SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs74989162 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971626 | TGAGACTCTGTCTCA[A/C/G]AAAAAAAAAAAAGAC | 4734 |
rs74998877 | snp | C/T | 0.142272 | 0.225598 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831192 | CCCAAAATGTTGAGA[C/T]TACAGGCATGAGCTA | 4734 |
rs75025094 | snp | A/G | 0.00375383 | 0.0431605 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915314 | CAGTTCATTTGTGCA[A/G]TCTCTGTTGCTGTCT | 4734 |
rs75051911 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849809 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCG | 4734 |
rs75097839 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925191 | GTCACTCATTTTCTA[G/T]TAGTTTCACAACAAC | 4734 |
rs75102172 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853800 | TCGAGGCCAGCCTGG[A/C]CAACATGGTGAAAAC | 4734 |
rs75137931 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985760 | TGTGTAGAGTACACA[C/T]ACACACACACACACA | 4734 |
rs75188997 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968624 | ATAGAATGGCTAAGA[A/C]ATACATGAAAAGATA | 4734 |
rs75200899 | in-del | -/C | 0.316485 | 0.240998 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920949 | TGGTAAACCGAGTTT[-/C]TCAAGAAAAGCTGTA | 4734 |
rs75252823 | snp | A/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899938 | TGGTGCTGTAGGAAA[A/T]TTTTTTTAGTAAAAC | 4734 |
rs75253477 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970355 | CTACTGCACTGAAAA[A/G]AAAGACCCAGTCCTG | 4734 |
rs75255309 | snp | A/G | 0.188 | 0.24219 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995613 | AGTGATGATACTTCT[A/G]AAGACCACTGATTTG | 4734 |
rs75258263 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955697 | TCTTTTTTTTTTCTT[C/T]TCATGTGAGATTGGT | 4734 |
rs75417626 | snp | C/T | 0.166506 | 0.235645 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866902 | TTCTTTATAAAATAA[C/T]TTTCTAAGTATCAAT | 4734 |
rs75418371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858702 | GGAAGAAAGGAAGGG[C/T]AGGAGGCAGGCAGGC | 4734 |
rs75434294 | snp | A/G | 0.209997 | 0.246779 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981405 | TGCTACATCACTTAC[A/G]GTGACCGTATTTTCC | 4734 |
rs75445703 | snp | A/T | 0.299158 | 0.245119 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963194 | TGGAGTGCAGTGGCA[A/T]AATCATGGCTCATTG | 4734 |
rs75488065 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956848 | CTGAAAAAACTTGCT[A/G]AGATTTTTATTGGGA | 4734 |
rs75598710 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990940 | CCAGGGTGATCTCTT[A/G]CTATAAGTCACTTAT | 4734 |
rs75599406 | snp | A/C | 0.0364509 | 0.129988 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895626 | AGACAGATTGCTGGG[A/C]TCTACCCCTAGAATT | 4734 |
rs75599547 | snp | A/C | 0.444444 | 0.157135 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988455 | AATGTGCACATGTAC[A/C]CTAAAACTTAGAGTA | 4734 |
rs75612702 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992143 | CCACAGGTGAAGTGC[G/T]GTATTATCTTCTGAT | 4734 |
rs75664361 | in-del | -/GCT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901403 | ATAGGACTTTCTGGC[-/GCT]TAATTATTTACTCCT | 4734 |
rs75705641 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940322 | TTGATTGTGGTGATG[A/G]TTTCACAGCTGTATG | 4734 |
rs75735268 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943915 | CAGAGACACAGGGGT[A/G]GAGACACCCAAGGCC | 4734 |
rs75760756 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928813 | ATCTCCCTACTGAGT[A/T]ATAAACATCACAAAT | 4734 |
rs75787525 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976327 | TTTGCAAACTATCCA[A/C]CAAGAGACTAATCAC | 4734 |
rs75934910 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884346 | AAATAAGCATAGACT[A/G]TGAAGACTATAATAA | 4734 |
rs75961102 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992414 | GTGTAAAATGTTTGA[C/T]GACACCAAGGTACTA | 4734 |
rs76006755 | snp | G/T | 0.298905 | 0.24517 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946926 | GGTACATAACGAAAT[G/T]AAGGCAGAAACAAAG | 4734 |
rs76009244 | snp | C/G | 0.0155312 | 0.0867431 | utr-variant-5-prime, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55966496 | CAATATATCCTTCTT[C/G]GCAAGGCCTATTCCG | 4734 |
rs76054130 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930431 | ATTTTCTGAGTCTGT[A/G]GTTCACATGAGGAAT | 4734 |
rs76067397 | in-del | -/T | 0.282895 | 0.247826 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856584 | GCAAGTCTTACTTCC[-/T]TAAGTCCATTCTCCA | 4734 |
rs76067919 | snp | C/T | 0.121717 | 0.214577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978557 | GATCCTGAGCACTAT[C/T]AACAGAAATCTGGAT | 4734 |
rs76156588 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956851 | AAAAAACTTGCTGAG[A/G]TTTTTATTGGGATTG | 4734 |
rs76156695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927070 | GCAACAGAGTGAGAC[C/T]ACGTCTCAAAAAAAA | 4734 |
rs76268348 | snp | A/G | 0.144632 | 0.226711 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842835 | CTTTTCCCTACCTCT[A/G]CTTTCCTCCCTGGAG | 4734 |
rs76297040 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985971 | GAACAACTTCTGCCA[G/T]AAAGTGTTCAAAGAA | 4734 |
rs76315495 | in-del | -/TA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967650 | ACATGTATATTTTTT[-/TA]AAAAAATTCACAAGT | 4734 |
rs76373288 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986621 | GTGAGACGGAGTCTC[A/G]CTCCGTCGCCGAGGC | 4734 |
rs76376152 | in-del | -/A | 0.342358 | 0.232314 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844396 | GCACACTGGTCAGTT[-/A]AAAGACCCCTGGAAT | 4734 |
rs76433825 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944482 | GTAAACAAAGCAGCC[A/G]GGAAGCTGAAACTAG | 4734 |
rs76461481 | snp | A/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980778 | GCTAGCATTCATTTT[A/T]AGTGTGTGTGTAGGG | 4734 |
rs76532952 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978924 | TTTCTTGACAACGCA[A/C]AAAAAAAAAAAAAAC | 4734 |
rs76541505 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913931 | AACGTTTCTTCTCAG[A/T]GCCACTTCATTTCTT | 4734 |
rs76544703 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898313 | AAAGGTAAATGAATC[G/T]AAAAGTTACAAACTA | 4734 |
rs76548200 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886865 | ATGATACAAAAACAT[C/T]GAAATTAAATAGTAT | 4734 |
rs76551155 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931524 | AAGCAGAAAAAAAAT[A/T]AAAATATCAGTGACA | 4734 |
rs76590316 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865715 | TTCCAAGATGGAAGA[C/G]AATTCTTCCACGTTG | 4734 |
rs76622553 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924475 | ATGGAAAGGGAGCGA[G/T]TAGGACCAGGAGGAA | 4734 |
rs76624857 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857274 | GTCTTTGACCACTAA[C/T]AGTAACTGAGGGAGC | 4734 |
rs76627205 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883225 | GAGCCCTGGGGCCTT[A/G]AGTGAACACTGGTGG | 4734 |
rs76651278 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989293 | CACTATATTTATTCA[C/T]TTCTTTAGTCCCTGC | 4734 |
rs76660025 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877493 | ACTTCAATCATTTGG[A/T]TAAGGTGCTGTCTTC | 4734 |
rs76664246 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963142 | TCTTTTTTATTTTTT[A/T]TTTTTTTGAGACAGG | 4734 |
rs76707347 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874943 | CATGCCACTGCACTC[C/T]AGCTTGGGTGACAGA | 4734 |
rs76744511 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923646 | GCGAGACTCCATCTC[A/C]AAAAAAAAAAAAAAT | 4734 |
rs76759606 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901792 | TACAGTTTACAGTGC[A/C]TTCAGACACTCTCAC | 4734 |
rs76764275 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967862 | CCCATCCCTCCAAAA[A/T]ATAAGCCAGGCATGA | 4734 |
rs76848811 | snp | A/C/G | 0.0387552 | 0.1337 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867764 | ATTTGAAGAAAAAAG[A/C/G]TTCTTTCCTGGCTGG | 4734 |
rs76851035 | snp | A/G | 0.117188 | 0.211804 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873444 | CTCACTTTTCTACAA[A/G]AGACGCCACTCTTAT | 4734 |
rs76867626 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851929 | TTATATAATAACAAG[C/T]GGTAATTCGTGTATA | 4734 |
rs76907282 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835442 | TTTTTTTTTTTTTCC[C/T]ATGCCCTAAACTGTC | 4734 |
rs76933679 | snp | A/G | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832185 | ACCCCTATCTTGAAA[A/G]AAAAAAAAAAAAAAG | 4734 |
rs76969006 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874990 | AAAGAAAAAAAAAAA[A/G]GAAATCAACTCTCCT | 4734 |
rs76990955 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862699 | AATTAAAAGGGTAGT[A/G]TCTAGAGTCAAGTAA | 4734 |
rs77000091 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931828 | TTTTAATATATTCAG[A/G]GAATGTGCAACCATC | 4734 |
rs77131479 | in-del | -/AT | 0.0166325 | 0.0896639 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901716 | TGGATTCATAATTAC[-/AT]ATATGATTCCATTTG | 4734 |
rs77184015 | snp | C/T | 0.375 | 0.216506 | intron-variant | NEDD4 | GRCh38.p7 | 15:55987953 | ATTGACTTGGCGATG[C/T]GGGCTCTTTTTTGGT | 4734 |
rs77197184 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921966 | ACAACATGCAAATAA[C/T]GCAAATAAAATAGTT | 4734 |
rs77199034 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881802 | AATACAGGCACAGAA[C/G]AGGGTTTCTCAGCTT | 4734 |
rs77205685 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923645 | AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 4734 |
rs77234137 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980780 | TAGCATTCATTTTTA[G/T]TGTGTGTGTAGGGGT | 4734 |
rs77351400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858051 | AAATTATACACATAT[C/T]TATGCTCTGCATTTA | 4734 |
rs77410538 | snp | G/T | 0.176219 | 0.238865 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930068 | ACAGAGTCAGTGAAA[G/T]AATTAACCCCTAATG | 4734 |
rs77518565 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972283 | TGAGCAGAAAGACTA[A/G]AAGATGAACCTATCA | 4734 |
rs77522108 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884344 | AAAAATAAGCATAGA[C/T]TGTGAAGACTATAAT | 4734 |
rs77532807 | in-del | -/TA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979080 | AAAATATATATATAT[-/TA]ACCCCATTTTTACTT | 4734 |
rs77591988 | in-del | -/ATACTAATAAAATAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838088 | TATCCAATAAAATAC[-/ATACTAATAAAATAC]TTACTAAATATATTC | 4734 |
rs77597799 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983629 | TTTTTTTTTTTTTTT[G/T]GAGACAGAGTGTTCT | 4734 |
rs77618750 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898651 | TTTTTTTTTTTTTTT[G/T]TTTGAGACAAGGTCT | 4734 |
rs77638506 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904131 | TGCACAACTGCACTC[C/T]AGGGACAAGAGCAAG | 4734 |
rs77652265 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865800 | TGTTTTTTGGTAGCA[A/G]GGAGAAATGGATAGG | 4734 |
rs77685364 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874988 | AAAAAGAAAAAAAAA[-/AA]GGAAATCAACTCTCC | 4734 |
rs77705462 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878655 | TAAAATACTTCTTCA[A/G]GAATGTTCACAGAAT | 4734 |
rs77761384 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971625 | GTGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAGA | 4734 |
rs77808902 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931629 | ATATCCAGTTTTCCA[A/G]AAAGAACAAAGGTGT | 4734 |
rs77838195 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921070 | AACGCGTTAAGTCTA[C/T]GAATGTTAAATGACA | 4734 |
rs77842879 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853977 | CCTGGGCAACTGAGC[A/C]AAACTCCGACTCAAA | 4734 |
rs77873281 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965216 | TGGTTGTTTGTTTTT[C/T]GAGACACGGTCTCAC | 4734 |
rs77913535 | in-del | -/GTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964289 | GTTGTTGTTGTTGTT[-/GTT]TTTCTCCAATCTTTG | 4734 |
rs77914199 | snp | A/G | 0.126494 | 0.217362 | utr-variant-5-prime, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55993523 | CACCTCGTCCTCCAG[A/G]AGCCCGAACACCTCC | 4734 |
rs77988972 | snp | C/T | 0.000150096 | 0.00866173 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856104 | GTTTTATATTTTTAT[C/T]GATTGATGGGAGAGG | 4734 |
rs78031481 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929682 | ATGTTTATGCATTTT[A/G]CCTAGAGAAACAACA | 4734 |
rs78063584 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982584 | CTATAGAGAGTAGAC[A/G]GGCAGAATTGACTGG | 4734 |
rs78074059 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890910 | TTGAGCATCTTTTCA[C/T]GTGCTTATTGTGCTT | 4734 |
rs78095626 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885190 | TTACCCTACAATAGT[A/G]TATCTGGCGAAAATG | 4734 |
rs78130532 | snp | C/T | 0.318415 | 0.240457 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903762 | CCCGGGAGGCGGAGG[C/T]TGCAATGAGCCGAGA | 4734 |
rs78248035 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950988 | GAGGCAGATGGGGTG[A/G]AAAGGCAGCAATGTC | 4734 |
rs78249086 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975946 | CGTACAAACCAATGG[A/G]ACAGAATAGAGAACC | 4734 |
rs78313911 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838376 | AAAGTACAAATTCTT[A/G]CTCAGAGACAGCTTT | 4734 |
rs78394999 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929577 | ACTTATAAGTGAGAA[C/T]ATGTGGTGGTTGGTT | 4734 |
rs78440815 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902478 | TTATGGGTACAATAT[G/T]TATTTTTTAAAAAAG | 4734 |
rs78499307 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974737 | ATGATAAAAAAAAAA[A/C]CCCTCAAAAACCTGA | 4734 |
rs78503266 | snp | A/C/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886761 | AGACTCCGTCTCAAA[A/C/G]AAAAAAAAAAAAATT | 4734 |
rs78560585 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898723 | TCAATGCAACTTGGA[A/C]TCCTGGGCTCAAGTG | 4734 |
rs78594972 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889708 | TGTTTTGTTTTGTTT[G/T]GTTTTTTTTGGAGAC | 4734 |
rs78596228 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917834 | AATATATGCAGATTA[A/G]AAAAAAAAAACTATA | 4734 |
rs78622558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843526 | ATATCTAAATATTTT[A/G]TTCCTCAGTACTTCA | 4734 |
rs78649755 | snp | A/G | 0.113685 | 0.209567 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917674 | ATAGGTTCAAGAAAA[A/G]AAGTTTAAGAGAAGC | 4734 |
rs78650601 | snp | A/T | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840626 | AACAGTTTGCCATGA[A/T]AAACTGCCATTCCAG | 4734 |
rs78698658 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939812 | ACAGTATAAAGGTTC[A/C]CCAAAAAATTAAAAA | 4734 |
rs78743831 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856441 | TCTCTTGAATGTTTC[A/T]CAGAAACCATTCTCA | 4734 |
rs78775641 | snp | A/G | 0.00611434 | 0.0549526 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915457 | GATAAGCTCCTCCCA[A/G]TGAAATACTTCTTCG | 4734 |
rs78777728 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826782 | TGTGGTTGAGAGTTT[A/G]TAATCATGTTAGTTC | 4734 |
rs78860764 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939120 | CGAAAACAACAACAA[A/C]AACAAACAAAAAAAC | 4734 |
rs78862027 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883694 | ACACACACACACACA[A/C]AAACACACACACACA | 4734 |
rs78907480 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929475 | CAGCTTTTCTATCCT[C/T]ACCCTCCTCCTCTCC | 4734 |
rs78910147 | in-del | -/A | 0.316485 | 0.240998 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920875 | GACTAGCAACAAATC[-/A]AGAGGACTAGAATGA | 4734 |
rs78916693 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956631 | TCTCACACACACATG[C/T]GCATGTATTTTTACA | 4734 |
rs78921563 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957434 | CTGGGTTTTTTCATA[G/T]ATACCCCTGATGAGG | 4734 |
rs78987200 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972848 | ATAGCTATATCAGAT[A/C]AAATAGATTTCAATA | 4734 |
rs78997053 | in-del | -/C | 0.436834 | 0.166111 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873701 | TATTTTCAAACTAAT[-/C]TTTTTTACACAATGT | 4734 |
rs79034884 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917463 | AATATAGGGACTGTT[A/T]ATTTTTTTTTTTTAA | 4734 |
rs79078233 | in-del | -/T | 0.323514 | 0.238947 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973634 | AGAGGAACTTGGAAA[-/T]TAATACAAACAAATG | 4734 |
rs79136313 | snp | A/G | 0.175254 | 0.238565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925342 | GACACCTTATGATCA[A/G]TTTTATTTACTTGCT | 4734 |
rs79213181 | snp | C/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967790 | CTTTGGGTGGCCAAC[C/G]TGAGAGAATTGCTTG | 4734 |
rs79303748 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984384 | ATCTCTAAAATGGGG[A/G]TAATACTTCCTACTT | 4734 |
rs79318015 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973136 | GTAAACCAAATGGAC[C/T]TAATAGATATTTACA | 4734 |
rs79377408 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856440 | TTCTCTTGAATGTTT[C/T]ACAGAAACCATTCTC | 4734 |
rs79390309 | snp | A/T | 0.138546 | 0.223781 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861694 | ACAGAAATTAAAATT[A/T]AAAAAAATCAGATTG | 4734 |
rs79449359 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990234 | AATGTGCTTGAATCA[C/G/T]CCTGAAACCACTGGA | 4734 |
rs79472037 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849796 | ATTTTAAGTAATTTT[C/T]TTTTTTTTTTTTTTG | 4734 |
rs79510775 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971639 | CAAAAAAAAAAAAAA[A/G]ACTTATTAGCTTTAA | 4734 |
rs79539337 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966887 | AAGTTCATAACCATT[G/T]GGCTTTTGGTTTTTT | 4734 |
rs79544621 | snp | A/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891039 | CATCTCCCTAAAAAA[A/T]TCACCTGTTTTTATT | 4734 |
rs79561431 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862394 | AATCACTGAGGAGAC[A/C]GAAGTTAGAATATGT | 4734 |
rs79617189 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917465 | TATAGGGACTGTTAA[A/T]TTTTTTTTTTTAATG | 4734 |
rs79634122 | snp | G/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835421 | CAGTCTCCTGTTCTG[G/T]TTTTTTTTTTTTTTT | 4734 |
rs79639088 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888924 | CAAACTAGACTCCTA[C/T]TTCTCACCTTATACA | 4734 |
rs79648055 | snp | C/T | 0.141258 | 0.225111 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904596 | GTGTGAGCCACCACA[C/T]CCGGCGTATTTCCAT | 4734 |
rs79648825 | snp | C/G | 0.103082 | 0.202275 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843382 | CTTAAGAAAGTCTTA[C/G]CTCCTGAGTCTGTGC | 4734 |
rs79659464 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884997 | ATAAGACTCCTCAAG[A/G]TATTTATTAACAAAA | 4734 |
rs79676491 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906640 | CCTGTTGTGGGGTGG[A/G]GGGCTGGGGGAGGGA | 4734 |
rs79693462 | snp | C/T | 0.132409 | 0.220618 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910200 | TATACCTTGCCTATG[C/T]TATCTCATGCTTATT | 4734 |
rs79722564 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897683 | TAAGGTTTGGGCTCC[A/G]GACTGGTTTATTAAT | 4734 |
rs79786260 | snp | G/T | 0.00795532 | 0.062565 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826734 | ACCAGACTTATGCAA[G/T]ACGACCTTTTTGTAA | 4734 |
rs79817948 | snp | C/G | 0.127599 | 0.217986 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965714 | TTTGTATGTATTTTT[C/G]TTTTTGAGACAGAGG | 4734 |
rs79821953 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931825 | GGTTTTTAATATATT[C/G]AGAGAATGTGCAACC | 4734 |
rs79851375 | snp | A/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835928 | CCCTCATTGAAATTC[A/T]GAGAAAACTCCGAAC | 4734 |
rs79865006 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944127 | CTGGTTCATCTCATT[A/G]GGACTGGTTGGACAG | 4734 |
rs79873736 | snp | A/G | 0.174288 | 0.23826 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950680 | AGAAGCAGAAATGAC[A/G]AGGGCAGACAACTCT | 4734 |
rs79913977 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963150 | ATTTTTTTTTTTTTT[G/T]AGACAGGGTCTCACT | 4734 |
rs79920149 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836237 | TCATTTCACTCTTTA[A/C]ATCATACATACCTTA | 4734 |
rs79927674 | in-del | -/AGAAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852687 | AGTTTTGCCTTTTCT[-/AGAAA]TATATATATATATAT | 4734 |
rs79970170 | snp | A/C/G | 0.000247921 | 0.0111311 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915708 | AAATGCACTGAAACA[A/C/G]AAGAATATCCTTCAG | 4734 |
rs80015860 | snp | C/T | 0.299158 | 0.245119 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949132 | aaccccatcaagaag[C/T]gggcgaaggatatga | 4734 |
rs80025455 | snp | C/G | 0.215446 | 0.2476 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982335 | TGAATGTTCACCGTA[C/G]GTTTATTCATAATAG | 4734 |
rs80034727 | snp | A/C | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837435 | TCACTCCGCGCTCAA[A/C]AAAAAAAAAAAAAGA | 4734 |
rs80077833 | snp | G/T | 0.00121871 | 0.024655 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916637 | TTCTTGAGACTGAAC[G/T]TTTTCCTTTATTAAC | 4734 |
rs80088766 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939443 | GTCAGTTAAACCTCC[C/T]TTGTTTATAAATTAC | 4734 |
rs80157989 | snp | G/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847693 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCG | 4734 |
rs80171128 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971212 | CGCAGAAGAAAGAAT[C/T]AGCGAGCTTGAAGAT | 4734 |
rs80178014 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881082 | TGATAATTTTTGAAA[C/T]GGGTAAGTTAGCTTT | 4734 |
rs80222656 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880695 | AAAGACAGGGAAAGG[A/T]AGTCTCAGAGTAACA | 4734 |
rs80243619 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940151 | CACAAAAAGTATCTA[A/C]AATAGTCAAATTCAT | 4734 |
rs80256079 | snp | C/G | 0.187685 | 0.242109 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993305 | TGTGGACCCGACAAG[C/G]TTGCTCCCTCCAGCG | 4734 |
rs80304445 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953006 | TTTTTTTCTTTTTTT[C/T]TGAGACAGAGTCTTG | 4734 |
rs80304948 | snp | C/G | 0.00677553 | 0.0578088 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980602 | AAGAAATTAAAGAAA[C/G]AGTAGATTCAACACA | 4734 |
rs80353034 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967308 | AATATCTTTGATATG[A/C]TGGCATAGAGGTTTT | 4734 |
rs111227291 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890623 | GTTTGGCTATTATAA[A/G]TAATGCCACTATGAA | 4734 |
rs111229634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846080 | GCATGAGCTACTGCA[C/T]CTGGCCCACAAAATT | 4734 |
rs111230340 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891770 | AAAATCCAAATTGCT[C/G]TTTTTGTAAAAACTT | 4734 |
rs111232474 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887188 | AATGAAGAAAATGAC[A/G]CAAAAGACCAACAAA | 4734 |
rs111247337 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831037 | GATTCTCATGCCTCA[A/G]CCCTCCCAAGAAGCT | 4734 |
rs111254925 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883900 | TTTTTTTTTTTTTGA[C/G]ACAGAGTCTCACCCT | 4734 |
rs111272686 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947738 | CAGAAAAGGCCTTTG[A/G]CAAAATTCAACAGCC | 4734 |
rs111308798 | snp | C/G | 0.00463607 | 0.0479223 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916624 | GAACAGATGATCTTT[C/G]TTGAGACTGAACGTT | 4734 |
rs111342199 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956372 | GGTACTGTTCACGTA[A/C]ACTTTGTGTAACCCA | 4734 |
rs111345705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975161 | GCCTCTCAAAGTGCT[A/G]GGATTACAGGCGTGT | 4734 |
rs111359928 | in-del | -/GC/GCGC/GTGC | 0.374375 | 0.216866 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983303 | TGTGTGTGTGTGCGT[-/GC/GCGC/GTGC]GCGCGCGCGTGCGTG | 4734 |
rs111381921 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833171 | CAAATTATCCTGAAA[C/T]ATAAGCTATCGGAAT | 4734 |
rs111410871 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859329 | AGTGAAAATGTCATC[G/T]ATCTCCTTGTTTAGT | 4734 |
rs111412940 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900323 | CTGAAGAGCACTTTA[C/T]AGCTGCTTGGGATCT | 4734 |
rs111418895 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938291 | TTGAACCTGGGAGGT[G/T]GTGGTTGCGGTGAGC | 4734 |
rs111421482 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886940 | GATATTGAAAATTTT[C/T]TTGAAACAAATAATG | 4734 |
rs111425596 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979285 | CAGAAAGATTAGAAG[A/G]AAATATGCAAAAATA | 4734 |
rs111428146 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871378 | ATAAAGTTCTTTCTA[C/T]ACTTGCAATAATATT | 4734 |
rs111454667 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848364 | AGCACACTGGCAGAG[A/G]GACTTACTGGTCCAG | 4734 |
rs111461665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880273 | CGCTAGTCTGGGTGA[C/T]GGAGTGAGACCCCGT | 4734 |
rs111479658 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830133 | TTTCACCAGGGGTAG[A/G]AGTAAGACGTAGGAC | 4734 |
rs111508989 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885782 | GAAGGAAGAAAAGAA[A/G]GAAGAAAAAACTATA | 4734 |
rs111537540 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843479 | ACACAACTATGCTTT[A/G]GGCAGAACTTATTGT | 4734 |
rs111538206 | snp | C/T | 0.303187 | 0.244277 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932426 | AACGGGGAAAGGATT[C/T]CCTATTTAATAAATG | 4734 |
rs111606373 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886492 | TTGAAATGGGCCAGG[A/C/T]GTGGTTGCTCACGCC | 4734 |
rs111612037 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850778 | TATTGTAATATTTTA[G/T]AGAGAGAACTCACAA | 4734 |
rs111633137 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911535 | TAGACTGAAAAAAAA[A/T]TTTTTTTTTTTTGAG | 4734 |
rs111639944 | in-del | -/TC | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940518 | TTCCCTCCTCCCCCT[-/TC]TCTCTCTCTCTCTCT | 4734 |
rs111673857 | snp | C/T | 0.48 | 0.0979796 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873270 | CTGTTATCTGGACAG[C/T]GATAACACTCAATCC | 4734 |
rs111693500 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830474 | AGAGGAATCTCACTC[G/T]CTGAGGCTTTGTTCT | 4734 |
rs111753441 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944780 | GCCCCTCTGGGACAA[A/G]GCTTCCAGAGGAAGG | 4734 |
rs111769211 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880469 | TATAAGAGAGTACTT[C/G]CTGCAAAATAATGAG | 4734 |
rs111784267 | in-del | -/C | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958875 | CAATGCCCCAGTTTT[-/C]ATTCTCATTACCAGT | 4734 |
rs111786740 | snp | A/G | 0.48 | 0.0979796 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905352 | CCTCAGAGAGAAGAC[A/G]CTAACAATTGGGGGG | 4734 |
rs111793255 | in-del | -/ACACAC | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836332 | ATGAAAAAGTATGTG[-/ACACAC]ACACACACACACACA | 4734 |
rs111825283 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55954887 | GTAAGAGGTTTCATA[C/T]ATATAGGGGGTTAAT | 4734 |
rs111862916 | snp | A/C | 0.0524604 | 0.153226 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980144 | GCCACGTTGGCCAGG[A/C]TGATCTTGAACGCCT | 4734 |
rs111889278 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955361 | TTTTTAATTGCACAT[A/G]CATTAATGTTAACTT | 4734 |
rs111900201 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881788 | ACTGTCACTAGAGTA[A/G]TACAGGCACAGAACA | 4734 |
rs111929657 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55948531 | ACAAAGCTGGAGGCA[A/T]CATGCTACCTGACTT | 4734 |
rs111937337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937304 | TTTTTATGGCGAATA[C/T]ATTCAGTTCAAAACA | 4734 |
rs111981760 | snp | A/C | 0.444444 | 0.157135 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868026 | GCACCACTGCACTCC[A/C]GCATGGGCCACAGAG | 4734 |
rs112000713 | snp | G/T | 0.306431 | 0.243548 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928205 | TTAGTAGAGACAGGG[G/T]TTCACCGTGTTGGCC | 4734 |
rs112041231 | snp | C/G | 0.5 | 0 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862995 | TATCCTGCCTCTCTT[C/G]CCACCCTGGAGGTAG | 4734 |
rs112049661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925464 | GTTGCTTTTACTATA[C/T]AAAGTACATAGCAGT | 4734 |
rs112082658 | snp | A/T | 0.444444 | 0.157135 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875113 | AAAAAAAAAACCCAG[A/T]AGGAAGAGAAAAAGT | 4734 |
rs112095011 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891342 | GGAACTATCCTGGAA[A/C]GTCTGGGACATATGG | 4734 |
rs112100247 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883281 | CTGTGGCAGGAGTGG[C/G]CACGGAGAGACTCTG | 4734 |
rs112113022 | snp | C/T | 0.5 | 0 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826497 | GCTGGCTTGAGTGGG[C/T]GGGAGTGGATTCCCT | 4734 |
rs112113638 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913540 | AACATTAAACGGGGG[A/G]ACAATTTAAATCTCC | 4734 |
rs112140888 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944654 | CTCCCAGCATGGGAT[C/G/T]TGAGCTCTGATAACA | 4734 |
rs112145764 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980009 | TCTGCCTCCTAGGCT[C/T]AAGTGATTCTCCTAC | 4734 |
rs112157443 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833811 | ACTAAGTGCCTGTCT[C/T]AGCCTGTCATTCCAC | 4734 |
rs112161618 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903605 | CGAGGTGGGTGGATC[A/T]CGAGGTCAGGAGATC | 4734 |
rs112196018 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55993203 | GGCGCGGTGATGTGG[A/G]TCCCCCGCCGACCGC | 4734 |
rs112215956 | in-del | -/A | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981005 | AACAAAATATTCAAC[-/A]AAAAAAAATTGCTAG | 4734 |
rs112218967 | in-del | -/C | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849796 | TTTTAAGTAATTTTT[-/C]TTTTTTTTTTTTTTG | 4734 |
rs112284488 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953995 | AGCCTATACTCTTAA[C/T]GACTATAGCATACCA | 4734 |
rs112301491 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980795 | GTGTGTGTGTAGGGG[G/T]GTGTGTGTGTGTGTG | 4734 |
rs112303909 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930419 | GTTAGTCAAACCATT[C/T]TCTGAGTCTGTGGTT | 4734 |
rs112306166 | in-del | -/AACAAACA | 0.495252 | 0.0484902 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939120 | GAAAACAACAACAAC[-/AACAAACA]AACAAACAAAAAAAC | 4734 |
rs112321416 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924586 | CTTACCCACTTCCCC[C/T]GGCTGCTCCACTGAA | 4734 |
rs112328055 | snp | A/G | 0.48 | 0.0979796 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899526 | TCAACAAACCCCTTT[A/G]AAACCAGTATTTTCT | 4734 |
rs112345489 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945136 | GCCCCTCGCCAGCAA[C/T]AGAACAAAGCTGGAA | 4734 |
rs112354322 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926991 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGGGA | 4734 |
rs112369236 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870529 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 4734 |
rs112379380 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840396 | TCTTCAAAATGTTCA[A/G]GCTGCTTGTTAAATT | 4734 |
rs112387115 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852827 | TGATCTCGGCTCACT[C/G]CAACCTCTGCTTCCT | 4734 |
rs112395032 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835778 | TGTAGCACTTTCCCA[A/G]CTCTGCTGGGAAGTC | 4734 |
rs112396167 | snp | C/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988554 | GACTGCAAAGACATG[C/G]CACGTAAAAGCAATA | 4734 |
rs112403529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951085 | TGGGGAGACATAAAT[A/G]TAATTTGCATCATCT | 4734 |
rs112432297 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833697 | TGATTGAATGGCATA[C/T]ATATTTCTCTATGAG | 4734 |
rs112474356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944860 | CCACTGGTGATACCC[A/G]AGCAAACAGGGTCTG | 4734 |
rs112572553 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908411 | GTATCTGAAGTATTA[C/T]TGATATGTTTTTAAT | 4734 |
rs112572912 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962258 | TTCTTTCAAATTAGC[C/T]ATGTCTTTATATTTT | 4734 |
rs112577898 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974540 | ACTAGCAAACCAAAT[C/T]TGACAACACATTGAA | 4734 |
rs112601437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935153 | GATTACAGGCATGAG[C/T]CACCATGTCTGGCCT | 4734 |
rs112639665 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840146 | AATGTTATCTATAAC[C/T]TACTCTGAAATGCAT | 4734 |
rs112643396 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827622 | CATTCTACATAATGA[C/G]GACATTTCCAAAATG | 4734 |
rs112664386 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950471 | TTTCCTTACTGAAAT[C/G]AAGTATGGTACCACA | 4734 |
rs112666660 | snp | A/G | 0.305186 | 0.243833 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927094 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAGAAAGA | 4734 |
rs112718968 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945128 | GGATCGCAGCCCCTC[A/G]CCAGCAACAGAACAA | 4734 |
rs112723169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950814 | ATCCAGAGAGGGGAA[A/T]TTCCTAAAATGCATC | 4734 |
rs112730270 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862733 | TGAATATTATCAAGT[C/T]ATTTAAAAAACGAAA | 4734 |
rs112730468 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847323 | CAGGTAGAGAAATAT[C/T]AGAAACAAAAATTTC | 4734 |
rs112740777 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882283 | GAAGAGGGTAGGAAA[C/G]ACAGTCTTCAGTTGC | 4734 |
rs112742276 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855169 | TCTGTGTCCCTTTCT[G/T]AGTGCAGGGTGTTAT | 4734 |
rs112753823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977697 | ATTTCAGTTTTCTGA[C/G]GGGAGGGATTCACAA | 4734 |
rs112767718 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880916 | TATTTAAAATACTGG[C/T]GTATATAATGAAACC | 4734 |
rs112771508 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906644 | TTGTGGGGTGGGGGG[A/C]TGGGGGAGGGATAGC | 4734 |
rs112782806 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836557 | TTGAGACGGAGTCTC[A/G]CTCTGTTGCCCAGGA | 4734 |
rs112821396 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875378 | GCAGTGGTGCAATCA[C/T]AGCTAACTGCAACCT | 4734 |
rs112829629 | snp | A/T | 0.167158 | 0.235875 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906710 | TGGGTGCAGCACACC[A/T]ACATGGCACATGTAT | 4734 |
rs112878344 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911675 | GCTGGGACTACAGGC[A/G]CGCGCCACCATGCCC | 4734 |
rs112897799 | snp | A/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928869 | TTCAGAAGCATATAA[A/T]AAATGCAAAAATATA | 4734 |
rs112969350 | snp | C/T | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918417 | CTCACCTAAATTTTA[C/T]AGCTGGAACTCCAGT | 4734 |
rs112980121 | snp | C/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942402 | CCTAATGTTGGAGGA[C/G]GGGCCAGATGGGAGG | 4734 |
rs113057139 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991435 | CCCTCAGTCCGAGGC[C/T]GAGACTGTCTTTTTT | 4734 |
rs113078695 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833755 | CCTAGGAATACCCTG[C/T]AGGTTATTACAAGTT | 4734 |
rs113079079 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862442 | TTGATCTGTGCGTGC[C/T]GGAAGTTATGTGGAC | 4734 |
rs113099843 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932799 | AATATCCAAAATCTA[C/G]AAAGAACTTAAACAA | 4734 |
rs113103087 | snp | A/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901306 | TCCATAAGTCAAAAT[A/T]TTCAATGGGGGATCA | 4734 |
rs113134364 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939331 | GTTCCTCCCCCTTCA[A/C]TTTCTCTTCTGTCTC | 4734 |
rs113136592 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55850142 | CAAGCACTAAACAAT[C/T]TTAAGCCTTATCTTA | 4734 |
rs113176671 | snp | A/C | 0.0473341 | 0.14638 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916265 | AAAAGTATAACTACT[A/C]CTGTCACTGATGACA | 4734 |
rs113188590 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913339 | TAATATATAATTATT[A/G]ATAAACACAAGATTA | 4734 |
rs113213665 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917862 | ATACCCCAAGATAGT[G/T]TGAACACACAGGATA | 4734 |
rs113222787 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889606 | AAGTAGAGATAAGTA[A/G]TGGCTACACAAAAAA | 4734 |
rs113248787 | in-del | -/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883804 | TCTGGGAGAAAGTAA[-/G]GGAGAAGAACAAGAG | 4734 |
rs113328503 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830185 | CTGCACAACTCCTTG[C/T]GGAGTGCTGCCCCCA | 4734 |
rs113360985 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980222 | TCAGGCGTGAGCCAC[C/T]GCACCTGGCCATCTT | 4734 |
rs113373526 | snp | C/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909739 | GGTGAGGCCTCACAA[C/G]AGCTAGCACATGGTA | 4734 |
rs113375036 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882860 | CACTTGCTGACTGAA[A/G]AGCCTTAGGTCCTGA | 4734 |
rs113375620 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862824 | TGGATCACTATACTG[C/T]TATGAATCCATCTGA | 4734 |
rs113389780 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833622 | GCTGAGATGGCACCA[C/T]TGCACTCCAGCCTGG | 4734 |
rs113397068 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958307 | TTTTTCTACTTTACT[A/G]TATTAATACAGTGAA | 4734 |
rs113446385 | snp | C/T | 0.265727 | 0.249505 | intron-variant | NEDD4 | GRCh38.p7 | 15:55987298 | TCTGTTCATGTCCTT[C/T]GCCCACTTTTTGATG | 4734 |
rs113452502 | snp | A/C | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832884 | TGGTATCACTTTCAA[A/C]ATCTTAATTCTTTTT | 4734 |
rs113452880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841717 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCT | 4734 |
rs113454298 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917201 | TGAATGAGTAACACA[A/G]GAACAACAATCTTCT | 4734 |
rs113467649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840224 | AGTAAATCTAGAAAA[A/C]AAGCAATTGTGAGTA | 4734 |
rs113491565 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943251 | AAAAGAAAGCCCCAT[C/T]TTGTGGGGAGGAATT | 4734 |
rs113502754 | snp | C/T | 0.00256718 | 0.0357351 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916547 | AAGATATCCACTGTA[C/T]CTTGTTGGCTGTAGT | 4734 |
rs113511224 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940641 | AAGAATTGTCTCCCA[C/T]GTCAGCCTCCAAAGT | 4734 |
rs113513290 | snp | C/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834934 | CCCACCGCAGTGCCG[C/G]CTCTTCTTTCAGGCT | 4734 |
rs113520194 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924919 | CTAAAAATACAAAAA[C/T]GAGCCAGGTATGGTG | 4734 |
rs113523545 | in-del | -/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900069 | GAATCATGACTCCAC[-/T]TTTTTTTTTTTTAAA | 4734 |
rs113548962 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986483 | TTCTATGATTCCTGC[C/G]AAGAGAGCGTGACCT | 4734 |
rs113574741 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946266 | AGGAGACCCACCTCA[C/T]GTGCAGAGACACACA | 4734 |
rs113602535 | snp | A/G | 0.298651 | 0.24522 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965750 | TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGCACA | 4734 |
rs113608159 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864938 | CACAGTGGTTCATGC[C/G]TGCAATCTCAGCACT | 4734 |
rs113623231 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895345 | ATGAAATCAGCAGAC[A/G]ACTGCTACTGTTGCA | 4734 |
rs113626549 | snp | G/T | 0.321292 | 0.23962 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974047 | ACTAGACTAAGGAGA[G/T]AAGGCCCAAATAAAT | 4734 |
rs113627583 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829199 | AATATGAATTTGCTT[C/T]ACATGTCTTATGAAC | 4734 |
rs113664064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920740 | TCAGCAGAATAAAGA[C/T]GGAATGACATTTATA | 4734 |
rs113680384 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838525 | TGTCCAAAAAGTTCT[C/T]CATCTATGATAAACC | 4734 |
rs113695209 | snp | G/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904635 | TAAACAGGTTGATTC[G/T]CTTCTTCTGAGTGAC | 4734 |
rs113701977 | in-del | -/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952996 | AATTCTTTTTTTTTT[-/C]TCTTTTTTTTTGAGA | 4734 |
rs113733285 | in-del | -/AC | 0.168135 | 0.236216 | intron-variant | NEDD4 | GRCh38.p7 | 15:55892640 | CAAAAAGAAAATGAA[-/AC]AGTTTCTACCCTCCA | 4734 |
rs113748713 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920692 | GAGAATTTGCTAGGA[A/G]AATGGTACATTTTAA | 4734 |
rs113766301 | snp | A/G | 0.48 | 0.0979796 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886603 | CCCCATCTCTACTAA[A/G]AATACAAAAAATTAG | 4734 |
rs113778248 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898645 | ACTTTTTTTTTTTTT[C/T]TTTTTTTTTGAGACA | 4734 |
rs113782468 | snp | A/G | 0.301081 | 0.244726 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945259 | GCAAGGAACCTAAAA[A/G]CCTTGAAAAAAGGTT | 4734 |
rs113798809 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864843 | ACAATTAAAGCTGTG[C/T]GGTTCTGGTGCATGC | 4734 |
rs113819591 | snp | C/T | 0.286564 | 0.247312 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976789 | GCCCGCCACCACACC[C/T]GGCTAATTTTTTTTT | 4734 |
rs113824884 | in-del | -/TAAAAAAAAC | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880712 | TCTCAGAGTAACAGT[-/TAAAAAAAAC]TATGTAACACCTAGA | 4734 |
rs113832270 | snp | C/T | 0.321053 | 0.23969 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971377 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA | 4734 |
rs113867444 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834301 | CCTAGAAAAAAGATG[C/T]ATTTAAAAACTTGAT | 4734 |
rs113868691 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956275 | TGGCTTGCATTTTCC[A/G]TAACCTTGTTTCTTA | 4734 |
rs113874414 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887067 | ACTTCAAATAAACAG[C/T]GTAAAAAGTGCATCT | 4734 |
rs113876054 | snp | C/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980030 | ATTCTCCTACCTCAG[C/T]CTCCTAGGCTCAAGT | 4734 |
rs113885354 | snp | A/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978137 | AAACCATCCATGTTA[A/G]CCTCGACTGAAACAC | 4734 |
rs113891541 | snp | C/G | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972547 | CAATAGATAAACCAA[C/G]AAATTAAAGCATACC | 4734 |
rs113900813 | snp | A/G/T | 0.0209421 | 0.100162 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968006 | AGACCTTATTTTAAA[A/G/T]AATTTATAAAATATT | 4734 |
rs113910146 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934341 | TCATTATATGTGTAT[A/G]TCTCATTTTGTTATC | 4734 |
rs114051376 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919868 | GGCCAAAGTCAGCTG[C/T]GGTGGTTAATTGTAT | 4734 |
rs114053579 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980625 | TCAACACAGAAAAGA[C/G]ATCGAGTGAATTCTC | 4734 |
rs114083214 | snp | A/C/G | 0.0142815 | 0.0833581 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960132 | ACTGACCCCATACCC[A/C/G]CAAAGGACTGCAGAA | 4734 |
rs114086893 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985076 | GCAAGATTCACCAAG[C/T]AAGTGACAGGGCCAG | 4734 |
rs114087436 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971246 | TTATTTGAAAATATA[C/T]CGTCAGAGGTGTAAA | 4734 |
rs114088528 | snp | C/G | 0.021333 | 0.101051 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971648 | AAAAAAGACTTATTA[C/G]CTTTAAAGAGGAGGT | 4734 |
rs114148312 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919923 | ACCCACTTGTTTGGT[C/G]AAACATCAGTATAGA | 4734 |
rs114166493 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942001 | ATTAGCTGTAGTGTA[C/T]TATACATGTCAAACA | 4734 |
rs114176861 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934838 | TTTACACAAATAATA[A/T]ATTCCTATATACAAT | 4734 |
rs114226470 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896906 | TTCTAAATTATTAAA[C/T]ATGATAATTTATAAA | 4734 |
rs114229345 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828641 | GCACAGCGCTAGGCA[C/T]GCAGCATTCAATAAA | 4734 |
rs114264654 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832696 | GCAGGATTACAGGTG[A/T]GAGCCACCCCTCCCG | 4734 |
rs114300493 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885380 | ATTTCACTGGTAACA[A/G]TAAGAACACAGAAAA | 4734 |
rs114334043 | snp | C/T | 0.138207 | 0.223612 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849914 | TCTCTAGCCTCAGCC[C/T]CCTGAACAGCTGGGA | 4734 |
rs114348256 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878328 | TGAATCAATAATAAA[C/T]AGAAAAACTGTCCCA | 4734 |
rs114348879 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836032 | TCTCTCACCCAGCAT[A/G]CTCAACTGCCTGTGG | 4734 |
rs114401399 | snp | A/C | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917961 | GGATTTAGCACATCA[A/C]ATAAACATGTCTCAA | 4734 |
rs114406078 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885881 | TAAACAGACTAAACG[C/T]TCCAATCAAAAGACA | 4734 |
rs114421233 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855055 | GAGAGTAAGGCTAGC[A/G]ATGATAGTCTTTCAA | 4734 |
rs114465327 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938673 | AAAGTGAAAAGGCAC[C/T]GTACAAAATGGGAAA | 4734 |
rs114481408 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923771 | TCTTTAGTTGCCAGT[A/G]TAATTACCATTTCTT | 4734 |
rs114483499 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976014 | TGACAAAGGTGCCAT[G/T]AACACACAATGGGGA | 4734 |
rs114502110 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882371 | CTTAGGGTTGGGAGA[A/G]CTCAGTGACAGTGGG | 4734 |
rs114535376 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905465 | AATATCAACAACAGA[C/T]ATCTGGAGGGAAATG | 4734 |
rs114566232 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919809 | GATTATCTACATGGT[A/G]TGGATAGGCTCTGGG | 4734 |
rs114568344 | snp | A/G | 0.0227299 | 0.104155 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973633 | AAGAGGAACTTGGAA[A/G]TTAATACAAACAAAT | 4734 |
rs114611656 | snp | A/G | 0.00931995 | 0.0676248 | utr-variant-5-prime, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55966511 | GGCAAGGCCTATTCC[A/G]GCTATAACTCTTACT | 4734 |
rs114641143 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870602 | ACAGTGGCTCAATTA[C/T]GGTTCACTGCAGCCT | 4734 |
rs114649998 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941146 | ATATAAGGCCAGCTG[C/T]TGTATATCAATTTCA | 4734 |
rs114654196 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893125 | TTTCTGAGTGAGCCA[A/C]GAAGCACAGATAAGT | 4734 |
rs114699141 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835901 | AATAGCCTTTAATGC[C/T]ACCTTCCTTCTCCCT | 4734 |
rs114708192 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919581 | TATAAAATGTAGTCT[C/G]TCAGTCCAGCAAATA | 4734 |
rs114709965 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861443 | TGAGTATTAAAAAAA[A/G]CAGAAAGAATGAATA | 4734 |
rs114712899 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896820 | GGAAAACTTTTATTC[C/T]TTGTTATAGCCCAAT | 4734 |
rs114792903 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972419 | TTAGTTTTCTCTTTT[C/T]CTGTTTGTTTTTGCA | 4734 |
rs114909729 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942988 | GTCCCTCTTGCTATG[A/C]TTCTACAAAGAGACT | 4734 |
rs114910958 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852728 | ATATATATATATTTA[C/T]CTTTTCTGAGAGAGT | 4734 |
rs114991606 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938632 | ACATTTAACTAAAAA[A/G]CTATATGACAAAAGA | 4734 |
rs115093591 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973389 | TAAAAACAAACAAAA[A/C]AACAACAACAAAAAA | 4734 |
rs115106841 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885107 | CAGGAAGCAGACTTT[G/T]CAGTGGAAACCTTAT | 4734 |
rs115132992 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968867 | AAATATGGAGGAGGA[A/G]GCGGAGCAAGATGGC | 4734 |
rs115206816 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870877 | TTCTAGTATCCTATG[A/T]TTTACTTAAGAAATC | 4734 |
rs115276894 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841664 | CTCGGCTCCGCCTTC[C/T]GGGTTCACGCCATTC | 4734 |
rs115294481 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976350 | CTAATCACTAGAAAA[C/T]ATATGAAGCTCAAAC | 4734 |
rs115310979 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882184 | AAATTTAAAAATCAC[A/C]CAAAAAGCACCTTCA | 4734 |
rs115330568 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908023 | AGTGCCACTCTTCCA[C/T]GCAAAGGATGAAGCA | 4734 |
rs115354156 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917850 | AAAAAAAAAACTATA[C/T]CCCAAGATAGTTTGA | 4734 |
rs115387329 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886485 | TAAAAAATTGAAATG[A/G]GCCAGGCGTGGTTGC | 4734 |
rs115484917 | snp | G/T | 0.0057033 | 0.0530954 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916745 | GCACATGTGAACATG[G/T]CTATCCAAGTCATCT | 4734 |
rs115491562 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929617 | TGTAAGCATCAGTTT[G/T]AATATATAAAATATA | 4734 |
rs115533752 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928058 | TCTGTCACCCTGGCT[G/T]GAGTACAGTGGTGCA | 4734 |
rs115577059 | snp | A/T | 0.0622301 | 0.165053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880456 | CACAAACCTGAAATA[A/T]AAGAGAGTACTTCCT | 4734 |
rs115585694 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896852 | TGCCTTACCTTTATA[G/T]TTTTAACATAATTTA | 4734 |
rs115590273 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965468 | CAGTCTCCCAAACCC[C/T]GTTTCTTAGGCAGTG | 4734 |
rs115682945 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979156 | TTAAAATCCTATATC[A/G]TCTAGGCAGAATCCT | 4734 |
rs115728824 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897501 | TCCTTTGACTTTTCA[A/G]TCACTAGATTCTTAA | 4734 |
rs115731768 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891886 | TAAGAGAATCCAAAG[A/T]AATAAAAAATCAGAA | 4734 |
rs115738078 | snp | C/T | 0.000115514 | 0.00759894 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915595 | TATGCATGAGCTTAA[C/T]ATACTCTGAATCAGA | 4734 |
rs115739669 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55936125 | AAGCATCCTAAATGA[C/T]ACACTTTGTCAGAGG | 4734 |
rs115759832 | snp | C/T | 0.132751 | 0.2208 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884238 | GGCTTGGAATGTCCC[C/T]TAACACACATATGGC | 4734 |
rs115777509 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849066 | AAAATCTATCACTGT[C/T]AGGCTATAATATCAA | 4734 |
rs115847759 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986928 | AACTGTCTAGGATAA[C/G]AAAAACTGTGCATGT | 4734 |
