/G]GACGCCATCATAAAT | 79023 |
rs554277139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102100036 | CCTGAGCAACTTTAA[C/T]AAACCCAGGTCCTCC | 79023 |
rs554315698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100650 | GTCTGTGCTCTTAAC[C/T]GCTTTGGAATTCTGC | 79023 |
rs554332595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121969 | TGACTTGTCATAAAA[A/C]CCTATGGGATAGGGT | 79023 |
rs554415729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113664 | AGGAATCTTCTGTGC[C/T]AACTACAGTTTTCTT | 79023 |
rs554466226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084654 | AACTACCAGATTAAA[G/T]GTTGGTTAATTGTGC | 79023 |
rs554505903 | snp | A/G | 2.56894e-05 | 0.00358386 | intron-variant | NUP37 | GRCh38.p7 | 12:102076896 | GTGTTAAACTCAAGT[A/G]GGTGAACTTAAGGTT | 79023 |
rs554516600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099968 | ACTGCTCACTATGTA[A/G]AAATGTAATATTAAA | 79023 |
rs554554588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121433 | CTATTTTCACACTAG[A/C]AGGTCAAAGTGAGTA | 79023 |
rs554631579 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100949 | TAAAAAGCCATTTTA[A/G]ATTGGAATAAATCCA | 79023 |
rs554641092 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120654 | CAGCCTCCCAAGGAA[A/C/G]CTTTGGGACTTGCAC | 79023 |
rs554979173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102112915 | GTGAATATGTAATAA[A/G]TAATCTGGCTAATTT | 79023 |
rs555014325 | snp | C/T | 0.0023697 | 0.03434 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077365 | AATCATTTCCTGCAA[C/T]GGCTCCAACTTTGAA | 79023 |
rs555042566 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102113633 | GAAGGCCAAATTTTC[A/G]CGACAAATTTGTCCA | 79023 |
rs555178360 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102095850 | GTAGATCTGCTCAGC[A/G]CTATGACACTGTAGA | 79023 |
rs555209574 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120090 | GGCAGGCTGGTCTTC[C/G]TTGGGGGCTGCCGCG | 79023 |
rs555242788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082515 | TGAGTGCTTACTATG[C/T]GCTTTTTAAAGGATT | 79023 |
rs555244522 | in-del | -/T | 0.00994209 | 0.0698011 | intron-variant | NUP37 | GRCh38.p7 | 12:102099028 | ATGTAAAAGTCACAT[-/T]TTTTTTTTCTCATTT | 79023 |
rs555318563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102076331 | AGCAGAAATAATGGC[G/T]TAAGGACCACACTAT | 79023 |
rs555322028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117403 | TATAGTGAGCCGAGG[C/T]TGACCTCCAGCCTGG | 79023 |
rs555425182 | in-del | -/CACGTGTAAGG | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121139 | CCTCCACCTAGGAAC[-/CACGTGTAAGG]CTTATGGCATAGGCT | 79023 |
rs555428360 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102101988 | TCTTGGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 79023 |
rs555443139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110590 | GGCTCATGCTGTCAT[A/C]CCAGCACTTTGGGAG | 79023 |
rs555510822 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102104004 | AAATAATACTGCAAG[G/T]TAGGTAATTCTATTT | 79023 |
rs555566513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086085 | AGAGTCACACACATT[C/T]TCCCTCTAATTAATC | 79023 |
rs555592449 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102108656 | ATACATGCAAATAAA[G/T]GGTAAGAAAAACTGT | 79023 |
rs555612816 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102100811 | TATTTCAATTTAATA[A/C]GAGATATCAGATTTA | 79023 |
rs555852095 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102086784 | CACATATAATTCTGA[A/T]CCTTAAGAACTGAAC | 79023 |
rs555920685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102078824 | ATGTTTAATACACTG[A/G]TAAGTTTTATGTGTG | 79023 |
rs555965218 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095417 | TATTTTTATCAACCT[A/G]TGTATATATGTGTGC | 79023 |
rs555966406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115975 | ATTGTATTTCCAATG[C/T]CTGATGCAGAATATA | 79023 |
rs555996190 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096219 | GTTAGAAAGGCAGTG[C/T]TGGAACTGATAAAGA | 79023 |
rs556160014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078727 | ACCTCAATGTAATGC[C/T]TGACAAATAGTAGCC | 79023 |
rs556194278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116257 | CCCTCAACATTTCTT[A/C]ATCATAAATGAGATA | 79023 |
rs556206560 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102116827 | CAACATGGTGAAACC[C/G]CGTCTCTACTAAAGA | 79023 |
rs556336256 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121361 | ATTTCAGTGTCCATA[A/C]AAAAAGTTTTATTGG | 79023 |
rs556350644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114450 | AAAAGGCCCGTGTGT[A/G]TGTGTGGTATAGGCA | 79023 |
rs556412431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115067 | CTCTGTCCATTCAAA[G/T]AGAGATGACAAATAA | 79023 |
rs556436360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086008 | AAGAAAATTATAACA[A/C]CACTTTTAAGTAATA | 79023 |
rs556439582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079292 | TGTTCTTTAAGAACG[C/T]ACTTTTGTACTTTCC | 79023 |
rs556586554 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079611 | TGAACAGTGCTATAA[C/T]TCATGCCTAAACAAA | 79023 |
rs556586567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101421 | TTTAAACGTTTTCTT[A/C]AAAGCATAAAAGGAT | 79023 |
rs556627396 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079844 | AGCTAAAATAAGAAG[C/G]CAGAGTTCACCTTGT | 79023 |
rs556695513 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102085442 | AACAAAAACAAAAAC[A/C]AAAGAAAAACCAAAA | 79023 |
rs556695868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102093045 | TTTTACTGACTTCAG[A/G]GCAAGAATTAAAAGG | 79023 |
rs556849863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105051 | TTTAACACTATGAAA[C/T]CTTTCAATCCATGAA | 79023 |
rs556974554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088461 | GAGTATTTCCAAGAC[C/T]CCAAAAGTTGTCTTG | 79023 |
rs556974674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080099 | AAAGATAAAGGACAT[A/G]ATCCTTGATCTCAAG | 79023 |
rs557094628 | snp | C/T | 1.67604e-05 | 0.00289481 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118528 | CTTCATCTTGTATGT[C/T]AAAATTCAAGCAGTT | 79023 |
rs557107566 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097441 | TTTACAAAATGATAG[G/T]GGTAGAAGGCAGTAA | 79023 |
rs557234343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102087404 | AAATGAACACAGATG[G/T]TTTTCAAAATGATTA | 79023 |
rs557259939 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102102578 | TTCACTCTGTTGTTT[C/T]CTTTGCTGTGCAGCT | 79023 |
rs557296788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102094667 | TTTAAACAACTATAT[C/T]ACTGGCTTAGTGAAT | 79023 |
rs557446171 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102073989 | TTCTCTTTTGATAAA[C/T]GTGTCCCTGAGAATT | 79023 |
rs557535787 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102104875 | TACGATTTGAAATAA[A/C]GAAGTGTGAGAACTT | 79023 |
rs557560804 | in-del | -/T | 0.00160417 | 0.0282756 | intron-variant | NUP37 | GRCh38.p7 | 12:102099028 | TATGTAAAAGTCACA[-/T]TTTTTTTTCTCATTT | 79023 |
rs557595183 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102095719 | CTTTTTCAACTTGAC[A/T]TCCTATGATTTATCT | 79023 |
rs557602211 | snp | A/T | 1.71469e-05 | 0.002928 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118347 | ACTGTCATTCGGTGC[A/T]GTTTTGTAGACTAAC | 79023 |
rs557764216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104098 | CAACAGTATAGAAAA[A/G]TTTCAATTTCTCCAC | 79023 |
rs557764819 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102073747 | TGCAGTGAAGTGGCA[C/T]GATCTTGGCTCACTG | 79023 |
rs557801249 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110534 | AAAAAAAAAAAGAAA[G/T]ATTGACAATAGCAAA | 79023 |
rs557892039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088787 | AGGGTCATAGGATAA[G/T]AGTGGAGAGAAGGTC | 79023 |
rs557949520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079433 | TTATTATAAAGTTGC[C/T]GCAAACACTCAACTA | 79023 |
rs557960095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102101521 | CTTAGTCTTTGCCCT[C/T]TTCTGTTATCCATAA | 79023 |
rs557999022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102102340 | AAAGCCACCAGGGAA[A/T]GATTCTTTGTCCAAG | 79023 |
rs558034047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102094502 | TTGTGATCTCAATTG[C/G]GGTGGGGGTGGAGGA | 79023 |
rs558050889 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102108809 | GTTGAGGGTCTCCTA[C/T]GGATTTCCTCAGTTA | 79023 |
rs558171044 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NUP37 | GRCh38.p7 | 12:102091395 | AGAGTGAGAGACTCC[A/G]TCTCAAAAAAAAAAA | 79023 |
rs558211635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102084505 | AAAAATTAGCCGAGT[A/G]TAGTGGTGCGTGCCT | 79023 |
rs558253667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079945 | CTGTGACTAAAGAAG[C/T]GCTATGAGCATTGAT | 79023 |
rs558362499 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084095 | GAGCTGGGAGGCATA[C/T]GTTCAAATACCTATT | 79023 |
rs558374709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102109834 | TGAATATGTAGATTA[A/C]AGAGGTATCACAAAA | 79023 |
rs558385703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102076986 | CTAAACAAGCAATCA[A/G]TTAAAACAGATGAAA | 79023 |
rs558430790 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119074 | CATAAGCAGGGCCAG[A/G]ATTTGGAAGACTTCA | 79023 |
rs558433695 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP37 | GRCh38.p7 | 12:102090617 | AAGAAAAAAAACTCA[C/T]TCATATTAGGTATGT | 79023 |
rs558596546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102076652 | ACAAAGGCAATGACT[C/T]AGTCGGGAAAGTAAA | 79023 |
rs558631915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075654 | AGTTCCAAAGTTACA[C/T]AAGGTTGATACAATC | 79023 |
rs558708292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105680 | AGCCTGGTCAACACG[A/G]CGAAATCCCATCTCT | 79023 |
rs558769090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113528 | AGGAAAGGTAAAAAA[C/G]AAAATGATAAAAAAA | 79023 |
rs558939433 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077191 | AAATCCATAGCTCTG[A/G]CCTTCTATAGGAAAG | 79023 |
rs559003580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082423 | ATGACTGAAAACGTA[C/T]GGCAGAGCACTGAAA | 79023 |
rs559009294 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111274 | ATCAATGGTTGCTTC[C/T]GCAGGGAGTGGGGTA | 79023 |
rs559026405 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084522 | AGTGGTGCGTGCCTA[C/T]AGTCCCAGCTACTCG | 79023 |
rs559117097 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102104388 | CCCTTGTTAGGTATA[C/T]GGGTTGCAAATATTT | 79023 |
rs559117166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096407 | TTTGATTCAGAATTT[A/G]GCAATTTTCAATACA | 79023 |
rs559217507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075160 | CAAGCTTTTCTGAAG[C/T]GGGCTTTTTCTTTTT | 79023 |
rs559235481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089326 | CCCAGACGGGGTGGC[A/G]GCCGGGCAGAGGCGC | 79023 |
rs559376549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103713 | GGATGCAACAATGTT[A/C]AACATATGCAAATAA | 79023 |
rs559438328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102074613 | CCTTACAGGTGAAAT[A/G]CACATTATTGATACG | 79023 |
rs559531584 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090358 | GACAGATTTTTCTTT[C/T]TTCCCCCTATAGAAG | 79023 |
rs559568113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089023 | GAGAGCACGGGGTTG[A/G]GGGTAAGGTTATAGA | 79023 |
rs559693776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117724 | TTTACATATACTAAA[A/T]TTCAAGCATTAGTTT | 79023 |
rs559770473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100399 | TGACCCAATCTGAGG[A/G]TTATTATTATAGTAA | 79023 |
rs559777459 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102115812 | ATTTACCTTTACTTA[C/G]TTTTCTCTCAAGACA | 79023 |
rs559888765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114625 | GGAAGGGCTATTATA[A/G]GGGTTTGAAACTGGC | 79023 |
rs559999209 | snp | A/G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094123 | GAGAGTTCTTTTAAC[A/G/T]ACAAAGAATCTCTAT | 79023 |
rs560163762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108132 | TGTATCTGGGTGTCA[A/G]GAGATTAACATCTGA | 79023 |
rs560196093 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106087 | AAGAGATTGAAGTGA[C/T]GCATCAACAAGGCAA | 79023 |
rs560307947 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120199 | TATTCAGCGGCGACA[C/G]CGGCGACTGCGGCGG | 79023 |
rs560379455 | snp | C/T | 3.83561e-05 | 0.0043791 | intron-variant | NUP37 | GRCh38.p7 | 12:102077228 | TTTCGCTTGACAGCA[C/T]AGTCTCAGGTATAAC | 79023 |
rs560436636 | in-del | -/T | 0.00524778 | 0.0509544 | intron-variant | NUP37 | GRCh38.p7 | 12:102103044 | CTCCGGGTTTGTTCT[-/T]TTTTTTTGCTCAAAA | 79023 |
rs560458377 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077943 | GGATCCTCAACCTAT[A/T]TTACAAATGGAAGAT | 79023 |
rs560527304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113083 | GTCGCTGGCAATGGA[A/G]ACAATAACCTGAAAA | 79023 |
rs560538683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102090943 | ACTTTTGGTCTAGAC[C/T]ACGTCAGACAACAGG | 79023 |
rs560564287 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NUP37 | GRCh38.p7 | 12:102090016 | GAATTGCTGGATCAC[A/G]GCTTACAAATATATT | 79023 |
rs560616102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106669 | CAATGAATTATAAAA[A/T]TAGGTGCTTTGATTT | 79023 |
rs560684674 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102105342 | CCAGCCTGGGTAACA[C/T]GGCAAAACCCCATCT | 79023 |
rs560723229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105772 | AGGCTGAGGCAGGGA[G/T]AATCACTTGAACCTG | 79023 |
rs560725692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102113948 | TCTGCATAATTCAGA[C/T]ACCCTTTGAAAATAA | 79023 |
rs560731203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102112523 | ACTGCTTGGTCAGGC[A/G]TGTTGGCTCACGTCT | 79023 |
rs560795229 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094965 | GAGGGATGAGGAGGA[G/T]GGATGGGATTTACTA | 79023 |
rs560831287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102076170 | AAGTCAGGATGTATC[G/T]TAACGATCCATGGCA | 79023 |
rs560835120 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102083795 | GGCTTTAAAAATCAA[A/C]CTAGCAGTTTCAAGA | 79023 |
rs561006196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114568 | TACAAATGATTATAC[A/G]AGGTTTCGGCATATT | 79023 |
rs561197971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098536 | TCCAATATGTTTGTG[G/T]TTTTTTTTTTTTTGA | 79023 |
rs561325766 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119494 | GGAAGTAGCATTCCC[A/C]CATGAGAATTATGGG | 79023 |
rs561369362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097916 | AGAATAATGGCCTAT[G/T]ACTCTATCACTTTAA | 79023 |
rs561382217 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084146 | GACCTTGGATAATTT[A/G]TTTAATTTCTCTGCG | 79023 |
rs561408002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102089508 | GCAGCCAGGCAGAGA[C/T]GCTCCTCACCTCCCA | 79023 |
rs561458233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110464 | AGTAAGCTGTGATTA[C/T]GGGTCTGGCTGTCAG | 79023 |
rs561525348 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119066 | GCCAAGCTCATAAGC[A/G]GGGCCAGGATTTGGA | 79023 |
rs561530296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102112493 | GGCATTTCATAATAA[C/G]TTCAATGAAAATGGA | 79023 |
rs561600076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102086554 | CACAGTAACAAGGAC[C/T]AGGTTACTCACCAAC | 79023 |
rs561662097 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094055 | CCCTATTTCACTGCA[C/T]TGAATTTAAAAATGT | 79023 |
rs561663011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101764 | CAGACTTGCTCTGTT[C/G]CCCAGGCTGGAGTGC | 79023 |
rs561699349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102102688 | GTTGTGGAGATTAAT[C/G]TTGTGAAGCTTTTTC | 79023 |
rs561725888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115653 | TCATTCAGAAGCTCA[C/T]ATGTCCATCATAATC | 79023 |
rs561793792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102094919 | GTTTTCTTTCACCAT[A/G]AACTTTTATCTAATA | 79023 |
rs561828424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086937 | AAACACATAAAAATT[A/G]GCCAGGCATAGTGAT | 79023 |
rs561869706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108423 | ACAGATTGAAGGCTG[C/G]AATGTTGGCTTTCCT | 79023 |
rs561925242 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102116349 | TAAAAATTAGTTTTA[A/C]CTGTAGGAGGCTGCT | 79023 |
rs561925978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107329 | TCAGAACTTTGCCCA[A/G]TTTAGTTCAACATCC | 79023 |
rs561931021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102109028 | TTAAAAAGAAAATTA[A/G]TAATCTTACTGGGAT | 79023 |
rs561978047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100382 | AAAACATGATGCAAT[G/T]TTGACCCAATCTGAG | 79023 |
rs562150691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078159 | ATGGTGAAACCCCGT[C/T]TCTACTAAAAAAAAA | 79023 |
rs562161608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085502 | ATTGTTGGAACACCA[C/G]TTTTTACACTGAAAT | 79023 |
rs562374052 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087835 | TTTTTTCTTTCAAAT[A/G]AAGGAAACAGAAGAG | 79023 |
rs562443430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108263 | CAGATGGAGGTGGAA[A/G]GAGATGACTTGCTGA | 79023 |
rs562653080 | in-del | -/TTTGTT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088682 | TGCATGTTGTTGTAA[-/TTTGTT]TTTGTTTTTGTTTTA | 79023 |
rs562673293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114727 | TTCAATTCTTTCCCC[C/T]CAATGCTTGAATCCC | 79023 |
rs562842963 | snp | C/T | 0.000329506 | 0.0128314 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077328 | AGAAAGTACCTGGAC[C/T]GAGTAATATCCCAAA | 79023 |
rs562857967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102091014 | CAGGTTTTAATATTT[C/T]CAAAATTATTACTAT | 79023 |
rs562891379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100219 | TTAACCAATCCATAC[A/T]GTACATTAAGCCCAC | 79023 |
rs562897899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084091 | TATGGAGCTGGGAGG[C/T]ATATGTTCAAATACC | 79023 |
rs562898149 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102091711 | GTAAAGCATCACTCC[G/T]CAAGTGAAATAAAAT | 79023 |
rs562933086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084856 | CATACAATAACTACA[A/G]TGATGACCAAGAGAA | 79023 |
rs563073779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105926 | AACCCCTGGTAACTA[C/T]GAGTGCTGCCTTATT | 79023 |
rs563321080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088978 | ACCACCCTTAATCCA[C/T]TTAACCCTGAGTTGA | 79023 |
rs563336463 | snp | A/G | 0 | 0 | intron-variant | NUP37 | GRCh38.p7 | 12:102102991 | ACCATGCTGTCTTGA[A/G]TACCATAGCTTTTAT | 79023 |
rs563404228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117594 | TCACCACAAAGCAAT[A/C]TTACTTTGGTGATTA | 79023 |
rs563406260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102110298 | CGAGCCTGGGTGCTC[A/G]AGACCAGCCTGGGCA | 79023 |
rs563413876 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094484 | TTAGGTATACTGCAT[A/G]TTTTGTGATCTCAAT | 79023 |
rs563418912 | snp | C/T | 0.000156695 | 0.00885002 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074443 | ACAGTCCAGATCCAA[C/T]GGCTACAGAACCCAT | 79023 |
rs563433950 | snp | A/C/T | 0.00279258 | 0.0372817 | intron-variant | NUP37 | GRCh38.p7 | 12:102113239 | AGACAAATCCTAGTG[A/C/T]CTGCACAAGGAAGGA | 79023 |
rs563446131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102097061 | TCCATATCTGCTCCA[C/T]GTGTTTCTCATTCTG | 79023 |
rs563566666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086375 | TGCTTATTCCTTCTA[C/T]CTTTAGGATTCCAAC | 79023 |
rs563605258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079005 | TAAGTGCATGAGTAG[C/T]TGATGCCTGAATAAA | 79023 |
rs563640873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079518 | GATGACTGATCAATA[C/T]GTAGCTTTTGAAAAT | 79023 |
