SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs249567 | snp | C/T | 0.209084 | 0.246629 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930960 | TTCAAACCTGAAAAA[C/T]CTCAACATATTTGTC | 121441 |
rs249568 | snp | C/T | 0.492484 | 0.0608394 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930848 | TACtgtgagtgcatg[C/T]gtacgtgtgtgtgca | 121441 |
rs249569 | snp | A/T | 0.499713 | 0.0119774 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928129 | CACTGTTAGAAAACA[A/T]CTTTCAAATAGCTTT | 121441 |
rs249570 | snp | C/T | 0.499703 | 0.0121769 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927908 | CATTTTATACCAATG[C/T]TCCTATATAACATAA | 121441 |
rs249571 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927433 | GTAGTCTGTCAGCCC[A/G]GGAGTTCTGCAGAAG | 121441 |
rs249572 | snp | A/G | 0.126564 | 0.217402 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932883 | GTTTTCTATTATGTA[A/G]ATGAGAACGCTGAGT | 121441 |
rs249573 | snp | C/T | 0.209084 | 0.246629 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934387 | ATAAAATGACAAATA[C/T]TAATAGGCTATTGAT | 121441 |
rs249574 | snp | A/C | 0.49934 | 0.0181589 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934592 | GCCCAGGCTGGAGTA[A/C]AATAGTGTGATCTTG | 121441 |
rs249575 | snp | C/T | 0.496034 | 0.0443518 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935761 | CTGGTGTACATAATC[C/T]TCTAAGCATTTGGGC | 121441 |
rs249576 | snp | A/T | 0.49607 | 0.0441545 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937587 | TTAATTTCAAAAATG[A/T]TAAAAGGCCCTTATT | 121441 |
rs249577 | snp | A/G | 0.496105 | 0.0439572 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940874 | ATTTTAGATGTTTTG[A/G]TATGCAAAAAAGTCT | 121441 |
rs249578 | snp | C/T | 0.207253 | 0.246318 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940953 | CCATAAAAAAGTTGG[C/T]ATAATAAAAAGCAAA | 121441 |
rs249579 | snp | A/G | 0.49614 | 0.0437598 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943421 | CATCAATTGCGGGGT[A/G]TATCTGAGAAACAAA | 121441 |
rs249580 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943832 | GGGTGGCTGCCAGTG[C/T]ATGTATCCTAATTAT | 121441 |
rs249581 | snp | C/T | 0.207253 | 0.246318 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943918 | AATACTTTGAAATCT[C/T]GCTTTGGATATGTTG | 121441 |
rs249582 | snp | G/T | 0.496034 | 0.0443518 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943956 | CAGCAGATGGAAAGT[G/T]GCAGTATTTTTCTAA | 121441 |
rs249583 | snp | A/G | 0.491316 | 0.0653198 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944330 | CAAATATTATTGACT[A/G]GTTACCACATGCATG | 121441 |
rs249584 | snp | C/T | 0.496034 | 0.0443518 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944492 | TCCAGTTCTCTTTTT[C/T]TTTTTCTTCTTCTAT | 121441 |
rs249585 | snp | A/G | 0.496517 | 0.0415876 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944918 | AAGAGTTTAAAGTTT[A/G]TGGACACTTCTGTTG | 121441 |
rs249586 | snp | G/T | 0.496382 | 0.0423778 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945084 | ACCCTTTGAAAAGGG[G/T]TGGTTAACTACCTGA | 121441 |
rs249587 | snp | A/G | 0.118933 | 0.212888 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945150 | CTTAGAGTTTGTGCT[A/G]CAGACCCATACAAAC | 121441 |
rs249588 | snp | A/G | 0.491421 | 0.0649309 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945265 | AAATATCTATATTTT[A/G]CTTGAAGTTTTCTGT | 121441 |
rs249589 | snp | C/G | 0.165527 | 0.235296 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945610 | AAGATTTGGCATGTG[C/G]AAACTTGAAAAACTG | 121441 |
rs249590 | snp | C/T | 0.164546 | 0.234942 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946754 | CAACAGTGTTCTATT[C/T]TACTGATCCCAAATG | 121441 |
rs249591 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947704 | TGTGCATTTCTGCCC[C/T]GCTGCCAGCTTTCGG | 121441 |
rs1044910 | snp | A/G | 0.499234 | 0.0195537 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953146 | CCAAAGATTTAAACT[A/G]TGTACCTTTGTATAG | 121441 |
rs1548947 | snp | C/T | 0.439085 | 0.163545 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910686 | AAACGTTTTGGGTTG[C/T]CACAACTAGAGGCTA | 121441 |
rs1610921 | in-del | -/GCTTATAA | 0.496385 | 0.0423584 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934937 | AATGTCCTTATGAAT[-/GCTTATAA]TTACATAAAATTTAT | 121441 |
rs1861632 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922503 | GCATAAAAATTGAAG[C/T]ATAAGAATATACATA | 121441 |
rs2024490 | snp | C/T | 0.116138 | 0.211142 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905586 | CTCTGTGCCTATGTA[C/T]ACACTGTTTCCTCAG | 121441 |
rs2052312 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936865 | TATAATTTCCATATT[C/G]TGAGTTAGatttatt | 121441 |
rs2304696 | snp | C/G | 0 | 0 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952117 | ACACAGAACTACATA[C/G]AATCAGTATTGTTTT | 121441 |
rs2304697 | snp | A/G | 0.183568 | 0.241012 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952177 | AGTAAGAGTAAAAGG[A/G]TGATGGGATTTTATA | 121441 |
rs2371354 | snp | A/G | 0.375 | 0.216506 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929603 | cacacacacacacat[A/G]tgtgtatatatatat | 121441 |
rs2888010 | snp | C/T | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929600 | acacacacacacaca[C/T]atatgtgtatatata | 121441 |
rs2888011 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929601 | cacacacacacacac[A/G]tatgtgtatatatat | 121441 |
rs2888021 | snp | A/G | 0.464523 | 0.128375 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908905 | ATAGTGGCTGGGCAC[A/G]GTGGCTCACGCCTGT | 121441 |
rs3035156 | in-del | -/TT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926032 | GGGATTTTTTTTTTT[-/TT]GATGGCTAAATGAGA | 121441 |
rs3217159 | in-del | -/AT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945488 | TTTATCTATATATAT[-/AT]AAACTGCCAGCTGTC | 121441 |
rs3741957 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937047 | TTTCCCTCTAAATTA[A/C]AATGTCTTTTAAAAT | 121441 |
rs3803093 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944564 | GGGACAAAAGAGAGA[A/G]GTAGGCAAAAATTAT | 121441 |
rs4469943 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929366 | TTGTATTTTTTTTTT[C/T]CTTAATGTCTTGTAT | 121441 |
rs4762167 | snp | A/C | 0.0573587 | 0.15934 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96907173 | AGAAGCCACAGCCGC[A/C]CGCAGCGCCTCGCCC | 121441 |
rs4762338 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911776 | GTAATATCTAGGTAG[C/G]AATGATTTGATTTGC | 121441 |
rs4762339 | snp | C/T | 0.499518 | 0.0155147 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917763 | TAAAAAAAATCTTCA[C/T]GAAAAAATGGATATC | 121441 |
rs4762341 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944129 | TATCATTGTTACTTT[C/G]TGCTAAAATATATAT | 121441 |
rs6538750 | snp | G/T | 0.497641 | 0.0342639 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905520 | ATAATTCATATATTA[G/T]CAAGGCTTCTAACAT | 121441 |
rs6538752 | snp | C/T | 0.11963 | 0.213316 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908535 | TCTTTAAAGTGCCTG[C/T]CTAGAGCAGCTTCTT | 121441 |
rs6538753 | snp | A/G | 0.499575 | 0.0145705 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926353 | GGAACAAATGGTTAT[A/G]TTTGTTTTGTGTACC | 121441 |
rs7136677 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932465 | aaaaaaaaAAAAAAa[A/T]atatatatatatata | 121441 |
rs7296608 | snp | C/T | 0.492484 | 0.0608394 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923314 | ttacaaggtagctac[C/T]gtgaatatttttgta | 121441 |
rs7296774 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930211 | cacacacacacacac[A/T]ctctctctctctctc | 121441 |
rs7296936 | snp | C/T | 0.499683 | 0.0125759 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916302 | ggtacatgtgcacat[C/T]gtgcaggttagttac | 121441 |
rs7300178 | snp | A/C/G | 0.0329836 | 0.124112 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908616 | TTACGTGTTTCAGCT[A/C/G]TATGCTCTGAATAAA | 121441 |
rs7302642 | snp | A/G | 0.0429648 | 0.14013 | intron-variant, synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924924 | tcaatttactaccaa[A/G]catgatagtcattgt | 121441 |
rs7307168 | snp | C/T | 0.496034 | 0.0443518 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950281 | CTGGTAATACTAAGT[C/T]TTGATGATATAGAGC | 121441 |
rs7350552 | snp | A/G | 0.078151 | 0.181571 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928141 | AAGATGTTTTCTAAC[A/G]GTGTTTCTATGTATA | 121441 |
rs7350633 | snp | C/G | 0.0788843 | 0.182262 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927101 | AGTCTGTTACTTAGG[C/G]CAATTTCTGTGATCA | 121441 |
rs7488730 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930243 | ctctctctctctctc[A/T]cacactctcACATGC | 121441 |
rs7955447 | snp | C/T | 0.426047 | 0.177503 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928969 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACCCC | 121441 |
rs7957384 | snp | A/C | 0.432357 | 0.171014 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941572 | GTGGAGAGAAAAGTG[A/C]CTAGTGCTGGAGTTG | 121441 |
rs7963782 | snp | A/G | 0.49681 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920571 | TTTTTGTTTTTGTAG[A/G]TATATGATAAAGTAT | 121441 |
rs7968624 | snp | C/T | 0.417196 | 0.185864 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905911 | AAATTATATATATAT[C/T]GCATACATACACATT | 121441 |
rs7970302 | snp | C/T | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932108 | ATATTTAGAAACAAT[C/T]TCCCTCCTCCACAAA | 121441 |
rs7970386 | snp | C/T | 0.00961516 | 0.0686668 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932135 | CAAACATGCAACATT[C/T]TTACACAATAATGTG | 121441 |
rs7971975 | snp | C/G | 0.499598 | 0.0141716 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922681 | gtgcagtgcatatat[C/G]ttaagtgtacagctt | 121441 |
rs7973062 | snp | C/T | 0.492287 | 0.0616198 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910353 | GGAGATAAAAAATTG[C/T]CCAATATCTCCATCT | 121441 |
rs7977313 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911560 | GTTAATGTGAGACAC[C/T]AGAGAGATTAGTTTT | 121441 |
rs7980370 | snp | A/G | 0.191147 | 0.242974 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952727 | CTTTACCTATAAAAA[A/G]TGTTTAAGGTTCATA | 121441 |
rs10431407 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922730 | cgtaaatacattggt[A/G]taactactaacaaaa | 121441 |
rs10431408 | snp | G/T | 0.0130429 | 0.0796953 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937441 | GTTTGTTTTTTTTTT[G/T]TTTTTTTGTTTTTGG | 121441 |
rs10431438 | snp | A/G | 0.492435 | 0.0610346 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922079 | AAAGACTTGTTTTGG[A/G]AGGTATTTAGGGAAA | 121441 |
rs10431439 | snp | A/G/T | 0.0213998 | 0.101213 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937442 | TTTGTTTTTTTTTTG[A/G/T]TTTTTTGTTTTTGGC | 121441 |
rs10492172 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925505 | TATTTTACATATCAG[C/G]TCTTCAGAAGTGGTA | 121441 |
rs10528785 | in-del | -/TGTGTGTGTGTG | 0.499539 | 0.0151687 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923789 | TCCTTAATACCTGTT[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 121441 |
rs10735350 | snp | A/C | 0.132751 | 0.2208 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96907106 | TAACTTCCCCCGCGG[A/C]TGCCCAGCGCCGCCC | 121441 |
rs10777820 | snp | A/C | 0.499653 | 0.0131743 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906762 | ATGTAGGAATCCTTT[A/C]CTAAATCCACATCCA | 121441 |
rs10777821 | snp | C/G | 0.491316 | 0.0653198 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906879 | CAGCTTCCTATAGTG[C/G]ATTGTAAGCTCCACA | 121441 |
rs10777822 | snp | A/T | 0.492484 | 0.0608394 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914785 | TGCACCTTGAGCAGT[A/T]CAGGATTCCTGTAAT | 121441 |
rs10777823 | snp | C/T | 0.496034 | 0.0443518 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951080 | AAAGGAATATAGTAT[C/T]GGAGAGTTCAGGGGT | 121441 |
rs10860103 | snp | A/G | 0.418007 | 0.185132 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906400 | TGAATGCAGATAACT[A/G]GGGCTGATGTACCTA | 121441 |
rs10860104 | snp | A/T | 0.459004 | 0.137176 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913257 | ATTCTGTCCACCTGT[A/T]CTGAGGGGCCTGTCT | 121441 |
rs10860105 | snp | C/T | 0.439918 | 0.162576 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918043 | ATGGTGTGTGGTCAT[C/T]AGGGATCTTTCCTTA | 121441 |
rs10860106 | snp | A/G | 0.439918 | 0.162576 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932546 | TATATATATAATTTA[A/G]TAAATCAGTGTTTTG | 121441 |
rs10860107 | snp | A/G | 0.499382 | 0.017561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948578 | AGGTTTGTTTTCGTT[A/G]TTAGAGTTGAGAAAT | 121441 |
rs11108732 | snp | C/G | 0.304937 | 0.243889 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905948 | ATATACACAAATACA[C/G]TGCTTAGTAAAGTGT | 121441 |
rs11108733 | snp | A/G | 0.206642 | 0.246211 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906909 | AAGGCCAAGGACCAC[A/G]AGAATTCACTGTACC | 121441 |
rs11108734 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908203 | ACTTTAATGGCTTTT[A/G]GTAGCACTGTATCGG | 121441 |
rs11108735 | snp | A/G | 0.414868 | 0.187932 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909744 | ACATTGTTTTAAACT[A/G]TTTGTAGGCGCAGTC | 121441 |
rs11108736 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915706 | ATAGCATAGTTACTG[A/G]TGGCACCACCAAATT | 121441 |
rs11108737 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96916412 | CCTCCCCCCTCCCCC[C/T]TCCCCACCACAGTCC | 121441 |
rs11108738 | snp | C/T | 0.439085 | 0.163545 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922315 | TTTGATAAAGAGAGA[C/T]ATAAAGTCTAAGCCT | 121441 |
rs11108739 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932489 | atatatatatatata[A/G]aatgcacacacacaa | 121441 |
rs11108740 | snp | A/T | 0.0777841 | 0.181223 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935619 | tattgtaggatattc[A/T]tcagcatccctggcc | 121441 |
rs11108741 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946420 | CAATTATTAAAATCA[C/T]TGGTGCCTTTTTTCC | 121441 |
rs11108742 | snp | C/T | 0.078151 | 0.181571 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948418 | TTACTCTGTCAAGGG[C/T]ATGAAGATGGGTCTC | 121441 |
rs11108743 | snp | A/T | 0.451732 | 0.147663 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96954134 | cacaggaaatgattt[A/T]aaaaaatgcctttag | 121441 |
rs11295574 | in-del | -/G | 0.499218 | 0.0197529 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936392 | GAAGTGAATAGAAAA[-/G]TAAGATGGAATGTTT | 121441 |
rs11333833 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917599 | TTAAATTAAGGTAAC[-/T]TTTTTTTTTTTTTTT | 121441 |
rs11613194 | snp | G/T | 0.078151 | 0.181571 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919266 | aggaagagaggcttt[G/T]gagtttgacatggaa | 121441 |
rs11830756 | snp | A/G | 0.414245 | 0.188477 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920223 | TGAAATGCTTGATTG[A/G]AAAACTTCAGCTATT | 121441 |
rs11830956 | snp | A/C/T | 0.0150606 | 0.0854603 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939548 | TTTTCAGTTTTTCAT[A/C/T]TGGGCCTGAGATGCC | 121441 |
rs11836610 | snp | A/G | 0.406814 | 0.194704 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932166 | GTATAAGAAAAAATA[A/G]CATTGCTGCTTATAC | 121441 |
rs12229713 | snp | C/G | 0 | 0 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953431 | TGACAGATTATGAAA[C/G]CATTATGACTTGTAA | 121441 |
rs12304966 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915235 | GTCCACAGAAGTGAA[C/T]ACAAATCTATTTGAT | 121441 |
rs12371968 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929465 | TGTGGGATATATCTG[C/T]GAAATTAGTTTTAGC | 121441 |
rs12580563 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912475 | CAGAGTAGTATTTCA[C/G]GTGGGTTAAATAGCT | 121441 |
rs12581454 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96916472 | catgtgatctcattg[G/T]tcaattcccacctat | 121441 |
rs12810959 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940268 | TAACTTTAGCTCTTG[G/T]CATATTCTGTTTTAT | 121441 |
rs12814203 | snp | C/T | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928679 | aggtacatagtgtgt[C/T]tcttttttttttttt | 121441 |
rs12815751 | snp | A/T | 0.403509 | 0.197319 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937926 | ATTTCTTGCTCACAA[A/T]AAAAAAATATTCTGT | 121441 |
rs12819482 | snp | C/T | 0.437542 | 0.165312 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938157 | ATGATTTTGCTATTT[C/T]CAAGTAGAAGCAAAA | 121441 |
rs17026100 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917380 | CTGTGTCGTCACCGG[C/T]CCACAGAAGTGAATG | 121441 |
rs17026103 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917863 | ATTGAACTAAGATTT[A/G]TTAGGGAAAATAAAG | 121441 |
rs17026118 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925909 | CGTGGTAAGTCCCAC[A/G]TTTATTTGGAGAGCA | 121441 |
