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 |