rs563787225 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087091 | GGTGACAGAGACCCT[A/G]TCTCAAAACAACAAC | 79023 |
rs563896048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102093398 | AGGAGAATTATTAAC[A/T]TCTCATTTAACTTAT | 79023 |
rs563917502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103476 | ACTAATCAGTTCTAA[C/T]AGTTTTTTGGTGGAG | 79023 |
rs563936706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116989 | CCTGGATGACAGAGC[A/G]AGACTCCGTCTCAAA | 79023 |
rs564042163 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104741 | TTGGAACCTTTGTCA[A/C]AGATCATTTGATGGC | 79023 |
rs564124338 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102109211 | ATTCTCTAGCCACTA[C/T]GCAAGAAAAGCAAGT | 79023 |
rs564138046 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102087691 | TAGTATGAATTTGTC[C/T]TGAAAATTCAGCAAG | 79023 |
rs564141109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101865 | AAGTAGCTGGGATTA[C/T]AGGCGCCCACCACCA | 79023 |
rs564148331 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078049 | AATTCAAGATTTGGC[C/T]GGGTGTGGTGGCTCA | 79023 |
rs564184660 | in-del | -/CCCTAAAA | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102106377 | GAGTATCAAGTTATC[-/CCCTAAAA]ATGTGCCATATTTTA | 79023 |
rs564213459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080319 | CCCAGATACTCAGGA[A/G]GCTGAGGCAGGAGGA | 79023 |
rs564222864 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081058 | CTTCAGGAGCTGTAA[C/G]ATCTTGGGCAAACGG | 79023 |
rs564276688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116398 | GTGGCTTGCATTAGA[A/G]AAATGGTTTTTCCTC | 79023 |
rs564331901 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102100903 | TAGTAGAGTAAATGA[A/G]ACTCTAAATTATATA | 79023 |
rs564400076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102084575 | CCTGAGCCCGGCATA[C/T]GAAGGTTGCAGTGAA | 79023 |
rs564546202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078974 | GGAGATAAGGTATGA[A/G]ATTGCTACGAGTATC | 79023 |
rs564563291 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120256 | CCTTCCGCACACTGA[A/G]GAGTACGTCTTCGGG | 79023 |
rs564564807 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102087275 | TATTTCAAAGAAAGT[A/G]GAGTATGTATTGGAC | 79023 |
rs564646299 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080730 | GTCTGTTTAACTACA[C/G]TGCACACATGTTCCC | 79023 |
rs564727465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097843 | GGGGCCCTAGAATCT[C/T]AATGTCATGTAAATC | 79023 |
rs564763812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089480 | CAGAGGCGCTCCTCA[C/T]TTCCCAGACGGGGCA | 79023 |
rs564766173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075982 | AAGTCCCAATCCTTG[A/C]CACTGAGAATAGCAG | 79023 |
rs564779619 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084783 | TGAACTTTAGAGAAC[A/C]GATGAAGAGTTAACT | 79023 |
rs564802428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089836 | CAGTACACAACAACA[C/T]ATATATTCATTCTAC | 79023 |
rs564804369 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102086230 | TAGTCATTTCAACTG[A/G]CGATAATTACTACTG | 79023 |
rs564848366 | snp | A/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119008 | ACCTCTGGTCTCCAT[A/T]TTGTAGATGGAGAAA | 79023 |
rs564991056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102097226 | CAAAGCTAGGGCTAA[C/T]TAGATGGGAAAATCT | 79023 |
rs565186492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102105158 | TTGGTTGTCTAGTGA[A/G]GGTTTATATGAAAGG | 79023 |
rs565262051 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119330 | CTTAATACCTAGGTG[A/G]TGGGTGTGCAAACCA | 79023 |
rs565279551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111489 | GTTGATAACTTTTAG[G/T]TCCTAAGTACTGTCT | 79023 |
rs565295396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104693 | TTCAACACCATTTGT[C/T]GAACAGACTATCCTT | 79023 |
rs565688442 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113939 | ACATCTTTCTCTGCA[A/T]AATTCAGATACCCTT | 79023 |
rs565691244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111146 | AAAGCACTGGTATAC[A/G]TAACAATGTGGAAAA | 79023 |
rs565753836 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102103052 | TTTGTTCTTTTTTTT[G/T]CTCAAAATTGCTTTG | 79023 |
rs565769542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088195 | GATGGCACAATTTAA[C/G]TTGTTAAGTCTTATT | 79023 |
rs565808167 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102080590 | ATTTAATCCCCTAAA[C/G]CACTGTATGAGGAAA | 79023 |
rs565821976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104042 | TCTGAGGAACCTTTG[A/G]AATGTTTTTCATAGC | 79023 |
rs565859370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102087268 | AAAAATTTATTTCAA[A/G]GAAAGTAGAGTATGT | 79023 |
rs565910697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079924 | TTCTGTGCTCCCTGC[A/G]TATGTCTGTGACTAA | 79023 |
rs565928974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110358 | TACAAAAAATTAGCC[G/T]GGAGTGGTGGTGCAT | 79023 |
rs565953335 | snp | A/C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111961 | TGATAAGCCTAAATT[A/C/T]TTAAGTAGTAGCAAA | 79023 |
rs565982858 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089209 | TCATGGCCCGTTCTC[A/G]ATGGTCGCTGTCTCT | 79023 |
rs566054842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085314 | ATAGTCCCAGCTACT[C/T]AGGAGGCTGAGGTGA | 79023 |
rs566100185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115986 | AATGTCTGATGCAGA[A/T]TATAATTTGTGTTTA | 79023 |
rs566185667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102091290 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 79023 |
rs566281674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116682 | CTATAAAATGCCAAA[C/T]TGCATTTTTGATGTC | 79023 |
rs566401028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102095125 | GTACTGTTTCTAATA[C/T]ACAAGAACATCTGTT | 79023 |
rs566459393 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102106830 | AATTACAGAGATTGA[C/T]TCTCCTGATCTTAAA | 79023 |
rs566622064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102112783 | ACTTTGGGACCTTAT[A/T]AAGACCTCAAAGTCT | 79023 |
rs566633818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120412 | TGGGACCGAAGTATT[A/C]TGGTGCAGTGACTTG | 79023 |
rs566743132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089653 | ACGATGAGCGGCTGG[A/G]CAGAGGCGCTCCTCA | 79023 |
rs566812641 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105304 | CCAAAATGGGCAGAC[C/T]ACTTGAGCCCAGGCG | 79023 |
rs566904957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105512 | TCCAGTCTGGGTGAC[A/G]GGAGCGAAACCCTGT | 79023 |
rs566943718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105981 | ATTAAATTAAAGGAT[A/G]CTAAGATGATCATCC | 79023 |
rs567125644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098176 | GATGCACTCATTTCA[C/T]TCCTGACTCCTCAGC | 79023 |
rs567238790 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089457 | ACTTCCCAGACGGGG[C/T]GGCCGGGCAGAGGCG | 79023 |
rs567272494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098318 | TGAGGTAGAAGAACA[C/T]AATAGTTAAATGTAT | 79023 |
rs567368129 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119909 | CGACACCTCTCCCCG[A/G]GCCAGGCGAGTTCCT | 79023 |
rs567409686 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119202 | CTATAATATAAACAG[A/G]TAGAAAATACAGGAT | 79023 |
rs567433403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102082314 | ATGAACTCATATCTT[C/T]CTTCTCTAGCTGCCT | 79023 |
rs567548263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097437 | TTCTTTTACAAAATG[A/T]TAGTGGTAGAAGGCA | 79023 |
rs567571276 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120195 | ACTGTATTCAGCGGC[A/G]ACAGCGGCGACTGCG | 79023 |
rs567786844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078582 | AAAGAGCACAGACAC[A/G]CCGCTTCCTTCACTT | 79023 |
rs567823463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102079133 | AATAGTAGTGGTAGA[C/T]TGGCAAGAATGTGGG | 79023 |
rs567827616 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078300 | CACGGCACTCTAGCC[A/G]GGGCAACAAGAGCGA | 79023 |
rs567851782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110967 | AACATACATCTACCC[G/T]GTGACTCAGCAATTC | 79023 |
rs567906279 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099438 | GTCTTTCTTTTCTAG[C/T]ATGCATTTCTTACAA | 79023 |
rs567907770 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102096828 | TCTGTTTTTAAAAAA[A/G]TCTTACCTATATTGC | 79023 |
rs567916867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102104770 | GCTATGTGAAGGTAT[A/T]TTTCCTAAGTTTTCC | 79023 |
rs568042091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092738 | GGACAAATCTTTACA[A/G]TGGGTATGGGTAGGT | 79023 |
rs568222193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102092267 | ACACATCTGTATCCA[C/T]TTGGCCCTAACTGGT | 79023 |
rs568255433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107856 | AACTATAAAAAAAAG[C/G]AAGGAGATGATTATC | 79023 |
rs568271495 | in-del | -/ACA | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102115675 | ATCATAATCAAAGGG[-/ACA]ACATGAGATTCTGAA | 79023 |
rs568318688 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102101170 | AGGTCTCCCCCTCCC[C/G]CCCATCCTTCCCTTC | 79023 |
rs568382691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114276 | GCTACTGTAACAATA[C/T]TGTTGACAATCAAGT | 79023 |
rs568511537 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085086 | CACAAGCGTGGATGA[A/T]GTAACTTAAAACAAA | 79023 |
rs568512577 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102091419 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAACCCAAA | 79023 |
rs568550299 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082369 | GAGGCTAACAATTCT[A/G]GGCTTGCAGAGCACT | 79023 |
rs568583615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085146 | CCTACTGGGCCAGGC[A/G]TGGTGGTTCATGCCT | 79023 |
rs568600394 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP37 | GRCh38.p7 | 12:102106975 | AGGCACCAGACCCCT[C/T]GTTTGTCATGACTGG | 79023 |
rs568671917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102091115 | TAAAAGCTCACAGCC[A/G]GCCAGGCACTGTGGC | 79023 |
rs568703405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102083466 | CACACACTTAGATAC[A/C]GTCTGGGGATTATCT | 79023 |
rs568740040 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102084282 | CGTATGTAAGCACTA[C/T]GTGCTTGTTATGATT | 79023 |
rs568834308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100431 | AGAAAACACACATAC[A/G]GCGTTTACTATGTAT | 79023 |
rs568879491 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094597 | AAAAACACATAGCTT[C/G]CATGTGGTACACAGA | 79023 |
rs568959319 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095715 | CTTACTTTTTCAACT[C/T]GACATCCTATGATTT | 79023 |
rs569097095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107793 | AAGAAAGTTCATAAG[A/C]AGGCAAAATTAAGCT | 79023 |
rs569400400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121083 | TTGTCTCATTGACTT[C/T]TCACAAGGGACTGGA | 79023 |
rs569400741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113559 | TTTTGCAATTTTAAA[A/C]ATAAGTAAATCATCC | 79023 |
rs569417987 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099017 | TCTATAGAATTTATG[C/T]AAAAGTCACATTTTT | 79023 |
rs569447306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102098669 | CCCGAGTAGCTGGAA[A/T]CACAAGTGCGCACTA | 79023 |
rs569508068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089696 | GGCAGCCGGGCAGAG[A/G]CGCTCCTCACTTCCC | 79023 |
rs569639591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114411 | CCTGTTTTCCTGGCA[A/G]CACTGTTTGCCACTG | 79023 |
rs569784903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102095240 | ACTTTTACCTTCTTT[C/T]GGAGGAGGAGATAAT | 79023 |
rs569830946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102094064 | ACTGCATTGAATTTA[A/C]AAATGTCTGCAAAAG | 79023 |
rs569909777 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077689 | GCTAACATGATACCA[C/T]AAGTGAAAAATTCCA | 79023 |
rs569939798 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102079318 | TTTCCTAAACACATA[A/C]AACATCATTTATTCT | 79023 |
rs570105017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121943 | AAAAGCTTTACTTGT[A/G]TTTATGTCGTTGACT | 79023 |
rs570221323 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120943 | AGTGACAATTTTCTG[G/T]CTCACAGTTTTTGCT | 79023 |
rs570277153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078461 | GTTATATTGTCTAGA[A/G]AGAATAGCTAAGTAT | 79023 |
rs570340859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078598 | CCGCTTCCTTCACTT[A/G]TAAGCTGAGTGACTG | 79023 |
rs570420963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079872 | TGTTCAATTTTAGGT[A/G]AGCAAGTGCACATAA | 79023 |
rs570430701 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076109 | TCATTGATTTTAAAA[C/T]TGATGGATACTTGCT | 79023 |
rs570452347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079262 | CAAAAACTTACTGTA[G/T]GGCTAAAATGTGACT | 79023 |
rs570534875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115721 | AAATTCAAATTCACT[A/T]TATCTACAACGTTTT | 79023 |
rs570604647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085925 | AAAATTAAATTTCCA[G/T]GAATTTATTCAAAGC | 79023 |
rs570637657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101360 | GATGTGCTTCTTCAG[C/T]AATAAAAGTGTAGAA | 79023 |
rs570712176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102093829 | GTAACCACATGAGGG[C/T]CACATAAAGCAAGCT | 79023 |
rs570718953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114949 | CCACACCAAATCAGT[C/T]TAACTTAATGATGAC | 79023 |
rs570780400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102107935 | TTGGAGAGGGGCACA[C/T]TGGCAGCCTCAAGTG | 79023 |
rs570795210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121273 | TAAGAAGGAGTGTTA[A/C]GTGTTTATATGGTTG | 79023 |
rs570857587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121864 | CTTTTAACTCAAAAC[A/G]ACTTAGAAACTCATA | 79023 |
rs570870975 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079309 | CTTTTGTACTTTCCT[-/A]AACACATAAAACATC | 79023 |
rs570874121 | snp | A/G | | | upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120146 | CGGAGGGCGAGCGCA[A/G]CGATTGGCTCCCGGG | 79023 |
rs570906192 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111124 | ACTGTAATGGAGTAC[C/T]ACTTAAAAAGCACTG | 79023 |
rs570960593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108504 | GACGCCTTATTGTGG[C/G]ACTTCATCTTGTGAT | 79023 |
rs570986996 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102076937 | TTTCTCTTTATAGGA[C/G]AGAATGTCCAATGTG | 79023 |
rs571057066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085073 | ACACAGTAGGGCTCA[C/T]AAGCGTGGATGATGT | 79023 |
rs571093851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077593 | ACTGTTGTACGGTAA[A/T]ATGTAAACATTTGCA | 79023 |
rs571096797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089175 | CCCCCTTTTCTTTTC[C/G]ACAAAACCGCCATCG | 79023 |
rs571108206 | in-del | -/TAAG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092355 | TGTGTATTGATTAAT[-/TAAG]TAAGAAAGAAAAGAA | 79023 |
rs571217226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102105406 | GCAGTGGCGTGTGCC[C/T]GTAGTCCCAGCCACT | 79023 |
rs571232731 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119143 | GCCTCCTGGCTTGAA[A/G]GAGACCACAGTTTAG | 79023 |
rs571321688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102087295 | ATGTATTGGACAATG[C/T]TACTATTCTGTGCCA | 79023 |
rs571359962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088366 | TTGAAGTATACCATA[A/T]ATAATAAAAATACAC | 79023 |
rs571379563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081391 | GAATCTAAAAATGCT[A/G]CAGGGGGAATTTTTC | 79023 |
rs571754747 | in-del | -/TTTTTTTTTTTTTTT | 0.373799 | 0.217195 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121546 | ACCATAGTAATGCTC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTAAGA | 79023 |
rs571797007 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104865 | AGCATTGCGATACGA[C/T]TTGAAATAAAGAAGT | 79023 |
rs571818389 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100185 | TTATATACTTGGTTA[C/T]TTCTGGTACAGCCTT | 79023 |
rs571831062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117123 | ACACTTCCAAATTAC[C/T]GTGCTCATTATAATT | 79023 |
rs571836073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110407 | TTGGGAGGCGGAGGT[A/G]AGAGGGAGGGTTGAG | 79023 |
rs571896594 | snp | C/G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090639 | TAGGTATGTGTGACA[C/G/T]TTTTAAAAGATTAAA | 79023 |
rs571991358 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105753 | ATAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 79023 |
rs572210584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096035 | ATGTCTTCATATGTA[A/G]TTGTTATCTGAGCTT | 79023 |
rs572260411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102079336 | CATCATTTATTCTAT[C/T]ATTCATCTAACAGGC | 79023 |
rs572275128 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109066 | AAACCAAACAAACAA[A/G]CCCAGAAAACTTTAT | 79023 |
rs572278695 | in-del | -/ATC | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102113568 | TTTAAAAATAAGTAA[-/ATC]ATCCTTCTGTTATTT | 79023 |
rs572299301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102117427 | AGCCTGGGCGACCAA[A/G]CAAAACTCTGTCTGA | 79023 |
rs572308674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102100863 | TTAGTTCTTAATAAT[A/G]TAGTAAGCTAGTTAT | 79023 |
rs572312368 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NUP37 | GRCh38.p7 | 12:102079919 | TGTTGTTCTGTGCTC[C/T]CTGCGTATGTCTGTG | 79023 |
rs572358853 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080614 | GAGGAAATTACTATC[A/G/T]TTAATCCCATTTTTC | 79023 |
rs572481077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102089757 | ACTTCCCAGAGGAGG[C/T]GGCCGGGCAGAGGCG | 79023 |
rs572511737 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115847 | GCATGAAACTGGGTG[A/C]AATGGAACTTGAAGG | 79023 |
rs572691385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092458 | ACCCTCAACATTCTT[A/G]GACAAGAAACATATT | 79023 |
rs572703303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097760 | TTATTTCCAGTGACC[A/G]AATTTTTACCTTAAA | 79023 |
rs572763363 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NUP37 | GRCh38.p7 | 12:102082625 | GAGATCACACAGCTA[A/G]TAAGTGGTGAAACTG | 79023 |
rs572847104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102083537 | TATGTCATCATTCTA[C/T]TTAATAGATTTTTTG | 79023 |
rs572857209 | snp | A/G | 2.41917e-05 | 0.00347782 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074303 | TATAGAAATTCTTCA[A/G]AATATGTACTAAAAA | 79023 |
rs573164869 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118780 | TGCTCCACAGCTCTT[G/T]CCCATATCTGTGATT | 79023 |
rs573249865 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102115 | AAAAAAATTTAAATT[A/T]TATTTATATACTGAA | 79023 |
rs573255354 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086814 | CTTGACTGGGTGCCA[C/T]GGCTCATGCCTGTAA | 79023 |
rs573306478 | snp | A/G | 4.95135e-05 | 0.00497537 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112218 | CTGAATGCCTTCAAC[A/G]TCTGCTTCTTCTTCC | 79023 |
rs573313800 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099329 | TAAATATTTCTTAAG[A/C]AATCCGCTATTTTTA | 79023 |
rs573361926 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119305 | GGATAAATAGCTAAT[A/G]CATGTGGAGCTTAAT | 79023 |
rs573375519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102088667 | TTTACCACCATTTGT[C/T]GCATGTTGTTGTAAT | 79023 |
rs573394362 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102084286 | TGTAAGCACTACGTG[C/G]TTGTTATGATTAACG | 79023 |
rs573403612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080185 | AAATGCTCTAGAGTA[C/T]AAAAAGGAATTATTT | 79023 |
rs573414426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102080954 | TACCTGAGCCTGGTC[C/T]GAAGGTAGTAGGGGC | 79023 |
rs573429538 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112596 | GAGCTCTGGAGTCTG[A/G]GACCAGACTGGGCAA | 79023 |