rs17026162 | snp | C/T | 0.0405363 | 0.136473 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944818 | CATGAAACTTCCTGA[C/T]GTTTGAAAGTGTTTG | 121441 |
rs17026165 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951013 | TCTAACCTAGTGAAT[C/T]TTCTGTATTTCATTG | 121441 |
rs17747759 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948811 | TCTGGAGTATTCACT[A/G]TCTTTTTTACCTTGG | 121441 |
rs28475124 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922739 | ATTGGTGTAACTACT[A/C]ACAAAATCAAGATAT | 121441 |
rs28587015 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922815 | TCACTACCTCATATT[C/T]TATGAAAGGAATCAT | 121441 |
rs34174920 | snp | G/T | 0.0298439 | 0.118454 | missense | NEDD1 | GRCh38.p7 | 12:96944764 | AGCCCAGTTGATATG[G/T]GAACCCCCAATCAAT | 121441 |
rs34236090 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935755 | TATGTACTGGTGTAC[A/C]TAATCTTCTAAGCAT | 121441 |
rs34248689 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926993 | AAAAAAAAAATTGTG[-/T]GTGTGTGTGTGTGTG | 121441 |
rs34255398 | in-del | -/A | 0.442926 | 0.158996 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942905 | CTGTTGGCTGGAGAT[-/A]ATCAGTTCCATGCCA | 121441 |
rs34446396 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931579 | ATCAATGAATTACAA[-/T]TTTTTTTCATAAATT | 121441 |
rs34499067 | in-del | -/A | 0.444799 | 0.156695 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909905 | GCAATAGTATCCTTT[-/A]AAAAAAAAAAACACA | 121441 |
rs34575410 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928682 | TACATAGTGTGTTTC[-/T]TTTTTTTTTTTTTTT | 121441 |
rs34602531 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929624 | TATATATATATATAT[-/A]TTTTTTTTTAATGGC | 121441 |
rs34653282 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934208 | TTGCTTTTTTTTTTT[-/T]CTCCCAGTATTCCCT | 121441 |
rs34688138 | in-del | -/AT | 0.314787 | 0.241459 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923350 | CTTTTTTTAAGATAC[-/AT]GTTTTTATTTATTTT | 121441 |
rs34995908 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947322 | AATCACAGAAAGGGA[-/C]GCAGTTCTTCTGTGG | 121441 |
rs35105640 | in-del | -/A | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905389 | TTCACCTATACACTT[-/A]AAAATTGATAATGGC | 121441 |
rs35154601 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925136 | AAAGCAATAAACTGC[A/G]GAGTTCCAAGGGAAC | 121441 |
rs35358198 | in-del | -/C | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96907119 | GGATGCCCAGCGCCG[-/C]CCTGACCAGACCCTC | 121441 |
rs35462225 | snp | A/T | 0.437824 | 0.164991 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949417 | AGAAAAACATTAAAA[A/T]TTTTTTTTGTTTAAA | 121441 |
rs35497488 | in-del | -/C | 0.439918 | 0.162576 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932566 | CAGTGTTTTGTTTAT[-/C]CCAGGATTCTTAGCT | 121441 |
rs35501175 | in-del | -/TTTC | 0.208474 | 0.246527 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913756 | ACTCTTTGAAAGCTA[-/TTTC]TTTTTTAAATAAGAT | 121441 |
rs35530798 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928589 | GGTTATTCAAAGGAA[-/T]TTTTTTTTTTCTTTA | 121441 |
rs35646887 | in-del | -/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941655 | TCTGGAGGAACTTTT[-/G]GCATTGAAGAATGTA | 121441 |
rs35746916 | in-del | -/C | | | utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96907474 | TGGGCTGGGAAGTGT[-/C]CCGGGGAGGCGCGGG | 121441 |
rs36031336 | in-del | -/C | 0.499575 | 0.0145705 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906110 | AGATTTAATTAATTG[-/C]CCTTTTTGTTTGAAG | 121441 |
rs55727280 | snp | C/T | 0.0926964 | 0.194308 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905919 | TATATATTGCATACA[C/T]ACACATTACGTCTAT | 121441 |
rs55765326 | in-del | -/AAT | 0.499609 | 0.0139722 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910231 | GTTGGTAGTTGTGGA[-/AAT]AATTCCAAAAGGTTT | 121441 |
rs55847672 | snp | A/G | 0.396182 | 0.202807 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930700 | GTGAGCCACTCTTAC[A/G]AGTTAAGGCAGTGGG | 121441 |
rs56027670 | in-del | -/ATT/ATTATT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96916262 | ATTATTATTATTATT[-/ATT/ATTATT]TTTAAATTATACTTT | 121441 |
rs56112144 | in-del | -/GAAAAATAT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918407 | AAAAAGTTTTAATAT[-/GAAAAATAT]AAACATATTTATATC | 121441 |
rs56762092 | in-del | -/ACACACACACACACACACACACACTC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930189 | CACACACACACACAC[-/ACACACACACACACACACACACACTC]TCTCTCTCTCTCTCT | 121441 |
rs56818741 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917806 | GAGTACTTACCAAGC[G/T]TTTATTTTTGAGCTT | 121441 |
rs57230931 | in-del | -/TGTGTGTGTGTG | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923819 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTG]AAACTGTATGCCTGT | 121441 |
rs57888505 | snp | A/C/G | 0.0111196 | 0.0737302 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914336 | AGCTTTTTTTTTAAA[A/C/G]TATAAAAATAACAGA | 121441 |
rs57918937 | in-del | -/TT/TTT | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921673 | GGGATTTTTTTTTTT[-/TT/TTT]CTTTCTTAGAGAGTC | 121441 |
rs58004376 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932462 | AAAAAAAAAAAAAAA[-/T]AATATATATATATAT | 121441 |
rs58112024 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932463 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 121441 |
rs58889639 | in-del | -/GAT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96916777 | TATGGAAGGAGACAT[-/GAT]CTGATTTACATTTTT | 121441 |
rs59074488 | snp | A/T | 0.084728 | 0.187577 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919557 | ATGATTTTTCTCTTT[A/T]CTCTAAGGTTGAACT | 121441 |
rs59844782 | in-del | -/TCTCTCTCAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938829 | CTCTCATTCTCTCTC[-/TCTCTCTCAC]ACACACACACATTTT | 121441 |
rs59941028 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928305 | GTATTTCATTATTCA[A/G]TGCCATCATTTACCT | 121441 |
rs60465508 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948055 | TCATCTACACCTATC[A/G]TTGGCAGGACAGAGA | 121441 |
rs60535832 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932461 | AAAAAAAAAAAAAAA[-/T]AAATATATATATATA | 121441 |
rs60826498 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921792 | TTTTTTTTTTTTTTT[-/T]AATATTAGAGACAGG | 121441 |
rs60955260 | in-del | -/TATATATATATATATATATATATATATAT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932460 | AAAAAAAAAAAAAAA[lengthTooLong]AAAATATATATATAT | 121441 |
rs61146311 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923358 | AAGATACATGTTTTT[A/G]TTTATTTTGAGTAAA | 121441 |
rs61348420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928451 | TCTCTTTCAATGTAA[C/T]TTAGTAGCAGGCTTA | 121441 |
rs61405089 | in-del | -/ACACACACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930203 | CACACACACACACAC[-/ACACACACAC]TCTCTCTCTCTCTCT | 121441 |
rs61407297 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909966 | AAACAACCACTGTCA[A/G]TGAAACTTTTGCATG | 121441 |
rs61564045 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921047 | TATCTGGGAATAAAA[C/T]AGGGAAAATTGAAAG | 121441 |
rs61648615 | snp | G/T | 0.0854556 | 0.188216 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941453 | AATTTCTATTTAAAT[G/T]GCTAAGTCAAACTGA | 121441 |
rs61735398 | snp | G/T | 0.498047 | 0.0311889 | missense | NEDD1 | GRCh38.p7 | 12:96936802 | TTCAGTACTCCACTG[G/T]TCTTACTAAGGTGAG | 121441 |
rs61938394 | snp | A/G | 0.396727 | 0.202413 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928926 | CGATCTCCTGACCTC[A/G]TGATCTGCCCGCCTC | 121441 |
rs61938396 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933019 | TTTTTTTTTTTTTAA[A/T]TAGTCTGCCATGTAG | 121441 |
rs61938397 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941420 | TATTGAGTATCTTCT[C/G]CCTTACCCTGGCCTG | 121441 |
rs61938398 | snp | A/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945889 | CTATCTAGACCTTAC[A/T]TGTTTTTTTTTTAGA | 121441 |
rs66735119 | in-del | -/C | 0.496616 | 0.0409947 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922308 | GACTTTATGTCTCTC[-/C]TTTATCAAAATATAA | 121441 |
rs67367047 | in-del | -/T | 0.498556 | 0.0268265 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937442 | TTTGTTTTTTTTTTG[-/T]TTTTTTGTTTTTGGC | 121441 |
rs71078436 | in-del | -/GTGTGTGTGTGTGTGT | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929557 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGT]ATACATGAAAACAAT | 121441 |
rs71078437 | in-del | -/TA/TATA | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929607 | ATATATATATATATA[-/TA/TATA]CACATATGTGTGTGT | 121441 |
rs71078438 | in-del | -/GTGTGTGTGTGTGT | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930163 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGT]GTGTGTTTTACAACA | 121441 |
rs71307519 | in-del | -/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909194 | TTCCTAATATCTGAA[-/T]TTTTTTTTTTTTTTT | 121441 |
rs71440803 | snp | A/T | 0.491104 | 0.0660973 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929625 | TATATATATATATAT[A/T]TTTTTTTTAATGGCT | 121441 |
rs71440804 | snp | A/T | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932463 | AAAAAAAAAAATATA[A/T]ATATATATATATATA | 121441 |
rs71443535 | in-del | AGAGAGA/TGTGTGTGTGT | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930211 | GAGAGAGAGAGAGAG[AGAGAGA/TGTGTGTGTGT]GTGTGTGTGTGTGTG | 121441 |
rs71460366 | snp | A/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909348 | TTGAGCTAAGACCTG[A/G]ATGATGAGAAGGAGA | 121441 |
rs71460367 | snp | A/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926992 | AAAAAAAAAAATTGT[A/G]TGTGTGTGTGTGTGT | 121441 |
rs73226537 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936525 | GAAGTGTTAATAACT[C/G]TGGTTTTGGTATATA | 121441 |
rs73226539 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942842 | CCAGAGCTTCATTCA[A/G]CTTAAGACTCAACTG | 121441 |
rs73368669 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908255 | ACATGAGTGAATTAC[A/G]TTAACTTTTTGTCTC | 121441 |
rs73368684 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918851 | GAACGATACCCAGAA[C/T]GTCTGCTCTTCCTTT | 121441 |
rs73368698 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923995 | ACTATTCTGTGTTTT[A/C]TTTTAGAAGCTTTGT | 121441 |
rs73370508 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932190 | CTTATACTGCCGGGA[C/T]TTTTTCCCCCCCATA | 121441 |
rs73370523 | snp | A/G/T | 0.00796298 | 0.0626859 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945950 | GGTTACTATTGTCTA[A/G/T]GTTCTGGTAATCCTA | 121441 |
rs74239044 | snp | A/C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913759 | CTTTGAAAGCTATTT[A/C/T]TTTTTTAAATAAGAT | 121441 |
rs74348293 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945168 | GACCCATACAAACTT[C/G]ATCACATTTAAAGGA | 121441 |
rs74359935 | in-del | -/TTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917612 | ACTTTTTTTTTTTTT[-/TTT]AAATAGCAAAAGCAG | 121441 |
rs74364287 | snp | A/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929607 | CACACACACATATGT[A/G]TATATATATATATAT | 121441 |
rs74375807 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914411 | TCCAAATTAGTTGCT[A/G]TGATTCTTAGCCCTC | 121441 |
rs74430986 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909639 | GGTGACTGCACTGTT[C/T]GGAACAAAAATGAAT | 121441 |
rs74497074 | snp | A/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917617 | TTTTTTTTTTTTTAA[A/T]TAGCAAAAGCAGACA | 121441 |
rs74559747 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953093 | GTTAAGTGAAGCTTG[G/T]GGGGGCTACTGACTT | 121441 |
rs74618322 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934518 | TTTTTTTTTTTAAGA[A/C]AGAGTTGGGTTTTTT | 121441 |
rs74809593 | snp | G/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928705 | TTTTTTTTTTTTTTT[G/T]AGGCAGAGTTTCGCT | 121441 |
rs74829058 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935321 | GGTCCTAAAGTTTGT[A/G]CAGTTGATGGATCTA | 121441 |
rs74829808 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923122 | ACCCTGTCTCAAAAG[-/A]AAAAAAAAAGCAAGG | 121441 |
rs74888935 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933336 | CGATAACTATATGAA[C/T]TCCTAAAGTGCTGTA | 121441 |
rs74925243 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919169 | CATAGTCCTTGTGAA[C/T]TCAGTTTGTTTAAAA | 121441 |
rs75007264 | in-del | -/CA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909933 | ACACACACACACACA[-/CA]AACCGCTTATTAGGT | 121441 |
rs75051870 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936357 | GTGCTGCTTCTATAA[C/G]ATGCAGAATGTACCT | 121441 |
rs75071256 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910233 | TGGTAGTTGTGGAAA[A/T]AATTCCAAAAGGTTT | 121441 |
rs75127005 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911739 | AGAAGTCAAGGAAAG[C/G]GAAATGGTTTTTCTC | 121441 |
rs75160794 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940847 | ATCTACTTCTAAATT[A/G]ATGTTCCTAAAATTT | 121441 |
rs75173252 | in-del | -/C | 0.206642 | 0.246211 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906821 | GCATCTTATACCTTT[-/C]CATTATCATAGTTTC | 121441 |
rs75267821 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935941 | AAGGTCCCACTGTCA[C/G]CCTTTATTATGATGC | 121441 |
rs75299109 | snp | A/G | 0.0410537 | 0.137264 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952822 | TCAATCAACATGACA[A/G]CTTATAATGAGTGGA | 121441 |
rs75301828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935892 | GCTTACCACTGTCTG[A/T]AGATCATGTGGAGTA | 121441 |
rs75319164 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951145 | TTACTGGTTGTGTGA[C/T]TTTGAACAAGTTATA | 121441 |
rs75336181 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938544 | TGTTTAACAAAGACA[A/G]CATTAATTTGCAAAT | 121441 |
rs75453831 | snp | A/T | 0.146314 | 0.227484 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945458 | ATTAATCCCTCTGTC[A/T]TGTGGTATTACATTA | 121441 |
rs75561987 | snp | A/C | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909914 | TCCTTTAAAAAAAAA[A/C]AACACACACACACAC | 121441 |
rs75583789 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929723 | ATCCTGTTCAGGTTT[A/G]CTTCCACTTCTAGCA | 121441 |
rs75591533 | snp | G/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948451 | TTCTCCTAGTCATGG[G/T]TCTCTTTTCTCCTAA | 121441 |
rs75608999 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933849 | TCAATACAAGTTTGA[C/T]AGTAACATTTTAGTA | 121441 |
rs75696243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925600 | TTCTGGAAACTTTAC[A/G]CTATTTTCTTGTCTC | 121441 |
rs75746227 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945142 | GTCTTATCCTTAGAG[G/T]TTGTGCTGCAGACCC | 121441 |
rs75793732 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941804 | AGCATTTGAGTCATA[C/T]GCCCTCCAGATTCAT | 121441 |
rs75794137 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915273 | AAGCATTTTTGACCC[C/G]CTTAAAAGCCGTTGG | 121441 |
rs75819629 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918512 | CCTGCATGGCAAAAT[G/T]TGATGATTTTTTCCA | 121441 |
rs75861789 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920191 | GTATCTTACATAAGA[C/T]TGTGAATTTAAGTTT | 121441 |
rs76299900 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946300 | AAAAAAATTCTTTCT[C/T]AGACTTATCCTTGTC | 121441 |
rs76300103 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918500 | ACTTACCCCATCCCT[A/G]CATGGCAAAATTTGA | 121441 |
rs76436327 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910934 | ATGTGACTGGTTCAG[A/G]AACAAAAATATTAAA | 121441 |
rs76505872 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947686 | GAGCAACTCTGAAAT[C/T]GCTGTGCATTTCTGC | 121441 |
rs76644025 | snp | A/G | 0.11963 | 0.213316 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948649 | TGTGCATCTGTTTCT[A/G]TTGTCTATTAAGAAG | 121441 |
rs76647098 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936168 | ACTGTACAACTAAGA[A/C]CAAAGTAACAGCTGC | 121441 |
rs76664116 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946772 | TAGAACACTGTTGAC[A/G]ATATGATGAGGAAAT | 121441 |
rs76669984 | snp | C/G | 0.209084 | 0.246629 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921533 | AACCATGGCCTGTTT[C/G]TTTGTCCTCAGTCTA | 121441 |
rs76693823 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946191 | ATAGATCTATTAGGT[A/G]TGCTGTGTGCAATAA | 121441 |
rs76697101 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928179 | CTTCTGTCCATATAG[C/T]TATACTCATTCTGTT | 121441 |
rs76788484 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937882 | TTATTGATGTGTTAT[A/G]TGATAAGCTTTCTCT | 121441 |
rs76837486 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928292 | TTAATGACTGGATGT[A/G]TTTCATTATTCAATG | 121441 |
rs76870169 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933109 | TTTAACTGGTTATCA[A/G]GTTGTGTTAAAGACA | 121441 |