rs115905701 | snp | G/T | 0.296109 | 0.245711 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977739 | TTTATTTAATCTTGT[G/T]TTTTTTTTTAATTTA | 4734 |
rs115910013 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936364 | TATAGAAAAAAATCA[C/T]GCCAAATTTGTGTGC | 4734 |
rs115920009 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877419 | GATGCTTGTGCCCTT[C/G]TCAGTGCATCATATC | 4734 |
rs115924533 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978705 | ACTCATGAGTAAAGA[C/G]AGCTTTATTGTTTTT | 4734 |
rs116053822 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944015 | AGCTTTAAGATGTAA[C/T]GATTGGAAGATGGCC | 4734 |
rs116071486 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907931 | TATGAATCAGACTCC[A/G]CTGTGGAAACTAATC | 4734 |
rs116090701 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884815 | AGATCTAGAAAATAG[C/G]CTCAAATGGGCAAAT | 4734 |
rs116137940 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973851 | AAAAAAAAAAACAAC[C/T]TAGCTATGCATCTTA | 4734 |
rs116178758 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830894 | TTCATTTTGTAGAGA[G/T]GGGGGTCTCACTATG | 4734 |
rs116184318 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869969 | AAGAGAAGCTGGCCT[A/T]TGAGTTGGGGTTAGA | 4734 |
rs116220048 | snp | A/C/T | 0.0154538 | 0.0865337 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854650 | AACTTTTGGGGGTGA[A/C/T]AGAAGTTTCTTAAAC | 4734 |
rs116323476 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866939 | TATTTAATTTCTAAC[C/T]GCAAAGCCAATATGT | 4734 |
rs116356716 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830097 | TTGATGAGAATGTTC[C/T]AACACCACCAAAATA | 4734 |
rs116403854 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927038 | CCAAGATCGTGCCGC[C/T]GCACTGTCCAGCCTG | 4734 |
rs116410082 | snp | A/G | 0.00835141 | 0.0640778 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826707 | TTTTATCTTCTGGCT[A/G]TTTCACTAACAACCA | 4734 |
rs116492893 | snp | A/C/T | 0.0422008 | 0.138995 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922392 | TTGGAGACAGAGTTT[A/C/T]GCTCTTGTCACCTAG | 4734 |
rs116540137 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983309 | GTGTGTGCGTGCGCG[C/T]GCGTGCGTGCATTTG | 4734 |
rs116566513 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896428 | GCCTCAAGGGATGCA[A/C]CTGCCTTGGCCTCCC | 4734 |
rs116572074 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852355 | ATCCTACAAAGTGAT[A/G]TAATAGTTTACATAG | 4734 |
rs116630372 | snp | C/T | 0.030278 | 0.119257 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963228 | CCTTGACCTCCTGGG[C/T]TCCAGCGATCCTCCA | 4734 |
rs116638471 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919897 | ATGTATCAACTTCGA[C/T]AGGTTATGGTACCCA | 4734 |
rs116639110 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870107 | TTGCAGTAGTTGAGT[C/T]TGGCTAGATTATAGG | 4734 |
rs116666885 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839091 | TGGAGTGCAGTGGGG[C/T]GACTGTGGCTCACTG | 4734 |
rs116706321 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936801 | ATTTCTTTTCTTTTT[C/T]TTTTTTTTGAGACAG | 4734 |
rs116739399 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905182 | GTTAAGAATTCTGTA[A/C]GTAAATATCACTTTT | 4734 |
rs116792818 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834340 | CCAATGGCCTTTCCT[A/G]TGCCTCAGCTTCTGG | 4734 |
rs116795225 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943780 | TGGAGCTGTGAGAAG[C/T]AGGCCACTATCGTCC | 4734 |
rs116819209 | snp | A/C | 0.021333 | 0.101051 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908128 | GTGTAGTCATCCTCA[A/C]CTATCAGGATTCTGC | 4734 |
rs116820411 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854127 | GCACTCCAGCCTGGA[C/T]AACAGAGCAAGACTC | 4734 |
rs116870870 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896413 | GGTCTCGAACTCCTG[A/G]CCTCAAGGGATGCAC | 4734 |
rs116942508 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961428 | ACAGAAACTGTGAGA[A/C]AATAAATGTACGTTC | 4734 |
rs116989483 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973269 | TTCAGCTAGGCACAA[C/T]GGTTCATGCCTGTAA | 4734 |
rs117097600 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897918 | TGAGCCACACTCCCA[C/T]CCTTGGCTGTGGAAT | 4734 |
rs117135970 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843696 | AACATAATAATGTAA[A/G]CAGTTGATATAAGCA | 4734 |
rs117140196 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986213 | TAAAACAAAATAGTG[A/G]TGTTTGGTTCAGATA | 4734 |
rs117156506 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943015 | GACTGGCAGCATTGT[A/G]CCCCTGCTCTAGAAA | 4734 |
rs117175563 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962324 | TGTTTTTTAATTTAT[C/T]CTAACAACATCTGTC | 4734 |
rs117206500 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973512 | CCACTGCAGTCCAGC[A/C]TGGTCAACAGAGTAG | 4734 |
rs117280067 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982793 | CAGACAAAAACAAAA[A/G]CTGAGAAAGTTCAAT | 4734 |
rs117328211 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966790 | GAATAAGAATTTATC[A/G]CTGCGCTCAAGAAAA | 4734 |
rs117329472 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983311 | GTGTGCGTGCGCGCG[C/T]GTGCGTGCATTTGAT | 4734 |
rs117352429 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970493 | GCTTCAGGTGTGACC[C/T]AACACAGTCCCAGTG | 4734 |
rs117447005 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862034 | TGAGGTATGCAACAG[C/T]GCAATTCTACAGAAT | 4734 |
rs117452990 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912070 | TTCTAAGAAATATAC[A/C]TGTACAAATATACAT | 4734 |
rs117522829 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970401 | GCTGACTGAAGAGCC[A/T]TTGGGTCTTAAATAA | 4734 |
rs117543599 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909655 | CCTACAAAGCCTCTT[C/G]TCCTGGCTTCTCCTG | 4734 |
rs117596592 | snp | G/T | 0.109814 | 0.206997 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896109 | ACAAAAGCCCCCCAA[G/T]AGCTGCAATGATCCT | 4734 |
rs117640519 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841415 | GAGGAGTCAAATTCA[C/T]AGGGACAGAAAGCAG | 4734 |
rs117665158 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912613 | TTTAGAAAACAACAG[A/G]TGGGGGAAACAAAAT | 4734 |
rs117666854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983320 | CGCGCGCGTGCGTGC[A/G]TTTGATTTCCATGCT | 4734 |
rs117668121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846424 | TTAGTTCCAAACATA[C/T]TGCATTTGTGGCGAT | 4734 |
rs117669478 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926004 | TGTATCATATACATA[C/T]ACAGTATGTAAAATA | 4734 |
rs117693137 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860110 | AAAACACCAATGGTG[C/T]GTGTTCTCCCTTGCT | 4734 |
rs117715237 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993122 | CAAATCAACAGCGGG[A/G]ATGCTGCGACCGTCT | 4734 |
rs117718855 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939106 | GTGAGACCGTGTCTC[A/G]AAAACAACAACAACA | 4734 |
rs117724097 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909940 | CCAAAATGAGGTGTG[A/T]ATATTCATAAGCGAT | 4734 |
rs117753040 | snp | C/G | 0.030278 | 0.119257 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944415 | GAGATCGACCTGCCA[C/G]TCTGCAGACTGGTGG | 4734 |
rs117811054 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907674 | CAAAAGTAAAGGTCA[C/T]TCTTAGCTGAAACAG | 4734 |
rs117847376 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886171 | ATAAGTCTATATGCA[C/T]CCAACACTGGAGCAC | 4734 |
rs117863613 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872323 | TAACTTATTTACAGA[C/G]GTTTAAACCCTGAAT | 4734 |
rs117864424 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928338 | TTTAATCTATCTTTC[A/G]TACTGTAATCGGACT | 4734 |
rs117892826 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962224 | TACTGTTTGCATGGC[A/G]TATCTTTTTGCGTCC | 4734 |
rs117927944 | snp | A/G | 0.121022 | 0.21416 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979326 | AGTAATAAGATCATG[A/G]AAGTTTTTACCTCTT | 4734 |
rs117958966 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973060 | CAATATCCCACTTTC[A/C/G]GCACTGGATAGATCA | 4734 |
rs117999366 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837006 | CTTAAGAAATGAGTG[A/C]TCTGACAATCTGTCT | 4734 |
rs118055931 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938883 | GGGCAAGGCAGGAGG[A/G]TCACTTGAATCCAGG | 4734 |
rs118174519 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974891 | CATTTCTTTTCCTTT[C/T]TTTTTTTTTTTTTTT | 4734 |
rs137880859 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876048 | AGAATAAGAATACAA[A/G]TAATGGTTGACTTCT | 4734 |
rs137893846 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910112 | AGACTGTACTCTCCC[G/T]GTAGAGAGGGAGTTT | 4734 |
rs137931812 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978474 | AATCTCTCACATGTT[-/T]GAAAAGGAGGGAAAG | 4734 |
rs137958804 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841082 | GGAATTACAGGCGCC[C/T]GCCACCATGCCTGGT | 4734 |
rs137961192 | snp | C/G/T | 0.00677167 | 0.0578647 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885439 | GGTGTGCTAACTACT[C/G/T]ATATGTTAAGTAGAA | 4734 |
rs137964612 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925983 | ATGTAAAAATACATA[C/T]ACATATGTATCATAT | 4734 |
rs137998259 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920951 | GTAAACCGAGTTTCT[A/C]AAGAAAAGCTGTATT | 4734 |
rs138004913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880765 | CAGGAAGACAGCTAC[A/G]AGAGAGATGTTTCCT | 4734 |
rs138012178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950965 | TGGAATTTGCTTTTA[C/T]GGTAAATGAGGCAGA | 4734 |
rs138032615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977225 | ATATGATGGTGGTCC[C/T]ATAAAATACCACATT | 4734 |
rs138054022 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949638 | ACAAAAGGATGAGTT[A/C]ATGTCTTTTGTAGGG | 4734 |
rs138063015 | snp | C/T | 0.000214537 | 0.0103548 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863030 | GAAGGTTCTTGTTGT[C/T]GCTGCAAATGGCAAG | 4734 |
rs138066287 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847894 | CACGTTGGCCGGGCC[A/G]GTCTCGAACTCCTGA | 4734 |
rs138070169 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929838 | AAACTATAAGGAGTA[A/T]CCTTAGAAACATTTA | 4734 |
rs138138988 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984543 | ACTTTCACTAAAGCA[G/T]CTTTATTGACGGCCA | 4734 |
rs138158780 | in-del | -/GCTGGGC | 0.304188 | 0.244057 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926619 | AAATAACAAAAATTA[-/GCTGGGC]GCTGGGCATCATGGC | 4734 |
rs138186256 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854039 | CGTCTGTAGTCCAGC[C/T]ACTCGGGAGGCTGAA | 4734 |
rs138242255 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863789 | GCACCTTGCTTACGG[C/T]AGAAATCAATAACTA | 4734 |
rs138277608 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935471 | CCAACAATGGGGTAG[C/G]AAATATGCACATTAC | 4734 |
rs138277913 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886942 | TATTGAAAATTTTCT[G/T]GAAACAAATAATGGA | 4734 |
rs138322442 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992668 | TCTCCAAGAACACAC[A/C]GAAGCCACATATCAT | 4734 |
rs138346814 | snp | A/G | 0.00146723 | 0.0270456 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916029 | GGACTCCTAGGAAAA[A/G]TGACTAAGGAGGAGT | 4734 |
rs138361942 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960673 | CTTCATATATATATC[A/T]ATCCTATTAGTTCTG | 4734 |
rs138366239 | snp | A/C | 0.126219 | 0.217206 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933115 | ACCATTGTGGAAGAC[A/C]GTGTGGCGATTCCTC | 4734 |
rs138369888 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921057 | TCAGAGAGCTACAAA[C/T]GCGTTAAGTCTACGA | 4734 |
rs138375681 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943198 | AAGGAAAGCAGAGCA[C/T]AAAAGTTGGGAATAT | 4734 |
rs138393120 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840133 | TAGTGGGATGTTTAA[C/T]GTTATCTATAACTTA | 4734 |
rs138400447 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860478 | TCAATTCTTCTGCAA[A/G]ATGAGTTGGAACATC | 4734 |
rs138425602 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950731 | AGGTGAACAGAGAAA[C/T]GACTCAACAGCTAAA | 4734 |
rs138463950 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55936196 | CTGTATTTACTCTCC[A/G]GTATCATTGTTTTCC | 4734 |
rs138463988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972641 | GAAGTCCTTACTTAT[C/T]AATAATAACAATGAA | 4734 |
rs138484838 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968674 | AGAGTTCTAAATGCA[C/T]TGTTGGTGGGAGTGT | 4734 |
rs138494293 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960672 | CCTTCATATATATAT[C/T]TATCCTATTAGTTCT | 4734 |
rs138512133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830075 | AAACAGAGCAATGCT[A/G]CTATTCTTGATGAGA | 4734 |
rs138562132 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880283 | GGTGACGGAGTGAGA[A/C]CCCGTCTCCAAAAAA | 4734 |
rs138577174 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844402 | CTGGTCAGTTAAAGA[A/C]CCCTGGAATAGCTGA | 4734 |
rs138585173 | snp | A/G | 0.165853 | 0.235413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947302 | AAGAATCAAATAGAC[A/G]CAATAAAAAATGATA | 4734 |
rs138587615 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871527 | TTGATATGCAGATGT[C/T]ACAATCAGTCTAAAA | 4734 |
rs138606065 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981271 | CTCACCACCATGTTG[A/G]CCAGGCTGGTCTGGA | 4734 |
rs138624646 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876902 | AAGAGATGGAGTCTT[A/G]CCATCTTACGCAGGA | 4734 |
rs138628831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955470 | CTTCCATTTCTACTT[A/G]CCCCTCACCCCTCAC | 4734 |
rs138634415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866111 | TAGAGATGGGGTCTC[A/G]TTATGTTGCCCAGGC | 4734 |
rs138650259 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992313 | AATTAAATTCTAATC[A/G]CATCACGTAAGCATT | 4734 |
rs138656092 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926536 | GCACTCCTAGGCTGA[A/G]GTGGGAGGATCACTT | 4734 |
rs138662542 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983909 | AGCCACTGCGCCCAG[A/C]CTGTTATAAATACTT | 4734 |
rs138682936 | snp | C/T | 0.295854 | 0.245759 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976687 | CAGGCTGGAGTGCAG[C/T]GGTGCAATCTCACTT | 4734 |
rs138742175 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923087 | TACTTGGAAGGCTGA[A/G]GCAGGAGAATAGCTT | 4734 |
rs138764182 | snp | G/T | 0.00034624 | 0.013153 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842115 | GGTAAGAGTCTTCAA[G/T]AACAGTTGCTCGGCG | 4734 |
rs138767007 | snp | A/C/G | 3.36356e-05 | 0.00410084 | missense, stop-gained, intron-variant | NEDD4 | GRCh38.p7 | 15:55837821 | TTTGCTTCTGGATTC[A/C/G]GTTTACAAATCGCCA | 4734 |
rs138768125 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893293 | CATGATTCCTCTGTA[C/T]AGATCATATAATTCT | 4734 |
rs138790556 | in-del | -/GTGT | 0.39709 | 0.20215 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964651 | TGAATTTTGCTGCTG[-/GTGT]GTGTGTGTGTGTGTG | 4734 |
rs138840707 | snp | A/C/T | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828945 | TGTAAACATGATAAA[A/C/T]CCTGTAAACATACAT | 4734 |
rs138845499 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859735 | AAAACCAACTTCAGC[A/G]TAACTGGGAGAGAGA | 4734 |
rs138910121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908276 | CAAATCTGAGCCCAG[A/G]AAAGATTTGCTTAAT | 4734 |
rs138946818 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939161 | CAATAATATGGTTTG[C/G]CTCTGTTGCCCACCC | 4734 |
rs138951402 | in-del | -/AATAAATAAATAAATAAATA | 0.0551013 | 0.156571 | intron-variant | NEDD4 | GRCh38.p7 | 15:55892267 | GCAAAACTCCAACTC[-/AATAAATAAATAAATAAATA]AATAAATAAATAAAT | 4734 |
rs138977557 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861233 | GTAGAGTACTCCATG[A/C]ATGAATGTGAAGGGC | 4734 |
rs138980842 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865197 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 4734 |
rs138998116 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899755 | TCTGTACTGATGGAA[A/C]TGTTCTGTACTACTG | 4734 |
rs139010560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849034 | CCTAAATATGTGACA[C/T]AATATTTTCTCCTTC | 4734 |
rs139021051 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930675 | CCAAATGTGTCAACG[A/G]CAGGGCTAGGTGGAG | 4734 |
rs139021155 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961580 | GGTTCATATCATTCT[C/G]CTGCCTCAGCCTCCC | 4734 |
rs139079378 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856003 | CCCTGAACATCACCA[C/T]CTGGAGCCTACATTC | 4734 |
rs139084289 | in-del | -/ATT | 0.0267878 | 0.112589 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968521 | TCTAAAATATACATC[-/ATT]GAGACAAATGATAAT | 4734 |
rs139095205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867424 | CTCCACAGAAACTCA[A/G]CTGTGAATAGGGTCC | 4734 |
rs139098949 | snp | C/T | 4.96833e-05 | 0.00498389 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915868 | GAAGTCCATTGACAG[C/T]TGTTGAAAGAAATCC | 4734 |
rs139123211 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934413 | TGAATAATGCTGCTA[C/T]GAACATTGGTGCGCA | 4734 |
rs139131290 | in-del | -/T | 0.142272 | 0.225598 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832175 | GAGATTCTCCACCCC[-/T]ATCTTGAAAAAAAAA | 4734 |
rs139142216 | snp | C/T | 0.000178158 | 0.00943648 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916851 | TCTCATTTCCAAACA[C/T]GTTAAGGGCTGAAAG | 4734 |
rs139163169 | snp | A/G/T | 9.88556e-05 | 0.00702987 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916562 | CCTTGTTGGCTGTAG[A/G/T]GAAATCTGTAGACAG | 4734 |
rs139209941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970826 | AAGGATGGGTACAAA[C/T]CAGCCCAGACTGTGA | 4734 |
rs139245513 | snp | A/C/T | 0.000990417 | 0.0222315 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842129 | AGAACAGTTGCTCGG[A/C/T]GAAGTTTCATTTCAA | 4734 |
rs139250178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924094 | CAATCATTTTATAAA[A/C]AGAACATCAGGTTTA | 4734 |
rs139269466 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952225 | TTTAGTCACAACTAC[G/T]CGGGAGGCTGAGGCA | 4734 |
rs139281238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836744 | CATTAGCCAGACTAG[A/T]CTCAAACTCCTGACC | 4734 |
rs139348860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844973 | CCACTGCACCTGGTG[C/T]TTTTAATATTCTTTA | 4734 |
rs139371902 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832616 | AGACGGGGTTTCACT[A/G]TGTTGGCTAGGCTCA | 4734 |
rs139377739 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877577 | CTTTGAGGTTATGTA[A/G]ATAGCCCATTTCTCA | 4734 |
rs139395127 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835204 | AACCCACTGCAATCG[G/T]ACTTCTACACTACAG | 4734 |
rs139396981 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888831 | ATTGGGTAAAGGTGC[C/T]GAGAACATACACTGG | 4734 |
rs139416324 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873448 | CTTTTCTACAAGAGA[C/T]GCCACTCTTATCTTC | 4734 |
rs139419957 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994236 | TCCCTAGGATTTGTA[A/T]ACAGTGCCAGTTCCT | 4734 |
rs139420567 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947589 | TCTACCAAAGGTACA[A/G]GGAGCTTATCCACCA | 4734 |
rs139422357 | in-del | -/GTC | 0.299158 | 0.245119 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958134 | AAAAAAAAGATGACT[-/GTC]TTCTTTTATTCTATT | 4734 |
rs139462920 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960674 | TTCATATATATATCT[A/G]TCCTATTAGTTCTGT | 4734 |
rs139477908 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895086 | CTAAGGTATAAAGTT[A/G]TAATTTAGCCAGGAA | 4734 |
rs139514179 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944973 | AGCATCAACATCAAC[A/G]AAAAGGACATACACA | 4734 |
rs139514549 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981437 | AACTAAACACTGGAA[C/T]CTATGGATTGACAGC | 4734 |
rs139522803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937365 | TGACAAAGAGGAAAA[C/T]AGAGGACCACACATA | 4734 |
rs139527779 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904764 | GTCTTTCTAGGAGTG[C/T]ATATGCTTCTAGAAT | 4734 |
rs139542357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831675 | CAGTTCTGCAAACTC[A/C]TATTAATGAGGCTTG | 4734 |
rs139554400 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978667 | AGGGCTCTTCACTAA[A/G]GCTTGAAACTTCCCT | 4734 |
rs139567385 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900710 | AAAATTGAGCTTTTA[C/T]GTATGTCTCAAAGAG | 4734 |
rs139634497 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940410 | GAACTATACCCCCAA[A/T]AAATCAGTTAAAATT | 4734 |
rs139657664 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940081 | ATGAACCTTGAGGAC[A/C]CTACCCTAGGTGAAA | 4734 |
rs139682945 | snp | A/G | 0.000153988 | 0.00877327 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916490 | CTTCAAGATACAAGT[A/G]AACGAAGCATCATCA | 4734 |
rs139684677 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878045 | AGAACCCTGATAAAT[G/T]TTACTGGAGAATCAT | 4734 |
rs139695240 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922384 | TGCTTTTTTGGAGAC[-/A]AGAGTTTCGCTCTTG | 4734 |
rs139709881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985660 | TTGAATTGGAAAAAA[C/T]CAGTATGAATTCATG | 4734 |
rs139714439 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874114 | GTAGAGTTTTTTTTT[-/T]ATTCAGTCATATGCA | 4734 |
rs139731640 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966718 | AAAGAAAATTATTTG[-/T]TAGATGACCTGATTA | 4734 |
rs139741605 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858225 | ACTATATGGTTGCCA[C/T]GTATTACTTTAAGTA | 4734 |
rs139747556 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927959 | ATATTGCTAAGAAAC[G/T]AATCTGCTGTCCTGG | 4734 |
rs139764003 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934014 | CAAAATTAGCTGGGT[A/G]TGGTGGCACACGCCT | 4734 |
rs139794785 | in-del | -/AT | 0.506463 | 0.0676264 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920188 | ATATATTGTGTGGAA[-/AT]ATATATATATTCATA | 4734 |
rs139810216 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932037 | TGGCTTCTGATATGG[G/T]TTGACTGTGTCCCCA | 4734 |
rs139811523 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964093 | CTTCATTGTGTTCTT[A/C]ATGTTTATTATCCTG | 4734 |
rs139830531 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960309 | AGACACACCCTCAAT[C/G]TGGGTGGGCACCATC | 4734 |
rs139880232 | in-del | -/A | 0.17138 | 0.237316 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885917 | TGGCTGAATAGATTT[-/A]AAAAAAAAAAATCAA | 4734 |
rs139911224 | in-del | -/C | 0.320575 | 0.239832 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967713 | AGAAATATAAAAAAA[-/C]CTTCATAGATAACAT | 4734 |
rs139947511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882459 | CTCAGCCATGGTCCA[C/T]GAAGGTGGCATTTAG | 4734 |
rs139975951 | snp | A/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917714 | GCATTTTCTCCTGTA[A/T]TTTTAAGGCCTTTTC | 4734 |
rs139987806 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878883 | GCTGGGGTGCAATGG[C/T]GCGATCTCGACTCAC | 4734 |
rs139996016 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837103 | GCAGCTATATGTCGT[C/T]ACATGTAAATATCCC | 4734 |
rs140007357 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851375 | CAAAGTTTTTTTTTT[-/T]ATCAAGCAGCACCTC | 4734 |
rs140022173 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912138 | GGCATCACATTTTAG[A/G]ATATTTATAAATTAC | 4734 |
rs140022527 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949710 | GCAGGGACAAAAAAC[A/C]AAACACCTCATGTTC | 4734 |
rs140034645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986100 | CTGATTACAACCTGC[A/T]GAATAAAGTGGGATT | 4734 |
rs140043649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925019 | ACTGCAGTGAGCCAA[A/G]ACTGTGCCATTGCAC | 4734 |
rs140078994 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928211 | GAGACAGGGTTTCAC[C/T]GTGTTGGCCAGGCTG | 4734 |
rs140081916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843327 | TATGCGAAAGCTACT[A/G]TTATTGTCTTCATTT | 4734 |
rs140118042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854596 | TAGAGAGCAGATGAG[C/T]GGTTGCTTGCAACTG | 4734 |
rs140126503 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982854 | GGGCTGGGGGTGGTG[A/G]CTCACACCTGTAATC | 4734 |
rs140183266 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894644 | GTCCTTTGAATTTCA[A/G]TTTCTTTGGAGTTCT | 4734 |
rs140189460 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959583 | TAAGCATGGGACAGA[G/T]CTATATATTCTAACC | 4734 |
rs140223805 | snp | C/T | 3.32851e-05 | 0.00407939 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55847031 | CCCTGGAGTAGGGCA[C/T]TGCCTTTAGTTGGAA | 4734 |
rs140250611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885118 | CTTTTCAGTGGAAAC[C/T]TTATTACCTTGGAGA | 4734 |
rs140275320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991442 | TCCGAGGCTGAGACT[A/G]TCTTTTTTCCCTCTC | 4734 |
rs140288025 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944263 | ATAAACTGTACCTGG[-/A]AAAACAGGACACTTC | 4734 |
rs140295093 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847227 | GTTTAAGATAAAATT[C/G]TATTCAGCAATTCCT | 4734 |
rs140298624 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880686 | GAATCTCAGAAAGAC[A/C]GGGAAAGGAAGTCTC | 4734 |
rs140317557 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929520 | GGCCGCGGTGTCTAT[C/T]GTTCCTGTCTTTGTA | 4734 |
rs140318097 | in-del | -/AC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883697 | CACACACACACACAA[-/AC]ACACACACACACACA | 4734 |
rs140333401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890313 | TTTAGAACATTTTCA[C/T]CACCCAAAAAGAACA | 4734 |
rs140341562 | snp | A/G/T | 0.0123139 | 0.0775937 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957889 | AGAAAACCAAACACC[A/G/T]CATGTTCTCACTCAT | 4734 |
rs140362771 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861654 | TCTCATGTACCCCAC[A/G]AACATATATACCTAC | 4734 |
rs140371823 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859281 | TACTTTATTCTGAAC[C/G]CTATGGACAACAGTT | 4734 |
rs140379278 | snp | C/T | 5.1181e-05 | 0.00505845 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55837843 | AAATCGCCATTGTAT[C/T]ACAAGACTAAAAAGA | 4734 |
rs140402189 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858845 | ATACTGGCTGTGGGC[C/T]ATATGGTTGCTGCTG | 4734 |
rs140406094 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911047 | CACATCCCCAGGCTA[A/C]CCTATGCTTGAGCCC | 4734 |
rs140409404 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827029 | ACATCAATCTTGATA[C/T]ATATATTTACTGTGT | 4734 |
rs140440361 | snp | C/T | 4.94605e-05 | 0.0049727 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860663 | AAACTACTTATACCT[C/T]GGAAGACTCTCGGTT | 4734 |
rs140454449 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920950 | GGTAAACCGAGTTTC[C/T]CAAGAAAAGCTGTAT | 4734 |
rs140455133 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969328 | GGCTAAAGCACTCCA[A/G]GATCCTAAATAAACT | 4734 |
rs140497718 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905544 | GAACCAGAGACAACA[C/T]AGGACCTGAAACAAA | 4734 |
rs140499972 | snp | C/T | 0.00898866 | 0.0664344 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55834252 | TTTTCATCAAAAATT[C/T]TGATGAGATCCTGTG | 4734 |
rs140505391 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913124 | TAGAAACCAGGTTCT[C/T]TGACCAAAGCAGTGA | 4734 |
rs140511198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938524 | GAAGAAAACAGAGAA[A/G]AAGCTTCTTGACTTT | 4734 |
rs140525099 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948356 | ATAGGAAGAATCAAT[A/G]TTGTGAAAATGGCCA | 4734 |
rs140550996 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941616 | GTCACCCAGGCTGGA[A/G]TCCAGCAGCACAATT | 4734 |
rs140610151 | in-del | -/TCCTTCCTCCCTCTCTCCC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940474 | CTAATTCCAAAGTAG[-/TCCTTCCTCCCTCTCTCCC]TCCTTCCTCCCTCTC | 4734 |
rs140619665 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859829 | GACCACTCTGTAATC[A/G]TGGCTGAATATAGAC | 4734 |
rs140623117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975603 | CTACAATGAAAACTA[C/T]AGATGAAAGAGATAG | 4734 |
rs140638728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908946 | TTAGGTATATCTGTA[C/T]TTAACTTCAGGTATA | 4734 |
rs140642756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972021 | TAGAATAGTATATCC[A/G]GTGAAAATACCCTTC | 4734 |
rs140659714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950653 | AGTACAGTGGGTTAA[C/T]GAGCGTCCCGGAGAA | 4734 |
rs140667871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976091 | TATATAGAAGAATCA[A/G]ACTAGACCCCTATCT | 4734 |
rs140700109 | in-del | -/ATTTCAG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910004 | ATTTGATATTGCTGA[-/ATTTCAG]ATTTCCTTTTCACTC | 4734 |
rs140700456 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880174 | GTACATGCCTTTAAT[C/T]CCAGCTACTCAGGAG | 4734 |
rs140783302 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844862 | ATTCAGGCTGGAGTG[C/T]AGTGGCATGATTATA | 4734 |
rs140785047 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892309 | AAATAAATAAATAAA[A/T]AAATAAATAAATAAT | 4734 |
rs140792200 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851635 | GCATGCGCCACCACG[A/C]CTGGCTAATTTTTGT | 4734 |
rs140800682 | snp | C/T | 0.00730654 | 0.059999 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834113 | TTCCCTCCAGTCATT[C/T]ACATCAACATCTCCC | 4734 |
rs140823423 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842448 | CTGGAGTGCAGTGGC[A/G]TGAACATGGCTTACT | 4734 |
rs140828345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886027 | GTACTTCATTAAAAC[A/G]GAAATCAAAAAAGGG | 4734 |
rs140828914 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956023 | CAGGGTCTTATCACC[A/G]GGCTGGTCTCGAACT | 4734 |
rs140833857 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928746 | TCAAAGTAGTTGATC[A/G]GATTTACTACATTTT | 4734 |
rs140836346 | in-del | -/AC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883679 | GTTCCAGGCATCTCA[-/AC]ACACACACACACACA | 4734 |
rs140854660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992246 | AGGGACTATGAGCCG[C/T]CACCATTTGTCCATC | 4734 |
rs140868475 | snp | A/C/G | 0.00110618 | 0.0234921 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856139 | AACTCACCACAGGAA[A/C/G]TGTAGGTTGTTCCTC | 4734 |
rs140869235 | snp | C/T | 0.000725833 | 0.0190365 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915961 | AAGTTTGATAGGATC[C/T]TTTGCTCAGAAGAGT | 4734 |
rs140874639 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846570 | AGAATGAATGACTTT[C/T]GCTGGAAAACAACAA | 4734 |
rs140875720 | in-del | -/TATCTATCC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960669 | TCCCCTTCATATATA[-/TATCTATCC]TATTAGTTCTGTCCC | 4734 |
rs140884430 | in-del | -/ATATATAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903846 | AAAAAAAAAACACAC[-/ATATATAT]ATATATATATATATA | 4734 |
rs140909650 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882701 | ACCAGTTGGAGTGGT[A/C]AAGGGAGTGCGTGTG | 4734 |
rs140918430 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952779 | TTTGGCTTTTTCTTT[G/T]ATCTAGGTTTCTCTA | 4734 |
rs140925562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926067 | TGTAAAATACATATA[C/G]GTATGTAAAAATACA | 4734 |
rs140925989 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957582 | TTCCTCAAGGATCTA[C/G]AACTAGAAATACCAT | 4734 |
rs140956528 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989631 | TCTCCATACCGATAG[C/T]GGAGACTCTGAACTC | 4734 |
rs140965590 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955154 | AGCCTCCCAAGTAGC[A/G]GGGACTACAGGCGCA | 4734 |
rs140975138 | snp | A/G | 4.9879e-05 | 0.0049937 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916784 | TTCTGACAAAGGGTA[A/G]GTATTGCTTCTTCTG | 4734 |
rs140978429 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967216 | TAACTACTTAGAAAA[G/T]GTTATTTTTTTAAAT | 4734 |
rs140994280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870642 | AGGCTCAGGTGATCT[C/T]CACACCTTAGCCTCC | 4734 |
rs141043242 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919807 | GTGATTATCTACATG[A/G]TATGGATAGGCTCTG | 4734 |
rs141174461 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980345 | AAGTAGCTGAAAATA[A/G]AAGCCTCATCCCCCA | 4734 |
rs141211068 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836682 | ACGTGCACGCCACCA[C/T]GTCCGGCTAATTTTT | 4734 |
rs141251902 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907305 | AAAAGACAGAAAATC[C/T]TCAAAGAAATAATAT | 4734 |
rs141281865 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828429 | ATAAGGATGAAACAA[C/T]ATAAGTATGAAATAT | 4734 |
rs141325621 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942160 | GTCAATTTTGACTTC[C/G]TAATTTTAAAGATTA | 4734 |
rs141395937 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951974 | TCTCAAGTTATCTCA[C/T]GGGTGTAAACTCTTC | 4734 |
rs141415497 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988896 | GTATGAGAAGAATAC[C/T]GGAGCTCTTTGTGTT | 4734 |
rs141446203 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857099 | GAGACAGCAAGTGAA[A/G]AAAGCAAGTTACCAA | 4734 |
rs141462074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935154 | ATTACAGGCATGAGC[C/T]ACCATGTCTGGCCTT | 4734 |
rs141498490 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888277 | GAACTGATACATTCA[C/G]TAAAGTTGCATGATA | 4734 |
rs141543647 | in-del | -/A | 0.328382 | 0.237395 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864387 | AACTGTATTATGATT[-/A]AAAAAAAAAATAGGC | 4734 |
rs141563688 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942854 | AGGATGATGGAAAGA[C/T]AGAATTTCCTAGAGA | 4734 |
rs141563734 | snp | A/C | 0.000115377 | 0.00759443 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916411 | TGGCTGGACTGCTTA[A/C]AAGGTGACCATCATT | 4734 |
rs141583170 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864738 | GTTCAACAGAAACAT[A/C]AACAAGCAGGAATAA | 4734 |
rs141675289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969034 | AGAGGCACTGAAGAG[A/G]GTAGGAAAGACAGTC | 4734 |
rs141692030 | snp | C/T | 0.000153988 | 0.00877327 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916019 | GGTAGTTGAAGGACT[C/T]CTAGGAAAAATGACT | 4734 |
rs141693007 | snp | C/T | 9.09546e-05 | 0.00674307 | missense, utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55872454 | TTAAATGTATATGGT[C/T]TCTCCAATCTTGGAT | 4734 |
rs141699267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877337 | TGACTAGTCATAGAA[C/G]ATCCTTCTAATATTT | 4734 |
rs141718031 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981090 | GTCGCCCAGGCTGGA[A/G]TGCAGTGGTATGATC | 4734 |
rs141742218 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874749 | GAGGCCGAGGTGGGC[A/G]GATCACCTGAGGTCA | 4734 |
rs141782603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871458 | GAAAGCATGTGACAA[A/C]TTGAAAAGCAGGCTG | 4734 |
rs141782645 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924880 | CGAGACGAGCCTGGC[C/T]AACATGGTGAAACCT | 4734 |
rs141787647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872799 | GGACTATGCACATGT[C/G]TGCAGGCTGGCTTGG | 4734 |
rs141787743 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927072 | AACAGAGTGAGACTA[C/T]GTCTCAAAAAAAAAA | 4734 |
rs141797053 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983934 | ATACTTTCATCTTAC[A/G]CTGTTTTCCTTAATA | 4734 |
rs141825349 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923140 | AGTGAGCTGAGACTG[C/T]GCCACTGCACTCCAG | 4734 |
rs141832191 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980089 | CTGGGATTACAGGCG[C/T]GTGCCACTATGCCCA | 4734 |
rs141837287 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981321 | CCACCCGCCTCAGCC[A/T]CCCAAAGTGCTGGGA | 4734 |
rs141854751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857235 | TGATTTATCACCAGC[A/C]AATCAGTATCATTTA | 4734 |
rs141916786 | snp | C/G | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842096 | TTGACACCCATAATT[C/G]TCCGGTAAGAGTCTT | 4734 |
rs141945279 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958575 | TTTTTTTTCCCTAAA[C/T]GTCTGATAGCTGCAT | 4734 |
rs141966149 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860998 | TTGTGAAAAGGTATA[A/G]CATGTCTGATTTGAT | 4734 |
rs141996991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972669 | GAATGTAAGTGAACT[A/G]AACTCTCCAATCAAA | 4734 |
rs142018487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909777 | TAGCCTGTAAGAAGC[C/T]GGCAACATAGACAGA | 4734 |
rs142040608 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855737 | TGAATGCCAGTGCAC[C/G]CCTGAGTGATGAAAC | 4734 |
rs142044619 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884988 | ATGACCTAAATAAGA[C/G]TCCTCAAGATATTTA | 4734 |
rs142047126 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953696 | ATCTGCCCGCCTTGG[C/T]CTCACAAAGTGCTGG | 4734 |
rs142067415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991057 | AGACACTGACTCAGC[A/G]ACTATTCACTATATA | 4734 |
rs142085803 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900662 | AAAAGCCCTATCAGA[C/G]CGACAAAATTGAGTT | 4734 |
rs142179890 | in-del | -/AAAAT | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884762 | ACAGTAAGAGGAGAC[-/AAAAT]AAAAAGAATAAAAAA | 4734 |
rs142185481 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903925 | AGCACTTTGTGAGGG[C/T]GAGGTGGGAGGATCA | 4734 |
rs142192275 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905738 | TGTTTTTTTCTTGTA[A/C]ATTTGTTTGAGTTCT | 4734 |
rs142193286 | in-del | -/AT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976627 | CCAATCTGGGCAAAA[-/AT]TTTTTTTTTTTTTTT | 4734 |
rs142195370 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967685 | AAACTATTAGAACAG[A/T]AATAAAATTAATAAG | 4734 |
rs142200598 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901331 | GGATCAAAGAAACAA[A/G]AGTTCGTTTTAGAAC | 4734 |
rs142205609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966098 | ATTCCCTTCTTCCAA[A/C]CATGAACTCCCCACC | 4734 |
rs142213582 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944702 | GTGGGTCCCTGACCC[C/T]CGTGTAGCCTAACTG | 4734 |
rs142222432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899795 | GCAGGAGCCAGTGAT[C/T]ACATGTAGCTATGGA | 4734 |
rs142286786 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896608 | TGCACTCCAACCAGA[C/T]GGTAAATTCCTTGAG | 4734 |
rs142294138 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833489 | AAGGTGAAACCCCGT[C/T]TCTACTAAAAATACA | 4734 |
rs142299011 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961561 | CTGCAACCTCCGCCT[C/G]CCGGGTTCATATCAT | 4734 |
rs142322580 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874225 | GATAACAATTATATT[A/C]TGTGACAAAATACTA | 4734 |
rs142364501 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982568 | GGTGACAAAAGGCTG[C/G]CTATAGAGAGTAGAC | 4734 |
rs142414802 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883696 | ACACACACACACACA[A/C]ACACACACACACACA | 4734 |
rs142432126 | in-del | -/ACACACACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836332 | ATGAAAAAGTATGTG[-/ACACACACAC]ACACACACACACACA | 4734 |
rs142518019 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922523 | GCCCACCATCACGCC[C/T]AACTAATTTTTGTAT | 4734 |
rs142529928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858599 | GGCGTGAGCCACCAC[A/G]CCTGGCCTAATGTAG | 4734 |
rs142564120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880010 | AAATAAAAGGGCTGG[C/T]TGGGCATGGTGTCTC | 4734 |
rs142568932 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834890 | ATCCCTGCGTCCCAA[C/T]CATCACCAACACCCA | 4734 |
rs142573482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949916 | GTAACAAACCTGCAC[A/G]TTGTGCACAGGTACC | 4734 |
rs142595461 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837027 | CAATCTGTCTACCAA[C/T]TGGAAAAATTTAAGT | 4734 |
rs142608757 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950979 | ATGGTAAATGAGGCA[G/T]ATGGGGTGGAAAGGC | 4734 |
rs142621799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960997 | TGTTTTGTTGAGTTG[A/C]CTCCCGTGTCTCACC | 4734 |
rs142641186 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862081 | CTTTGCAGTCTGTAC[A/G]TCACTCTATGAAGAC | 4734 |
rs142648314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949653 | CATGTCTTTTGTAGG[A/G]ACATGGATGAAGCTG | 4734 |
rs142651788 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875371 | CTGGAGTGCAGTGGT[C/G]CAATCACAGCTAACT | 4734 |
rs142671797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871829 | CAGTAAATCCACACA[C/T]GTTTTCACTAGATTT | 4734 |
rs142674363 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911654 | CCTGCCTCAGCCTCC[C/T]GTGTAGCTGGGACTA | 4734 |
rs142680915 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974436 | GCCAATATTACTCTG[A/T]TATCAAAACCAGACA | 4734 |
rs142685907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877732 | TAATTATTATTCTGC[C/T]TAAGCAAAGAATTTT | 4734 |
rs142706313 | in-del | -/T | 0.118933 | 0.212888 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843886 | ATGGGGAATAAAGGG[-/T]AATAAAAACATAGGG | 4734 |
rs142716772 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866212 | AGCCACTGTGCCCAA[C/G]CTTTCTTCTTTTTTT | 4734 |
rs142722029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943530 | TAGAAGGTTCAAACC[A/G]TAAGTCTTGGTGGCT | 4734 |
rs142789307 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974098 | AGACATTACAACTGA[C/T]ACCACAGAAACTCAA | 4734 |
rs142815278 | in-del | -/AA | 0.324145 | 0.238752 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969888 | AGGAGAGGGAAAAGT[-/AA]AAAAAAAAAAATTGT | 4734 |
rs142847474 | in-del | -/AC/ACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985760 | GTGTAGAGTACACAT[-/AC/ACAC]ACACACACACACACA | 4734 |
rs142859883 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839382 | TGTTTATACCCAGCC[C/T]GAGTTAAAGAAAAAT | 4734 |
rs142861794 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919446 | CATGCACTTCCTAGC[A/G]CTCTAGTCTGAGTTT | 4734 |
rs142908237 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949895 | ATATGGCACGTGTAT[A/G]CATATGTAACAAACC | 4734 |
rs142909749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899454 | ACTGAAGACTATAAC[A/T]TATCAATGAAAACAG | 4734 |
rs142989118 | in-del | -/CCCTGTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835964 | CACTTCACACACAGG[-/CCCTGTA]TAAGCTGGTCTGTTA | 4734 |
rs142994143 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852822 | TGGTATGATCTCGGC[C/T]CACTGCAACCTCTGC | 4734 |
rs142999433 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938741 | TCCAAACTTCAAAAT[A/T]ACATACAAAAGGAAC | 4734 |
rs142999564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894534 | TACGGCCCTTAGAAA[C/T]CCTCACATCTTTAAA | 4734 |
rs143020253 | snp | A/G | 1.65113e-05 | 0.00287322 | stop-gained, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842127 | CAAGAACAGTTGCTC[A/G]GCGAAGTTTCATTTC | 4734 |
rs143030927 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836283 | TCTTTTGGCCTGGTA[C/T]AGCACCATACACATA | 4734 |
rs143032795 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849526 | CCTGGACCACATGAT[A/G]TTTCTAAGCCCCAGA | 4734 |
rs143040781 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936481 | TGGTGGTTTATCGAG[A/G]TGAAATTATGGCTGA | 4734 |
rs143045794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930819 | GCTACCATGTATGAT[A/G]TGCCTTTGCTTCTCC | 4734 |
rs143073113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876448 | TGGGTTTAAAATATA[C/T]GTAGATGTAATAAAA | 4734 |
rs143077885 | snp | C/G | 0.270621 | 0.249148 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949380 | AGTTCAACCATTGTG[C/G]AAGACAGTGTGGCGA | 4734 |
rs143087964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958305 | GTTTTTTCTACTTTA[C/T]TGTATTAATACAGTG | 4734 |
rs143099072 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983902 | AGGTGTGAGCCACTG[C/T]GCCCAGCCTGTTATA | 4734 |
rs143116874 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889975 | CCCAAAGCGCTAGGA[C/T]TACAGGCATGAACCA | 4734 |
rs143131685 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934139 | GCCTGGGCAACAAGA[C/G]TGAAACTCTGTCTCA | 4734 |
rs143172046 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932142 | ATCATGGGGGCGGTT[A/T]CCTGCATGCTGTTTT | 4734 |
rs143177167 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956063 | AAGTGATCCTCCCAC[A/C]TTGGCCTCCCAAAGT | 4734 |
rs143199945 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930674 | TCCAAATGTGTCAAC[A/G]GCAGGGCTAGGTGGA | 4734 |
rs143205746 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988640 | CATTTATCAAAATTT[C/G]GATGGTATCTGTGGA | 4734 |
rs143239652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859728 | CAAACAAAAAACCAA[C/T]TTCAGCATAACTGGG | 4734 |
rs143252347 | snp | A/G/T | 0.000132682 | 0.00814401 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915788 | TTTCTTCTGTAACGA[A/G/T]CCCTTCCTGTGAAGC | 4734 |
rs143341910 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864574 | TAAATCCCAGTTATT[C/T]GGGAGGCTGAGGCAG | 4734 |
rs143372577 | snp | A/T | 0.00206058 | 0.0320319 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916278 | CTACTGTCACTGATG[A/T]CACTGTTAGTATATG | 4734 |
rs143389547 | in-del | -/A | 0.404733 | 0.196361 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864688 | ACTCTGTCTCATAAG[-/A]AAAAAAAAAAAAAAA | 4734 |
rs143393003 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975969 | AGAGAACCCAGAAGT[A/G]AATCTATACATCTAT | 4734 |
rs143450184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872183 | AGGAGAACGAATCTT[C/T]CCCAAAAGGCTGTGA | 4734 |
rs143454804 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831209 | ACAGGCATGAGCTAC[C/T]GCACCCAGCCGCCTT | 4734 |
rs143464681 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910739 | ACATAAACTTCATAC[A/G]TGATTTCTTCTTCAC | 4734 |
rs143495741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922245 | GAAAATTATGCATCA[C/T]TGAAATGTGTAATCA | 4734 |
rs143502463 | snp | A/G | 0.298905 | 0.24517 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947091 | cctaacatcacaatt[A/G]aaagaactagagaag | 4734 |
rs143533500 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852233 | CCCAGGAGGCAGAGG[C/T]GCAGTGAGCCACGAT | 4734 |
rs143537347 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932548 | GACTTAAATGTTAGA[C/G]CTAAAACCATAAAAA | 4734 |
rs143552786 | snp | A/G | 0.000490972 | 0.0156603 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862892 | TTCCAGATTAAAATT[A/G]TGAAAGCCATCAGCA | 4734 |
rs143558835 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977987 | TAATTGAAAGTGACA[A/G]CAGCAAATAATGTTA | 4734 |
rs143584252 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845527 | CATGGTTTTTTTTTT[-/T]GTATTTTGAGGCCTG | 4734 |
rs143591116 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912937 | CATCTTCACTCTAAG[C/T]TGTAAACACAGAACA | 4734 |
rs143601055 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975365 | CCCAAAAGCTATTAG[A/T]ACTGATAAGCACATT | 4734 |
rs143621723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955715 | ATGTGAGATTGGTAA[C/T]CTGCCCATGTTGTAA | 4734 |
rs143637092 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857117 | AGCAAGTTACCAAAA[A/T]GTATGTTTAAGATGA | 4734 |
rs143748221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848307 | GGTTATGCCCGTGAC[C/T]ATCTGCTCTTGAAGA | 4734 |
rs143767758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909677 | CTTCTCCTGGTCTGT[C/G]TTGTTTCCCTGTCAC | 4734 |
rs143782911 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55892093 | CAAAACGGCCAAACC[C/T]CGTCTCTACTAAAAA | 4734 |
rs143789171 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830072 | AGCAAACAGAGCAAT[A/G]CTGCTATTCTTGATG | 4734 |
rs143789706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844625 | TCCTCATCTATAAAA[C/T]AGGGATAATAATAAT | 4734 |
rs143804803 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843290 | GAATGGCAGGTTAAC[A/G]TGTTTAACCTCATAA | 4734 |
rs143815507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946139 | ATAATTACAGGATCA[A/G]ATTCACACATAACAA | 4734 |
rs143883316 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939277 | GCTGTTCTCATGACA[C/G]TGAGTTCATTCTCTG | 4734 |
rs143884132 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955909 | TAGCCTCAACTTCCT[A/G]GGCTCAAGTGATCTT | 4734 |
rs143906083 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992715 | TTTCCAAATGGTCGT[A/T]CAATATTTTTAATAA | 4734 |
rs143922942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850473 | ATACATACTTAAAGA[C/T]TTTAAGGAACTATAC | 4734 |
rs143961536 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846042 | TCCACCCACCTCGAC[C/T]TCCCAAAGTGCTGGG | 4734 |
rs143963563 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894941 | TTGTATGCTCCTAAA[C/G]TAGATGACTACTAAA | 4734 |
rs143964435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989279 | TTATTTTAAAAATAC[A/G]CTATATTTATTCACT | 4734 |
rs143967420 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826542 | TAATTCTCATGCCTG[A/G]GAGGAAGGAGGAAAA | 4734 |
rs143993863 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957158 | TTGCATTTTGTGGTG[C/G]TGTTAAATTCATTTA | 4734 |
rs144014357 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889510 | CACTTATTTGTGGGA[A/G]CTAAAAATTAAAACA | 4734 |
rs144056473 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867515 | ATTTTTTCAAGTTAC[C/T]AAATAAATAATTTTC | 4734 |
rs144061443 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991494 | TGCATGGTACAGAGC[A/T]AACAGTAAATGAATG | 4734 |
rs144062955 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944588 | AAATGCAGCAGAAAC[C/T]TCTACAGACTTAAAT | 4734 |
rs144101702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977540 | TAAATTAACACAACA[C/T]AAAAAACTCTGACTG | 4734 |
rs144113886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830105 | AATGTTCCAACACCA[C/T]CAAAATATGTCTTTT | 4734 |
rs144134464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881366 | GGCTGGTCTTGAACT[A/C]CTGACCTCCAGTAAT | 4734 |
rs144159953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832755 | TGCATACTGGGCATA[A/G]AATTTGAAGTTAAAG | 4734 |
rs144179817 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827713 | CCATATACAGATATA[C/T]ACATGTGTATCCATA | 4734 |
rs144185018 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947602 | CAAGGAGCTTATCCA[C/T]CATGATCAAGTGGGC | 4734 |