rs573454486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102096860 | TAGGTTTTGGCCTAA[A/G]AGGTTTGGCTTTAAT | 79023 |
rs573458132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111376 | GTTGTACAAATATAC[C/G]TATTTGTCAAAACTG | 79023 |
rs573508998 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100951 | AAAAGCCATTTTAAA[C/T]TGGAATAAATCCAAT | 79023 |
rs573518741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102111976 | ATTAAGTAGTAGCAA[A/G]TATCAAAATATCTAA | 79023 |
rs573576204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102089416 | GCAGCCGGGCAGAGG[C/T]GTTCCTCACTTCCGA | 79023 |
rs573642839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102105058 | CTATGAAATCTTTCA[A/C]TCCATGAACACAGGC | 79023 |
rs573692088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080103 | ATAAAGGACATAATC[A/C]TTGATCTCAAGAAAC | 79023 |
rs573728738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080757 | TCCCTGCTACAAGGC[A/T]AGGCTGCTGAAGACT | 79023 |
rs573737578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102081985 | TTACAGGCATGAGCC[A/G]CTGCTCCCGGCCACA | 79023 |
rs573871691 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114003 | AGTTAACAGCAAAAA[A/G]TTTTTCCACAAATGA | 79023 |
rs573921306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102097071 | CTCCACGTGTTTCTC[A/G]TTCTGGGATCAGTAG | 79023 |
rs574025033 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074132 | CTGCTGAGTCAATAT[A/G]ATTTTGTAAGATTAA | 79023 |
rs574094805 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118581 | CTGGACAAGGTCACG[A/C]AACTGTGGATTAGAG | 79023 |
rs574129397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077901 | TCCAAAATCTGAAAC[C/G]CTTCTAGTTCCAAGA | 79023 |
rs574134680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102103290 | CATCAATGTTTTATC[A/G]TTTCTGTGTACAGAT | 79023 |
rs574159413 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102094721 | TTATACAGTGATTTG[A/G]TTACATTCTAATATC | 79023 |
rs574173274 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102095827 | ACATGAGCTTTTATC[C/T]TAAAACTGTAGATCT | 79023 |
rs574272233 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095480 | GAGTGCATCTGCATA[A/T]GGTAGACATGATGAG | 79023 |
rs574324775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121434 | TATTTTCACACTAGA[A/C]GGTCAAAGTGAGTAG | 79023 |
rs574380895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102093525 | CCATATGGTAGTTTT[C/T]AAACAGACCATGTGT | 79023 |
rs574435273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102114571 | AAATGATTATACAAG[C/G]TTTCGGCATATTTGA | 79023 |
rs574456449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121983 | ACCCTATGGGATAGG[G/T]TTTTCATTTTCATTA | 79023 |
rs574520439 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102115391 | CAGATTTCTAAGTCT[A/T]TTCAAGGGGTCTTCA | 79023 |
rs574563671 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102083839 | CAGTGTAAAACACTG[G/T]CTGGAGAATAAGAAT | 79023 |
rs574630450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102084656 | CTACCAGATTAAAGG[C/T]TGGTTAATTGTGCCA | 79023 |
rs574732840 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102113635 | AGGCCAAATTTTCGC[A/C/G]ACAAATTTGTCCAAG | 79023 |
rs574746845 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | NUP37 | GRCh38.p7 | 12:102117453 | TCTGAAAAAAAAAAA[-/T]AAAAATAATAATAAT | 79023 |
rs574814363 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103926 | TTAATGGTGAGAAGA[C/T]GGTGGTCTCTCTTTT | 79023 |
rs574906162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106194 | AACCAACCCCACTGA[A/T]AACTTGATTTTGAAT | 79023 |
rs575007848 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102079759 | CAGTAAAATTACCCA[C/T]AAAAAGTACAAAAAT | 79023 |
rs575030295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102099030 | TGTAAAAGTCACATT[A/T]TTTTTTCTCATTTTA | 79023 |
rs575081129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082531 | GCTTTTTAAAGGATT[C/T]TACACGTTAGCACAT | 79023 |
rs575083114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075282 | CTGGGCTCAAGTGAT[C/G]TTCCCACCTCAGCCT | 79023 |
rs575121372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075756 | CTGCCCCTTTTCCAT[A/G]CTAAGTGAAGCCTAA | 79023 |
rs575124270 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120676 | GACTTGCACTCGAAC[A/G]CTGATAATGATGTTG | 79023 |
rs575157608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102090622 | AAAAAACTCACTCAT[A/G]TTAGGTATGTGTGAC | 79023 |
rs575157701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102082663 | ACTCCAGGCAGTTAA[C/T]TCAAGAGTCCACACT | 79023 |
rs575195571 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098937 | TGAGGACTATCTCAC[C/T]GGTTTTGAAACTCAT | 79023 |
rs575272952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102077056 | TCATGCAACAGGGTC[A/T]GTGTTTTTCTTATTT | 79023 |
rs575331005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102098451 | CACAAACTTATCATA[C/T]AGCATCTGTAAAGTA | 79023 |
rs575332100 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096895 | AATCAGAGTTGTTTA[G/T]TTTTGGTTGGTGAAC | 79023 |
rs575341346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121366 | AGTGTCCATAAAAAA[A/G]GTTTTATTGGAGCAC | 79023 |
rs575381322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106040 | AATGAATGAACACAA[A/T]AAAGGATAAACACAG | 79023 |
rs575661450 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120077 | GGAACCGACCAGAGG[C/T]AGGCTGGTCTTCCTT | 79023 |
rs575699669 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102075575 | GGAATTCCAGGAAAA[C/T]ATTCCATAAATATTT | 79023 |
rs575724157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102112881 | AATAATTCATCTGAA[A/C]TATTATTGTTTATGA | 79023 |
rs575727016 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109594 | ACAAGATTGTGCCTT[C/T]AGGTTGCTCTAAAAA | 79023 |
rs575820103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102075161 | AAGCTTTTCTGAAGC[A/G]GGCTTTTTCTTTTTC | 79023 |
rs575985560 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113321 | AGGAAAAAACAGACA[A/G]ACAAAAAGAAAATCC | 79023 |
rs576062642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108942 | GTAAAGAGGTATTAA[C/T]AGCAAAATGAAGCCA | 79023 |
rs576064355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102116829 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAGATA | 79023 |
rs576102413 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106784 | AACTGGCCCAACTTC[A/C]CCACAGAACTAATGT | 79023 |
rs576123387 | in-del | -/T | 0.00631972 | 0.0558562 | intron-variant | NUP37 | GRCh38.p7 | 12:102085886 | ACAGTATAATGTTAA[-/T]TGTTCTTGATATATC | 79023 |
rs576246107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102115085 | AGATGACAAATAACA[C/T]AAAATCCATTTACCA | 79023 |
rs576298901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078099 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACTTGAG | 79023 |
rs576342496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102078758 | ACCCACTCAAAAAAT[A/G]GTAGCTATTACTTCA | 79023 |
rs576377537 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | NUP37 | GRCh38.p7 | 12:102117447 | CTCTGTCTGAAAAAA[-/T]AAAAATAAAAATAAT | 79023 |
rs576404046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092416 | GGATTAGCAGGCACT[A/T]TACAATGTCACTGGT | 79023 |
rs576419374 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102093050 | CTGACTTCAGAGCAA[G/T]AATTAAAAGGGCAAA | 79023 |
rs576563590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102085445 | AAAAACAAAAACAAA[A/G]GAAAAACCAAAACAA | 79023 |
rs576777279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102108152 | TTAACATCTGAGTCA[A/G]TGGAGTGGGAGGGGA | 79023 |
rs576804729 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119231 | ATCTGTTGTTAAGGA[A/G]TACCAAAATGTGTGA | 79023 |
rs576836101 | snp | C/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119205 | TAATATAAACAGATA[C/G]AAAATACAGGATCTG | 79023 |
rs576926715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP37 | GRCh38.p7 | 12:102116224 | CTCTTTTCCTAATTT[A/G]TTCTCCACTGACTTT | 79023 |
rs576976048 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120715 | TTTTAAATTGAGCAC[C/T]TACTAAATGCCTGGC | 79023 |
rs577087537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102092382 | AAAAGAACAAAGTAA[C/T]ACAGAGATGTAGTTA | 79023 |
rs577288529 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105469 | CGGGAGGCGGAGGTT[A/G]TAGTGAGCTGATATC | 79023 |
rs577516029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102106338 | AAATATATGACTGTT[G/T]CATTAAATTGCTTAA | 79023 |
rs577592767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086881 | TTGAGCCCAGGAGTT[C/T]AAGACCAGCCTGGCA | 79023 |
rs577691831 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087191 | ATATCTCATTAGGGA[A/C]CCAATGAGGTTAAAC | 79023 |
rs577697081 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102096205 | ATTATAAAATGTTTG[C/T]TAGAAAGGCAGTGTT | 79023 |
rs577715193 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121800 | CCTCGGCTTCCCAAA[A/G]TGCTGGGATTACAAG | 79023 |
rs577737721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102096927 | AAGCTGTAAATTCTA[A/G]AAATACTCCTAGTTT | 79023 |
rs577748730 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NUP37 | GRCh38.p7 | 12:102107775 | TAGTATTATTATATT[C/G]ATAAGAAAGTTCATA | 79023 |
rs577781712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102110646 | TCAGGAGTTTGAGGC[C/T]AGCCTGGGCAACAGG | 79023 |
rs577877175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102086231 | AGTCATTTCAACTGA[C/T]GATAATTACTACTGG | 79023 |
rs577916134 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP37 | GRCh38.p7 | 12:102103552 | ATTTAACTTCTTCCT[C/T]TCCTATTTGGATGCG | 79023 |
rs577937884 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092464 | AACATTCTTAGACAA[G/T]AAACATATTTTCCAC | 79023 |
rs577972634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP37 | GRCh38.p7 | 12:102111398 | TCAAAACTGATCAAA[C/T]TATACCCTTAAGAGC | 79023 |
rs577999255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102080042 | GATCTACTGTATACA[C/T]ACATACATACACAAA | 79023 |
rs578113646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP37 | GRCh38.p7 | 12:102101549 | TAATCCTTAGTTTTT[C/T]CTATTCCTCCAAATA | 79023 |
rs578213701 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096731 | TTATCACATATGTCC[C/T]CTTAGAATTCCTTCT | 79023 |
rs745309686 | snp | A/G | 3.32369e-05 | 0.00407644 | intron-variant | NUP37 | GRCh38.p7 | 12:102099209 | CTAAAACCTGACAGA[A/G]AGAGAAACAGAAAGC | 79023 |
rs745428605 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085469 | AAAACAAAAAAAATC[C/G]CTGCCTACTGCTACT | 79023 |
rs745437760 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117124 | CACTTCCAAATTACC[A/G]TGCTCATTATAATTT | 79023 |
rs745467040 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111911 | ATGGTCAAGGCATCA[C/T]AGTCATGGCTGTATA | 79023 |
rs745469170 | in-del | -/CTGCAG | 0.000162456 | 0.0090112 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120511 | GTCCTGAGGGTTCGT[-/CTGCAG]CTTGGAAGACAGGCC | 79023 |
rs745516310 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077325 | TCAAGAAAGTACCTG[A/G]ACCGAGTAATATCCC | 79023 |
rs745561969 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099086 | AATTTAAAAATGTGG[C/T]TATAACATAAGCAAC | 79023 |
rs745599588 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110754 | GGAGGCTGAGGTGGG[-/A]AGACGGCTTGAGCCT | 79023 |
rs745633246 | snp | C/T | 1.96273e-05 | 0.00313261 | intron-variant | NUP37 | GRCh38.p7 | 12:102077216 | GGAAAGACTTGCTTT[C/T]GCTTGACAGCATAGT | 79023 |
rs745689652 | in-del | -/CCCA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104407 | TTGCAAATATTTTCC[-/CCCA]TTCTATGGGTTGCCT | 79023 |
rs745693371 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107232 | TAACAATGGCAACAC[A/G]TTAAGAAAAAAAATA | 79023 |
rs745697360 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093882 | TGGTGATATATTTTA[C/T]TAAGCACTTGTTTTG | 79023 |
rs745712366 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086806 | GAACTGAACTTGACT[A/G]GGTGCCATGGCTCAT | 79023 |
rs745837774 | snp | C/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119678 | ATCAGGGACTGGAGA[C/G]TTTTGAAGGGTGACC | 79023 |
rs745871506 | snp | C/T | 1.67153e-05 | 0.00289091 | intron-variant | NUP37 | GRCh38.p7 | 12:102112247 | CCTAAGCATACACAG[C/T]AAATGTTTTAATAAG | 79023 |
rs745900755 | in-del | -/A | 2.2771e-05 | 0.00337416 | intron-variant | NUP37 | GRCh38.p7 | 12:102076878 | TGCATTTTATGAATT[-/A]ATGTGTTAAACTCAA | 79023 |
rs745914168 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099842 | AGTTGAAATCCTAAA[C/T]AGGCCTGTCAGATAA | 79023 |
rs746001381 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103358 | TTGATGCTTTTGTAA[A/G]TCATATTACCTTAAT | 79023 |
rs746087561 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083020 | GTCATGGAAACATCA[C/T]AAAAGAAAGGAGATG | 79023 |
rs746108334 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115703 | CTGAAAAATGCTTTA[C/T]TGAAATTCAAATTCA | 79023 |
rs746110321 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102597 | TGCTGTGCAGCTCTT[G/T]AGTTTAATACAATTC | 79023 |
rs746341112 | snp | A/G | 1.69292e-05 | 0.00290935 | stop-gained, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074419 | ACAGAGGGAGAGTTC[A/G]ATGCCAGGACAGTCC | 79023 |
rs746344644 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090445 | GTATGAAGAGGGAAT[A/G]CAGCTTCTTTGCTTA | 79023 |
rs746362193 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092032 | ATACTGGGGATATCC[C/T]AGATATTCTCAAAGG | 79023 |
rs746371076 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091154 | GTAATCCCAACACCT[G/T]GGGAGGCTGAGGCAG | 79023 |
rs746444664 | snp | C/T | 2.16106e-05 | 0.00328707 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101044 | TACCTTATATTCATT[C/T]TTATCCTGAAGATCT | 79023 |
rs746511535 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079924 | TCTGTGCTCCCTGCG[-/T]TATGTCTGTGACTAA | 79023 |
rs746627416 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087087 | CCTGGGTGACAGAGA[A/C]CCTGTCTCAAAACAA | 79023 |
rs746636200 | snp | A/G | 2.10418e-05 | 0.00324352 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101055 | CATTTTTATCCTGAA[A/G]ATCTGAAGTAAATAA | 79023 |
rs746684295 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110412 | AGGCGGAGGTGAGAG[A/G]GAGGGTTGAGGCTGA | 79023 |
rs746771646 | snp | C/T | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102073917 | CAAGTGATCCACTCC[C/T]TTCAGCCTCCCAAAG | 79023 |
rs746905939 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084373 | TGGAGATGGCCGGTA[C/T]GGTGGCTCACAACTG | 79023 |
rs746967746 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116974 | ACCACTGCACTCCAG[C/G]CTGGATGACAGAGCG | 79023 |
rs746968649 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085214 | CATCTGAGCTCAGGA[C/G]TTTGAGAGCACCCTG | 79023 |
rs746979579 | snp | G/T | 1.64985e-05 | 0.0028721 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118485 | CTTCACAATCCACAG[G/T]GTAGGCAGCATTTCT | 79023 |
rs747002881 | snp | A/G | 1.93287e-05 | 0.00310869 | intron-variant | NUP37 | GRCh38.p7 | 12:102077224 | TTGCTTTCGCTTGAC[A/G]GCATAGTCTCAGGTA | 79023 |
rs747032433 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075747 | ACAGCCATTCTGCCC[C/T]TTTTCCATGCTAAGT | 79023 |
rs747058764 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082762 | CTCTTAGTCTAGTAG[G/T]CAAGAAGAATCAAAG | 79023 |
rs747176960 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114297 | ACAATCAAGTCCTTT[A/C]ATTTGTTACCCAAAT | 79023 |
rs747219956 | snp | C/T | 3.53995e-05 | 0.00420696 | intron-variant | NUP37 | GRCh38.p7 | 12:102099070 | TTCTCATTAAAATGG[C/T]AATTTAAAAATGTGG | 79023 |
rs747240438 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081261 | ATTAAAACTCAGTTC[C/T]AACAAAAGATTTTTG | 79023 |
rs747290534 | snp | C/T | 1.981e-05 | 0.00314716 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085819 | CAGGAGAATGAAGAA[C/T]AAAATGAGCTGTTTG | 79023 |
rs747402614 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120864 | ACAGGTCATAAAGGG[A/G]GAGCCTGGAAGTGAT | 79023 |
rs747454259 | in-del | -/T | 1.65943e-05 | 0.00288043 | intron-variant | NUP37 | GRCh38.p7 | 12:102077281 | GCAACAGTTACTGCC[-/T]TTTTTTTGGTGTGTA | 79023 |
rs747489274 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102496 | AGTTCCCTACATATT[A/G]TTGATATTAGCCCCT | 79023 |
rs747498408 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103451 | TGTATCATGCAACCT[G/T]ACTGAATTCACTAAT | 79023 |
rs747548111 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089886 | TGTTTCCAATTTTTG[C/G]TCGTCACCAAGAATG | 79023 |
rs747562052 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078490 | ATGTATCTCTCAAGA[C/G]AGACAGACATTTATG | 79023 |
rs747584054 | in-del | -/T | 1.65696e-05 | 0.00287828 | intron-variant | NUP37 | GRCh38.p7 | 12:102101143 | TACCAATTTTTAGCC[-/T]TTGTAAGTGAAAGGT | 79023 |
rs747626722 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087708 | GAAAATTCAGCAAGT[C/T]CCATGAGAGGATGGT | 79023 |
rs747697705 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108859 | AACTTTGTTCAAAAT[A/G]TCATCTCTAAAACAG | 79023 |
rs747732666 | snp | C/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119891 | AGTCTCTGCAATGAG[C/G]GCCGACACCTCTCCC | 79023 |
rs747774400 | snp | A/C | 1.67217e-05 | 0.00289147 | intron-variant | NUP37 | GRCh38.p7 | 12:102074988 | CGTATGTTACAAAAC[A/C]TTTCCACATTACCTG | 79023 |
rs747800853 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089803 | TTTCTTAATGCCTTA[C/T]ACGGTCTTCAATTAA | 79023 |
rs747870614 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant | NUP37 | GRCh38.p7 | 12:102112094 | AGGAATGCATTTGGT[A/G]CTGTTAAACTTACTT | 79023 |
rs747929257 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084300 | GCTTGTTATGATTAA[C/T]GAAACTTATCTTCTC | 79023 |
rs748025979 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097359 | TAAAAAATTAAATTT[A/T]TTTAAACTAAAAGAC | 79023 |
rs748042434 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083094 | TAAGTTAAAGCATAT[C/G]GAAGAAAGAGATAAA | 79023 |
rs748043209 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115972 | TTAATTGTATTTCCA[A/G]TGTCTGATGCAGAAT | 79023 |
rs748048601 | snp | A/G | 4.9708e-05 | 0.00498513 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077478 | TCATAAAACCGGATT[A/G]TTCCATTCTTCTCTG | 79023 |
rs748122766 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098087 | AACATTATGCAAAAC[A/G]GCAGAGCAGCAGTTT | 79023 |
rs748176836 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081170 | GTATGAGTTAGTAAA[C/T]ATAAAGCACTTAGAA | 79023 |
rs748190257 | snp | A/C/T | 0.000233878 | 0.0108115 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118375 | AACCTGAAACGTACA[A/C/T]GTGCCAATGACCACA | 79023 |
rs748324319 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093636 | ACTACCCAGGAAATA[C/T]TAGCATTTCATTTTT | 79023 |
rs748349511 | in-del | -/TTTTATTTAGTATA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117694 | ATGCCCTCTTGGAAT[-/TTTTATTTAGTATA]TTTTATTTAGTATAT | 79023 |
rs748369402 | in-del | -/AAGA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112363 | AGCAAATTACATATT[-/AAGA]TTTAACTAGTTCATT | 79023 |
rs748388835 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092411 | TATAAGGATTAGCAG[A/G]CACTTTACAATGTCA | 79023 |
rs748430672 | in-del | -/AATAT | 0.000208326 | 0.0102039 | intron-variant | NUP37 | GRCh38.p7 | 12:102112277 | GTAATGAGAACAAAC[-/AATAT]AATATTCTGTATTTC | 79023 |
rs748574106 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087068 | TTGCACCTCTGCACT[C/G]CAGCCTGGGTGACAG | 79023 |
rs748575999 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102306 | GTAATTTGTCAAGAG[C/T]TGTTAGAGAAAACAG | 79023 |
rs748634155 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112823 | GTGTCAATGATTTTC[A/G]TGTAGTGTTACATGT | 79023 |