rs76901495 | snp | C/T | 0.0577344 | 0.159793 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905938 | CATTACGTCTATATA[C/T]ACAAATACAGTGCTT | 121441 |
rs76977905 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938924 | GGCCAGGATGCTTTT[A/G]GGCAATTCTCTTAAC | 121441 |
rs77110098 | snp | A/C | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926973 | GCCTGGGTGACAGAG[A/C]GAAAAAAAAAAAAAT | 121441 |
rs77203721 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918699 | CTGGTGATTAACACA[A/G]TTTCTGGCACTTAGT | 121441 |
rs77275962 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934499 | TTCTTTTCTTTTCTT[C/T]TCTTTTTTTTTTTTA | 121441 |
rs77543090 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914470 | ATGCTGTTGGATAAA[A/G]GTAAGATTAGTTGAG | 121441 |
rs77544329 | snp | A/C | 0.0948562 | 0.196037 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909915 | CCTTTAAAAAAAAAA[A/C]ACACACACACACACA | 121441 |
rs77673365 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920395 | TTGTTAATAGGTTAA[A/G]TGTAAAAAATGGATA | 121441 |
rs77802446 | snp | A/G | 0.0573587 | 0.15934 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906679 | ATGGGTTTTGAAGTA[A/G]GTTAGTGCAGACGCC | 121441 |
rs77884884 | snp | C/T | 0.0123036 | 0.0774623 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905671 | CAGCATCAGTGAGGA[C/T]AGAGGAATGGAGGTT | 121441 |
rs78012855 | snp | A/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926974 | CCTGGGTGACAGAGC[A/G]AAAAAAAAAAAAATT | 121441 |
rs78013157 | snp | G/T | | | missense | NEDD1 | GRCh38.p7 | 12:96934990 | GTCTGTTCGGCACTT[G/T]AAGTACTCCTTGTTT | 121441 |
rs78114324 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923214 | GTTCATACTGTATTA[A/C]TTCTGTGTAGTGTTT | 121441 |
rs78140821 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914893 | AGGGTTAGCCAGCTC[C/T]AAATATAATTTTTAT | 121441 |
rs78165489 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918177 | GTTTGTGTTTTTTTT[G/T]TGTGTGTGTGTGTTT | 121441 |
rs78174451 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950733 | ATGACTTCTTTCTTG[A/G]GCTTTTTCCCAAGAG | 121441 |
rs78543463 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941281 | TCAACAGCAGGATCT[A/C/T]GAAGTTGTTTCATCC | 121441 |
rs78569440 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948714 | TCCTTTGGTTACTAG[A/G]TTCAGGTTTTCTTAG | 121441 |
rs78574017 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920306 | TTATGGTGCTTATAT[A/T]AATTTGATTATGTAA | 121441 |
rs78623950 | snp | C/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937003 | TTTTTCTTTTTTTTT[C/T]CTCCTTATATATCTC | 121441 |
rs78632932 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916084 | TATAGGGTTGTATAT[C/T]TAAGGAATGGAAGGT | 121441 |
rs78657464 | snp | A/C | | | stop-gained | NEDD1 | GRCh38.p7 | 12:96945741 | TTGCCAGTTCACTCT[A/C]AGAAAAAATAGCCGA | 121441 |
rs78683922 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950352 | ACCTTTGGAAAACAA[C/T]TTGCATGATTTTGTA | 121441 |
rs78878997 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923186 | TACATTTGCTTTGTT[A/G]CATGGAATAGTAGTT | 121441 |
rs78910947 | snp | A/G | 0.0150747 | 0.0854992 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940381 | TTTAGATGTAATAAC[A/G]TTGATTTTTATATCT | 121441 |
rs78923952 | snp | C/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949815 | TCAGTAAGTTGTGTT[C/G]TGACATTTGTTTTTT | 121441 |
rs78971586 | snp | C/G | 0.0573587 | 0.15934 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905279 | TCTATGAATTACTGA[C/G]AAAATTCTGTCAGTC | 121441 |
rs79024542 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950055 | AGAGTGAAGGGATAA[C/G]AAGATACCTGCAGTT | 121441 |
rs79049646 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943818 | TATCAGTAGAAAGTG[C/G]GTGGCTGCCAGTGCA | 121441 |
rs79115305 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939213 | CTAAACTTGTTATTG[C/G]TACTTAGTTTTAGAA | 121441 |
rs79171111 | snp | A/T | 0.0573587 | 0.15934 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906936 | TACCCCTGTATCCCC[A/T]GGCTAAACCATCACT | 121441 |
rs79336777 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923315 | TACAAGGTAGCTACT[A/G]TGAATATTTTTGTAC | 121441 |
rs79380851 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944194 | TCAAAATGATCAAAA[A/G]TTACCAGGAAGGCCA | 121441 |
rs79440468 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926604 | CAGTACTGCCTGTTT[C/T]ATCTGATTGTGGCCC | 121441 |
rs79464821 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948255 | TTGTCCCTACTTTTT[A/T]TACATGAGCGCTGAA | 121441 |
rs79533977 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910659 | TATTGGTCTTCACCC[A/G]TTAGGTACCAATAGC | 121441 |
rs79558706 | snp | A/C | 0.0737376 | 0.17729 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953216 | ACTAAAATTAAAAAA[A/C]AAAAAACAAAAAACA | 121441 |
rs79772654 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927293 | GCATCATACTGAATT[A/G]TATATATTGAAATAA | 121441 |
rs79923927 | snp | A/G | 0.209388 | 0.246679 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923669 | TATGTTGGGTTATTC[A/G]TGTTTTTAAAATTTA | 121441 |
rs80186010 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930784 | TGGGACTTTTTAAAG[A/G]TAGACAGTCTCAGGC | 121441 |
rs80190824 | snp | A/C | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926975 | CTGGGTGACAGAGCG[A/C]AAAAAAAAAAAATTG | 121441 |
rs80231105 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947941 | CTTTGACCATAGGCA[A/G]CCTCTGCCTGGGACG | 121441 |
rs80238813 | snp | C/T | 4.95225e-05 | 0.00497582 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96943645 | AGTATTGCATTCTAG[C/T]CCTCTTAATGTTTTT | 121441 |
rs80272596 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929946 | GGCTGTTATGGGCTG[C/T]TTCTGTTCTCAGATC | 121441 |
rs111247297 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914690 | TACTGATTTTAAAAT[C/T]TTAGAGTAGAACTTT | 121441 |
rs111338569 | snp | G/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913147 | ACTAGGTTGACCTGA[G/T]CATATAAACTCTAAT | 121441 |
rs111411238 | in-del | -/TG | 0.492871 | 0.0592773 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926989 | GAAAAAAAAAAAAAT[-/TG]TGTGTGTGTGTGTGT | 121441 |
rs111423351 | snp | A/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928970 | GCTGGGATTACAGGC[A/G]TGAGCCACCACCCCC | 121441 |
rs111574522 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941459 | TATTTAAATTGCTAA[A/G]TCAAACTGAAAGAGG | 121441 |
rs111585765 | in-del | -/CTCTCTCTCA | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938828 | TCTCTCATTCTCTCT[-/CTCTCTCTCA]CACACACACACATTT | 121441 |
rs111620890 | snp | C/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940127 | TTCCAACAAAATGGC[C/T]AAAATAAGGTATTAC | 121441 |
rs111775462 | snp | C/T | 0 | 0 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952959 | TTTCTGTACTGTGTA[C/T]AATATTTTTATATTA | 121441 |
rs111807514 | in-del | -/TT | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921663 | GCTTTAGAAGAGGGA[-/TT]TTTTTTTTTTTCTTT | 121441 |
rs111871143 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913016 | AAAATAGTTTTGAAT[A/T]TAGGGGAACAATTGA | 121441 |
rs112018832 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929341 | AATTTATGTTTTTTT[C/T]CTTAATGTCTTGTAT | 121441 |
rs112128759 | snp | C/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917916 | TTTTTATGTCTTTTT[C/T]CTTACATGTGTAGCA | 121441 |
rs112131402 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939270 | ATAAGACTTTAGCGC[C/T]GTTTTCAAATGATAC | 121441 |
rs112236261 | snp | C/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942336 | GTTACACTATACCTT[C/G]CTGCCTCATTAAATG | 121441 |
rs112309525 | snp | A/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934596 | AGGCTGGAGTACAAT[A/G]GTGTGATCTTGGCTC | 121441 |
rs112328392 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929613 | CACATATGTGTATAT[A/G]TATATATATATTTTT | 121441 |
rs112358985 | snp | G/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952233 | ATGTATATTTTTATA[G/T]TAAAAATTGTACAGT | 121441 |
rs112564114 | snp | C/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943415 | AATACACATCAATTG[C/T]GGGGTGTATCTGAGA | 121441 |
rs112599630 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923780 | CTGTTTTACTCCTTA[A/G]TACCTGTTTGTGTGT | 121441 |
rs112622130 | snp | C/T | 0.0818113 | 0.184966 | upstream-variant-2KB, intron-variant | NEDD1 | GRCh38.p7 | 12:96907335 | GAGGTCAGCGGGCCC[C/T]CGCCCGCCGCGTCCG | 121441 |
rs112685038 | snp | A/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932896 | TAGATGAGAACGCTG[A/T]GTTTTGGAGAGTTTA | 121441 |
rs112959763 | snp | A/T | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920656 | GGAAAATAAGTCAAT[A/T]TTTTTCCTCTATAAA | 121441 |
rs112961742 | snp | C/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922891 | AGGCTGAGGCAGGCA[C/G]ATCCCTTGAGCCCAG | 121441 |
rs112980154 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917467 | ATGTGGAAGAAAGAC[A/C/G]ATGAGAGAGTGGCTC | 121441 |
rs113163735 | snp | A/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945045 | TGTGTCTTTAATATG[A/G]TAGAGATAGAATTAT | 121441 |
rs113164146 | snp | C/G | 0.00236369 | 0.0342966 | missense | NEDD1 | GRCh38.p7 | 12:96945695 | TTCTTTATTTTAGAT[C/G]CAAAGATAGCATCTT | 121441 |
rs113248634 | in-del | -/CA | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909917 | TTTAAAAAAAAAAAA[-/CA]CACACACACACACAC | 121441 |
rs113284349 | snp | C/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940611 | AAAAGATGTGAATAA[C/T]AGCTTCAGTCCAACT | 121441 |
rs113288975 | snp | C/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915616 | AATCCAAGGATGCAC[C/T]GTGGAAGTTCCAACT | 121441 |
rs113303198 | in-del | -/ATT | 0.016326 | 0.0888619 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937158 | TGTATAGTATGAAAC[-/ATT]AGTAACCTGAGCTTT | 121441 |
rs113436652 | snp | A/C/G | 9.96943e-05 | 0.00705955 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942662 | TTCGTGAAAATGAAA[A/C/G]GTGAATTGTATTATC | 121441 |
rs113472978 | in-del | -/TATT | 6.81559e-05 | 0.00583723 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909743 | TACATTGTTTTAAAC[-/TATT]TGTAGGCGCAGTCAT | 121441 |
rs113492714 | snp | A/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915892 | TTGGTAAGTTATCAT[A/G]CAGATAACTAAAATA | 121441 |
rs113493649 | snp | G/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912479 | GTAGTATTTCACGTG[G/T]GTTAAATAGCTTTTG | 121441 |
rs113573973 | snp | A/C | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940807 | TGAAGGAAGTTTTTA[A/C]CTTCATAGGCAATCT | 121441 |
rs113585010 | snp | C/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951907 | CCTGCCAAATAAATG[C/T]GAAATATCAATAATT | 121441 |
rs113654868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921145 | CTCTTTGCCAATTAT[C/T]TGTTTCTAACTTGTA | 121441 |
rs113808367 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947765 | CCTGTTCCTGGCTTT[C/T]TGTGCCTCAGGAGAA | 121441 |
rs113821271 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920738 | ACTTTCCATAAGATT[A/C/T]GCCATAGAAATTTCC | 121441 |
rs113848947 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951826 | AAGTTGTTAAGTACA[A/G]GAAATATCATTCACC | 121441 |
rs113858974 | in-del | -/TT | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937159 | GTATAGTATGAAACA[-/TT]AGTAACCTGAGCTTT | 121441 |
rs113890248 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929612 | ACACATATGTGTATA[C/T]ATATATATATATTTT | 121441 |
rs113893590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934815 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACCACG | 121441 |
rs113960667 | snp | A/G | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942253 | TTGTCCAAGGTCACA[A/G]AGCTATTAAGTGGTA | 121441 |
rs113965229 | snp | A/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918041 | CTATGGTGTGTGGTC[A/T]TCAGGGATCTTTCCT | 121441 |
rs114156231 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942978 | GGTTTACCTCAGAGC[C/T]GGTGAACAAGAGAAT | 121441 |
rs114489494 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915080 | TCTTAGTCTCCCTCA[A/G]CTAAAGTCAATTCCT | 121441 |
rs114539251 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910658 | TTATTGGTCTTCACC[C/T]GTTAGGTACCAATAG | 121441 |
rs114549992 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920474 | GATTTTGTCAGCTGC[A/G]AGACAGATACACTCA | 121441 |
rs114664835 | snp | C/T | 0.00745081 | 0.0605796 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942649 | ACTTAGAAGTATTTT[C/T]GTGAAAATGAAAAGT | 121441 |
rs114712390 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906978 | AGTCTAGCACAGTGC[C/T]TGGCACACAGTAAAC | 121441 |
rs114790480 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928612 | TTTCTTTAAAGCCAC[A/G]TAATTTTTCTAGAAT | 121441 |
rs114853873 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931786 | TTCTGTTGATACTCT[A/G]CTGAATACACAGAAG | 121441 |
rs114854249 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951873 | AGAGAAATGATAGCT[C/G]AAAGTATATTAAACA | 121441 |
rs114936675 | snp | A/G | 0.0126979 | 0.078662 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953407 | AGGGATGTTAATGTG[A/G]TCTTTTCCTGACAGA | 121441 |
rs114938913 | snp | A/G | 0.000560276 | 0.0167279 | intron-variant, missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924874 | GTGATGATAGTGGAC[A/G]TCTTTATTTTGTCCC | 121441 |
rs115042864 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947955 | AGCCTCTGCCTGGGA[C/T]GCAGTGAAGACCCAG | 121441 |
rs115130239 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915371 | GAACGTGCAATGGGG[G/T]AAGGGCTAGAGGAAG | 121441 |
rs115330326 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909468 | GGCAGAGAGAAGGCC[A/G]GTGAAAAGAAAGAGG | 121441 |
rs115401195 | snp | C/T | 0.000197814 | 0.00994324 | missense | NEDD1 | GRCh38.p7 | 12:96937310 | TTGTCAGAGAAGCAC[C/T]TGCCACGTCCATTGC | 121441 |
rs115631209 | snp | G/T | 0.0107246 | 0.0724382 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953583 | TAATGTATATTAAAA[G/T]AGGTGGGATGAAATA | 121441 |
rs116042821 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931449 | TGCAAATTAGTATTT[A/T]AAAAATCTTCATAGC | 121441 |
rs116057209 | snp | A/G | 0.00408557 | 0.0450121 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944829 | CTGATGTTTGAAAGT[A/G]TTTGATTGAAAAATC | 121441 |
rs116242113 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942735 | AAATAAACATTTATC[A/G]TCTCATAATTTCTGT | 121441 |
rs116322130 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930843 | ATACATGCACACACA[C/T]GTACACATGCACTCA | 121441 |
rs116332402 | snp | C/T | 0.0520825 | 0.152737 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952501 | TAAAATGGCAATTGG[C/T]GTTTCTAAGCCATTG | 121441 |
rs116465712 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918805 | GTCATAGAAATTACA[C/T]TGGACCCCATGTTCT | 121441 |
rs116520904 | snp | C/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905664 | GAGGCCGCAGCATCA[C/G]TGAGGACAGAGGAAT | 121441 |
rs116630556 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924334 | AATTTTAGAATCAGC[G/T]TGCCCATTTCTAACA | 121441 |
rs116695984 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929627 | TATATATATATATTT[A/T]TTTTTTAATGGCTGC | 121441 |
rs117059376 | snp | A/C | 0.0126979 | 0.078662 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953524 | ATGGTGTATTTAAAT[A/C]TATTAATATTTTCCT | 121441 |
rs117089985 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926988 | CGAAAAAAAAAAAAA[A/T]TGTGTGTGTGTGTGT | 121441 |
rs117117309 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940036 | GTAGATGATCATGAG[A/T]CAGTCAATAGCAAAA | 121441 |
rs117217525 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940667 | TTCTCCATCCCTGGG[C/G]TGGTATCTTTTTCTT | 121441 |
rs117291911 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906705 | ACGCCTACTCTTTGG[A/G]TTATTTCTCAGCCTG | 121441 |
rs117663197 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937065 | ATTTAGAGGGAAACT[C/T]AGGTCTGCCAGCAAG | 121441 |
rs117666345 | snp | A/G | 0.0165278 | 0.0893908 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905538 | AGGCTTCTAACATTT[A/G]GCATCTATTGTTCGT | 121441 |
rs117878496 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933985 | TCCACTACCTGCAGG[G/T]ATTTGTGTTTAGAGA | 121441 |
rs117918845 | snp | C/T | 0.00580176 | 0.0535464 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937408 | GGTAAATGTTGCTTA[C/T]ATATTGTTGGAGGGT | 121441 |
rs118008596 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935935 | CAAGGGAAGGTCCCA[C/T]TGTCAGCCTTTATTA | 121441 |
rs118120574 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921467 | ATTACAGGTATGAGC[C/T]ACTGCACCCAGCCAG | 121441 |
rs137877242 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921873 | CTCCTGCCTCAGTCT[C/G]CCAAAGTGCTGGGAT | 121441 |