rs144204491 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945012 | CCATCTGTATGTCAC[G/T]AACGTCAAAGATGAA | 4734 |
rs144233451 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870092 | GTGCAATTAAGGAAA[C/T]TGCAGTAGTTGAGTT | 4734 |
rs144263518 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924337 | GAGTAGGAACCAGGG[A/G]TCATGGGCGAGTGAG | 4734 |
rs144267521 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982103 | CAGGAGTAGGAGGAG[A/G]GCTTTGGCTGAAACT | 4734 |
rs144284755 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979626 | CCAAAGTGCTGGGAT[G/T]ACAGGCGTGAGCCAC | 4734 |
rs144322621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854315 | ACACGGGAGTCCTAC[A/G]TACTTTGGGGACAGT | 4734 |
rs144327996 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861680 | CCTACTAGGGACCCA[A/C]AGAAATTAAAATTAA | 4734 |
rs144336652 | in-del | -/GTAT/GTATGTAT/GTATGTATGTAT | 0.119889 | 0.215463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965653 | TACTAATACTATTTG[-/GTAT/GTATGTAT/GTATGTATGTAT]GTATGTATGTATGTA | 4734 |
rs144348977 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963088 | CCACAACCGGCCTCC[A/G]TTACTTTTTTAAATC | 4734 |
rs144358167 | snp | G/T | 0.000362343 | 0.0134551 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850602 | ATTTGGTGCATGCCG[G/T]ACTTCCCAGCCTTTA | 4734 |
rs144365735 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858950 | CAATGGTAATTATTC[A/G]TAACAGGCAGCTGCT | 4734 |
rs144380134 | snp | A/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937415 | AGATATTTCACCGTA[A/T]GTTTTCAGTTTTTTT | 4734 |
rs144406930 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858573 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 4734 |
rs144419274 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969754 | CCTTGAATAAACATC[A/G]GGGTAGCCAGGCAGC | 4734 |
rs144449030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904647 | TTCTCTTCTTCTGAG[G/T]GACAGGTATGCATAT | 4734 |
rs144452683 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960676 | CATATATATATCTAT[C/T]CTATTAGTTCTGTCC | 4734 |
rs144455175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968870 | TATGGAGGAGGAGGC[A/G]GAGCAAGATGGCTCA | 4734 |
rs144485134 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889103 | GGACAAATGGGATCA[C/G]ATCAAGGTAAAAAGC | 4734 |
rs144492954 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961257 | CCTAGAGTCTCATCA[-/G]GGCAGGGCTAGAGTT | 4734 |
rs144512809 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966286 | ATCATTTGTACTTCT[A/G]CCTAATTTCACAAAT | 4734 |
rs144554083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832496 | CTTGGCTCACTGCAA[C/T]GTCCGCCTCCTGGGT | 4734 |
rs144600467 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844469 | GTAGTGGAAGAAGAG[A/G]GGGGTACAAGAGAAC | 4734 |
rs144608484 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927218 | GAATTTAAATGAGAA[G/T]GTATAGAGAACATGC | 4734 |
rs144659506 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846606 | TAAAAAAATCCAGAC[C/T]GTCCTCCAACACAGT | 4734 |
rs144663496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928987 | AGTCTATTTAAATCA[A/T]AGGTAATAGTTTGTA | 4734 |
rs144699173 | snp | C/G | 0.00835444 | 0.0641245 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926487 | AAAATAGTGTTAAGA[C/G]GGCCGGATGTGCTGG | 4734 |
rs144700139 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928011 | TATAACAGGATTCAC[C/T]ACCTCAACTATCTTT | 4734 |
rs144700623 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957685 | CATGTATGTTTATTA[C/T]GGCACTATTCACAAT | 4734 |
rs144709362 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949877 | AATGGGTGCAGCACA[C/G/T]CAATATGGCACGTGT | 4734 |
rs144719426 | snp | C/G | 0.303438 | 0.244222 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932577 | AACCCTAGAAGAAAA[C/G]CTAGGCAATACCATT | 4734 |
rs144727004 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849533 | CACATGATATTTCTA[A/T]GCCCCAGAACATGCA | 4734 |
rs144740740 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844010 | GACAATTGCTGATGA[C/T]AGAGATGGAAGCAAT | 4734 |
rs144746077 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844966 | GCATGAACCACTGCA[A/C]CTGGTGTTTTTAATA | 4734 |
rs144748768 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893972 | GCTTATTTAAAACAT[C/T]TTCCTAGAAGTTCAA | 4734 |
rs144753611 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958326 | TAATACAGTGAATTG[C/T]ATTAATTAATTTTTT | 4734 |
rs144756989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986085 | ATTTAATGACAGTAA[C/G]TGATTACAACCTGCT | 4734 |
rs144785069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842452 | AGTGCAGTGGCGTGA[A/G]CATGGCTTACTGCAG | 4734 |
rs144789161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924404 | CTCCTGTCACAAGAG[G/T]TCTTGAGTAAGACCT | 4734 |
rs144792170 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955223 | AAACAGGGTTTCACC[A/G]TGTTGCCCAAGATGG | 4734 |
rs144829633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952782 | GGCTTTTTCTTTGAT[C/T]TAGGTTTCTCTAGGC | 4734 |
rs144858093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899837 | GTGTCTAGTGCAAAT[G/T]AGGTTCTGAATTTTA | 4734 |
rs144866037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989781 | AAATTTTTGGAAGAG[C/T]TGGAAGAGTAGGTGC | 4734 |
rs144916239 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833034 | GCAAATCCATTCATA[A/G]GCACCCGAGATGTGC | 4734 |
rs144918087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950263 | ATGTCATACTACATA[C/G]AGTGGGGAAAATCTT | 4734 |
rs144932707 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983673 | CTGGAGTGCAGTGGC[A/G]CAGTCTCGGTTCACT | 4734 |
rs144942835 | in-del | -/GAC | 0.212728 | 0.247206 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983276 | AATAATGTTGATGAT[-/GAC]CGACAATGGTGTGTG | 4734 |
rs144970052 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934426 | TACGAACATTGGTGC[A/G]CAAGTTTTCTGTGCA | 4734 |
rs145049625 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907889 | AGACACCCAGTTATA[C/T]GGTACCAGTTAGTGG | 4734 |
rs145114818 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942633 | CCTGTACAGCCTGTG[G/T]AACTGTGAGTCAATT | 4734 |
rs145128555 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859570 | GGCGTGGTGGTGTGC[A/G]CCTGTAATCTCAGCT | 4734 |
rs145196288 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900772 | AATTACTTTGCTTTT[A/G]CCCTGTCAACAACTG | 4734 |
rs145203909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873773 | CTGGGGTTCATGAAC[A/G]GAAATCTTAAAGAGA | 4734 |
rs145235983 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940083 | GAACCTTGAGGACAC[C/T]ACCCTAGGTGAAATA | 4734 |
rs145292427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843408 | TGTGCTCTTAATTAA[C/T]GGAGCTACATTGCCT | 4734 |
rs145322103 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914845 | GCATTCTAAATTTTA[C/T]TCTATTTCATAATGA | 4734 |
rs145328125 | snp | A/C/T | 0.000463995 | 0.0152246 | synonymous-codon, missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840688 | GTGATCTTCGTTACA[A/C/T]AATCCAGAGTTTGGA | 4734 |
rs145332045 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885437 | GTGGTGTGCTAACTA[C/T]TCATATGTTAAGTAG | 4734 |
rs145335389 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975738 | TTCAATGCAACTCCT[A/G]TCACAATACCAATGA | 4734 |
rs145340461 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55954859 | GGCTTTTTAATTATA[G/T]TATTACTGAGTTGTA | 4734 |
rs145384888 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928276 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 4734 |
rs145426537 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882489 | GATCAGCCAGAGCCG[A/G]TGGAGAATTGTCCAT | 4734 |
rs145482517 | snp | A/T | 3.3145e-05 | 0.0040708 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838577 | CATTTTCAAGAATCC[A/T]TCTTAGGGAATTGTA | 4734 |
rs145488813 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852061 | AGCACTTTAGGAGGC[C/T]GAGGTGGGTGGATCA | 4734 |
rs145513040 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984542 | TACTTTCACTAAAGC[A/G]TCTTTATTGACGGCC | 4734 |
rs145517932 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878951 | CCTCAGCCTCGCAAG[C/T]AGCTGAGATTACAGG | 4734 |
rs145533910 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895286 | TTTCGAAGAGGTGGA[C/T]GCTAACATTCTCTGG | 4734 |
rs145549988 | in-del | -/AAC | 0.438526 | 0.164189 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917203 | AATGAGTAACACAAG[-/AAC]AACAATCTTCTAACA | 4734 |
rs145556884 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928263 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 4734 |
rs145562599 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920949 | TGGTAAACCGAGTTT[C/T]TCAAGAAAAGCTGTA | 4734 |
rs145565453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986301 | GGCATAATCTTACGA[C/T]ATGTCCCCTGAAAAT | 4734 |
rs145645599 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924897 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 4734 |
rs145647343 | snp | A/G | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848861 | TTTCCTCTCAGATGG[A/G]CTGGAATTTTCAATC | 4734 |
rs145668583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902322 | ATTTTGTCAATACTA[A/G]AATGACATAGTGACT | 4734 |
rs145684286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863664 | AAGTACTGAGAAATT[A/G]AGAAGTATAGTTTAA | 4734 |
rs145686285 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941825 | TGATATGCCTGCATC[A/G]GCTTCCCAAAGTGCG | 4734 |
rs145699377 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941083 | ATCTGTAGGTTCCCT[A/C]CTCTGATTCCTAATA | 4734 |
rs145712820 | in-del | -/TG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964702 | TGCTGGTGTGTGTGT[-/TG]GTGTGTGTGTGTGTG | 4734 |
rs145713922 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837620 | TGTTTATTGTCTAGA[C/T]TTCTTGAATGACTGA | 4734 |
rs145725382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938593 | AAACAAAGGCAATGA[A/G]AGCAAAAATTGACAA | 4734 |
rs145768630 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860065 | AACAGGAGCCCAAAT[C/T]CCTGAAGTCTTTTCT | 4734 |
rs145779563 | snp | A/C/T | 0.00021427 | 0.0103485 | | | GRCh38.p7 | 15:55916413 | GCTGGACTGCTTACA[A/C/T]GGTGACCATCATTCA | 4734 |
rs145787870 | snp | A/G | 0.0547245 | 0.156101 | | | GRCh38.p7 | 15:55976666 | ACGGAGGCTCGCTCT[A/G]TGGCCCAGGCTGGAG | 4734 |
rs145814401 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972535 | ACAACAGACATACAA[C/T]AGATAAACCAAGAAA | 4734 |
rs145824169 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871127 | GTAGTCAGTGAAATC[A/C]TGATGCTTATTCCCA | 4734 |
rs145840193 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883351 | TTATGGTTTGTGTGT[C/T]CACTCAGCTGCAGCA | 4734 |
rs145886076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932034 | AATTGGCTTCTGATA[C/T]GGTTTGACTGTGTCC | 4734 |
rs145916287 | in-del | -/CCA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890361 | TCACTGCCCATTTCC[-/CCA]CCCCTCCTTCAGTCC | 4734 |
rs145932819 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960269 | CAAAGGAGATTAACA[G/T]TTGAATCAGTGGACT | 4734 |
rs146000620 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841283 | ATTCTGCCTTAAAAA[A/G]GAAGGACATTCTGAT | 4734 |
rs146015874 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917308 | TATACTTTCTCCAGC[C/T]GACTTTGCCCACTAA | 4734 |
rs146027903 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837041 | ATTGGAAAAATTTAA[C/G]TAACTTTTTAATTTA | 4734 |
rs146047431 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856893 | TTTACAATGCACATA[C/T]AAATTGAATCAGAAT | 4734 |
rs146053378 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947651 | GGCTGGTTCAACATA[C/T]GCAATCAATAAACGT | 4734 |
rs146060722 | in-del | -/ATATATATATATATAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852691 | TTGCCTTTTCTAGAA[-/ATATATATATATATAT]ATATATATATATATA | 4734 |
rs146081341 | in-del | -/AATAAATAAATC/AATAAATC | 0.493432 | 0.0569306 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869889 | ATAAATAAATAAATA[-/AATAAATAAATC/AATAAATC]AATAATTGTTATGAC | 4734 |
rs146102554 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974886 | ATGTCCATTTCTTTT[C/T]CTTTCTTTTTTTTTT | 4734 |
rs146116364 | snp | A/G | 0.00248143 | 0.0351363 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852576 | AGAAGAATTAAATAC[A/G]TCAAGTTTAAGAATC | 4734 |
rs146126184 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899664 | CAATACACTGGATCA[C/T]TGTGAAAGTACAGGG | 4734 |
rs146152545 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938881 | GAGGGCAAGGCAGGA[C/G]GATCACTTGAATCCA | 4734 |
rs146152659 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894551 | CTCACATCTTTAAAG[G/T]GGCTTTTACCTCACA | 4734 |
rs146163321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936719 | AAATAACATGTGCAT[C/T]GCACCTAATGTGTTG | 4734 |
rs146190209 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934216 | CATATCTTATGAGCA[G/T]TGTGAGAATGGGCTA | 4734 |
rs146216406 | snp | C/G | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916548 | AGATATCCACTGTAC[C/G]TTGTTGGCTGTAGTG | 4734 |
rs146246672 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877445 | ATATCAGGAGGCACA[C/T]GATACTGATTTGTTG | 4734 |
rs146270802 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873009 | AGTATTTTTTCTCTT[G/T]CTTTAAAATTCAGCA | 4734 |
rs146285888 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981412 | TCACTTACGGTGACC[A/G]TATTTTCCAAACTAA | 4734 |
rs146296128 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978346 | TAAAAACTTCTTTCA[A/G]AATTAAGTGCCATTT | 4734 |
rs146369896 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55936153 | AGGGGTCCCTCCTAA[A/G]CCTCCTAGACTAAGT | 4734 |
rs146372591 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893275 | TCCTCTATGCGCAAA[C/T]GTCATGATTCCTCTG | 4734 |
rs146380659 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933951 | CTGAGGTCAGGAGTT[C/T]GAGACCATTCTGGCC | 4734 |
rs146393136 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854940 | CTTCCACATATTCAT[C/T]GTATAGAGGACATTA | 4734 |
rs146402026 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958100 | TTGTGCACATGTACC[C/T]TAGAACTTAACGTAT | 4734 |
rs146406058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963949 | TTTTCTCCTGGTCTC[C/T]GTAGTTTTGGGTAGG | 4734 |
rs146423976 | in-del | -/AATAAATA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892267 | GCAAAACTCCAACTC[-/AATAAATA]AATAAATAAATAAAT | 4734 |
rs146454403 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995065 | ACCTCAATTGTCGTA[C/T]TTTATGATTGGTAGG | 4734 |
rs146482959 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991659 | GAACTGACAGCCAGA[A/T]CTCCCAGAATGTGAA | 4734 |
rs146550864 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827827 | GTGGTCAATTTGCAC[A/G]CCTGACTTGACACAA | 4734 |
rs146553620 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907247 | CAATCCAGGAAGTGC[A/T]AACTTTGGCTAACAG | 4734 |
rs146565479 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945118 | CTCCTCCAAAGGATC[A/G]CAGCCCCTCGCCAGC | 4734 |
rs146591156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942018 | ATACATGTCAAACAG[G/T]TTAACATGATTGGTA | 4734 |
rs146646361 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889246 | AGAAAGGAAATCAGC[A/G]TATTGAAAGGATATG | 4734 |
rs146646973 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963551 | GTCTATAACTTATAC[-/C]TGCTCCATCCTTTAT | 4734 |
rs146672648 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885038 | TCAGGGGTAAAGAAC[A/G]GATCCTAAAAGCAGC | 4734 |
rs146680025 | snp | C/T | 4.97748e-05 | 0.00498848 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915807 | TTCCTGTGAAGCGGC[C/T]GTATGTCTCTTACTT | 4734 |
rs146710301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929134 | GAAGCTGAAAACCAC[C/T]GAAAGAACAGAGTGT | 4734 |
rs146766995 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869034 | TGCTTACTCCAGATG[C/T]ATGTAACTCTACACA | 4734 |
rs146777146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919921 | GTACCCACTTGTTTG[C/G]TCAAACATCAGTATA | 4734 |
rs146793302 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918959 | CTAATAGGCTAATCA[A/C]TGAGATCTAATTGTT | 4734 |
rs146795229 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903841 | AAAAAAAAAAAAAAA[A/C]ACACATATATATATA | 4734 |
rs146804100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913082 | AGCTAAACATATAAG[A/C]AAAGAAGTTGTAGAC | 4734 |
rs146806394 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975367 | CAAAAGCTATTAGAA[A/C]TGATAAGCACATTCA | 4734 |
rs146817673 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971594 | TGCGCCACTGCACTC[C/T]AGCCTGGGCAACACG | 4734 |
rs146882270 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859258 | CATCGTGGAAGCATA[-/T]GCTGGGATACTTTAT | 4734 |
rs146888635 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850892 | TTTCAAATGTAGTTA[C/T]GGCATGTTAATATTT | 4734 |
rs146900173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835106 | AACAAAAACTAATGA[C/T]TCTCTTTTTCCCTTC | 4734 |
rs146902633 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915394 | GTAACTGAGATGGTC[C/T]CCCTTTAGAACAATT | 4734 |
rs146944700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980662 | ATGGCAAATGGAAGC[C/T]CACAGATGATGGCTA | 4734 |
rs146972216 | snp | C/T | 0.000692692 | 0.0185975 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916758 | TGGCTATCCAAGTCA[C/T]CTCCGGAGGTTTCTG | 4734 |
rs146984055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895958 | AACCTATCTGTCAAT[A/G]GGGTAGGTTTTATAC | 4734 |
rs147040338 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933000 | ATCTCACACCAGTTA[C/G]AATGGCGATCATTAA | 4734 |
rs147042166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992468 | ATATTACAATACTTA[A/G]GCAAGCAGTATAAAT | 4734 |
rs147056900 | in-del | -/GAATGCCCAA | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937240 | AATTTCCATTTGGCC[-/GAATGCCCAA]GAACCAAGTTTTTGC | 4734 |
rs147060928 | snp | A/G | 0.000494698 | 0.0157196 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916023 | GTTGAAGGACTCCTA[A/G]GAAAAATGACTAAGG | 4734 |
rs147070220 | in-del | -/TCTT | 0.314301 | 0.241589 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865935 | GGAGGGGAATTTCTC[-/TCTT]TCTTCTCTCTCTCAA | 4734 |
rs147100438 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874841 | TAGCCAGGTGTGGTG[A/G]CACATGCCTGTAATC | 4734 |
rs147110381 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871484 | GGCTGCTAGGACAAT[C/T]AAATAAGAAAAAACA | 4734 |
rs147122912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980213 | GCTGGGATTTCAGGC[A/G]TGAGCCACTGCACCT | 4734 |
rs147155353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973610 | GAATAACACTAGAAA[C/T]CAATAACAAGAGGAA | 4734 |
rs147166155 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910975 | CCTTCTTTGTCTTCA[A/G]CATGAAGCACCAGGC | 4734 |
rs147177650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969125 | GAATCTATGCCTTTG[C/T]GGGACGAAGGGCAAA | 4734 |
rs147220471 | in-del | -/ACACACACACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836332 | ATGAAAAAGTATGTG[-/ACACACACACAC]ACACACACACACACA | 4734 |
rs147238613 | snp | C/G | 0.000906163 | 0.0212664 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848783 | TAGCCAAGTTAGATG[C/G]GTTAGCATTTCTATA | 4734 |
rs147248492 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844696 | AAAATGCTTAAACAG[C/T]ATCTGGCATATGGTA | 4734 |
rs147248690 | in-del | -/ATG | 0.0391387 | 0.134304 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878225 | GACAAATTAGATTTC[-/ATG]ATGATGAGTATTACC | 4734 |
rs147271127 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887964 | AAAACACTACAAAAA[A/C]TGGTATCGAAGAAAT | 4734 |
rs147281311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882698 | GACACCAGTTGGAGT[A/G]GTCAAGGGAGTGCGT | 4734 |
rs147283524 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952673 | AACCTAGTGAGTCAG[C/G/T]AGTCCTCTTGTTTTG | 4734 |
rs147283530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992851 | TCTTTATAAAGTATT[C/T]ATACTTTTTTGGCTT | 4734 |
rs147345090 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830382 | TCGTTGGGTGTCACC[A/G]ACTCCTTCTTACCCA | 4734 |
rs147365706 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943913 | TGCAGAGACACAGGG[A/G]TGGAGACACCCAAGG | 4734 |
rs147385705 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55861832 | TATTTAATGCGACAT[C/G]AGCTCAGGCTAGTCA | 4734 |
rs147389100 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977089 | AAAATATGCATATCA[C/G/T]AGATTATTTATTTTA | 4734 |
rs147438262 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886523 | TCTAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 4734 |
rs147450625 | snp | A/G/T | 0.000232224 | 0.0107732 | stop-gained, synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55847023 | TTTGTAATCCCTGGA[A/G/T]TAGGGCACTGCCTTT | 4734 |
rs147461380 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882350 | ATGGCATGGAGAATC[C/T]GTGCACTTAGGGTTG | 4734 |
rs147466701 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915438 | GATAGACAGGAAATA[C/T]TTGGATAAGCTCCTC | 4734 |
rs147470936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931016 | TACATACAAGGCATA[C/T]AACTGTGAAATTTTA | 4734 |
rs147516562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956228 | TTAGGTTGTTTCCAG[A/C]TATATGTCTAAAGAT | 4734 |
rs147531337 | in-del | -/ATT | 0.320814 | 0.239761 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967637 | AAAATATTATAAAAC[-/ATT]ATGTATATTTTTTAA | 4734 |
rs147587181 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858754 | TATTCACGTACAACT[A/G]TCTACTGTGAAGCTT | 4734 |
rs147596980 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856566 | CTAAGAGGTTTCCCC[A/G]TTGCAAGTCTTACTT | 4734 |
rs147620064 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900932 | CCTAAAGATCAAGAG[C/T]AAGATAAAAACCAAG | 4734 |
rs147629890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896572 | TTGTATCTGTTTTTA[A/G]TATCTGTATTATAGT | 4734 |
rs147653133 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938289 | ATTTGAACCTGGGAG[A/G]TGGTGGTTGCGGTGA | 4734 |
rs147696976 | snp | A/T | 0.000165497 | 0.00909512 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916772 | ATCTCCGGAGGTTTC[A/T]GACAAAGGGTAAGTA | 4734 |
rs147702814 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839651 | CTAGGAACCTAACCA[A/T]AACGCTTTGCCTTTC | 4734 |
rs147724913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879366 | AAGAAAATTCCTCTC[C/T]GGAACAACTAAGCAA | 4734 |
rs147736577 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986613 | TTTTTTTTGTGAGAC[A/G]GAGTCTCGCTCCGTC | 4734 |
rs147745854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983075 | TGCAGTGAACCGAGA[C/T]TGCGCCATTGCACTT | 4734 |
rs147818405 | snp | C/T | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938086 | CAAATGGTGGCCAGG[C/T]GCAGTGGCTCACACC | 4734 |
rs147827846 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859213 | AATCTCCCTTGATGA[C/T]ACATATTAGACAGCT | 4734 |
rs147836888 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916743 | AAGCACATGTGAACA[C/T]GGCTATCCAAGTCAT | 4734 |
rs147837503 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857069 | CTATCTGTACTGAAA[C/T]GGTTCAATGTCTAAG | 4734 |
rs147840465 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970323 | ATTTCTAGAACCACC[A/G]TGGGCCAGAAGGGAA | 4734 |
rs147840893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935113 | CCTCAGGTGATCCAC[C/T]CTCCTCGGCCTCCCA | 4734 |
rs147850546 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966794 | AAGAATTTATCGCTG[C/T]GCTCAAGAAAATCTA | 4734 |
rs147935033 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842553 | ATCATGCCTGACTAA[G/T]TTTTTAAGTTTTTGA | 4734 |
rs147936010 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924810 | TGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 4734 |
rs147944768 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839848 | GAGTGTGGTGGTGCG[C/T]GCCTGTAGTCCCAGC | 4734 |
rs147946627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920609 | ACTTACATTACAAAC[A/G]TTTTCCAGATGACTA | 4734 |
rs147946686 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953290 | CATAGCGCTGAGCCC[A/G]TATATTAATTCTTTG | 4734 |
rs147998250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872389 | TAAAAAATTTAATAT[C/G]CTATTATTATTTTAT | 4734 |
rs148008436 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922303 | AAAAAGCATATCAGA[A/G]GAATGTCTATAGAGA | 4734 |
rs148010425 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980784 | ATTCATTTTTAGTGT[A/G]TGTGTAGGGGTGTGT | 4734 |
rs148017681 | in-del | -/GT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980794 | AGTGTGTGTGTAGGG[-/GT]GTGTGTGTGTGTGTG | 4734 |
rs148044096 | snp | C/T | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860690 | GGTTGTCAACACTTT[C/T]TGTTTCCTCGGATAT | 4734 |
rs148061683 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927296 | GCTCTAAGGAAATGA[C/G]ACAGACAAAGACGAC | 4734 |
rs148073069 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844488 | GTACAAGAGAACTTC[A/T]GTGTTTGAACTGAGT | 4734 |
rs148084634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955780 | ATGGACACCCCATCA[A/T]GACACTTAAAAACTA | 4734 |
rs148092577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857224 | ATGTATGCATGTGAT[G/T]TATCACCAGCAAATC | 4734 |
rs148102831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903291 | CCCAGTGCCCGATGA[C/G]AGTCCTTTTGGCTAG | 4734 |
rs148157289 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909696 | TTTCCCTGTCACCTG[A/T]GATGTAAAGGGAGAG | 4734 |
rs148221210 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949405 | TGGCGATTCCTCAAG[G/T]ATCTAGAACAAGAAA | 4734 |
rs148230984 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847192 | ACAAAACTTTAAACT[C/T]TAAAATATTTAATTT | 4734 |
rs148275263 | snp | C/T | 0.00371997 | 0.0429668 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55951530 | TTAATGGTTTTTGTT[C/T]GCACACTTGTAAGAA | 4734 |
rs148285418 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882056 | AATGTTCCAACAAAC[A/G]TGCAGAAGTCTCTTC | 4734 |
rs148294090 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897194 | TACCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 4734 |
rs148297865 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988883 | AGTTGCAGAATCTGT[A/G]TGAGAAGAATACTGG | 4734 |
rs148316623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938317 | TGAGCCGAGATCGTG[C/T]CACTGCATTCCAGTG | 4734 |
rs148331249 | snp | C/T | 0.00168059 | 0.0289391 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915392 | GAGTAACTGAGATGG[C/T]CCCCCTTTAGAACAA | 4734 |
rs148336468 | in-del | -/A | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916924 | GCACTGCATCAAAAG[-/A]AAAAATCATTTGTGG | 4734 |
rs148350620 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993073 | CAGACCGAAGTCCGT[A/C]AAGTTAAGTCGGCCC | 4734 |
rs148365691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864638 | GGTGAGCCGAAATCA[C/T]GCCATTGCACTCCAG | 4734 |
rs148369236 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942655 | GAGTCAATTACAGCC[A/G]TTTTCTTTATAAACT | 4734 |
rs148389813 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956999 | ATAGTTTTCAGTGTC[C/T]ATTTATTACAAATCT | 4734 |
rs148397282 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847659 | GGGCATTTACAATGA[-/T]TTTCTTTTTCTTTTT | 4734 |
rs148400474 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936914 | TCTCCTGCCTCACCC[A/T]CTTGAGTAGTTGGGA | 4734 |
rs148411050 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968903 | AGAACCCTCCAGTGA[C/G]AGTCCCCACCAAGGA | 4734 |
rs148451260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861833 | ATTTAATGCGACATG[A/G]GCTCAGGCTAGTCAG | 4734 |
rs148464498 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974360 | AGAATTAATACCAAT[C/T]CTACTCAAACTATTT | 4734 |
rs148514642 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55919109 | TAAGCATCAGTTCCA[C/T]GTCCCCTAACTAGAT | 4734 |
rs148526982 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838265 | TTATACGAGAAACTT[C/G]GTGTTTTAAATTAAG | 4734 |
rs148529539 | in-del | -/AG | 0.0622301 | 0.165053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880452 | ATACACAAACCTGAA[-/AG]ATATAAGAGAGTACT | 4734 |
rs148537925 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949888 | CACACCAATATGGCA[C/T]GTGTATACATATGTA | 4734 |
rs148545649 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849574 | TATCTGTTCAAGGGT[C/T]GATTAATATTTTTGA | 4734 |
rs148552628 | in-del | -/GC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940546 | TCTCTCTCTCTCTCT[-/GC]CTCTCTGCCTCTCTC | 4734 |
rs148600293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990168 | GCTGTATAATTACTT[C/T]ATTACATATCACAAT | 4734 |
rs148608949 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900088 | TTTTTTTTTAAACTA[A/G]TTTGGCTCATCATAC | 4734 |
rs148618904 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939380 | GGTGCCCGCTTCCTG[A/T]TCATCTTCTGCCATG | 4734 |
rs148660935 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826727 | ACTAACAACCAGACT[G/T]ATGCAATACGACCTT | 4734 |
rs148694822 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977820 | AAATATTCCATGGGC[A/C]CTGATGGTCAAATTC | 4734 |
rs148700559 | snp | C/T | 0.000115324 | 0.00759268 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916705 | GAACAACGTTAGACG[C/T]TGAAATCCGTGTTGG | 4734 |
rs148736733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874137 | CATATGCAGCATCAA[C/T]GGAAAATAAAAAGTA | 4734 |
rs148743910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888013 | AGTCATACATGACAG[A/T]CCCATAGTGAATATC | 4734 |
rs148746954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924341 | AGGAACCAGGGGTCA[C/T]GGGCGAGTGAGAGGG | 4734 |
rs148749138 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982195 | AAAATGGTACAATCG[C/T]GTTGGGAGACTGTTA | 4734 |
rs148769096 | snp | C/T | 0.00684659 | 0.058107 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850653 | TTCAGATGGCTGGGT[C/T]ACCTGCTGGCCTGAA | 4734 |
rs148785640 | in-del | -/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994984 | GCTTGAGCTTGGGAG[-/G]GAGGAGGTTACAGTG | 4734 |
rs148801306 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928406 | TAAAAGTTGTCCCCA[A/G]TGGTCTAAATAACAA | 4734 |
rs148856602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950736 | AACAGAGAAACGACT[C/G]AACAGCTAAAGGGGA | 4734 |
rs148864425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960744 | ATGACTCCATGAAAT[C/T]TATGCCTACTTGCTC | 4734 |
rs148919973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992449 | AAGGAACTATACAAC[C/T]TAAATATTACAATAC | 4734 |
rs148928487 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902883 | GCAGGTGCCTGTAAT[C/T]GCCGCTAGTCAGGAG | 4734 |
rs148947752 | in-del | -/CCT | 0.0337553 | 0.125452 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929478 | CTTTTCTATCCTCAC[-/CCT]CCTCCTCTCCTCTAC | 4734 |
rs148999128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842805 | CCTGCTAGCTGTTGT[A/G]CCTGTCTGTTCAGGC | 4734 |
rs149044341 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949321 | AGCTGGAGAGGATGT[A/G]GAGAAATAGGAATAC | 4734 |
rs149061862 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889665 | AGAATAGGGTAACTT[C/T]AGTCAAAAATAATTT | 4734 |
rs149074681 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995105 | ATTCATATAATATGT[A/G]TCAAAATTCTGTTAA | 4734 |
rs149085180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934535 | GAATAGAAAGTATTC[C/T]GGCATTTTAATTTAA | 4734 |
rs149088239 | snp | C/T | 1.65209e-05 | 0.00287405 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863039 | TGTTGTTGCTGCAAA[C/T]GGCAAGCAGCATCTG | 4734 |
rs149189977 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864285 | AATAAGGGAAAGACA[C/T]AGTCTGTTCTTGGCT | 4734 |
rs149201508 | snp | A/T | 1.8609e-05 | 0.00305027 | intron-variant | NEDD4 | GRCh38.p7 | 15:55915251 | AGTTATTCTCATATA[A/T]ATTAACATTTACCAA | 4734 |
rs149202946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975955 | CAATGGAACAGAATA[C/G]AGAACCCAGAAGTAA | 4734 |
rs149219044 | snp | A/C/G | 0.0150606 | 0.0854603 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845889 | CTCCTGGGTTCAAGC[A/C/G]GTTCTCCTGCCTCAG | 4734 |
rs149233897 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904602 | GCCACCACACCCGGC[A/G]TATTTCCATACACAT | 4734 |
rs149236129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968791 | CCCTAGATAAATGTA[C/T]ATCTATGTACACAAG | 4734 |
rs149287342 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911473 | AGATAAATAATGTCA[C/T]ATCTTTCTACTTTTT | 4734 |
rs149299658 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934977 | AGACTCAAGTGATTC[C/T]CCTGCCTCAGCCTCC | 4734 |
rs149306778 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844440 | AAGACAGAGGGACCT[A/G]TGAAGGAGCAATGGT | 4734 |
rs149307952 | in-del | -/TTT | 0.178465 | 0.239547 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870530 | TTCTTCTTCTTCTTC[-/TTT]TTTTTTTTTTTTTTG | 4734 |
rs149317789 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955523 | CACTCTTTGATTCTA[A/T]GAATTTGACTATTTT | 4734 |
rs149383822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893810 | ATACTACATACTAGA[C/T]ATAGATAGAAAAAAG | 4734 |
rs149393500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935929 | TCTTTGGAACTGCTG[A/T]AAGTATCTGTGACCA | 4734 |
rs149420186 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892308 | TAAATAAATAAATAA[A/T]TAAATAAATAAATAA | 4734 |
rs149444667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861425 | ATCAGATTGGACGGT[A/T]AATGAGTATTAAAAA | 4734 |
rs149448142 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939194 | ATCTCATCTCGATCC[A/G]TAATCCCCACGTGTC | 4734 |
rs149457308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836265 | TTAATAACAGGACCT[A/G]TGTCTTTTGGCCTGG | 4734 |
rs149466275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876323 | GAGAGTAATAAAGAG[A/C]ACCAGAAAATGGTAA | 4734 |
rs149477349 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841644 | CTGGAGTGCAGTGGC[A/C/G]TGATCTCGGCTCCGC | 4734 |
rs149511196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977457 | CTAATGACACATTTC[G/T]CAGAATGTATCCGTT | 4734 |
rs149519660 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881332 | TTTTAGTAGAGACAG[C/G]GTTTCACCATGTTGG | 4734 |
rs149522564 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917179 | ATTATACCTTCTCCA[A/G]TTTGCATGAATGAGT | 4734 |
rs149542353 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930340 | CTGTATGTTATCTAT[C/T]AATTTCTCTCATGTA | 4734 |
rs149582146 | snp | C/G | 0.299916 | 0.244966 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933520 | AACATCACACACTGG[C/G]GCCTGTCGTGGGGTG | 4734 |
rs149592369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854223 | ATAAGCCCTGGTTTG[C/G]TGTGGCTCCCTAAGG | 4734 |
rs149604968 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962780 | TTGTTCCTCCTTTTC[C/T]GACTTTTATTTTTTT | 4734 |
rs149646680 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858505 | TAGTGACAAGGTTTC[A/G]CCATGTTGCCCAGGC | 4734 |
rs149688235 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895107 | TAGCCAGGAAATACT[C/T]ACAGCTAGGTAACTG | 4734 |
rs149696600 | in-del | -/TT | 0.401924 | 0.198543 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847677 | TCTTTTTCTTTTTCC[-/TT]TTTTTTTTTTTTTTT | 4734 |
rs149707636 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832445 | TTTGAGACAGGGTCT[C/T]AGTCTGTCACCCAGG | 4734 |
rs149742038 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902210 | AAAGAGAAAATCCTA[C/T]GGTAAATAACTGACA | 4734 |
rs149758664 | in-del | -/TGTG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964676 | GTGTGTGTGTGTGTG[-/TGTG]AATTTTGCTGCTGGT | 4734 |
rs149759503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837356 | AATTGCTTGAACCTG[A/G]GAGGTGCAGGTTGCA | 4734 |
rs149782920 | snp | C/T | 0.040671 | 0.13668 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878844 | TTTGTTTTTTTGAGA[C/T]GGAGTTTCGCTCTTG | 4734 |
rs149837013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882898 | GCAGCAGTAACCAGA[A/T]AGTATACATCATGGG | 4734 |
rs149846819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931922 | CCCATTTTCCCTCAA[C/T]CTTCCCAGGAAACCA | 4734 |
rs149849851 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989727 | CATTCTAGATGCTTT[A/C]AGAAGAAAGAAGCTA | 4734 |
rs149899893 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856344 | GCAGGCTGAGTCATG[C/T]GGTCGCTCTCAGCCC | 4734 |
rs149900771 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934425 | CTACGAACATTGGTG[C/T]GCAAGTTTTCTGTGC | 4734 |
rs149901812 | snp | C/T | 0.000164766 | 0.00907502 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55830580 | AATGACTGTGGTCCA[C/T]TTGAACCTATAAGGA | 4734 |
rs149920572 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867448 | AGGGTCCTATGATGC[A/G]TGCATGTGGGCAAAA | 4734 |
rs149924312 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965697 | GTATGTATGCATGCA[G/T]GTTTGTATGTATTTT | 4734 |
rs149951632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859290 | CTGAACCCTATGGAC[A/G]ACAGTTTTTACAGTG | 4734 |
rs149974613 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906855 | AATCCCAATGCTTTG[A/G]GAGGCTGAGGCAGGT | 4734 |
rs149994169 | in-del | -/AT | 0.294832 | 0.245947 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979068 | AGTCTATTTTTAAAA[-/AT]ATATATATATATACC | 4734 |
rs149994307 | snp | C/T | 5.0363e-05 | 0.00501787 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842162 | TTGTTTGGAATGTCA[C/T]TCTGAAAATCCAGAG | 4734 |
rs149996187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924121 | TTTAACTTTGCTTTT[C/T]GCTTCTGTAAGAGCT | 4734 |
rs150037696 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948715 | GGGAAAGGATTCCCT[A/G]TTTAATAAATGGTGC | 4734 |
rs150045933 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845486 | AGAAGAACGCCTGGT[A/G]TGCAATGAGAGATCA | 4734 |
rs150058800 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956430 | TTCCTATAGAAGTTT[A/T]ATCATTTTAGCTCAT | 4734 |
rs150068324 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994414 | ACTAGGACCTCCTGT[A/G]GAATAACTCCTCCTG | 4734 |
rs150079421 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839931 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 4734 |
rs150090998 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950663 | GTTAACGAGCGTCCC[A/G]GAGAAGCAGAAATGA | 4734 |
rs150141366 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886215 | GAAAATATTATTAGC[A/G]ATAAAGAGAGAGACA | 4734 |
rs150154289 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992292 | TTCTGGCAGCAATAG[A/C]TAGGAAATTAAATTC | 4734 |
rs150200430 | snp | A/G | 5.14231e-05 | 0.0050704 | stop-gained, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916816 | CTGCAAAGTGCAATC[A/G]TAAGCTTTGTGCCAT | 4734 |
rs150212864 | snp | C/T | 0.0252325 | 0.109451 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828786 | CATAGTAAACAGTAT[C/T]TTAAAAGGCATAAGA | 4734 |
rs150216881 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857256 | GTATCATTTATTCTT[C/T]AGGTCTTTGACCACT | 4734 |
rs150235949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870890 | TGATTTACTTAAGAA[A/G]TCCTTACTTGTCTCA | 4734 |
rs150277777 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909846 | AAAACCTTGACTTGT[G/T]TTCTACATGGAAGCT | 4734 |
rs150280553 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973205 | TCCTGGCATATGGAT[A/C]ATTCTCAAGGATAAA | 4734 |
rs150289426 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875543 | GTCTGGTCTCAAACT[C/G]CTGACCTCAGGTGAT | 4734 |
rs150299553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925091 | CAAAACAAAACAAAC[A/G]AACAAAAAGAAGTTG | 4734 |
rs150301589 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983602 | ATAAAATTAATTAAT[A/T]TTTAGATATACTTTT | 4734 |
rs150347474 | snp | C/T | 0.126909 | 0.217598 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947450 | GACACATACACCCTC[C/T]CAAGACTAAACCAGG | 4734 |
rs150375599 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957898 | AACACCGCATGTTCT[C/T]ACTCATAGGTGGGAA | 4734 |
rs150416184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962126 | ATTGACTTTATTCTT[A/T]ATCATCATGAAATGT | 4734 |
rs150427254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897528 | TTAAAGTCCCACTTT[A/G]CCCATTTCAAAAGGG | 4734 |
rs150444960 | snp | A/G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834409 | CCACTACACAATCAC[A/G/T]GGCTCTTCACTGAGA | 4734 |
rs150447707 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913314 | TTACAATATACCACT[A/G]TAATTAGATTAATAT | 4734 |
rs150473505 | in-del | -/GTGTGTGA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964673 | TGTGTGTGTGTGTGT[-/GTGTGTGA]ATTTTGCTGCTGGTG | 4734 |
rs150534269 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831245 | ACTTTTTATTGGCTA[C/T]CTAATATTGTAATTT | 4734 |
rs150543024 | snp | A/G | 0.000831908 | 0.020378 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872493 | TAGAATAAAATAGTG[A/G]GTTTTCAAAATATAT | 4734 |
rs150545722 | snp | C/T | 0.127254 | 0.217792 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947255 | ACAAAACTGATAGAC[C/T]GCTACCAAGACTAAT | 4734 |
rs150568373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981144 | ACCTCCCAGGTTCAA[A/G]CAATTCTCCTGCCTC | 4734 |
rs150596721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877909 | GGTTAGTTTTTGTGC[A/C]TTTCTGATATCTTCT | 4734 |
rs150608556 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985531 | TGCGTGGTCAGGAAG[C/T]TAGTTACACTGAACA | 4734 |
rs150619746 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927763 | TGGACTGGAGACAGA[C/T]CCTGGTGTCTACAGG | 4734 |
rs150641951 | snp | C/T | 9.88989e-05 | 0.00703134 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842102 | CCCATAATTCTCCGG[C/T]AAGAGTCTTCAAGAA | 4734 |
rs150672635 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931727 | GGTTGTGGGAACAAA[A/C]AATACAGATACATCT | 4734 |
rs150677409 | in-del | -/GA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852743 | CTTTTCTGAGAGAGT[-/GA]GAGAGAGAGAGAGAG | 4734 |
rs150681604 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958857 | TTTCCACAGGGTCTA[C/T]AGCAATGCCCCAGTT | 4734 |
rs150689676 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861232 | AGTAGAGTACTCCAT[G/T]CATGAATGTGAAGGG | 4734 |
rs150693011 | snp | A/C | 0.000307953 | 0.0124049 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915559 | CTACATTTTGGGAGG[A/C]TGGCAAACATGCAGA | 4734 |
rs150732136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900688 | GAGTTGCTTATATGA[A/C]TCATACAAAATTGAG | 4734 |
rs150752813 | snp | C/G | 0.000168893 | 0.00918793 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916803 | TTGCTTCTTCTGGCT[C/G]CAAAGTGCAATCGTA | 4734 |
rs150763469 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836700 | CCGGCTAATTTTTTT[A/G]TATTTTTAGTAGAGA | 4734 |
rs150776157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949625 | ACTATGCAGCCATAC[A/G]AAAGGATGAGTTCAT | 4734 |
rs150824112 | in-del | -/TTCTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870527 | TTCTTCTTCTTCTTC[-/TTCTT]TTTTTTTTTTTTTTT | 4734 |
rs150858069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844972 | ACCACTGCACCTGGT[A/G]TTTTTAATATTCTTT | 4734 |
rs150886795 | snp | C/T | 0.000692167 | 0.0185904 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916447 | CATTCAATTCATTAT[C/T]GACCACAGCACTACT | 4734 |
rs150924874 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928492 | TCTGGCCTTGTGTCC[C/T]ACAAATGTCCCCCTG | 4734 |
rs150936951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894971 | ATATGAGAAAAAGGT[A/T]TTGCATTTGTTTCAA | 4734 |
rs150959218 | snp | A/C | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852488 | TAATATGATCTTCCT[A/C]TTTCATCTTGTTTTT | 4734 |
rs150990234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852256 | GCCACGATCACGCCA[C/T]TGGACTCCAGCCTGG | 4734 |
rs150997820 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862554 | AAAAATAGAGTACTA[C/T]AGAAATTAACATTTT | 4734 |
rs150998865 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940118 | AGTCCCAGAAGAACA[A/C]ATACTGACTATCTTA | 4734 |
rs151022159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975130 | ACTCCTGACCTCAGG[C/T]AATCCACCCACCTCG | 4734 |
rs151049924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870438 | AGTTGTCTAAGCTAA[A/C]GGCTGCTGCCTGCTG | 4734 |
rs151055629 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967200 | CCATAATAATTTGTA[A/G]TAACTACTTAGAAAA | 4734 |
rs151074707 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919481 | TCTAGGGAGGCTGAA[C/T]AATTTGCATTGCTGG | 4734 |
rs151076189 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979696 | AATTTTACATTCTAT[A/T]TTTTCTTTAAAGAAA | 4734 |
rs151125181 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843316 | CATAACAACACTATG[C/T]GAAAGCTACTATTAT | 4734 |
rs151125420 | in-del | -/TGT | 0.118584 | 0.212673 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964288 | AAATCCTCAAGGCTC[-/TGT]TGTTGTTGTTGTTGT | 4734 |
rs151138595 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954335 | AAATACTGATATTCC[C/T]TAAGTATTGCCCCAG | 4734 |
rs151147895 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855921 | ACCACCCACAGTCAC[C/G]AGCATGCAGAGACTT | 4734 |
rs151189767 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890232 | CATACAATTAACCCA[C/T]TTAGAGTGTACAATT | 4734 |
rs151209943 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906224 | TGGAAGACAGTGTGG[C/T]GATTCCTCACGGATC | 4734 |
rs151283525 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874628 | ACTGATTTCAGCTGA[G/T]GTTCACCAAAAGGGA | 4734 |
rs151285734 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948278 | CAAGGAGAACTACTC[A/T]AACTACTGCTCAATG | 4734 |
rs151295682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982627 | GGGAGCATTCTGGAA[C/T]GATGGGAATATTCTG | 4734 |
rs151336103 | snp | A/C/G | 0.00994615 | 0.0699428 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880104 | CGAGACCAGCCTGAC[A/C/G]TACATGGTGAAACCC | 4734 |
rs180702487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938070 | AGGACAGTCTCTTCA[A/T]CAAATGGTGGCCAGG | 4734 |
rs180705255 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958621 | GGGCCTGGAGTTTTC[A/T]TTGTGGGAAGGACAA | 4734 |
rs180709591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977759 | TTTTTAATTTAAAAA[G/T]ATTATCCTTTTTTTC | 4734 |
rs180713774 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928501 | GTGTCCTACAAATGT[C/G]CCCCTGCCCAACCAA | 4734 |
rs180718124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984422 | AATGTTGTGATGATT[A/C]CAGCTAAAGTATGAA | 4734 |
rs180733047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877200 | TCTGCCTAATTTTAG[G/T]CCAGGGTCCAATTCA | 4734 |
rs180744256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920888 | TCAAGAGGACTAGAA[C/T]GACACACACCACCAT | 4734 |
rs180746072 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968140 | AATACTATTCCCATT[C/T]TCCCTTCAAATTTTT | 4734 |
rs180749304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946072 | ATTATAAAGATCATC[A/G]ATGCTATGAAGAAAC | 4734 |
rs180751216 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898464 | TCCTCCTGCAAACTT[C/T]CTTAATTCACGGGCA | 4734 |
rs180753400 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837355 | GAATTGCTTGAACCT[C/G]GGAGGTGCAGGTTGC | 4734 |
rs180755642 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865769 | CCTCAGGGAAAAGAG[C/G/T]TGGGAAGGAAAGGAA | 4734 |
rs180760882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858201 | TCTTCAATGGCTGCA[C/T]AGTATTACACTATAT | 4734 |
rs180765853 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905022 | GCTTGAACCCAGGAG[G/T]CAGAGGCTGCAGTGA | 4734 |
rs180771737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884915 | ACAGAGAACTGTCCA[A/G]ACCTAGAGAAAGAGA | 4734 |
rs180775514 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827244 | AAAGTTATATGCTTG[G/T]AATTTCTAGAAACAT | 4734 |
rs180783774 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846706 | AACCCCACAGGGATA[C/T]ACCAGGTTAGAGCTC | 4734 |
rs180838964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852880 | TCAGCCTCCTGAGTA[G/T]CTGGGATTACAGGCA | 4734 |
rs180854329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872233 | AATGTTTTGCAATGT[A/G]CATACAGTACTTTTA | 4734 |
rs180855906 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833553 | GTAATCCCAGCTACT[C/G]GGGAAGCTGAGGCAA | 4734 |
rs180879237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902697 | AGGTAGTTTATAACA[C/T]TTATTAAATAAAAAG | 4734 |
rs180894609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861826 | ACTGTTTATTTAATG[C/T]GACATGAGCTCAGGC | 4734 |
rs180902294 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880602 | GTAATGGAGGATATA[A/C]TTCACCAAAATGAGG | 4734 |
rs180927333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841728 | AGGCGCCCGCCACCA[C/T]GCCTGGGTAAGTTTT | 4734 |
rs181155368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981180 | CCTGAGTAGCTGAGA[C/G]TACAGGTGCCCACCA | 4734 |
rs181161120 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953222 | CTTGAACTCCTGACC[A/T]CAGGTGATCCGCCCG | 4734 |
rs181166308 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974402 | GGAGGAGGAATACTT[G/T]CCATACTGATTCTAT | 4734 |
rs181196448 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914835 | TTTTAAATAAGCATT[C/T]TAAATTTTACTCTAT | 4734 |
rs181232290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992974 | CCTGCTCTCCCATCC[C/T]TGTCTCTAGTTAGGG | 4734 |
rs181256316 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942119 | GTAAAATCAACTATT[A/G]TGGATTTGTTTATTT | 4734 |
rs181281248 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957627 | CCATTACTGGGTATA[G/T]ACCCAAAGGATTATA | 4734 |
rs181281444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937226 | CAACTTCTGACCACA[A/G]TTTCCATTTGGCCGA | 4734 |
rs181297177 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977314 | ACAGTATTCAGTACA[A/G]TATCATGCTGTAAAG | 4734 |
rs181302183 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897208 | TCGATCTCCTGACCT[C/T]GTGATCCGCCCGCCT | 4734 |