rs748638941 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113953 | ATAATTCAGATACCC[C/T]TTGAAAATAACTTCA | 79023 |
rs748648808 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082073 | CCAATTCTTTGATCC[C/T]GTGACATCCTGAATC | 79023 |
rs748807575 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119016 | TCTCCATTTTGTAGA[C/T]GGAGAAACTGAGGCT | 79023 |
rs748814951 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119819 | TCACCGTACACGTTG[G/T]ACAGGACTTGCCCCT | 79023 |
rs748861633 | snp | C/T | 2.13018e-05 | 0.0032635 | intron-variant | NUP37 | GRCh38.p7 | 12:102076864 | TAAAAGATAATATTT[C/T]GCATTTTATGAATTA | 79023 |
rs748882435 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085640 | TAGACTAATCCAAAT[A/G]CCTTTGTGCTGACTA | 79023 |
rs749030709 | in-del | -/ACTC | 3.41023e-05 | 0.00412917 | intron-variant | NUP37 | GRCh38.p7 | 12:102077529 | GAAAAATAAAAAGAA[-/ACTC]AATCACTTATCTCAC | 79023 |
rs749095643 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111191 | CCAGACACAAAAGAC[A/T]TTCTGTATGATCCCA | 79023 |
rs749139501 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082238 | TTTTCCTGATCTTAC[A/G]GCTTTTTTTATGGTT | 79023 |
rs749151611 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081276 | TAACAAAAGATTTTT[A/G]TTATTTACTGTCTGT | 79023 |
rs749239810 | in-del | -/GATA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103148 | TGACATTGGAGTTTT[-/GATA]GATAGGCATTGCATT | 79023 |
rs749265650 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095572 | TGGGAATTTCTTTTA[C/T]TAAACACATCTATCA | 79023 |
rs749280452 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108552 | CTTAATAAACTCCCC[C/T]TCATATATACATCTA | 79023 |
rs749288960 | snp | C/T | 0.0009745 | 0.0220522 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120499 | TGGAGCTGGTAGGTC[C/T]TGAGGGTTCGTCTGC | 79023 |
rs749348908 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077350 | TATCCCAAATTAACC[A/G]ATCATTTCCTGCAAC | 79023 |
rs749376130 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084708 | GCCAGGCTGTGTCTC[-/A]AAAAAAAAAAAAAAA | 79023 |
rs749504716 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104992 | TGCCACAGAGATTGA[G/T]AAAGACGTCATTGAA | 79023 |
rs749524333 | snp | C/G | 1.67959e-05 | 0.00289787 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074403 | TCTCCTCCAATTACA[C/G]ACAGAGGGAGAGTTC | 79023 |
rs749756429 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113997 | TTAAGAGTTAACAGC[-/A]AAAAAGTTTTTCCAC | 79023 |
rs749765365 | snp | G/T | 3.3066e-05 | 0.00406595 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099193 | AAATCGGTATGGCCC[G/T]CTAAAACCTGACAGA | 79023 |
rs749791950 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093450 | GGATGGAAATTGTGA[G/T]AAATTTTGTCACATT | 79023 |
rs749833451 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111984 | GTAGCAAATATCAAA[A/G]TATCTAATATCTTGG | 79023 |
rs749852340 | snp | A/C/G/T | 6.61963e-05 | 0.00575281 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099111 | AGCAACATACCTGCA[A/C/G/T]GTGTGATCGTCACTC | 79023 |
rs749987837 | snp | A/G | 4.89321e-05 | 0.00494607 | intron-variant | NUP37 | GRCh38.p7 | 12:102085738 | AGTCTTTTCAATTTG[A/G]TAAGAGAGTTAAATT | 79023 |
rs750016867 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094593 | TATGAAAAACACATA[C/G]CTTGCATGTGGTACA | 79023 |
rs750021412 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100682 | TGTGCTATGCTGTAC[C/T]GATCATTTGTTCCCA | 79023 |
rs750062669 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080818 | GTGGGGAAGGATCAG[A/G]AAAGGTAAGAGATCG | 79023 |
rs750067964 | snp | C/G | 1.65083e-05 | 0.00287296 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077454 | AAAATAGCCTGTTGG[C/G]CCAAAAGATCATAAA | 79023 |
rs750086456 | snp | C/T | 1.70851e-05 | 0.00292271 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118560 | TGAAAATTAAATAGC[C/T]TTCTACTGGACAAGG | 79023 |
rs750104195 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081688 | GCATTCAACAAATGT[C/T]GGCTGTTAAACCTAT | 79023 |
rs750155448 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113243 | AAATCCTAGTGCCTG[C/T]ACAAGGAAGGATGCC | 79023 |
rs750224569 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120281 | TTCGGGTCTACCCCT[A/G]ATCACGTAAGTCTCG | 79023 |
rs750280255 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115914 | TAGCTAGATAAAAAA[C/T]AACTCCACAGAAAAG | 79023 |
rs750376683 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088309 | AGCTCATCTGGTTAA[C/T]ATTACTTACATGAGA | 79023 |
rs750493584 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085009 | AATAGGAATTGAACA[A/C]TACTGTAGCTAAGAC | 79023 |
rs750541415 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116662 | AGCTTTATATATTCA[C/T]TGTGCTATAAAATGC | 79023 |
rs750574253 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105399 | GCCGGGTGCAGTGGC[A/G]TGTGCCTGTAGTCCC | 79023 |
rs750602108 | snp | C/T | 1.77222e-05 | 0.0029767 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076819 | AGCAGGCTCGATCCA[C/T]GTGAACAGGTCTCTT | 79023 |
rs750607469 | in-del | -/AAGTA | 2.08488e-05 | 0.00322861 | frameshift-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101061 | TATCCTGAAGATCTG[-/AAGTA]AATAATCTAATTTTC | 79023 |
rs750654123 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111271 | CAGATCAATGGTTGC[C/T]TCTGCAGGGAGTGGG | 79023 |
rs750673367 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097924 | GGCCTATGACTCTAT[C/T]ACTTTAAAAAGATGA | 79023 |
rs750676321 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098729 | TAGAAATGGAGTTTC[A/G]CCATGTTGGTCAGGC | 79023 |
rs750689837 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083802 | AAAATCAAACTAGCA[A/G]TTTCAAGAAGGAGGT | 79023 |
rs750748100 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112138 | AATGAATCAAGTCTA[A/G]TCTCTGGGCTCCAAG | 79023 |
rs750860673 | snp | G/T | 3.59099e-05 | 0.00423717 | intron-variant | NUP37 | GRCh38.p7 | 12:102101152 | TTAGCCTTTGTAAGT[G/T]AAAGGTCTCCCCCTC | 79023 |
rs750915006 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104880 | TTTGAAATAAAGAAG[C/T]GTGAGAACTTCAGCT | 79023 |
rs750917164 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117857 | TCATGCTCTTAATGG[C/T]TATGCTTAACTGCCT | 79023 |
rs750935054 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105489 | GAGCTGATATCATGC[C/T]ATTGCACTCCAGTCT | 79023 |
rs750961558 | in-del | -/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100229 | CATACAGTACATTAA[-/G]CCCACTGTAAATAGC | 79023 |
rs751107659 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111562 | GCAAGGCTAGTGTTT[C/T]GTAACAGATCTTAAA | 79023 |
rs751173272 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116199 | ACTTCTCCCTCTCTC[A/G]TCTTTGCCTCTCTTT | 79023 |
rs751199788 | snp | C/T | 2.89047e-05 | 0.00380151 | intron-variant | NUP37 | GRCh38.p7 | 12:102085872 | CTAATAAAAGAATAA[C/T]AGTATAATGTTAATT | 79023 |
rs751216479 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091749 | TTCATCCAATTTGAA[C/T]GATAATTATAATTAA | 79023 |
rs751227623 | in-del | -/TAA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100856 | TAAGAACTTAGTTCT[-/TAA]TAATATAGTAAGCTA | 79023 |
rs751268453 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079679 | CACAGCCTTCTTGCA[C/T]TTAGAACACTAGCCA | 79023 |
rs751302054 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101502 | AATATTGTTATACAT[A/C]TACCTTAGTCTTTGC | 79023 |
rs751424560 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091620 | AGGGAAATTTAAAAG[A/G]AAAAGCTTTTATGGG | 79023 |
rs751547525 | snp | C/G | 7.22587e-05 | 0.00601033 | intron-variant | NUP37 | GRCh38.p7 | 12:102074498 | AGAATTAAAGAAGCA[C/G]AGTAAGTCCCCAAAA | 79023 |
rs751547976 | snp | A/T | 1.65053e-05 | 0.0028727 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099174 | AAACACCAAACCATT[A/T]ATGAAATCGGTATGG | 79023 |
rs751601446 | in-del | -/GCGGCGACT | | | cds-indel, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120199 | TATTCAGCGGCGACA[-/GCGGCGACT]GCGGCGGCCGCGGGA | 79023 |
rs751639027 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097844 | GGGCCCTAGAATCTT[A/T]ATGTCATGTAAATCT | 79023 |
rs751738279 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110325 | GGCAACATGGCGAAA[C/T]CCCATCACTGCAAAA | 79023 |
rs751762227 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077982 | AAGGAAGAGGCTATG[C/T]AAAAATCTCTAGAGA | 79023 |
rs751791601 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121472 | TGCCTCAAATATTTA[C/G]TGTTTGTTCCTTTAG | 79023 |
rs751800569 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104699 | ACCATTTGTTGAACA[C/G]ACTATCCTTTTCCCC | 79023 |
rs751833430 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109587 | TTTGAAAACAAGATT[C/G]TGCCTTCAGGTTGCT | 79023 |
rs751976319 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083681 | AGTGACAATTAACCC[C/T]TGAAGCAATTCACAA | 79023 |
rs752004071 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104825 | TTATCTTTATGCCAG[C/T]ACCATACTGTTTTGA | 79023 |
rs752007926 | snp | C/T | 1.83273e-05 | 0.00302709 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076834 | TGTGAACAGGTCTCT[C/T]ATTTTGAGGATAACT | 79023 |
rs752009194 | snp | A/G | 5.0929e-05 | 0.00504598 | intron-variant | NUP37 | GRCh38.p7 | 12:102075146 | CCTATGGATAATGAC[A/G]AGCTTTTCTGAAGCG | 79023 |
rs752090005 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116608 | CTGAAACTTTCAATT[C/G]ACACTTCCTCTTAAA | 79023 |
rs752129050 | snp | C/T | 3.29554e-05 | 0.00405914 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112166 | AAGCTATGCCATCAA[C/T]CCTGACTCCATGGTG | 79023 |
rs752206953 | snp | C/T | 1.73156e-05 | 0.00294236 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118333 | AGTGAAATATGTTCA[C/T]TGTCATTCGGTGCAG | 79023 |
rs752247106 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121836 | ACCACCATGCCCAGG[C/T]AATGCTCTTTTACTT | 79023 |
rs752274777 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116429 | AGTCTTTTTCAAGTA[C/T]GTAACATTGTCTTAA | 79023 |
rs752306115 | in-del | -/ATCTT | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118239 | CATCTTTCTCTATGG[-/ATCTT]ATCTTTTTTTTTTTT | 79023 |
rs752358415 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108405 | CTCTTGGGCCTTAGG[-/C]CCACAGATTGAAGGC | 79023 |
rs752399155 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104384 | TTATCCCTTGTTAGG[C/T]ATATGGGTTGCAAAT | 79023 |
rs752413170 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090574 | TGAAACTAAGTCAAT[A/G]CCAACTAACTAAAGG | 79023 |
rs752632530 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080613 | TGAGGAAATTACTAT[C/T]GTTAATCCCATTTTT | 79023 |
rs752644185 | in-del | -/A | 1.697e-05 | 0.00291285 | intron-variant | NUP37 | GRCh38.p7 | 12:102074982 | AAGCACGTATGTTAC[-/A]AAAACATTTCCACAT | 79023 |
rs752647571 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079554 | TTCTTTTTAAAGATA[G/T]CTTACTTAATATATA | 79023 |
rs752676161 | snp | C/G | 2.16997e-05 | 0.00329384 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085783 | TAAAAGTCTCCTCAG[C/G]ATGCCAGCACACACT | 79023 |
rs752730992 | in-del | -/A | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120280 | TTCGGGTCTACCCCT[-/A]AATCACGTAAGTCTC | 79023 |
rs752765211 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108143 | GTCAAGAGATTAACA[G/T]CTGAGTCAGTGGAGT | 79023 |
rs752790445 | in-del | -/AC | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089964 | CATACGATCACATAC[-/AC]ACACACACACACCTG | 79023 |
rs752833011 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075457 | GAAGTGCTGGGATTA[C/T]AGGTATGAGCCATAG | 79023 |
rs752870047 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095361 | ACGTATTTATATTTT[A/T]CTGTGCATATGCATA | 79023 |
rs752872370 | snp | A/G | 2.29671e-05 | 0.00338866 | intron-variant | NUP37 | GRCh38.p7 | 12:102101111 | GTACAAAATCTGGAA[A/G]CAAAAAAACAAAAAT | 79023 |
rs752904793 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085919 | TACTAAAAAATTAAA[C/T]TTCCATGAATTTATT | 79023 |
rs752995966 | snp | G/T | | | upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120162 | CGATTGGCTCCCGGG[G/T]CCTCCCGCGAGGTTT | 79023 |
rs753151546 | snp | A/C | 4.94474e-05 | 0.00497205 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118411 | ATTGCCACCATATGC[A/C]ATTAGGTTTCCTGAA | 79023 |
rs753233602 | snp | G/T | 5.05992e-05 | 0.00502962 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118543 | CAAAATTCAAGCAGT[G/T]GTGAAAATTAAATAG | 79023 |
rs753241776 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088434 | AAAGAATGGCACCTA[A/T]ATCAAGAAACAGAGT | 79023 |
rs753261484 | snp | A/G | 1.9932e-05 | 0.00315684 | intron-variant | NUP37 | GRCh38.p7 | 12:102076853 | TTGAGGATAACTAAA[A/G]GATAATATTTTGCAT | 79023 |
rs753268501 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104956 | TGAATTTTAGGATGG[C/T]TTTTCTGTTTCTGTA | 79023 |
rs753338331 | snp | A/G | 1.65127e-05 | 0.00287334 | intron-variant | NUP37 | GRCh38.p7 | 12:102077292 | CTGCCTTTTTTTGGT[A/G]TGTAATAGACAAACA | 79023 |
rs753353236 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102997 | CTGTCTTGAATACCA[C/T]AGCTTTTATTTTGAA | 79023 |
rs753497796 | snp | A/C | 1.64773e-05 | 0.00287026 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118426 | AATTAGGTTTCCTGA[A/C]TCCCCATTCTCAAAG | 79023 |
rs753511283 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079477 | CACTGGGGAAATACA[C/G]AGTTAGGTTCCCTGC | 79023 |
rs753545383 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101878 | TACAGGCGCCCACCA[C/T]CACACGTGGCTAATT | 79023 |
rs753549040 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114942 | TCTGGAACCACACCA[A/C]ATCAGTCTAACTTAA | 79023 |
rs753553793 | in-del | -/AC | 1.65228e-05 | 0.00287422 | intron-variant | NUP37 | GRCh38.p7 | 12:102100985 | AAAAGCAAAAAACAA[-/AC]ACGTTTTAAAATAAG | 79023 |
rs753554593 | snp | C/T | 2.10928e-05 | 0.00324745 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074330 | AAAATACAAAGTTTG[C/T]GAATCTAAGGTACAG | 79023 |
rs753596844 | in-del | -/ATGTACTGAGA | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119603 | AAGCACCTTAAGAGT[-/ATGTACTGAGA]ATGAGTCCCACCTCG | 79023 |
rs753626209 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109839 | ATGTAGATTAAAGAG[G/T]TATCACAAAACTTAA | 79023 |
rs753660633 | in-del | -/TAAA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078327 | GCGAAATTCCTTCTT[-/TAAA]AAAAAAAAAAAGATT | 79023 |
rs753738077 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115097 | ACATAAAATCCATTT[A/C]CCATTGAGTCTAATA | 79023 |
rs753773714 | in-del | -/AATT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109023 | CTTACTTAAAAAGAA[-/AATT]AATAATCTTACTGGG | 79023 |
rs753777864 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090368 | TCTTTTTTCCCCCTA[C/T]AGAAGTGCCAAGAAT | 79023 |
rs753780538 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091496 | ATGAAAAGATGATAG[A/G]CCATTTCTCAAAGCA | 79023 |
rs753804864 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121691 | CCCAAGTAGCTGGGG[C/T]TAGAGGCACACACCA | 79023 |
rs753818503 | snp | G/T | 1.65023e-05 | 0.00287244 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099142 | ACACTTGCAATTTCT[G/T]GGCCTTCTTTGGGAT | 79023 |
rs753836967 | snp | C/T | 3.58096e-05 | 0.00423125 | intron-variant | NUP37 | GRCh38.p7 | 12:102099057 | TTTAAAAATGTAATT[C/T]TCATTAAAATGGCAA | 79023 |
rs753966632 | snp | C/T | 1.66832e-05 | 0.00288814 | intron-variant | NUP37 | GRCh38.p7 | 12:102075111 | TAAGAAATAAGGAAG[C/T]GTAAAATTAAGTATC | 79023 |
rs754002670 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105730 | GCTGGGCATGGTGAT[A/G]TGCACCTATAATCCC | 79023 |
rs754007624 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088730 | TTTTTTTTTAGTATT[C/T]ATTGAACATTCTTGG | 79023 |
rs754054963 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112134 | AGGCAATGAATCAAG[C/T]CTAGTCTCTGGGCTC | 79023 |
rs754124083 | in-del | -/AC | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099457 | ATTTCTTACAAAAAC[-/AC]ACACACACACACACA | 79023 |
rs754163254 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081831 | CCAGAGTAGCTGGGA[A/C]TACGGTCGAGCACCA | 79023 |
rs754163576 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096596 | AAATTTTCTTAAGTA[A/T]GCACTGGGTCTGCTC | 79023 |
rs754177472 | in-del | -/A | 5.0104e-05 | 0.00500494 | intron-variant | NUP37 | GRCh38.p7 | 12:102075114 | GAAATAAGGAAGCGT[-/A]AAATTAAGTATCGTA | 79023 |
rs754179785 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102290 | ACTACACCCCTTTCC[A/G]GTAATTTGTCAAGAG | 79023 |
rs754238206 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076917 | ACTTAAGGTTTAAAC[A/G]GTATTTTCTCTTTAT | 79023 |
rs754299643 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106859 | AAGCCTGAAAACTTG[C/T]ATTTGTCTCCTCTGA | 79023 |
rs754303245 | snp | C/T | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077446 | CAAGAGATAAAATAG[C/T]CTGTTGGGCCAAAAG | 79023 |
rs754357465 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094945 | TAATATTTTAAAAGA[C/T]TATTGAGGGATGAGG | 79023 |
rs754512932 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090379 | CCTATAGAAGTGCCA[A/G]GAATGAGAAGGCTAT | 79023 |
rs754515126 | in-del | -/CATG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092689 | TCAGAGGTGGGGAAC[-/CATG]TAACTGAAAGCCCAA | 79023 |
rs754526814 | snp | C/T | 4.9436e-05 | 0.00497148 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112177 | TCAACCCTGACTCCA[C/T]GGTGAAATGTTCGAA | 79023 |
rs754580714 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076859 | ATAACTAAAAGATAA[C/T]ATTTTGCATTTTATG | 79023 |
rs754702894 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102118042 | AGGATGTAGAAAAAC[C/T]GTAATTAATTGGATC | 79023 |
rs754746162 | snp | A/C | 2.59622e-05 | 0.00360284 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085771 | AAATAATAACCTTAA[A/C]AGTCTCCTCAGGATG | 79023 |
rs754824708 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108841 | AGCATAATGAAATCA[C/T]AAAACTTTGTTCAAA | 79023 |
rs754954471 | in-del | -/GTGACTGCCAT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078607 | TCACTTATAAGCTGA[-/GTGACTGCCAT]GTGACTGGCAGCTTT | 79023 |
rs754958670 | snp | C/T | 0.000204714 | 0.0101151 | intron-variant | NUP37 | GRCh38.p7 | 12:102101015 | AGCTCTAAAGATTTA[C/T]ATGGTTGTCAACATA | 79023 |
rs755059539 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119326 | GGAGCTTAATACCTA[A/G]GTGATGGGTGTGCAA | 79023 |
rs755109858 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102118145 | ATTAATGATCATGAG[A/G]CAAAAGTGAAGCCTC | 79023 |
rs755119006 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080498 | CTAATGCTACTAACA[A/G]TAAGTACAATGAGGT | 79023 |
rs755119076 | snp | A/G | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099175 | AACACCAAACCATTA[A/G]TGAAATCGGTATGGC | 79023 |
rs755147516 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106913 | TTCAGGCCTCCCAGA[C/T]AGCATAAAGGAACTA | 79023 |
rs755179160 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075370 | TGTTTTTTGTAGGAA[C/T]GGGGTCTTGCTATCT | 79023 |
rs755184139 | snp | C/G | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102073717 | TTTGAGATAGTCTCG[C/G]TCTGTCGCCCAGGCT | 79023 |
rs755204019 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082682 | AGAGTCCACACTCTT[A/C]ACCACTTCTCTGTAT | 79023 |
rs755228051 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087299 | ATTGGACAATGCTAC[C/T]ATTCTGTGCCAAAAC | 79023 |
rs755232387 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121142 | CCACCTAGGAACCAC[C/G]TGTAAGGCTTATGGC | 79023 |
rs755401636 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082624 | AGAGATCACACAGCT[A/G]GTAAGTGGTGAAACT | 79023 |
rs755420894 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096969 | TCAACCCGAAAATCT[C/T]GGTGGTTTACAGAAA | 79023 |
rs755469075 | in-del | -/TAAGGAA | 1.65119e-05 | 0.00287327 | intron-variant | NUP37 | GRCh38.p7 | 12:102112076 | ATCAAAGTACATTAG[-/TAAGGAA]TAAGGAATGCATTTG | 79023 |