rs137964230 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933475 | CATTCATGTAGTTTA[G/T]TTTTTCTTGAATATG | 121441 |
rs138031125 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938464 | CAAAATAAAGATTCT[C/T]TCATTCACTGTAAAC | 121441 |
rs138059846 | snp | A/G | 6.61737e-05 | 0.00575174 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909845 | TGGTGGATAAATTCA[A/G]CCCACACACATCACC | 121441 |
rs138059932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919354 | CTCAGTGTCTCATGT[A/G]CTTCATTTATAAAAT | 121441 |
rs138081476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926385 | TTTTATTTCATTTTT[A/C]TTCAATAAGTTATAC | 121441 |
rs138232366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951053 | TTTGTGTCTTAATGA[C/T]AATTTCTATATAAAG | 121441 |
rs138280236 | in-del | -/TATC | 0.00557542 | 0.0525036 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911764 | TTCTCGCTATGGTAA[-/TATC]TATCTAGGTAGGAAT | 121441 |
rs138297518 | snp | A/G | 5.15619e-05 | 0.00507723 | missense | NEDD1 | GRCh38.p7 | 12:96944661 | AGTTGGTCACATCTG[A/G]TGCTGAAAGTGGAAA | 121441 |
rs138339183 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944301 | AGTACAAAAACATCT[A/T]TTGATTTATTTTGCA | 121441 |
rs138347006 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910241 | GTGGAAATAATTCCA[A/G]AAGGTTTTGGAATGA | 121441 |
rs138373842 | snp | A/C | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933041 | GCCATGTAGGTCCCA[A/C]GAACTTGAAGTAAGA | 121441 |
rs138392345 | in-del | -/GT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923850 | TGTATGCCTGTTTGC[-/GT]GTGTGTGTGTGTTTT | 121441 |
rs138406250 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914698 | TTAAAATTTTAGAGT[A/T]GAACTTTAAGTTCAT | 121441 |
rs138610076 | in-del | -/G | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909501 | GTTACATGGGGGCCA[-/G]GGACATGTAAGGCAG | 121441 |
rs138696171 | snp | C/T | 0.000401573 | 0.0141642 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96943726 | GTCTAAGAAAATATA[C/T]ATGGGAAAACAGGAA | 121441 |
rs138808248 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944885 | AGAAATAGAGTAATC[A/G]TAGACTAAAAATGTT | 121441 |
rs138823534 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905374 | TCAAAATTCTCTTAC[A/G]TTCACCTATACACTT | 121441 |
rs138991234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949009 | TTAGTTTTCTGCAGG[C/T]CTCCTCTCTTCAAGA | 121441 |
rs139111568 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953343 | ATAAAAACAGGAATA[C/T]TACTTTTACCCAGTG | 121441 |
rs139159493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913231 | CAGCTGATGGTAGCT[C/T]TCTGCTTCAGATTCT | 121441 |
rs139227251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917171 | TTAAAAAAAAACTTA[C/T]CCCATCGGTAAAATG | 121441 |
rs139230489 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939629 | TGGCAGACTTTAATC[A/T]AAATTTTTGAACCTC | 121441 |
rs139251179 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935437 | AGATGACATCTTAAT[A/G]ATTTCACATTTTAAT | 121441 |
rs139494296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922595 | ACATTAGGTTTGACT[A/G]TACCTTTTGGCCTAA | 121441 |
rs139533062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908332 | ATGGCTTATACTAGA[C/T]GTAGGTGTGCTGTTG | 121441 |
rs139568846 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942364 | ATGACTGTACTATAG[A/G]ATTATCTGTTCATAT | 121441 |
rs139724150 | snp | C/T | 0.000517732 | 0.016081 | intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907648 | CACTTGAGCTGTTGT[C/T]CTGCAAGTAAAGTGT | 121441 |
rs139753561 | snp | A/G | 0.000798403 | 0.0199641 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96945736 | TGGAGTTGCCAGTTC[A/G]CTCTCAGAAAAAATA | 121441 |
rs139789496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910830 | TGAAACTCATACGCT[A/G]TTTCTTAACAAATTA | 121441 |
rs139890132 | snp | A/T | 3.30338e-05 | 0.00406397 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936782 | ATCTGTGCAGTGTAT[A/T]GCATTTCAGTACTCC | 121441 |
rs139965273 | snp | A/C/T | 0.000776032 | 0.0196828 | synonymous-codon, missense | NEDD1 | GRCh38.p7 | 12:96936696 | GCTATTGGATCTTCC[A/C/T]GGGGGAAAATATATC | 121441 |
rs140058219 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936290 | GCCCCTGTTTGTGGC[A/G]TAATAGACAGTTCTG | 121441 |
rs140074862 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928402 | ATAAGTATGTATCTT[C/G]TGATTTTTGATTCTT | 121441 |
rs140210892 | in-del | -/TTA/TTATTA | 0.473451 | 0.112115 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916230 | GAAGCCGTTGAAGAT[-/TTA/TTATTA]TTATTATTATTATTA | 121441 |
rs140215753 | in-del | -/TT | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911274 | TATTTTTTGGTTGAC[-/TT]TTGTTTTAAGTTTTA | 121441 |
rs140240362 | snp | A/T | 0.000434717 | 0.0147367 | missense | NEDD1 | GRCh38.p7 | 12:96951975 | TTCTTTGCTGGAAAG[A/T]TACTCAGTGAATGAA | 121441 |
rs140288438 | snp | A/G | 0.000153988 | 0.00877328 | missense | NEDD1 | GRCh38.p7 | 12:96940516 | AGTAGTTTAGGTGAC[A/G]TGTTCTCACCTATCA | 121441 |
rs140342241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931614 | GTTTTAAAAAAGGAT[A/G]GTAATCAGAGTACTT | 121441 |
rs140446302 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925660 | CCTCTTCCTCACACC[A/G]GTATCTTTTAAAATT | 121441 |
rs140482567 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923657 | GTTGCCCATTTTTAT[G/T]TTGGGTTATTCGTGT | 121441 |
rs140495748 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906306 | TGCCACTCCCCCATG[A/G]ACCTCAGTAACTTGG | 121441 |
rs140554986 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943919 | ATACTTTGAAATCTC[G/T]CTTTGGATATGTTGA | 121441 |
rs140586470 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918330 | TTTTTTTGGAATTCT[A/G]CTTTTCATTATATTG | 121441 |
rs140663913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908834 | CTGTGTGCCAGGAAT[A/G]TTTCAAGACTCTGGT | 121441 |
rs140680808 | snp | C/T | 3.30622e-05 | 0.00406571 | missense | NEDD1 | GRCh38.p7 | 12:96934982 | TTTTTATAGTCTGTT[C/T]GGCACTTGAAGTACT | 121441 |
rs140732441 | snp | A/G | 0.000280244 | 0.011834 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937335 | CATTGCCACAGTTCT[A/G]CCACAACCTATGACA | 121441 |
rs140839320 | snp | A/G | 9.91129e-05 | 0.00703894 | missense | NEDD1 | GRCh38.p7 | 12:96943589 | CCGCAGTTGAACTCA[A/G]TGTTTCCTCCAAGAA | 121441 |
rs141085126 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932892 | TATGTAGATGAGAAC[A/G]CTGAGTTTTGGAGAG | 121441 |
rs141101403 | in-del | -/AATATGAAA | 0.499642 | 0.0133738 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918402 | TCTTAAAAAAGTTTT[-/AATATGAAA]AATATAAACATATTT | 121441 |
rs141115229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914023 | TTCAGTTCTAACCCA[C/T]AGATGTTGGAGACTG | 121441 |
rs141192311 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927405 | CTTTCTACAGGGGAA[A/G]AGAGCCTTGCTGCTT | 121441 |
rs141200505 | in-del | -/TT | 0.0785177 | 0.181917 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920925 | ATACAGGAAAAAGTC[-/TT]TTTTAAGTTTCATAT | 121441 |
rs141352387 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96954128 | TCGCACCACAGGAAA[G/T]GATTTAAAAAAATGC | 121441 |
rs141469417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948789 | TTTCTAGGACATCAG[C/T]TGAATGTCTGGAGTA | 121441 |
rs141565734 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934671 | GCCTCCCAAGTAGCT[A/G]TAATTACAGGCGCCT | 121441 |
rs141810465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915834 | AAACTGACATTCTGG[C/T]GGGGGACAGGCAGTA | 121441 |
rs141825006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920855 | GGAAGTAGTTTTTTT[A/G]AATTATTACTTGAAT | 121441 |
rs141847584 | snp | C/T | 0.00154212 | 0.0277251 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96940443 | CACAGACACTTTATC[C/T]AAGGAAACAGACAGT | 121441 |
rs141961331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947561 | TGCTGTCTATTTATT[A/G]CCCATTTATTCAACA | 121441 |
rs142089490 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945052 | TTAATATGGTAGAGA[G/T]AGAATTATTATGTAG | 121441 |
rs142104628 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943488 | GTTAATCTGCCTATC[A/G]TGTTAAATGCTTTTC | 121441 |
rs142139676 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913010 | TTAGGTAAAATAGTT[C/T]TGAATATAGGGGAAC | 121441 |
rs142175766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946253 | TCTGAATGTTTTCCA[A/G]TAGAATGCATCAGAA | 121441 |
rs142341448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923288 | AGCAGTGAATTGTCT[C/T]GTTTTAGCTGTTACA | 121441 |
rs142362184 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926489 | AGTGAGGAAAGACAG[C/T]TTTCATGATTTTACA | 121441 |
rs142378138 | snp | A/G | 0.0380574 | 0.132591 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917781 | AAAAATGGATATCTT[A/G]ATGCATTTAGAGTAC | 121441 |
rs142472316 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918786 | ACACTTGCCTCTTTA[A/T]AAAGTCATAGAAATT | 121441 |
rs142503770 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922044 | GAATATAGTATTGAT[G/T]TAAGACTGAATGTCA | 121441 |
rs142518711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908116 | TTGTTCCTTGACTTG[A/G]GAACCAAGGGGGCAC | 121441 |
rs142708932 | in-del | -/T | 0.0410537 | 0.137264 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952882 | ATTATTTCTATTTTC[-/T]TTTTTCCAAATAAGA | 121441 |
rs142810820 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910334 | GGCAGAAGCAAGTTG[A/G]GGAGGAGATAAAAAA | 121441 |
rs142830273 | in-del | -/AATT | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950196 | GATATTCAACTTCAC[-/AATT]AATCAGAGAACTAAA | 121441 |
rs143026492 | snp | A/G | 0.000153988 | 0.00877328 | missense | NEDD1 | GRCh38.p7 | 12:96935120 | GCTCCAGCGTCAGGC[A/G]TCTGTTTTTCTCCTG | 121441 |
rs143149300 | snp | C/T | 1.64977e-05 | 0.00287203 | missense | NEDD1 | GRCh38.p7 | 12:96937352 | CACAACCTATGACAT[C/T]AGCTATGGGGAAAGG | 121441 |
rs143496804 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933236 | AAACTTTATGAACTT[A/C/T]GAGAATCTACCAGGT | 121441 |
rs143499929 | snp | C/G | 1.65236e-05 | 0.00287429 | missense | NEDD1 | GRCh38.p7 | 12:96942612 | AGTGATGAGTCCATA[C/G]GCAAAGGAGATGGTA | 121441 |
rs143560922 | in-del | -/TACATTTTA | 0.084728 | 0.187577 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912109 | GAAGGTAAATAAAAT[-/TACATTTTA]TTTAAAAATTAAAAC | 121441 |
rs143562580 | in-del | -/CTCTCTCTCTCTCT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930212 | ACACACACACACACA[-/CTCTCTCTCTCTCT]CTCTCTCTCTCTCTC | 121441 |
rs143579860 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951702 | AGCCTTCTTTTTTCC[A/G]TGGCTTTCTTCCTGA | 121441 |
rs143679219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941783 | GCTATGTTTAAAAAT[A/G]TTACTAGCATTTGAG | 121441 |
rs143778712 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948527 | CCATTCTCAGCTCTC[A/G]GTTGAATTTAAAATA | 121441 |
rs143853915 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926565 | ATTTTTTTTTTTTTT[C/G]AAATTAGTTTTTTTT | 121441 |
rs143897198 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911802 | TTTGCATCATGTATC[A/G]TAATAAAATTACAGT | 121441 |
rs143899807 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915113 | AATGGTATCTGCAGG[A/C]GAATTACAGCAACTA | 121441 |
rs143967501 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929366 | TTGTATTTTTTTTTT[-/C]CTTAATGTCTTGTAT | 121441 |
rs144004755 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933829 | CCGCCTAGTAAATGA[C/T]AACATCAATACAAGT | 121441 |
rs144073178 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905794 | TTCTGAATCTACCAT[G/T]TATTAAACTTGTAAC | 121441 |
rs144108328 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936464 | TCAAATTCTGAAATT[A/G]TGCTTTAAACAAATA | 121441 |
rs144139862 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935905 | GTAGATCATGTGGAG[-/T]TATGAATGTTACTAC | 121441 |
rs144147794 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928776 | ACTGCAAGCTCCGCC[A/T]CCTGGGTTCACACCA | 121441 |
rs144154513 | snp | C/T | 0.00163827 | 0.0285736 | missense | NEDD1 | GRCh38.p7 | 12:96934977 | TTTCATTTTTATAGT[C/T]TGTTCGGCACTTGAA | 121441 |
rs144157309 | snp | A/G | 0.031825 | 0.122064 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947676 | CTGAGTGCTGGAGCA[A/G]CTCTGAAATCGCTGT | 121441 |
rs144224603 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952538 | AAAACATAGGGTTGG[C/T]TAGTAATTATTTTGT | 121441 |
rs144294186 | snp | C/T | 0.000135444 | 0.00822822 | missense | NEDD1 | GRCh38.p7 | 12:96944784 | CCCCAATCAATGGAT[C/T]CTCAACTCCAAGTAA | 121441 |
rs144422652 | snp | C/G | 0.0252911 | 0.109967 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913404 | TTTGAGATGGAGTCT[C/G]GCTCTGTTGCCCAGG | 121441 |
rs144557667 | snp | C/T | 0.000214644 | 0.0103574 | missense | NEDD1 | GRCh38.p7 | 12:96945773 | AGCATTGGAAATAAC[C/T]GGCAAAATGCACCAT | 121441 |
rs144564488 | snp | C/T | 0.0271762 | 0.113356 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906359 | GAAAAAATGCACTTA[C/T]TAGAATTTTCCAATT | 121441 |
rs144568275 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951328 | ATTATAGTAATTATT[A/G]ACATTCAGTAATTTG | 121441 |
rs144574993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923478 | GCTGGCTGTGAGATC[C/T]AGTTGCTCCACATTT | 121441 |
rs144771840 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922754 | AACAAAATCAAGATA[C/T]AGAACATTGCCAGCA | 121441 |
rs144840414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939952 | GGGAAGAAAAGTAAC[A/G]TTAATTGAATCCTGC | 121441 |
rs145054077 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943305 | TATTTTCACAAATAA[C/T]ATCTTTGAAGCCTTA | 121441 |
rs145143963 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926989 | GAAAAAAAAAAAAAT[A/T]GTGTGTGTGTGTGTG | 121441 |
rs145161026 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948958 | ATTGCTTAGAAGTCA[A/G]CAGATGTCTTGAGGG | 121441 |
rs145225409 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936887 | AAATTATATGTGGTC[-/A]AATTAAACAGTATAG | 121441 |
rs145290611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946434 | ATTGGTGCCTTTTTT[C/T]CTTTCTAACCTATAG | 121441 |
rs145378677 | snp | A/G | 0.0154538 | 0.0865337 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953727 | TCATTGTTGGCCAAA[A/G]TGATATGAGAGATTT | 121441 |
rs145407266 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932075 | TTCCCCCCACCTTTA[C/G]TGAGTGGTATGTTTT | 121441 |
rs145495750 | snp | A/G | 3.30218e-05 | 0.00406323 | missense | NEDD1 | GRCh38.p7 | 12:96936709 | CCCGGGGGAAAATAT[A/G]TCAATATGATTTAAG | 121441 |
rs145520438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947875 | TGCTGCCCTGTGCTG[C/T]ATGTCTGCACCTAGG | 121441 |
rs145556049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926366 | ATATTTGTTTTGTGT[A/G]CCATTTTATTTCATT | 121441 |
rs145621373 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950540 | AATGATATACAGATA[C/T]ATAAAACATGAATCT | 121441 |
rs145636369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942795 | GTACCTTTGCCTTCA[A/G]GTCTATCTTCCTGCT | 121441 |
rs145647212 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922968 | AAAAATATAAAGAAA[C/T]TCACCAGGCATGGTG | 121441 |
rs145733461 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914197 | TCTTTGGATCTTTGT[A/G]TCCTAAGATGTTCAA | 121441 |
rs145751989 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908871 | AGACAGACATTATAA[G/T]AACAAATAAAAATTT | 121441 |
rs145866211 | snp | C/T | 0.00390147 | 0.0439945 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96943708 | CCGTGATCTAACAGC[C/T]GAGTCTAAGAAAATA | 121441 |
rs145947210 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918047 | GTGTGGTCATCAGGG[-/A]ATCTTTCCTTAGGGC | 121441 |
rs146012004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942263 | TCACAAAGCTATTAA[G/T]TGGTATAGGCAGAAC | 121441 |
rs146051503 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941121 | AGCAATATTAATAAC[A/G]TGGATACATTTCTAG | 121441 |
rs146072419 | snp | C/T | 1.65789e-05 | 0.0028791 | missense | NEDD1 | GRCh38.p7 | 12:96944706 | CATCATCTAACCAAA[C/T]AAGAAATTCTGAGAA | 121441 |
rs146135363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917405 | TGAATGCAAATCTAT[C/T]TGATTTCCTTGAAGC | 121441 |
rs146173796 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917053 | ATGGTGTCTTTACAG[A/T]GATGGGGAACAGTTG | 121441 |
rs146192348 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921357 | CAGCTAATTTTTGTA[C/T]TTTAGTAGAGATGGG | 121441 |
rs146252155 | in-del | -/A | 0.0850919 | 0.187897 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945062 | AGAGATAGAATTATT[-/A]TGTAGGACCCTTTGA | 121441 |
rs146280315 | in-del | -/AA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935839 | CTAAAAAACAAAAAC[-/AA]AAAAACAAAAGAATG | 121441 |