rs181306602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875831 | AAAGGGGATAGGTAA[C/T]AGGGCAGAAAAATAT | 4734 |
rs181314443 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918119 | CGAAGTACATACTTG[C/T]TTACATTTTTGAGAG | 4734 |
rs181319212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857713 | TAAAATAGGTAACAC[C/T]CATACATGTTATAAA | 4734 |
rs181334793 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924255 | TGGATACAGGTAACC[C/T]TAAGAAAGGCCACTG | 4734 |
rs181337918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964107 | TAATGTTTATTATCC[C/T]GCTTGGTGTTTTTAA | 4734 |
rs181348165 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969558 | GACTATGTTCTCCAA[A/C/T]TTGGATACCAGCACA | 4734 |
rs181398891 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929572 | CTTCCACTTATAAGT[C/G]AGAACATGTGGTGGT | 4734 |
rs181417230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886048 | CAAAAAAGGGCATGA[A/G]TAGCTGTATCAGATA | 4734 |
rs181439569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965415 | CCATATTGCCCAGGC[C/T]GGTCTCAAACTCCTG | 4734 |
rs181442686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981976 | ATCATTACTTTACAT[C/G]TTATCACTACTTTTA | 4734 |
rs181443404 | snp | C/T | 0.00809717 | 0.0631112 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832966 | ATGAAAAAGACAATA[C/T]GCATTATTCCATTTT | 4734 |
rs181449253 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851880 | CAAAGACGAGATCAT[C/T]TGCTTTTTCCTCTTA | 4734 |
rs181473174 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948583 | AGTAACCAAAACAGC[A/T]TGGTACTGGTATCAA | 4734 |
rs181481901 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985878 | GTAAAAACCATTTTA[A/T]ACTAAATAGGACCAG | 4734 |
rs181493192 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953001 | CTTTTTTTTTTTCTT[C/T]TTTTTTGAGACAGAG | 4734 |
rs181495719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906895 | GAGGTCAGAGGTTCA[A/T]GACCAGCCTGGCCAA | 4734 |
rs181511225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991863 | AACAGAGAAATTACT[A/G]AAGTAGATAATTAAA | 4734 |
rs181516364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914367 | CAAATACAGAAATTT[A/T]AAAAATCTATTTCAG | 4734 |
rs181571424 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871581 | ATTCCAGACATCTAC[A/G]GAAATTAAATGTGAC | 4734 |
rs181573750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836905 | CTCAAGCAATCCTCC[C/T]GCCTCAGCCTCCTCA | 4734 |
rs181577594 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875107 | GAAATAAAAAAAAAA[A/C]CCCAGTAGGAAGAGA | 4734 |
rs181578387 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836586 | GATGGAGTGCAGTGG[C/T]GTAATCTTGGCTCAC | 4734 |
rs181582256 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856269 | TGACAGCTAAGGTAG[C/T]GAGGGTAAATATGAC | 4734 |
rs181658119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841559 | TGTATGTAATGACTC[A/T]AAATTGTATATTTAA | 4734 |
rs181661205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890457 | GGAATTATATAATAC[A/G]TGGTCCTTTATGACT | 4734 |
rs181662519 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933590 | ACCTAATGCAAATGA[C/T]GAGTTAATGGGTGCA | 4734 |
rs181723536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866584 | TAATAAAATAGTTCT[C/T]ACTACTGCTGTAAAG | 4734 |
rs181728083 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896404 | GGTTAGGCTGGTCTC[A/G]AACTCCTGGCCTCAA | 4734 |
rs181745694 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827821 | GGGAGTGTGGTCAAT[A/T]TGCACACCTGACTTG | 4734 |
rs181889150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969033 | AAGAGGCACTGAAGA[C/G]GGTAGGAAAGACAGT | 4734 |
rs181901971 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985255 | TTCTGTTCCTGGCGC[A/G/T]GAGCAGTCAATCACA | 4734 |
rs181915540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905824 | CCCATTCTGTAGGTT[C/G]CCTGTTCACTCTGAT | 4734 |
rs181916683 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55946942 | AAGGCAGAAACAAAG[A/T]TGTTCTTTGAAACCA | 4734 |
rs181935571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846838 | AAAAAATGAGCATCC[C/T]TTCTCTAGGAAAAAC | 4734 |
rs181935804 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885639 | AGTTTAAAACAATAA[A/C]TTATAAAATATTTGC | 4734 |
rs182005156 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924535 | TGCCCAGAGTCTCCA[A/C/T]AACCACCCCCAAGCC | 4734 |
rs182028835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862156 | GGAAGGATTTGAGAA[C/T]AGAAAATATCTGTAA | 4734 |
rs182035240 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902937 | ACCCAGGAAGTGGAG[A/G]TTGCAGTGAACCGAG | 4734 |
rs182036846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952468 | TTACTTGTCCATTGT[C/T]AAATTTCTCCTGTTT | 4734 |
rs182038643 | snp | A/C | 0.299916 | 0.244966 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933230 | AAAGACACATGCACA[A/C]GTATGTTTATTGCAG | 4734 |
rs182041216 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881827 | CAGCTTGGGCACTAC[G/T]GACAATTCGAGCCAG | 4734 |
rs182048793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842521 | ATTCCTAAGTAACTG[A/G]ACCACAGGCGCATGC | 4734 |
rs182052838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948698 | GACAAAAACAAGAAA[C/T]GGGGAAAGGATTCCC | 4734 |
rs182067091 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886465 | AAATAAGCCTTAAAA[C/T]GTTTTAAAAAATTGA | 4734 |
rs182075989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930603 | TCATTAGACTGAAAT[A/G]CTTACTGATATGGTT | 4734 |
rs182079061 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908129 | TGTAGTCATCCTCAC[C/G]TATCAGGATTCTGCA | 4734 |
rs182098183 | snp | A/G | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868437 | TTCTATAATCCCCTC[A/G]TGTCGTGGTAGGCAC | 4734 |
rs182098944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830370 | CAAAACACCTGTTCG[C/T]TGGGTGTCACCAACT | 4734 |
rs182103052 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848250 | ATGGGAAATGGGGGA[A/G]AGGAGAGAACGGCCA | 4734 |
rs182237510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965041 | GCCTGAGGCCCTCAC[G/T]AGATGCAAAGGCCCA | 4734 |
rs182302770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890312 | TTTTAGAACATTTTC[A/G]TCACCCAAAAAGAAC | 4734 |
rs182308464 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851517 | GTTTCGCTCTTGTTG[C/T]CCAGGCTGGAGTGCA | 4734 |
rs182350286 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922017 | ATCAGGCAAAATTCA[C/T]ATCGGTATCAGTGGC | 4734 |
rs182366800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986236 | TTCAGATAGAATTCA[C/T]CAATGGATGCTAAAA | 4734 |
rs182393503 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879532 | ATATTATACATTATG[G/T]GCAGTTATGGACTAC | 4734 |
rs182473154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981466 | GCAGTTTTCTTCCTC[C/T]GGTATGTAAATTTAT | 4734 |
rs182482162 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979866 | TCTCCACTTTTAAAA[A/C]TGAGATTTTGGAAAC | 4734 |
rs182505143 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942825 | ACAGTTTGGAGAGAT[C/G]AGAAGAAGAAAGGAG | 4734 |
rs182523626 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913096 | GAAAAGAAGTTGTAG[A/G]CTCTCAGTGCTTTAG | 4734 |
rs182575129 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871148 | CTTATTCCCAAGGCC[A/G]CTAATGTGGCTTGTG | 4734 |
rs182585201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832371 | ACACTTAGTAACATT[A/C]TGTGAAACTTCAAAT | 4734 |
rs182595174 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975513 | AAAGAAATCAAGAAT[A/G]TAACTCCCAGTTACA | 4734 |
rs182610142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901689 | GCATTTCCCATTACT[G/T]AACTGTTCATGTGGA | 4734 |
rs182617887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939937 | CATTACAGCATTATT[A/C]ACAGTAGCCAAGATA | 4734 |
rs182619379 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970442 | TAGCCAGGAAATAGT[C/T]ACCACAAGCCTTAGG | 4734 |
rs182624411 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55936229 | TCCATAAAGCTCAGC[A/C]CACTGGTAATAATTA | 4734 |
rs182625912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956222 | GGACATTTAGGTTGT[C/T]TCCAGATATATGTCT | 4734 |
rs182657315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847512 | TATTTTTATGAATTA[G/T]AAAACAAAATCTGAA | 4734 |
rs182657431 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859833 | ACTCTGTAATCGTGG[C/T]TGAATATAGACAAAA | 4734 |
rs182676993 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828969 | CATACATTTACTACA[C/T]AATTGTACAAGTGTA | 4734 |
rs182729307 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979652 | GCCACCGCGCCCGGC[A/G]AAAGTTTTTACTTCT | 4734 |
rs182743912 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960206 | GTCAACTTCATTAGA[A/C]TGAAGGATGCAAAGT | 4734 |
rs182744586 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921723 | ATCTATAAATATCCA[A/G]CTGTTAATATCAAAG | 4734 |
rs182762487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939649 | CAAATCAAAACCACA[C/T]CTGTTAGGATGACTA | 4734 |
rs182780280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901062 | TCTAACTTTTTTTAA[C/T]TTTTAATTTTTGTGG | 4734 |
rs182788432 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878811 | TCTCAAAGAAAAGTG[G/T]TTTTTTTGTTTGTTT | 4734 |
rs182879058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925716 | TGTGACAAAGATATC[A/T]AGATACCTAACTCAG | 4734 |
rs182879114 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873728 | ATGTTTTCACAATGC[C/T]AACAAACATCAGAAA | 4734 |
rs182885432 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902984 | CCAGCCTGGGTGACA[A/G]AGCGAGACTCCATCT | 4734 |
rs182891728 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894284 | TTAAAAAACAATGCA[A/G]CACAAGTATTTACAT | 4734 |
rs182896219 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943347 | TAGAGATCTTTGTGG[A/C]AGCTCCTCCTATCAC | 4734 |
rs182898604 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834791 | CAAGCCTCCACATCA[C/G]CCCTTCTTTACAGTA | 4734 |
rs182921296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982498 | CAAGACACAAAAGAG[C/T]ACATAATGTACATTC | 4734 |
rs182953110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903472 | ACAGTTTCCTAAAAT[A/G]TGGCACATGAAGTAT | 4734 |
rs182963436 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943859 | AAACCCTTAGGCACT[C/G]AACACTAGCCTGTGA | 4734 |
rs182999245 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863400 | CCCATCTCAAAACAA[C/T]AATAAAACAGAACTT | 4734 |
rs183041082 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55840041 | ATATATATATATATA[A/T]AACATTCATCATAAA | 4734 |
rs183122869 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859145 | AAAGGCAGGGAAACC[A/T]CAACTGGAAATGACA | 4734 |
rs183158981 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986843 | CTCGTGATCCACCCG[A/T]CTCGGCCTCCCAAAG | 4734 |
rs183176390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950446 | TGAAGTACAGAAGAA[C/T]GGCTTCTGTTTTCCT | 4734 |
rs183180682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931072 | AAATTTTTCAGAGAA[A/G]GAGAAGGAAAGAGGG | 4734 |
rs183191611 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971094 | ACAAAGAGATTAAAA[A/C]CCTCTTTGATTCTTA | 4734 |
rs183206873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965787 | GCTCGCTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 4734 |
rs183240171 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955321 | AGGCATCAGCCACCA[C/T]ACCTGGCAGCTCTAC | 4734 |
rs183242321 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926627 | AAAAATTAGCTGGGC[A/G]TCATGGCACATGCCT | 4734 |
rs183248634 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949881 | GGTGCAGCACACCAA[C/T]ATGGCACGTGTATAC | 4734 |
rs183266135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882437 | TGGAAAGCAACACCA[G/T]GCAGAACTCAGCCAT | 4734 |
rs183271744 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844646 | TAATAATAATGATAG[C/T]TACCCACATGGAGTT | 4734 |
rs183286053 | snp | A/C | 0 | 0 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994897 | CTGTCTCTACTAAAA[A/C]CACAAAAATTAGCTG | 4734 |
rs183304787 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988604 | TTAGACCAGAAAAGG[A/G]AAAAGAGAAATTATT | 4734 |
rs183305499 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882143 | AAATAGAAGCCTCCA[A/C/T]TGATCATCCTACCTG | 4734 |
rs183317936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843289 | GGAATGGCAGGTTAA[C/T]GTGTTTAACCTCATA | 4734 |
rs183329812 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945003 | ACCAAAACCCCATCT[A/G]TATGTCACGAACGTC | 4734 |
rs183348711 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903655 | ACGGTGAAACCTCAG[A/C]TCTACTAAAAATACA | 4734 |
rs183350382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877985 | TTCAGGTTCAGCATA[C/T]ACTCTTCTTATCCCT | 4734 |
rs183358444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883260 | CTGGCAGTACTCCCC[A/G]TAGCCCTGTGGCAGG | 4734 |
rs183359219 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858443 | CTCCCAAGTAGCTGG[C/G]ATTACAGGTGTGCAC | 4734 |
rs183361262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927212 | TGGGAAGAATTTAAA[C/T]GAGAAGGTATAGAGA | 4734 |
rs183361829 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899862 | ATTTTAAATCCAATT[C/T]AATTTAAGCTAATTT | 4734 |
rs183363550 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55954895 | TTTCATATATATAGG[G/T]GGTTAATGGCCTTCT | 4734 |
rs183369026 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975132 | TCCTGACCTCAGGCA[A/G]TCCACCCACCTCGGC | 4734 |
rs183391976 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864564 | CGCATGCCTGTAAAT[C/G]CCAGTTATTCGGGAG | 4734 |
rs183393960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844784 | GTTAAAGACAGTGCA[C/T]GGCTTTCAAGCACCG | 4734 |
rs183404613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840204 | GACAGATAGGTATGT[G/T]ATAAAGTAAATCTAG | 4734 |
rs183415662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867681 | GAGAAAAATACCTAA[C/T]AAAAAGTTAATCAAA | 4734 |
rs183467410 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935424 | GCTGAATTTTGATTC[C/T]TCTAAGCCTTAGGGT | 4734 |
rs183510055 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862851 | CTGAGACATGACTTC[A/G]AAATGAAAATTCGTA | 4734 |
rs183597267 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870514 | TGCTGCTTTTTTTTT[C/T]TTCTTCTTCTTCTTC | 4734 |
rs183610865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851325 | CAGAGCTTTAAAACA[A/G]TGTTAAGCAAAAAGG | 4734 |
rs183614722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889116 | CACATCAAGGTAAAA[A/C]GCTTTTGCACAGCCC | 4734 |
rs183798948 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979327 | GTAATAAGATCATGA[A/C]AGTTTTTACCTCTTT | 4734 |
rs183820086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938790 | AAAAAAAAACAAGCA[C/T]CAACAACAACAACAA | 4734 |
rs183827307 | snp | C/T | 0.000121271 | 0.00778593 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869593 | CCTCTAATTCCTCAG[C/T]CTGTTCTGCATTATC | 4734 |
rs183838052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975220 | CACTATTATTGAATA[C/T]AGTACTGGAAGTCCT | 4734 |
rs183839471 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909591 | AACCACCTTCCTGAC[C/G]TCAACACATCGCCTG | 4734 |
rs183870894 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831294 | TCTTCCTATAAATAC[A/C]TAAGAATTTGACTTT | 4734 |
rs183931492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972576 | CCACTAAAGAAAACA[C/T]TTTCACAAAAAGGAG | 4734 |
rs183940286 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966145 | GTTCACTCTCCACTG[A/C]CTTCAGGTTGCTGCT | 4734 |
rs183958379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932737 | GTGAACAGGCAACCT[A/G]CAGAATGGGAGAAAA | 4734 |
rs183958671 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912784 | AAGTATTTATTTTCA[A/G]ATCAAAAGTCATTAT | 4734 |
rs183965926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935151 | GGGATTACAGGCATG[A/G]GCCACCATGTCTGGC | 4734 |
rs183970423 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952143 | ACCGTCCTGGCTAAC[A/G]TGGTGAAACCCCGTC | 4734 |
rs183997431 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893288 | AATGTCATGATTCCT[C/T]TGTATAGATCATATA | 4734 |
rs184010925 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887605 | TTCTGAAAAACAGAG[A/G]AGGAGGGAATACTTC | 4734 |
rs184013561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921491 | CATCAGGCCTGGCTA[A/C]ATTTTGTATTTTTAG | 4734 |
rs184021391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941858 | GATTATAGGCGTGAG[C/T]CATTGCGCCCAGCCA | 4734 |
rs184024592 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963152 | TTTTTTTTTTTTTGA[C/G]ACAGGGTCTCACTCT | 4734 |
rs184025817 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959052 | TATTATTTCTTCCCT[C/G]TACTTATTTTAGAAT | 4734 |
rs184026709 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980828 | TGTTACATTTTTACC[A/G]CACTGAATGGTTTTA | 4734 |
rs184029513 | snp | A/G | 0.000115381 | 0.00759455 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848774 | TATTTGAGATAGCCA[A/G]GTTAGATGGGTTAGC | 4734 |
rs184034617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853559 | CCAGGTAATCTAACA[A/C]CAGAAATCATGCTTA | 4734 |
rs184057159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902488 | AATATGTATTTTTTA[A/G]AAAAGATTCTAGAAA | 4734 |
rs184103668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865516 | TTGATAACAAAACAC[C/T]CACATTTGTATATGG | 4734 |
rs184103907 | snp | C/T | 9.89283e-05 | 0.00703238 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916751 | GTGAACATGGCTATC[C/T]AAGTCATCTCCGGAG | 4734 |
rs184119987 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983169 | AGGCAGAAAAAGTGA[C/T]CCTAGATGGAAAGGT | 4734 |
rs184135900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845942 | AGGTGTGCGCCATCA[C/T]ACCTAACTAATTTTT | 4734 |
rs184141217 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840325 | TGTTGAGGAAAAAGT[A/T]CATTTGTATTTTGAA | 4734 |
rs184142033 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854500 | AAAACAGCATGCTAA[A/G]TGAAAAAGGTCAGAC | 4734 |
rs184143434 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895076 | AACAAGAGAACTAAG[G/T]TATAAAGTTATAATT | 4734 |
rs184147517 | snp | C/T | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826583 | TCTGAATTAACACTC[C/T]GAACTCTTTTTCTCA | 4734 |
rs184147657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874381 | ATTCTACAGTCCACA[A/T]AATGCAGAGAGCCTA | 4734 |
rs184161205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872814 | CTGCAGGCTGGCTTG[A/G]TTAGAGCATAGAGAT | 4734 |
rs184164611 | snp | A/G | 0.000873384 | 0.0208789 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915443 | ACAGGAAATATTTGG[A/G]TAAGCTCCTCCCAAT | 4734 |
rs184168817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856412 | CCCCGTGCTGGACTG[C/G]CTCCTGGACACCTTC | 4734 |
rs184180671 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875613 | GTTAGCCACCACGGC[C/T]GGCCAGATGTACATT | 4734 |
rs184181095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836675 | GGACTGCACGTGCAC[A/G]CCACCACGTCCGGCT | 4734 |
rs184182823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927322 | ACGACAAGATTCTTT[C/T]TTTTTTGAGATAGAG | 4734 |
rs184253999 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870355 | ACATCTCTTTGGCAG[C/T]TGTTTGAATCTGTCA | 4734 |
rs184268484 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831796 | ATTTCCTAGGCAGCA[G/T]TCCCGACTTGTAGTC | 4734 |
rs184273121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849472 | TCAGGTGATCCACCC[A/G]CCTTGGCCTCCCAAA | 4734 |
rs184275552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832336 | TTCAACCATGACTCT[A/G]TTTTTATTTTTTTAA | 4734 |
rs184469109 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983376 | AACACGGCATGCCAG[C/G]CTTGCCTGATCAGGC | 4734 |
rs184490198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945230 | CAAGCTAAAGAAGCA[A/T]GTTCTAACCCATTGC | 4734 |
rs184498110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896497 | CACAATGCCATTTTA[A/G]TAAAAATTTACCTGA | 4734 |
rs184505235 | snp | C/T | 0.00151847 | 0.0275123 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55966536 | CTTACTCTCACAATT[C/T]GTGAATTTTCCTAAA | 4734 |
rs184509624 | snp | C/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917980 | AACATGTCTCAATGC[C/T]AATTCTGTTCTGAAA | 4734 |
rs184517445 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990507 | CAATATGTACAAAGC[A/T]AGTTACCAGATACTG | 4734 |
rs184523872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964238 | GTAAGATATTATATA[A/G]TGATATCCATGTTAG | 4734 |
rs184611183 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981181 | CTGAGTAGCTGAGAC[G/T]ACAGGTGCCCACCAC | 4734 |
rs184627511 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983953 | TTTTCCTTAATAACA[C/T]TTATAAAATATTGAT | 4734 |
rs184638974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902092 | AAGATGTGGTTAGAT[A/G]ATAAATTCCAAATCT | 4734 |
rs184658574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923070 | GTGCCTGTAATCCCA[A/G]CTACTTGGAAGGCTG | 4734 |
rs184662579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860296 | GTCCCTAATGTATTA[C/T]TACATATTATTGCAT | 4734 |
rs184665572 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945697 | AAGAGCAACCCCAAG[A/G]CACATAATTGTCAGA | 4734 |
rs184671330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879931 | AAAGAAAAGAGGAAA[G/T]GGAGGACATTATCAA | 4734 |
rs184676755 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841364 | GCTGGTCACAAAAAG[A/C]CAAATATTGAATGAT | 4734 |
rs184690727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904293 | CTTGTTCTATTTCCA[C/T]ACACCTTTTATTTTA | 4734 |
rs184745990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835393 | GCCTCTGTTAATTTC[C/T]TTATTTCCTTTGCAG | 4734 |
rs184790061 | snp | A/C | | | intron-variant, utr-variant-5-prime, splice-donor-variant | NEDD4 | GRCh38.p7 | 15:55952653 | CAGAATCCATCCTTA[A/C]CCCTAACCTAGTGAG | 4734 |
rs184793642 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973394 | ACAAACAAAAAAACA[A/G]CAACAAAAAAACAGG | 4734 |
rs184796643 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991231 | GCCTATTTCCAGACT[A/G]GTCTGTGAGTTTTAG | 4734 |
rs184804791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928349 | TTTCGTACTGTAATC[A/G]GACTTACCTAGAAGA | 4734 |
rs184812563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968008 | ACCTTATTTTAAAAA[A/T]TTTATAAAATATTGA | 4734 |
rs184815131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884868 | AAGTAGAGACAGAGA[C/T]TGAAGTAGAAAGTTT | 4734 |
rs184827482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931474 | TATGCTCACAAAAAA[C/T]AGAGTTTATAAGATG | 4734 |
rs184843676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971929 | TACATCTGGCAGCAG[A/G]TTTCTGAGTGGACAC | 4734 |
rs184861365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861140 | TTTGCCATGTTATTA[C/T]AAGAGTAATAGAGTT | 4734 |
rs184874584 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888315 | AACATACAAATATCA[A/G]TAGCATTTCTCAATG | 4734 |
rs184919459 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968602 | TTAACCTAGTACAAG[A/T]TACCATATAGAATGG | 4734 |
rs184939839 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928941 | TACTAATTAAAACAT[C/G]AACATAAACAGCTAT | 4734 |
rs184943323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880455 | ACACAAACCTGAAAT[A/G]TAAGAGAGTACTTCC | 4734 |
rs184947374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905335 | CTGGAGAAACAAATT[A/G]ACCTCAGAGAGAAGA | 4734 |
rs184947451 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976225 | GCATAACTGGACAAA[C/T]TGGATCACATCAACT | 4734 |
rs184961253 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946218 | GACTGGCGAATTAGA[C/T]AAAGAGTCAAGACCC | 4734 |
rs184976243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910385 | GTGGTACTGTCTGCT[C/T]TCCTCCTTCCCTCAC | 4734 |
rs184978856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884229 | GCATTACTGGGCTTG[A/G]AATGTCCCCTAACAC | 4734 |
rs184982823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841667 | GGCTCCGCCTTCCGG[A/G]TTCACGCCATTCTCC | 4734 |
rs184999709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845668 | TTCTATTCCTCCAGC[A/G]TATTCTCATTAACAA | 4734 |
rs185101185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903926 | GCACTTTGTGAGGGC[A/G]AGGTGGGAGGATCAC | 4734 |
rs185118422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842221 | CATAATAACAAACCC[A/C]TCTCTCATAAAGTTA | 4734 |
rs185121617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864824 | AAACACATTATAAAT[C/G]ACAACAATTAAAGCT | 4734 |
rs185177568 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993308 | GGACCCGACAAGCTT[A/G]CTCCCTCCAGCGAGC | 4734 |
rs185201378 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934855 | TTCCTATATACAATG[G/T]TCTGCTTTTTTTTTT | 4734 |
rs185203488 | snp | A/C/T | 0.00518061 | 0.050666 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953721 | TGCTGGGATTACAGG[A/C/T]ATGAGCCAACATGCC | 4734 |
rs185209887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974448 | CTGATATCAAAACCA[A/G]ACAAAGATCCATTGA | 4734 |
rs185224745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891979 | TCTATTAAATATGAA[G/T]TATAGGCTGGGCACG | 4734 |
rs185242219 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55915191 | GGACCAGGAAAATAT[A/G]TAAAACTGCTTGGTT | 4734 |
rs185257199 | snp | A/G | 0.000373797 | 0.013666 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872511 | TTTCAAAATATATCT[A/G]TAACACCAAAAGCAT | 4734 |
rs185328773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957539 | GTTTTCTGCTTTTAT[C/T]AAGATGACTGTCTTC | 4734 |
rs185350846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957686 | ATGTATGTTTATTAC[A/G]GCACTATTCACAATA | 4734 |
rs185352159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886057 | GCATGAGTAGCTGTA[G/T]CAGATAAAATAGACT | 4734 |
rs185353916 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937298 | CAGACATTTTTATGG[C/T]GAATACATTCAGTTC | 4734 |
rs185366530 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977440 | CACAATGATGAAATT[C/G]CCTAATGACACATTT | 4734 |
rs185368465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897209 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 4734 |
rs185381372 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55919036 | ATTATTAACATATAA[A/C]ATAATGAACTCCAAG | 4734 |
rs185383081 | snp | A/T | 0.000398652 | 0.0141127 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829894 | CAGATTGTTATTTGT[A/T]ATCTAATCAACTCCA | 4734 |
rs185387290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867999 | AGGCAGAGGCTGCAG[A/C]GAGCTGAGATTGCAC | 4734 |
rs185387558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847513 | ATTTTTATGAATTAG[A/T]AAACAAAATCTGAAT | 4734 |
rs185451648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977119 | AACCTTCTTTCTTCT[A/G]AAGACTTACAAACAT | 4734 |
rs185458902 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913779 | AAAAGCATCCACAAC[A/C]AACTATAATTATTAC | 4734 |
rs185464930 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940790 | GCCTCTCGAAGTGCT[G/T]GTATTATAGGCATGA | 4734 |
rs185471758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980562 | AAGCCACCAAACAAA[C/G]GAATAAATTTGGAAA | 4734 |
rs185479837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937009 | TATTGGCCGGGCTGG[C/T]CTTGAACTCCTGACC | 4734 |
rs185501070 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890729 | AAAATCTGCCAGACC[A/G]TTTTCCAAAGTTGCT | 4734 |
rs185504825 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871178 | GTCTCCATACTGAAG[A/G]AGATGTGAACATTCT | 4734 |
rs185535833 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833101 | AATCCATCATTAAAA[C/G]AGCCTGAATAAGATA | 4734 |
rs185538289 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871651 | TCCTTTTCATTTTTT[A/T]AATATTTACATTACA | 4734 |
rs185544994 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851966 | ATTCATAGGAAAAGG[C/T]AGACACTTAACATCA | 4734 |
rs185572801 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867643 | AATACTTGAAAACTT[C/T]AAAAACAATTATACG | 4734 |
rs185596644 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961673 | GACAGGTTTCAAAGT[A/G]TTAGCCAGGATGGTC | 4734 |
rs185610376 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933304 | ATCAATGATAGACTG[G/T]ATTAAGAAAATGTGG | 4734 |
rs185614597 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896119 | CCCAATAGCTGCAAT[G/T]ATCCTATATTTTGCC | 4734 |
rs185626639 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936841 | CTTGTCACCCAGGCT[G/T]GAGCACAATGGTGTG | 4734 |
rs185628394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890392 | CCTAGGCAACCACCA[A/G]CCACTTTCTGTCTTT | 4734 |
rs185632566 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851726 | AGGTGATCCTCCCAC[C/T]TTGGCCTCCCAAAGT | 4734 |
rs185649545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855624 | GGCTGGGACAGCACT[C/G]AGCAGGAAGCAGAAG | 4734 |
rs185694055 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984860 | TGCCACAGAATTCAG[A/C]AGAACAATGGGTTCA | 4734 |
rs185707010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925837 | CTAATTTTTGAAAAC[C/T]GAAGTACAACACATA | 4734 |
rs185714084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957193 | TTCTTCCAGTAGTTT[C/T]TTCTGTAGATTCCTT | 4734 |
rs185715563 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943681 | AGGGGCAGAGCCCTC[A/T]TGGAGAACTTCTATT | 4734 |
rs185743810 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55917085 | AAATGCCTTCACTTA[A/C]AAAGCACTTGATTTC | 4734 |
rs185780871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874670 | GAGTTCAGCTATGTT[A/G]ACTTGCTAGAACAAA | 4734 |
rs185796666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836496 | CTCAGCCTCCCAAGT[A/G]GCTGTGACCATATGC | 4734 |
rs185934433 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978118 | GTGGAGCTCCTGATA[C/T]TAAAAACCATCCATG | 4734 |
rs186071829 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965665 | TTTGGTATGTATGTA[C/T]GTATGTATGTATGTA | 4734 |
rs186086411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982331 | TAGATGAATGTTCAC[C/T]GTAGGTTTATTCATA | 4734 |
rs186095185 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995200 | AAATTACAGAATGGT[C/T]AGGAATTGTTGGCTT | 4734 |
rs186109155 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924324 | TCCCAGAGCCATGGA[A/G]TAGGAACCAGGGGTC | 4734 |
rs186129717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975144 | GCAATCCACCCACCT[C/T]GGCCTCTCAAAGTGC | 4734 |
rs186131429 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853499 | AGTAATGGAAGTAAC[C/T]TGTTAAGCGACATGG | 4734 |
rs186131625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880899 | ACATGTTAGCTAATA[C/T]ATATTTAAAATACTG | 4734 |
rs186211946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948588 | CCAAAACAGCATGGT[A/G]CTGGTATCAAAACAG | 4734 |
rs186224556 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986017 | ACGAAGACCTAGGAA[A/C]CTCCTTGAAAGGGCT | 4734 |
rs186227304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969052 | AGGAAAGACAGTCTT[A/G]AATTGCCCACACCAC | 4734 |
rs186227548 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921545 | GGCCAGGCTGGTGTC[A/G]AACTCCTGACATCAG | 4734 |
rs186233129 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907104 | TCTCAAAAATAAAAA[A/G]AAATAAAAATAAAAA | 4734 |
rs186233788 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985273 | GCAGTCAATCACAGG[C/T]CACTACAGAAAATGT | 4734 |
rs186235667 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939332 | TTCCTCCCCCTTCAC[G/T]TTCTCTTCTGTCTCC | 4734 |
rs186238253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942510 | AAAAGTGTGTAGTAC[C/T]TCCCCCTTCATTCTC | 4734 |
rs186241804 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878079 | TAGATATAAAGATCC[A/G]GGTTCAAGGTGCTTA | 4734 |
rs186256208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947092 | CTAACATCACAATTG[A/G]AAGAACTAGAGAAGC | 4734 |
rs186257690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900274 | GGATTTGTTTTAGAG[C/T]GCATGGGAGCCATGC | 4734 |
rs186262289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876823 | CTATCATTATTGTTT[A/G]AAAATATTTTATTAA | 4734 |
rs186273668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862047 | AGCGCAATTCTACAG[A/C]ATTTTATAGTGTCTT | 4734 |
rs186285409 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902844 | AGGAAGGAAATATTT[C/G/T]AGAGAAATTAGGTCA | 4734 |
rs186288084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833644 | CCAGCCTGGGAGACA[C/G]AGCGAGACTCCATCT | 4734 |
rs186306115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837036 | TACCAATTGGAAAAA[C/T]TTAAGTAACTTTTTA | 4734 |
rs186334448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924820 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 4734 |
rs186354679 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943204 | AGCAGAGCATAAAAG[G/T]TGGGAATATGTGCAG | 4734 |
rs186359982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970050 | CCTAAAGGGAGAGAC[C/T]CAGGCCTGGCAGGAC | 4734 |
rs186360694 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903119 | GGCCATAAGAAAACA[C/T]TTGATCTGGACTATA | 4734 |
rs186363537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862316 | AAAAATGGAAGGGGA[C/T]TTGAGAATAAATATG | 4734 |
rs186366756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973928 | AAAAGAAATAATAAA[A/G]ATCAGAGCAGAAATA | 4734 |
rs186369179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902944 | AAGTGGAGGTTGCAG[C/T]GAACCGAGATCGTGC | 4734 |
rs186374050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862869 | ATGAAAATTCGTAGT[G/T]AAAGTGTTTCCAGAT | 4734 |
rs186383243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933614 | GGGTGCAGCACACCA[A/G]CATGGCACATGTATA | 4734 |
rs186387286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842762 | AGTTCCAATGAACAC[C/T]GTTCTGTGACCTGTA | 4734 |
rs186414843 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929760 | ATCACGAACGTACAA[A/G]TTAGAAAAACTGTCC | 4734 |
rs186439787 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857783 | TTACAAAAATTTTTT[A/T]AAAAAATTAGCAGGG | 4734 |
rs186476617 | snp | C/T | 0.0001059 | 0.00727592 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837750 | ACTTATAGGTTATAC[C/T]GTGACATTATGGAAG | 4734 |
rs186493030 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885281 | ATCAATACCAGACCT[C/G]TCCTACAAGAAATGC | 4734 |
rs186497540 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827461 | TCTCATTTAACATCA[G/T]GTTCTATGAGTCACA | 4734 |
rs186506076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846766 | TATATTATAAAATAT[A/G]CTGAAAAATAAAGAC | 4734 |
rs186554164 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953064 | GTGCAGTCTTGGCTC[A/T]CTGCAACCTCTGCCT | 4734 |
rs186573864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992536 | GATAAAAGGTACATG[G/T]GGCAGCTTAGTCAGC | 4734 |
rs186583343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914489 | CTGAATTGTCAAAAA[A/T]ATGAAAAGGTAAATA | 4734 |
rs186596291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843329 | TGCGAAAGCTACTAT[G/T]ATTGTCTTCATTTTA | 4734 |
rs186601014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882301 | AGTCTTCAGTTGCTG[A/C]CACCCACCCCCTCCA | 4734 |
rs186632401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949097 | TACAAAGAACACAAA[C/T]AAATTTACAAGAAAA | 4734 |
rs186642401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970631 | AAGAGAACAAGAGTC[C/T]CTGCCTGGTAATCCA | 4734 |
rs186648106 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986518 | ATGGTCATCAAGAAA[A/C]ACTAAACAGACCCAA | 4734 |
rs186774390 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828772 | AAAAACATTGTCTTC[A/G]TAGTAAACAGTATTT | 4734 |
rs186804731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844649 | TAATAATGATAGCTA[C/T]CCACATGGAGTTGTT | 4734 |
rs186806332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863620 | AAAGGACAAAAAATC[A/G]TTTAAATAAACAACC | 4734 |
rs186877714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975578 | ACTTAACCAAAGAAG[C/T]GAGAGATCTCTACAA | 4734 |
rs186893284 | snp | A/G | 0.00159617 | 0.0282053 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916827 | AATCGTAAGCTTTGT[A/G]CCATTTGTTCTCATT | 4734 |
rs186909210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956939 | TGAAAACAGCATATG[C/T]ATCCATTGATTTATG | 4734 |
rs186910482 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936304 | TTGAGGGTAGGTACT[A/G]TGGCCATCTCATTAA | 4734 |
rs186925512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959319 | TTTTTCTAGATCTTA[A/G]TATTATTGGTTTCCA | 4734 |
rs186925913 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895232 | ATTTTTTTCTTTTTA[A/G]AAATGTCTGCCAAGC | 4734 |
rs186950983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929485 | ATCCTCACCCTCCTC[C/T]TCTCCTCTACCCTCA | 4734 |
rs186970475 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847249 | GCAATTCCTATGGCT[A/G]TAATTTTCATTATGC | 4734 |
rs186972522 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885688 | AAATAAAAAGACATA[A/C]AAAAGATACACAAAA | 4734 |
rs187005132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959795 | GGCAGCATGCAAGGA[A/G]CTGAATGCCACCAGC | 4734 |
rs187007280 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979688 | ATTTTGTAAATTTTA[C/T]ATTCTATTTTTTCTT | 4734 |
rs187030630 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921957 | TCCTTGTGGACAACA[C/T]GCAAATAACGCAAAT | 4734 |
rs187035935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870381 | TGTCACACATTAATT[C/T]ACCTAATCTATTTTT | 4734 |
rs187044736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981717 | AGTATGAACATCACA[C/T]GGAAATTTGTTACAT | 4734 |
rs187046644 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911623 | CAAGCTCTGCCTCCC[A/G]GGTCCACGCCATTCT | 4734 |
rs187050551 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888912 | ATGCAAAAGAAACAA[A/C]CTAGACTCCTATTTC | 4734 |
rs187053848 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939681 | TACAAAAATTTTTAG[A/T]TTTTTTTAGTTAACA | 4734 |
rs187055612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55954939 | TTTAATTGTTTCTCT[C/T]GTGGTAAGAATATTT | 4734 |
rs187060989 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849733 | TTAGTATTATTTAAG[C/T]TATGTTGGTCTTTTA | 4734 |
rs187073210 | snp | A/G | 0.030278 | 0.119257 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979402 | CCCAGGCCGGACTGC[A/G]GACTGCAGTGGCGCA | 4734 |
rs187131622 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905968 | CATCAACAAGTGGGC[A/G]AAGGATATGAACAGA | 4734 |
rs187152019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832873 | AGTGTCCCTAATGGT[A/G]TCACTTTCAAAATCT | 4734 |
rs187169422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867195 | TAGTAGAATTTTATA[C/T]ATACAGTCACAAACT | 4734 |
rs187178321 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873798 | AAGAGAAAATGGAAA[C/T]GGAAAATTGAAATGA | 4734 |
rs187183791 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938307 | GTGGTTGCGGTGAGC[C/T]GAGATCGTGCCACTG | 4734 |
rs187186023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854304 | ACTTACTAAATACAC[C/G]GGAGTCCTACGTACT | 4734 |
rs187192542 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894602 | CAGGAGAAACTACTT[C/T]CTAAATCAGTTTCAC | 4734 |
rs187199648 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835202 | TCAACCCACTGCAAT[C/T]GGACTTCTACACTAC | 4734 |
rs187228348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898499 | GCCTTGATGCTTACA[A/G]TAATTTCAACACTCT | 4734 |
rs187266721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965127 | TTAGGAATTCTGTTA[C/T]AGCAACACTAAACAT | 4734 |
rs187268637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858267 | AGGAAGAAGGGGAAT[G/T]GGATCGTATGTGATT | 4734 |
rs187308551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983409 | TCCTCTCCAGCCTCA[G/T]CTGCTGACGTTGTGC | 4734 |
rs187325551 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945490 | AAAGAAGCAAAGAAA[G/T]CCTCCAAGAAATATG | 4734 |
rs187339274 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966795 | AGAATTTATCGCTGC[A/G]CTCAAGAAAATCTAA | 4734 |
rs187423089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877261 | TATTTAATTTCTTTA[A/G]ATCTGGAAAGTACCT | 4734 |
rs187432655 | snp | A/C/T | 0.00279258 | 0.0372817 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920942 | GTTTTGCTGGTAAAC[A/C/T]GAGTTTCTCAAGAAA | 4734 |
rs187441780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986926 | AAAACTGTCTAGGAT[A/G]AGAAAAACTGTGCAT | 4734 |
rs187480398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971427 | GTCAGGAGTTCGAGA[C/T]TAGTCTGTCCAACAT | 4734 |
rs187503526 | snp | G/T | 4.97038e-05 | 0.00498492 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915863 | TAACCGAAGTCCATT[G/T]ACAGCTGTTGAAAGA | 4734 |
rs187565897 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945011 | CCCATCTGTATGTCA[C/T]GAACGTCAAAGATGA | 4734 |
rs187571168 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980215 | TGGGATTTCAGGCGT[A/G]AGCCACTGCACCTGG | 4734 |
rs187581699 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901918 | GTTTCATAAATTTTA[A/T]ATTATATAAATATAA | 4734 |
rs187586300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903680 | AATACAAAAAATTAG[C/T]TGGGCGTGGTGGCAG | 4734 |
rs187588486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940103 | TAGGTGAAATAAGCT[A/G]GTCCCAGAAGAACAA | 4734 |
rs187600619 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883261 | TGGCAGTACTCCCCA[C/T]AGCCCTGTGGCAGGA | 4734 |
rs187604694 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927294 | GTGCTCTAAGGAAAT[A/G]AGACAGACAAAGACG | 4734 |
rs187641498 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864639 | GTGAGCCGAAATCAC[A/G]CCATTGCACTCCAGC | 4734 |
rs187648422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845377 | ATTACCTATTCTCTC[G/T]GTGCCTCAGTTTCCT | 4734 |
rs187657965 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858986 | GGCCCACCGGTTGTA[A/C/G]TTTGCTTTCCTCTGC | 4734 |
rs187671007 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840103 | ATATAACTTGGTATA[A/G]CCTATTGAAGTATTT | 4734 |
rs187687798 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965839 | TATTTTTAGTAGAGA[C/T]AGGGTTTCACCATGT | 4734 |
rs187718887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854703 | AACTGTATAAATTTA[C/T]AAAAACTCTTTAATT | 4734 |
rs187722271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926873 | TTGAGTTCAGGAGTC[A/T]GAAACCAGCCTGGCC | 4734 |
rs187741635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882675 | TTGGGGGGCAGGTGA[G/T]CTAGTGAGACACCAG | 4734 |
rs187758715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860019 | ATGTAGAGCAAAGTC[C/T]TGCTTCCTAAAACCC | 4734 |
rs187763181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887431 | AACCTATTAAGATTG[A/G]GCCATGAAGAAATCC | 4734 |
rs187773317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840917 | GTCCTTTGGCAGATG[A/G]ATGTATAAACAAAGT | 4734 |
rs187773453 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931037 | TGAAATTTTAAAACA[A/C/T]GGGCGTAAAGATAAT | 4734 |
rs187775263 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909118 | CAAGAGAAGGCCTAC[G/T]CTCTTTCTTCACCAA | 4734 |
rs187790636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989817 | TGGACTTCTAGAGCA[C/G]GGGTCCCCAACCTTA | 4734 |
rs187796285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868807 | CTCAACGAGCAGGTG[A/T]TTTTTTGACCCCTTT | 4734 |
rs187829433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961287 | TTACAGCCACTCTCA[C/T]GTGAGAGACTTCAAG | 4734 |
rs187862966 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922043 | GTGGCAACAGGAAAA[A/G]TAACAGTAATACCAT | 4734 |
rs187878694 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879071 | CCAGGTGATCCACCT[A/G]ACTTGGACTCCCAAA | 4734 |
rs187974062 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944081 | GATTGACGCAGAAGA[C/T]GGGTGATTTCTACAT | 4734 |
rs187982091 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983061 | CAGAAGGCAGAGGTT[A/G]CAGTGAACCGAGATT | 4734 |
rs187995501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903483 | AAATGTGGCACATGA[A/G]GTATGCTGTTTTAAA | 4734 |
rs188013851 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874454 | AGAAGGCCTAGTTTG[A/G]GGTTGACAGCATATC | 4734 |
rs188069967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971940 | GCAGGTTTCTGAGTG[C/G]ACACCTAATAGGCAG | 4734 |
rs188091863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931736 | AACAAACAATACAGA[C/T]ACATCTTTAAAATAG | 4734 |
rs188123850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901258 | GAAGAGAAAAAAGTC[C/T]ACAATTTTATGTTTT | 4734 |
rs188159236 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859501 | GAGTTCAAGACTAGC[C/G]TGGCCAACAGGGTGA | 4734 |
rs188214822 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972795 | AATAAAGGCACACAG[A/G]AAATATTCCATGCCA | 4734 |
rs188215678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937884 | GAAGAACAAAGCTAG[A/G]GGCATAATAGTTCCT | 4734 |
rs188222173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958397 | GTGGTGATATATTGC[C/T]ACATAATGTTTAATT | 4734 |
rs188230093 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990736 | ATATCACAGGGAGGT[A/G]CATGGGAAGGAGGTG | 4734 |
rs188238172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881067 | TAGAACATGAGTTGA[A/T]GATAATTTTTGAAAT | 4734 |
rs188240783 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919642 | GTGTAGAAGAACTGG[A/G]GGGACATGGCAGCCC | 4734 |
rs188248055 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912970 | GACAGTGTCCCAGAT[A/T]CAGGTAAAAGTTCTC | 4734 |
rs188252529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862077 | TCAGCTTTGCAGTCT[A/G]TACGTCACTCTATGA | 4734 |
rs188256873 | snp | C/G | 0.299916 | 0.244966 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933208 | GGATTATAAATCATG[C/G]TGCTATAAAGACACA | 4734 |
rs188258902 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952238 | ACTCGGGAGGCTGAG[A/G]CAGGAGAATGGCATG | 4734 |
rs188266977 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842376 | AATCACTTAGTAATA[C/T]AGACTTCTTTACATC | 4734 |
rs188280432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889918 | GTGTTGCCCAGGCTG[A/G]TCTCAAACTCCTGAG | 4734 |
rs188333576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975325 | GAATGATATGAACTT[A/G]TATTTGGAAAAGCTA | 4734 |
rs188356977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935470 | ACCAACAATGGGGTA[A/G]GAAATATGCACATTA | 4734 |
rs188365134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963609 | ACCAACAATATAAAT[C/G]CTAAAAAACAATGTT | 4734 |
rs188371174 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981005 | AACAAAATATTCAAC[A/C]AAAAAAAATTGCTAG | 4734 |
rs188390898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865741 | CGTTGGAAGGCTAGA[A/C]CTGAAAACGAGGCCT | 4734 |
rs188403538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884897 | TTACTCAAAGGGATA[A/G]TAACAGAGAACTGTC | 4734 |
rs188415577 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846085 | AGCTACTGCACCTGG[C/T]CCACAAAATTATCCT | 4734 |
rs188427514 | snp | G/T | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826831 | GATTGCACTGAAAAT[G/T]TAACGTGCTGCTGTG | 4734 |
rs188487543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931209 | GCCAAACATAAGTTG[A/G]CTATTTATTCATCTA | 4734 |
rs188501906 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887726 | AGCATTGATACAAAA[A/C]TCCTCAACAAAATAC | 4734 |
rs188530726 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848820 | CAGGTAAAGGCCCTA[C/G]ATCATTGGAAGTATC | 4734 |
rs188554241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831917 | TTTCCTTAAAAGCAA[A/G]TAAATATCATTCCAA | 4734 |
rs188660170 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955486 | CCCCTCACCCCTCAC[C/T]CCAACACAGCAACCA | 4734 |
rs188661620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873208 | AATGGCTGGCCCTCC[A/G]TTCTTATCTCTTTCA | 4734 |
rs188669610 | snp | G/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915573 | GATGGCAAACATGCA[G/T]ATGTCCTATGCATGA | 4734 |
rs188699559 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834383 | GAATCCCACATCCAC[A/C]CAAGTTTCTACCACT | 4734 |
rs188756423 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980747 | TGTCTTCAACAAGAA[C/G]AAGGAAAAGGAAATG | 4734 |
rs188765102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950584 | GAACTTGGCAGCAGG[A/G]AAGTCACTGGTGACC | 4734 |
rs188793395 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870145 | AAGGGGACTACAGGA[G/T]ATTGGGATGGTCCAG | 4734 |
rs188797924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909778 | AGCCTGTAAGAAGCC[A/G]GCAACATAGACAGAA | 4734 |
rs188817118 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830403 | TTCTTACCCATAATC[C/G]ATACCTGCCACCGAC | 4734 |
rs188831445 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831389 | GCCCCAAATTTCAAA[C/G/T]AGTGCATGAAATCAG | 4734 |
rs188873945 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937018 | GGCTGGTCTTGAACT[A/C]CTGACCTCAGGCAAT | 4734 |
rs188875997 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957607 | TACCATTTGACCCAG[A/C/T]GATCCCATTACTGGG | 4734 |
rs188893044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896509 | TTAATAAAAATTTAC[C/G]TGATGATACTAAATT | 4734 |
rs188913419 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918060 | TTTAGCTGTTTGATA[A/T]CTATAAAGAAATACA | 4734 |
rs188916733 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856935 | TACTGTTTATAATAG[A/T]ACTGTAAACAATCTA | 4734 |
rs188924222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875672 | TAAAAAAATTCAATA[A/C]ATGGGTTTAAAAGAC | 4734 |
rs188931850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836832 | CGCGCCCAAATTTTT[A/T]ATTTTTTATAGAGAT | 4734 |
rs188952321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893418 | TAAGCTAACAGATCA[A/G]GAAATACTTCAGAGA | 4734 |
rs188963746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853646 | TTTATCATAGTTTGT[C/T]ACAAATGAATAAAGA | 4734 |
rs189018110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962236 | GGCATATCTTTTTGC[A/G]TCCGCTTTCTTTCAA | 4734 |