rs755551389 | snp | C/G | 1.79313e-05 | 0.00299421 | intron-variant | NUP37 | GRCh38.p7 | 12:102076747 | ATCCCAGTGGTGGCA[C/G]AGCAACGTCAAAAGA | 79023 |
rs755610975 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092079 | TTAATAAAGAAAGAT[A/G]TTCTGTCCGAGGATT | 79023 |
rs755616370 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100689 | TGCTGTACTGATCAT[C/T]TGTTCCCATGAAGTT | 79023 |
rs755634769 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108717 | CCTTTGAATTTGTCC[-/A]ATTATTATTTTGGGA | 79023 |
rs755655884 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113659 | GTCCAAGGAATCTTC[C/T]GTGCTAACTACAGTT | 79023 |
rs755675214 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086917 | AGTGAAACTTCGTCT[C/G]TACAAAACACATAAA | 79023 |
rs755933358 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120326 | GCCCTGTCGCATTTT[C/T]AAGTGGTGATTCAGG | 79023 |
rs755942277 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088392 | TACACAAATCTTAAA[A/T]GTACAATTCAAAGAG | 79023 |
rs755966307 | snp | A/G | 4.54907e-05 | 0.00476899 | intron-variant | NUP37 | GRCh38.p7 | 12:102085897 | TTAATTGTTCTTGAT[A/G]TATCATTACTAAAAA | 79023 |
rs755983902 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108330 | CTTCCTGCCATTGAA[A/C]ATCAGACTCAAGTTC | 79023 |
rs755996106 | in-del | -/GG | 1.65556e-05 | 0.00287707 | frameshift-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102075005 | TTCCACATTACCTGA[-/GG]GTGTCCTAAATGATG | 79023 |
rs756054669 | snp | A/C | 2.08527e-05 | 0.00322892 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085788 | GTCTCCTCAGGATGC[A/C]AGCACACACTCATGC | 79023 |
rs756090214 | snp | A/C | 4.79008e-05 | 0.00489368 | intron-variant | NUP37 | GRCh38.p7 | 12:102074499 | GAATTAAAGAAGCAC[A/C]GTAAGTCCCCAAAAT | 79023 |
rs756144999 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116687 | AAATGCCAAATTGCA[G/T]TTTTGATGTCAGAAT | 79023 |
rs756202667 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104908 | GCTTTCTCAAGATTG[A/T]TTTGGTCATTTGGGG | 79023 |
rs756224759 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098750 | TTGGTCAGGCTGGTC[A/G]TTAACTCCTGACCTC | 79023 |
rs756232376 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117879 | TAACTGCCTGCTCAA[C/T]TAATATGACTCCATA | 79023 |
rs756240742 | snp | G/T | 1.67919e-05 | 0.00289753 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074388 | AACAACAGCTTGTGG[G/T]CTCCTCCAATTACAC | 79023 |
rs756251468 | in-del | -/TTAAG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078433 | TGGGAAAAGTTACTT[-/TTAAG]TTATGTTAGTTATAT | 79023 |
rs756264929 | in-del | -/TAAG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086015 | TTATAACACCACTTT[-/TAAG]TAATATGAAAGTAGG | 79023 |
rs756342138 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083990 | GGTACAAGTGATGGA[G/T]TCAAACATTTAGAAA | 79023 |
rs756370547 | snp | C/T | 2.41987e-05 | 0.00347833 | intron-variant | NUP37 | GRCh38.p7 | 12:102101024 | GATTTATATGGTTGT[C/T]AACATACCTTATATT | 79023 |
rs756376364 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099396 | ATCTTGGGAAAAAAA[C/T]TGATCATTCAACACA | 79023 |
rs756452274 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093280 | GGATAAAAATTTTAT[C/G]AATTTGTATGCTGTT | 79023 |
rs756458335 | snp | A/G/T | 3.30306e-05 | 0.00406377 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099183 | ACCATTAATGAAATC[A/G/T]GTATGGCCCTCTAAA | 79023 |
rs756505027 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080833 | AAAAGGTAAGAGATC[A/G]AGGAAAATTCACCAG | 79023 |
rs756571057 | in-del | -/TTAG | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120555 | CCTGCTTAACTTCCA[-/TTAG]TTAGGCAGGAAACCT | 79023 |
rs756576827 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092162 | CATTTTTGGCAGCTC[A/C]TTGTTTGCTAGGAAA | 79023 |
rs756725810 | snp | C/T | 1.66236e-05 | 0.00288297 | intron-variant | NUP37 | GRCh38.p7 | 12:102077275 | TCATTTAGCAACAGT[C/T]ACTGCCTTTTTTTGG | 79023 |
rs756730460 | snp | G/T | 1.65042e-05 | 0.0028726 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077452 | ATAAAATAGCCTGTT[G/T]GGCCAAAAGATCATA | 79023 |
rs756745819 | snp | C/T | 1.6489e-05 | 0.00287128 | intron-variant | NUP37 | GRCh38.p7 | 12:102077308 | TGTAATAGACAAACA[C/T]ATCAAGAAAGTACCT | 79023 |
rs756768639 | in-del | -/ACTT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115951 | TTTATTTTGAAATGG[-/ACTT]ACTTAATTGTATTTC | 79023 |
rs756812303 | in-del | -/CTGCTAG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096490 | TCCTAGGGCAAAATT[-/CTGCTAG]CTGATTATAATATAG | 79023 |
rs756900316 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079692 | CACTTAGAACACTAG[C/T]CAGCACTACATTACT | 79023 |
rs756904951 | snp | C/T | 3.29533e-05 | 0.00405901 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118431 | GGTTTCCTGAATCCC[C/T]ATTCTCAAAGGGATT | 79023 |
rs756988285 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080776 | CTGCTGAAGACTGGT[A/G]AGTGGTCTAGTGTGC | 79023 |
rs757020204 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086804 | AAGAACTGAACTTGA[C/G]TGGGTGCCATGGCTC | 79023 |
rs757069966 | snp | A/G/T | 6.82109e-05 | 0.00583965 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118356 | CGGTGCAGTTTTGTA[A/G/T]ACTAACCTGAAACGT | 79023 |
rs757105990 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087919 | ATTCCTGTCCAATGA[A/T]CCAAAGTTTTACCTA | 79023 |
rs757118597 | snp | A/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119406 | CACGTATCCCGGAAC[A/T]TAAAAATTAAAATAA | 79023 |
rs757144706 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085240 | CCCTGGGTAACATGG[A/C]GAAACCTCAGCCCTA | 79023 |
rs757145632 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075483 | CATAGCACCTAGACA[C/G]AAACAGGTTTCTTTT | 79023 |
rs757258385 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082906 | GAAGGAAAAATTAAA[A/C]GACCTGGAATAGTTT | 79023 |
rs757330180 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115374 | AAGTGTAAAATACAT[A/T]CCAGATTTCTAAGTC | 79023 |
rs757392192 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097847 | CCCTAGAATCTTAAT[A/G]TCATGTAAATCTTTC | 79023 |
rs757406957 | in-del | -/A | 1.76184e-05 | 0.00296797 | intron-variant | NUP37 | GRCh38.p7 | 12:102076781 | AATCACAGCTCCAAC[-/A]AAAACGGTACATTAC | 79023 |
rs757508167 | snp | A/T | 0.000328353 | 0.0128089 | intron-variant | NUP37 | GRCh38.p7 | 12:102074957 | TCAAAAACACAAATT[A/T]AAAAAAAAAAAAGCA | 79023 |
rs757510723 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096961 | GTTGTGCATCAACCC[A/G]AAAATCTCGGTGGTT | 79023 |
rs757536527 | in-del | -/AAAG | 2.70676e-05 | 0.00367873 | intron-variant | NUP37 | GRCh38.p7 | 12:102101006 | TTTAAAATAAGCTCT[-/AAAG]ATTTATATGGTTGTC | 79023 |
rs757546350 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102074991 | ATGTTACAAAACATT[C/T]CCACATTACCTGAGG | 79023 |
rs757564707 | in-del | -/TTTG | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121393 | GCACAGCTATACTCA[-/TTTG]TTTGTTTATGTATGT | 79023 |
rs757604427 | snp | C/G | 3.36242e-05 | 0.00410012 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074407 | CTCCAATTACACACA[C/G]AGGGAGAGTTCGATG | 79023 |
rs757604441 | snp | A/T | 2.56453e-05 | 0.00358078 | intron-variant | NUP37 | GRCh38.p7 | 12:102101128 | AAAAAAACAAAAATA[A/T]ACCAATTTTTAGCCT | 79023 |
rs757620868 | snp | C/T | 2.27897e-05 | 0.00337555 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101034 | GTTGTCAACATACCT[C/T]ATATTCATTTTTATC | 79023 |
rs757728973 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103541 | GGAAACAGACAATTT[A/C]ACTTCTTCCTTTCCT | 79023 |
rs757754255 | in-del | -/A | 0.0341008 | 0.126046 | intron-variant | NUP37 | GRCh38.p7 | 12:102074957 | TCAAAAACACAAATT[-/A]AAAAAAAAAAAAGCA | 79023 |
rs757796846 | in-del | -/CTA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089991 | CTGCTGGGTACATAC[-/CTA]CTAGGCATGGAATTG | 79023 |
rs757902882 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121841 | CATGCCCAGGCAATG[C/T]TCTTTTACTTTTAAC | 79023 |
rs757919494 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110239 | GCACAGTGGCTCATG[C/T]CTGTAATCCTAACAC | 79023 |
rs757958794 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078585 | GAGCACAGACACGCC[A/G]CTTCCTTCACTTATA | 79023 |
rs757987483 | in-del | -/GAT | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102073854 | TATTTTTTTAGTAGA[-/GAT]GATAGGGTTTCACCA | 79023 |
rs758046724 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079584 | ACTGATTCATTAATA[C/T]AGACCTCACCATGAA | 79023 |
rs758090817 | snp | C/T | 1.65299e-05 | 0.00287483 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077463 | TGTTGGGCCAAAAGA[C/T]CATAAAACCGGATTG | 79023 |
rs758135832 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116078 | TTGCTAATCTCACAG[G/T]TATGAGGGTAACTGA | 79023 |
rs758161588 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089931 | CTTGCATATGTCTTT[C/T]AGTGAATATAGATAC | 79023 |
rs758170550 | in-del | -/GT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116284 | GATAAACATTTTTCA[-/GT]GTTTGCGAATACAAT | 79023 |
rs758178904 | snp | A/G | 3.45012e-05 | 0.00415324 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118570 | ATAGCCTTCTACTGG[A/G]CAAGGTCACGAAACT | 79023 |
rs758191245 | snp | A/G | 1.64776e-05 | 0.00287028 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118465 | TTCTACCACATGCAC[A/G]TAATCTTCACAATCC | 79023 |
rs758192647 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098844 | GTCCAATATAGATTT[C/G]GATTTCATAAATGTG | 79023 |
rs758230836 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098165 | TTCCAATGACTGATG[A/C]ACTCATTTCACTCCT | 79023 |
rs758270454 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085135 | ACAAAAAACTGCCTA[C/T]TGGGCCAGGCATGGT | 79023 |
rs758295395 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111518 | CTACTAAAAGAAGAC[A/G]CATCTTTTAGATTTG | 79023 |
rs758377469 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095379 | GTGCATATGCATATA[C/T]AAACACACACATAAA | 79023 |
rs758417802 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101112 | ACAAAATCTGGAAGC[-/A]AAAAAAACAAAAATA | 79023 |
rs758460746 | in-del | -/CACCCACT | 2.32924e-05 | 0.00341257 | intron-variant | NUP37 | GRCh38.p7 | 12:102076881 | ATTTTATGAATTATG[-/CACCCACT]TGTTAAACTCAAGTG | 79023 |
rs758464434 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082083 | GATCCCGTGACATCC[G/T]GAATCCTTGGTCCTG | 79023 |
rs758478568 | snp | C/T | 0.000100976 | 0.00710478 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074378 | AGTCACCCAAAACAA[C/T]AGCTTGTGGTCTCCT | 79023 |
rs758495238 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076525 | AGCACAGAACAATCA[A/G]GAAGCATAATATATT | 79023 |
rs758517404 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108234 | TGGCTGCCAGCACAA[C/G]TAGAAAAAACAGACA | 79023 |
rs758530597 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105485 | TAGTGAGCTGATATC[A/C]TGCCATTGCACTCCA | 79023 |
rs758535797 | snp | A/T | 1.78417e-05 | 0.00298673 | intron-variant | NUP37 | GRCh38.p7 | 12:102099058 | TTAAAAATGTAATTC[A/T]CATTAAAATGGCAAT | 79023 |
rs758590913 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107404 | ATCTCCCCAACCATT[C/T]TTCACACTTCTTTCA | 79023 |
rs758629406 | snp | C/T | 3.36661e-05 | 0.00410267 | intron-variant | NUP37 | GRCh38.p7 | 12:102075135 | AAGTATCGTATCCTA[C/T]GGATAATGACAAGCT | 79023 |
rs758642668 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107147 | TTCTTCCCTTGCAAT[A/G]CTTGTTGTCTTAGTC | 79023 |
rs758660673 | in-del | -/TCTT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105076 | CATGAACACAGGCTG[-/TCTT]TCTATTTATTTGTGT | 79023 |
rs758664689 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077588 | GATTCACTGTTGTAC[A/G]GTAAAATGTAAACAT | 79023 |
rs758682573 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115045 | CTGAAAGCATTATAA[G/T]CAACAACTCTGTCCA | 79023 |
rs758697168 | in-del | -/TC | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092117 | AATATTCTGTAATAT[-/TC]TGTTTATTTGTTCAT | 79023 |
rs758717611 | snp | C/T | 1.6477e-05 | 0.00287024 | stop-gained, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112149 | TCTAGTCTCTGGGCT[C/T]CAAGCTATGCCATCA | 79023 |
rs758818981 | snp | A/T | 1.72169e-05 | 0.00293396 | intron-variant | NUP37 | GRCh38.p7 | 12:102074972 | AAAAAAAAAAAAAGC[A/T]CGTATGTTACAAAAC | 79023 |
rs758893327 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113969 | TTGAAAATAACTTCA[A/C]ATTTCAGGTGAACTT | 79023 |
rs758990450 | snp | A/G | 3.30404e-05 | 0.00406437 | intron-variant | NUP37 | GRCh38.p7 | 12:102112057 | ACTTCCAATCATGTA[A/G]CACAATCAAAGTACA | 79023 |
rs759001255 | in-del | -/AA | 4.85519e-05 | 0.00492683 | intron-variant | NUP37 | GRCh38.p7 | 12:102085740 | TCTTTTCAATTTGAT[-/AA]GAGAGTTAAATTATA | 79023 |
rs759011994 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120508 | TAGGTCCTGAGGGTT[C/G]GTCTGCAGCTTGGAA | 79023 |
rs759068498 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081335 | TTTTTGGGTGATAAG[A/T]ACAGATAGGGTAGAA | 79023 |
rs759106967 | snp | C/T | 1.6525e-05 | 0.00287441 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099119 | ACCTGCAGGTGTGAT[C/T]GTCACTCACACTTGC | 79023 |
rs759178882 | snp | C/T | 6.42075e-05 | 0.00566565 | intron-variant | NUP37 | GRCh38.p7 | 12:102085880 | AGAATAACAGTATAA[C/T]GTTAATTGTTCTTGA | 79023 |
rs759185821 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104248 | TTTTATATGCCTGTT[A/G]GCCATTCATATACCT | 79023 |
rs759227294 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114954 | CCAAATCAGTCTAAC[G/T]TAATGATGACAAATA | 79023 |
rs759236438 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120086 | CAGAGGCAGGCTGGT[C/T]TTCCTTGGGGGCTGC | 79023 |
rs759252411 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105861 | GCGGGACTCCCTCTC[-/A]AAAAAAAAAAAAAAA | 79023 |
rs759289635 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080381 | GAATTATGATTGTCC[C/G]ACTGCATCCAGCCTG | 79023 |
rs759412586 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092491 | CCACTGAGCTTGTGA[C/G]AGCAAAACTAGGATT | 79023 |
rs759461222 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091570 | AAAACCTAGGATCTA[C/T]ATTAACATACATAGT | 79023 |
rs759571743 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089940 | GTCTTTTAGTGAATA[C/T]AGATACCCACATACG | 79023 |
rs759583886 | snp | G/T | 1.65381e-05 | 0.00287555 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102075089 | TTTTCACTAATTGTG[G/T]ACCACCTAAGAAATA | 79023 |
rs759687035 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101277 | GTAAAAAGTATTATA[C/T]AGCCATCACAGAAAG | 79023 |
rs759824504 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087513 | GAGACAATTACAATT[G/T]AATTGAAGAGAGAAA | 79023 |
rs759920355 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109063 | ATAAAACCAAACAAA[C/G]AAACCCAGAAAACTT | 79023 |
rs759939054 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085370 | GAGGCTGCAATGAGC[C/G]AAGATCACACCACTG | 79023 |
rs759944077 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077746 | TTTCATGCACAAAAT[C/T]ATTAAAAAAAGTTAT | 79023 |
rs760002567 | snp | A/T | 1.64882e-05 | 0.00287121 | upstream-variant-2KB, stop-gained, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118405 | ATAATTATTGCCACC[A/T]TATGCAATTAGGTTT | 79023 |
rs760010525 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097595 | ACATAGACTACTGAG[C/T]GTGATCCTAGGTCTC | 79023 |
rs760091797 | snp | C/T | 4.63446e-05 | 0.00481354 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074321 | TATGTACTAAAAATA[C/T]AAAGTTTGTGAATCT | 79023 |
rs760263430 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096343 | TCTTCCATAATAACA[C/T]TTTGTATTATCAGAG | 79023 |
rs760321559 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114802 | ACACTTCCAGTGACA[C/G]GGAACTAGCTATTTC | 79023 |
rs760328279 | snp | A/C | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099128 | TGTGATCGTCACTCA[A/C]ACTTGCAATTTCTTG | 79023 |
rs760349784 | snp | C/T | 4.36024e-05 | 0.00466897 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074327 | CTAAAAATACAAAGT[C/T]TGTGAATCTAAGGTA | 79023 |
rs760428386 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091315 | AGGCAGGAGAACTGC[C/T]TGAATCTGGGAGGCG | 79023 |
rs760437794 | snp | A/C | 1.70697e-05 | 0.00292139 | intron-variant | NUP37 | GRCh38.p7 | 12:102099240 | TTAGCAAGAAAACAG[A/C]AAAATAACCTACAAT | 79023 |
rs760556992 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104119 | ATTTCTCCACATCCC[A/G]GGTCAACATTTGTTA | 79023 |
rs760594947 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102930 | GAATTTATTTCTGGG[A/C]TCTCTATCTTATTCT | 79023 |
rs760683374 | in-del | -/ATA | 8.95456e-05 | 0.00669065 | intron-variant | NUP37 | GRCh38.p7 | 12:102085876 | TAAAAGAATAACAGT[-/ATA]ATGTTAATTGTTCTT | 79023 |
rs760688421 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112115 | AAACTTACTTGATTA[C/T]TGGAGGCAATGAATC | 79023 |
rs760688780 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090250 | TCTTTTTTTTTTTGC[A/G]TTTTATTTGCAGTAT | 79023 |
rs760774176 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101112 | TACAAAATCTGGAAG[A/C]AAAAAAACAAAAATA | 79023 |
rs760877608 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086265 | GCTTACAAACACACA[C/T]ACGCATGCAAGCCGA | 79023 |
rs760886383 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112421 | TCTAAGCCTCACAAA[A/G]TAACTCTCTAAGGCA | 79023 |
rs760928535 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088477 | CCAAAAGTTGTCTTG[C/T]GCTCCCTTCTACTCA | 79023 |
rs761081286 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119992 | GGAATAGAGTGGCAA[A/G]GCTGGGCGGCCGGCA | 79023 |
rs761099099 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094687 | GCTTAGTGAATAGCT[C/T]AGGTAATTTAGTATT | 79023 |
rs761099203 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107864 | AAAAAAGCAAGGAGA[C/T]GATTATCCTAATAAA | 79023 |
rs761124984 | snp | G/T | 1.68547e-05 | 0.00290294 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118541 | GTCAAAATTCAAGCA[G/T]TTGTGAAAATTAAAT | 79023 |
rs761141591 | snp | G/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077421 | GACATTAATGGCACT[G/T]GTTCTGATTCAAGAG | 79023 |
rs761306931 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106402 | GTGCCATATTTTAAC[A/G]ACATTTTCATTTGAT | 79023 |
rs761340411 | snp | A/C | 1.69668e-05 | 0.00291258 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118554 | CAGTTGTGAAAATTA[A/C]ATAGCCTTCTACTGG | 79023 |
rs761365981 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075905 | TTGTTTAATTGTTCG[A/G]CAAATGGAGTACTTC | 79023 |
rs761430741 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096010 | TTGTAAAGAAGAAGA[A/C]AGACTACCTATGTCT | 79023 |
rs761490591 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114579 | ATACAAGGTTTCGGC[A/G]TATTTGAGGTTGGGG | 79023 |
rs761611731 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100606 | AAGTAATAACACTGG[A/C]GTTTAAATGCAAGGA | 79023 |
rs761636412 | snp | A/T | 2.07394e-05 | 0.00322013 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101068 | AAGATCTGAAGTAAA[A/T]AATCTAATTTTCATA | 79023 |
rs761638403 | snp | A/G | 1.8887e-05 | 0.00307297 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074340 | GTTTGTGAATCTAAG[A/G]TACAGAAAACACTTT | 79023 |
rs761661368 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102810 | TTCAATTTCATTCTT[C/G]TGTGTGTAAATACAG | 79023 |
rs761726223 | snp | A/G | 0.000113257 | 0.00752433 | intron-variant | NUP37 | GRCh38.p7 | 12:102100989 | GCAAAAAACAAACAC[A/G]TTTTAAAATAAGCTC | 79023 |
rs761800645 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082354 | CAAGGCCAAGCATAA[C/G]AGGCTAACAATTCTG | 79023 |
rs761810674 | snp | C/T | 5.26367e-05 | 0.00512987 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076812 | CTGAATAAGCAGGCT[C/T]GATCCATGTGAACAG | 79023 |