rs146407974 | in-del | -/TA | 0.0185938 | 0.0946107 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945487 | CAGTTTATATATATA[-/TA]GATAAATGACTATTA | 121441 |
rs146521457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932829 | CTGTACAGAAATGCT[A/G]TTTAATCCTCAAAAT | 121441 |
rs146536976 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918994 | TGTAATATAAGTGGA[A/C]TATCATAGCTATTAT | 121441 |
rs146599403 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913866 | ATTATGAATTGTCAT[A/T]ATTTTACACACTGGG | 121441 |
rs146651626 | snp | A/T | 1.6504e-05 | 0.00287258 | missense | NEDD1 | GRCh38.p7 | 12:96945822 | GTTTTATTCAGAACA[A/T]GATACAGGAAACGTT | 121441 |
rs146696807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913114 | GCTGCTATTTTAGGA[C/T]GATATCCCACATAGG | 121441 |
rs146832162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939122 | TATTTTAAGCTTTGT[A/G]TAAAATTAAAGTTCA | 121441 |
rs146860196 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908595 | TGTGAAATCACCTTG[G/T]TAGAATTACGTGTTT | 121441 |
rs147061088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909987 | CTTTTGCATGTGCCT[C/T]ATACTGAGTAATGTG | 121441 |
rs147069264 | in-del | -/GTAT | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931755 | GCTGTTTATAATGAA[-/GTAT]GTATGATTCCAGGTT | 121441 |
rs147290580 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933977 | AGAATATCTCCACTA[A/C]CTGCAGGGATTTGTG | 121441 |
rs147431717 | snp | C/G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906431 | GTTCAGAAACACACC[C/G/T]CATGTAGTTGTGATG | 121441 |
rs147455751 | snp | A/G | 0.00151464 | 0.0274777 | missense | NEDD1 | GRCh38.p7 | 12:96944642 | TTAAATATAAAGTTA[A/G]CAAAGTTGGTCACAT | 121441 |
rs147465310 | snp | C/G | 4.97418e-05 | 0.00498682 | missense | NEDD1 | GRCh38.p7 | 12:96936627 | CTAGTGAAAACTTTA[C/G]TGGCTGACACTCCTC | 121441 |
rs147557583 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943339 | CTCTGGGAGATGGAT[A/G]TCATCATTTACATTT | 121441 |
rs147574073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947554 | TAATGGGTGCTGTCT[A/G]TTTATTACCCATTTA | 121441 |
rs147992304 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941747 | AAATGAATAAATTAC[-/T]TTTTTTCTTTAATTA | 121441 |
rs148023951 | snp | C/T | 0.000677949 | 0.0183988 | missense | NEDD1 | GRCh38.p7 | 12:96943575 | GCTTTGACTTTCTAC[C/T]GCAGTTGAACTCAGT | 121441 |
rs148030645 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915738 | GTGACACTCAAAGAT[A/G]CTCACTGAGAAGAAC | 121441 |
rs148135973 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948604 | GAAATTATACTTTTG[A/C]ACCAACCTAATACAT | 121441 |
rs148226206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927303 | GAATTGTATATATTG[A/G]AATAAGATTTCCTGA | 121441 |
rs148294738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909647 | CACTGTTTGGAACAA[A/T]AATGAATGAGTTAGA | 121441 |
rs148453961 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951594 | TATTTTAGTTGTTTT[C/G]TTTAGTTTCTAAGAT | 121441 |
rs148542228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930841 | ACATACATGCACACA[C/G]ACGTACACATGCACT | 121441 |
rs148593109 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922845 | TATGTGGGCCAGACG[C/T]GGTGGCTACCTGTAA | 121441 |
rs148610093 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912540 | TCTTCCCTGCAGTAG[C/T]AGCAAAGAGAATTAG | 121441 |
rs148769567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917525 | TATTTAATTTAACCA[A/G]TATTTATCATATGCT | 121441 |
rs148894729 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942942 | TTCTTTATATATGGG[A/G]CAGCCAACAACATGG | 121441 |
rs148929499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914247 | ATCAAAACAATTTCA[A/G]CTTCTACTCTACCAC | 121441 |
rs149087331 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919808 | ATAATCTCTCTCTCT[C/T]GTAAAGTGCCTGGAC | 121441 |
rs149210002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909612 | TTTTAGGAAAATCAC[C/T]TCAACTGCTTTGGTG | 121441 |
rs149282432 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933190 | TGTTTTAAGGATGTT[A/G]TAGGAAAATTCCTGC | 121441 |
rs149370678 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905655 | AGATTTGATGAGGCC[A/G]CAGCATCAGTGAGGA | 121441 |
rs149443078 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939651 | TTGAACCTCTAAAAC[A/T]GTCGTTACTCCAGTA | 121441 |
rs149524438 | snp | C/T | 0.000945658 | 0.0217241 | synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917635 | GCAAAAGCAGACATG[C/T]GTCAATTTAAATTCT | 121441 |
rs149530944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911340 | AGTCTAACAACAAAA[A/C]TGATGTAGCTATGAG | 121441 |
rs149577441 | snp | A/C | 0.000199498 | 0.00998545 | missense | NEDD1 | GRCh38.p7 | 12:96944690 | AATCTAAATACCTCT[A/C]CATCATCTAACCAAA | 121441 |
rs149583688 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951321 | TTTTATTATTATAGT[A/C]ATTATTAACATTCAG | 121441 |
rs149689333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908508 | CACTTATCGTTCATT[A/G]CTACCTGTTGCTCTT | 121441 |
rs149707195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942677 | AGTGAATTGTATTAT[C/T]TATGCTGTGTAACAA | 121441 |
rs149829081 | snp | C/G/T | 0.00597694 | 0.0544006 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922606 | GACTATACCTTTTGG[C/G/T]CTAATTTTGTGTAAA | 121441 |
rs149842178 | snp | A/G | 1.6504e-05 | 0.00287258 | missense | NEDD1 | GRCh38.p7 | 12:96937267 | GTTAATGTGAATGCT[A/G]CTAGTGGAGGAGTTC | 121441 |
rs149896388 | snp | C/T | 5.01383e-05 | 0.00500666 | missense | NEDD1 | GRCh38.p7 | 12:96952007 | GTTTAGTGGCTGAAA[C/T]TGAAAGACTACGAGA | 121441 |
rs149902497 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953554 | TGTTGCTTTTTTAAA[A/C]AAATAAATACACATA | 121441 |
rs149970974 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935461 | TTTTAATTTTAGCAT[A/C]TTTTCCACAATATGA | 121441 |
rs150147171 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924719 | CTTTTGAAAGAATTT[A/G]TAGTATTTACAGTTT | 121441 |
rs150160326 | snp | A/G/T | 0.000181565 | 0.00952624 | missense | NEDD1 | GRCh38.p7 | 12:96943607 | TTTCCTCCAAGAAAA[A/G/T]ATCCAGTAACTTCAA | 121441 |
rs150268546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914118 | AGCAGAATCAAGGCA[C/T]AGAATGTCTCTGGTC | 121441 |
rs150286959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938086 | TATATCCATGTCTTT[A/T]AAATTTTTCAGGATA | 121441 |
rs150446438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944243 | TATGTCTGTATTTTC[A/G]TATTTATTGTTTAGA | 121441 |
rs150536570 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922384 | TCAAATATCTTTTTT[A/C]AGGACATAGAGTAAC | 121441 |
rs150570331 | in-del | -/G | 0.029116 | 0.117091 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908421 | TTTCCATACTAGGAA[-/G]GTGTGGGAGGTATAA | 121441 |
rs150588602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915901 | TATCATGCAGATAAC[C/T]AAAATAAGATATTGT | 121441 |
rs150681746 | in-del | -/TTG | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933137 | ACAGTGGTAAGCTCC[-/TTG]TTGTTTGATAGATGC | 121441 |
rs150764904 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946308 | TCTTTCTCAGACTTA[C/T]CCTTGTCTGTCTCAT | 121441 |
rs150834909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935333 | TGTACAGTTGATGGA[C/T]CTAGTAAGAAAGAAT | 121441 |
rs150887088 | snp | G/T | 1.65575e-05 | 0.00287724 | missense | NEDD1 | GRCh38.p7 | 12:96945723 | CTTCTGTCACTGCTG[G/T]AGTTGCCAGTTCACT | 121441 |
rs151076741 | snp | A/G | 1.65059e-05 | 0.00287275 | missense | NEDD1 | GRCh38.p7 | 12:96936741 | ATGTTGAAATCACCA[A/G]TTAAGACCATCAGTG | 121441 |
rs151137222 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952791 | TTAGTAACATGCAAC[A/G]TTGTACTGCAAAATT | 121441 |
rs151155751 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937585 | TATTAATTTCAAAAA[C/T]GATAAAAGGCCCTTA | 121441 |
rs151207457 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931355 | CTTCTGACAAAAAGC[A/G]AGGCAAAAATTCACA | 121441 |
rs151277457 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923552 | TGGTTATGTAGTGCT[G/T]TCTCATGGTGGTTTT | 121441 |
rs151328270 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918203 | TGTTTGTATTTTTAA[C/T]TTGGTAATATTTTGT | 121441 |
rs180797463 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940093 | AGAGCAGCAAAGTAT[A/G]TAAATTATTTTAGAA | 121441 |
rs180840556 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916073 | CTTGAGGCAAATATA[G/T]GGTTGTATATTTAAG | 121441 |
rs180934258 | snp | A/C/G | 0.000549016 | 0.0165592 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934972 | TATTCTTTCATTTTT[A/C/G]TAGTCTGTTCGGCAC | 121441 |
rs180946474 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909142 | GATCACACCATTGCA[C/T]TCCAGCCTGGACAAC | 121441 |
rs180961978 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922919 | CAGGAGTTCAAGACC[A/C]CCTTGGGCAATGTGG | 121441 |
rs181089020 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913726 | TAATACTGGCTTCTT[C/T]ATTTCTAGTCACACA | 121441 |
rs181105493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939792 | TGTCTACCTTACTAT[G/T]CTTTATGAGTTTGGT | 121441 |
rs181464568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945070 | AATTATTATGTAGGA[C/T]CCTTTGAAAAGGGTT | 121441 |
rs181465733 | snp | C/T | 0.0006003 | 0.0173144 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951389 | ATGACCTAGAATTGG[C/T]TAAACTATTGTAATT | 121441 |
rs181593308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950011 | ATATTTGAGCACATT[A/G]ATAAGAACTATTTAT | 121441 |
rs181595482 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928446 | CAAGTTCTCTTTCAA[A/T]GTAATTTAGTAGCAG | 121441 |
rs181597702 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916705 | ATTGTGAGTAATGCC[A/G]CAATAAACATACGTG | 121441 |
rs181604167 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927366 | GCTGAATTAAAGTTA[C/T]TAGCTTTATGTGGAT | 121441 |
rs181680400 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934454 | CCACTGAATGACACC[A/G]TGGTTGTCATGATTG | 121441 |
rs181722996 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923202 | CATGGAATAGTAGTT[A/C]ATACTGTATTAATTC | 121441 |
rs181791154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908910 | GGCTGGGCACGGTGG[C/T]TCACGCCTGTGGTCC | 121441 |
rs182038373 | snp | A/T | 1.66832e-05 | 0.00288814 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940545 | CAGAGATGGTAAGTC[A/T]GTTCAGAGGATCCTG | 121441 |
rs182178105 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952195 | ATGGGATTTTATACC[A/G]ACAACTGTTTCATCT | 121441 |
rs182193565 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929294 | AATTTCTAATTCTTT[C/G]CCAAGTTCTGACATC | 121441 |
rs182224477 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912188 | TATTTGCAAGTTACT[G/T]TAATAGTCATTCTTA | 121441 |
rs182232139 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937841 | GTAATTGGCGAAACA[A/G]TTCTGAAACAGGATT | 121441 |
rs182463692 | snp | C/T | 3.31428e-05 | 0.00407066 | missense | NEDD1 | GRCh38.p7 | 12:96943694 | GAGGAAAATGAAAAC[C/T]GTGATCTAACAGCTG | 121441 |
rs182581128 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936218 | GTCCTCATGAGGCCT[A/G]AGCAGGTCAATAAAT | 121441 |
rs182631111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924263 | GTAGCTTTATGGTAG[A/G]TCGTGATATTTTTAA | 121441 |
rs182680156 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942179 | CAATTTTGTGAGCTT[A/C]TCTGGACATTATCCC | 121441 |
rs182693851 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917801 | ATTTAGAGTACTTAC[C/G]AAGCTTTTATTTTTG | 121441 |
rs182738113 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919916 | TAATGTATGGTATTT[A/G]CAGAAACATGAAAAT | 121441 |
rs182815091 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910826 | TTTGTGAAACTCATA[C/T]GCTATTTCTTAACAA | 121441 |
rs182892859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946712 | AGTGTGTTCTGCCAT[C/G]TGTGTTTCTCTTAAT | 121441 |
rs182927485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947738 | GGCTGGAGCTTGTTT[A/T]TCACTATCTAACCTG | 121441 |
rs183061876 | snp | G/T | 0.00398564 | 0.0444627 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953835 | CCTAAGAAACTCAAT[G/T]AACCTCAAACACAAG | 121441 |
rs183420461 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931894 | TGGATGGTTTTTCTT[C/G]TTTGTGATAAAAAAA | 121441 |
rs183485319 | snp | A/C/G/T | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930557 | GGTTTTTATTGGGGG[A/C/G/T]GCTGGTTATATCTAG | 121441 |
rs183531621 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906958 | ACCATCACTGTACAC[G/T]CAAGAGTCTAGCACA | 121441 |
rs183545091 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924607 | TTATTTTCCTATTCT[A/T]TGTGGCTTGTAGAGA | 121441 |
rs183548487 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947346 | TCTGTGGGGGCAGAT[A/T]TAGAAAGGTACACTG | 121441 |
rs183562482 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925014 | TTACTATTTATGTTG[G/T]AAGTTTTACATCATT | 121441 |
rs184086048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910258 | AGGTTTTGGAATGAG[G/T]TTTTGCATCTACATT | 121441 |
rs184161487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915359 | TTTATAGTATTTGAA[C/T]GTGCAATGGGGGAAG | 121441 |
rs184163511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944391 | CTATTTTAAATGATA[C/T]TTAACAGCAGGTGCT | 121441 |
rs184175621 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939902 | CTCCCACTGTTAGTG[A/G]AAGAAAAGACAGAAA | 121441 |
rs184287597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944104 | AACTGATGGTGCTGA[A/G]AATGGAATTTATCAT | 121441 |
rs184297627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922846 | ATGTGGGCCAGACGC[A/G]GTGGCTACCTGTAAT | 121441 |
rs184323651 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923134 | AAGAAAAAAAAAAGC[A/G]AGGAATCATATGTGT | 121441 |
rs184350170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925720 | TTGAAAGGATTTTCA[C/T]TGATAACTGCACAGG | 121441 |
rs184406829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939071 | ACACTATGGTGTTGA[C/T]ACTATCATTGTGGTC | 121441 |
rs184424756 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913357 | ATGAAGCTCTCACTA[A/C/T]GTACTGTTGCCTTAT | 121441 |
rs184486541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948268 | TTTTACATGAGCGCT[A/G]AATGAAGGCTTGTGG | 121441 |
rs184548813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921681 | TTTTTTTTCTTTCTT[A/G]GAGAGTCTTACTCTA | 121441 |
rs184556594 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943870 | GCTATGCACTTATTC[A/C/G]TAAGTCTTGATGTCA | 121441 |
rs184803194 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949261 | ATGGTTCCCTGATAC[A/C]GTGTTTTTGTTTGTT | 121441 |
rs184815480 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926169 | TACCTTTTGTGATTT[A/C]CTTCTCTAAAATGGT | 121441 |
rs185000933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934721 | TTTTGTATTTTTAAT[A/G]AAGATGGGGTTTCAC | 121441 |
rs185155302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909289 | TAAGGAAGGGACTGC[A/G]TTAGCCAGGGTGGTC | 121441 |
rs185161765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935246 | ATTTAGTAACAAATA[G/T]CTATTATTCCATTAA | 121441 |
rs185286202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908838 | GTGCCAGGAATGTTT[C/G]AAGACTCTGGTGTGG | 121441 |
rs185544374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933128 | GTGTTAAAGACAGTG[A/G]TAAGCTCCTTGTTGT | 121441 |
rs185696577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916972 | TTAGAGAGCTTACTG[A/G]TAGATTGGAGGGGAG | 121441 |
rs185705260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941059 | TCTTTTTGGTACTAA[C/T]ATCCATAATGTTTTT | 121441 |
rs185712551 | snp | A/T | 0.0102689 | 0.0709155 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912848 | TTTTTTTAAACTTTT[A/T]AAAATCTTAGTTTTG | 121441 |
rs185775339 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946807 | TTTGTTCGTGTAATA[A/G]CAGCCAAAATAAAGT | 121441 |
rs185823981 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938875 | CCTCTGAAACATTGA[G/T]AATAGTAGACTCAGT | 121441 |
rs185834446 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908947 | TTTGGGAGGCTGAGG[C/G]GGGCAGATCACCTGA | 121441 |
rs185901243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924288 | TTTTAAGTTCACTTT[C/G]ACTACTATGGGCCTT | 121441 |
rs186236906 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923373 | ATTTATTTTGAGTAA[A/G]TACTTAGGAGTGGAA | 121441 |
rs186242918 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96944695 | AAATACCTCTCCATC[A/G]TCTAACCAAACAAGA | 121441 |
rs186317044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928474 | CAGGCTTACATTTCC[C/T]TTAAGGAGCTTAAGT | 121441 |
rs186462738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912656 | GCTTTTATAATCGCA[A/G]TTCTTATAATAGTCT | 121441 |
rs186469461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938078 | GAAATACATATATCC[A/G]TGTCTTTTAAATTTT | 121441 |