rs189020112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941121 | TCTGAGTACTCTCTC[G/T]GTCTCTCTCATATAA | 4734 |
rs189035779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902310 | TATCCATCTTGAATT[C/T]TGTCAATACTAAAAT | 4734 |
rs189047979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880094 | GTCAGGAGTTCGAGA[A/C]CAGCCTGACCTACAT | 4734 |
rs189050033 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923785 | TATAATTACCATTTC[G/T]TGAGGGCAAAAAAAA | 4734 |
rs189064451 | snp | A/T | 4.94743e-05 | 0.0049734 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860595 | ATGAACAGAATAAGC[A/T]TGAGCCACACATACT | 4734 |
rs189068637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832938 | ATGATGGAAGCTTGC[A/G]GATTCGTCAGCCATG | 4734 |
rs189072174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879601 | ACCTAAATGAAAGAC[A/G]GGAGTCTGATGAATA | 4734 |
rs189073212 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981306 | CTGACCTCAGGTGAT[C/G]CACCCGCCTCAGCCT | 4734 |
rs189079053 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841461 | GGAATGGGGAGCGAG[G/T]GCTTACTGGGTATAG | 4734 |
rs189080482 | snp | A/G | 0.0020215 | 0.031728 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848619 | TTAGGAGAGGGGCGT[A/G]GATGAATGGATAGAA | 4734 |
rs189103036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942718 | AAGAACAAACTAATA[C/T]AGAAAATTGGTAATG | 4734 |
rs189138969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902887 | GTGCCTGTAATCGCC[A/G]CTAGTCAGGAGGCTG | 4734 |
rs189142430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991787 | CCCCAGTTCCTTACC[A/G]ACCACCCATTAACTG | 4734 |
rs189147216 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870716 | TTTTTGTATTTTTTT[A/G]TAGAGACAGGGTTTT | 4734 |
rs189193713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836556 | TTTGAGACGGAGTCT[C/T]GCTCTGTTGCCCAGG | 4734 |
rs189248209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897277 | TGCGCCCGGCCGATA[C/T]GGCATGTCTTAATGG | 4734 |
rs189257267 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928432 | AACAAAATCCAAAAG[C/G]CTGAGTATGGAATGA | 4734 |
rs189269704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968071 | ATCCACTATGTTTAC[A/G]TGTGAAAATATTTAA | 4734 |
rs189276348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929030 | CCATTACAGCAAAGA[A/T]GATGAGAGGGCCATC | 4734 |
rs189276771 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905505 | AAAGAGAAATAACAA[C/T]AACAACAGCAAAGGG | 4734 |
rs189282719 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946746 | TTCCAAAATTGACCA[A/C]ATAGTTGGAAGTAAA | 4734 |
rs189297633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866417 | ACCTAAAATTTAGTC[C/T]TGCATATATTGAATC | 4734 |
rs189314757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885327 | AGTCTGAAAGAAAAG[C/G]ATATTAATGAGCAAC | 4734 |
rs189393417 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924394 | TTTCTGTCCTCTCCT[G/T]TCACAAGAGGTCTTG | 4734 |
rs189403901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880542 | ACCTTTTTCAATTAT[C/G]ATGGTAGAATAAAGA | 4734 |
rs189404676 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964942 | AAAAAGAGGCTGGCA[C/T]ACCTCCCCCTTGCTT | 4734 |
rs189412154 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923931 | CTTTGCACACATAAC[A/G]CTGTTTCTATACTTA | 4734 |
rs189422145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841716 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 4734 |
rs189445382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851478 | ATTTTACATTTTCTT[C/T]TCTGTTTTTTTTTTT | 4734 |
rs189517536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984160 | AAGAAAAGACAGAAG[A/T]TGTGGAAATGAGAGC | 4734 |
rs189551735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945952 | ACCCTTTATAGACAA[C/G]CTGAGAGATTTTGTC | 4734 |
rs189570708 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904833 | GCATTTTGGCCAGGC[A/G]TGTAATCCCAGCACT | 4734 |
rs189583808 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865106 | GAGAGGCTGGGGCAG[A/G]AGAATTGCTTGAGCC | 4734 |
rs189593497 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994319 | TCCAATCTCCAGGCT[A/G]ACCCTCTAAACCTGC | 4734 |
rs189624852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953790 | CAATGGCACGATCTC[A/G]GCTCACTGCAACCTC | 4734 |
rs189625065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934995 | TGCCTCAGCCTCCCA[A/G]GTAGCTGTAATTAGA | 4734 |
rs189627982 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968647 | AAAAGATAATCTCAC[C/T]GGTCAGCAGAAAGAG | 4734 |
rs189634332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985125 | TCCCATTTTCTATAC[C/G]CCTGCTCACCCTAAA | 4734 |
rs189639679 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974506 | TGATAAACATTGATG[C/T]AAAAATCCGTAATAA | 4734 |
rs189697997 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902565 | GATATATTTTAGAAC[A/G]GGATGAGGCATACAT | 4734 |
rs189706672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861716 | ATCAGATTGAACACC[C/G]TTACCCCAGTCATTT | 4734 |
rs189765688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907620 | GTTTCCAGTAAGCTC[C/T]GTGACTGTTTAAGAG | 4734 |
rs189773574 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886245 | AGACCCCAATACAAT[C/T]ATAGCTTGAGAATTC | 4734 |
rs189780740 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953151 | CACACCACCACGCCC[A/G]GCTAATTTTTGTATT | 4734 |
rs189789008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992801 | TCAAATCCCAGAGCT[C/T]AATCTAGTTTTCAAA | 4734 |
rs189800710 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830160 | GGACTGGGTTCTGGG[A/C]ATGGATACTCTGCAC | 4734 |
rs189804916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868142 | ATTTAAAATTTTCCC[A/T]GAAAGCTCTGCTGCA | 4734 |
rs189808961 | snp | A/C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847937 | CACCTGCCTTGGCCT[A/C/T]CCAAAGTGCTGGGAT | 4734 |
rs189848069 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845768 | TTTCCAGGGAAATTT[C/T]GACACAAAGTTATTC | 4734 |
rs189919943 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891252 | CTGTATTTCCAATAT[A/T]TGAAAAATGAAAAAA | 4734 |
rs189926164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934066 | GCTGAGACAGGAGAA[C/G]AGCTTGAACCCAGGA | 4734 |
rs189927774 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977211 | ATGATGGACAGCATA[C/T]ATGATGGTGGTCCCA | 4734 |
rs189930374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914710 | TGCTTTAAACATGCA[G/T]CATAATAGTTTTTAT | 4734 |
rs189950266 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872083 | CGTCGAGTTAGGTAA[C/T]GGTTTTAGATGAATT | 4734 |
rs189952374 | snp | C/G/T | 0.00360943 | 0.0423289 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833148 | AACAGCACTGGGAAA[C/G/T]AGGTAAACAAATTAT | 4734 |
rs189982829 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903967 | GAGTTTGAGACCAGC[C/T]TGGCCAACACGGTGA | 4734 |
rs190035447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974159 | TATGCCAATAAATTA[C/T]AAAACCTAAAGGAAA | 4734 |
rs190047130 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973443 | TCATCAGGAGGCTGA[A/G]GTGGGAGGATCACTT | 4734 |
rs190074177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890408 | CCACTTTCTGTCTTT[A/G]TGGATTTGCCTATTC | 4734 |
rs190087820 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933495 | GAGAACACTTGGACA[C/T]GGGAAGGGGAACATC | 4734 |
rs190108482 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851876 | TACCCAAAGACGAGA[C/T]CATTTGCTTTTTCCT | 4734 |
rs190189343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957438 | GTTTTTTCATAGATA[C/T]CCCTGATGAGGTTTA | 4734 |
rs190216019 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917154 | CTCAAACACAGCCAA[C/T]CTTGTTTCAATTATA | 4734 |
rs190220622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884704 | AGAATTTATCAAGCA[C/G]AAGAAAGAATAGTGA | 4734 |
rs190225963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846781 | ACTGAAAAATAAAGA[C/G]ATAAACTAATTATGG | 4734 |
rs190254533 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875049 | CTATTAGTTACTATA[C/T]TCATTGTCCAGCCCA | 4734 |
rs190293165 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952733 | ACTTTGGAGCCTTGC[A/G]TCATCTGTTCTCACT | 4734 |
rs190312947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914060 | AGAATTTGAAATCTG[A/T]TCTTTTTTTATCCTT | 4734 |
rs190358416 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871296 | TTTTCAATTGGAAAA[G/T]AAGCCTCAAGGTTTT | 4734 |
rs190391318 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832338 | CAACCATGACTCTGT[C/T]TTTATTTTTTTAAAA | 4734 |
rs190396564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965769 | TGCAGTGGCACAATC[G/T]TGGCTCGCTGCAACC | 4734 |
rs190412443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982464 | AAACAACCCCATGGA[C/T]GACTCTCAAAAAAAG | 4734 |
rs190452189 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976354 | TCACTAGAAAATATA[C/T]GAAGCTCAAACAACT | 4734 |
rs190472484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896403 | TGGTTAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 4734 |
rs190474269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936916 | TCCTGCCTCACCCTC[C/T]TGAGTAGTTGGGATT | 4734 |
rs190490769 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827695 | GAATTATGATGGTAA[A/G]ATCCATATACAGATA | 4734 |
rs190508994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855701 | AAGGACTGATAAACT[A/C]CAGCCTGGCTGCCGG | 4734 |
rs190523969 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979500 | CTGGGACTACAGGCG[C/T]CCGCCACCGCGCCCG | 4734 |
rs190548192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921717 | TTATCCATCTATAAA[C/T]ATCCAACTGTTAATA | 4734 |
rs190552587 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985454 | GGGATGCTGCATAGA[C/G]AATAGCAATATTCCC | 4734 |
rs190558904 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959455 | TACCATGTGCATTTC[A/T]AAAGAATGTGGTTTA | 4734 |
rs190560625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939589 | ACAAATGGCCCACTC[C/T]TTATGTAAAAAGGTG | 4734 |
rs190575472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900507 | AATATATTTCGGCAA[C/T]TTTACCACCTGTTGC | 4734 |
rs190578938 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859001 | GTTTGCTTTCCTCTG[A/C]ACTAGAATGTAAGTC | 4734 |
rs190585453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878235 | ATTTCATGATGATGA[A/G]TATTACCACAAATAA | 4734 |
rs190593362 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840190 | CAGACTGATGGATAG[A/G]CAGATAGGTATGTGA | 4734 |
rs190666208 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944487 | CAAAGCAGCCGGGAA[C/G]CTGAAACTAGGCAGA | 4734 |
rs190666528 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965398 | TGTAGAGACAGGTTT[A/C]ACCATATTGCCCAGG | 4734 |
rs190668673 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981968 | AACAACTCATCATTA[C/T]TTTACATCTTATCAC | 4734 |
rs190679904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983087 | AGATTGCGCCATTGC[A/C]CTTCAGCCTGGGCAA | 4734 |
rs190708848 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943287 | CAGCTGCTGGAGCTG[A/C]ATGTTCATAGCCAAG | 4734 |
rs190712985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834408 | ACCACTACACAATCA[C/T]GGGCTCTTCACTGAG | 4734 |
rs190715261 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862459 | GAAGTTATGTGGACA[C/T]TGACCAGACTGTCAA | 4734 |
rs190718656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872783 | CATCCCAAAAGAACA[C/T]GGACTATGCACATGT | 4734 |
rs190719378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853698 | TTACTTAAAATAGTC[A/C]TAAATCCAGGCTGGG | 4734 |
rs190724263 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902955 | GCAGTGAACCGAGAT[C/G]GTGCTATTGCATTCC | 4734 |
rs190730721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881985 | TTTGTCAAATATCCC[C/T]TGGGTGGCAAGATCA | 4734 |
rs190752086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833949 | TGTATCAGTTAAATG[C/T]AATCCACCAGTATAG | 4734 |
rs190822378 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970147 | GCCACAGGTCTGGGG[A/C]AGTGGTGGCCATGGG | 4734 |
rs190842255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930507 | AACTAGTTGGAATCC[C/T]CAAATGATAATACAA | 4734 |
rs190865577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839691 | TTAAAAAATATACAC[C/T]ATTTGGCCAGGTGCG | 4734 |
rs190871439 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858334 | TTTCTTGAGACGGAG[A/T]TTCACTCTGTCACCC | 4734 |
rs190887102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857903 | TATGATCATGCTACT[A/G]CACTCCAGCCTGGGC | 4734 |
rs190919524 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966101 | CCCTTCTTCCAAACA[C/T]GAACTCCCCACCAGA | 4734 |
rs190961206 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55892623 | TACACCGAGTACAAA[A/C]TCAAAAAGAAAATGA | 4734 |
rs190987057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853508 | AGTAACTTGTTAAGC[A/G]ACATGGCTTCTAAGG | 4734 |
rs190997135 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882304 | CTTCAGTTGCTGACA[C/T]CCACCCCCTCCATCC | 4734 |
rs190998925 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844207 | GAGGAAGGGAAAGAA[C/G]GCAGGGATTATAGGG | 4734 |
rs191015982 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986690 | TGCCTCCCAGGTTCA[C/T]GCCATTCTCCGGCCT | 4734 |
rs191038111 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949742 | CACTCATAGGTGGGA[A/C]TTGAACAATGAGAAC | 4734 |
rs191043933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931042 | TTTTAAAACACGGGC[A/G]TAAAGATAATTATTA | 4734 |
rs191048357 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970934 | CATGATCTCACCAAA[A/C]AAACTAAATAGGGCA | 4734 |
rs191063551 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948613 | AAACAGAGATACAGA[A/C]CAATGGAACAGAAAA | 4734 |
rs191064883 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887579 | AACTAATACCAATCC[C/T]ACTCAAACAATTCTG | 4734 |
rs191078326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986131 | TTACAAGTCTATGCT[A/G]ATATAAATAAATGAC | 4734 |
rs191086327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909413 | CTTGTTTTGAAATTA[A/C]TGTATCTCTAAGTAT | 4734 |
rs191111685 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876913 | TCTTGCCATCTTACG[C/T]AGGATGGTCTCAAAC | 4734 |
rs191148451 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837168 | AGCACGGTGGCTCAC[A/G]CTGGTAACCCCAGCA | 4734 |
rs191187334 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903548 | AATATACTGGGGCCG[G/T]GCAAGGTGGCTCACG | 4734 |
rs191193243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882982 | CAGCTGTGTTGGCTA[C/T]AGAGACTCCTGCGTG | 4734 |
rs191227332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863756 | TTCTTATTGGTCATT[A/G]TCTTTCCTACAGAGA | 4734 |
rs191228085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863212 | GACAGAATAAACAAT[C/T]CTCAACTTTTAAGAC | 4734 |
rs191229026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844660 | GCTACCCACATGGAG[C/T]TGTTTCAACTCCATG | 4734 |
rs191280971 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957078 | CGTTTTTAAATTGTA[C/T]TTTCCAATGGCCCAA | 4734 |
rs191285220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976209 | AGCACAGGCAACCAA[A/G]GCATAACTGGACAAA | 4734 |
rs191325332 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936406 | AGTTTTTTCCCCCTA[A/T]CCATAAAAATACAAA | 4734 |
rs191377883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926525 | CTGTCATCCCAGCAC[A/T]CCTAGGCTGAGGTGG | 4734 |
rs191430861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959807 | GGAACTGAATGCCAC[C/T]AGCAACCACATTAGC | 4734 |
rs191433322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931773 | TAGCTATAATTCACA[G/T]AGCATACACTCATCC | 4734 |
rs191435263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979822 | TATCACATACTATCT[C/T]GTATCTGAGGCAATA | 4734 |
rs191436916 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912044 | TCTGTCTGAAATTAA[C/T]AATTCCTCAGTTCTA | 4734 |
rs191453426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951312 | AAAATGAGAATTTAT[C/T]ATTCTAACCTCCTAA | 4734 |
rs191457351 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870389 | ATTAATTTACCTAAT[C/G]TATTTTTATATTGTA | 4734 |
rs191473446 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889033 | TCTGCAGACATTGGA[C/G]AAGGCAAAGATTTCT | 4734 |
rs191481699 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832057 | ATAGAATACATAGAA[A/T]CTTACTTTACCGAAA | 4734 |
rs191487427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850263 | TCATATAAAAGCAAA[C/G]GATTATTCCTATGTA | 4734 |
rs191507921 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906234 | TGTGGCGATTCCTCA[A/C]GGATCTAGAACTAGA | 4734 |
rs191522972 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948564 | AACTATACTACAAGG[A/C]TACAGTAACCAAAAC | 4734 |
rs191553939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867474 | CAAAACTTGGAGCAG[A/G]TTACTAAATAATGAA | 4734 |
rs191561637 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828834 | TACAAATTATGCATT[A/T]TAACAACTCTTTGGT | 4734 |
rs191605445 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903285 | GATTCTCCCAGTGCC[C/T]GATGAGAGTCCTTTT | 4734 |
rs191606216 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935379 | TGACTATGTCTGTCA[A/G]GGATAGACAGCAACT | 4734 |
rs191618132 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835340 | TTAAAACCATCTTTT[C/G]TATTGAAACTCTGTC | 4734 |
rs191626875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975188 | GTGTGCCACTGTGCC[C/T]GGCCGCCCACTTTTA | 4734 |
rs191660381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894161 | TTCTGGTAGATCTGA[C/G]TATAAGACATAAACT | 4734 |
rs191746135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969153 | AAAGTGATTGTGGGA[C/G]TTTGCATTGGAACTC | 4734 |
rs191783979 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929566 | GTTTAACTTCCACTT[A/G]TAAGTGAGAACATGT | 4734 |
rs191785176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983756 | CCTGAGACTACAGGT[A/G]TATGCTACCATGCCT | 4734 |
rs191790105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877304 | GTCTTTCATAATCTT[A/G]ACATTTTTGAGCAGT | 4734 |
rs191801259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886001 | GACTAAAAACAAAGG[A/G]ATGGAAAAAGGTACT | 4734 |
rs191806842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847431 | AGGAGTTGCCTTTTT[A/G]AGCCATTAAAGGACT | 4734 |
rs191884807 | snp | A/C | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995424 | AATTCAGTGTCATTT[A/C]AGGGCACAATTACAA | 4734 |
rs191907062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55936195 | CCTGTATTTACTCTC[C/T]GGTATCATTGTTTTC | 4734 |
rs191914819 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916616 | AGATGAGGGAACAGA[C/T]GATCTTTCTTGAGAC | 4734 |
rs191916232 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955238 | ATGTTGCCCAAGATG[G/T]TCTCAAATTTGCAGG | 4734 |
rs191925209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955630 | TAATCCATATTGTCA[C/T]ATGAATTTCCTTCTT | 4734 |
rs191928951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873952 | ATCATGGACACCTAT[A/G]CCAACCGGTAATGGA | 4734 |
rs191933810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873343 | TCAGCAGTCTACTTT[A/G]AACTTTCATTTTCTT | 4734 |
rs191941511 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854436 | GATATATCTCTACAG[C/T]GGAATACCGTGCACT | 4734 |
rs191942085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941510 | TGATATACATACGTG[A/T]GTTACTGAATTGTAA | 4734 |
rs191943171 | snp | C/T | 0.000759816 | 0.0194764 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915691 | CTGCTTTTCGTTGGG[C/T]GAAATGCACTGAAAC | 4734 |
rs191943437 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894714 | TACCTTGTCAAGTTT[A/G]TCTTTACATGCTCTA | 4734 |
rs191949615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962414 | TACAGGTTTATTGTT[G/T]GTTTTCCATTGTCAC | 4734 |
rs191958517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902326 | TGTCAATACTAAAAT[A/G]ACATAGTGACTTAGA | 4734 |
rs191989093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842763 | GTTCCAATGAACACC[A/G]TTCTGTGACCTGTAG | 4734 |
rs191994974 | snp | A/G | 0.000148315 | 0.00861021 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860700 | ACTTTCTGTTTCCTC[A/G]GATATCTGCCGCCTG | 4734 |
rs192093868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945067 | GGAGAAACCAGAGCA[A/G]AAAAGCTGAAAATTC | 4734 |
rs192100828 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869050 | ATGTAACTCTACACA[A/G]ATCTTGACTTGGACT | 4734 |
rs192105248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831695 | AATGAGGCTTGGCAA[A/G]CTGACCAGATTTGCC | 4734 |
rs192107161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899084 | ACAATAAACACACTG[A/C]AAGAAGTATGTGTAA | 4734 |
rs192112137 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966335 | AGAGATTTAGTAAAC[C/T]ACCAACTGGTAATAT | 4734 |
rs192116250 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983316 | CGTGCGCGCGCGTGC[A/G]TGCATTTGATTTCCA | 4734 |
rs192119661 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921471 | CCGGGACTACAGGTG[A/C]GCACCATCAGGCCTG | 4734 |
rs192123764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958766 | GTCTTTCAAGAATAT[C/T]ATCTACTTCACTAAA | 4734 |
rs192129775 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883659 | CTTGTGTCATCCCTC[C/T]CCTAGTTCCAGGCAT | 4734 |
rs192138809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927311 | GACAGACAAAGACGA[C/T]AAGATTCTTTTTTTT | 4734 |
rs192143049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903750 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGGTTGC | 4734 |
rs192202649 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916888 | CAAAGATCTCTGTCC[A/G]TAGACAGGCTAGAAG | 4734 |
rs192242237 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874539 | ATCTATATATAAACT[C/G]TTACCTAAATCCCTA | 4734 |
rs192255533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836147 | TCCCTCTAGTCCTTC[C/T]TTGTCCCTTCCTTTG | 4734 |
rs192359739 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901479 | CCAGTGTTGACACTG[A/T]CCCTAAGAATACATC | 4734 |
rs192363001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939682 | ACAAAAATTTTTAGA[C/T]TTTTTTAGTTAACAA | 4734 |
rs192391618 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859521 | CAACAGGGTGAAACT[C/T]CTCCATCTCTACTAA | 4734 |
rs192462118 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979162 | TCCTATATCATCTAG[A/G]CAGAATCCTTTGAAG | 4734 |
rs192489901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938669 | CAACAAAGTGAAAAG[C/G]CACCGTACAAAATGG | 4734 |
rs192604582 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973384 | TCTCTTAAAAACAAA[C/G]AAAAAAACAACAACA | 4734 |
rs192604775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990800 | CCACACTGCTCTCCA[A/G]TAAAGATCAGTGCAT | 4734 |
rs192646821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895974 | GGGTAGGTTTTATAC[A/G]AGGCATCTTACAGAC | 4734 |
rs192651287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855276 | AAAGCTGATATCTAG[A/G]CTGCCATTCAAAGTT | 4734 |
rs192652885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926984 | GGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 4734 |
rs192679772 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860238 | TCTGGTCCATACTAC[C/T]AATGAGGATATTTGA | 4734 |
rs192691496 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972439 | TTGTTTTTGCAATCA[A/G]AGTTAAACTGTTATC | 4734 |
rs192693852 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879662 | TCAGAAAAACCGTAA[A/T]ATTCCCAGAGATAAG | 4734 |
rs192695119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841223 | AGGCATGAGCCACCA[C/T]GCCCAGCCTAAACAA | 4734 |
rs192724787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921977 | ATAACGCAAATAAAA[C/T]AGTTCACCAATAATA | 4734 |
rs192747995 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840312 | TTTCATAATAAAATG[A/T]TGAGGAAAAAGTTCA | 4734 |
rs192750729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879248 | CAGAGAGATAAGTGA[A/G]AGAATGAGTGAAAGT | 4734 |
rs192770747 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927543 | CTCAAGTGTTCCTCC[C/T]GTCATGGCCTCACAA | 4734 |
rs192779081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967286 | TATTATAATGTATCA[A/G]ATATTAAATATCTTT | 4734 |
rs192779991 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884793 | AAAACAATGAAGCAC[A/C]CCTACAAGATCTAGA | 4734 |
rs192794468 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845913 | GCCTCAGCCTCCGGA[A/G]TAGCCGGGATTAAAG | 4734 |
rs192851307 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950685 | CAGAAATGACGAGGG[C/G]AGACAACTCTCCCAT | 4734 |
rs192858327 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870328 | AGGCCTGATCAGTGT[C/T]TGAAACCTGCTACAT | 4734 |
rs192860268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909935 | GCTGTCCAAAATGAG[A/G]TGTGAATATTCATAA | 4734 |
rs192904661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990126 | GAAAACAAGCTCAGG[A/G]CTCCCACTAATTCTA | 4734 |
rs192911445 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936973 | GATTTTTGTATTTTT[A/G]GCAGAGATGAGGTTT | 4734 |
rs192935939 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864656 | CATTGCACTCCAGCC[C/T]GGACAACAAGAGTGA | 4734 |
rs192976239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975395 | TCAGTAAAGTTGCAG[A/G]ATACAAAATCAATAC | 4734 |
rs192977335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945646 | CAACATTCAAATTCA[A/G]GAAATACAGATAACA | 4734 |
rs192992605 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865177 | CATACCAGCCTGGGC[A/G]ATAGAGCAAGACTCT | 4734 |
rs192994737 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904093 | TTTGAACTCTGGAGG[C/T]GGAGGTCACAGAGAG | 4734 |
rs193002604 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848698 | TCTTAGAAGGTATCA[A/G]CATTTTAATAATAAC | 4734 |
rs193053200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931407 | TCATTTTAAAACTAT[A/G]TGCAAATTCTTTCAC | 4734 |
rs193057865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971453 | AACATGGTTAAACCC[C/T]GTCTCCACTAAAAAT | 4734 |
rs193071237 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888140 | TCCTAGCTACAGCAA[C/T]CAGGCAAGAAAAAGA | 4734 |
rs193075388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849402 | GCTAATTTTTGTATA[G/T]TTAATAGAGACGGGG | 4734 |
rs193095454 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976531 | AATGAGATATCATCT[C/G/T]ACCCCAGTTAAAATG | 4734 |
rs193134644 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961646 | CGGATAATTTTTTGT[A/G]TTTTTAGTAGAGACA | 4734 |
rs193143608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922135 | AGACATAAAAATGTT[C/T]ATCAATTTGTAAGAG | 4734 |
rs193159969 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917924 | TTAAGAGAGTGTTGT[A/G]GTAAGTAAAGAAGTC | 4734 |
rs193167620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845557 | TTGAGGCCTGTAATG[A/G]CATTGTCTCCCATCT | 4734 |
rs193209407 | snp | A/G | 0.00133537 | 0.025805 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830626 | TCATTTACTCTCTAC[A/G]AGGATCTCCAGGCAT | 4734 |
rs193247437 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957474 | TTTCCATCTATTCCT[A/G]GTTTGCAGAGAGTGT | 4734 |
rs193287466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980409 | CTAAACAGAAGATTG[A/G]GCGAACTGGGTGATC | 4734 |
rs193291324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901969 | TATAATAGGAACTAA[C/T]AGAGTTACTTCAACA | 4734 |
rs193295159 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940705 | GTGAAGAGGGTCGTT[C/T]TTTTTTGGTAGAGAT | 4734 |
rs199511074 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839582 | GGCTATTCAGCAGCA[A/C]AGGAAACAACACGGC | 4734 |
rs199512355 | snp | A/T | 0.000116054 | 0.00761668 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840691 | ATCTTCGTTACACAA[A/T]CCAGAGTTTGGATTT | 4734 |
rs199524276 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958134 | AAAAAAAAGATGACT[G/T]TCTTCTTTTATTCTA | 4734 |
rs199530416 | snp | A/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916131 | TCCTGGACAAAAGGA[A/T]CTGTACTTGTACTTC | 4734 |
rs199531649 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55850063 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCA | 4734 |
rs199535782 | snp | A/G | 0.00127742 | 0.0252405 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833109 | ATTAAAACAGCCTGA[A/G]TAAGATAAAAACATC | 4734 |
rs199539849 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957280 | TTTTTGACTGTGTGA[-/T]TTTTTTTTTCTTTGC | 4734 |
rs199632907 | in-del | -/C | 0.0138799 | 0.0821421 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911036 | CACCGCCTCCCACAT[-/C]CCCCAGGCTACCCTA | 4734 |
rs199644161 | snp | C/G/T | 0.000164905 | 0.00907884 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860764 | TTGCCATTCTCAGCA[C/G/T]CTGTTAGGTTGTCCC | 4734 |
rs199650621 | snp | A/C/T | 9.89587e-05 | 0.00703358 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860607 | AGCTTGAGCCACACA[A/C/T]ACTTTATTGCTATAG | 4734 |
rs199703832 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992856 | ATAAAGTATTTATAC[-/T]TTTTTGGCTTCACTT | 4734 |
rs199714618 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977748 | CTTGTTTTTTTTTTT[-/T]AATTTAAAAAGATTA | 4734 |
rs199718541 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865552 | ACTACTAAATAACAT[A/T]AAAAAAAAAAAGACC | 4734 |
rs199761730 | snp | C/T | 3.3716e-05 | 0.00410571 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847041 | GGGCACTGCCTTTAG[C/T]TGGAAATTTTGGAAA | 4734 |
rs199790562 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962205 | ACTTCAGTCTTTTTA[C/T]GCTTACTGTTTGCAT | 4734 |
rs199792098 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944146 | CTGGCTGGACAGTGG[A/G]TGCAGCCCACAGAGG | 4734 |
rs199800611 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865549 | AAAACTACTAAATAA[A/C]ATTAAAAAAAAAAAG | 4734 |
rs199802166 | in-del | -/C | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917208 | GTAACACAAGAACAA[-/C]AATCTTCTAACATTT | 4734 |
rs199802208 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880292 | TGAGACCCCGTCTCC[-/A]AAAAAAAAAGAATAA | 4734 |
rs199805881 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934697 | CTCTGTCTTACCTTT[A/G]TCCCACCCCCAGAGC | 4734 |
rs199840988 | snp | A/G | 0.208169 | 0.246476 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983499 | TTCTATTTACTCAAT[A/G]GGGTTCTATTGCCCC | 4734 |
rs199842511 | snp | A/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917476 | TTAATTTTTTTTTTT[A/T]AATGTGTGAATTCAA | 4734 |
rs199852397 | in-del | -/CGCG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983304 | GTGCGTGCGCGCGCG[-/CGCG]TGCGTGCATTTGATT | 4734 |
rs199857460 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966604 | TTAACTAAGACACAA[-/T]TTTTTTAAAAAATAT | 4734 |
rs199857470 | snp | C/T | 7.03309e-05 | 0.00592963 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869579 | TTTATAAAATCTCAC[C/T]TCTAATTCCTCAGCC | 4734 |
rs199861047 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866221 | CTTCTTTTTTTTTTT[-/T]AAATTTTTACCTCTT | 4734 |
rs199891346 | in-del | -/C | 0.0410537 | 0.137264 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979927 | ATTACTTTTTTTTTT[-/C]TGAGATGGAGTCTCG | 4734 |
rs199894826 | snp | A/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850684 | TCACTGGTGGAGGCT[A/T]GTGATTGAGGGCCTG | 4734 |
rs199902876 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967713 | AAGAAATATAAAAAA[A/C]CTTCATAGATAACAT | 4734 |
rs199915202 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935742 | GTCCCAGCTACTCGG[A/G]AGGCTGCGGCAGGAG | 4734 |
rs199950548 | snp | A/T | 0.00441178 | 0.0467592 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850496 | AACTATACATAAGAG[A/T]TGATTATTGTTGTTA | 4734 |
rs199985462 | snp | C/G/T | 0.000183013 | 0.00956426 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916785 | TCTGACAAAGGGTAA[C/G/T]TATTGCTTCTTCTGG | 4734 |
rs199993115 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955834 | TTTTTTTTTTTTTTT[-/G]AGGCAGGGTCTCGCT | 4734 |
rs200027398 | in-del | -/A | 0.104149 | 0.203046 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988875 | TTAACAGTTGCAGAA[-/A]TCTGTATGAGAAGAA | 4734 |
rs200055696 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834138 | TCTCCCAGTCCACAC[A/G]TAAGAAGCTACATAA | 4734 |
rs200090404 | in-del | -/C | 0.0360663 | 0.129354 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976642 | TTTTTTTTTTTTTTT[-/C]TTTTTGAGACGGAGG | 4734 |
rs200103497 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863980 | GGCAAGGCATTTTAT[A/C]AAGTCATAAAACAGC | 4734 |
rs200164901 | snp | A/T | 0.0721875 | 0.175735 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951595 | GTAAGGATCACTGTT[A/T]AAAAAAAAAAAAAAA | 4734 |
rs200188204 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957770 | AATGTGGCACATATA[C/T]ACCATGGAATACTAT | 4734 |
rs200224565 | snp | A/G | 1.66101e-05 | 0.0028818 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852546 | AAGTAGGCAAAAGCT[A/G]AAGTGAAGAATAACA | 4734 |
rs200243140 | snp | C/T | 0.000329603 | 0.0128333 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842099 | ACACCCATAATTCTC[C/T]GGTAAGAGTCTTCAA | 4734 |
rs200257962 | in-del | -/TATCAAGTGTTCT | 0.0178098 | 0.0926698 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940234 | TGTGAAGAGGGTACA[-/TATCAAGTGTTCT]TACCACAAAAAAGGG | 4734 |
rs200265653 | in-del | -/AAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978937 | CAAAAAAAAAAAAAA[-/AAC]AAGAACAGAAAACAC | 4734 |
rs200302173 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840516 | TGGGCGGATGAAAAA[A/G]CCTTGCAAAAAACCA | 4734 |
rs200302839 | snp | C/G | 0.0193698 | 0.0964867 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869581 | TATAAAATCTCACCT[C/G]TAATTCCTCAGCCTG | 4734 |
rs200334089 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883700 | ACACACACACAAACA[A/C]ACACACACACACACA | 4734 |
rs200353248 | snp | A/G | 0.000956953 | 0.0218532 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840547 | AATACATTTAGGATG[A/G]TTACCAAGTGAAAGA | 4734 |
rs200355988 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900069 | ACTTTTTTTTTTTTT[-/T]AAACTAGTTTGGCTC | 4734 |
rs200363177 | snp | A/G/T | 0.000427328 | 0.0146112 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993525 | CCTCGTCCTCCAGGA[A/G/T]CCCGAACACCTCCAC | 4734 |
rs200370285 | snp | C/T | 0.000280262 | 0.0118344 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915396 | AACTGAGATGGTCCC[C/T]CTTTAGAACAATTGT | 4734 |
rs200377508 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957574 | TGTGGCGATTCCTCA[A/G]GGATCTAGAACTAGA | 4734 |
rs200384528 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911081 | TGGACTATTTACAGT[G/T]GAGATTCTTTCACAT | 4734 |
rs200417584 | snp | C/T | 0.000511252 | 0.0159801 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860413 | GCATCTTACTGAGCT[C/T]GATGCTGGCTGGCTC | 4734 |
rs200464629 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837335 | CTCAGGAGGCTGAGG[C/T]AGGAGAATTGCTTGA | 4734 |
rs200475260 | in-del | -/CGCA | 0.0189856 | 0.0955633 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983306 | GTGTGTGTGCGTGCG[-/CGCA]CGCGCGTGCGTGCAT | 4734 |
rs200500843 | snp | A/G | 0.0039919 | 0.0444974 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951606 | TGTTAAAAAAAAAAA[A/G]AAAAAGAAAGAAAAA | 4734 |
rs200514829 | snp | C/G | 6.59239e-05 | 0.00574087 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860529 | GTGATGGGAAGGCCT[C/G]GTTGCTATACATGGT | 4734 |
rs200519542 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870547 | TTTTTTTTTTTTTTT[G/T]TTTTGAGACAGCATC | 4734 |
rs200569269 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852303 | TCCATCTCAAAAAAA[A/T]AAAAAAAAAAAAGAA | 4734 |
rs200591357 | in-del | -/AA | 0.497211 | 0.037236 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832182 | TCCACCCCTATCTTG[-/AA]AAAAAAAAAAAAAAA | 4734 |
rs200608517 | snp | G/T | 3.2975e-05 | 0.00406035 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915506 | GTTCATCTGTGAATG[G/T]GGTCTTTCCAATTCT | 4734 |
rs200649067 | snp | A/G | 0.00060945 | 0.0174457 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848436 | CTTTTTATATCTGAA[A/G]GGAAGAAAAAGAAAA | 4734 |
rs200653183 | snp | A/G | 9.88875e-05 | 0.00703093 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834080 | ATTTGCACTGTAGCC[A/G]TTTTTATACTTTGTA | 4734 |
rs200667839 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945507 | CTCCAAGAAATATGG[C/G]ACTATGTGAAAAGAC | 4734 |
rs200669435 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874979 | ACTCCGCTCAAAAAG[-/A]AAAAAAAAAAGGAAA | 4734 |
rs200691419 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949566 | CAAATGTCCATCAAT[A/G]ATAGACTGGATTAAG | 4734 |
rs200711137 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983497 | GGTTCTATTTACTCA[A/G]TGGGGTTCTATTGCC | 4734 |
rs200723498 | snp | C/G | 3.30715e-05 | 0.00406628 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862925 | TACTGAGGGGTTGGT[C/G]TTTTCCACTGTGTTC | 4734 |
rs200727276 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853260 | AGTACTTCACTTGGG[A/G]AAAAAAACACTAGAA | 4734 |
rs200737525 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924715 | CTAAGAAAAACACAA[C/T]CTTTATTTAAAAACA | 4734 |
rs200765053 | in-del | -/A | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917835 | ATTAGAAAAAAAAAA[-/A]CTATACCCCAAGATA | 4734 |
rs200777260 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872372 | AAGGTGTAATGAAGA[C/G]ATAAAAAATTTAATA | 4734 |
rs200788423 | in-del | -/TGTGTGTG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967441 | TGAACATAACTATGC[-/TGTGTGTG]TGTGTGTGTGTGTGT | 4734 |
rs200791863 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55915058 | AAATCACTTAGGAAG[A/G]TTTTTAAAAATATAC | 4734 |
rs200797359 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865548 | CAAAACTACTAAATA[A/C]CATTAAAAAAAAAAA | 4734 |
rs200812282 | snp | A/C | 0.000634242 | 0.0177966 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830045 | AGACACTGACAAAGC[A/C]AGTACCACCACAGCA | 4734 |
rs200826776 | snp | A/C | 1.65231e-05 | 0.00287424 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848917 | AAATAAAGAACAATA[A/C]ACACAAATTTTAAAA | 4734 |
rs200830834 | snp | C/T | 0.343254 | 0.231956 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903867 | ATATATATATATATA[C/T]ACACACATTGGCTGG | 4734 |
rs200832080 | in-del | -/C | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889469 | GAAATAAGCAAGGCA[-/C]CAGAAAGACAAACTT | 4734 |
rs200846676 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965490 | TAGGCAGTGACTGTG[A/G]TCTCTGTTCAGATCT | 4734 |
rs200853618 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911079 | ACTGGACTATTTACA[G/T]TGGAGATTCTTTCAC | 4734 |
rs200856171 | snp | A/G | 0.000889489 | 0.0210702 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830589 | GGTCCATTTGAACCT[A/G]TAAGGAAGAATTTAT | 4734 |
rs200891809 | in-del | -/GTGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964693 | TGAATTTTGCTGCTG[-/GTGT]GTGTGTGTGTGTGTG | 4734 |
rs200895510 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906395 | CCCAAATGTCCATCA[A/G]TGATAGACTGGATTA | 4734 |
rs200900512 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848815 | ACTTACAGGTAAAGG[C/T]CCTAGATCATTGGAA | 4734 |
rs200912483 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952998 | ATTCTTTTTTTTTTT[C/T]TTTTTTTTTGAGACA | 4734 |
rs200943726 | in-del | -/ATA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872275 | ATAATAATAATAATA[-/ATA]TTTAGAAGTAACTTA | 4734 |
rs200979318 | snp | C/T | 0.000132758 | 0.00814625 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860399 | AACAAAATCTAAGAG[C/T]ATCTTACTGAGCTCG | 4734 |
rs200987917 | in-del | -/TC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983504 | TTTACTCAATGGGGT[-/TC]TATTGCCCCACTCTT | 4734 |
rs200998083 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55987427 | TGTTGTAGGTTGCCT[C/G]TTCACTCTGATGGTA | 4734 |
rs201001664 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966373 | ATACTTTCCACAACA[A/G]TTTACTAATACTATT | 4734 |
rs201022349 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988485 | ATAATAAAAAAAAAA[A/T]TTAAAAAAAAAAAAA | 4734 |
rs201023183 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865938 | GGGGAATTTCTCTCT[C/T]TCTTCTCTCTCTCAA | 4734 |
rs201050473 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955815 | AGGATCTATACTACA[G/T]TTTTTTTTTTTTTTT | 4734 |
rs201051306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856218 | AAAAAACAAGACAAC[A/G]GAAGAATACCTTGAT | 4734 |
rs201059295 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870544 | CTTTTTTTTTTTTTT[G/T]TTGTTTTGAGACAGC | 4734 |
rs201063976 | in-del | -/G | 0.0162398 | 0.0886349 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922818 | GGTTTCAAAGATTTT[-/G]GTAATGTTCTAGTTC | 4734 |
rs201078950 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55833503 | CTCTACTAAAAATAC[-/A]AAAAAAAAATAACTA | 4734 |
rs201080792 | snp | C/G | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917205 | TGAGTAACACAAGAA[C/G]AACAATCTTCTAACA | 4734 |
rs201091245 | snp | C/T | 0.00149456 | 0.0272956 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55834235 | GTCTTACCTCTAGTT[C/T]ATTTTCATCAAAAAT | 4734 |
rs201091807 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988488 | ATAAAAAAAAAAATT[A/T]AAAAAAAAAAAAAAA | 4734 |
rs201093932 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963138 | CACTCTTTTTTATTT[-/A]TTTTTTTTTTTGAGA | 4734 |
rs201096724 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869858 | TAGAGAAAAGGCAAA[A/C]ATATATAAATAAATA | 4734 |
rs201100393 | snp | G/T | 0.208169 | 0.246476 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983502 | TATTTACTCAATGGG[G/T]TTCTATTGCCCCACT | 4734 |
rs201109651 | in-del | -/AATAAATAAATAAATA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892267 | GCAAAACTCCAACTC[-/AATAAATAAATAAATA]AATAAATAAATAAAT | 4734 |
rs201121993 | in-del | -/ATATATATAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852691 | TTGCCTTTTCTAGAA[-/ATATATATAT]ATATATATATATATA | 4734 |
rs201127147 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856607 | ATTCTCCATGCTGCA[C/T]GCTGCAGGCTCAGAG | 4734 |
rs201132661 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843623 | GAAGGTTAGCTCTAA[-/G]GGAAAAAAAATCAAT | 4734 |
rs201144694 | in-del | -/T | 0.164219 | 0.234823 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955993 | CTAATTTTTCAAAAA[-/T]TTTTTTTGTAGAGAC | 4734 |
rs201147279 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858311 | TCAATATGGTTTATT[C/T]TTTTTTTTTTCTTGA | 4734 |
rs201155304 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983496 | GGTTCTATTTACTCA[-/G]ATGGGGTTCTATTGC | 4734 |
rs201162493 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930117 | GGCAAATTATGGCTT[G/T]TGTGCTAAATCCAGC | 4734 |
rs201172446 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964797 | AAATTTGATTTCCAA[C/T]GTGGGAATATTGAAA | 4734 |
rs201215909 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827787 | TCTTAGAAGTCACTT[A/G]ACTTTTAAATGATTC | 4734 |
rs201231776 | snp | A/C/G | 0.00284592 | 0.037617 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838219 | ATATGTTATTTTAGC[A/C/G]AGAAAAATTTAAAAA | 4734 |
rs201250020 | snp | C/G | 0.000135093 | 0.00821754 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850767 | TAATGAAATCATATT[C/G]TAATATTTTATAGAG | 4734 |
rs201283622 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852087 | GATCACCTGAGGTCA[C/G]GAGTTTCAGATCAGC | 4734 |
rs201295772 | snp | C/T | 0.000181865 | 0.00953411 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55846988 | TTCTTCAACTTTCTT[C/T]GGAAGAACTCATACT | 4734 |
rs201328988 | snp | A/C/T | 6.60638e-05 | 0.00574703 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840566 | CCAAGTGAAAGAAAA[A/C/T]AGGTAATTATATTGT | 4734 |
rs201340191 | snp | A/T | 0.00199801 | 0.0315438 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848497 | TACAAAAAATAACAT[A/T]ATGAAAAATCGCACT | 4734 |
rs201363710 | in-del | -/AT/TA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979069 | AAATATATATATATA[-/AT/TA]CCCCATTTTTACTTA | 4734 |
rs201375826 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834533 | CGCAGTGGCTCATTC[C/T]GTAATCCCAGCACTT | 4734 |
rs201395884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924597 | CCCCTGGCTGCTCCA[C/G]TGAAATGTACCCTTA | 4734 |
rs201400016 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963149 | ATTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC | 4734 |
rs201402509 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954541 | TGCCTTTTTTTTTTT[-/T]GAGATGGAGTTTCAC | 4734 |
rs201413155 | snp | A/C | 0.00199792 | 0.0315431 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915540 | TTGATATTTATTTGA[A/C]AATCTACATTTTGGG | 4734 |
rs201436638 | snp | A/G | 0.324619 | 0.238604 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967474 | TGTGTGTGTGTGTGT[A/G]TATGTGTGTGTATAC | 4734 |
rs201455596 | in-del | -/A | 0.419456 | 0.183806 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868057 | CAAGACTCTGACTCC[-/A]AAAAAAAAAAAAAAA | 4734 |
rs201458222 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865547 | CCAAAACTACTAAAT[A/T]ACATTAAAAAAAAAA | 4734 |
rs201471317 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957638 | TATATACCCAAAGGA[G/T]TATAAATCATGCTGC | 4734 |
rs201495371 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939136 | AACAAACAAAAAAAC[A/C]CACCACCAACAATAA | 4734 |
rs201497786 | snp | A/C | 0.00299769 | 0.0385987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833154 | ACTGGGAAAGAGGTA[A/C]ACAAATTATCCTGAA | 4734 |
rs201509966 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837433 | ACTCACTCCGCGCTC[-/AA]AAAAAAAAAAAAAAG | 4734 |
rs201547754 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933290 | CAACCCAAATGTCCA[A/T]CAATGATAGACTGGA | 4734 |
rs201551324 | snp | A/T | 0.00199797 | 0.0315435 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829983 | ATTCATAAGGTGGCA[A/T]GTCCAGGCGATTAAA | 4734 |
rs201569707 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881227 | GCTCACTGCAACCTC[C/T]ACCTCCCGGGTTCCG | 4734 |
rs201583414 | in-del | -/AAT | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878319 | TCAATAATATGAATC[-/AAT]AATAAACAGAAAAAC | 4734 |
rs201589405 | snp | G/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841945 | TTACGTAGCAGAATA[G/T]TCAAACAACCCATAA | 4734 |
rs201616822 | in-del | -/TGTGTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967471 | GTGTGTGTGTGTGTG[-/TGTGTA]TGTGTGTGTATACAA | 4734 |
rs201653409 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875107 | AAATAAAAAAAAAAA[-/A]CCCAGTAGGAAGAGA | 4734 |
rs201655397 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980431 | TGGGTGATCCAAGGG[A/G]AAAAAAAATGCTATA | 4734 |
rs201668319 | snp | C/T | 0.000379309 | 0.0137663 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833039 | TCCATTCATAGGCAC[C/T]CGAGATGTGCCAGTG | 4734 |
rs201682687 | snp | C/T | 1.6543e-05 | 0.00287597 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848548 | AGAAGATTCTTCCAT[C/T]TGTGTGAGTTCTCTC | 4734 |
rs201695400 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865550 | AAACTACTAAATAAC[A/T]TTAAAAAAAAAAAGA | 4734 |
rs201712441 | snp | A/G | 6.60818e-05 | 0.00574774 | stop-gained, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915685 | ATGTAGCTGCTTTTC[A/G]TTGGGTGAAATGCAC | 4734 |
rs201769294 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829939 | GTTTTCAATTGCCAT[C/G]TGAAGTTTATCCCAT | 4734 |
rs201805356 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910017 | TGAATTTCCTTTTCA[C/G]TCATCATACTTGCTT | 4734 |
rs201805609 | snp | A/T | 0.350109 | 0.229081 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963135 | CTGGCACTCTTTTTT[A/T]TTTTTTTTTTTTTTG | 4734 |
rs201822413 | snp | A/G | 0.00199795 | 0.0315433 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55846990 | CTTCAACTTTCTTCG[A/G]AAGAACTCATACTTT | 4734 |
rs201829007 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911080 | CTGGACTATTTACAG[G/T]GGAGATTCTTTCACA | 4734 |
rs201848122 | snp | A/G | 0.00157106 | 0.0279833 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852556 | AAGCTAAAGTGAAGA[A/G]TAACAGAAGAATTAA | 4734 |
rs201849594 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980076 | GCCTCCCAAGTAGCT[G/T]GGATTACAGGCGCGT | 4734 |
rs201852150 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935640 | ATCATGAGGTCAGGA[C/G]ATCGAGACCATCCTG | 4734 |
rs201865264 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845526 | ATTGCTTTTATCATG[G/T]TTTTTTTTTTGTATT | 4734 |
rs201876442 | in-del | -/AC | 0.499996 | 0.00139776 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903839 | AAAAAAAAAAAAAAA[-/AC]ACACACATATATATA | 4734 |
rs201880688 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952999 | TTCTTTTTTTTTTTC[C/T]TTTTTTTTGAGACAG | 4734 |
rs201885262 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965687 | ATGTATGTATGTATG[C/T]ATGCATGCATGTTTG | 4734 |
rs201886052 | snp | A/T | 0.208169 | 0.246476 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983498 | GTTCTATTTACTCAA[A/T]GGGGTTCTATTGCCC | 4734 |
rs201896190 | in-del | -/C | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975628 | AGATAGAAGACGACA[-/C]CAAAAAAAAAACAAA | 4734 |
rs201906568 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872918 | TCCTGCACCCTGTTT[-/A]AAAAAAAAAAAAAAA | 4734 |
rs201914804 | in-del | -/AG | 0.136847 | 0.222927 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847863 | TTTTGCATTTTTAGT[-/AG]AGACAGGGTTTCACC | 4734 |
rs201917673 | snp | C/T | 1.65274e-05 | 0.00287462 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860803 | AAGTATAAAAAGCCA[C/T]CATCCATGTCTTAAG | 4734 |
rs201950392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871304 | TGGAAAAGAAGCCTC[A/G]AGGTTTTGACTTAAT | 4734 |
rs201967452 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911527 | TCACATATTAGACTG[-/A]AAAAAAATTTTTTTT | 4734 |
rs201996136 | snp | A/C/G | 0.00182925 | 0.0301881 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916022 | AGTTGAAGGACTCCT[A/C/G]GGAAAAATGACTAAG | 4734 |