rs761856279 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115338 | TGTGGCTAGTTCTAT[C/T]TGATATGTGTACACT | 79023 |
rs761891905 | in-del | -/TAAG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081355 | ATAGGGTAGAAAAGT[-/TAAG]TAAGTTTGGGAGTAG | 79023 |
rs761931916 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111118 | TGATACACTGTAATG[C/G]AGTACTACTTAAAAA | 79023 |
rs761951937 | in-del | -/CAA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105530 | AGCGAAACCCTGTCT[-/CAA]CAACAACAAGAATTC | 79023 |
rs762055166 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098712 | AATTTTTGTATGTTT[A/C]GTAGAAATGGAGTTT | 79023 |
rs762224016 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119093 | TGGAAGACTTCATTG[C/T]GTGTGGAGAACCAGC | 79023 |
rs762295005 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105462 | TTGAGCCCGGGAGGC[A/G]GAGGTTGTAGTGAGC | 79023 |
rs762356005 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084867 | TACAGTGATGACCAA[C/G]AGAAGATACTGGCAA | 79023 |
rs762356025 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100254 | AATAGCTTACAGCAT[A/T]ATTTTTACTATTTTC | 79023 |
rs762358966 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109781 | AGAGGACAGGAAAAC[A/T]AGTACTAAGCAACAA | 79023 |
rs762385668 | snp | C/G | 5.02462e-05 | 0.00501204 | splice-acceptor-variant | NUP37 | GRCh38.p7 | 12:102085857 | TCCAAGTTCCAAATC[C/G]TAATAAAAGAATAAC | 79023 |
rs762449245 | in-del | -/AA | 0.0245391 | 0.108016 | intron-variant | NUP37 | GRCh38.p7 | 12:102074957 | TCAAAAACACAAATT[-/AA]AAAAAAAAAAAGCAC | 79023 |
rs762475317 | snp | A/G | 0.000154595 | 0.00879055 | intron-variant | NUP37 | GRCh38.p7 | 12:102085754 | TAAGAGAGTTAAATT[A/G]TAAATAATAACCTTA | 79023 |
rs762558223 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104678 | ATGATACTCAGTTTA[C/T]TCAACACCATTTGTT | 79023 |
rs762589517 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106261 | TTGTTTTAAGTCATC[A/G]TGTTTGTGGTGGTTT | 79023 |
rs762594784 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102074704 | TGCAGTCTACACCAA[C/T]CAAACAAGCAAAATT | 79023 |
rs762614978 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092904 | TGTGTGTGTCCAAAT[A/G]TATTTAGAAAATAAG | 79023 |
rs762616573 | snp | A/T | 1.65141e-05 | 0.00287346 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102075020 | GGGTGTCCTAAATGA[A/T]GAATTTGAAACTGGC | 79023 |
rs762772644 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117612 | ACTTTGGTGATTAAA[C/G]CTGAGAGTGTTACCA | 79023 |
rs762791004 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113237 | AGAGACAAATCCTAG[A/T]GCCTGCACAAGGAAG | 79023 |
rs762923921 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080630 | TTAATCCCATTTTTC[A/G]GATGAGATTGAGGCT | 79023 |
rs762930586 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119489 | ATTCTGGAAGTAGCA[C/T]TCCCACATGAGAATT | 79023 |
rs762962992 | snp | A/G | 2.01501e-05 | 0.00317406 | intron-variant | NUP37 | GRCh38.p7 | 12:102074475 | AGGATGGGCTATAAA[A/G]TATGTGAAGAATTAA | 79023 |
rs762968208 | in-del | -/AACA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085106 | TTAAAACAAACAACA[-/AACA]AACAAACAAACAAAC | 79023 |
rs762995671 | snp | C/T | | | intron-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102079163 | GATTTGGCATCAAAA[C/T]TCCTGAGCTGTACCA | 79023 |
rs762996841 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091389 | GGAAACAGAGTGAGA[C/G]ACTCCGTCTCAAAAA | 79023 |
rs763013349 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081506 | CGTATTTGAACCAGA[C/T]TGAGTTCAAATCTGT | 79023 |
rs763015035 | snp | A/C | 2.06699e-05 | 0.00321474 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101075 | GAAGTAAATAATCTA[A/C]TTTTCATATCAGCAG | 79023 |
rs763065337 | snp | C/T | 1.90743e-05 | 0.00308817 | intron-variant | NUP37 | GRCh38.p7 | 12:102077232 | GCTTGACAGCATAGT[C/T]TCAGGTATAACAGGA | 79023 |
rs763092372 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121259 | GCCAGCTCCTGAGCT[A/G]AGAAGGAGTGTTACG | 79023 |
rs763116557 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113950 | TGCATAATTCAGATA[-/C]CCTTTGAAAATAACT | 79023 |
rs763155034 | snp | A/G | 6.61124e-05 | 0.00574907 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118390 | CGTGCCAATGACCAC[A/G]TAATTATTGCCACCA | 79023 |
rs763182989 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109279 | TTTAAGGCAACTACA[C/T]GCTAATGATAAGCCA | 79023 |
rs763196810 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091199 | GTCAGGAGTTCGAGA[A/C]CAGCCTGACCAATAT | 79023 |
rs763306109 | snp | C/T | 1.77868e-05 | 0.00298213 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076821 | CAGGCTCGATCCATG[C/T]GAACAGGTCTCTTAT | 79023 |
rs763322636 | snp | A/T | 3.58205e-05 | 0.0042319 | intron-variant | NUP37 | GRCh38.p7 | 12:102112281 | TGAGAACAAACAATA[A/T]AATATTCTGTATTTC | 79023 |
rs763390434 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083661 | TACAATAAAGGGTAC[A/C]GTGTAGTGACAATTA | 79023 |
rs763410750 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084617 | AGAGTTACTGGAAAT[A/G]AAACTTGGGGCCATG | 79023 |
rs763485497 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110924 | ATGGTAGAACCACTT[C/T]AGAAACTGGCATTTT | 79023 |
rs763601948 | snp | C/T | 2.15348e-05 | 0.0032813 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074328 | TAAAAATACAAAGTT[C/T]GTGAATCTAAGGTAC | 79023 |
rs763618635 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095612 | TTTTTGTTTCAGTAA[C/T]GGCACCTTTTTCATA | 79023 |
rs763673297 | snp | A/G | 1.65239e-05 | 0.00287431 | intron-variant | NUP37 | GRCh38.p7 | 12:102077289 | TTACTGCCTTTTTTT[A/G]GTGTGTAATAGACAA | 79023 |
rs763679469 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093059 | GAGCAAGAATTAAAA[A/G]GGCAAAAATGAGATA | 79023 |
rs763697956 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080638 | ATTTTTCAGATGAGA[C/T]TGAGGCTCAAAGTGA | 79023 |
rs763699712 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094328 | CAGTATAATAAATCA[C/T]GTAAATTATCCTGAT | 79023 |
rs763815689 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113257 | GCACAAGGAAGGATG[C/T]CAGATCAGAGATTTC | 79023 |
rs763817829 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100502 | ATGCTCATAATCCTA[C/T]AAGGCAGCTGCTATG | 79023 |
rs763834884 | in-del | -/CAAGA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115821 | TACTTAGTTTTCTCT[-/CAAGA]CAAGAGGCATGAAAC | 79023 |
rs763847071 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105424 | AGTCCCAGCCACTTG[A/G]GAGACTGAGGTAGGA | 79023 |
rs763878168 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091684 | CAGACCAAATCAAAG[A/G]GCACTGGGTAAGTAA | 79023 |
rs763913060 | in-del | -/A | 1.65072e-05 | 0.00287286 | frameshift-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102075067 | ATAACCAGTGGTTGC[-/A]AACAGATTTTCACTA | 79023 |
rs763979594 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086749 | CCGGTGACAGAACTC[A/G]GTGGGAGGCTGGCAA | 79023 |
rs764035370 | snp | C/T | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099140 | TCACACTTGCAATTT[C/T]TTGGCCTTCTTTGGG | 79023 |
rs764291515 | snp | A/T | 3.3507e-05 | 0.00409297 | intron-variant | NUP37 | GRCh38.p7 | 12:102074515 | GTAAGTCCCCAAAAT[A/T]AATAAATAAAAATGA | 79023 |
rs764297304 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097797 | CCATTTACTCTTCAG[A/G]TCACTATACAAACTT | 79023 |
rs764387238 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102120277 | CGTCTTCGGGTCTAC[C/T]CCTAATCACGTAAGT | 79023 |
rs764563639 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106847 | CTCCTGATCTTAAAG[A/C]CTGAAAACTTGTATT | 79023 |
rs764605496 | in-del | -/TGATA | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120875 | GGGGGAGCCTGGAAG[-/TGATA]TGATATCTGACTCGG | 79023 |
rs764620563 | snp | C/T | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077443 | ATTCAAGAGATAAAA[C/T]AGCCTGTTGGGCCAA | 79023 |
rs764707350 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083662 | ACAATAAAGGGTACA[A/G]TGTAGTGACAATTAA | 79023 |
rs764708249 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077453 | TAAAATAGCCTGTTG[A/G]GCCAAAAGATCATAA | 79023 |
rs764776886 | snp | C/T | 4.99363e-05 | 0.00499657 | intron-variant | NUP37 | GRCh38.p7 | 12:102085735 | ATAAGTCTTTTCAAT[C/T]TGATAAGAGAGTTAA | 79023 |
rs764799654 | snp | C/T | 3.41565e-05 | 0.00413244 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118559 | GTGAAAATTAAATAG[C/T]CTTCTACTGGACAAG | 79023 |
rs764958782 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111410 | AAACTATACCCTTAA[C/G]AGCTGAGAATTTCAG | 79023 |
rs765024861 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103165 | TAGATAGGCATTGCA[C/T]TGAATCTGTGGATTG | 79023 |
rs765031496 | in-del | -/TA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078327 | GCGAAATTCCTTCTT[-/TA]AAAAAAAAAAAAAGA | 79023 |
rs765050066 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112485 | TCTTAGGAGGCATTT[A/C]ATAATAAGTTCAATG | 79023 |
rs765084878 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115440 | TAGTAGAACTTGGAT[A/G]AGAACATTGATTTAG | 79023 |
rs765136118 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079495 | TTAGGTTCCCTGCCA[A/G]CCTTTTTGATGACTG | 79023 |
rs765141248 | snp | C/T | 5.61193e-05 | 0.00529684 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074341 | TTTGTGAATCTAAGG[C/T]ACAGAAAACACTTTA | 79023 |
rs765229165 | snp | A/G | 2.76201e-05 | 0.00371609 | intron-variant | NUP37 | GRCh38.p7 | 12:102101001 | CACGTTTTAAAATAA[A/G]CTCTAAAGATTTATA | 79023 |
rs765230174 | snp | C/G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076453 | TAGTTTCATTTAACA[C/G/T]ATAATAATAAAGTTT | 79023 |
rs765234824 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117375 | GAATCAACTGAACCC[G/T]GGAGATGAAGGTTAT | 79023 |
rs765309619 | snp | A/G | 1.75832e-05 | 0.00296501 | stop-gained, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076813 | TGAATAAGCAGGCTC[A/G]ATCCATGTGAACAGG | 79023 |
rs765314832 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092715 | AAGCCCAAATCTAGA[A/G]ATTAGATGGACAAAT | 79023 |
rs765369606 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077788 | ATCAGGTCATGTGTA[C/T]AAGGTATACATGAAA | 79023 |
rs765378073 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108102 | TGGTTCTGGGTGTAT[C/T]TGGGTGTTTCTGGGT | 79023 |
rs765405852 | in-del | -/T | 2.63536e-05 | 0.00362989 | intron-variant | NUP37 | GRCh38.p7 | 12:102101011 | AATAAGCTCTAAAGA[-/T]TTATATGGTTGTCAA | 79023 |
rs765456891 | snp | A/T | 1.73815e-05 | 0.00294795 | intron-variant | NUP37 | GRCh38.p7 | 12:102112277 | GTAATGAGAACAAAC[A/T]ATATAATATTCTGTA | 79023 |
rs765492869 | snp | A/C | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112137 | CAATGAATCAAGTCT[A/C]GTCTCTGGGCTCCAA | 79023 |
rs765505192 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097621 | GTCTCTCCGGCTTTC[A/G]TTCACTATTCAGAGG | 79023 |
rs765546217 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114992 | ATAGCTGATCTCCTC[C/T]AGGTGAAGACACACT | 79023 |
rs765571793 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082630 | CACACAGCTAGTAAG[C/T]GGTGAAACTGGGATC | 79023 |
rs765699687 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109079 | AAACCCAGAAAACTT[G/T]ATGGCCAGCCTTGTG | 79023 |
rs765838632 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102932 | ATTTATTTCTGGGCT[C/T]TCTATCTTATTCTAT | 79023 |
rs765888995 | snp | A/T | 5.21608e-05 | 0.00510663 | intron-variant | NUP37 | GRCh38.p7 | 12:102085859 | CAAGTTCCAAATCCT[A/T]ATAAAAGAATAACAG | 79023 |
rs766008310 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082488 | CAACGATGACCAGCA[A/G]CTAAAATTGACTGAG | 79023 |
rs766175651 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079442 | AGTTGCTGCAAACAC[C/T]CAACTAGTGAATACT | 79023 |
rs766178358 | snp | C/G | 4.16658e-05 | 0.00456412 | intron-variant | NUP37 | GRCh38.p7 | 12:102074481 | GGCTATAAAATATGT[C/G]AAGAATTAAAGAAGC | 79023 |
rs766193280 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091480 | ACACATAATTAAGCA[C/T]ATGAAAAGATGATAG | 79023 |
rs766201160 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113738 | GCAGGTGAAACTTGA[G/T]ATTTAATGAAATACG | 79023 |
rs766220148 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109620 | AAAAATAGTCTAAAA[C/T]TAATGGCCTGCTAAT | 79023 |
rs766280130 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090287 | ATGGACAAATGTGCC[A/T]AAGTTTTAAAATGTT | 79023 |
rs766304869 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102118074 | CATTTATATTGTTTT[C/T]TTCCTGTACATACCA | 79023 |
rs766366122 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086471 | GCTGGCCATGGTTGA[C/T]GATTAAAGCTGGGTT | 79023 |
rs766391866 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104205 | TTTTGATTTGTATTT[C/T]TTTAATGATTAGGGA | 79023 |
rs766483866 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087358 | TAGAAATTATTGGGT[C/T]TCTAAATGTTGAAAT | 79023 |
rs766523950 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110287 | GGTGAATTGCTCGAG[C/T]CTGGGTGCTCGAGAC | 79023 |
rs766541433 | snp | A/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099157 | TGGCCTTCTTTGGGA[A/T]CAAACACCAAACCAT | 79023 |
rs766560816 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100415 | TTATTATTATAGTAA[C/T]AGAAAACACACATAC | 79023 |
rs766575802 | snp | C/T | 3.76187e-05 | 0.00433681 | intron-variant | NUP37 | GRCh38.p7 | 12:102077238 | CAGCATAGTCTCAGG[C/T]ATAACAGGATGGATG | 79023 |
rs766580195 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075316 | TAGTAGCTGGGACTA[C/T]AGGTGTGTACTACGA | 79023 |
rs766658934 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081829 | CTCCAGAGTAGCTGG[A/G]ACTACGGTCGAGCAC | 79023 |
rs766717751 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094810 | TAGAACATGACAACT[A/G]CAAATATTTCATGTT | 79023 |
rs766816578 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083761 | TACGCAAAGTTGCTC[A/G]AGAGGACTCAGATAA | 79023 |
rs766845598 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112157 | CTGGGCTCCAAGCTA[C/T]GCCATCAACCCTGAC | 79023 |
rs766868658 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078856 | AATACTTTATCAAAC[A/G]CACAAATTAATTATA | 79023 |
rs766912334 | snp | A/C/T | 5.2133e-05 | 0.00510531 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118314 | TTGTGTAAGTTCTCT[A/C/T]AGTAGTGAAATATGT | 79023 |
rs766916025 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106740 | AAAGCCAAAACCCAA[C/T]CAGGTCCGCTTTGTG | 79023 |
rs766944969 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076371 | TATTATGAAAAAGAA[A/C]AAGGTAGACATGTAT | 79023 |
rs766984716 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112556 | AATCCCAACACTTTG[C/T]GGGGCTGAGGTGGAA | 79023 |
rs767035951 | snp | A/G | 4.95659e-05 | 0.004978 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099120 | CCTGCAGGTGTGATC[A/G]TCACTCACACTTGCA | 79023 |
rs767053868 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081684 | GAAAGCATTCAACAA[A/G]TGTTGGCTGTTAAAC | 79023 |
rs767088315 | in-del | -/AG | 4.81916e-05 | 0.00490851 | intron-variant | NUP37 | GRCh38.p7 | 12:102085741 | CTTTTCAATTTGATA[-/AG]AGAGTTAAATTATAA | 79023 |
rs767114782 | snp | C/T | 3.47451e-05 | 0.0041679 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118317 | TGTAAGTTCTCTTAG[C/T]AGTGAAATATGTTCA | 79023 |
rs767283688 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088291 | TCTGTGTCTTTACTA[C/T]ATAGCTCATCTGGTT | 79023 |
rs767321509 | snp | C/T | 3.90694e-05 | 0.00441963 | intron-variant | NUP37 | GRCh38.p7 | 12:102085890 | TATAATGTTAATTGT[C/T]CTTGATATATCATTA | 79023 |
rs767332094 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102900 | TTGTAAATAATCGAT[C/T]GACCATAAATGCATG | 79023 |
rs767465099 | snp | A/C | 8.45219e-05 | 0.00650029 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101091 | TTTTCATATCAGCAG[A/C]TGAAGTACAAAATCT | 79023 |
rs767531651 | in-del | -/T | 1.73727e-05 | 0.00294721 | intron-variant | NUP37 | GRCh38.p7 | 12:102074969 | TTAAAAAAAAAAAAA[-/T]GCACGTATGTTACAA | 79023 |
rs767605689 | snp | A/G | 1.6823e-05 | 0.00290021 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074379 | GTCACCCAAAACAAC[A/G]GCTTGTGGTCTCCTC | 79023 |
rs767695608 | snp | C/T | 5.05357e-05 | 0.00502646 | intron-variant | NUP37 | GRCh38.p7 | 12:102101017 | CTCTAAAGATTTATA[C/T]GGTTGTCAACATACC | 79023 |
rs767741106 | snp | C/T | 3.3592e-05 | 0.00409815 | intron-variant | NUP37 | GRCh38.p7 | 12:102075130 | AAATTAAGTATCGTA[C/T]CCTATGGATAATGAC | 79023 |
rs767811494 | snp | A/C | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119100 | CTTCATTGTGTGTGG[A/C]GAACCAGCGCTAATG | 79023 |
rs767961584 | snp | A/G/T | 4.94249e-05 | 0.00497096 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077366 | ATCATTTCCTGCAAC[A/G/T]GCTCCAACTTTGAAG | 79023 |
rs768008501 | snp | A/G | 1.79583e-05 | 0.00299647 | intron-variant | NUP37 | GRCh38.p7 | 12:102077246 | TCTCAGGTATAACAG[A/G]ATGGATGAGTGGATC | 79023 |
rs768026133 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075799 | CACAGTGTGTCCTAC[C/T]CTAGGGGATGAGACA | 79023 |
rs768036272 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106280 | TTGTGGTGGTTTGTT[A/T]TGGCAACAGTGGGAA | 79023 |
rs768049604 | in-del | -/TATTT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114477 | GGCAGAGACAAATGC[-/TATTT]TGGATTTAGTTTGGG | 79023 |
rs768079301 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117790 | AAGGTCTCATAGCTA[C/G]TAAGAAGTAAGTAAA | 79023 |
rs768098577 | snp | C/T | 1.64844e-05 | 0.00287087 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118408 | ATTATTGCCACCATA[C/T]GCAATTAGGTTTCCT | 79023 |
rs768140901 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119832 | TGGACAGGACTTGCC[C/T]CTGTAAAACTACAAC | 79023 |
rs768156691 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102086961 | TAGTGATGCACACTT[A/G]TAGCCCCAGCTATTA | 79023 |
rs768213245 | snp | G/T | 1.82944e-05 | 0.00302438 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074458 | CGGCTACAGAACCCA[G/T]GAGGATGGGCTATAA | 79023 |
rs768215388 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107460 | AGGGGAAAAGGAGGC[A/G]AAAGAAAAGGCCTAA | 79023 |
rs768288516 | snp | A/C/G | 8.25803e-05 | 0.00642528 | intron-variant | NUP37 | GRCh38.p7 | 12:102112068 | TGTAACACAATCAAA[A/C/G]TACATTAGTAAGGAA | 79023 |
rs768337183 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119028 | AGATGGAGAAACTGA[A/G]GCTTCAGTAGGTTAA | 79023 |
rs768370562 | snp | G/T | 2.09567e-05 | 0.00323696 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101057 | TTTTTATCCTGAAGA[G/T]CTGAAGTAAATAATC | 79023 |
rs768469774 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114474 | ATAGGCAGAGACAAA[C/T]GCTATTTTGGATTTA | 79023 |
rs768547106 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105746 | TGCACCTATAATCCC[A/G]GCTACTCGGGAGGCT | 79023 |
rs768591758 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095631 | ACCTTTTTCATAAAG[A/T]TACATATTTCTTCAT | 79023 |
rs768632037 | snp | A/C | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077334 | TACCTGGACCGAGTA[A/C]TATCCCAAATTAACC | 79023 |
rs768633683 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083061 | GAATTTTAATGATAT[A/G]TAGGAGAAAAAACAA | 79023 |
rs768691385 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088704 | TTGTTTTTGTTTTAA[-/T]TTTTTTTTTTTTTTT | 79023 |
rs768695110 | snp | A/G | | | intron-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102079213 | CTGGAGTTATCTTTC[A/G]TATCTGTAAAATGGA | 79023 |
rs768695238 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092359 | TATTGATTAATTAAG[A/T]AAGAAAGAAAAGAAC | 79023 |
rs768708232 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075774 | AAGTGAAGCCTAACT[C/T]TGTTCAGGGCACAGT | 79023 |
rs768812000 | in-del | -/TG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104717 | TATCCTTTTCCCCAT[-/TG]TGTAGCCTTGGAACC | 79023 |