rs186475016 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923827 | GTGTGTGTGTGTGTG[C/T]GTGAAACTGTATGCC | 121441 |
rs186499238 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952198 | GGATTTTATACCAAC[A/T]ACTGTTTCATCTTAA | 121441 |
rs186511312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930064 | CTCAGCATGTGTTTG[A/G]GGGTTCATGGGGATA | 121441 |
rs186511529 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951636 | TTTATAGACTAAATA[A/G]GTAAAATAGATTTTA | 121441 |
rs186584978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950287 | ATACTAAGTCTTGAT[A/G]ATATAGAGCAAGAAG | 121441 |
rs186836182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927803 | ATCTATTCTAAATTG[A/G]TTTATTTCATTGACT | 121441 |
rs186941281 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931911 | TTGTGATAAAAAAAA[A/T]TTTTTTCTATTAAAT | 121441 |
rs186953905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942830 | TCAGGATGTCAACCA[G/T]AGCTTCATTCAACTT | 121441 |
rs186961599 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905831 | CAAGTTACTTAACCT[C/G]TATTTCCTCATATGT | 121441 |
rs187087419 | snp | G/T | | | missense | NEDD1 | GRCh38.p7 | 12:96937354 | CAACCTATGACATCA[G/T]CTATGGGGAAAGGAA | 121441 |
rs187099198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911238 | ACTATATAAGAGAAA[A/G]GTAGCAATTTGTAGT | 121441 |
rs187144325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936410 | AGATGGAATGTTTAG[C/T]AGTTCTCTATATGCC | 121441 |
rs187328152 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916127 | AGAATTAGTGGATGA[A/G]GAAGAAAATGGTAAC | 121441 |
rs187358080 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910583 | GAACCCTGTGCTATT[A/G]ACTTTTTGGGGCAGA | 121441 |
rs187577561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940161 | ATGAACAAATAAGCT[G/T]TTTTCTTTTGAGGAA | 121441 |
rs187673235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922038 | AAATATGAATATAGT[A/G]TTGATGTAAGACTGA | 121441 |
rs187682643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943926 | GAAATCTCGCTTTGG[A/G]TATGTTGAAGGTTAC | 121441 |
rs187821692 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947457 | GAGAAGGCACCGTGG[C/T]AAGAGACCAGGCCTG | 121441 |
rs187837907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, splice-acceptor-variant | NEDD1 | GRCh38.p7 | 12:96924832 | TTATTGCGTTGACTA[C/G]GCTCTCCAATCCAGT | 121441 |
rs188053806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925202 | GGAAAAGCATTTTAA[A/G]GGAAATGATGTCTCA | 121441 |
rs188183814 | snp | C/T | 0.00557542 | 0.0525036 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953948 | TAGAGAAAAAACACA[C/T]AGAAGGACAGAGAGA | 121441 |
rs188217427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917818 | AGCTTTTATTTTTGA[A/G]CTTTTATGATAAAAA | 121441 |
rs188317655 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948105 | CTCAGCCATCCTCCC[A/G]TGGCTGCCATCTTCT | 121441 |
rs188326011 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925992 | TCTCAAGCCTCCTTT[A/T]CCTTATCTTTCAAGT | 121441 |
rs188485178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930870 | CTCACAGTATTGACG[A/G]TCATTCAGAAACTCT | 121441 |
rs188586091 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909021 | GTCTCTACTAAAAAT[A/G]CAAAATTAGCCGGGT | 121441 |
rs188693715 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938978 | TGTACACATTTAAGA[A/T]GACATTTAACTGTTA | 121441 |
rs188717002 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913589 | ATGTTGGCCAGGCTG[A/G]TCTTGAACTCCTGAC | 121441 |
rs188721318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939517 | ATGCAGGCTGTTCTT[C/T]GTTTTCATCTCAGAC | 121441 |
rs188862384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920296 | TCATACTAGATTATG[G/T]TGCTTATATAAATTT | 121441 |
rs188986075 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912926 | TTTTTAAAAGCATTA[A/T]TTTTAACTTAAGCTC | 121441 |
rs189070907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944877 | TGTAAAGGAGAAATA[C/G]AGTAATCATAGACTA | 121441 |
rs189125682 | snp | A/C | 3.45644e-05 | 0.00415704 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96943753 | GGAATCTAAAGACTC[A/C]TTCAAACAGGTATTT | 121441 |
rs189222275 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949736 | TAAGCTGGAAAGAAA[A/C]CTATGCATATATGGA | 121441 |
rs189236821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926326 | GTCTGTTGGTTTTTT[C/T]CCCCTTTCCCTGGAA | 121441 |
rs189339021 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915611 | TGAAGAATCCAAGGA[C/T]GCACTGTGGAAGTTC | 121441 |
rs189360500 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948575 | ATCAGGTTTGTTTTC[A/G]TTATTAGAGTTGAGA | 121441 |
rs189376392 | snp | G/T | 0.00914312 | 0.0669923 | utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96907512 | CGCGCACCTCCCGGA[G/T]CCTTGTGGGGTGTGC | 121441 |
rs189384226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932218 | ATAAGCTTCTTGATT[G/T]AATTCTTTTCTTATA | 121441 |
rs189475296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944227 | CCAGTTGGGTATACA[A/G]TATGTCTGTATTTTC | 121441 |
rs189605974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939973 | TGAATCCTGCTGTAT[G/T]TTAGGCATCGCTCTA | 121441 |
rs189607377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927931 | ATAAAATGTTTATAT[A/G]ATAACATTTCTTTGA | 121441 |
rs189767264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922878 | TCAGCACTTTGGGAG[G/T]CTGAGGCAGGCAGAT | 121441 |
rs189836538 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924519 | GTAGAGGGCTTGCAT[A/T]TCTTTTAGTAGATTT | 121441 |
rs189864495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951012 | TTCTAACCTAGTGAA[C/T]TTTCTGTATTTCATT | 121441 |
rs189966449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937502 | CATAGAACTCAAATT[C/T]ATTTGAGTACTTAGG | 121441 |
rs189981411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911614 | GTTCCTCACTTTCTC[A/G]TGATTTCTAAAACTA | 121441 |
rs189990316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928628 | TAATTTTTCTAGAAT[A/G]TGTCTTGATGTTGGT | 121441 |
rs190105600 | snp | A/G | 1.65203e-05 | 0.002874 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917715 | GGGATTTAAAATCAA[A/G]AAGAGTTCATCGATC | 121441 |
rs190117769 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941301 | TTGTTTCATCCACTC[A/G]TTATCTTATACAATT | 121441 |
rs190164837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908849 | GTTTCAAGACTCTGG[C/T]GTGGGGAGACAGACA | 121441 |
rs190399960 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933760 | ACATTTTAGAATTAA[A/G]TAGAATATAAATTCA | 121441 |
rs190435809 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923141 | AAAAAAGCAAGGAAT[C/T]ATATGTGTCTGGTTT | 121441 |
rs190651137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923610 | GTTAAGTATATTTTT[A/G]TATGCCTCTTGTGAA | 121441 |
rs190669150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944542 | CATTTCTATTAACCT[A/G]CATACTGGGACAAAA | 121441 |
rs190888033 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952642 | ACAAATTACATGATA[C/T]CTTTTGCATTTATGT | 121441 |
rs190903940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930298 | ATTTGGTCATTCTCT[A/G]GGAGAACTCACAGGA | 121441 |
rs190912330 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918292 | GAAAATAAAAATATT[C/T]AGCACAAGAAAGTCT | 121441 |
rs191027203 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947295 | TAATACAGTGTGAGC[A/C]AAGTGATGTTGAAAT | 121441 |
rs191048557 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946163 | AATTGGGTTCTTAAC[C/G]TGCAGTATGTTCATA | 121441 |
rs191056574 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935459 | CATTTTAATTTTAGC[A/G]TCTTTTCCACAATAT | 121441 |
rs191144112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943125 | CCAAGCCACGTTCAA[A/G]GGGAGGAGATTACCC | 121441 |
rs191220896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948612 | ACTTTTGCACCAACC[G/T]AATACATCCTAAGTG | 121441 |
rs191237520 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926112 | AGGTCAGTGGATGTT[A/T]GCTATTACTGTGAGC | 121441 |
rs191311738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924216 | TATTTTGTTCCGTTG[A/G]TCTAGTTTGACTGTT | 121441 |
rs191388940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932145 | ACATTCTTACACAAT[A/C]ATGTGGTATAAGAAA | 121441 |
rs191399281 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906427 | CCTAGTTCAGAAACA[C/G]ACCCCATGTAGTTGT | 121441 |
rs191734575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910635 | TGTATGTTGTACCAC[G/T]TGGAGGTTTATTGGT | 121441 |
rs191865441 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940188 | GGAACCTTTTGTTCC[A/G]TGAAAATCCTGGTTA | 121441 |
rs192012104 | snp | C/T | 0.000167479 | 0.00914939 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936605 | ACTTTGTTCTCCTTT[C/T]CAAAGGCTAGTGAAA | 121441 |
rs192107702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944100 | AGCAAACTGATGGTG[C/T]TGAGAATGGAATTTA | 121441 |
rs192125097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922649 | TTTAAAACAATTGAG[A/G]TGTAACTTACAATAA | 121441 |
rs192185270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916239 | TGAAGATTTATTATT[A/T]TTATTATTATTATTA | 121441 |
rs192262883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947622 | CAGATGATTTGAGGA[C/G]AGTGGGCTCAGGGCC | 121441 |
rs192280414 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, synonymous-codon | NEDD1 | GRCh38.p7 | 12:96924942 | TGATAGTCATTGTAA[A/G]GTTTGTTTTGTAGAT | 121441 |
rs192281343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938352 | TCTACTTAAGGAAGA[A/T]ATTATTTTTGAAATA | 121441 |
rs192311114 | snp | A/G | 0.00065005 | 0.0180167 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909918 | TTAAAAAAAAAAAAC[A/G]CACACACACACACAC | 121441 |
rs192403904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921193 | TTGCTTGTTTGTTTG[G/T]TTTTTTGAGGCGGAG | 121441 |
rs192554506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948264 | CTTTTTTTACATGAG[C/T]GCTGAATGAAGGCTT | 121441 |
rs192704375 | snp | C/T | 0.00028029 | 0.011835 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912754 | AGCATCTTCCAGTGG[C/T]GACAAAATAGTTGTC | 121441 |
rs192756029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944318 | TGATTTATTTTGCAA[A/G]TATTATTGACTGGTT | 121441 |
rs192837936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925338 | CAGCATAGAATGCTT[A/G]CCACCATTTATTGTG | 121441 |
rs192892120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931203 | CTTACTGCTTTATAG[G/T]GCCTAGTAAGAAAAT | 121441 |
rs192958583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913174 | TAATGACACAGCACT[A/G]CTTTACTGATCTTGG | 121441 |
rs193016929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908563 | CTTTGCCTTCTGTTT[C/T]CTAGACTTCCTTGGT | 121441 |
rs193024891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943839 | TGCCAGTGCATGTAT[C/T]CTAATTATTAGCATT | 121441 |
rs193144485 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953989 | ACACTGGAGCAACAT[C/T]TTTAAAGTACTGAAA | 121441 |
rs193177473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939029 | TAAAATGTATTGGAA[A/G]TACCTGGCACATGGT | 121441 |
rs193212695 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932803 | TGGTGATGGCTACTG[G/T]GTACCTGATTCTGTA | 121441 |
rs199518242 | snp | C/T | 3.30404e-05 | 0.00406437 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96942602 | TAACAAGGGAAGTGA[C/T]GAGTCCATAGGCAAA | 121441 |
rs199556266 | snp | A/C | 0.0483689 | 0.1478 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909913 | ATCCTTTAAAAAAAA[A/C]AAACACACACACACA | 121441 |
rs199614751 | in-del | -/CTTAATGTCTTGTATTTTTTTTTTC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929342 | ATTTATGTTTTTTTT[-/CTTAATGTCTTGTATTTTTTTTTTC]CTTAATGTCTTGTAT | 121441 |
rs199642694 | in-del | -/A | 0.0429648 | 0.14013 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919310 | TGTCACTTAGCAGTT[-/A]ACGTGAGCTTGCGCA | 121441 |
rs199729117 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909916 | CTTTAAAAAAAAAAA[A/C]CACACACACACACAC | 121441 |
rs199732274 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938830 | TCTCATTCTCTCTCT[C/T]TCTCTCACACACACA | 121441 |
rs199782850 | in-del | -/GACACAC | 0.0520825 | 0.152737 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929772 | CTCTGACCTGAGAGG[-/GACACAC]TTTGGCTGGTCAGTT | 121441 |
rs199796284 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949413 | TTGTAGAAAAACATT[-/A]AAAATTTTTTTTGTT | 121441 |
rs199799857 | snp | A/C | 0.00582401 | 0.0536478 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909917 | TTTAAAAAAAAAAAA[A/C]ACACACACACACACA | 121441 |
rs199862948 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936392 | GAAGTGAATAGAAAA[A/G]TAAGATGGAATGTTT | 121441 |
rs199889686 | snp | C/T | 6.59196e-05 | 0.00574068 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96935023 | GAAATCACTACTGGG[C/T]AGTGTTTCGGATAAT | 121441 |
rs199926276 | in-del | -/ATG | 0.0414363 | 0.137845 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916775 | GGTATGGAAGGAGAC[-/ATG]ATCTGATTTACATTT | 121441 |
rs200008061 | snp | A/G | 0.00199792 | 0.0315431 | missense | NEDD1 | GRCh38.p7 | 12:96937348 | CTACCACAACCTATG[A/G]CATCAGCTATGGGGA | 121441 |
rs200042769 | in-del | -/TACT | 0.0232847 | 0.105357 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946274 | TGCATCAGAATGTAA[-/TACT]TAATCTAAAAAAAAT | 121441 |
rs200067303 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915808 | GCATGGATATGGGCC[C/T]TGTGCTAGTGAAACT | 121441 |
rs200076088 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934944 | TTATGAATGCTTATA[A/T]TTACATAAAATTTAT | 121441 |
rs200081942 | snp | A/G | 6.6246e-05 | 0.00575488 | missense | NEDD1 | GRCh38.p7 | 12:96951436 | ATTCTTCCTAGAGAA[A/G]CATGCCATAGGGACA | 121441 |
rs200098098 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906112 | ATTTAATTAATTGCC[C/T]TTTTTGTTTGAAGTT | 121441 |
rs200101373 | snp | A/G/T | 9.95808e-05 | 0.0070556 | missense | NEDD1 | GRCh38.p7 | 12:96944750 | GAGAATGAAATTGAA[A/G/T]CCCAGTTGATATGTG | 121441 |
rs200102327 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929367 | TGTATTTTTTTTTTC[C/T]TTAATGTCTTGTATT | 121441 |
rs200130884 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921678 | TTTTTTTTTTTCTTT[C/T]TTAGAGAGTCTTACT | 121441 |
rs200183138 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938831 | CTCATTCTCTCTCTC[A/T]CTCTCACACACACAC | 121441 |
rs200217415 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923350 | CTTTTTTTAAGATAC[A/G]TGTTTTTATTTATTT | 121441 |
rs200323444 | snp | A/G | 5.04037e-05 | 0.00501989 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942541 | TATGGTTTCTTTTTC[A/G]CTAGTTTTAAAATTT | 121441 |
rs200348451 | snp | A/C/T | 0.00011551 | 0.00759893 | missense | NEDD1 | GRCh38.p7 | 12:96945806 | ACTTCCATTCAAATT[A/C/T]GTTTTATTCAGAACA | 121441 |
rs200439414 | in-del | -/ATT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910235 | GTAGTTGTGGAAATA[-/ATT]CCAAAAGGTTTTGGA | 121441 |
rs200471521 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929626 | ATATATATATATATT[A/T]TTTTTTTAATGGCTG | 121441 |
rs200577458 | snp | A/C | 9.95124e-05 | 0.00705311 | missense | NEDD1 | GRCh38.p7 | 12:96944701 | CTCTCCATCATCTAA[A/C]CAAACAAGAAATTCT | 121441 |
rs200584281 | snp | A/G | 0.000764927 | 0.0195417 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935241 | TCTTAATTTAGTAAC[A/G]AATAGCTATTATTCC | 121441 |
rs200588882 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926990 | AAAAAAAAAAAAATT[G/T]TGTGTGTGTGTGTGT | 121441 |
rs200657764 | in-del | -/C | 0.00103048 | 0.0226755 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909913 | TCCTTTAAAAAAAAA[-/C]AAACACACACACACA | 121441 |
rs200691517 | in-del | -/CTCT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930248 | TCTCTCTCTCTCACA[-/CTCT]CACATGCTGTGTTGG | 121441 |
rs200718756 | in-del | -/ATT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926987 | CGAAAAAAAAAAAAA[-/ATT]TTGTGTGTGTGTGTG | 121441 |
rs200755650 | in-del | -/GGC | 0.0520825 | 0.152737 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929782 | AGAGGGACACACTTT[-/GGC]TGGTCAGTTTTGGAA | 121441 |
rs200764548 | snp | A/T | 4.96241e-05 | 0.00498092 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912718 | CTCCATAACTCCTCA[A/T]TTAGATAACTTTTTA | 121441 |
rs200832974 | snp | A/C/G | 8.23806e-05 | 0.00641753 | missense | NEDD1 | GRCh38.p7 | 12:96935093 | TACCATAACTTTGAC[A/C/G]GTGTACACAAAGCTC | 121441 |
rs201048692 | in-del | -/A | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953222 | TTAAAAAAAAAAAAA[-/A]CAAAAAACAAACCTT | 121441 |
rs201100341 | snp | C/T | 1.6599e-05 | 0.00288084 | missense | NEDD1 | GRCh38.p7 | 12:96945711 | CAAAGATAGCATCTT[C/T]TGTCACTGCTGGAGT | 121441 |
rs201146185 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916630 | ATGGTGTATATGTGC[C/T]ACATTTTCTTAATCC | 121441 |