rs201998900 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971625 | GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAGAC | 4734 |
rs201999631 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939119 | TCGAAAACAACAACA[A/C]CAACAAACAAAAAAA | 4734 |
rs202007394 | in-del | -/ACAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883693 | AACACACACACACAC[-/ACAA]ACACACACACACACA | 4734 |
rs202024771 | snp | G/T | 3.84897e-05 | 0.00438672 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55834281 | TGGTATTAGTTCAAA[G/T]AATCCCTAGAAAAAA | 4734 |
rs202028119 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983507 | ACTCAATGGGGTTCT[A/T]TTGCCCCACTCTTCA | 4734 |
rs202038700 | snp | C/G | 0.000108126 | 0.00735195 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869618 | ATTATCATCTTCTGA[C/G]CCACTGGTTTTAGGT | 4734 |
rs202048175 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932893 | TCTCAAAAGAAGACA[-/TT]TATGCAGCCAAAAGA | 4734 |
rs202073134 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963140 | CTCTTTTTTATTTTT[-/A]TTTTTTTTTGAGACA | 4734 |
rs202084343 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882558 | TGTGGGCTAAAGCAC[-/T]TCTGGGGTTCTAAAT | 4734 |
rs202095078 | snp | C/T | 9.88989e-05 | 0.00703134 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852451 | CTTTGTCCAAGTAGT[C/T]GTTCTGGAATTGTGA | 4734 |
rs202122804 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971362 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 4734 |
rs202142120 | snp | A/G | 1.70316e-05 | 0.00291813 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841887 | ACTCTTACTTTTAAA[A/G]CAGTGATTTTTCTTT | 4734 |
rs202144074 | in-del | -/T | 0.0539704 | 0.155153 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889709 | TTTTGTTTTGTTTTG[-/T]TTTTTTTTGGAGACA | 4734 |
rs202155849 | in-del | -/AAAT | 0.095934 | 0.196885 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888155 | TCAGGCAAGAAAAAG[-/AAAT]AAGGGGCATCCAAAT | 4734 |
rs202189245 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881138 | CAGTAAGTTTCTTTT[C/T]TTTTCTTTTTTTTTT | 4734 |
rs202228155 | snp | A/T | 0.0696718 | 0.173152 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869862 | GAAAAGGCAAACATA[A/T]ATAAATAAATAAATA | 4734 |
rs202233875 | in-del | -/AAAC | 0.0138799 | 0.0821421 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859693 | GAGTGAGATGTCTCA[-/AAAC]AAACAAACAAACAAA | 4734 |
rs202235439 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957732 | CAACCCAAATGTCCA[A/T]CAATGATAGACTGGA | 4734 |
rs202245255 | in-del | -/TT | 0.427727 | 0.175821 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983614 | AATTTTTAGATATAC[-/TT]TTTTTTTTTTTTTTG | 4734 |
rs367566868 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972889 | AAAAGAGACAAAAAA[-/A]GGTTATTACACAATG | 4734 |
rs367581365 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55848179 | CCCTCACTGCTATTG[C/T]GTAGGGTAAGGATAA | 4734 |
rs367635737 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904290 | CTCCTTGTTCTATTT[A/C]CATACACCTTTTATT | 4734 |
rs367643447 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991465 | TCCCTCTCTATCCCT[C/G]GTGCCTAGCACAATG | 4734 |
rs367649746 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979223 | AATAATTATATTAAT[A/T]GAAAAAATAAGAATG | 4734 |
rs367697468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939495 | TGCTTGTATTAGTCC[A/G]TTTTCACACTATGAT | 4734 |
rs367702107 | snp | A/G | 2.20855e-05 | 0.00332299 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834307 | AAAAAGATGTATTTA[A/G]AAACTTGATGGGCAG | 4734 |
rs367779463 | in-del | -/TATTATTATTAT | 0.260504 | 0.249779 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961465 | CAACTAAGTTTGTGG[-/TATTATTATTAT]TATTATTATTATTAT | 4734 |
rs367818000 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866984 | TAATCAAGTCAAAGA[A/G]GGTCAGAAAGAAAGC | 4734 |
rs367834563 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924743 | ACAAGTAAACATCAA[C/T]CCACAGATACTCAGA | 4734 |
rs367845994 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971609 | CAGCCTGGGCAACAC[A/G]GTGAGACTCTGTCTC | 4734 |
rs367855430 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947008 | GACACATTTAAAGCA[C/G]TGTGTAGAGGGAAAT | 4734 |
rs367875084 | snp | C/T | 6.59837e-05 | 0.00574348 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916300 | TAGTATATGAACCTC[C/T]ACTTGTGATACTTGC | 4734 |
rs367880527 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973835 | AAAGTAGAAAAACTT[A/C]AAAAAAAAAAACAAC | 4734 |
rs367891617 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916079 | TGTGTTCCTGCTCAC[C/T]GGCAATTTCATAATC | 4734 |
rs367899129 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949306 | TCAGGAAACAACAGG[A/T]GCTGGAGAGGATGTG | 4734 |
rs367914118 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935227 | ATTATCTATAACAAC[A/G]TATAAACCTGCCTCT | 4734 |
rs367919667 | snp | A/G | 0.000175985 | 0.00937877 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55951569 | ATTGGGTCATATAAC[A/G]TCACTCTCACGTAAG | 4734 |
rs367941564 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902767 | AGAAAACAAAGTATG[G/T]GTTAATCAATAAAAG | 4734 |
rs367947745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881900 | GATATTTACCAACAT[G/T]CCTGGCCTCTACCCA | 4734 |
rs367987874 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976866 | TCTCGATCTCCTGAC[C/T]TCCTGATCCACCCGC | 4734 |
rs368007709 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903418 | AATTTCTGGGCCTTT[C/T]TACTTATTTCTAATA | 4734 |
rs368043458 | in-del | -/AACT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830865 | CCACCACGCCTGGCT[-/AACT]GTTAAAAAAATTCAT | 4734 |
rs368093506 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841773 | AGACGGGGTTTCACC[A/G]TGTTAGCTAGGATGG | 4734 |
rs368106742 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876977 | TTCAAAGTGCTGGGA[C/T]TACAGGTGTGAGCCA | 4734 |
rs368121909 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963135 | CTGGCACTCTTTTTT[-/A]TTTTTTTTTTTTTTG | 4734 |
rs368148733 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953955 | TCAATCTCTTGACCT[C/T]GTGACCCTCCTGCCT | 4734 |
rs368172324 | snp | C/T | 0.000477598 | 0.0154457 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850600 | CCATTTGGTGCATGC[C/T]GGACTTCCCAGCCTT | 4734 |
rs368172394 | snp | C/T | 0.000237244 | 0.0108888 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915335 | GTTGCTGTCTCTTGA[C/T]AAATTATCCACTTTA | 4734 |
rs368192257 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982139 | TGTTGCTGAAACAAT[C/G]TGCAGCAACTAGAAC | 4734 |
rs368218471 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988390 | GATGACACGTTAGTG[A/G]GTGCAGCACACCAGC | 4734 |
rs368227544 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880623 | CAAAATGAGGGAGTG[C/T]GCCGTGATATGGAAG | 4734 |
rs368231362 | snp | A/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994758 | GGTTTGTTACGTAAG[A/T]TTTTTCTCGTACTTG | 4734 |
rs368320427 | snp | A/C | 1.64781e-05 | 0.00287033 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848325 | CTGCTCTTGAAGAGA[A/C]AGGTGAGCGGACAGT | 4734 |
rs368324825 | snp | C/T | 0.000153988 | 0.00877327 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916147 | CTGTACTTGTACTTC[C/T]TGAAAAAATTTCACA | 4734 |
rs368393793 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965469 | AGTCTCCCAAACCCC[A/G]TTTCTTAGGCAGTGA | 4734 |
rs368412958 | snp | A/T | 1.80781e-05 | 0.00300645 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916878 | AAAGTCATAACAAAG[A/T]TCTCTGTCCGTAGAC | 4734 |
rs368417413 | snp | C/T | 1.65091e-05 | 0.00287303 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915374 | TCCAGATGCAAACTT[C/T]ATGAGTAACTGAGAT | 4734 |
rs368466032 | in-del | -/AGT | 0.00280111 | 0.037319 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980603 | AGAAATTAAAGAAAC[-/AGT]AGATTCAACACAGAA | 4734 |
rs368490718 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867782 | CTTTCCTGGCTGGGT[G/T]CCGTGGCTCACGCCT | 4734 |
rs368497552 | snp | C/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917208 | GTAACACAAGAACAA[C/T]AATCTTCTAACATTT | 4734 |
rs368539991 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882358 | GAGAATCCGTGCACT[G/T]AGGGTTGGGAGAGCT | 4734 |
rs368588677 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845667 | CTTCTATTCCTCCAG[C/T]GTATTCTCATTAACA | 4734 |
rs368605449 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876121 | ATAAGTGCTGAAATG[A/G]AAAATGTACCAAGAA | 4734 |
rs368619204 | in-del | -/AGC | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979262 | TATGACAACTGTAAA[-/AGC]ACACACAGAAAGATT | 4734 |
rs368620459 | snp | A/G | 0.000173985 | 0.00932535 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55966515 | AGGCCTATTCCGGCT[A/G]TAACTCTTACTCTCA | 4734 |
rs368656606 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854099 | GAGGTTGCAGTGAGC[C/G]GAGATCGCCTGGGCA | 4734 |
rs368711330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844540 | TGGAATCTGGTCCTG[C/T]GTTATTGACTCCACC | 4734 |
rs368711779 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949437 | ACCATTTGACCCAGC[A/C]ATCCCATTACTGGGT | 4734 |
rs368712798 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892315 | ATAAATAAATAAATA[A/T]ATAAATAATAAATAT | 4734 |
rs368738664 | in-del | -/GTCT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837018 | GTGCTCTGACAATCT[-/GTCT]ACCAATTGGAAAAAT | 4734 |
rs368765924 | snp | A/G | 1.65149e-05 | 0.00287353 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848495 | ATTACAAAAAATAAC[A/G]TAATGAAAAATCGCA | 4734 |
rs368788676 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944519 | CCCACCTCAGCTCAT[C/G]AAGGCCTACTGCCTA | 4734 |
rs368789363 | snp | C/T | 2.57676e-05 | 0.00358931 | utr-variant-5-prime, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55924667 | GTTTTCGTCAAACAC[C/T]TCAAAAAGAAGCCGG | 4734 |
rs368801081 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892302 | AATAAATAAATAAAT[-/A]AATAAATAAATAAAT | 4734 |
rs368808867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957735 | CCCAAATGTCCATCA[A/G]TGATAGACTGGATTA | 4734 |
rs368840688 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848361 | CAGAGCACACTGGCA[A/G]AGAGACTTACTGGTC | 4734 |
rs368905903 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904785 | CTTCTAGAATATACA[A/C]AAGGTATGTCAGACC | 4734 |
rs368913229 | in-del | -/AA | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921878 | AGTCACGCAAATACT[-/AA]AGTTACTGGCAAAAT | 4734 |
rs368941612 | snp | A/C | 1.64947e-05 | 0.00287177 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915578 | CAAACATGCAGATGT[A/C]CTATGCATGAGCTTA | 4734 |
rs368960297 | snp | G/T | 1.65113e-05 | 0.00287322 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916243 | AAAAAGTATCATCAC[G/T]TGGTGGAAAAGTATA | 4734 |
rs368965709 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947641 | TGGGATGCAAGGCTG[C/G]TTCAACATACGCAAT | 4734 |
rs369022480 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909050 | GTAATGTATTTTTCT[A/G]CTAAGGTAATCAAAA | 4734 |
rs369028368 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926052 | TATACATATACAGTA[C/T]GTAAAATACATATAC | 4734 |
rs369039492 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982630 | AGCATTCTGGAATGA[C/T]GGGAATATTCTGTAT | 4734 |
rs369074443 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961185 | GACACTTAGGCATGA[A/G]GGCACTTGCCTAAGA | 4734 |
rs369077103 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869021 | TCTGCCTCCTACTTG[C/G]TTACTCCAGATGCAT | 4734 |
rs369081212 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940297 | GGAGGTGATGGATAT[A/G]TTTATGACTTTGATT | 4734 |
rs369102365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842471 | GGCTTACTGCAGCCT[C/T]GACCTCATGGGCTCA | 4734 |
rs369108664 | snp | A/G | 6.66967e-05 | 0.00577442 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841911 | TTTCTTTTTCTGCCG[A/G]TAATCATTGTAAAGG | 4734 |
rs369110317 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949695 | TCTCAGCAAACTGTC[C/G]CAGGGACAAAAAACC | 4734 |
rs369164881 | in-del | -/ATATATATATATATATATATATATATATATATA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55840010 | AAAAAATATATATAT[lengthTooLong]ACATTCATCATAAAA | 4734 |
rs369165660 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55860055 | AAAATCACCTAACAG[A/G]AGCCCAAATCCCTGA | 4734 |
rs369171296 | snp | A/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994840 | GCGGTGAATCACCTT[A/T]GGTCAGGAGTTCGAG | 4734 |
rs369181075 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863070 | GTTGGTCCAAAACAA[C/T]CCAGCCAGGCTGAAA | 4734 |
rs369182977 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872071 | TGGCTTTGTGCACGT[C/T]GAGTTAGGTAATGGT | 4734 |
rs369201753 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904463 | GTGCACCAACACGCC[C/T]GGCTAATTTTTCTGT | 4734 |
rs369225348 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879092 | GACTCCCAAAGTGCT[C/G]GGATTATAGGCATGA | 4734 |
rs369285459 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953416 | GCACCTGGCTCCAGA[A/G]GCCATACTCTTCTTT | 4734 |
rs369292477 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872798 | GGACTATGCACATGT[-/G]CTGCAGGCTGGCTTG | 4734 |
rs369299652 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849647 | CAGAATGTTAAAAAA[C/G]AGAACAAAATTAAAT | 4734 |
rs369309250 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889433 | CAACAACTGGATAAA[A/T]CTGAAGGTCATTATG | 4734 |
rs369312559 | snp | C/T | 0.000187126 | 0.00967098 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966586 | ATTTTCATGTACTTA[C/T]AAGTTAACTAAGACA | 4734 |
rs369316566 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925972 | ACAGTATGTATATGT[A/G]AAAATACATATACAT | 4734 |
rs369327462 | snp | A/G | 0.000148342 | 0.00861099 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852452 | TTTGTCCAAGTAGTC[A/G]TTCTGGAATTGTGAT | 4734 |
rs369333047 | snp | A/C/G | 7.79849e-05 | 0.00624391 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924748 | TAAACATCAACCCAC[A/C/G]GATACTCAGAAATAA | 4734 |
rs369359614 | snp | C/T | 3.3048e-05 | 0.00406484 | splice-donor-variant | NEDD4 | GRCh38.p7 | 15:55841933 | TTGTAAAGGTACTTA[C/T]GTAGCAGAATATTCA | 4734 |
rs369365267 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922324 | TCTATAGAGATATAC[C/T]ATTTTTACAAATTAA | 4734 |
rs369378356 | snp | C/T | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860728 | CTGGTGGTAAATGCA[C/T]GTTGTGCTTGCAGTT | 4734 |
rs369408197 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846333 | TGCAGGCAAAGGAGG[A/T]CAGGATGAGCAAGTA | 4734 |
rs369451357 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868806 | CCTCAACGAGCAGGT[A/G]TTTTTTTGACCCCTT | 4734 |
rs369468383 | snp | A/C | 1.64841e-05 | 0.00287085 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916474 | TACTGTAAATACCAT[A/C]CTTCAAGATACAAGT | 4734 |
rs369474221 | snp | A/C/G | 0.000172756 | 0.00929256 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993500 | GCCCCGCAGCCCCGC[A/C/G]GTCCCCGCACCTCGT | 4734 |
rs369523947 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862864 | TCAAAATGAAAATTC[A/G]TAGTTAAAGTGTTTC | 4734 |
rs369530203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968639 | AATACATGAAAAGAT[A/C]ATCTCACCGGTCAGC | 4734 |
rs369558901 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974375 | CCTACTCAAACTATT[A/T]CAAAAAATAGAGGAG | 4734 |
rs369568485 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986847 | TGATCCACCCGTCTC[A/G]GCCTCCCAAAGTGCT | 4734 |
rs369601726 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957701 | GGCACTATTCACAAT[A/C]GCAAAGACTTGGAAC | 4734 |
rs369618436 | in-del | -/TTGAAAAAAGGTTAGCC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945262 | AGGAACCTAAAAACC[-/TTGAAAAAAGGTTAGCC]CAATGGCTAACTAGA | 4734 |
rs369653649 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978467 | AGATTGTAATCTCTC[A/C]CATGTTTGAAAAGGA | 4734 |
rs369688513 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913277 | TGGGAAATATTTTGG[C/G]AGCTGTTTATTTATA | 4734 |
rs369712873 | snp | A/C/G | 0.0360663 | 0.129354 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979479 | CTGCCTCAGCCTCCC[A/C/G]AGTAGCTGGGACTAC | 4734 |
rs369721795 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846007 | GGCCAGGCTGGTCGT[A/G]AACTCCTGACCTCAA | 4734 |
rs369731702 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949515 | ACATATGTTTATTGC[A/G]GCACTATTCACAATA | 4734 |
rs369741044 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983613 | AATTTTTAGATATAC[-/T]TTTTTTTTTTTTTTT | 4734 |
rs369744901 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963801 | GGACTTTAAGATATC[C/T]TACAGCACAGGTCTG | 4734 |
rs369748295 | snp | C/T | 0.000106136 | 0.00728402 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842184 | AATCCAGAGGAGAGA[C/T]GTACTGTTTAAATCA | 4734 |
rs369749022 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855433 | ATGAAGGCAGCAGGA[A/G]GCTTCTGTTGGGGGA | 4734 |
rs369753821 | snp | C/G | 8.24287e-05 | 0.00641931 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830608 | GGAAGAATTTATTTG[C/G]TTTCATTTACTCTCT | 4734 |
rs369757766 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926964 | ACCTGTAACCCCAGC[C/T]AGTTGGGAGGCTGAG | 4734 |
rs369767716 | in-del | CTA/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836538 | CACCAGGCTAATTTT[CTA/TT]TTTTGAGACGGAGTC | 4734 |
rs369773552 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828264 | AACCAAGAACCAGAG[G/T]TACTTTTTACAGTTC | 4734 |
rs369789188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836548 | ATTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 4734 |
rs369857011 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933405 | GAAGCTAGAAACCAT[C/G]ATTCTGAGCAAACTA | 4734 |
rs369882104 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929368 | AGTTTTGGGAGTACA[C/T]GTACAAGTTGGTTCT | 4734 |
rs369913873 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854959 | TAGAGGACATTATAA[C/T]GTGCAGAGGGAAAAA | 4734 |
rs369974971 | snp | A/C/G | 0.000223269 | 0.0105634 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838098 | AATACATACTAATAA[A/C/G]ATACTTACTAAATAT | 4734 |
rs369984184 | snp | A/G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55850080 | TGGGATTACAGGCAT[A/G/T]AGCCACTGCACCCGG | 4734 |
rs370009623 | snp | A/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850636 | AGGAATCCTTGCTCA[A/T]TTTCAGATGGCTGGG | 4734 |
rs370018498 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969186 | TGCTGCCCTGTCGCA[A/G]TGGAAGGCAACAGAG | 4734 |
rs370020188 | snp | A/T | 1.65089e-05 | 0.00287301 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848483 | CACATAAAATTTATT[A/T]CAAAAAATAACATAA | 4734 |
rs370079903 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993610 | CCCAGGGCAGGCAAC[A/T]GTGGAGGAGGAGGAG | 4734 |
rs370100375 | snp | C/T | 9.88761e-05 | 0.00703052 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834118 | TCCAGTCATTCACAT[C/T]AACATCTCCCAGTCC | 4734 |
rs370103713 | snp | C/T | 0.000168591 | 0.00917972 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55951555 | TAAGAACTCCATTCA[C/T]TGGGTCATATAACGT | 4734 |
rs370123066 | snp | C/T | 3.29565e-05 | 0.00405921 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916536 | TTGCTAGACTGAAGA[C/T]ATCCACTGTACCTTG | 4734 |
rs370132620 | snp | A/G | 0.000117215 | 0.00765464 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860382 | TAAACTACTGAAGCC[A/G]TAACAAAATCTAAGA | 4734 |
rs370149970 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978939 | AAAAAAAAAAAAAAA[-/C]AAGAACAGAAAACAC | 4734 |
rs370231347 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857536 | CCATGTTGGCCAGGC[C/T]GGTCTCGAACTCCTA | 4734 |
rs370236231 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911080 | TGGACTATTTACAGT[-/T]GGAGATTCTTTCACA | 4734 |
rs370289872 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931660 | TGGTAAGTATATGAT[C/T]CTATTGTGTTCATAA | 4734 |
rs370296034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946209 | AAAGACACAGACTGG[C/T]GAATTAGATAAAGAG | 4734 |
rs370340599 | snp | C/T | 5.46732e-05 | 0.00522816 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869623 | CATCTTCTGAGCCAC[C/T]GGTTTTAGGTAAATA | 4734 |
rs370348851 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843568 | CCAGGGGAAACCAGT[A/G]AGAGAAAACATGCCA | 4734 |
rs370368436 | snp | C/G | 0.133777 | 0.221342 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906036 | ACATGAAAAAATGCT[C/G]ATCATCACTGGCCAT | 4734 |
rs370395676 | snp | A/T | 0.000151163 | 0.00869244 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840431 | TTCGTCTATACTATA[A/T]GTGAAAAAGACATAC | 4734 |
rs370435572 | in-del | -/TCAAGTGTTCTTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940236 | TGAAGAGGGTACATA[-/TCAAGTGTTCTTA]CCACAAAAAAGGGGG | 4734 |
rs370448885 | in-del | -/TGCCCAAGAA | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937243 | TTCCATTTGGCCGAA[-/TGCCCAAGAA]CCAAGTTTTTGCTGT | 4734 |
rs370465939 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828011 | GAGGTTAAGTAAGCT[A/G]CTTCAGTTCACATGG | 4734 |
rs370523436 | snp | A/G/T | 8.39778e-05 | 0.00647942 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863112 | AGCAATTAAGTTTAC[A/G/T]CATGATTTTTTTAAC | 4734 |
rs370529041 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855715 | TCCAGCCTGGCTGCC[A/G]GGCATGTGAATGCCA | 4734 |
rs370532851 | snp | A/T | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840459 | TACCACAGATTCCAT[A/T]TCATGAAGGGTTATT | 4734 |
rs370536170 | snp | A/C | 4.94328e-05 | 0.00497131 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916593 | CTGCTCTTTTTATTA[A/C]CATTTTCAGATGAGG | 4734 |
rs370543174 | snp | C/G/T | 3.44407e-05 | 0.00414963 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993595 | ACGCGCTCGCCCCCG[C/G/T]CCAGGGCAGGCAACT | 4734 |
rs370549044 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874503 | GTCCCAGAAAAAAAG[A/G]AGCCACCAGAGTTCT | 4734 |
rs370554209 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897742 | ACTGTGGCTTATGTT[C/T]CTGCATCGTTTACTG | 4734 |
rs370624316 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951026 | TGTGGATAAAAAGAA[A/G]TGCATTCACTTGATA | 4734 |
rs370666865 | snp | G/T | 1.64996e-05 | 0.0028722 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915951 | AACTGGTGTGAAGTT[G/T]GATAGGATCCTTTGC | 4734 |
rs370701101 | snp | A/G/T | 6.63708e-05 | 0.00576029 | synonymous-codon, missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915808 | TCCTGTGAAGCGGCC[A/G/T]TATGTCTCTTACTTC | 4734 |
rs370710185 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55840003 | AAAAAAAAAAAAATA[A/T]ATATATATATATATA | 4734 |
rs370725074 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969538 | GGAGAGGTAAGAGTA[C/G]AGGAGACTATGTTCT | 4734 |
rs370740947 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949227 | ACTGGCCATCAGAGA[A/T]ATGCAAATCAAAACC | 4734 |
rs370742322 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972734 | ACCCAACAATCTGTT[C/G]CATACAAGAAACACA | 4734 |
rs370759464 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980585 | TTTGGAAAGAAGAAA[A/T]CAAGAAATTAAAGAA | 4734 |
rs370764955 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971365 | CATGGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 4734 |
rs370767610 | snp | A/G | 0.000324555 | 0.0127347 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850770 | TGAAATCATATTGTA[A/G]TATTTTATAGAGAGA | 4734 |
rs370772033 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990262 | GGACCGCATCCCCGG[C/T]CCATGGAAAAACTAT | 4734 |
rs370778504 | snp | C/G | 1.66123e-05 | 0.00288199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833113 | AAACAGCCTGAATAA[C/G]ATAAAAACATCATTT | 4734 |
rs370785559 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956178 | TATGTATTTATGGGG[A/T]ACATGAGATTACCCA | 4734 |
rs370844427 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55915037 | TGTAGAAAAGTTTTA[C/T]AGCTTAAATCACTTA | 4734 |
rs370853036 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915809 | CTGTGAAGCGGCCGT[-/T]ATGTCTCTTACTTCT | 4734 |
rs370860739 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55946747 | TCCAAAATTGACCAC[A/T]TAGTTGGAAGTAAAG | 4734 |
rs370879386 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847657 | ACTGGGCATTTACAA[A/T]GATTTCTTTTTCTTT | 4734 |
rs370903517 | snp | C/G | 8.44488e-05 | 0.00649748 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55951548 | ACACTTGTAAGAACT[C/G]CATTCATTGGGTCAT | 4734 |
rs370922125 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896095 | GCAGCCTTCTATTAA[-/C]AAAAGCCCCCCAATA | 4734 |
rs370932901 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887068 | CTTCAAATAAACAGC[A/G]TAAAAAGTGCATCTT | 4734 |
rs370936247 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828316 | ATATTTAAGAAGATT[C/T]GTAACATATATTTAC | 4734 |
rs370943667 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988331 | GACTGTGGTGGGGTC[A/G]GGGGAGGGGGGAGGG | 4734 |
rs370943831 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843864 | GTGGTATTGTAGTAG[A/G]GCCAACGATGGGGAA | 4734 |
rs371011003 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939602 | TCTTTATGTAAAAAG[A/G]TGCTCAAAAATCACT | 4734 |
rs371015037 | in-del | -/TG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967441 | TGAACATAACTATGC[-/TG]TGTGTGTGTGTGTGT | 4734 |
rs371016990 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955814 | AGGATCTATACTACA[-/T]TTTTTTTTTTTTTTT | 4734 |
rs371039998 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831758 | TGGTCAGCTTCTATT[G/T]GCACAAAAAATTCAG | 4734 |
rs371054999 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862967 | TGGTTTACATAATAG[A/G]TCCTTCCAAGGATAT | 4734 |
rs371060325 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863917 | TCTAGTGATGGAAAA[A/G]TCATTCTCATTCCCT | 4734 |
rs371061106 | snp | A/G | 0.000181829 | 0.00953317 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916210 | TGGAGGTGCTGTCAG[A/G]AGGTAAGTTTCCACC | 4734 |
rs371075944 | snp | C/T | 0.000263609 | 0.0114776 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848333 | GAAGAGACAGGTGAG[C/T]GGACAGTCCCATCAG | 4734 |
rs371093679 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952844 | GACTTTCCCTCCCTT[C/T]TCCAGCAAAGCAAAA | 4734 |
rs371102805 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898628 | TGTATTTCACAAAAA[A/G]AACTTTTTTTTTTTT | 4734 |
rs371115025 | snp | A/C | 3.30513e-05 | 0.00406504 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848923 | AGAACAATACACACA[A/C]ATTTTAAAATAATCA | 4734 |
rs371145990 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943087 | TGGCAGAAGAAATTT[C/G]TAAGCAGCAAAGTGT | 4734 |
rs371166391 | snp | C/T | 0.000666433 | 0.018242 | utr-variant-5-prime, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55993526 | CTCGTCCTCCAGGAG[C/T]CCGAACACCTCCACC | 4734 |
rs371173210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901288 | TACATTTATGAAATC[A/G]TCTCCATAAGTCAAA | 4734 |
rs371174487 | in-del | -/GTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55878827 | TTTTTTTGTTTGTTT[-/GTTT]TGTTTTTTTGAGACG | 4734 |
rs371178481 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935802 | CAGTGAGTTGAGATC[A/G]TGCCACTACACTCCA | 4734 |
rs371187317 | snp | A/C | 1.6477e-05 | 0.00287024 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848801 | TAGCATTTCTATACA[A/C]TTACAGGTAAAGGCC | 4734 |
rs371201299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848035 | TGCTGCTTCCTCATC[C/T]GCATACACTCTCTGC | 4734 |
rs371210456 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957097 | CCAATGGCCCAATGA[C/T]AGGATACAGAAATAT | 4734 |
rs371218721 | in-del | -/GTAT | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925960 | ATACTGTATCATACA[-/GTAT]GTATATGTAAAAATA | 4734 |
rs371247022 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899671 | CTGGATCATTGTGAA[A/C]GTACAGGGGTATCAA | 4734 |
rs371293287 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947010 | CACATTTAAAGCAGT[C/G]TGTAGAGGGAAATTT | 4734 |
rs371324882 | in-del | -/TCTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831245 | ACTTTTTATTGGCTA[-/TCTA]ATATTGTAATTTTAA | 4734 |
rs371331305 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901196 | GCATTTATCCTTTGT[A/G]ATATCTTAACTATTG | 4734 |
rs371344503 | snp | A/G | 5.12807e-05 | 0.00506337 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840774 | TTGAAAAACTTTAAT[A/G]TGACAAATAATTACA | 4734 |
rs371362175 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854789 | CTTAAAAAAAACCCC[A/G]ATCAATGTATTGAGG | 4734 |
rs371366507 | snp | C/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918495 | TTCCGTTGTTTATAC[C/T]ACATGCTACTACACC | 4734 |
rs371366820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984423 | ATGTTGTGATGATTA[C/T]AGCTAAAGTATGAAA | 4734 |
rs371369119 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973405 | AACAACAACAAAAAA[A/G]CAGGCAGAGTGGTAC | 4734 |
rs371369154 | snp | A/T | 0.000153988 | 0.00877327 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916261 | GTGGAAAAGTATAAC[A/T]ACTACTGTCACTGAT | 4734 |
rs371386464 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911998 | ACAGAGAATACAAAA[C/T]GTTTTCAAGCAAACA | 4734 |
rs371388916 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954234 | CTCATTTTGCTTCTA[C/T]GACACATCTCTTCTA | 4734 |
rs371395399 | in-del | -/TA | 0.0699101 | 0.1734 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923838 | AACAGACTTTTTTTT[-/TA]AAAAAAAAAGCTAGT | 4734 |
rs371397348 | snp | C/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852498 | TTCCTCTTTCATCTT[C/G]TTTTTCTTCCCAACC | 4734 |
rs371401529 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857477 | GGGATTACAGACACA[C/T]GCCACTGCACTCGGC | 4734 |
rs371401869 | in-del | C/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881148 | CTTTTCTTTTCTTTT[C/TT]TTTTTTTTTGAGATG | 4734 |
rs371411186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949357 | CACTGTTGGTGGGAC[C/T]GTAAACTAGTTCAAC | 4734 |
rs371443400 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882204 | AAGCACCTTCATAAG[A/T]ACCAAAAATCAGGTG | 4734 |
rs371446987 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985213 | ATTCCTAATTACCTA[C/T]AAAAGAAATTATAGT | 4734 |
rs371476688 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874104 | CACAGAAAATGTAGA[G/T]TTTTTTTTTTATTCA | 4734 |
rs371484519 | snp | A/G | 1.65108e-05 | 0.00287317 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834178 | AATTATAAACAAGGA[A/G]AATAATGGGTTCACA | 4734 |
rs371566051 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842253 | AACATTCCCTCTACA[A/C]CCTGTGTCCAAGTCT | 4734 |
rs371575217 | snp | C/T | 3.3915e-05 | 0.00411781 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862890 | GTTTCCAGATTAAAA[C/T]TGTGAAAGCCATCAG | 4734 |
rs371579579 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868895 | TCACTCTGCAAACAA[A/G]ATCCTGAGGTTCGGA | 4734 |
rs371588498 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957975 | GGCCTGTCGTGGAGT[C/G]GGGGAAGGGGTGAGG | 4734 |
rs371595612 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55833634 | CCATTGCACTCCAGC[C/G]TGGGAGACAGAGCGA | 4734 |
rs371597066 | in-del | -/AACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883696 | ACACACACACACACA[-/AACAC]ACACACACACACACA | 4734 |
rs371600515 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989635 | CATACCGATAGCGGA[A/G]ACTCTGAACTCTTTC | 4734 |
rs371608803 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908626 | AGACCTACTGAACCA[C/G]AACCAGAATCTGCAT | 4734 |
rs371627092 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867386 | CTGAGACATGAGACC[A/G]CAAAATGAAGTGAAG | 4734 |
rs371627343 | in-del | -/TGTG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967440 | TGAACATAACTATGC[-/TGTG]TGTGTGTGTGTGTGT | 4734 |
rs371641320 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906853 | ATAATCCCAATGCTT[A/T]GGGAGGCTGAGGCAG | 4734 |
rs371686094 | snp | A/G | 9.8837e-05 | 0.00702914 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848401 | CTACATTCTCCAACC[A/G]AGGATCTTCCCATTG | 4734 |
rs371693265 | snp | A/G | 4.94548e-05 | 0.00497242 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916448 | ATTCAATTCATTATC[A/G]ACCACAGCACTACTG | 4734 |
rs371726943 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933399 | ATGGATGAAGCTAGA[A/C]ACCATCATTCTGAGC | 4734 |
rs371727402 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55878770 | ATGAAATGAAATGAA[C/T]GGATATACAAAATAA | 4734 |
rs371728867 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957198 | CCAGTAGTTTTTTCT[A/G]TAGATTCCTTGGGGC | 4734 |
rs371735605 | snp | C/T | 4.94784e-05 | 0.00497361 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916306 | ATGAACCTCCACTTG[C/T]GATACTTGCACATGA | 4734 |
rs371736636 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55946937 | AAATGAAGGCAGAAA[C/T]AAAGATGTTCTTTGA | 4734 |
rs371738514 | in-del | -/TTCTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870527 | TTCTTCTTCTTCTTC[-/TTCTTT]TTTTTTTTTTTTTTG | 4734 |
rs371779512 | snp | C/G | 1.64738e-05 | 0.00286995 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848363 | GAGCACACTGGCAGA[C/G]AGACTTACTGGTCCA | 4734 |
rs371779979 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842569 | TTTTTAAGTTTTTGA[G/T]GTCTTGCCATCTTGC | 4734 |
rs371814444 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908124 | CTGTGTGTAGTCATC[C/T]TCACCTATCAGGATT | 4734 |
rs371829779 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939508 | AACGGACTAATACAA[A/G]CAACAAAGAACCTAA | 4734 |
rs371836927 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978060 | TATGACCTTAACTGA[G/T]AAAAGAGATTACCAT | 4734 |
rs371845577 | snp | A/C/G | 7.67136e-05 | 0.00619281 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838074 | AAAGTACAAAATTAT[A/C/G]TCCAATAAAATACAT | 4734 |
rs371862486 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992020 | CCTGTGAATATAGCA[C/G]GGAAAGAAAGTCCAA | 4734 |
rs371887202 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972842 | GCAGGAATAGCTATA[A/T]CAGATCAAATAGATT | 4734 |
rs371897398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839000 | TGCCTATGTGACTTC[A/G]TGTTAAATGTTTTAT | 4734 |
rs371915436 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854303 | CACTTACTAAATACA[C/T]GGGAGTCCTACGTAC | 4734 |
rs371928017 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942245 | AATCATGAAATGCCC[C/T]CTTTATCTCTGGCAA | 4734 |
rs371936158 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848616 | ATTTTAGGAGAGGGG[C/T]GTAGATGAATGGATA | 4734 |
rs371940281 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921307 | TTTCTTAGTCCTTAG[C/T]GTGGGGATCTATAAT | 4734 |
rs371958508 | snp | A/C/G | 3.29751e-05 | 0.00406038 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830488 | CTCTGAGGCTTTGTT[A/C/G]TATCAAGGTCCAAAC | 4734 |
rs372102930 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923661 | AAAAAAAAAAAAAAA[A/T]ATATATATATATAGC | 4734 |
rs372105917 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829646 | TCTAAAGCCAGGTGT[A/G]GTGGTGCCTGGCTTT | 4734 |
rs372140386 | snp | A/C | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936610 | TCTAATATATTGAGT[A/C]TGAATGCTAAAAATA | 4734 |
rs372154240 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871299 | TCAATTGGAAAAGAA[C/G]CCTCAAGGTTTTGAC | 4734 |
rs372170524 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910695 | ACTGCCCTACTTGAA[A/G]ACAGCACTATCAGGG | 4734 |
rs372180874 | in-del | -/ACC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979335 | ATCATGAAAGTTTTT[-/ACC]TCTTTTTTTTTTTTT | 4734 |
rs372200770 | snp | G/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994781 | CGTACTTGGCCGGGC[G/T]CGGTGGCTCACGCCT | 4734 |
rs372210470 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982692 | AATCATCAAATTATA[C/G]ATTTATAATCTGTGC | 4734 |
rs372223131 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838848 | AATTGGTGCCTACTT[A/G]AAAGTTTAGAATCTA | 4734 |
rs372245807 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979648 | GTGAGCCACCGCGCC[C/T]GGCGAAAGTTTTTAC | 4734 |
rs372254819 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984626 | TTGAAGCCAGACATT[G/T]GAGTCCAGCCATGAG | 4734 |
rs372315897 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864485 | TAGGGAGTTTGAGAC[C/T]AGCCTGACCAACATG | 4734 |
rs372323374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836686 | GCACGCCACCACGTC[C/T]GGCTAATTTTTTTGT | 4734 |
rs372328923 | in-del | -/GTGTGTGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964651 | TGAATTTTGCTGCTG[-/GTGTGTGT]GTGTGTGTGTGTGTG | 4734 |
rs372338327 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55936073 | TTATTGTGAAGGCAG[C/T]TTTCATTGCTACTTC | 4734 |
rs372348326 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949546 | GCAAAGACTTGGAAC[C/G]AACCCAAATGTCCAT | 4734 |
rs372374960 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936796 | TGCTATTTCTTTTCT[-/T]TTTTTTTTTTTTTGA | 4734 |
rs372376809 | snp | C/T | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840638 | TGATAAACTGCCATT[C/T]CAGCTACCCGACCAA | 4734 |
rs372379610 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943790 | AGAAGTAGGCCACTA[A/T]CGTCCAGACCCCAGA | 4734 |
rs372393808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960293 | GTGGACTGGGAGAGG[C/T]AGACACACCCTCAAT | 4734 |
rs372407335 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965579 | CTGCCATGTTTTCTT[C/G]AGATTCAGAGATTCA | 4734 |
rs372414054 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828161 | TGCTGTGGTGTTTGG[A/T]AAGTAGAAAGTGGTT | 4734 |
rs372464389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925594 | CTTGTGGGAATGTTT[C/T]GATATCAAAATAAAA | 4734 |
rs372470866 | snp | C/T | 4.94279e-05 | 0.00497107 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916557 | CTGTACCTTGTTGGC[C/T]GTAGTGAAATCTGTA | 4734 |
rs372477240 | in-del | -/TC | 0.145642 | 0.227177 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940519 | TTCCCTCCTCCCCCT[-/TC]TCTCTCTCTCTCTCT | 4734 |
rs372477892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909134 | CTCTTTCTTCACCAA[C/T]AGACATCCTCGGGCC | 4734 |
rs372486083 | snp | G/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953499 | CAGGCTGGAGTGCAG[G/T]GGCGCGATCTTGGCT | 4734 |
rs372490650 | snp | C/G/T | 6.59711e-05 | 0.00574298 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860620 | CATACTTTATTGCTA[C/G/T]AGCATGTGTCTTTCA | 4734 |
rs372493803 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849382 | GGCATGCACCACCAT[C/G]CCTAGCTAATTTTTG | 4734 |
rs372513438 | in-del | -/TG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892310 | ATAAATAAATAAATA[-/TG]AATAAATAAATAATA | 4734 |
rs372550422 | snp | A/G | 8.75848e-05 | 0.006617 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55966506 | TTCTTGGCAAGGCCT[A/G]TTCCGGCTATAACTC | 4734 |
rs372567961 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830177 | TGGATACTCTGCACA[A/G]CTCCTTGTGGAGTGC | 4734 |
rs372571492 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902764 | GGCAGAAAACAAAGT[A/T]TGTGTTAATCAATAA | 4734 |
rs372583639 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845829 | GACACTCTGTTGCCC[A/G]GGCTGGAGTGCAGTG | 4734 |
rs372592968 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882474 | TGAAGGTGGCATTTA[A/G]ATCAGCCAGAGCCGG | 4734 |
rs372597783 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903966 | GGAGTTTGAGACCAG[C/T]CTGGCCAACACGGTG | 4734 |
rs372610168 | snp | A/G | 9.07071e-05 | 0.00673389 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966438 | AATTAACAAATGCAA[A/G]GTTTTAAAATTATAA | 4734 |
rs372616439 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922744 | AAACAAAATTGAGGA[C/T]AGTGGCTAGTACTTG | 4734 |
rs372619673 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852953 | CAGGGTTTCACCATA[C/T]TGGCCAGGCTGGTCT | 4734 |
rs372625815 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994799 | GTGGCTCACGCCTGT[A/G]ATCCCAGCACTTTGG | 4734 |
rs372638702 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979972 | TTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 4734 |
rs372671966 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981330 | TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGTG | 4734 |
rs372677077 | snp | C/T | 0.000167986 | 0.00916323 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55924699 | GCTGCTGAGGATGAA[C/T]CTAAGAAAAACACAA | 4734 |
rs372702159 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985616 | TTAGAAAAGGTACTT[A/C]TGGCTATAAAGGAAC | 4734 |
rs372716185 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988507 | AAAAAAAAAAAAAAA[-/G]AAAAACTGAGGAAAT | 4734 |
rs372734809 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957662 | ATGCTGCTATAAAGA[A/C]ACATGCACATGTATG | 4734 |
rs372751271 | snp | A/C/G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890221 | GATGTAATTCACATA[A/C/G/T]AATTAACCCACTTAG | 4734 |
rs372762418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832052 | ATTTGATAGAATACA[C/T]AGAATCTTACTTTAC | 4734 |
rs372824709 | snp | A/C/T | 0.000468639 | 0.0153005 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841909 | TTTTTCTTTTTCTGC[A/C/T]GATAATCATTGTAAA | 4734 |
rs372832889 | snp | A/C/T | 4.94616e-05 | 0.0049728 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915458 | ATAAGCTCCTCCCAA[A/C/T]GAAATACTTCTTCGT | 4734 |
rs372902866 | snp | A/G | 4.9525e-05 | 0.00497595 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860783 | TTAGGTTGTCCCTAT[A/G]TTGGAAGTATAAAAA | 4734 |
rs372945728 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942604 | AGTTTCCTGAGGCCC[C/G]CTCATCCAGGCTTCC | 4734 |
rs372947474 | snp | A/G | 1.70516e-05 | 0.00291985 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993570 | TTTCCGAACGCTTCC[A/G]GCAAACCGGACGCGC | 4734 |
rs372959320 | snp | A/G | 3.30322e-05 | 0.00406387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848500 | AAAAAATAACATAAT[A/G]AAAAATCGCACTGCA | 4734 |
rs372996740 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841026 | GCAACCTCCGCCTCC[A/C]AGGTTCAAGTGATTC | 4734 |
rs373006751 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915582 | CATGCAGATGTCCTA[C/T]GCATGAGCTTAATAT | 4734 |
rs373014669 | snp | C/G | 1.67739e-05 | 0.00289597 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833143 | TAGGGAACAGCACTG[C/G]GAAAGAGGTAAACAA | 4734 |
rs373076525 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945561 | AAAGTGACAGGGAGA[A/G]TGGAACCAAGGTGGA | 4734 |
rs373109599 | in-del | -/AAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952335 | AAGACTCCGTCTCAA[-/AAT]AAAATAAAATAAAAT | 4734 |
rs373111567 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977652 | CCTCAGGTATCAGAA[A/G]TAAAGATGGAATTGA | 4734 |
rs373123879 | snp | C/T | 0.000186716 | 0.00966039 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863111 | CAGCAATTAAGTTTA[C/T]GCATGATTTTTTTAA | 4734 |
rs373126286 | snp | G/T | 3.29924e-05 | 0.00406142 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830468 | ACTAACAGAGGAATC[G/T]CACTCTCTGAGGCTT | 4734 |
rs373174073 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953654 | GCCATCTTGGCCAGG[C/T]TGGTCTCAAACTCTT | 4734 |
rs373175029 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958991 | TACAATAATTTTTTT[-/T]CTACCATTGTCCACT | 4734 |
rs373202349 | in-del | -/ATT | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918757 | AAACTTAGTAATACA[-/ATT]ATTATGTTATTTTTG | 4734 |
rs373208726 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55850116 | AGGTAATTTTTCTAT[G/T]AGTAGTAAGCCAAGC | 4734 |
rs373209674 | in-del | -/ACAC | 0.490343 | 0.0688145 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883697 | CACACACACACACAA[-/ACAC]ACACACACACACACA | 4734 |
rs373217200 | in-del | -/AG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883737 | CACACAGAAAGAGAA[-/AG]AGAGAGAGAGAGACT | 4734 |
rs373242677 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927073 | ACAGAGTGAGACTAC[A/G]TCTCAAAAAAAAAAA | 4734 |
rs373255323 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827537 | TTTTCTCATGCTTAG[A/G]TAGTTCACAAACATA | 4734 |
rs373278157 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844694 | TAAAAATGCTTAAAC[A/G]GTATCTGGCATATGG | 4734 |
rs373302336 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974626 | CAACATACACAAATG[A/G]AAGTCAAATGTCATA | 4734 |
rs373305896 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854597 | AGAGAGCAGATGAGC[A/G]GTTGCTTGCAACTGA | 4734 |
rs373370531 | snp | A/C/G | 4.94787e-05 | 0.00497366 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833051 | CACCCGAGATGTGCC[A/C/G]GTGACAAACTGAAGT | 4734 |
rs373386541 | snp | C/T | 1.65671e-05 | 0.00287807 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915761 | TCTGGGAGTATTATT[C/T]GAAAGAACAATTTTC | 4734 |
rs373389193 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972666 | AATGAATGTAAGTGA[A/G]CTAAACTCTCCAATC | 4734 |
rs373396780 | snp | A/C | 5.64042e-05 | 0.00531027 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837896 | AACCAAGACAAAATT[A/C]TGAGGCACAATTATT | 4734 |
rs373405299 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989860 | ACAGCAGGAGGTGAG[C/T]GGCAGGCCAGTGAGC | 4734 |
rs373449401 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886758 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 4734 |
rs373466742 | snp | C/T | 3.3561e-05 | 0.00409626 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850727 | TTGAGGTCAGCTGAC[C/T]GGTCTCCACTGTGGC | 4734 |
rs373470424 | snp | C/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850650 | AATTTCAGATGGCTG[C/G]GTCACCTGCTGGCCT | 4734 |
rs373473133 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989282 | TTTTAAAAATACACT[A/G]TATTTATTCACTTCT | 4734 |
rs373476330 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953809 | CACTGCAACCTCCTC[C/T]TCCTGGGTTCAAGCA | 4734 |
rs373519434 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55840042 | TATATATATATATAT[-/A]ACATTCATCATAAAA | 4734 |
rs373533638 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980219 | ATTTCAGGCGTGAGC[C/T]ACTGCACCTGGCCAT | 4734 |
rs373541674 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961563 | GCAACCTCCGCCTCC[C/T]GGGTTCATATCATTC | 4734 |
rs373543013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945167 | GGAGAATGACTTTGA[C/T]GAGTTGACAGAAGTA | 4734 |
rs373553712 | snp | A/C | 0.000184775 | 0.00961005 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951443 | AACATAGTATAACTA[A/C]ATAAGGTTTTGTCTT | 4734 |
rs373566590 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864213 | AGCATTAGAAACTGA[A/G]ATAAACTGGTGAAGA | 4734 |
rs373579426 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923376 | GGCCAGGCTGGGCAT[A/G]GCAGCTCATGCCTGT | 4734 |
rs373595353 | snp | C/T | 3.71202e-05 | 0.00430798 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863096 | TGAAAAACAGGATGG[C/T]AGCAATTAAGTTTAC | 4734 |
rs373614012 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973054 | AAATTTCAATATCCC[A/C]CTTTCGGCACTGGAT | 4734 |
rs373654655 | snp | C/T | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829991 | GGTGGCAAGTCCAGG[C/T]GATTAAAACTGAAAG | 4734 |
rs373663853 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958119 | AACTTAACGTATAAT[-/A]AAAAAAAGATGACTG | 4734 |
rs373718024 | snp | A/G | 0.000911914 | 0.0213337 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829931 | CCCTGGGTGTTTTCA[A/G]TTGCCATCTGAAGTT | 4734 |
rs373752895 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855958 | TAACATGGGAGAGAC[A/G]GTTCTCCATGTTTTG | 4734 |
rs373763592 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916521 | CTATCAGCTAAGACA[C/T]TGCTAGACTGAAGAT | 4734 |
rs373790620 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940619 | TATCCTCGAATTCCT[G/T]GGCTCAAAGAATTGT | 4734 |
rs373798130 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854996 | GGAACTCAGCTTGAG[C/T]GGGCTCTGATCTAAT | 4734 |
rs373824433 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882665 | ACCAGTGGACTTGGG[A/G]GGCAGGTGATCTAGT | 4734 |
rs373858258 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904960 | AGCCGGGTACGGTGG[C/T]ACATGCCTGTAATCC | 4734 |
rs373913900 | snp | C/T | 1.73957e-05 | 0.00294916 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915315 | AGTTCATTTGTGCAA[C/T]CTCTGTTGCTGTCTC | 4734 |
rs373926798 | snp | A/C/G | 0.000908632 | 0.0212966 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951449 | GTATAACTAAATAAG[A/C/G]TTTTGTCTTATAAAA | 4734 |
rs373943992 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981312 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 4734 |
rs373960008 | snp | C/T | 8.87414e-05 | 0.00666054 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842186 | TCCAGAGGAGAGACG[C/T]ACTGTTTAAATCAGT | 4734 |
rs373960838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977193 | AGAATGATATTTTGG[C/T]CAATGATGGACAGCA | 4734 |
rs373971755 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994962 | TGGGTGGCTGAGGCA[A/G]GGGAATCGCTTGAGC | 4734 |
rs373988556 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827232 | AGATTGTAGGCTAAA[C/G]TTATATGCTTGTAAT | 4734 |
rs374022021 | in-del | -/TT | 0.448316 | 0.15222 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976796 | ACCACACCTGGCTAA[-/TT]TTTTTTTTTGTATTT | 4734 |
rs374080596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840343 | TTTGTATTTTGAAAC[A/G]TGATAATATATTAAT | 4734 |
rs374086309 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935024 | GAGGCACCCACCACC[A/C]TGCCTGGCTAATTTT | 4734 |
rs374096436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950419 | AGAAGACAAACAAAA[A/T]ATCTTTAAACATGAA | 4734 |
rs374097037 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874322 | TCAAAGAAGGAACTA[C/T]ACTAGGTAAGATTCA | 4734 |
rs374099573 | in-del | -/AG | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927334 | TTTTTTTTTTGAGAT[-/AG]AGTCTCACTCTGTCA | 4734 |
rs374113595 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949280 | CAGTTAGAATGGCGA[A/T]CATTAAAAAGTCAGG | 4734 |