rs768821998 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091257 | CAAAAATTAGCTGGG[C/T]ATGGTGGTTAGGCAC | 79023 |
rs768886927 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110982 | TGTGACTCAGCAATT[C/T]TACTCCTAAATTAAA | 79023 |
rs768912996 | snp | C/T | 3.3442e-05 | 0.004089 | intron-variant | NUP37 | GRCh38.p7 | 12:102085719 | GATGTCTTATATCTC[C/T]ATAAGTCTTTTCAAT | 79023 |
rs769016172 | in-del | -/AT | 1.64901e-05 | 0.00287137 | intron-variant | NUP37 | GRCh38.p7 | 12:102077307 | GTGTAATAGACAAAC[-/AT]ATCAAGAAAGTACCT | 79023 |
rs769057413 | snp | A/G | 1.98375e-05 | 0.00314934 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085820 | AGGAGAATGAAGAAC[A/G]AAATGAGCTGTTTGC | 79023 |
rs769123718 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117184 | GCTAGGCCAGGCAGG[A/G]TGGCTCACACCTGTA | 79023 |
rs769140595 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099791 | ACAGTGGAGGACTGT[A/G]TGAGCAGATAAAGTT | 79023 |
rs769160591 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100821 | TAATAAGAGATATCA[A/G]ATTTATAATCTGCAG | 79023 |
rs769259244 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085483 | CCCTGCCTACTGCTA[C/T]TAGATTGTTGGAACA | 79023 |
rs769278835 | snp | C/G | | | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099126 | GGTGTGATCGTCACT[C/G]ACACTTGCAATTTCT | 79023 |
rs769290398 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090345 | CTGAACTGACTCTGA[C/T]AGATTTTTCTTTTTT | 79023 |
rs769336820 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112019 | TGGAAAATGGAAATT[A/G]AGAAAAAAGTATCTA | 79023 |
rs769355420 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074203 | ATAATTTTTCAAACC[A/G]TCAACATTTTATTTA | 79023 |
rs769374363 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118660 | TCAAAATAAGGTTGT[A/G]GTGTTACAATGAGAC | 79023 |
rs769384264 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084568 | AGGATCACCTGAGCC[C/T]GGCATACGAAGGTTG | 79023 |
rs769472950 | snp | C/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112110 | CTGTTAAACTTACTT[C/G]ATTACTGGAGGCAAT | 79023 |
rs769647711 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106094 | TGAAGTGATGCATCA[A/G]CAAGGCAAAGAAAGT | 79023 |
rs769657011 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075620 | TTTTATGAAGTGCTT[A/C]TTTTGTGTCATTTCA | 79023 |
rs769707112 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102094016 | CTTTACTGACTTCTA[C/T]TCTATTACAGTCTTT | 79023 |
rs769720411 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095547 | ATGACTAGCAACCCC[A/G]TGCTTTACTTGGGAA | 79023 |
rs769722723 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096469 | AGATTGTTTTAAAAT[-/A]AGTGTTCCTAGGGCA | 79023 |
rs769728712 | snp | A/C | 4.1395e-05 | 0.00454926 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101070 | GATCTGAAGTAAATA[A/C]TCTAATTTTCATATC | 79023 |
rs769858720 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103896 | TCTATGACGAGCCCA[C/T]AGGTAACATCATTCT | 79023 |
rs769860541 | in-del | -/GAA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117382 | CTGAACCCGGGAGAT[-/GAA]GGTTATAGTGAGCCG | 79023 |
rs769888292 | in-del | -/TTT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112797 | AAAGACCTCAAAGTC[-/TTT]TTTATAATCAGTGTC | 79023 |
rs769908878 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089999 | GTACATACCTAGGCA[C/T]GGAATTGCTGGATCA | 79023 |
rs769917057 | snp | A/G | 1.65214e-05 | 0.0028741 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118492 | ATCCACAGTGTAGGC[A/G]GCATTTCTTGAGGCA | 79023 |
rs770012756 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121146 | CTAGGAACCACGTGT[A/G]AGGCTTATGGCATAG | 79023 |
rs770050736 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102620 | TACAATTCCACTTGT[C/G]TAGTTTTGCTTTTGT | 79023 |
rs770057814 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111946 | AATCACAAATTCAGA[C/T]GATAAGCCTAAATTA | 79023 |
rs770103189 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115817 | CCTTTACTTAGTTTT[C/G]TCTCAAGACAAGAGG | 79023 |
rs770155748 | snp | C/T | 2.24077e-05 | 0.00334714 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085843 | CTGTTTGCACTCCTT[C/T]CAAGTTCCAAATCCT | 79023 |
rs770155885 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079001 | TATCTAAGTGCATGA[A/G]TAGTTGATGCCTGAA | 79023 |
rs770156086 | in-del | -/AACCTGA | 1.70003e-05 | 0.00291545 | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118360 | GCAGTTTTGTAGACT[-/AACCTGA]AACGTACACGTGCCA | 79023 |
rs770176778 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079823 | GACACATATTTACAG[C/T]ATGAAAGCTAAAATA | 79023 |
rs770195045 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098464 | TACAGCATCTGTAAA[A/G]TAACTTGACAACTGC | 79023 |
rs770203221 | snp | A/T | 1.67217e-05 | 0.00289147 | intron-variant | NUP37 | GRCh38.p7 | 12:102099095 | ATGTGGTTATAACAT[A/T]AGCAACATACCTGCA | 79023 |
rs770209695 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114360 | AAGAAATCTCAGGGA[-/C]CTGTACAGCCTGGGC | 79023 |
rs770422892 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098440 | TCATTATTCCACACA[A/C]ACTTATCATACAGCA | 79023 |
rs770423007 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083383 | ATGCACATATGCAGA[C/G]TATAATTCTACTGAT | 79023 |
rs770441248 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084391 | TGGCTCACAACTGTA[A/G]TCCCAGCAATATGGG | 79023 |
rs770468613 | in-del | -/A | 1.71102e-05 | 0.00292486 | intron-variant | NUP37 | GRCh38.p7 | 12:102077532 | AATAAAAAGAAACTC[-/A]AATCACTTATCTCAC | 79023 |
rs770593744 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106221 | GAATATGTGCCTCCA[A/G]AACTGTGATAATAAA | 79023 |
rs770598484 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116214 | ATCTTTGCCTCTCTT[C/T]TCCTAATTTGTTCTC | 79023 |
rs770644003 | snp | C/G | 1.6531e-05 | 0.00287493 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112229 | CAACGTCTGCTTCTT[C/G]TTCCTAAGCATACAC | 79023 |
rs770646476 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092448 | CAGGAAAGGGACCCT[C/T]AACATTCTTAGACAA | 79023 |
rs770663344 | snp | C/T | 2.32e-05 | 0.0034058 | intron-variant | NUP37 | GRCh38.p7 | 12:102076880 | GCATTTTATGAATTA[C/T]GTGTTAAACTCAAGT | 79023 |
rs770734624 | in-del | -/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104059 | TGTTTTTCATAGCAG[-/C]CTGCACCATTGCTAC | 79023 |
rs770765282 | snp | C/T | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102075026 | CCTAAATGATGAATT[C/T]GAAACTGGCTTGCCA | 79023 |
rs770790508 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081293 | TATTTACTGTCTGTA[C/T]AACTGTGCTCAATTA | 79023 |
rs770849443 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105132 | TTTGTAGCTTTTAGT[C/T]TTTGGCTTCGTTGGT | 79023 |
rs770853497 | snp | A/C/G | 3.29605e-05 | 0.00405948 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112114 | TAAACTTACTTGATT[A/C/G]CTGGAGGCAATGAAT | 79023 |
rs770916259 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102549 | ATATTTTCTCACAAT[A/C]TGTAGGTTGCATCTT | 79023 |
rs770922167 | snp | C/T | 3.29511e-05 | 0.00405887 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077359 | TTAACCAATCATTTC[C/T]TGCAACGGCTCCAAC | 79023 |
rs770983014 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114331 | ATATGGAATTACTGG[G/T]TGGTCATGGGGATAA | 79023 |
rs771028838 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101172 | GTCTCCCCCTCCCCC[C/G]CATCCTTCCCTTCAG | 79023 |
rs771030996 | snp | A/G | 1.68258e-05 | 0.00290045 | intron-variant | NUP37 | GRCh38.p7 | 12:102077511 | ACCATTAGCTGTAAG[A/G]CAGAAAAATAAAAAG | 79023 |
rs771229944 | snp | C/T | 1.66916e-05 | 0.00288886 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118521 | CATCTTGCTTCATCT[C/T]GTATGTCAAAATTCA | 79023 |
rs771278091 | in-del | -/TTA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099512 | CACCTCCTTTCTCAC[-/TTA]TTATATAAAGCCTAA | 79023 |
rs771288556 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112360 | AAAAGCAAATTACAT[A/G]TTAAGATTTAACTAG | 79023 |
rs771289715 | snp | A/T | 2.39616e-05 | 0.00346124 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074311 | TTCTTCAAAATATGT[A/T]CTAAAAATACAAAGT | 79023 |
rs771292710 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091105 | AGAAATGCTTTAAAA[A/G]CTCACAGCCGGCCAG | 79023 |
rs771317305 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120908 | GTGTAGTTCTTTCAA[C/T]CATTTCACACTGCCT | 79023 |
rs771322739 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114183 | CTGACTTCACAGTTT[C/G]GATTACATCTATTTT | 79023 |
rs771333755 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108995 | ATAGAGGAGTTACAG[C/T]AATCAAAGAATACTT | 79023 |
rs771474318 | snp | C/T | 2.14466e-05 | 0.00327457 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101046 | CCTTATATTCATTTT[C/T]ATCCTGAAGATCTGA | 79023 |
rs771477404 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078851 | TGTGAAATACTTTAT[C/T]AAACGCACAAATTAA | 79023 |
rs771500334 | in-del | -/ACAATTATGT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109446 | TACTATAGTATAATC[-/ACAATTATGT]ACAATTATGTACAAA | 79023 |
rs771563760 | snp | A/G | 2.26914e-05 | 0.00336826 | utr-variant-3-prime, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074323 | TGTACTAAAAATACA[A/G]AGTTTGTGAATCTAA | 79023 |
rs771569687 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108922 | CATCCCAACTAAAAG[C/G]GTTTGTAAAGAGGTA | 79023 |
rs771590170 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111403 | ACTGATCAAACTATA[C/G]CCTTAAGAGCTGAGA | 79023 |
rs771623975 | snp | C/G | 3.32745e-05 | 0.00407875 | intron-variant | NUP37 | GRCh38.p7 | 12:102099211 | AAAACCTGACAGAAA[C/G]AGAAACAGAAAGCTT | 79023 |
rs771625713 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097376 | TTAAACTAAAAGACT[C/T]ACTCTTTAGTTATTC | 79023 |
rs771692720 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083982 | AGTTAAAAGGTACAA[A/G]TGATGGATTCAAACA | 79023 |
rs771741929 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084321 | TTATCTTCTCATGCA[A/G]ACTTGAGGACAGAAC | 79023 |
rs771761860 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107763 | AAAAAATACATATAG[C/T]ATTATTATATTCATA | 79023 |
rs771945736 | snp | A/G | 1.74677e-05 | 0.00295526 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102076803 | GTACATTACCTGAAT[A/G]AGCAGGCTCGATCCA | 79023 |
rs772007956 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083360 | TAATAAGTTAGAACA[C/T]TTCACTCATGCACAT | 79023 |
rs772242199 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080282 | TTCTTATTAGCCAGG[A/C]GAGGTGGCAAGCACT | 79023 |
rs772282309 | snp | A/C | 2.01209e-05 | 0.00317176 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085796 | AGGATGCCAGCACAC[A/C]CTCATGCCAGGAGAA | 79023 |
rs772282684 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100277 | CTATTTTCTAAATGA[C/T]TGGAAAGGTTTGTAA | 79023 |
rs772286325 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093732 | CAATAAGGGAAAGTA[C/T]TCCTTTATCATTCAC | 79023 |
rs772532265 | in-del | -/AG | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118676 | GTGTTACAATGAGAC[-/AG]AAAGCTCAAAAGAAA | 79023 |
rs772624406 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089805 | TCTTAATGCCTTATA[C/T]GGTCTTCAATTAATT | 79023 |
rs772643654 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097399 | AGTTATTCCTTTCCT[A/T]CTTTTTAGAGTAATA | 79023 |
rs772670010 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093031 | ATTATTATTAGAAGT[C/T]TTACTGACTTCAGAG | 79023 |
rs772713016 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082419 | GTAAATGACTGAAAA[C/T]GTATGGCAGAGCACT | 79023 |
rs772868584 | in-del | -/A | 1.87968e-05 | 0.00306562 | intron-variant | NUP37 | GRCh38.p7 | 12:102074951 | AAAAGTCAAAAACAC[-/A]AAATTAAAAAAAAAA | 79023 |
rs772910612 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108933 | AAAGGGTTTGTAAAG[A/C]GGTATTAATAGCAAA | 79023 |
rs772943724 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104620 | CTTATGTTTAGGTCC[C/T]ATTTTGAGCTCATTT | 79023 |
rs773019736 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114716 | AGTTTCTCTAGTTCA[A/G]TTCTTTCCCCCCAAT | 79023 |
rs773020371 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104116 | TCAATTTCTCCACAT[C/T]CCGGGTCAACATTTG | 79023 |
rs773023340 | snp | G/T | 1.65436e-05 | 0.00287602 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102075007 | CCACATTACCTGAGG[G/T]TGTCCTAAATGATGA | 79023 |
rs773031527 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076200 | ATTCTTACATTTAGT[C/T]GAATGTATTTTATTC | 79023 |
rs773031794 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106135 | TGGCTACCATCAGAA[A/T]CTAGAAAACAGGCAT | 79023 |
rs773067825 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117425 | CCAGCCTGGGCGACC[A/T]AGCAAAACTCTGTCT | 79023 |
rs773100014 | snp | C/G/T | 3.29621e-05 | 0.00405958 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112113 | TTAAACTTACTTGAT[C/G/T]ACTGGAGGCAATGAA | 79023 |
rs773183009 | snp | C/T | 0.000157381 | 0.00886938 | intron-variant | NUP37 | GRCh38.p7 | 12:102074471 | CATGAGGATGGGCTA[C/T]AAAATATGTGAAGAA | 79023 |
rs773191031 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078204 | GTTGTGGTGGCATGC[A/G]CGTAATCCTAGCTAC | 79023 |
rs773216663 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116147 | TGTTTATACTAGTTC[C/T]TTTTTCTCATGTTAG | 79023 |
rs773282073 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093880 | TTTGGTGATATATTT[C/T]ATTAAGCACTTGTTT | 79023 |
rs773314505 | snp | A/G | 3.51482e-05 | 0.004192 | intron-variant | NUP37 | GRCh38.p7 | 12:102112280 | ATGAGAACAAACAAT[A/G]TAATATTCTGTATTT | 79023 |
rs773324749 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112368 | ATTACATATTAAGAT[C/T]TAACTAGTTCATTGA | 79023 |
rs773402465 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119981 | AAGAACTCCTGGGAA[C/T]AGAGTGGCAAGGCTG | 79023 |
rs773460569 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102080372 | AACTGCAGTGAATTA[C/T]GATTGTCCCACTGCA | 79023 |
rs773472753 | snp | A/G | 3.33545e-05 | 0.00408364 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118376 | ACCTGAAACGTACAC[A/G]TGCCAATGACCACAT | 79023 |
rs773519327 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110125 | AAAGATTTCTAATAG[A/G]AGAAACAAATATACC | 79023 |
rs773652861 | snp | C/T | 4.9894e-05 | 0.00499445 | intron-variant | NUP37 | GRCh38.p7 | 12:102099101 | TTATAACATAAGCAA[C/T]ATACCTGCAGGTGTG | 79023 |
rs773653489 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102076094 | TATAAGTACCATAGC[G/T]CATTGATTTTAAAAT | 79023 |
rs773696915 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107568 | GGACATTATGATATA[C/T]ACACACAGTAATGCT | 79023 |
rs773723768 | in-del | -/A/AA | 0.493319 | 0.0923796 | intron-variant | NUP37 | GRCh38.p7 | 12:102074956 | TCAAAAACACAAATT[-/A/AA]AAAAAAAAAAAAAGC | 79023 |
rs773742822 | snp | C/G | 2.48487e-05 | 0.00352473 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085856 | TTCCAAGTTCCAAAT[C/G]CTAATAAAAGAATAA | 79023 |
rs773748582 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101013 | TAAGCTCTAAAGATT[C/T]ATATGGTTGTCAACA | 79023 |
rs773748644 | in-del | -/TCA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106256 | TGTTGTTGTTTTAAG[-/TCA]TCATGTTTGTGGTGG | 79023 |
rs773952883 | in-del | -/TT | 5.22343e-05 | 0.00511023 | intron-variant | NUP37 | GRCh38.p7 | 12:102085727 | ATATCTCTATAAGTC[-/TT]TTCAATTTGATAAGA | 79023 |
rs774051010 | in-del | -/AT | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074150 | TTTGTAAGATTAAAA[-/AT]ATATATATATACACA | 79023 |
rs774054245 | in-del | -/GT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081334 | TTTTTGGGTGATAAG[-/GT]AACAGATAGGGTAGA | 79023 |
rs774064425 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102106387 | TTATCCCCTAAAAAT[C/G]TGCCATATTTTAACA | 79023 |
rs774090905 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075904 | TTTGTTTAATTGTTC[A/G]GCAAATGGAGTACTT | 79023 |
rs774136315 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095809 | TTCATTGTATTACTA[C/T]TAACATGAGCTTTTA | 79023 |
rs774142536 | snp | C/G | 3.30246e-05 | 0.0040634 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102075070 | ACCAGTGGTTGCAAA[C/G]AGATTTTCACTAATT | 79023 |
rs774239848 | snp | A/T | 7.00354e-05 | 0.00591716 | intron-variant | NUP37 | GRCh38.p7 | 12:102076790 | TCCAACAAAAACGGT[A/T]CATTACCTGAATAAG | 79023 |
rs774405496 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081588 | CATCTACAAAATACA[A/C]TACTACTACTGTCTC | 79023 |
rs774461652 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099617 | GCTGTTCTGCATACT[C/T]ACTACTTAACAAACA | 79023 |
rs774461798 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112378 | AAGATTTAACTAGTT[A/C]ATTGAATTAAAAAAA | 79023 |
rs774470212 | snp | A/G | 1.86712e-05 | 0.00305536 | intron-variant | NUP37 | GRCh38.p7 | 12:102077239 | AGCATAGTCTCAGGT[A/G]TAACAGGATGGATGA | 79023 |
rs774524461 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111097 | AATAAACAGACTATG[A/G]TCTATTGATACACTG | 79023 |
rs774538856 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091280 | TTAGGCACCTGTAAT[A/C]CCAGCTACTCGGGAG | 79023 |
rs774597592 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102074903 | AACGTAAATGTCTTC[A/G]GTCAACAAATTACAA | 79023 |
rs774624996 | snp | C/T | 0.000186029 | 0.00964261 | intron-variant | NUP37 | GRCh38.p7 | 12:102079258 | GATTCAAAAACTTAC[C/T]GTATGGCTAAAATGT | 79023 |
rs774745369 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117619 | TGATTAAACCTGAGA[C/G]TGTTACCACTGCTCG | 79023 |
rs774927422 | snp | C/G | | | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074455 | CAACGGCTACAGAAC[C/G]CATGAGGATGGGCTA | 79023 |
rs774984299 | in-del | -/TATC | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118243 | TTTCTCTATGGATCT[-/TATC]TTTTTTTTTTTTAAC | 79023 |
rs774988008 | snp | A/C | 1.70203e-05 | 0.00291716 | intron-variant | NUP37 | GRCh38.p7 | 12:102099238 | GCTTAGCAAGAAAAC[A/C]GAAAAATAACCTACA | 79023 |
rs775059797 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100234 | AGTACATTAAGCCCA[A/C]TGTAAATAGCTTACA | 79023 |
rs775199693 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084258 | ATGAAATGCTGACTA[C/T]AGGCCTGGCGTATGT | 79023 |
rs775210135 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102117194 | GCAGGGTGGCTCACA[C/T]CTGTAATCCCAGCAC | 79023 |
rs775212162 | snp | A/C | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099123 | GCAGGTGTGATCGTC[A/C]CTCACACTTGCAATT | 79023 |
rs775237165 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074411 | ATTACACACAGAGGG[-/A]AGAGTTCGATGCCAG | 79023 |
rs775356512 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081371 | AAGTAAGTTTGGGAG[C/T]AGCTGAATCTAAAAA | 79023 |
rs775362144 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077818 | ACATAAATGAATTTC[A/G]TGTTTAGACTTGGGT | 79023 |
rs775434853 | snp | C/T | 0.000234734 | 0.0108311 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118371 | GACTAACCTGAAACG[C/T]ACACGTGCCAATGAC | 79023 |
rs775444488 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082237 | GTTTTCCTGATCTTA[C/T]GGCTTTTTTTATGGT | 79023 |
rs775484143 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091195 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 79023 |
rs775571480 | in-del | -/A | 0.000104811 | 0.0072384 | intron-variant | NUP37 | GRCh38.p7 | 12:102085862 | GTTCCAAATCCTAAT[-/A]AAAGAATAACAGTAT | 79023 |
rs775666299 | snp | G/T | | | intron-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102079085 | GTTCTTTTAATTCTG[G/T]TTCTATTAAGTTGAA | 79023 |
rs775673146 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098522 | ATTGAAGAATTTGAT[C/G]CAATATGTTTGTGTT | 79023 |
rs775673887 | in-del | -/TCCA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097045 | ATAATGCCATATGGG[-/TCCA]TCCATATCTGCTCCA | 79023 |