rs201152071 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938837 | CTCTCTCTCTCTCTC[A/T]CACACACACACATTT | 121441 |
rs201201629 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933016 | TTTTTTTTTTTTTTT[-/T]AAATAGTCTGCCATG | 121441 |
rs201249479 | snp | G/T | 0.000149282 | 0.00863822 | missense, utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96909754 | AAACTATTTGTAGGC[G/T]CAGTCATGCAGGAAA | 121441 |
rs201301191 | snp | C/T | 0.000616885 | 0.0175517 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940382 | TTAGATGTAATAACA[C/T]TGATTTTTATATCTA | 121441 |
rs201335305 | snp | A/G | 1.66183e-05 | 0.00288251 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937407 | AGGTAAATGTTGCTT[A/G]TATATTGTTGGAGGG | 121441 |
rs201372474 | in-del | -/A | 0.0414363 | 0.137845 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946283 | TGTAATACTTAATCT[-/A]AAAAAAAATTCTTTC | 121441 |
rs201379106 | snp | A/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953209 | AGTATTTACTAAAAT[A/T]AAAAAAAAAAAAACA | 121441 |
rs201464037 | snp | A/G | 0.000694732 | 0.0186248 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920025 | TAACATACAATTGGA[A/G]TGATTGCTACATTGC | 121441 |
rs201498213 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923351 | TTTTTTTAAGATACA[C/T]GTTTTTATTTATTTT | 121441 |
rs201546373 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929623 | TATATATATATATAT[-/A]TTTTTTTTTTAATGG | 121441 |
rs201613446 | snp | A/T | 0.000377819 | 0.0137392 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919947 | GGGCTGTTCGAGGAT[A/T]ATGGGGCAGTGTACT | 121441 |
rs201624976 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938829 | CTCTCATTCTCTCTC[A/T]CTCTCTCACACACAC | 121441 |
rs201645365 | snp | A/C/T | 3.91445e-05 | 0.00442391 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909944 | CACACAAACCGCTTA[A/C/T]TAGGTTAAACAACCA | 121441 |
rs201734013 | snp | C/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906110 | AGATTTAATTAATTG[C/G]CCTTTTTGTTTGAAG | 121441 |
rs201744935 | snp | G/T | 0.00199809 | 0.0315444 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909732 | TGTTTTTAAAATACA[G/T]TGTTTTAAACTATTT | 121441 |
rs201752385 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921674 | GGGATTTTTTTTTTT[C/T]TTTCTTAGAGAGTCT | 121441 |
rs201753561 | in-del | -/TATG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931756 | TTATAATGAAGTATG[-/TATG]ATTCCAGGTTTTCTG | 121441 |
rs201788008 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945046 | GTGTCTTTAATATGG[A/T]AGAGATAGAATTATT | 121441 |
rs201789472 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918407 | AAAAAGTTTTAATAT[A/G]AAAAATATAAACATA | 121441 |
rs201790884 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937926 | ATTTCTTGCTCACAA[-/T]AAAAAAATATTCTGT | 121441 |
rs201797374 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924616 | TATTCTTTGTGGCTT[A/C]TAGAGAGAAACACAG | 121441 |
rs201820077 | in-del | -/ACACACACACACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929557 | ATTGTTTTCATGTAT[-/ACACACACACACAC]ACACACACACACACA | 121441 |
rs201827829 | in-del | -/CA | 0.031825 | 0.122064 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938835 | TCTCTCTCTCTCTCT[-/CA]CACACACACACACAT | 121441 |
rs201937631 | snp | C/T | 0.000291118 | 0.0120613 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945685 | ATTTTCTTCATTCTT[C/T]ATTTTAGATCCAAAG | 121441 |
rs201945642 | in-del | -/T | 0.0558544 | 0.157504 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913808 | ATAGCTTTTTTTTTT[-/T]AATTTCAAAGTTTTT | 121441 |
rs201968415 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934937 | AATGTCCTTATGAAT[G/T]CTTATAATTACATAA | 121441 |
rs202132836 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944486 | TTGCCTCCAGTTCTC[-/T]TTTTTCTTTTTCTTC | 121441 |
rs202220504 | snp | A/G | 1.64974e-05 | 0.00287201 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937278 | TGCTGCTAGTGGAGG[A/G]GTTCAGAATTCCGGA | 121441 |
rs367598384 | snp | C/T | 1.65252e-05 | 0.00287443 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936665 | GGTAGATTTCATGCC[C/T]GATGGAGCCACTTTG | 121441 |
rs367623226 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931224 | GTAAGAAAATGATGT[A/G]AATGTATGTTCTTAT | 121441 |
rs367647597 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917910 | AACTTATTTTTATGT[C/G]TTTTTTCTTACATGT | 121441 |
rs367688375 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951346 | ATTCAGTAATTTGGC[-/A]AATGAAAAAGTTTAG | 121441 |
rs367735912 | snp | A/G | 3.30879e-05 | 0.00406729 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917657 | TTAAATTCTACATCT[A/G]TGTATTTGGTAAGCG | 121441 |
rs367758655 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941500 | TTCTTTCAGGATGAA[A/G]AGAAGTCGAACTACA | 121441 |
rs367773746 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927021 | GTGTATAATATATAT[C/G]ATGTTCATTTAAACA | 121441 |
rs367875455 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944545 | TTCTATTAACCTACA[C/T]ACTGGGACAAAAGAG | 121441 |
rs367934915 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912556 | AGCAAAGAGAATTAG[A/T]CTTAGTAATTATTAA | 121441 |
rs367957450 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931557 | CTGAGAACCTTTAAG[A/G]CATGAACATCAATGA | 121441 |
rs368008254 | snp | A/G | 1.83102e-05 | 0.00302568 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943780 | ATTTGCCTGAAAATG[A/G]TACTGAACTCACTGT | 121441 |
rs368201005 | snp | A/T | 3.30376e-05 | 0.0040642 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912731 | CATTTAGATAACTTT[A/T]TAGTAACAGCATCTT | 121441 |
rs368275713 | in-del | -/CTCTCT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930212 | ACACACACACACACA[-/CTCTCT]CTCTCTCTCTCTCTC | 121441 |
rs368328556 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931961 | GAAAAACTATAACCT[A/G]TGGTCTAGCCAACTT | 121441 |
rs368371111 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907259 | GAGCCGGAAGCCCAG[C/T]GCGGAGCCGGCCGCG | 121441 |
rs368465501 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923788 | CTCCTTAATACCTGT[G/T]TGTGTGTGTGTGTGT | 121441 |
rs368626327 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937169 | AAACATTAGTAACCT[C/G]AGCTTTTAAATATTC | 121441 |
rs368698486 | snp | A/G | 0.00176301 | 0.0296378 | missense | NEDD1 | GRCh38.p7 | 12:96937340 | CCACAGTTCTACCAC[A/G]ACCTATGACATCAGC | 121441 |
rs368756184 | snp | C/T | | | missense | NEDD1 | GRCh38.p7 | 12:96943626 | CAGTAACTTCAAGTA[C/T]TTCAGTATTGCATTC | 121441 |
rs368857968 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942907 | TGTTGGCTGGAGATA[A/T]CAGTTCCATGCCAAT | 121441 |
rs368930274 | snp | A/C | 1.67747e-05 | 0.00289605 | missense | NEDD1 | GRCh38.p7 | 12:96944772 | TGATATGTGAACCCC[A/C]AATCAATGGATCCTC | 121441 |
rs368990981 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920940 | TTTTTTAAGTTTCAT[A/G]TATATTGGGGAATAA | 121441 |
rs369353365 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949671 | TTATTAAAGTATAAT[A/T]AAGATATATAGCATG | 121441 |
rs369354471 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914887 | ATCAACAGGGTTAGC[C/T]AGCTCTAAATATAAT | 121441 |
rs369613626 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96916525 | GTTTTTTGTTCTTGC[A/G]ATAGTTTACTGAGAA | 121441 |
rs369634125 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921422 | CTGACCTCAGGTGAT[A/C]CACCTCCCTCGGCCT | 121441 |
rs369800376 | snp | A/G | 1.66765e-05 | 0.00288756 | missense | NEDD1 | GRCh38.p7 | 12:96944763 | AAGCCCAGTTGATAT[A/G]TGAACCCCCAATCAA | 121441 |
rs369948541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942921 | ATCAGTTCCATGCCA[A/G]TGAGCTTCTTTATAT | 121441 |
rs369952853 | snp | C/T | 0.000133558 | 0.00817076 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917771 | ATCTTCATGAAAAAA[C/T]GGATATCTTAATGCA | 121441 |
rs369958664 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914284 | TATGTACTACTGTTA[C/T]GCATTATGCCTTAGG | 121441 |
rs370007120 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928681 | GTACATAGTGTGTTT[-/C]TTTTTTTTTTTTTTT | 121441 |
rs370055157 | snp | C/T | 1.66793e-05 | 0.0028878 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909746 | ATTGTTTTAAACTAT[C/T]TGTAGGCGCAGTCAT | 121441 |
rs370092261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945076 | TATGTAGGACCCTTT[A/G]AAAAGGGTTGGTTAA | 121441 |
rs370177580 | snp | C/T | 5.4752e-05 | 0.00523192 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951524 | CAAATTTTATTTTAA[C/T]ATTTTAAATGAAAGT | 121441 |
rs370399590 | snp | A/G | 0.0123036 | 0.0774623 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952347 | AGAAGAAAATTGTGC[A/G]TAAAAATTGGTTATG | 121441 |
rs370590429 | snp | C/T | 1.68414e-05 | 0.0029018 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943529 | AAAATTGGAGGACAC[C/T]ATATGCACATGCAGT | 121441 |
rs370594363 | snp | C/G | 0.000207799 | 0.010191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936585 | ACACTAACATTTCTA[C/G]ACATACTTTGTTCTC | 121441 |
rs370677886 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931613 | AGTTTTAAAAAAGGA[G/T]AGTAATCAGAGTACT | 121441 |
rs370769829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916929 | AGATAAAGGGGAGCC[C/T]ATGTGGGATTCATTC | 121441 |
rs370791655 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914458 | AATTGTATCATAATG[A/C]TGTTGGATAAAAGTA | 121441 |
rs370854915 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942642 | AAGAACTACTTAGAA[C/G]TATTTTCGTGAAAAT | 121441 |
rs370879571 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936419 | GTTTAGCAGTTCTCT[A/C]TATGCCATTTTATTA | 121441 |
rs370886402 | in-del | -/TTA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937159 | GTATAGTATGAAACA[-/TTA]GTAACCTGAGCTTTT | 121441 |
rs370936307 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944297 | AAGAAGTACAAAAAC[A/G]TCTTTTGATTTATTT | 121441 |
rs370940142 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918906 | CTCAAGATAGCAAGT[A/G]TTCCTTGGTTTTGGG | 121441 |
rs371018670 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930423 | CATAGGAAACCAGAT[A/G]TTAACTTCCAAGGGT | 121441 |
rs371057887 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946448 | TCCTTTCTAACCTAT[A/G]GTTAATGTTGTAGCT | 121441 |
rs371188637 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912224 | AGATTGAAACATTCT[A/G]TCACAAAAATTCATG | 121441 |
rs371252365 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924091 | AAGAGGGTCCTATAG[A/G]TATCTAATTGTACCA | 121441 |
rs371278745 | snp | A/G | 0.000214598 | 0.0103563 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936725 | TCAATATGATTTAAG[A/G]ATGTTGAAATCACCA | 121441 |
rs371366525 | snp | A/G | 0.000165857 | 0.00910499 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912707 | ATTGTTTGATGCTCC[A/G]TAACTCCTCATTTAG | 121441 |
rs371426574 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906020 | CATATAATATGTATA[C/T]ATTATATTACATGTA | 121441 |
rs371431356 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941549 | GGTAAACAGAGGGAC[A/G]GATGTAGGTGGAGAG | 121441 |
rs371493817 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943508 | AAATGCTTTTCTTCA[A/G]TGTCCAAAATTGGAG | 121441 |
rs371517383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928140 | AAAGATGTTTTCTAA[C/T]AGTGTTTCTATGTAT | 121441 |
rs371540570 | in-del | -/TAT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951639 | TAGACTAAATAAGTA[-/TAT]AAATAGATTTTAACT | 121441 |
rs371627906 | snp | A/T | 1.96558e-05 | 0.00313489 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943807 | CTGTATGTGTTTATC[A/T]GTAGAAAGTGGGTGG | 121441 |
rs371698956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934435 | TGGTATGTCATCTTA[C/T]GGTCCACTGAATGAC | 121441 |
rs371712075 | snp | A/G | 0.000183721 | 0.00958262 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96944680 | TGAAAGTGGAAATCT[A/G]AATACCTCTCCATCA | 121441 |
rs371791472 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929380 | TCCTTAATGTCTTGT[A/T]TTTTTTTTTTCTTTC | 121441 |
rs371814471 | snp | A/G | 3.32055e-05 | 0.00407451 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917634 | AGCAAAAGCAGACAT[A/G]TGTCAATTTAAATTC | 121441 |
rs372142255 | snp | C/T | 1.76173e-05 | 0.00296788 | missense | NEDD1 | GRCh38.p7 | 12:96944655 | TAGCAAAGTTGGTCA[C/T]ATCTGGTGCTGAAAG | 121441 |
rs372215467 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929204 | TTTTAACCTGTCTTT[-/T]AAGGTATTGTCTGTT | 121441 |
rs372334792 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943947 | TGAAGGTTACAGCAG[A/T]TGGAAAGTTGCAGTA | 121441 |
rs372351101 | snp | A/G | 4.95765e-05 | 0.00497853 | missense | NEDD1 | GRCh38.p7 | 12:96937247 | CAACAGTGAACAAAC[A/G]AAGTGTTAATGTGAA | 121441 |
rs372376583 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927462 | ACTTAGGTTATAATT[A/G]CATGTCACTCTTTAG | 121441 |
rs372409516 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942100 | CTACCATGGAAATAA[A/G]CACTAATAAAACTTT | 121441 |
rs372449216 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909902 | GCAGCAATAGTATCC[C/T]TTAAAAAAAAAAAAC | 121441 |
rs372543480 | snp | A/G | 3.36434e-05 | 0.00410129 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917786 | TGGATATCTTAATGC[A/G]TTTAGAGTACTTACC | 121441 |
rs372548046 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950600 | ATAAGCTATATGGTA[C/T]CCTTTTTTGTAATGC | 121441 |
rs372584752 | in-del | -/T | 0.428937 | 0.17459 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921775 | TGGGAGCCTGGCTAA[-/T]TTTTTTTTTTTTTTT | 121441 |
rs372610979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913335 | GCTTAGGTCCCAGGG[C/T]GTTTAAATGAAGCTC | 121441 |
rs372642467 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96907998 | CCTCAGTGATCTACC[C/G]ACTACACCCCGCAGC | 121441 |
rs372685534 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928294 | AATGACTGGATGTAT[G/T]TCATTATTCAATGCC | 121441 |
rs372703485 | snp | C/T | 4.95569e-05 | 0.00497755 | synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917671 | TATGTATTTGGTAAG[C/T]GGAGGCCTAAATAAC | 121441 |
rs372876408 | snp | C/G/T | 3.33824e-05 | 0.00408538 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96919994 | TTTCAGGATCATAAA[C/G/T]ATCAAGTAACTTGTG | 121441 |
rs372913646 | snp | C/T | 1.93493e-05 | 0.00311035 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909938 | CACACACACACAAAC[C/T]GCTTATTAGGTTAAA | 121441 |
rs372998065 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933389 | TTTGCCTTATATTTT[C/G]ATATGTTGTGTATGA | 121441 |
rs373011385 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914414 | AAATTAGTTGCTATG[A/G]TTCTTAGCCCTCTTT | 121441 |
rs373064033 | snp | A/G | 5.02601e-05 | 0.00501274 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912678 | TAATAGTCTAGTGCT[A/G]TAGATGTTCATGGAT | 121441 |
rs373067055 | snp | C/T | 5.17085e-05 | 0.00508445 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919940 | TGAAAATGGGCTGTT[C/T]GAGGATTATGGGGCA | 121441 |
rs373118109 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942908 | GTTGGCTGGAGATAT[C/T]AGTTCCATGCCAATG | 121441 |
rs373151026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949041 | CTTGGCTCTTACAGC[C/T]TTGGCTACCTTGGTA | 121441 |
rs373274960 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946342 | TCGAATTGTGAACAT[G/T]CTAAGAATGTGTTCT | 121441 |
rs373333698 | snp | A/G | 1.66893e-05 | 0.00288867 | missense | NEDD1 | GRCh38.p7 | 12:96937226 | AAGGCTGTTCAAATA[A/G]GCCCACAACAGTGAA | 121441 |
rs373391483 | snp | A/G | 0.000153988 | 0.00877328 | missense | NEDD1 | GRCh38.p7 | 12:96935187 | AAAGAATCATCCTCT[A/G]TGACACTTCAAGTAA | 121441 |
rs373405333 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923145 | AAGCAAGGAATCATA[C/T]GTGTCTGGTTTCTTT | 121441 |
rs373435855 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909634 | GCTTTGGTGACTGCA[C/T]TGTTTGGAACAAAAA | 121441 |
rs373458377 | snp | A/G | 1.65329e-05 | 0.0028751 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909828 | TGCTTCATCTATGAC[A/G]TTGGTGGATAAATTC | 121441 |
rs373463504 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950660 | TACAGATTATATGTT[A/T]TACAAATGTATTAAA | 121441 |
rs373562175 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926839 | AAAAAATACAAAAAT[C/T]AGCCAGGTGTGGTGG | 121441 |
rs373657679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941358 | TTTCCAAATGTTCTA[C/T]AATTTTATAGTCAGA | 121441 |
rs373693876 | snp | C/T | 0.000363236 | 0.0134717 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940362 | TAGCTTATGATAAAA[C/T]TTATTTAGATGTAAT | 121441 |
rs373706184 | snp | C/T | 0.000153988 | 0.00877328 | missense | NEDD1 | GRCh38.p7 | 12:96943596 | TGAACTCAGTGTTTC[C/T]TCCAAGAAAAAATCC | 121441 |
rs373754552 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911082 | ACTCTGTTAATCAAA[C/T]TCATGGTGAAGTGAC | 121441 |