rs374113929 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844450 | GACCTGTGAAGGAGC[A/G]ATGGTAGTGGAAGAA | 4734 |
rs374117100 | in-del | -/CCCA | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846220 | GAAACTCTGAGGTGG[-/CCCA]CCCACCATCTTGAAT | 4734 |
rs374126705 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910332 | CTCTTGCTAATGGAC[C/T]TCCTAACTGACACAT | 4734 |
rs374140193 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962132 | TTTATTCTTTATCAT[C/G]ATGAAATGTTTGAAA | 4734 |
rs374146463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866067 | TTTAGGTGTGTACTA[C/T]CATCCCAAGCTAATT | 4734 |
rs374176986 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856759 | CGCAATCTACCCCCT[G/T]GACATTCCAGACTAC | 4734 |
rs374180380 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841762 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 4734 |
rs374184981 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876201 | TACTTTCGGATAAAG[G/T]AGAGATAATTTGTCA | 4734 |
rs374190272 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858413 | TTGGGTTCAAGCCAT[C/T]CTTCCAATCTCAGCC | 4734 |
rs374190381 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975251 | AGCTAGAGAAATCAG[A/G]TAAGAAAAAGAAAGG | 4734 |
rs374195130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938228 | GCTGGGCATGGTGGC[A/G]TGTGCCTGTAGTCCC | 4734 |
rs374196076 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842877 | TCACTCATTAACAGA[C/T]GGTGACATTTACAGA | 4734 |
rs374202589 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932224 | AAGACAATCCTAAGC[A/C]AAAAGAACAAAGCTG | 4734 |
rs374227315 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832073 | CTTACTTTACCGAAA[-/A]CTGCATTAACTATTC | 4734 |
rs374244236 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905092 | AGCGAAATTCCGTCT[A/C]AAAAAAAAAAAAAAG | 4734 |
rs374273351 | in-del | -/GTG | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829652 | CCAGGTGTGGTGGTG[-/GTG]CCTGGCTTTAGGCAG | 4734 |
rs374292830 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843969 | ACAAGTGTAAATGAT[A/G]CTAATTCTGAGACTT | 4734 |
rs374309997 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895356 | AGACGACTGCTACTG[C/T]TGCAAATATAGAGTG | 4734 |
rs374348662 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897618 | CAATCTGACTGCCTT[C/T]TTCAACCTGGCCTTA | 4734 |
rs374355340 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931732 | TGGGAACAAACAATA[C/T]AGATACATCTTTAAA | 4734 |
rs374374181 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906392 | CAACCCAAATGTCCA[A/T]CAATGATAGACTGGA | 4734 |
rs374400257 | snp | A/C/G | 4.94338e-05 | 0.00497141 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848819 | ACAGGTAAAGGCCCT[A/C/G]GATCATTGGAAGTAT | 4734 |
rs374402245 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887115 | AAGAGCAAACCAAAC[C/T]CAAAATTAGTAGAAT | 4734 |
rs374453796 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871053 | GCCTCCCCTAATCTT[C/T]TTAGCTCTTCTCTGT | 4734 |
rs374552942 | snp | G/T | 8.54606e-05 | 0.00653628 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840775 | TGAAAAACTTTAATA[G/T]GACAAATAATTACAA | 4734 |
rs374556866 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927847 | GCCCCAGTTGGAGTA[C/G]GGAGGGAGACAGGGC | 4734 |
rs374615901 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933411 | AGAAACCATCATTCT[C/G]AGCAAACTATCACAG | 4734 |
rs374630991 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962990 | GGATTTCACCATGTT[A/G]GCCAGGCTGGTCTCA | 4734 |
rs374650583 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929229 | GTACATGTACACACA[A/T]GCACGAGCACGCACG | 4734 |
rs374656229 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944178 | CAAGCCGAAGCAGGA[C/T]GGGGCATTGCCTCAC | 4734 |
rs374671290 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955244 | CCCAAGATGGTCTCA[A/C]ATTTGCAGGCTCAAG | 4734 |
rs374724978 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894821 | TGAAGCAGGCAAGAC[A/G]TAACAGGAATCAGAG | 4734 |
rs374758649 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875195 | AGGAAAATAAAGCAG[A/C]TATTATAAAGATGTT | 4734 |
rs374804562 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951612 | AAAAAAAAAAAAAAA[-/G]AAAGAAAAATTTTAA | 4734 |
rs374826704 | snp | A/G | 0.000116933 | 0.00764543 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841910 | TTTTCTTTTTCTGCC[A/G]ATAATCATTGTAAAG | 4734 |
rs374842608 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896850 | TGTGCCTTACCTTTA[C/T]AGTTTTAACATAATT | 4734 |
rs374901705 | snp | A/T | 1.65214e-05 | 0.0028741 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850519 | TGTTGTTATAAATTT[A/T]AATGGAAAAGTATCA | 4734 |
rs374906059 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947001 | TCTCTGGGACACATT[C/T]AAAGCAGTGTGTAGA | 4734 |
rs374910058 | snp | C/T | 1.64917e-05 | 0.00287151 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830476 | AGGAATCTCACTCTC[C/T]GAGGCTTTGTTCTAT | 4734 |
rs374914589 | snp | G/T | 0.000153988 | 0.00877327 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834334 | GCAGGGCCAATGGCC[G/T]TTCCTATGCCTCAGC | 4734 |
rs374946047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921458 | GTCTCCAGAGTAGCC[A/G]GGACTACAGGTGCGC | 4734 |
rs374971497 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971197 | TGGCAGAATTGATCA[C/T]GCAGAAGAAAGAATT | 4734 |
rs374978359 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857382 | TGCCCAGGCTGGAGT[A/G]TGGTGGTGCGATCTT | 4734 |
rs374978563 | snp | G/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848384 | TACTGGTCCAGTTAT[G/T]GCTACATTCTCCAAC | 4734 |
rs374995949 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946787 | GCAAATGTAAAAGAA[A/C/T]AGAAATTATAACAAA | 4734 |
rs375051994 | snp | A/G | 0.000153988 | 0.00877327 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860497 | AGTTGGAACATCCAA[A/G]TTACTTGACGGTGGA | 4734 |
rs375080176 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939760 | GCAATGTAAAATGCT[C/G]CAGCCTCTACAGAAA | 4734 |
rs375088434 | snp | A/C/G | 0.000131792 | 0.00811666 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848427 | CATTGTGTTCTTTTT[A/C/G]TATCTGAAGGGAAGA | 4734 |
rs375108649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847762 | GCTCACCACAACCTC[C/T]GCCTCCTGGGTTCAA | 4734 |
rs375115312 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836726 | AGAGACAGGGTTTCA[C/T]CACATTAGCCAGACT | 4734 |
rs375189652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838955 | CCTAACTTCTCTGGA[C/T]ATCCAGGAGCACTTA | 4734 |
rs375213194 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934502 | GACAAGTATTTTCAT[A/T]AGCATAAAACAATAT | 4734 |
rs375226645 | in-del | -/GT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964651 | TGAATTTTGCTGCTG[-/GT]GTGTGTGTGTGTGTG | 4734 |
rs375240202 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972121 | AGCCTTCAAGAAATG[C/G]TAAAGGGTGTCCCAC | 4734 |
rs375276458 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984977 | TCCTGCATGTCTCCA[A/G]ATGCTATAGAATATT | 4734 |
rs375278672 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928258 | CTCAGGTGATCCACC[C/T]ACCTCGGCCTCCCAA | 4734 |
rs375290272 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965613 | AATCAACAATTGGAA[A/G]TATTATTCTACTTTC | 4734 |
rs375305648 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926995 | GCAGGAGAATCGCTT[A/G]AACCTGGGGGACAGA | 4734 |
rs375322043 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872090 | TTAGGTAATGGTTTT[A/G]GATGAATTCATGTTT | 4734 |
rs375385004 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986626 | ACGGAGTCTCGCTCC[A/G]TCGCCGAGGCTGGAG | 4734 |
rs375393261 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974218 | TCCAAGATTGAACCA[C/T]GAAGAAATCCAAAAC | 4734 |
rs375420746 | snp | C/T | 0.000378853 | 0.013758 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850655 | CAGATGGCTGGGTCA[C/T]CTGCTGGCCTGAATC | 4734 |
rs375422609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988963 | AAAATAGGACGGGCG[C/T]GGTGCCTCACGCCTA | 4734 |
rs375430736 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953504 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 4734 |
rs375457839 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978205 | CAAAAACAATTCCAG[G/T]GGAATTATAAATAAC | 4734 |
rs375461504 | snp | G/T | 0.00139503 | 0.0263736 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852372 | AATAGTTTACATAGG[G/T]ATGTGACAGTTTAAA | 4734 |
rs375463297 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992850 | TTCTTTATAAAGTAT[C/T]TATACTTTTTTGGCT | 4734 |
rs375490840 | in-del | -/CAA | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917208 | GTAACACAAGAACAA[-/CAA]TCTTCTAACATTTCA | 4734 |
rs375539729 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892314 | AATAAATAAATAAAT[-/A]AATAAATAATAAATA | 4734 |
rs375563116 | snp | A/G | 3.29973e-05 | 0.00406172 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916046 | GACTAAGGAGGAGTA[A/G]CGTTTTAGTGGAATT | 4734 |
rs375572629 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863718 | TTCTCTAAATTATCA[A/G]CTGAATGAAGGGCAA | 4734 |
rs375641757 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976902 | CCTCCCGAAGTGCTG[C/G]GATTACAGGTGTGAG | 4734 |
rs375669327 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829174 | GCTTTAATACTTTTT[A/T]CCCATTGCAAATATG | 4734 |
rs375696290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898870 | TGGTCTTGAACTCCT[A/G]GGCTAAAGTGATCCT | 4734 |
rs375697799 | snp | C/T | 0.000153988 | 0.00877327 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915342 | TCTCTTGATAAATTA[C/T]CCACTTTACCTTCAT | 4734 |
rs375737490 | snp | C/T | 9.17894e-05 | 0.00677394 | splice-acceptor-variant, intron-variant | NEDD4 | GRCh38.p7 | 15:55872478 | CTTGGATTTTCTGTC[C/T]AGAATAAAATAGTGG | 4734 |
rs375785168 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929817 | AACAAAAGAAAAGAG[G/T]TTTAAAAACTATAAG | 4734 |
rs375831020 | snp | A/T | 0.000148676 | 0.00862065 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840657 | CTACCCGACCAATAA[A/T]CTTGAAGTAAGAGAG | 4734 |
rs375840599 | snp | A/G | 1.80289e-05 | 0.00300235 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829974 | CTTCAAATGATTCAT[A/G]AGGTGGCAAGTCCAG | 4734 |
rs375849305 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969988 | CCTGGCCTTAGCTCC[A/G]AGAGGGCATTTCTAG | 4734 |
rs375869653 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863250 | TAAATACTTTATGAT[A/C]ATGAAGACTCTTTTT | 4734 |
rs375873855 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916299 | TTAGTATATGAACCT[C/T]CACTTGTGATACTTG | 4734 |
rs375967325 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827848 | CTTGACACAATCTGA[C/T]GGTCAGCACAAAGCA | 4734 |
rs376007297 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55993419 | GGGCTGACAGCAGAG[C/T]CTCCGGTCGTGGCCG | 4734 |
rs376034146 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841081 | TGGAATTACAGGCGC[C/T]CGCCACCATGCCTGG | 4734 |
rs376040036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954447 | CAAAATGTAAATGTA[A/G]TTATGTATCTATCCC | 4734 |
rs376041890 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875044 | TGTCTCTATTAGTTA[C/G]TATATTCATTGTCCA | 4734 |
rs376065121 | snp | A/C | 2.89406e-05 | 0.00380388 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924713 | ACCTAAGAAAAACAC[A/C]ATCTTTATTTAAAAA | 4734 |
rs376094634 | snp | A/C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983032 | GAGGCTGAGGGAGGA[A/C/G]AATCACTTGAACCCA | 4734 |
rs376116558 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963551 | GTCTATAACTTATAC[C/G]TGCTCCATCCTTTAT | 4734 |
rs376127769 | snp | C/G/T | 8.29615e-05 | 0.00644012 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841918 | TTCTGCCGATAATCA[C/G/T]TGTAAAGGTACTTAC | 4734 |
rs376129835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940090 | GAGGACACTACCCTA[A/G]GTGAAATAAGCTAGT | 4734 |
rs376163731 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55954871 | ATATTATTACTGAGT[A/T]GTAAGAGGTTTCATA | 4734 |
rs376204569 | snp | C/G | 1.72154e-05 | 0.00293384 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993592 | CGGACGCGCTCGCCC[C/G]CGCCCAGGGCAGGCA | 4734 |
rs376222979 | snp | C/T | 3.79492e-05 | 0.00435582 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863099 | AAAACAGGATGGCAG[C/T]AATTAAGTTTACGCA | 4734 |
rs376270403 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925326 | ATACAGATTAGATTT[G/T]GACACCTTATGATCA | 4734 |
rs376290329 | in-del | -/CA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892641 | AAAAAGAAAATGAAA[-/CA]GTTTCTACCCTCCAG | 4734 |
rs376297046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975042 | GGACTACAGGTGTGC[A/G]ATACCACACCCGGGT | 4734 |
rs376311673 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925950 | TTACATATACATACT[A/G]TATCATACAGTATGT | 4734 |
rs376367756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972952 | AATTGTAAATACATA[C/T]GCATCCAACACTGAA | 4734 |
rs376377663 | snp | G/T | 1.65266e-05 | 0.00287455 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915907 | TAGTGCCATCCTCAT[G/T]ATGTGCAATTTCACT | 4734 |
rs376399663 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937970 | AAGACAGACAGAGAC[A/G]GATGAAATAGATAGC | 4734 |
rs376419090 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950654 | GTACAGTGGGTTAAC[A/G]AGCGTCCCGGAGAAG | 4734 |
rs376425274 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830130 | TCTTTTCACCAGGGG[C/T]AGAAGTAAGACGTAG | 4734 |
rs376427568 | snp | A/C | 9.90066e-05 | 0.00703516 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830632 | ACTCTCTACAAGGAT[A/C]TCCAGGCATATCAAA | 4734 |
rs376434288 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884728 | ATAGTGAATTTTAAG[A/G]AAGGCTATTTTAAAA | 4734 |
rs376454952 | in-del | -/AAT | 0.0611083 | 0.163768 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872274 | CAATGAAGCTTTTAA[-/AAT]AATAATAATAATAAT | 4734 |
rs376461438 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859978 | TACAAAATCATAGAA[C/G/T]TATCCCTGCTTCCCA | 4734 |
rs376462283 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892384 | AGGCAAAGGATTATA[C/G]AAAGAATAATTTCTT | 4734 |
rs376466897 | snp | A/G | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826737 | AGACTTATGCAATAC[A/G]ACCTTTTTGTAAAGT | 4734 |
rs376470305 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926698 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 4734 |
rs376472798 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944115 | CACCTGAGGTGCCTG[A/G]TTCATCTCATTTGGA | 4734 |
rs376474493 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941650 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 4734 |
rs376475028 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858329 | TTTTTTTTCTTGAGA[C/T]GGAGTTTCACTCTGT | 4734 |
rs376492020 | snp | A/G | 5.0671e-05 | 0.00503318 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860366 | TATAATATGCATAAT[A/G]TAAACTACTGAAGCC | 4734 |
rs376502688 | snp | A/G | 8.43277e-05 | 0.00649282 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55951554 | GTAAGAACTCCATTC[A/G]TTGGGTCATATAACG | 4734 |
rs376503322 | snp | C/G/T | 0.000164808 | 0.00907628 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830597 | TGAACCTATAAGGAA[C/G/T]AATTTATTTGGTTTC | 4734 |
rs376603419 | snp | A/G | 0.000134771 | 0.00820776 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838483 | CACAATTTATGTGCC[A/G]TTTTAACTGATCAAA | 4734 |
rs376603841 | in-del | -/TCTAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972517 | CATCAAGTTAAAAAA[-/TCTAC]AACAGACATACAATA | 4734 |
rs376648343 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933402 | GATGAAGCTAGAAAC[A/C]ATCATTCTGAGCAAA | 4734 |
rs376673983 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944559 | AACCTCTGTGAGCAG[C/G]GCATAGCTGAACAAA | 4734 |
rs376711620 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979478 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 4734 |
rs376715455 | snp | C/T | 1.65056e-05 | 0.00287272 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848481 | CACACATAAAATTTA[C/T]TACAAAAAATAACAT | 4734 |
rs376721336 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913090 | ATATAAGAAAAGAAG[A/T]TGTAGACTCTCAGTG | 4734 |
rs376746187 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957810 | AAAAAGGATGAGTTC[A/G]TGTCCTTTGCAGGGA | 4734 |
rs376746405 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910266 | CTGCTTCCTTACCTG[-/T]TTTGATTCTTTCTTC | 4734 |
rs376762760 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933159 | TAGAAATACCATTTG[A/G]CCCAGCCATCCCATT | 4734 |
rs376770872 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941711 | TGGTATTACAGGTGC[A/G]CACCATCACACCCAG | 4734 |
rs376775758 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854693 | ATGTCTCCATAACTG[C/T]ATAAATTTACAAAAA | 4734 |
rs376810890 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901507 | ATCCAATCAAAATTC[A/G]TGAGTATAAGTAAAA | 4734 |
rs376829711 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942242 | TATAATCATGAAATG[C/T]CCTCTTTATCTCTGG | 4734 |
rs376846663 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970419 | GGGTCTTAAATAAAC[A/C]CAAGTGGTAGCCAGG | 4734 |
rs376856302 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949642 | AAGGATGAGTTCATG[C/T]CTTTTGTAGGGACAT | 4734 |
rs376858792 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852715 | TATATATATATATAT[A/T]TATATATATTTACCT | 4734 |
rs376862716 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992778 | GAAAAGAAACAGCTT[G/T]GCCTTCTTCAAATCC | 4734 |
rs376872433 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883767 | CTCTATTTGTGTGTG[A/T]GAGAGAGAGACACTC | 4734 |
rs376876347 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856028 | ACATTCTGTGCTGTA[C/T]TGGCTCCCTGTAAGG | 4734 |
rs376879211 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922814 | GGAGGGTTTCAAAGA[C/T]TTTGGTAATGTTCTA | 4734 |
rs376937793 | snp | A/C | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917197 | TGCATGAATGAGTAA[A/C]ACAAGAACAACAATC | 4734 |
rs376942630 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855323 | GAAAATGAGAAAGCC[A/G]TTCCAAGTGGGGAAA | 4734 |
rs376971017 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902399 | CCATTAATTTTGTCA[C/T]GACTGCATGGTGGCT | 4734 |
rs376973985 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938900 | CACTTGAATCCAGGA[C/G]TCTGAGACCAGCCTG | 4734 |
rs376979917 | snp | A/G | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917167 | AACCTTGTTTCAATT[A/G]TACCTTCTCCAATTT | 4734 |
rs376995564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880242 | GGTTGCAGTGAGCCG[A/C]GATCGCACCATTGCA | 4734 |
rs377007917 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952030 | CACTTAAAAAAAAAA[A/C]AACAAAAACTAGGTG | 4734 |
rs377016349 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947710 | AAAAACCATATGATT[A/G]TCTCAATAGATGCAG | 4734 |
rs377038385 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842208 | TAAATCAGTTCAACA[C/T]AATAACAAACCCATC | 4734 |
rs377041774 | snp | A/G | 6.59044e-05 | 0.00574002 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916563 | CTTGTTGGCTGTAGT[A/G]AAATCTGTAGACAGC | 4734 |
rs377080366 | in-del | -/AT/TA | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920197 | GTGGAAATATATATA[-/AT/TA]TTCATATATTATACA | 4734 |
rs377106860 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984037 | AGTATATTCTATATC[A/G]TTATACCTCATGCCC | 4734 |
rs377123486 | in-del | -/CTGC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964731 | TGTGTGTGTGTGTGT[-/CTGC]TTATCATTCTATGGT | 4734 |
rs377162621 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898769 | TCCCTGAGTAGCTGG[A/G]ACTATAGGCAAGCGC | 4734 |
rs377175991 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956412 | AGATTTTTTTCCTAT[C/G]TGTTCCTATAGAAGT | 4734 |
rs377202001 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875859 | ATTTGGGGAAAAAAA[-/C]CAGCCAAAATATTCA | 4734 |
rs377202085 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949463 | TGGGTATATACCCAA[A/C]GGATTATAAATCATG | 4734 |
rs377222105 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862246 | CACATTAAAAAATTA[C/T]GAGTATGTTTCAAAC | 4734 |
rs377222326 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882622 | CAATTCCTAGTTAAG[A/T]CCTAGTTCGTACTGG | 4734 |
rs377235963 | snp | A/C | 0.00065962 | 0.0181487 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860623 | ACTTTATTGCTATAG[A/C]ATGTGTCTTTCAAGG | 4734 |
rs377265437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850373 | CAATATTAAAAAGAC[A/G]CATAAGCATTCTCCT | 4734 |
rs377271420 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893706 | GTATTTTAAAAATAA[A/G]AAACCATATTTTTCT | 4734 |
rs377276334 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927275 | GCATGGGGGCAGAAT[A/G]AGCGTGCTCTAAGGA | 4734 |
rs377295315 | snp | C/T | 6.6036e-05 | 0.00574575 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850700 | GTGATTGAGGGCCTG[C/T]AGAACTCTGGCTTGA | 4734 |
rs377309836 | snp | A/C | 0.000389924 | 0.0139574 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848754 | CTATACCCGAAAATG[A/C]AAAATATTTGAGATA | 4734 |
rs377369914 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877384 | GATTATGCATTTTTT[-/T]GCAAGAATACCATAA | 4734 |
rs377433653 | snp | C/T | 1.65386e-05 | 0.00287559 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848544 | ATGTAGAAGATTCTT[C/T]CATCTGTGTGAGTTC | 4734 |
rs377434155 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980379 | TGGGTCTGAGAACAG[C/T]GGCTGCTGTACCCAC | 4734 |
rs377441208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967045 | GCATGCGCCACCATG[C/T]CCAGATAATTTTTCT | 4734 |
rs377461942 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931147 | AATTGTAAAAGATGA[C/T]AAAGCAATGTCTTCA | 4734 |
rs377518999 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894585 | TGGGGTGAGGTGGAA[C/G]TCAGGAGAAACTACT | 4734 |
rs377544053 | snp | C/T | 4.97442e-05 | 0.00498695 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915851 | AATTGTTTTAGATAA[C/T]CGAAGTCCATTGACA | 4734 |
rs377547946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947596 | AAGGTACAAGGAGCT[A/T]ATCCACCATGATCAA | 4734 |
rs377583850 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930365 | CATGTATCTAGAATG[A/G]TACTGGTTAAGACTA | 4734 |
rs377587799 | snp | A/C/G/T | 6.59105e-05 | 0.00574038 | stop-gained, missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916617 | GATGAGGGAACAGAT[A/C/G/T]ATCTTTCTTGAGACT | 4734 |
rs377603445 | in-del | -/G | 0.0637235 | 0.166737 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947320 | ATAAAAAATGATAAA[-/G]GGGATATCACCACCA | 4734 |
rs377613328 | in-del | -/TA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920189 | TATATTGTGTGGAAA[-/TA]TATATATATTCATAT | 4734 |
rs377622838 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939409 | TGACTGAGGCCTCCC[C/T]AGCCATGTGGAACTG | 4734 |
rs377635604 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843633 | TCTAAGGAAAAAAAA[-/A]TCAATTTCATTCTCA | 4734 |
rs377672502 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55840001 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 4734 |
rs377690346 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55987754 | CCATTGCTTGTTTTT[C/G]TCAGGTTTGTCAAAG | 4734 |
rs377696902 | in-del | -/CTC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929485 | ATCCTCACCCTCCTC[-/CTC]TCCTCTACCCTCAAG | 4734 |
rs386784276 | in-del | ATCTCTAT/CTCTCTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866261 | TTTATAAGAATTGTT[ATCTCTAT/CTCTCTA]TTTTTTCTTTTTATT | 4734 |
rs386784277 | in-del | CTTC/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870514 | TGCTGCTTTTTTTTT[CTTC/T]TTCTTCTTCTTCTTT | 4734 |
rs386784278 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904910 | CTAGCCTGACCAACA[CA/TG]GAGAAACCCCGTCTC | 4734 |
rs386784279 | multinucleotide-polymorphism | AC/GT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935574 | CAGCAAAGGCTGGGC[AC/GT]GGTGGCTCATGCCTG | 4734 |
rs386784280 | multinucleotide-polymorphism | ACT/GCC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969701 | AAAGGACCCAGTCCT[ACT/GCC]AGATTTCACTACCTG | 4734 |
rs386784281 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970424 | TTAAATAAACACAAG[CA/TG]GTAGCCAGGAAATAG | 4734 |
rs386784282 | multinucleotide-polymorphism | AAAAAGAGAAGCTTATAGCTATAAA/TAAAAGAGAAGCTTATAGCTATAAG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973783 | GAGCAAAAGCAGTAC[lengthTooLong]TACCTACATGAAAAA | 4734 |
rs386784283 | in-del | AG/GGGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980792 | TTAGTGTGTGTGTAG[AG/GGGT]GTGTGTGTGTGTGTG | 4734 |
rs386784284 | in-del | ATGGGGTTCTA/GAAGGCTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983497 | GGTTCTATTTACTCA[ATGGGGTTCTA/GAAGGCTTT]TTGCCCCACTCTTCA | 4734 |
rs397731134 | in-del | -/ACTTT | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827788 | CTTAGAAGTCACTTT[-/ACTTT]TAAATGATTCTTTGG | 4734 |
rs397735251 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981376 | GCCTCCTTTTTTTTT[-/T]CTTTTGAGCAACATG | 4734 |
rs397748735 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942073 | TACTATTTTTTTTTT[-/T]GTCTAGTTGTTGTAT | 4734 |
rs397751121 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905106 | CAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 4734 |
rs397753863 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835442 | TTTTTTTTTTTTCCC[-/C]ATGCCCTAAACTGTC | 4734 |
rs397770149 | in-del | -/G | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834532 | AGTGCTGGGATTACA[-/G]GAATGAGCCACTGCG | 4734 |
rs397772604 | in-del | -/A | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858321 | AAACTCCGTCTCAAG[-/A]AAAAAAAAAGAATAA | 4734 |
rs397788614 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841027 | AACCTCCGCCTCCCA[-/A]GGTTCAAGTGATTCT | 4734 |
rs397933250 | in-del | -/TGGA/TGGG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881192 | TTTGCCCAGGCTGGA[-/TGGA/TGGG]GTGCAATGGCGTGAT | 4734 |
rs397934837 | in-del | -/AAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923660 | AAAAAAAAAAAAAAA[-/AAA]TATATATATATATAG | 4734 |
rs398027400 | in-del | -/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837448 | TGACTTACTTTCTTC[-/T]TTTTTTTTTTTTTTT | 4734 |
rs398027402 | in-del | -/A | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881158 | GTAAAACTGCATCTC[-/A]AAAAAAAAAAAAAAG | 4734 |
rs398027403 | in-del | -/A | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983628 | GAACACTCTGTCTCA[-/A]AAAAAAAAAAAAAAG | 4734 |
rs398027404 | in-del | -/C | 0 | 0 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995152 | AAGTGCCATCTCTTT[-/C]CCCCTAATACGGATA | 4734 |
rs398043333 | in-del | -/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881157 | TCTTTTTTTTTTTTT[-/T]TGAGATGCAGTTTTA | 4734 |
rs398043334 | in-del | -/T | 0.5 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898654 | TTTTTTTTTTTTTTT[-/T]GAGACAAGGTCTTAC | 4734 |
rs398043335 | in-del | -/T/TC | 0.5 | 0 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952997 | ATTCTTTTTTTTTTT[-/T/TC]CTTTTTTTTTGAGAC | 4734 |
rs398057718 | in-del | -/AT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901720 | TTCATAATTACATAT[-/AT]GATTCCATTTGTACA | 4734 |
rs398070668 | in-del | -/GCT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901404 | TAGGACTTTCTGGCT[-/GCT]AATTATTTACTCCTG | 4734 |
rs398070669 | in-del | -/GTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964310 | GTTGTTGTTGTTGTT[-/GTT]TTTCTCCAATCTTTG | 4734 |
rs398078209 | in-del | -/A | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918596 | TTGTTAAAAAAAAAA[-/A]ACTGCTTAAGATAGA | 4734 |
rs398099820 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910942 | TTGCCCAACTACTTA[-/A]CTATCAGCCGAAGAC | 4734 |
rs398099822 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973635 | GAGGAACTTGGAAAT[-/T]AATACAAACAAATGG | 4734 |
rs398118877 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845536 | CATGGTTTTTTTTTT[-/T]GTATTTTGAGGCCTG | 4734 |
rs398118878 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851384 | CAAAGTTTTTTTTTT[-/T]ATCAAGCAGCACCTC | 4734 |
rs527245504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969524 | TCATAGCTCCAGGAG[A/G]AGAGGTAAGAGTAGA | 4734 |
rs527253086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909308 | CAGTTCGCTTCAATC[C/T]TAGTGTGGGTAAAAT | 4734 |
rs527284896 | snp | A/G | 0.000798881 | 0.01997 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969008 | CCTAGTTTCAACATC[A/G]TATCAAGGAAAGAGG | 4734 |
rs527362593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881393 | TAATCTACCCACCTC[C/G]GCCTTCCAAAGTGCT | 4734 |
rs527371410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974469 | GATCCATTGAAAAAA[A/G]AAAACTACAGGCCAA | 4734 |
rs527389223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931910 | TAACAGACACTCCCC[A/G]TTTTCCCTCAACCTT | 4734 |
rs527398132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939055 | AGGCTGCAATAAGCC[A/G]TGATTGTGCCACTGC | 4734 |
rs527409183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973992 | CAACAAAATGAAATG[C/T]TGGTGTTTTGAAAAG | 4734 |
rs527431136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889140 | ACAGCCCACAATAAA[C/T]AATCAACAAAGTGGG | 4734 |
rs527433647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899277 | AAAAGTTTTACTTTT[C/T]GAAATGAATAGCCTT | 4734 |
rs527448455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944703 | TGGGTCCCTGACCCC[C/T]GTGTAGCCTAACTGG | 4734 |
rs527487669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853727 | GGCATGATGGCTCAC[C/T]CCTGTAATCCCAGCA | 4734 |
rs527494557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898149 | AAGAATGTTTACACA[A/G]TGTTCCAAAAGGAAG | 4734 |
rs527494888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980133 | TTTTTAGCTTTGCCA[C/T]GTTGGCCAGGCTGAT | 4734 |
rs527508143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986177 | CTTCTTACATAGAAT[A/G]CCAACTAACAGAGAT | 4734 |
rs527509911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944209 | CTCGGAAGTGCAAGG[A/G]GTCAGGGGATTTCCC | 4734 |
rs527593934 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853315 | CCCTAATAAAACATA[C/G/T]CAACAATAACAAGCA | 4734 |
rs527595477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949599 | AATGTGGCACATATA[C/T]ACCATGGAATACTAT | 4734 |
rs527596752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840943 | AAAGTTTTGTTTGTT[C/G]GTTTGTTTTTGAGAT | 4734 |
rs527618651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992965 | ATTTATGTTCCTGCT[C/T]TCCCATCCCTGTCTC | 4734 |
rs527647362 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961592 | TCTCCTGCCTCAGCC[A/T]CCCGAGCAGCTGGGA | 4734 |
rs527665902 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983204 | AAGCAAGAAGAAATA[A/C]AGAAATAACTAGCAA | 4734 |
rs527687545 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981576 | CTGGAGTCTATGATA[A/C]CCACATGCATGAGTC | 4734 |
rs527703527 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981989 | ATCTTATCACTACTT[C/T]TAAGTGTGATAACAC | 4734 |
rs527722251 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964756 | TTCTATGGTTTGGAT[-/A]TTTGTATCCTTCAAA | 4734 |
rs527726554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945842 | CAAGCCAGAAGACAG[G/T]GGGGGCCAATATTCA | 4734 |
rs527730944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939782 | CTACAGAAAATAGTA[A/T]AGCCTCTATAGAAAA | 4734 |
rs527737176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988005 | TTTTTTCCAATTCTG[C/T]GAAGAAAGTCATTGC | 4734 |
rs527743313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852251 | AGTGAGCCACGATCA[A/C]GCCATTGGACTCCAG | 4734 |
rs527755528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900407 | TGTATCTACTGGTCC[C/T]TGCAGGCTGGTGAAG | 4734 |
rs527757357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907073 | GCACTCCAGCCTGGG[C/T]GACAGAGCCAGACTG | 4734 |
rs527774499 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965371 | CATGCCCAGCTGATT[G/T]TTTGTACTTTTTGTA | 4734 |
rs527811197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983027 | CTCGGGAGGCTGAGG[A/G]AGGAGAATCACTTGA | 4734 |
rs527813055 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963501 | TTAATCTTTTATTCA[A/G]CTTATACTTAGTATT | 4734 |
rs527816424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906621 | GGAACATCACACACC[A/G]GGGCCTGTTGTGGGG | 4734 |
rs527823832 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995033 | GCACTCCAGCCTGGG[C/T]GACAGAACAAGACTC | 4734 |
rs527825694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986885 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCAAGGCC | 4734 |
rs527832686 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928061 | GTCACCCTGGCTGGA[A/G]TACAGTGGTGCAATC | 4734 |
rs527851347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860323 | GCATTTAAGACAAAA[C/T]TTTACATAAAAGTTA | 4734 |
rs527868771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839416 | TTAATAAATATAGAG[A/G]CTCAATGAACCAACT | 4734 |
rs527876678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913524 | AAAGAGAAGTCTAAT[A/G]AACATTAAACGGGGG | 4734 |
rs527920461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867080 | CAAATGGTACAAAAA[A/T]CAAATGTTACATAAT | 4734 |
rs527935316 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839941 | GATCACGCCACTGCA[C/T]TCCAGCTTGGCAACA | 4734 |
rs527974570 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926120 | GATACATACGTATAT[A/G]TATCAAACCCAGATA | 4734 |
rs527984876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956682 | TATATCTATTCTCAT[A/G]CCACTGCCACTCTGT | 4734 |
rs527997618 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927157 | AAAGAAGATGTAGAA[A/G]AACTTTTGAGGAGAT | 4734 |
rs528055925 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989033 | CTGAGGTCAGGAGTT[A/C/T]GAGACCAGCCTGGCC | 4734 |
rs528066716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848664 | GTATGGTTAATTTAA[C/G]TTGCATATTCCATTC | 4734 |
rs528091393 | snp | C/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993824 | GCGTGCGGCGGGGCT[C/T]GGGTGGGATGAGCGC | 4734 |
rs528110226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928241 | GGTCTCGAACCCCTG[A/G]CCTCAGGTGATCCAC | 4734 |
rs528116978 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867784 | TTCCTGGCTGGGTGC[C/T]GTGGCTCACGCCTGT | 4734 |
rs528142754 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849197 | AAAACTGGTGAAAGA[G/T]TAGGACATTAAATTG | 4734 |
rs528160013 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866375 | CTTTTCCTTTCTCTT[A/G]AATTATGATAATACA | 4734 |
rs528169325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868848 | AATTTTTTTGCTGGA[A/C]GAAACCCTCGAGGTC | 4734 |
rs528170321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958293 | AAATGACCATGTGTT[C/T]TTTCTACTTTACTGT | 4734 |
rs528190578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849963 | ATGCCTGACTAATTA[G/T]TTTGTATTTTTAGTA | 4734 |
rs528213449 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894698 | GTGAAAACAGATGAT[G/T]TACCTTGTCAAGTTT | 4734 |
rs528213825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922265 | ATGTGTAATCACAGA[G/T]CTCACAAATATAATG | 4734 |
rs528229514 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890258 | CAATTCAATGTTTTT[C/T]AGTATTTTCACAGAG | 4734 |
rs528231515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868183 | CTGTTCTAGAGCTTT[G/T]CTTTCTCAAGGTACA | 4734 |
rs528237416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964999 | GTACGCTAGGTCCCC[C/T]TCCCGTTTCTGTCAT | 4734 |
rs528237784 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994119 | GGTGTCATTCCCATA[A/G]GAAGCTGGACCTGGG | 4734 |
rs528246786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876106 | AACTGAATGATATCT[A/G]TAAGTGCTGAAATGG | 4734 |
rs528262074 | in-del | -/AGGGCCTTGGAGCAAACAG | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883519 | TGATTGTAGAGCCCT[-/AGGGCCTTGGAGCAAACAG]AGGTGGCAGCTAGCG | 4734 |
rs528273141 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971129 | GAATCAAGCAGAATT[C/G]TGAAGTTGAAAAAAT | 4734 |
rs528274163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843349 | TCTTCATTTTACACA[A/T]AAAACTGAAGAAGAC | 4734 |
rs528274561 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928212 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 4734 |
rs528352088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927766 | ACTGGAGACAGACCC[C/T]GGTGTCTACAGGAGC | 4734 |
rs528372720 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914244 | ACATAATGGATGTTA[C/G]AAAAACACAGATTAA | 4734 |
rs528379914 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976182 | GCAAAACTTTCTTGA[C/G]TAATACCCAAAAGCA | 4734 |
rs528393976 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910608 | CTTATCTGAGGCTTT[C/G]ACTATACTCCTGACT | 4734 |
rs528402961 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969359 | TAAAAGGCAGTCTAG[A/G]CCATAAGGACTGCAG | 4734 |
rs528404130 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939204 | GATCCGTAATCCCCA[C/T]GTGTCAAGGGAGGGA | 4734 |
rs528406434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975641 | CACCAAAAAAAAAAC[A/G]AAAGGGAAAAATATT | 4734 |
rs528435034 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959670 | TCCATCTTGCTAGGA[G/T]ACTCTTGCTAGCTTT | 4734 |
rs528439116 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879729 | GCAAAAAAGAAGCAA[C/T]TAGAGGACAAGAAAT | 4734 |
rs528460893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966819 | AATCTAAAGCCAAAG[C/T]ATTGCAACTAATAGG | 4734 |
rs528461853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924098 | CATTTTATAAAAAGA[A/C]CATCAGGTTTAACTT | 4734 |
rs528491065 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973573 | AATTAAAATCTTAAA[A/T]GTATCTTCTCTGACT | 4734 |
rs528510051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878731 | TAAAACTGTGGGATA[C/T]ACAACTAGTAGAATT | 4734 |
rs528517523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834454 | AGAAAATGTACATGT[A/G]CACAGTCTGTTCTCT | 4734 |
rs528556444 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875903 | ACACAAGCTGAGACA[G/T]TCAATAAAGTCAGTG | 4734 |
rs528561662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877510 | AAGGTGCTGTCTTCC[A/G]TGTTTCTCAATATTT | 4734 |
rs528568271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886293 | ATTGGACAGATATCC[A/G]GACAGAAAATCAACA | 4734 |
rs528579064 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826663 | TGAGCAGCAAGGTGC[C/T]TGAAATCCAGTCCAT | 4734 |
rs528587964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972136 | CTAAAGGGTGTCCCA[A/C]AGTCTAAAAGAAAAG | 4734 |
rs528597184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929045 | AGATGAGAGGGCCAT[C/T]AGCAGCTGAGTAATT | 4734 |
rs528608302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895594 | TGTGTGTTAAAATCA[C/G]CTGATAGGCTATTTA | 4734 |
rs528616822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977422 | TACACTCTATGACAT[C/T]TGCACAATGATGAAA | 4734 |
rs528628915 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991028 | TTTTAGCATACTTCA[A/G]TGCTAATATGCTCAG | 4734 |
rs528657941 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827331 | TTGAGACACTTTTCT[A/C]TCTGGGATAAGGGGC | 4734 |
rs528694516 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976823 | TATTTTTAGTACAGA[C/T]GGGGTTTCACCGTGT | 4734 |
rs528725869 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55840599 | AAAGTTTATACTTAA[C/T]ACTAACCATCCAACA | 4734 |
rs528730778 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855123 | GAGCAATGATGCATA[C/G]GTGGGCGACCTCTCA | 4734 |
rs528799076 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989641 | GATAGCGGAGACTCT[C/G]AACTCTTTCCTCTTT | 4734 |
rs528810952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855383 | AGAATCAGGACATGG[C/G]AACAGTCTGCTTGGA | 4734 |
rs528813993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908657 | TTTAATAAGATCGCC[A/G]TGTTATTTACATGCA | 4734 |
rs528838151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838399 | ACAGCTTTTGTTACT[A/G]GGAAATGAATGTAAA | 4734 |
rs528843428 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901036 | AAGAATGCTATTAGC[A/G]AAAACTGGTATCTAA | 4734 |
rs528863004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937727 | TGGAAGAACTTAATA[C/T]TGTTAAAATGTCCAT | 4734 |
rs528886826 | in-del | -/TGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967245 | TCCCATTCAACAGAC[-/TGT]AACAGAGTATATAAT | 4734 |
rs528896212 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55860074 | CCAAATCCCTGAAGT[A/C]TTTTCTAACATTCTG | 4734 |
rs528899333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839269 | CCTGACCTCAAGTGA[G/T]CCACCTGCCTCAGCT | 4734 |
rs528902246 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949084 | AATATCCAGAATCTA[C/T]AAAGAACACAAACAA | 4734 |
rs528904479 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897161 | TTGTATTTTTGTAGA[G/T]ATGGGGTTTCACTGT | 4734 |
rs528905520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943691 | CCCTCATGGAGAACT[C/T]CTATTAGGGCAGTGT | 4734 |
rs528912585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887660 | TTACTCAGAGACCAA[A/C]ACCAAACAGACACAA | 4734 |
rs528926381 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831220 | CTACCGCACCCAGCC[G/T]CCTTAACATACTTTT | 4734 |
rs528962687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943228 | TGTGCAGCCTGATCA[G/T]GTGGTAGAAAAGAAA | 4734 |
rs528991157 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949113 | AAATTTACAAGAAAA[A/C]AACAACCCCATCAAG | 4734 |
rs529027859 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903977 | CCAGCCTGGCCAACA[A/C/T]GGTGAAACCCCATCT | 4734 |
rs529037810 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931003 | ATTTTAAAAACTGTA[C/T]ATACAAGGCATATAA | 4734 |
rs529039147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992278 | TCACTTTATTTCTCT[C/T]CTGGCAGCAATAGCT | 4734 |
rs529051170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955058 | CAGAGTCTTGCAACG[G/T]TGCCCAGGCTGGAGT | 4734 |
rs529091126 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910427 | GCCTCTATGCCTCCA[C/T]GCCTCCATGCTCTCC | 4734 |
rs529112693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856629 | GGCTCAGAGCATCCT[A/G]CAATGCACAGCCAGT | 4734 |
rs529120431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954426 | ATATACTATTAAATA[C/T]AAATACAAAATGTAA | 4734 |
rs529138217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863992 | TATCAAGTCATAAAA[C/G]AGCCAAAGAAAGATT | 4734 |
rs529170681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953783 | TGGAGTGCAATGGCA[C/T]GATCTCGGCTCACTG | 4734 |
rs529181327 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965904 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAATTACT | 4734 |
rs529184623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845466 | ATAACATATGTAAAC[G/T]TCTAAGAAGAACGCC | 4734 |
rs529186240 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874739 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 4734 |
rs529200998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871286 | GTTTCATGTCTTTTC[A/C]ATTGGAAAAGAAGCC | 4734 |
rs529205814 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938694 | AAATGGGAAAAATAT[C/T]TGCAGACCATGTATA | 4734 |
rs529209714 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954707 | TTTTGTATTTTTAGT[A/G]GAGATGGCATTTCTC | 4734 |
rs529213860 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852276 | CTCCAGCCTGGGCGA[C/T]AATACTGAGACTCCA | 4734 |
rs529223615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859585 | GCCTGTAATCTCAGC[C/T]ATTCAGGAGGCTGAG | 4734 |
rs529232096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985804 | GCTTAACTGTTCAGA[C/G]ATGGTCCAAGAGTAT | 4734 |
rs529238553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830373 | AACACCTGTTCGTTG[A/G]GTGTCACCAACTCCT | 4734 |
rs529291727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905473 | CAACAGATATCTGGA[A/G]GGAAATGTCCAGTAT | 4734 |
rs529304830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956597 | TCATATATATGTGTA[A/T]ATATTCTCTCTCTCG | 4734 |
rs529310500 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912333 | TATAATCTTGAGATT[A/T]GTGTTAAAGGCTTTG | 4734 |
rs529343103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962409 | TAGTCTACAGGTTTA[C/T]TGTTTGTTTTCCATT | 4734 |
rs529354248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911690 | GCGCGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 4734 |
rs529362332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993100 | GCCCGGCCTCCGCCA[C/G]AGCAAGCAAATCAAC | 4734 |
rs529376046 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945171 | AATGACTTTGATGAG[C/T]TGACAGAAGTAGGCT | 4734 |
rs529376871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920369 | GCTCCTAAAACCGGT[A/G]GCTGAATGTGTACAG | 4734 |
rs529404499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961787 | TTGTGGTAATATTAT[G/T]ATGAAGCAATAAACT | 4734 |
rs529427513 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872618 | GTTTATCAAATGCTA[A/C]CTTGACAGTGCTTTC | 4734 |
rs529450323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968369 | ATACAATCTTAATAG[A/C]AAAAATTATTAAATT | 4734 |
rs529465805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961094 | GGTAGGAACAAACTG[A/G]ACACAGACAAGAGCT | 4734 |
rs529497008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844019 | TGATGATAGAGATGG[A/T]AGCAATGTTCTGCAG | 4734 |
rs529513103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872085 | TCGAGTTAGGTAATG[G/T]TTTTAGATGAATTCA | 4734 |
rs529515976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851554 | TAATCTTGGCTCACC[A/G]CAACCTCCGCCTCCC | 4734 |
rs529559176 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844507 | TTTGAACTGAGTAGT[A/G]GACAAGTGCATGCAT | 4734 |
rs529562985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938308 | TGGTTGCGGTGAGCC[A/G]AGATCGTGCCACTGC | 4734 |
rs529588145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979909 | AACTTTTATAATTAT[A/C]ATTATTACTTTTTTT | 4734 |
rs529588558 | in-del | -/T | 0.139564 | 0.224285 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866220 | GCCCAACCTTTCTTC[-/T]TTTTTTTTTTTAAAT | 4734 |
rs529621906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867248 | ACTCCTCTAGTCATT[A/G]GCTACACAGAAGGTA | 4734 |
rs529633212 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977029 | AATGATTCCACTGGC[A/T]AGCAGTAGCTTGTAT | 4734 |
rs529638661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920995 | AGAGCATCTAACACA[A/G]TAGATATACTAAATG | 4734 |
rs529653311 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874974 | GTAAGACTCCGCTCA[A/C]AAAGAAAAAAAAAAA | 4734 |
rs529655408 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826513 | GGGAGTGGATTCCCT[C/T]CTAACTGGGAAACTA | 4734 |
rs529660362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888362 | TGTAAAATAAATCAA[A/G]AAGGCAATCCTATTT | 4734 |
rs529668516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957195 | CTTCCAGTAGTTTTT[C/T]CTGTAGATTCCTTGG | 4734 |
rs529672336 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857189 | GCATGTTTATGAATA[A/T]ACAGAAAAAGTTTCT | 4734 |
rs529682676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963950 | TTTCTCCTGGTCTCC[A/G]TAGTTTTGGGTAGGA | 4734 |
rs529683193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874154 | GAAAATAAAAAGTAA[C/T]GTGGTACAACTTCTG | 4734 |
rs529688180 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927600 | AGAAAAGTTTGGTTA[G/T]TTAGGGTAGAGCCAG | 4734 |
rs529698387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970129 | AGTAGCCAGACTATA[A/G]TAGCCACAGGTCTGG | 4734 |
rs529732762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963234 | CCTCCTGGGCTCCAG[C/T]GATCCTCCAACCTCA | 4734 |
rs529747022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969604 | AGCAGCAACCAGAGT[C/T]CTGAAGCCCCCATTC | 4734 |
rs529775208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933210 | ATTATAAATCATGCT[A/G]CTATAAAGACACATG | 4734 |
rs529792079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890728 | AAAAATCTGCCAGAC[C/T]GTTTTCCAAAGTTGC | 4734 |
rs529795998 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933294 | CCAAATGTCCATCAA[C/T]GATAGACTGGATTAA | 4734 |
rs529807312 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951017 | TCAATGACGTGTGGA[A/T]AAAAAGAAATGCATT | 4734 |
rs529833962 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879511 | ACCCTTCCAATAAAT[A/T]TTGGAATATTATACA | 4734 |
rs529838054 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847864 | TTTGCATTTTTAGTA[C/G]AGACAGGGTTTCACC | 4734 |
rs529855650 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956574 | ATTTTTTGTTAAACA[A/G]GAGCTGATCATATAT | 4734 |
rs529872839 | in-del | -/C | 0.208169 | 0.246476 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983505 | TTACTCAATGGGGTT[-/C]TATTGCCCCACTCTT | 4734 |
rs529904268 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855194 | TGTTATTTAGACAGA[A/T]AACCCACTCATGGGA | 4734 |
rs529918411 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974515 | TTGATGCAAAAATCC[A/G]TAATAAAATACTAGC | 4734 |
rs529921408 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880251 | GAGCCGAGATCGCAC[C/T]ATTGCACGCTAGTCT | 4734 |
rs529925242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899358 | AATTTGATTACCTGG[C/T]TATCTGATCAAATGT | 4734 |
rs529932141 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55954923 | TCTTCAGATATCTTT[A/G]TTTAATTGTTTCTCT | 4734 |
rs529941051 | in-del | -/T | 0.327914 | 0.237549 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839033 | TATTTTTTAATTTAA[-/T]TTTTTTTTTTTTTGA | 4734 |
rs529958774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945197 | AGGCTTCAGAAGGTC[A/G]GTAAAAACAAACTTC | 4734 |
rs529965092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939099 | TAATAGAGTGAGACC[A/G]TGTCTCGAAAACAAC | 4734 |
rs529981780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986270 | AGGATGAAGACTTGA[C/T]GAGAAATAGGATATT | 4734 |