rs775745315 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102090017 | AATTGCTGGATCACA[A/G]CTTACAAATATATTC | 79023 |
rs775884249 | snp | A/G | 1.71196e-05 | 0.00292567 | intron-variant | NUP37 | GRCh38.p7 | 12:102077534 | ATAAAAAGAAACTCA[A/G]TCACTTATCTCACTA | 79023 |
rs775884290 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102088407 | TGTACAATTCAAAGA[G/T]AATACACTCAAAAAG | 79023 |
rs776083515 | snp | A/G | 1.74339e-05 | 0.0029524 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074444 | CAGTCCAGATCCAAC[A/G]GCTACAGAACCCATG | 79023 |
rs776094055 | snp | C/G | 3.7219e-05 | 0.00431371 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074461 | CTACAGAACCCATGA[C/G]GATGGGCTATAAAAT | 79023 |
rs776133279 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109095 | ATGGCCAGCCTTGTG[C/T]TGCCCCACTTTTCTT | 79023 |
rs776233028 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097583 | AAACAAACAAAAACA[C/T]AGACTACTGAGTGTG | 79023 |
rs776323091 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083398 | GTATAATTCTACTGA[C/T]GAAAGACTCAATGGG | 79023 |
rs776333246 | in-del | -/AT | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074151 | TGTAAGATTAAAAAT[-/AT]ATATATATATACACA | 79023 |
rs776349770 | snp | A/T | 1.68049e-05 | 0.00289865 | intron-variant | NUP37 | GRCh38.p7 | 12:102074984 | AGCACGTATGTTACA[A/T]AACATTTCCACATTA | 79023 |
rs776422423 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075804 | TGTGTCCTACCCTAG[C/G]GGATGAGACATAATT | 79023 |
rs776457822 | snp | C/T | 2.0922e-05 | 0.00323428 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101058 | TTTTATCCTGAAGAT[C/T]TGAAGTAAATAATCT | 79023 |
rs776459315 | snp | C/T | 1.64765e-05 | 0.00287019 | stop-gained, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077349 | ATATCCCAAATTAAC[C/T]AATCATTTCCTGCAA | 79023 |
rs776530671 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102087371 | GTCTCTAAATGTTGA[A/T]ATATCATAGTTACAT | 79023 |
rs776682162 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104242 | ACATCTTTTTATATG[C/G]CTGTTGGCCATTCAT | 79023 |
rs776682339 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116997 | ACAGAGCGAGACTCC[A/G]TCTCAAAACAAAACA | 79023 |
rs776730778 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101257 | AAGAATGTTGTGGCT[C/G]TACTGTAAAAAGTAT | 79023 |
rs776770092 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105234 | TTATACATTGCACAA[C/G]AATGCCATGGCCGGG | 79023 |
rs776808454 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102109031 | AAAAGAAAATTAATA[A/T]TCTTACTGGGATCTA | 79023 |
rs776896891 | snp | A/G | 2.02055e-05 | 0.00317842 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085826 | ATGAAGAACAAAATG[A/G]GCTGTTTGCACTCCT | 79023 |
rs776938480 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091002 | AATTTGAAAATTCAG[G/T]TTTTAATATTTCCAA | 79023 |
rs776978101 | in-del | -/T | 1.64751e-05 | 0.00287007 | frameshift-variant, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077384 | CCAACTTTGAAGGTG[-/T]TTTTTTAAGCACCAG | 79023 |
rs777004961 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120909 | TGTAGTTCTTTCAAC[C/T]ATTTCACACTGCCTG | 79023 |
rs777029984 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093462 | TGAGAAATTTTGTCA[A/C]ATTTAAAAATAAACT | 79023 |
rs777177947 | snp | A/C/G | 0.000105742 | 0.00727047 | intron-variant | NUP37 | GRCh38.p7 | 12:102085720 | ATGTCTTATATCTCT[A/C/G]TAAGTCTTTTCAATT | 79023 |
rs777288077 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092392 | AGTAATACAGAGATG[C/T]AGTTATAAGGATTAG | 79023 |
rs777342791 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102077632 | GTTCAGCATTCCTCA[C/T]CTGAAAATCTGCAAT | 79023 |
rs777351545 | snp | A/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102122105 | CCAAGTGAGTCTTCA[A/T]TCATAGCAATCAAAT | 79023 |
rs777460634 | snp | A/G | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102073724 | TAGTCTCGCTCTGTC[A/G]CCCAGGCTGCAGTGA | 79023 |
rs777500522 | snp | A/G | 1.77043e-05 | 0.0029752 | intron-variant | NUP37 | GRCh38.p7 | 12:102076773 | AAAGATCAAATCACA[A/G]CTCCAACAAAAACGG | 79023 |
rs777608451 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078654 | TCTAAAATGGAGATG[A/G]GAGGATAAGAATGGC | 79023 |
rs777742702 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082750 | GATATTCTAAGACTC[A/T]TAGTCTAGTAGGCAA | 79023 |
rs777752427 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098916 | GGAAGTTTTCATTAA[C/T]GGTGATGAGGACTAT | 79023 |
rs777759155 | snp | A/T | 1.66774e-05 | 0.00288763 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118518 | AGGCATCTTGCTTCA[A/T]CTTGTATGTCAAAAT | 79023 |
rs777788189 | snp | C/G | 2.04866e-05 | 0.00320045 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085791 | TCCTCAGGATGCCAG[C/G]ACACACTCATGCCAG | 79023 |
rs777806585 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084356 | TCAACAGAGAAAAAG[C/G]ATGGAGATGGCCGGT | 79023 |
rs777818201 | snp | A/G | 5.03259e-05 | 0.00501601 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102074397 | TTGTGGTCTCCTCCA[A/G]TTACACACAGAGGGA | 79023 |
rs777847860 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102110934 | CACTTTAGAAACTGG[A/C]ATTTTCTTAAAATGT | 79023 |
rs777848049 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081270 | CAGTTCTAACAAAAG[A/C]TTTTTGTTATTTACT | 79023 |
rs777849392 | snp | C/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082120 | GTATGCATTGAAATC[C/G]TAGCTCCTATTGAGT | 79023 |
rs777864249 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083391 | ATGCAGAGTATAATT[C/T]TACTGATGAAAGACT | 79023 |
rs777895968 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121259 | GCCAGCTCCTGAGCT[-/AAG]AAGGAGTGTTACGTG | 79023 |
rs777949390 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102009 | GGATTACAGGCATGA[A/G]CCACTGCGCCTGGCC | 79023 |
rs778059008 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099413 | GATCATTCAACACAC[C/T]ATTAGCTTAGTCTTT | 79023 |
rs778090459 | snp | A/G | 7.07639e-05 | 0.00594785 | intron-variant | NUP37 | GRCh38.p7 | 12:102101028 | TATATGGTTGTCAAC[A/G]TACCTTATATTCATT | 79023 |
rs778107522 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102114080 | ACTTCGTAATTTGTG[G/T]GTATAATAGTTGTAT | 79023 |
rs778116411 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107214 | CAACCCCTTGTATTT[C/T]GGTAACAATGGCAAC | 79023 |
rs778176628 | snp | A/C | 3.3065e-05 | 0.00406588 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099191 | TGAAATCGGTATGGC[A/C]CTCTAAAACCTGACA | 79023 |
rs778199371 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102414 | GTCTTCTTTCAAGAA[A/T]TGTCTGTCTACTCAG | 79023 |
rs778272787 | snp | A/C/G | 0.00015649 | 0.00884434 | intron-variant | NUP37 | GRCh38.p7 | 12:102077217 | GAAAGACTTGCTTTC[A/C/G]CTTGACAGCATAGTC | 79023 |
rs778398062 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115245 | ATTACTGTCGATTTA[C/T]AGAGGAAGATGCAGA | 79023 |
rs778430561 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111373 | TGGGTTGTACAAATA[A/T]ACGTATTTGTCAAAA | 79023 |
rs778454749 | in-del | -/G | 0.000162351 | 0.00900828 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120444 | CGCTCGAGCCTGGTT[-/G]GGCCTGGGGGCTGTA | 79023 |
rs778514395 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102098029 | TAGTTTTATATGTAC[A/G]TAAGTACTAATAAAT | 79023 |
rs778520083 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083675 | CAGTGTAGTGACAAT[G/T]AACCCTTGAAGCAAT | 79023 |
rs778554776 | snp | C/T | 1.64768e-05 | 0.00287021 | upstream-variant-2KB, missense, nc-transcript-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118436 | CCTGAATCCCCATTC[C/T]CAAAGGGATTAAATT | 79023 |
rs778559475 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | NUP37 | GRCh38.p7 | 12:102077319 | AACATATCAAGAAAG[C/T]ACCTGGACCGAGTAA | 79023 |
rs778801903 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102121764 | GGCCAGGTTGGTCTC[A/G]AACTCCTAACCTTAG | 79023 |
rs778898569 | snp | G/T | 1.69444e-05 | 0.00291066 | intron-variant | NUP37 | GRCh38.p7 | 12:102077520 | TGTAAGACAGAAAAA[G/T]AAAAAGAAACTCAAT | 79023 |
rs778978891 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097296 | AACAATAATATCAAC[A/C]ACCAGTCTGGCAAAA | 79023 |
rs778984498 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105040 | AGCACAGACACTTTA[A/G]CACTATGAAATCTTT | 79023 |
rs778995013 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093541 | AAACAGACCATGTGT[A/C]ATGATTTCATCTTTA | 79023 |
rs778996186 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081096 | TTCTGTGTTTCGGGT[A/T]CTTATCACTAAGAAG | 79023 |
rs779097322 | in-del | -/A | 1.76184e-05 | 0.00296797 | intron-variant | NUP37 | GRCh38.p7 | 12:102076780 | AATCACAGCTCCAAC[-/A]AAAAACGGTACATTA | 79023 |
rs779223668 | snp | A/T | 1.73706e-05 | 0.00294703 | intron-variant | NUP37 | GRCh38.p7 | 12:102074964 | CACAAATTAAAAAAA[A/T]AAAAAGCACGTATGT | 79023 |
rs779230001 | snp | C/T | 4.45127e-05 | 0.00471745 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101038 | TCAACATACCTTATA[C/T]TCATTTTTATCCTGA | 79023 |
rs779259289 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102118182 | TTCTTTTTCACTATC[C/T]ATATAATGTTTACAT | 79023 |
rs779273857 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102113753 | TATTTAATGAAATAC[A/G]TATGTCTATATTGAT | 79023 |
rs779314083 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091963 | TACCATATGGTATTT[-/A]AATGTTATTGTCCCA | 79023 |
rs779357506 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102100856 | TAAGAACTTAGTTCT[C/T]AATAATATAGTAAGC | 79023 |
rs779396864 | snp | G/T | 3.4641e-05 | 0.00416165 | intron-variant | NUP37 | GRCh38.p7 | 12:102101150 | TTTTAGCCTTTGTAA[G/T]TGAAAGGTCTCCCCC | 79023 |
rs779435667 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082028 | TTAACCTCTTTTTTC[G/T]TAGGGTCAGAGACTG | 79023 |
rs779446328 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102055 | AACTAGTTTATCTTT[A/C]ATCCTAAATTTTCTA | 79023 |
rs779559312 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102101720 | AACAAAACCTAAGCA[G/T]CAAACACTCCTTTTT | 79023 |
rs779566516 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102075695 | CAACCAAAGGGGTAA[C/T]AGTGTGGTAGAAGAA | 79023 |
rs779622109 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102112760 | TACATTCTCACTACA[C/T]GGAAAATACTTTGGG | 79023 |
rs779627245 | in-del | -/TG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079277 | TGGCTAAAATGTGAC[-/TG]TTCTTTAAGAACGTA | 79023 |
rs779651428 | snp | A/C | 2.11423e-05 | 0.00325126 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102101053 | TTCATTTTTATCCTG[A/C]AGATCTGAAGTAAAT | 79023 |
rs779754105 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092593 | GTGTATTTCCTTAGC[-/A]AATGAGCACACAATT | 79023 |
rs779806104 | snp | A/G | 3.30846e-05 | 0.00406709 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077465 | TTGGGCCAAAAGATC[A/G]TAAAACCGGATTGTT | 79023 |
rs779867063 | in-del | -/CAGA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116579 | CTGTCATATTCTACT[-/CAGA]CAGCAACAAACTGAA | 79023 |
rs779913757 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120352 | TCAGGCTGTGGCTTT[G/T]GAGGGTGTTTTGCAC | 79023 |
rs779925163 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102095561 | CATGCTTTACTTGGG[A/C]ATTTCTTTTATTAAA | 79023 |
rs780014984 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097014 | TTGCACATGGGTCTA[C/T]GGGAAGCTCTGTTTC | 79023 |
rs780042199 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103648 | AGCAAACTGTATTCA[A/G]GAGTACATTAAAAAG | 79023 |
rs780043200 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102104930 | CATTTGGGGTCCTTT[A/G]AGGTTCCATCTGAAT | 79023 |
rs780045126 | in-del | -/AAA | 4.75037e-05 | 0.00487335 | intron-variant | NUP37 | GRCh38.p7 | 12:102101113 | ACAAAATCTGGAAGC[-/AAA]AAAACAAAAATATAC | 79023 |
rs780107055 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115949 | AATTTATTTTGAAAT[G/T]GACTTACTTAATTGT | 79023 |
rs780272313 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079920 | GTTGTTCTGTGCTCC[C/T]TGCGTATGTCTGTGA | 79023 |
rs780344413 | snp | A/G | 1.77678e-05 | 0.00298054 | intron-variant | NUP37 | GRCh38.p7 | 12:102099065 | TGTAATTCTCATTAA[A/G]ATGGCAATTTAAAAA | 79023 |
rs780362863 | snp | C/T | 1.99583e-05 | 0.00315892 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085799 | ATGCCAGCACACACT[C/T]ATGCCAGGAGAATGA | 79023 |
rs780445104 | snp | A/G | 1.65206e-05 | 0.00287403 | intron-variant | NUP37 | GRCh38.p7 | 12:102112059 | TTCCAATCATGTAAC[A/G]CAATCAAAGTACATT | 79023 |
rs780455848 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102081046 | GCCCAGCTCTGCCTT[C/T]AGGAGCTGTAAGATC | 79023 |
rs780469730 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102079849 | AAATAAGAAGCCAGA[A/G]TTCACCTTGTTCAAT | 79023 |
rs780475221 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085062 | GTTTTTTGTTCACAC[A/G]GTAGGGCTCACAAGC | 79023 |
rs780524414 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102111962 | GATAAGCCTAAATTA[C/T]TAAGTAGTAGCAAAT | 79023 |
rs780558637 | in-del | -/CA | 2.35841e-05 | 0.00343387 | intron-variant | NUP37 | GRCh38.p7 | 12:102076883 | TTTATGAATTATGTG[-/CA]TTAAACTCAAGTGGG | 79023 |
rs780582987 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102093393 | CTCAGAGGAGAATTA[C/T]TAACATCTCATTTAA | 79023 |
rs780612467 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119274 | GTTCAGGGGGTTGGG[C/T]GGAGGGAGAGCATCA | 79023 |
rs780696085 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120713 | ATTTTTAAATTGAGC[A/G]CCTACTAAATGCCTG | 79023 |
rs780699692 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102085430 | CTGTCTAAAAAAAAC[A/C]AAAACAAAAACAAAA | 79023 |
rs780805458 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102116317 | CTATGTTGTTATTAA[G/T]TTTAAAAGTAATGAA | 79023 |
rs780814655 | snp | C/T | | | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099194 | AATCGGTATGGCCCT[C/T]TAAAACCTGACAGAA | 79023 |
rs780828979 | snp | A/G | 1.78605e-05 | 0.0029883 | intron-variant | NUP37 | GRCh38.p7 | 12:102076751 | CAGTGGTGGCACAGC[A/G]ACGTCAAAAGATCAA | 79023 |
rs780834653 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091726 | TCAAGTGAAATAAAA[A/T]GACAGTTTTCATCCA | 79023 |
rs780890285 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096364 | ATTATCAGAGGTACC[-/T]TTGTTCACAGTACGA | 79023 |
rs780907314 | snp | A/C | 4.83267e-05 | 0.00491539 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102085775 | AATAACCTTAAAAGT[A/C]TCCTCAGGATGCCAG | 79023 |
rs780920838 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102112179 | AACCCTGACTCCATG[A/G]TGAAATGTTCGAAGT | 79023 |
rs781013186 | in-del | -/AA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102102846 | CAACATCATTCATTG[-/AA]GACACTGTCCTTTCT | 79023 |
rs781015586 | in-del | -/AT | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119496 | AAGTAGCATTCCCAC[-/AT]GAGAATTATGGGTTT | 79023 |
rs781090787 | snp | A/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105979 | TGATTAAATTAAAGG[A/T]TACTAAGATGATCAT | 79023 |
rs781092481 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119464 | CTTAACCTGTCAGGG[A/G]CTAGTGTGCATTCTG | 79023 |
rs781120093 | snp | C/T | 4.97055e-05 | 0.00498501 | synonymous-codon, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102077477 | ATCATAAAACCGGAT[C/T]GTTCCATTCTTCTCT | 79023 |
rs781208329 | snp | C/T | 3.30147e-05 | 0.00406279 | missense, nc-transcript-variant | NUP37 | GRCh38.p7 | 12:102099176 | ACACCAAACCATTAA[C/T]GAAATCGGTATGGCC | 79023 |
rs781212645 | snp | C/T | 0.000162509 | 0.00901267 | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120481 | GTTCACAGTATCTAG[C/T]GATGGAGCTGGTAGG | 79023 |
rs781233027 | snp | C/T | | | downstream-variant-500B | NUP37 | GRCh38.p7 | 12:102074030 | CATATACTCAAAGTA[C/T]AGAAAACAGGATACA | 79023 |
rs781262711 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105848 | GCCTGGGTGACAGAG[C/T]GGGACTCCCTCTCAA | 79023 |
rs781281239 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102107930 | GCTGATTGGAGAGGG[A/G]CACACTGGCAGCCTC | 79023 |
rs781350578 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108305 | TCATCTTTCTCCTGT[-/A]AGTTGGATGCTTCCT | 79023 |
rs781351728 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102078166 | AACCCCGTCTCTACT[-/A]AAAAAAAAAAAAAAA | 79023 |
rs781503857 | snp | A/G | 1.67868e-05 | 0.00289709 | intron-variant | NUP37 | GRCh38.p7 | 12:102099093 | AAATGTGGTTATAAC[A/G]TAAGCAACATACCTG | 79023 |
rs781546080 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099019 | TATAGAATTTATGTA[A/C]AAGTCACATTTTTTT | 79023 |
rs781559271 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102091963 | TACCATATGGTATTT[A/G]AATGTTATTGTCCCA | 79023 |
rs781588592 | in-del | -/A | 1.65119e-05 | 0.00287327 | intron-variant | NUP37 | GRCh38.p7 | 12:102112078 | TCAAAGTACATTAGT[-/A]AGGAATGCATTTGGT | 79023 |
rs781601611 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102082948 | AAGAAGAATTAAAGA[C/T]GATTTTAGGATTCTG | 79023 |
rs781648208 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103744 | ATATATGTGGTTCAC[G/T]TTATTAACAGAATGA | 79023 |
rs781725368 | in-del | -/GTTTCCATAATGCC | | | intron-variant | NUP37 | GRCh38.p7 | 12:102097024 | TCTATGGGAAGCTCT[-/GTTTCCATAATGCC]GTTTCCATAATGCCA | 79023 |
rs796096731 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102083294 | TCTCAGGGAGAAATG[C/T]AGGCATAAAACAAAA | 79023 |
rs796171528 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102105361 | AAACCCCATCTCTAC[-/A]AAAAAAAAAAATACA | 79023 |
rs796190713 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARPBP, NUP37 | GRCh38.p7 | 12:102120655 | AGCCTCCCAAGGAAC[A/C]TTTGGGACTTGCACT | 79023 |
rs796200660 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089481 | AGAGGCGCTCCTCAC[C/T]TCCCAGACGGGGCAG | 79023 |
rs796205596 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103066 | TGCTCAAAATTGCTT[C/T]GGCTATCTGGGGTGT | 79023 |
rs796237468 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102092244 | GAAAGAATGGATGAC[A/G]TTAAATGACACATCT | 79023 |
rs796280139 | snp | A/C | | | intron-variant | NUP37 | GRCh38.p7 | 12:102099627 | ATACTCACTACTTAA[A/C]AAACACACACAGGAT | 79023 |
rs796355737 | in-del | -/TAAG | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096594 | TTAAATTTTCTTAAG[-/TAAG]CACTGGGTCTGCTCT | 79023 |
rs796423823 | snp | C/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089526 | TCCTCACCTCCCAGA[C/T]GGGGCGGCCAGGCAG | 79023 |
rs796500727 | snp | G/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089500 | CAGACGGGGCAGCCA[G/T]GCAGAGACGCTCCTC | 79023 |
rs796517464 | in-del | -/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102096663 | ATGATATACTCTCTT[-/G]TCACATATGTGATAA | 79023 |
rs796601829 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089501 | AGACGGGGCAGCCAG[A/G]CAGAGACGCTCCTCA | 79023 |
rs796647562 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089532 | CCTCCCAGACGGGGC[A/G]GCCAGGCAGAGGCGC | 79023 |
rs796665502 | in-del | -/T | | | upstream-variant-2KB, intron-variant | PARPBP, NUP37 | GRCh38.p7 | 12:102119361 | CCATAGCACACGTTT[-/T]ACCTTTGTAATAAAC | 79023 |
rs796708869 | in-del | -/A | | | intron-variant | NUP37 | GRCh38.p7 | 12:102084709 | GCCAGGCTGTGTCTC[-/A]AAAAAAAAAAAAAAA | 79023 |
rs796764052 | in-del | -/AA | | | intron-variant | NUP37 | GRCh38.p7 | 12:102115356 | ATATGTGTACACTTT[-/AA]AAAGTGTAAAATACA | 79023 |
rs796821306 | in-del | -/TT | | | intron-variant | NUP37 | GRCh38.p7 | 12:102108847 | ATGAAATCATAAAAC[-/TT]TGTTCAAAATGTCAT | 79023 |
rs796892687 | snp | A/G | | | intron-variant | NUP37 | GRCh38.p7 | 12:102089509 | CAGCCAGGCAGAGAC[A/G]CTCCTCACCTCCCAG | 79023 |
rs796901249 | in-del | -/T | | | intron-variant | NUP37 | GRCh38.p7 | 12:102103051 | GTTTGTTCTTTTTTT[-/T]GCTCAAAATTGCTTT | 79023 |