rs373814176 | snp | A/T | 8.28851e-05 | 0.00643705 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936806 | GTACTCCACTGTTCT[A/T]ACTAAGGTGAGACAT | 121441 |
rs373850588 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944543 | ATTTCTATTAACCTA[C/T]ATACTGGGACAAAAG | 121441 |
rs373922592 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947658 | TTCAGCAGACCCAGG[C/G]ATCTGAGTGCTGGAG | 121441 |
rs374054564 | snp | C/T | 0.000153988 | 0.00877328 | missense | NEDD1 | GRCh38.p7 | 12:96936625 | GGCTAGTGAAAACTT[C/T]AGTGGCTGACACTCC | 121441 |
rs374308635 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917338 | GCCCTGATGGGAGAC[C/T]AGGACTGCCAGTGTT | 121441 |
rs374310011 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941854 | TAAGGAAGCTAATAA[C/T]TTCTAAAAGTGTGCA | 121441 |
rs374338359 | snp | G/T | 0.000103493 | 0.00719276 | utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96907611 | TTTGGCAGGTACTTG[G/T]ATGCATTTTACAGGT | 121441 |
rs374351119 | snp | C/G | 4.96676e-05 | 0.00498311 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945859 | CTTTAGGTAGTAATT[C/G]AGAAACTACTCCTTC | 121441 |
rs374405549 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940319 | TAATATTACCAACAA[C/T]ATGAGTGATACATTA | 121441 |
rs374425199 | snp | C/T | 0.000153988 | 0.00877327 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952103 | GGAAGTTTCTGGCAA[C/T]ACAGAACTACATAGA | 121441 |
rs374483926 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922265 | AAGCAGGAACTTATT[A/G]TATTTTGTTTTGGTG | 121441 |
rs374493100 | snp | A/G | 1.66432e-05 | 0.00288467 | missense | NEDD1 | GRCh38.p7 | 12:96940429 | CCTCGAAGCATAAAC[A/G]CAGACACTTTATCTA | 121441 |
rs374502121 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920347 | ACATCCTTCTAGACT[A/G]TAACTATATACAGCA | 121441 |
rs374553588 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917527 | TTTAATTTAACCAAT[A/G]TTTATCATATGCTTA | 121441 |
rs374578508 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911121 | TGAAGGACTTTCCAG[A/G]TGTGTAATAGGGAAA | 121441 |
rs374739361 | snp | G/T | | | missense | NEDD1 | GRCh38.p7 | 12:96943650 | TGCATTCTAGTCCTC[G/T]TAATGTTTTTATGGG | 121441 |
rs374767934 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934341 | TTTTTCCTCTGAAAG[G/T]AGAAGATTGAGGTAG | 121441 |
rs374812773 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909233 | AAAAAAATGAAATCA[A/G]GTATTGGGATATAGG | 121441 |
rs374836743 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928272 | AGTCTTCATAACCAT[A/G]ATTTTTAATGACTGG | 121441 |
rs374898267 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928369 | TATAATAAATGAGCA[C/T]ATGTTAATATTGTTT | 121441 |
rs375022252 | snp | A/G | 1.73966e-05 | 0.00294924 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952061 | ACTTTTGAAATTTCA[A/G]TGAATACCTTAATGT | 121441 |
rs375155040 | snp | G/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905285 | AATTACTGAGAAAAT[G/T]CTGTCAGTCTCCAAC | 121441 |
rs375169575 | in-del | -/TT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915418 | TTTAAAGAATCTCTT[-/TT]GAGCAGAGGATATTT | 121441 |
rs375177708 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930637 | TAGGTGTTCAGCTGT[C/G]GTTCAGCCTTAAACC | 121441 |
rs375214691 | snp | A/G | 4.9476e-05 | 0.00497348 | missense | NEDD1 | GRCh38.p7 | 12:96937345 | GTTCTACCACAACCT[A/G]TGACATCAGCTATGG | 121441 |
rs375269332 | snp | A/G | 0.000275217 | 0.0117274 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919941 | GAAAATGGGCTGTTC[A/G]AGGATTATGGGGCAG | 121441 |
rs375295556 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914575 | TGTTTACAGAAACAT[A/G]TTAATGTGCTAATAA | 121441 |
rs375309990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938111 | AGGATAAATACTTGG[G/T]CAAAAATATTTATTG | 121441 |
rs375370164 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948856 | CAGCCTCTATTTTGC[C/T]AGCATCACAAGACTT | 121441 |
rs375424950 | snp | A/G | 0.000349939 | 0.013223 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937146 | ATAAAATATTAATGT[A/G]TAGTATGAAACATTA | 121441 |
rs375430029 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917598 | GTTAAATTAAGGTAA[A/C]TTTTTTTTTTTTTTT | 121441 |
rs375466917 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931836 | ATACTTAAAGGATAC[C/T]CCCTCAAAATGTCAA | 121441 |
rs375472744 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920806 | AATCTCTTTGGCCAT[A/G]ACTATTATAAAATAT | 121441 |
rs375567960 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942754 | CATAATTTCTGTGTA[G/T]TAAGAACTGAGCATG | 121441 |
rs375577755 | in-del | -/TGTGTGTGTG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923789 | TCCTTAATACCTGTT[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 121441 |
rs375608122 | in-del | -/ACACACACACACACACACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930157 | ATTATCTGTTGTAAA[-/ACACACACACACACACACAC]ACACACACACACACA | 121441 |
rs375614936 | snp | C/G | 1.77858e-05 | 0.00298205 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936569 | GCTAATATACCTGTA[C/G]ACACTAACATTTCTA | 121441 |
rs375745431 | snp | A/C | 3.31022e-05 | 0.00406817 | synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917653 | CAATTTAAATTCTAC[A/C]TCTATGTATTTGGTA | 121441 |
rs375876499 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953256 | CTCACTAACTTTATG[A/G]GTTTCTGAAGTGATG | 121441 |
rs375903785 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924691 | TCACTTAATAGTTTG[C/G]ACAGTCTTGATTCTT | 121441 |
rs375928589 | snp | A/G | 1.94649e-05 | 0.00311963 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909943 | ACACACAAACCGCTT[A/G]TTAGGTTAAACAACC | 121441 |
rs376026591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942683 | TTGTATTATCTATGC[C/T]GTGTAACAAATCTCT | 121441 |
rs376069489 | snp | A/G | 0.000283086 | 0.0118938 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952104 | GAAGTTTCTGGCAAC[A/G]CAGAACTACATAGAA | 121441 |
rs376202935 | snp | C/T | 0.00117041 | 0.0241627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912687 | AGTGCTATAGATGTT[C/T]ATGGATTGTTTGATG | 121441 |
rs376249320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922063 | GACTGAATGTCACAC[A/G]AAAGACTTGTTTTGG | 121441 |
rs376258540 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946773 | AGAACACTGTTGACA[A/G]TATGATGAGGAAATT | 121441 |
rs376318549 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945946 | TGTTGGTTACTATTG[G/T]CTAGGTTCTGGTAAT | 121441 |
rs376342043 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941982 | AGTAAATTCGTTAAT[G/T]ACTTTGGCTCATTTT | 121441 |
rs376366987 | snp | C/G | 1.67483e-05 | 0.00289377 | missense | NEDD1 | GRCh38.p7 | 12:96944771 | TTGATATGTGAACCC[C/G]CAATCAATGGATCCT | 121441 |
rs376505455 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929625 | ATATATATATATATT[-/A]TTTTTTTTAATGGCT | 121441 |
rs376541803 | snp | A/G | 7.29847e-05 | 0.00604045 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944606 | GAGTAAAAAAATTGT[A/G]TATTAAAGTCATTAT | 121441 |
rs376543598 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947990 | GCTCAGAGGATTTCC[A/G]TAAATTCACTTGTTT | 121441 |
rs376554829 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933690 | CTTAGCATTTGGTTT[C/G]TGTATTTCCTAGACA | 121441 |
rs376599182 | in-del | -/GTG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912885 | TGGCAATTGCTTATT[-/GTG]GTGCTTGCGACTAAA | 121441 |
rs376601103 | snp | A/T | 1.68983e-05 | 0.00290669 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96944782 | ACCCCCAATCAATGG[A/T]TCCTCAACTCCAAGT | 121441 |
rs376668036 | snp | C/T | 6.97642e-05 | 0.00590569 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940401 | TTTTTATATCTAATT[C/T]CTATAAGGTTTGCCT | 121441 |
rs376801876 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930199 | CACACACACACACAC[A/T]CACACACACACACTC | 121441 |
rs376812489 | in-del | -/CTTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913759 | CTTTGAAAGCTATTT[-/CTTT]TTTAAATAAGATAAG | 121441 |
rs377021557 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928523 | GTCTCAAATGTGTGA[C/T]GTGATTTCATAGCTT | 121441 |
rs377088622 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919298 | TGAGTCCTGGCCCTG[C/T]CACTTAGCAGTTACG | 121441 |
rs377226839 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913643 | TCCCAAAGTGCTGGG[A/T]TTACAGGCATGAGCC | 121441 |
rs377235303 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945514 | ATAAATGACTATTAG[A/G]AATAATGTTATAGAA | 121441 |
rs377251687 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96916071 | GCCTTGAGGCAAATA[C/T]AGGGTTGTATATTTA | 121441 |
rs377295844 | snp | C/T | 1.67435e-05 | 0.00289335 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940559 | CTGTTCAGAGGATCC[C/T]GTTCTCTTGCTGGTA | 121441 |
rs377421365 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940915 | AAAAATTGTGTGTGT[A/G]TAGGTGTACACCTCC | 121441 |
rs377708251 | snp | G/T | 3.37302e-05 | 0.00410658 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935214 | GTAAGAAGTAAGTGT[G/T]ACATGCTTATTTCTT | 121441 |
rs386377489 | in-del | -/TT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921672 | AGGGATTTTTTTTTT[-/TT]TCTTTCTTAGAGAGT | 121441 |
rs386765545 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923314 | TTACAAGGTAGCTAC[CA/TG]TGAATATTTTTGTAC | 121441 |
rs386765546 | in-del | GACACACTTTGGC/TTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929772 | CTCTGACCTGAGAGG[GACACACTTTGGC/TTT]TGGTCAGTTTTGGAA | 121441 |
rs397753233 | in-del | -/C | 0.5 | 0 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906112 | ATTTAATTAATTGCC[-/C]TTTTTGTTTGAAGTT | 121441 |
rs397776684 | in-del | -/T | 0.375 | 0.216506 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909916 | GTGTGTGTGTGTGTG[-/T]TTTTTTTTTTTAAAG | 121441 |
rs397783900 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932568 | GTGTTTTGTTTATCC[-/C]AGGATTCTTAGCTAA | 121441 |
rs397835769 | in-del | -/TT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926042 | gggattttttttttt[-/TT]gatggctaaatgaga | 121441 |
rs398020740 | in-del | -/A | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917614 | CTGCTTTTGCTATTT[-/A]AAAAAAAAAAAAAAA | 121441 |
rs398020741 | in-del | -/AC | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927008 | CATGATATATATTAT[-/AC]ACACACACACACACA | 121441 |
rs398039986 | in-del | -/T | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942906 | TTGGCATGGAACTGA[-/T]TATCTCCAGCCAACA | 121441 |
rs398039987 | in-del | -/A | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934218 | AGGGAATACTGGGAG[-/A]AAAAAAAAAAAGCAA | 121441 |
rs398044697 | in-del | -/AAT | 0.5 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910234 | GGTAGTTGTGGAAAT[-/AAT]TCCAAAAGGTTTTGG | 121441 |
rs398116782 | in-del | -/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922309 | TATATTTTGATAAAG[-/G]AGAGACATAAAGTCT | 121441 |
rs527423669 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906804 | CTTATTATGGGTCTT[C/G]GTGCATCTTATACCT | 121441 |
rs527425544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913877 | TCATAATTTTACACA[C/T]TGGGATAGGTAAAGT | 121441 |
rs527461704 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907233 | CCGCCGAAGTTTAAC[A/G]GTCCAGGCGGGAGCC | 121441 |
rs527566424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945315 | TTAAACTCTAAGGCT[C/T]TTCCTGTAGCAGTAC | 121441 |
rs527596553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938907 | TCAGATCTGTCACTT[C/G]CGGCCAGGATGCTTT | 121441 |
rs527602796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945968 | TCTGGTAATCCTAAA[A/G]CCATAGAAAACATAA | 121441 |
rs527658025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912584 | TAATAGTAATGTGAG[C/T]CATTTTTGAAAGCTA | 121441 |
rs527743700 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927191 | TCTACTTTTGCTTCT[A/G]TGAACAATCACAAAT | 121441 |
rs527984347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937524 | GTACTTAGGTAAAAT[C/T]AGTAGAAGTGAAAAT | 121441 |
rs528018932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929191 | TTTTAAAAATTTCTT[C/T]TTAACCTGTCTTTAA | 121441 |
rs528071946 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912048 | TAGTTTTAAAATAGT[A/T]ACTGTTTTGTGTTTA | 121441 |
rs528144764 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913619 | CCTCATGATCCGCCC[C/G]CCTCAGCCTCCCAAA | 121441 |
rs528204352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926667 | TTAATTAAAAAAAGT[G/T]TTGTTAAGATTTCTC | 121441 |
rs528262268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918817 | ACATTGGACCCCATG[G/T]TCTTAATTTCCCAAA | 121441 |
rs528263867 | in-del | -/AC | 0.00279162 | 0.0372561 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952603 | TGTACATTTGATAAG[-/AC]AATTTTTGGAATTTT | 121441 |
rs528430549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911345 | AACAACAAAACTGAT[A/G]TAGCTATGAGATAGT | 121441 |
rs528560821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917307 | TTTATCAAGAGGAGA[C/T]AGGATGGGCAAACAA | 121441 |
rs528620907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909555 | TCATTACTGTGAGGA[A/G]CCATTGGAAGGGTCA | 121441 |
rs528622991 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923987 | TTGAAGATACTATTC[-/TG]TGTTTTCTTTTAGAA | 121441 |
rs528778676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949155 | TGTGGAATCAGCACA[C/T]ACTCTAGAAGGAAAA | 121441 |
rs528806488 | snp | C/T | | | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953745 | ATATGAGAGATTTAC[C/T]TTCCCACCTGAAATT | 121441 |
rs528863580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915597 | GTCTCCTTTGAATTT[C/G]AAGAATCCAAGGATG | 121441 |
rs528941233 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953803 | CAGATATTGATCCTT[A/G]AGAGAAACAAATGAG | 121441 |
rs529016522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946804 | TTGTTTGTTCGTGTA[A/C]TAGCAGCCAAAATAA | 121441 |
rs529131095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940601 | TATTCTGGCTAAAAG[A/G]TGTGAATAATAGCTT | 121441 |
rs529144742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947619 | CTTCAGATGATTTGA[A/G]GACAGTGGGCTCAGG | 121441 |
rs529291157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945236 | AACTCTTTGTTTACA[A/G]TCAACTCTCATATAA | 121441 |
rs529409426 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930681 | ATAAGTTTAGGCAGA[A/G]TGAGTGAGCCACTCT | 121441 |
rs529425758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931155 | ATATATGTGTGTATG[A/T]TCATATGTATGTTAA | 121441 |
rs529549264 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931077 | GATGATTTGTGCTTG[A/G]TGTAAGGCCCTGGGA | 121441 |
rs529646025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914809 | CTGTAATAACCACAC[A/G]ATTTCCATTAATTAT | 121441 |
rs529789220 | snp | A/G | 3.31521e-05 | 0.00407123 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912817 | AGAGCTTGCTGAAGG[A/G]GTAAGTGATTTTTTT | 121441 |
rs529894374 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917556 | TACTAAGTGTTGGAT[C/G]AGACCTGAAAGTCAG | 121441 |
rs529902933 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943096 | TTACTTTTGTTAGAA[A/G]CAAGTTACTAGGTCC | 121441 |
rs529905558 | snp | A/G | 3.67566e-05 | 0.00428683 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951929 | TCAATAATTTAAAAA[A/G]CATTTTCCTGTTTTT | 121441 |
rs529989001 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96907170 | GCCAGAAGCCACAGC[C/T]GCACGCAGCGCCTCG | 121441 |
rs530015997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910588 | CTGTGCTATTGACTT[C/T]TTGGGGCAGAAAATT | 121441 |
rs530088800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919389 | AAAATGACCTTGCCC[C/G]TCAGGCTTTTCTAAG | 121441 |
rs530117829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911228 | TTTCCCTCTTACTAT[A/G]TAAGAGAAAGGTAGC | 121441 |
rs530220819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950250 | CACACCGAGTAAATG[A/G]GAAAATATAAAAAAT | 121441 |
rs530401435 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939369 | AGGAGAGGAAATTTC[G/T]TCTTTGTAACAACTG | 121441 |
rs530401686 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906767 | GGAATCCTTTCCTAA[A/G]TCCACATCCACAATA | 121441 |
rs530416309 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936395 | GTGAATAGAAAAGTA[A/C]GATGGAATGTTTAGC | 121441 |
rs530463576 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909262 | GGGTAAACTGCTAAG[G/T]CCCTTACCAGGTAAG | 121441 |
rs530477785 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935314 | GTCCAGGGGTCCTAA[A/C]GTTTGTACAGTTGAT | 121441 |
rs530507665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942470 | CACTCATATTTAGCT[G/T]TTTAAGATTGTTAGT | 121441 |
rs530625762 | in-del | -/T | 0.039378 | 0.134679 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917600 | AAATTAAGGTAACTT[-/T]TTTTTTTTTTTTTTA | 121441 |