rs530017275 | snp | C/T | 1.65348e-05 | 0.00287526 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842136 | TTGCTCGGCGAAGTT[C/T]CATTTCAAATTTGTT | 4734 |
rs530022462 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934612 | CAATAAATATAAAAA[A/T]AAACTGTAGATATAC | 4734 |
rs530023076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944836 | GCAATATTTGCTGTT[C/T]TGCAGCCTCCACTGG | 4734 |
rs530045159 | in-del | -/CTGGT | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964648 | GACTGAATTTTGCTG[-/CTGGT]GTGTGTGTGTGTGTG | 4734 |
rs530068232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884946 | TCAATATTCAAGTAC[A/C]AGAAGGTTATAGAAC | 4734 |
rs530081111 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832068 | AGAATCTTACTTTAC[C/T]GAAAACTGCATTAAC | 4734 |
rs530081258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941373 | CTGAAATAGCTTCAT[C/T]CCACATTTGGTATGT | 4734 |
rs530113944 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984266 | AATTATTTTATTTGC[A/G]TATTAGTAGCAGGAA | 4734 |
rs530132370 | in-del | -/AT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923657 | CTCAAAAAAAAAAAA[-/AT]AAATATATATATATA | 4734 |
rs530137334 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843683 | AAAGCCCTATAGAAA[C/T]ATAATAATGTAAGCA | 4734 |
rs530174837 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982497 | TCAAGACACAAAAGA[C/G]TACATAATGTACATT | 4734 |
rs530178129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901281 | TATGTTTTACATTTA[C/T]GAAATCGTCTCCATA | 4734 |
rs530190210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902079 | TTAAGGCTTAGATAA[A/G]ATGTGGTTAGATGAT | 4734 |
rs530192352 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906346 | ACGTATGTTTATTGC[A/G]GCACTATTCACAATA | 4734 |
rs530199510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55892126 | CAAAAATTAGCCAGG[C/T]GTGGTGGTGGCCACC | 4734 |
rs530204561 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946067 | GCCAAATTATAAAGA[A/T]CATCGATGCTATGAA | 4734 |
rs530220420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946394 | TTCAACCAACAAAGA[C/T]CAAAAGAGACAAAGA | 4734 |
rs530264556 | snp | A/G/T | 0.000105037 | 0.00724619 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55951405 | CTTCATTCCACTTTG[A/G/T]ATTCAAACTCTAAAA | 4734 |
rs530271660 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55878610 | TTCTGCTCCTTGTAT[A/T]TTCTTAAGAGAATAA | 4734 |
rs530303067 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995082 | TTATGATTGGTAGGA[C/T]CCATTTCATTCATAT | 4734 |
rs530354950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913837 | CTACAAATATTTCTA[A/C]ATGAATTATTCCTTT | 4734 |
rs530381204 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905283 | GTCACTAACCATGGC[C/T]GTAAAACATAACTGG | 4734 |
rs530419640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867964 | GGGAGGCTGAGGCAT[A/G]AGAATTACTTGAACC | 4734 |
rs530452509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947317 | GCAATAAAAAATGAT[A/T]AAGGGGATATCACCA | 4734 |
rs530473429 | in-del | -/CCTTGAAAAAAGGTTAG | 0.0121561 | 0.0770084 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945260 | CAAGGAACCTAAAAA[-/CCTTGAAAAAAGGTTAG]CCCAATGGCTAACTA | 4734 |
rs530487661 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843331 | CGAAAGCTACTATTA[A/T]TGTCTTCATTTTACA | 4734 |
rs530492205 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979225 | TAATTATATTAATTG[-/A]AAAAATAAGAATGCT | 4734 |
rs530492610 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989790 | GAAGAGCTGGAAGAG[A/T]AGGTGCTAGGCTGGA | 4734 |
rs530493357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947733 | AGATGCAGAAAAGGC[C/G]TTTGACAAAATTCAA | 4734 |
rs530522846 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909665 | CTCTTGTCCTGGCTT[A/C]TCCTGGTCTGTCTTG | 4734 |
rs530530983 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977291 | TTTACATTGTATTAC[C/T]AATGCATACAGTATT | 4734 |
rs530533178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843844 | AAAGGCCTACTCTGG[A/G]CCAGGTGGTATTGTA | 4734 |
rs530557194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953697 | TCTGCCCGCCTTGGC[C/T]TCACAAAGTGCTGGG | 4734 |
rs530565284 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882066 | CAAACGTGCAGAAGT[C/T]TCTTCCTAATTTTGG | 4734 |
rs530585150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909061 | TTCTACTAAGGTAAT[C/T]AAAATGTTTCCTAGT | 4734 |
rs530626467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965578 | ACTGCCATGTTTTCT[C/T]CAGATTCAGAGATTC | 4734 |
rs530634531 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869774 | ACCCACTAGGTACCA[A/G]GGGGTCTACAAAGGG | 4734 |
rs530668196 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994730 | TGGGAACAAGGCTAT[A/G]GCCCATATTACTGGT | 4734 |
rs530693630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869816 | CAAGTTCCAGGGCAG[A/C]AGATATCTAGGGAAA | 4734 |
rs530696318 | snp | C/G/T | 0.000140263 | 0.0083734 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830009 | TTAAAACTGAAAGAA[C/G/T]AGAGAGGAAGTGGTT | 4734 |
rs530701730 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943703 | ACTTCTATTAGGGCA[A/G]TGTGGATGGGAAATG | 4734 |
rs530736760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928242 | GTCTCGAACCCCTGA[C/G]CTCAGGTGATCCACC | 4734 |
rs530747809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971213 | GCAGAAGAAAGAATT[A/T]GCGAGCTTGAAGATA | 4734 |
rs530777162 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896386 | ATGGGGTTTTGCCAC[A/G]TTGGTTAGGCTGGTC | 4734 |
rs530810133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925173 | AGAGCAGACTAGTCA[C/T]GTGTCACTCATTTTC | 4734 |
rs530813507 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917777 | TTTATATTTTGACTA[C/T]TAAAACTGCCAAGAA | 4734 |
rs530818229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967365 | CACATATTGAAGTGC[A/T]TAGGAATAAAGTATC | 4734 |
rs530829159 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971516 | TGTAATCCCAGCTAC[A/T]CAGGAGGCTGAGGCA | 4734 |
rs530844515 | in-del | -/A | 0.165853 | 0.235413 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917834 | ATATATGCAGATTAG[-/A]AAAAAAAAAACTATA | 4734 |
rs530851481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836033 | CTCTCACCCAGCATA[C/T]TCAACTGCCTGTGGG | 4734 |
rs530868747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976700 | AGTGGTGCAATCTCA[C/G]TTCACTGCAAGCTCT | 4734 |
rs530881776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954611 | CTCACCGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 4734 |
rs530885910 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939231 | GGGAACTGGTGGGAG[C/G]TGATTGGATCACGGG | 4734 |
rs530899633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864140 | CTTTTATATGAGAAA[C/T]CTCACAAAAGAAAAG | 4734 |
rs530961961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871342 | ACACAAATTTAGGAA[C/T]GTAGTACATTTTCTA | 4734 |
rs530967121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887372 | GACCAAGTATATGCA[A/C]TAAATTGGAAAATCT | 4734 |
rs531029150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978247 | AGATACATTTAACTT[C/T]TAACCTTTCTCCTTG | 4734 |
rs531030440 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896334 | ATTAGAGACATGCAC[A/C]GGTATGCCTGGCTAA | 4734 |
rs531034782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972216 | AAAAGTAAGTACACA[C/G]ACAAATACAGAATAT | 4734 |
rs531037544 | in-del | -/T | 0.491247 | 0.065573 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976797 | CCACACCTGGCTAAT[-/T]TTTTTTTTTGTATTT | 4734 |
rs531056377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930310 | AAGTTCACTGACCCT[C/T]GTCCTAGACAATCAC | 4734 |
rs531059112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943095 | GAAATTTCTAAGCAG[C/T]AAAGTGTTCAAGAAG | 4734 |
rs531064297 | snp | A/G | | | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834074 | CTGATGATTTGCACT[A/G]TAGCCATTTTTATAC | 4734 |
rs531066025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983794 | TTTTGTATTTTTGGT[A/G]GAGACAGGGTTTCAC | 4734 |
rs531066394 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975018 | CTGCCTCAGCCTCCC[A/G]ACTAGCTGGGACTAC | 4734 |
rs531071827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977470 | TCTCAGAATGTATCC[A/G]TTGTTAAGCAATGCA | 4734 |
rs531071935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856049 | CCCTGTAAGGCAAAC[A/G]TTCACACTCAATCTT | 4734 |
rs531111887 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936957 | GCCATGATGCCCAGC[C/T]GATTTTTGTATTTTT | 4734 |
rs531127552 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850486 | GATTTTAAGGAACTA[C/T]ACATAAGAGATGATT | 4734 |
rs531133847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856502 | TTTTATTGTTGTTTT[A/T]ACTTCAAGTTTCATC | 4734 |
rs531158403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983367 | CAAATCCTTAACACG[A/G]CATGCCAGGCTTGCC | 4734 |
rs531212829 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895674 | GGTATAATGTGTGAG[A/C]ATTTGCAGTTCTTGG | 4734 |
rs531222025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889099 | AAATGGACAAATGGG[A/T]TCACATCAAGGTAAA | 4734 |
rs531245385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938519 | CCATAGAAGAAAACA[A/G]AGAAGAAGCTTCTTG | 4734 |
rs531274973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903579 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 4734 |
rs531281129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897992 | TGAATTTCTATTATT[C/G]AAATGCCATGATATT | 4734 |
rs531287616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881290 | GGGATTACAGGCACA[C/T]GCCACCACTCCCGCC | 4734 |
rs531305444 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952665 | TTACCCCTAACCTAG[C/T]GAGTCAGGAGTCCTC | 4734 |
rs531306216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937926 | ATATCACAAAGCTAC[A/G]GTAATTAAAACAGTA | 4734 |
rs531311686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944162 | TGCAGCCCACAGAGG[A/G]CAAGCCGAAGCAGGA | 4734 |
rs531346219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905179 | CATGTTAAGAATTCT[A/G]TAAGTAAATATCACT | 4734 |
rs531355041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985431 | GGAGGGGAGGACGGC[A/G]TTGCACAGGGATGCT | 4734 |
rs531375812 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983681 | CAGTGGCGCAGTCTC[A/G]GTTCACTGCAACCCC | 4734 |
rs531411001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888489 | GAAAGGTATGTTCAT[A/G]GATCAGAAGAATCAA | 4734 |
rs531414352 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983076 | GCAGTGAACCGAGAT[G/T]GCGCCATTGCACTTC | 4734 |
rs531461054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853129 | TGTTTGCTTTAAAAC[A/C]AATTATATTTTATTT | 4734 |
rs531465193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911072 | GAGCCCCACTGGACT[A/G]TTTACAGTGGAGATT | 4734 |
rs531481653 | snp | C/G | 0.021333 | 0.101051 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979527 | CCCGGCTAATTTTTT[C/G]TATTTTTAGTAGAGA | 4734 |
rs531523343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853724 | CTGGGCATGATGGCT[C/G]ACCCCTGTAATCCCA | 4734 |
rs531544128 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918554 | TTTCCTAAGTAAAAG[A/C]AAATATGTAAAACAT | 4734 |
rs531546996 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981378 | CCTCCTTTTTTTTTC[C/T]TTTGAGCAACATGCT | 4734 |
rs531565566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949151 | CGAAGGATATGAACA[G/T]ACACTTCTCAAAAGA | 4734 |
rs531575465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945252 | ACCCATTGCAAGGAA[C/T]CTAAAAACCTTGAAA | 4734 |
rs531576683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857991 | CATTCTTTGCCTCTC[C/T]TCAGAGGCAAGCAAA | 4734 |
rs531593533 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986751 | CCCACCACCACACCC[A/G]GCTAATTTTTTTTTT | 4734 |
rs531605014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992375 | AATTGCCCACCCTTT[A/G]TAAACAAAGAACTCT | 4734 |
rs531624740 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854114 | CGAGATCGCCTGGGC[A/G]CTCCAGCCTGGACAA | 4734 |
rs531629347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955124 | CCTCCCGGGCTCAAG[A/C]AATCCTCCCACCTCA | 4734 |
rs531639782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857395 | GTATGGTGGTGCGAT[C/T]TTGTCTCACTGCAAC | 4734 |
rs531649992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985677 | AGTATGAATTCATGA[C/T]TTTTAAATTTATGTA | 4734 |
rs531655372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845934 | GGGATTAAAGGTGTG[C/T]GCCATCACACCTAAC | 4734 |
rs531673011 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902114 | TCCAAATCTGAACTC[G/T]AATCTCTTGGTTTTA | 4734 |
rs531680878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950125 | ATCAAGTCTGGAATT[C/T]ATTCTGGTTAAATAG | 4734 |
rs531681879 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994410 | GTGAACTAGGACCTC[C/T]TGTAGAATAACTCCT | 4734 |
rs531708732 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900249 | CCTGGAAATACTGCT[C/T]CACAGGACTGGATTT | 4734 |
rs531712372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925904 | GGAAGAAAAAAGTAT[A/G]CTAATCTTAACTATA | 4734 |
rs531715795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859611 | CTGAGGCATGAGAAT[C/T]GCCTGAAGCTGGAGA | 4734 |
rs531739729 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906591 | GAACAATGAGAACAC[C/T]TGGACACAAGAAGGG | 4734 |
rs531741550 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899461 | ACTATAACATATCAA[A/T]GAAAACAGGAAAAAC | 4734 |
rs531744894 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923997 | AAGATGCTAAGATGA[-/G]GGTTTGAGATTGGAT | 4734 |
rs531756931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944932 | GAACTGAGTGTTAGA[C/T]GGAAAACTAACAAAC | 4734 |
rs531769645 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947557 | AAGTCCAGGACCAGA[C/T]GTATTCACAGCTGAA | 4734 |
rs531771269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860111 | AAACACCAATGGTGC[A/G]TGTTCTCCCTTGCTG | 4734 |
rs531783994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986406 | TAAGGTCACTGACAG[C/T]GTTGGGACAAGTCAG | 4734 |
rs531801073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920512 | ATCACCATAATGAAA[C/T]GACAATATTTTATAA | 4734 |
rs531814430 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906219 | CATTGTGGAAGACAG[C/T]GTGGCGATTCCTCAC | 4734 |
rs531834801 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982967 | TCTCTACTAAAAATA[C/T]AAAAATTAGCAAGGC | 4734 |
rs531873846 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993637 | GGAGGAGAAGCGGGA[A/G]GAGGCGGGGAAGAGT | 4734 |
rs531896913 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932376 | ACCACACATCTACAA[A/C]CATGTGATCTTTGAC | 4734 |
rs531960927 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995176 | GGCACTTAATCAAAC[A/G]TGACTACAAAATTAC | 4734 |
rs531980097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860948 | CATGGGTAGGCAGAC[A/T]GGTATATTTAGAGTA | 4734 |
rs532010210 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914571 | ACTTAGAATTCAATA[A/T]TGTTGAAAGAGTGAG | 4734 |
rs532024717 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872679 | CATCACAACTCAAAT[A/G]AAAACTAGCTGAGCA | 4734 |
rs532028986 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945344 | GGAGCTGAAAACCAT[A/G]GCACAAGAACTTTGT | 4734 |
rs532045321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926006 | TATCATATACATATA[A/C]AGTATGTAAAATACA | 4734 |
rs532047513 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931799 | CATCCCTTTGAAGTA[C/T]ACAATTCAATGGTTT | 4734 |
rs532048100 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863460 | CAAAAAAGTAATAAA[A/G]GTATGTGAGGTGATT | 4734 |
rs532054878 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889759 | AGGCTGGAGTGCAGT[G/T]GTGTGATCTCAGCTC | 4734 |
rs532062507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921806 | ACAGTAAATGCTTAA[A/G]GAATGTTAATTCACT | 4734 |
rs532066121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968522 | CTAAAATATACATCA[C/T]TGAGACAAATGATAA | 4734 |
rs532095422 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55951428 | CTCTAAAAAATAATA[A/T]ACATAGTATAACTAA | 4734 |
rs532097387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958115 | CTAGAACTTAACGTA[A/T]AATAAAAAAAAGATG | 4734 |
rs532098229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868627 | CCTTCCACCATGATT[A/G]TGAGACCTCCCCAGC | 4734 |
rs532122254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922205 | TAAATACATAAATTA[C/T]AGCATTATGATTTTT | 4734 |
rs532129867 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883740 | ACAGAAAGAGAAAGA[C/G]AGAGAGAGAGACTCT | 4734 |
rs532144548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964889 | CCCTCCCTCGGAAGT[A/G]AGTGAGTTCTCATTC | 4734 |
rs532190518 | snp | C/G | 5.89026e-05 | 0.00542659 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842214 | AGTTCAACATAATAA[C/G]AAACCCATCTCTCAT | 4734 |
rs532191249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882824 | CAACCTGGATACCAG[C/T]TCAGCCATAGTAGGC | 4734 |
rs532203101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855311 | ATGGTTGGGGAAGAA[A/T]ATGAGAAAGCCATTC | 4734 |
rs532210056 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55946449 | ATCAATTCAACAAGA[A/G]GAGCTAACTATCCTA | 4734 |
rs532228892 | in-del | -/AAAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925082 | AAGAAAAACAAAACA[-/AAAC]AAACAAACAAACAAA | 4734 |
rs532234986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981917 | ATTTAAAATACTAGA[C/T]TTTATTCAATCAATA | 4734 |
rs532266721 | snp | A/G | 1.64789e-05 | 0.0028704 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848442 | ATATCTGAAGGGAAG[A/G]AAAAGAAAAAAGATG | 4734 |
rs532266809 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827337 | CACTTTTCTATCTGG[G/T]ATAAGGGGCTGTGTT | 4734 |
rs532282771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890793 | TTTCAATTCCTCCCC[C/T]TTCTTACCAACAATG | 4734 |
rs532306909 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920342 | ACAGGGTCTCCACCC[A/G]GAATATAGGTGGCTC | 4734 |
rs532321537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933828 | TCAGCCATGCTAAAC[C/T]GTGAGTCAATTAAAA | 4734 |
rs532329590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849092 | ATCAAAAGGAATAAC[G/T]ATCAGTTCTCAGGGA | 4734 |
rs532343128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900346 | TGGGATCTTTTATGA[C/G]AAGAGAAGAGCTAAG | 4734 |
rs532357842 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846619 | ACCGTCCTCCAACAC[A/T]GTCAAAGACTAGGCC | 4734 |
rs532381704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842641 | CCTTGGCCTCCCAAA[G/T]TGCTGAGATTACAGG | 4734 |
rs532387287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933298 | ATGTCCATCAATGAT[A/G]GACTGGATTAAGAAA | 4734 |
rs532413480 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935337 | TCTTCCTAGCTAAAA[G/T]AATTATAATTTTATT | 4734 |
rs532443956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836150 | CTCTAGTCCTTCTTT[A/G]TCCCTTCCTTTGCCC | 4734 |
rs532475862 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934850 | ATATATTCCTATATA[A/C]AATGTTCTGCTTTTT | 4734 |
rs532518202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902760 | AGGAGGCAGAAAACA[A/C]AGTATGTGTTAATCA | 4734 |
rs532546684 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893910 | ATTGCATTTGTATAG[A/C]TGCTTCTTTCCTACT | 4734 |
rs532560722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941394 | TTTGGTATGTTATGC[G/T]TTAACAATCAATCAG | 4734 |
rs532561425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885560 | AAGAGGACAAAGTTA[C/G]AGTTTTTATTAGTTT | 4734 |
rs532562013 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970890 | AGACATTAGTGAACA[A/T]CCACAAGCATCAACA | 4734 |
rs532569570 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835974 | ACAGGCCCTGTATAA[A/G]CTGGTCTGTTAGCTC | 4734 |
rs532577507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902230 | AATAACTGACATGCT[A/C]CATCCCAAAGAGATG | 4734 |
rs532620956 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946460 | AAGAAGAGCTAACTA[C/T]CCTAAATATATATGC | 4734 |
rs532637416 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883319 | AAAGAGAAGGGAAGA[A/G]TGGGAAGAACTTTGT | 4734 |
rs532641881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907927 | AGGCTATGAATCAGA[A/C]TCCACTGTGGAAACT | 4734 |
rs532649636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988951 | TAAAATAATTTTAAA[A/G]TAGGACGGGCGCGGT | 4734 |
rs532667146 | snp | G/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983019 | CCCAGCTACTCGGGA[G/T]GCTGAGGGAGGAGAA | 4734 |
rs532680662 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976404 | AATCTGATATTAAAA[A/T]GGGCAAAAGATCTGA | 4734 |
rs532708124 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995718 | TAGAGTAATTATTGT[A/G]TCCCGGTCAACAGCT | 4734 |
rs532748452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843941 | AGTTTCTCATCTGGC[A/G]TATATGTGAAAAACA | 4734 |
rs532785561 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826576 | ACTTCGTTCTGAATT[A/T]ACACTCCGAACTCTT | 4734 |
rs532801896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895792 | TTGTTAATAGCTGAA[A/G]ATAAATGAGCAGGCC | 4734 |
rs532815791 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942878 | CTAGAGACTTGTTGA[A/T]TGGTTGTGACCAAAA | 4734 |
rs532831752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857166 | TCTACAAATATATGT[A/G]TATGCATGCATGTTT | 4734 |
rs532845516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952130 | TCAGGAGATCAAGAC[C/T]GTCCTGGCTAACATG | 4734 |
rs532848613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859273 | TGCTGGGATACTTTA[C/T]TCTGAACCCTATGGA | 4734 |
rs532851027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954280 | CTCGAACTGTTCCTT[C/T]GGTGGCTTACTTAGG | 4734 |
rs532852203 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847421 | TTGAACTCCAAGGAG[C/T]TGCCTTTTTGAGCCA | 4734 |
rs532854762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947796 | AGGTATTGATGGGAC[A/G]TATCTCAAAATAATA | 4734 |
rs532861752 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932604 | CATTCAGGCCATAGG[C/T]ATGGGCAAGGACTTC | 4734 |
rs532870998 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906550 | AAAAACCAAACACCC[C/T]ATGTTCTCACTCATA | 4734 |
rs532885347 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896377 | TTTGTAGAGATGGGG[C/T]TTTGCCACGTTGGTT | 4734 |
rs532892223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838330 | ATACTAGTTTTACTA[A/C]AATAAATATGGAACG | 4734 |
rs532905111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943197 | AAAGGAAAGCAGAGC[A/G]TAAAAGTTGGGAATA | 4734 |
rs532913228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953728 | ATTACAGGCATGAGC[C/T]AACATGCCCGGCTTA | 4734 |
rs532958080 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964394 | TTTAAGTTCAGTTAA[C/T]CTTTCCTCTTCTCCA | 4734 |
rs532978211 | in-del | -/CT | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970169 | GGCCATGGGCAGAGA[-/CT]CTGTCTGCTTGAGAA | 4734 |
rs532988337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837179 | TCACACTGGTAACCC[C/T]AGCACTTTGGGAGGC | 4734 |
rs533014624 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991373 | ATAAATGGCAAATGA[C/T]AGTGGAGAGGGCAAC | 4734 |
rs533017697 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956849 | TGAAAAAACTTGCTG[A/G]GATTTTTATTGGGAT | 4734 |
rs533031832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910299 | TCTGGCTTTTAACCC[C/T]GCATTCTCCTGAGCC | 4734 |
rs533053973 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958961 | ATTGATGTCTTCAAA[A/T]AACAAGCTTTTGATT | 4734 |
rs533055097 | snp | C/T | 1.6489e-05 | 0.00287128 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830486 | CTCTCTGAGGCTTTG[C/T]TCTATCAAGGTCCAA | 4734 |
rs533071517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929550 | ATCCATGTGTACTCA[C/T]GTTTAACTTCCACTT | 4734 |
rs533089191 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923458 | CAGGACCATCCTGGC[A/C]AACATGGTGAAACCC | 4734 |
rs533094230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909722 | GAGAGTGGACACAAA[C/T]GGGTGAGGCCTCACA | 4734 |
rs533098336 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979377 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 4734 |
rs533164256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959531 | CTCCTATTATCCCCA[C/T]CTCCTAATATTCATG | 4734 |
rs533208889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961645 | CCGGATAATTTTTTG[C/T]ATTTTTAGTAGAGAC | 4734 |
rs533238250 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899447 | GATTTTTACTGAAGA[A/C]TATAACATATCAATG | 4734 |
rs533248738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872068 | AATTGGCTTTGTGCA[C/T]GTCGAGTTAGGTAAT | 4734 |
rs533257376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869909 | ATTGTTATGACACAA[A/G]GAAGATGCTAAGGAA | 4734 |
rs533279065 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896757 | AAATCTGTGTAAAAA[C/T]TGCAAAGGAAAAGGA | 4734 |
rs533292174 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939505 | GAAAACGGACTAATA[C/T]AAGCAACAAAGAACC | 4734 |
rs533301526 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972086 | AACAAAAGCTGAGGG[A/T]TTTAATCAACATCAG | 4734 |
rs533309029 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880459 | AAACCTGAAATATAA[A/G]AGAGTACTTCCTGCA | 4734 |
rs533327823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858224 | CACTATATGGTTGCC[A/G]TGTATTACTTTAAGT | 4734 |
rs533349207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973311 | TGGGACGCCAAGATG[A/G]GAGGACTTCTTGGGC | 4734 |
rs533357859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911388 | GATGAACTCCAGTTT[A/G]CCTATCAAGACTCGG | 4734 |
rs533384343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888331 | TAGCATTTCTCAATG[C/G]CAAGAGTAAACAATT | 4734 |
rs533402318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937602 | GGAAGTTATAGAAAA[C/T]AAAATAAAAAATAAG | 4734 |
rs533402843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850147 | ACTAAACAATTTTAA[A/G]CCTTATCTTAAAATA | 4734 |
rs533418976 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918738 | GAATGCGTACAATAG[C/T]TGAAAACTTAGTAAT | 4734 |
rs533434645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972914 | ACAATGATAAAGGCA[C/T]CATTTCAACAAGAAG | 4734 |
rs533443508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938793 | AAAAAACAAGCATCA[A/T]CAACAACAACAATAA | 4734 |
rs533448640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979394 | CTCTGTCGCCCAGGC[C/T]GGACTGCGGACTGCA | 4734 |
rs533466117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961026 | CCTGACTGATACACT[C/T]GACCCTAACTTGTTT | 4734 |
rs533467416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843423 | TGGAGCTACATTGCC[G/T]CACTAATCTTTTGTA | 4734 |
rs533480961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925254 | TTTTTCTAACAGAAC[A/G]AAAGGAAGTAAAAGA | 4734 |
rs533498961 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55936070 | TGCTTATTGTGAAGG[C/G]AGTTTTCATTGCTAC | 4734 |
rs533516455 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975142 | AGGCAATCCACCCAC[C/T]TCGGCCTCTCAAAGT | 4734 |
rs533545058 | snp | C/G/T | 0.000112177 | 0.00748838 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55924650 | ATATAACTTACCAAT[C/G/T]GGTTTTCGTCAAACA | 4734 |
rs533617445 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852466 | CGTTCTGGAATTGTG[A/G]TCTACATAATATGAT | 4734 |
rs533626891 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55993103 | CGGCCTCCGCCAGAG[A/C]AAGCAAATCAACAGC | 4734 |
rs533660851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925542 | ATGAATAAAAATTAC[A/G]AGCAATATTTTGTTT | 4734 |
rs533678829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866274 | TTCTCTCTATTTTTT[A/C]TTTTTATTGCCCAAA | 4734 |
rs533682885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937001 | TTTCACCATATTGGC[C/T]GGGCTGGTCTTGAAC | 4734 |
rs533728228 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865976 | TCATTCTGACACCCA[G/T]GTTGGAGTGCAGTGG | 4734 |
rs533729667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846010 | CAGGCTGGTCGTGAA[C/T]TCCTGACCTCAAGTG | 4734 |
rs533730224 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881838 | CTACTGACAATTCGA[A/G]CCAGATAATTTTTTT | 4734 |
rs533731649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839793 | CCATCCTGGTGAACA[C/T]GGTGAAACCCCGTCT | 4734 |
rs533737787 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886197 | AGCACTCAGATATAA[A/T]AAGAAAATATTATTA | 4734 |
rs533742003 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858406 | CTGCCTCTTGGGTTC[A/G]AGCCATTCTTCCAAT | 4734 |
rs533754746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888693 | AAATCACATTACCTG[A/T]CATCAAATTACATTA | 4734 |
rs533775377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911552 | TTTTTTTTTTTGAGA[C/T]GGGGTTTCGCTCTGT | 4734 |
rs533783393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930705 | GATAATTGAATCATG[A/G]GGGTAGTTTCCCCCA | 4734 |
rs533790555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872778 | GTTAACATCCCAAAA[G/T]AACACGGACTATGCA | 4734 |
rs533792648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865338 | CCTACCTCATGCCTT[A/G]TATCAGGATAAGTTA | 4734 |
rs533800942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979575 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 4734 |
rs533803725 | in-del | -/GTATGTAT | 0.128076 | 0.218254 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965654 | TACTAATACTATTTG[-/GTATGTAT]GTATGTATGTATGTA | 4734 |
rs533807343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897255 | TGGGATTACAGGCGT[G/T]AGCCACTGCGCCCGG | 4734 |
rs533858635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872298 | TAATAATAATAATAA[A/T]ATTTAGAAGTAACTT | 4734 |
rs533861441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833323 | TGGGATTATAACCTA[C/G]TGAAGTAACAAAATT | 4734 |
rs533871898 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879217 | AAAAAAGGGAGACTG[C/G]AAGAGTAGATGACAG | 4734 |
rs533876274 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949394 | GGAAGACAGTGTGGC[A/G]ATTCCTCAAGGATCT | 4734 |
rs533883597 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906844 | CTCACGCCCATAATC[C/T]CAATGCTTTGGGAGG | 4734 |
rs533885174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984874 | GCAGAACAATGGGTT[A/C]AGCAATTCAAATCAG | 4734 |
rs533903478 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967879 | TAAGCCAGGCATGAT[A/G]ACTTGTGTCTGTAAT | 4734 |
rs533917302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853206 | TTAGTGAAATAAACC[A/G]CATTTTAAATATCTT | 4734 |
rs533951533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882312 | GCTGACACCCACCCC[C/T]TCCATCCCCTGGCAG | 4734 |
rs533956724 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981499 | GAAACGATCTATAAA[A/G]ATATAAGTGGAAGAT | 4734 |
rs533985649 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55826978 | CAAGATTTTAAAAAA[-/T]GATTTTACACTTTAA | 4734 |
rs533986219 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974727 | ACATCTCTTCATGAT[A/T]AAAAAAAAAACCCTC | 4734 |
rs533994748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973602 | CTACAACAGAATAAC[A/G]CTAGAAATCAATAAC | 4734 |
rs534007852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890360 | TTCACTGCCCATTTC[A/C]CCACCCCTCCTTCAG | 4734 |
rs534050329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838737 | CTTTACTTACACACA[C/T]ATATAAACAAAAATG | 4734 |
rs534063149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887972 | ACAAAAAATGGTATC[A/G]AAGAAATATAGCTCA | 4734 |
rs534066229 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891098 | TTTGGGAACAAAAGA[A/G]CAAAAATCCCACATG | 4734 |
rs534089083 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872803 | TATGCACATGTCTGC[A/G]GGCTGGCTTGGTTAG | 4734 |
rs534101077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944989 | AAAAGGACATACACA[C/T]CAAAACCCCATCTGT | 4734 |
rs534101809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937239 | CAATTTCCATTTGGC[C/T]GAATGCCCAAGAACC | 4734 |
rs534160779 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950195 | ATCCAATTGATTCAA[A/T]ACCATTTCCTCAAGA | 4734 |
rs534181991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933406 | AAGCTAGAAACCATC[A/G]TTCTGAGCAAACTAT | 4734 |
rs534220822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949743 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 4734 |
rs534230518 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942232 | ATTCACTCTTTATAA[C/T]CATGAAATGCCCTCT | 4734 |
rs534243965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911810 | TGGGATTACAGGCGT[A/G]AGCCACCGCGCCCGG | 4734 |
rs534254728 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898116 | AAACTACCCCACTTA[A/G]TAGTTTAAGTATAAT | 4734 |
rs534260230 | snp | C/G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924374 | GGCAGGACAAAGAGG[C/G/T]TGGTTTTCTGTCCTC | 4734 |
rs534316564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830742 | TATCCCTCTGTCACC[C/G]AGACTGGAGTGCAGT | 4734 |
rs534322217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901390 | CTTGTGGCCCACATA[C/T]AGGACTTTCTGGCTA | 4734 |
rs534336253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889528 | AAAAATTAAAACAAT[C/T]GAACTGAGATAGAGA | 4734 |
rs534365699 | in-del | -/AA | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988508 | AAAAAAAAAAAAAAG[-/AA]AAACTGAGGAAATGT | 4734 |
rs534371100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834926 | GCCTCCTTCCCACCG[C/T]AGTGCCGCCTCTTCT | 4734 |
rs534371416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986464 | GCGAAGAACACAGCA[C/T]CATTTCTATGATTCC | 4734 |
rs534386057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988401 | AGTGGGTGCAGCACA[A/C]CAGCATGGCACATGT | 4734 |
rs534410706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860973 | AGAGTACCTTACGGA[A/G]TTTAAGGTTTTGTGA | 4734 |
rs534422561 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986989 | TGGGTATATACCCAG[G/T]AATGGGATGGCTGGG | 4734 |
rs534422614 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995234 | TAAATCGAAAAAGCC[A/G]TGAGAGCATTAATTT | 4734 |
rs534432640 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863684 | TATAGTTTAAACTAC[-/T]TAGTGTAATCTTAGG | 4734 |
rs534438632 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837113 | GTCGTCACATGTAAA[-/T]ATCCCTAATAAATAT | 4734 |
rs534450848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906826 | TTAGGCTGGGCGCAG[C/T]GGCTCACGCCCATAA | 4734 |
rs534451859 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905703 | AAATTTTATATCCTT[C/G]GCCCACTTGTTGATG | 4734 |
rs534459722 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993894 | GGCGCGCCCTCGGTC[C/T]CTTCCCGGGAGGTGG | 4734 |
rs534472010 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886436 | CTCAAGGACAGACCA[C/T]TTATTAGGCCACAAA | 4734 |
rs534472695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985958 | CAAGAGAAGCCTGGA[A/T]CAACTTCTGCCAGAA | 4734 |
rs534477219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920384 | GGCTGAATGTGTACA[A/G]GTGTATATCTTAGAC | 4734 |
rs534490803 | in-del | -/CCTG | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964463 | GCTGTATTTTTCACT[-/CCTG]CCTGGAATTTTCATT | 4734 |
rs534519816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934025 | GGGTGTGGTGGCACA[C/T]GCCTGTAATCCCAGC | 4734 |
rs534538632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957290 | GTGTGATTTTTTTTT[C/G]TTTGCCATACTACAT | 4734 |
rs534556320 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866231 | TCTTCTTTTTTTTTT[A/T]AAATTTTTACCTCTT | 4734 |
rs534589229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841754 | GTTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 4734 |
rs534591927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866886 | TATGTATCAGCTGCT[A/G]TTCTTTATAAAATAA | 4734 |
rs534635205 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885861 | AACAATAATAACACT[A/G]AATATAAACAGACTA | 4734 |
rs534648402 | in-del | -/GT | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874364 | GCTTTTCCTCTAGTA[-/GT]ATTCTACAGTCCACA | 4734 |
rs534661126 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842311 | AAAACACAACTAGGT[A/G]TATTGTCTTGGTTTC | 4734 |
rs534700355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908203 | AATTTAATAAATATC[C/T]ATTAAGTGTCTATTT | 4734 |
rs534728269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | NEDD4 | GRCh38.p7 | 15:55952583 | TCATACCACGTTACC[C/T]CTTAATTGGCCAAAC | 4734 |
rs534753388 | snp | C/G | 6.63724e-05 | 0.00576036 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915806 | CTTCCTGTGAAGCGG[C/G]CGTATGTCTCTTACT | 4734 |
rs534753448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923516 | GCCAGGTGTGGTGGT[A/G]AGCGCCTGTGGTCCC | 4734 |
rs534767350 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950969 | ATTTGCTTTTATGGT[A/G]AATGAGGCAGATGGG | 4734 |
rs534789576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958440 | CTATGTTGACAGATA[C/T]TGGTTTTAAGTTTTC | 4734 |
rs534792615 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827770 | GTTCCTACTTCCTTG[C/T]CTCTTAGAAGTCACT | 4734 |
rs534873280 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921130 | TCCAAGTATTTTCAT[A/C]GTCATTGTCTCATTT | 4734 |
rs534935583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928013 | TAACAGGATTCACTA[C/T]CTCAACTATCTTTTT | 4734 |
rs534938055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920789 | TGCTATACAATCAGG[A/T]CTGTTACTCCACCAA | 4734 |
rs534957719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893999 | TCAAAATTTACTGAG[C/T]CAATCTTTCTATATG | 4734 |
rs534977267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862480 | AGACTGTCAAATGCG[C/T]GTTTAACGTAATACC | 4734 |
rs534993037 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832710 | GTGAGCCACCCCTCC[C/T]GGCCAAGGTAATGCT | 4734 |
rs534997328 | snp | C/G | 3.35194e-05 | 0.00409372 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834016 | CAAAAAGTAAGTTAT[C/G]AAAATAGAAGTTTCA | 4734 |
rs535042018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870016 | TTACCTGTGGCAGTA[A/G]AGGAAAAGGCATATG | 4734 |
rs535091465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930479 | GAAAATCACTCTAGG[C/T]GACCTTCCATTCAAC | 4734 |
rs535108078 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869317 | CTTTAATGGAGAATA[C/T]ACAGTTTTAGAAAAC | 4734 |
rs535153712 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965382 | GATTTTTTGTACTTT[C/T]TGTAGAGACAGGTTT | 4734 |
rs535168986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876523 | TTGTTGCAAGACTTA[C/T]ATTTTATATAAAGTG | 4734 |
rs535209095 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971190 | CTCTCAATGGCAGAA[C/T]TGATCACGCAGAAGA | 4734 |
rs535230976 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885139 | ACCTTGGAGATAGTG[A/G]CATGACATTTTAGAA | 4734 |
rs535241434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942908 | ATGCTGATAGTGATA[G/T]GAACAGGAAAGTCCA | 4734 |
rs535249543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971340 | CAAAGTTAACAGTTA[C/T]TGGGCCGGGCATGGT | 4734 |
rs535265678 | in-del | -/A | 0.00459937 | 0.047734 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873913 | AGTATTTATTAAATT[-/A]AAAAAAATAAGCCCA | 4734 |
rs535268742 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935803 | AGTGAGTTGAGATCG[A/T]GCCACTACACTCCAG | 4734 |
rs535278055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976518 | AAATCAAAACTACAA[A/T]GAGATATCATCTCAC | 4734 |
rs535297662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947981 | AAAAAGAAATAAAGG[G/T]TATTCAATTAGGAAA | 4734 |
rs535299065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942356 | GGTTTGGAATTATGT[C/T]TCTGCCAAAATCTCA | 4734 |
rs535350157 | snp | C/G | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941509 | GTGATATACATACGT[C/G]TGTTACTGAATTGTA | 4734 |
rs535350686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851807 | TAATAGATCCCAATC[A/G]CCAAGATTATCTGTT | 4734 |
rs535364067 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854824 | AAAAAGGCATGGAAA[C/G]AACTTTTCTGGTACT | 4734 |
rs535367765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848135 | CAGCCCACACTGCCT[C/T]AGCATTCTGACTGTC | 4734 |
rs535384741 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900861 | AAATGTATTAATAAT[A/G]TTTTGTTTAAAATAT | 4734 |
rs535409631 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926278 | AATGAAGCCAACCTA[A/G]TGCCAGTCACTCCTC | 4734 |
rs535427367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924345 | ACCAGGGGTCATGGG[C/T]GAGTGAGAGGGAAGG | 4734 |
rs535482635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929795 | AGGAAAAAGAGATAA[C/T]TTAGGAAACAAAAGA | 4734 |
rs535490512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972482 | TGCATTGTAAGATGT[G/T]AATTGCAACCCTCAT | 4734 |
rs535501758 | snp | C/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994658 | AAATCTAATTTTTAT[C/T]TTCCTCAATGATTTC | 4734 |
rs535521399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886562 | ACGAGGTCAGAGATC[A/G]AGACCATCCTGCCAA | 4734 |
rs535526177 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984978 | CCTGCATGTCTCCAA[A/T]TGCTATAGAATATTT | 4734 |
rs535544509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904736 | CATTTTCTACTTGAG[A/G]GTGTTTACTTCAGTC | 4734 |
rs535556783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890263 | CAATGTTTTTTAGTA[A/T]TTTCACAGAGTTGTT | 4734 |
rs535561060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984382 | TTATCTCTAAAATGG[A/G]GGTAATACTTCCTAC | 4734 |
rs535573129 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949283 | TTAGAATGGCGAACA[C/T]TAAAAAGTCAGGAAA | 4734 |
rs535581608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843158 | ATTGTGAGGCCTCCC[C/T]AGCCATGTAGAACTG | 4734 |
rs535601765 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850302 | AGCATTTATGGCTAG[A/T]GAGCTAAAAACTGGA | 4734 |
rs535603153 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911446 | TTCCTCTACCAACCA[C/G]GTCCTCTCTCCAGAT | 4734 |
rs535615855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857520 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC | 4734 |
rs535620120 | in-del | -/CAC | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970442 | TAGCCAGGAAATAGT[-/CAC]CACAAGCCTTAGGCA | 4734 |
rs535632513 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955334 | CATACCTGGCAGCTC[C/T]ACCCTCTTAAATTTT | 4734 |
rs535642216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836551 | TTTTTTTTGAGACGG[A/G]GTCTCGCTCTGTTGC | 4734 |
rs535646752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991809 | CATTAACTGCCACAA[A/T]TAGTTTTATTTCAGC | 4734 |
rs535651268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895180 | ACTCTCGACTGAAAA[C/T]AGAGATTCACACTTC | 4734 |
rs535658561 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939673 | ATGACTATTACAAAA[A/G]TTTTTAGATTTTTTT | 4734 |
rs535678651 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864513 | ATGGAGAAACCCCAT[C/G]TCTACTAAAAATACA | 4734 |
rs535681819 | snp | C/T | 0.000445093 | 0.0149113 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915522 | GGTCTTTCCAATTCT[C/T]CATTGATATTTATTT | 4734 |
rs535702374 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836947 | TTTAGGCGTCAGCCA[A/C]CATGCCCAGCCAGAT | 4734 |
rs535705215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844338 | GTTCTCAGAAGCTGA[C/T]GGGACAGGGTGTAAA | 4734 |
rs535707196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903011 | ATCTCAAATAAAAAA[A/T]AAATAAATAAATAAA | 4734 |
rs535719239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990925 | ATCCTGCACATGCAG[A/C]CAGGGTGATCTCTTA | 4734 |
rs535735668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863638 | TAAATAAACAACCAC[A/G]GAAAGTTGGAAAGTA | 4734 |
rs535762222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871459 | AAAGCATGTGACAAA[C/T]TGAAAAGCAGGCTGC | 4734 |
rs535767771 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843547 | CAGTACTTCATGGGC[-/A]AATTTCCAGGGGAAA | 4734 |
rs535770958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909229 | ATCGAGCTACAAGGT[A/G]CACATACACACTAGC | 4734 |
rs535776997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967036 | AGATTACAGGCATGC[A/G]CCACCATGCCCAGAT | 4734 |
rs535787644 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978294 | AATCAGAACTAGTTA[C/T]TTTAAATGCTAAGAT | 4734 |
rs535788980 | snp | A/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937870 | TGCATCTTGAGAAAG[A/T]AGAACAAAGCTAGAG | 4734 |
rs535789101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959866 | CTCAGCTAAGACCAC[A/G]GCCCTACCAATACCT | 4734 |
rs535806914 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841811 | ATCCTGACCTTGTGA[A/T]CCGCCCGCCTCGGCC | 4734 |
rs535807305 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979367 | TTTTTTTTTTTTTGA[-/G]ACGGAGTCTCGCTCT | 4734 |
rs535819440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944354 | CATGCCTGGATTGGC[A/G]GGTACCATGCCCACA | 4734 |
rs535831141 | in-del | -/TTGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55987317 | CACTTTTTGATGGGG[-/TTGT]TTGTTTTTTTCTTGT | 4734 |
rs535834874 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912944 | ACTCTAAGTTGTAAA[C/T]ACAGAACACAGACAG | 4734 |
rs535843709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856253 | GTGATTTGCCTTTGA[G/T]TGACAGCTAAGGTAG | 4734 |
rs535866217 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993980 | AGCTGCAGTGTTCCT[C/T]AGCAACAAGTCTCGC | 4734 |
rs535867994 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985424 | GTACTGAGGAGGGGA[A/G]GACGGCGTTGCACAG | 4734 |
rs535870156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853366 | TAACGTCATTTACTT[C/G]CCACCTGAATTTCAA | 4734 |
rs535895535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911860 | TGTTTACAAGCATGT[C/T]CCTATTACTAGAATG | 4734 |
rs535905409 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920723 | ATTTAGTTGTGAGTG[C/T]CTCAGCAGAATAAAG | 4734 |
rs535906574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849540 | TATTTCTAAGCCCCA[A/G]AACATGCATTTTGCC | 4734 |
rs535949545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943418 | AGGCCCAGGGCCCTG[C/G]TGCCCTACACAACCT | 4734 |
rs535964943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840237 | AAAAAGCAATTGTGA[A/G]TAGTTGATATACAAC | 4734 |
rs535975789 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895365 | CTACTGTTGCAAATA[G/T]AGAGTGCCTTCAATT | 4734 |
rs536002827 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948744 | GCTGGGAAAACTGGC[G/T]AGCCATATGTAGAAA | 4734 |
rs536015419 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874076 | AAGAGTTTGATGAGA[C/T]AGTGCCACCATTCAC | 4734 |
rs536015451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906966 | CCAGACAGGTGGCAC[A/G]TACCTGTAATCCCAG | 4734 |
rs536017858 | snp | C/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918465 | TCATTCATAGGAAAG[C/T]AAAAGGTAAAATAGT | 4734 |
rs536024573 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841016 | ACAGCTCACTGCAAC[A/C]TCCGCCTCCCAGGTT | 4734 |
rs536038215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910735 | ATACACATAAACTTC[A/G]TACATGATTTCTTCT | 4734 |
rs536046194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926105 | ACTGTACATGTATAT[A/G]ATACATACGTATATG | 4734 |
rs536071553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881568 | TCAATCAGGATGACT[A/G]AGGAATAAAATATTT | 4734 |
rs536104481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931978 | TTTGCCTATTCTGGA[C/T]ATTTCATGTAAGTGG | 4734 |
rs536121600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889347 | CCATCAACAGACATA[C/T]AAAGAAAATACGGTA | 4734 |
rs536174783 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929316 | TAATGAAAATATAAG[A/C]ATCAGATTTTTTTCC | 4734 |
rs536178503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924798 | TTTGGTCGGGCATGG[G/T]GGCTCATGCCTGTAA | 4734 |
rs536204963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867588 | TATTCGAGATACTCT[C/G]GTACACCAAAAAGCC | 4734 |
rs536217780 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969813 | GTATTATGCTGACTT[C/T]GGGTGTGATCCAACA | 4734 |
rs536217853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859832 | CACTCTGTAATCGTG[C/G]CTGAATATAGACAAA | 4734 |
rs536250411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963506 | CTTTTATTCAACTTA[C/T]ACTTAGTATTGTACC | 4734 |
rs536261067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949868 | TGACAAGTTAATGGG[G/T]GCAGCACACCAATAT | 4734 |
rs536263886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874810 | GAAACCTCATCTCTA[C/T]GAAAAATACAAAAAT | 4734 |
rs536299213 | snp | C/T | 0.000898571 | 0.0211773 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55837837 | GTTTACAAATCGCCA[C/T]TGTATTACAAGACTA | 4734 |
rs536326415 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884943 | AGATCAATATTCAAG[C/T]ACAAGAAGGTTATAG | 4734 |
rs536326581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956330 | GAAGTTCCTTTCAAC[A/T]TTTTTCTTTTATGGC | 4734 |
rs536331683 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855345 | GTGGGGAAATGGAAT[A/G]CACACAGACTCAGAA | 4734 |
rs536368949 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827718 | TACAGATATACACAT[A/G]TGTATCCATATTATT | 4734 |
rs536369948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926787 | TCCACCACACCCCCC[A/C]AAAAAAGGGTGGGCA | 4734 |
rs536370245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846842 | AATGAGCATCCTTTC[C/T]CTAGGAAAAACTGTT | 4734 |
rs536393788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975261 | ATCAGATAAGAAAAA[A/G]AAAGGGAAGCTAAAT | 4734 |
rs536413553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939906 | CTGCAATTAAAGTTA[C/T]CTGCCCTCCCACGTT | 4734 |
rs536431683 | in-del | -/AGATAAGT | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905783 | TATTAGCTCTTTGTC[-/AGATAAGT]AGATTGCAAAAATTT | 4734 |
rs536524211 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880770 | AGACAGCTACGAGAG[A/G]GATGTTTCCTAGAAG | 4734 |
rs536538859 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905659 | TAGGACTAGGAAATC[A/G]TCAGAAACAAGAAAG | 4734 |
rs536540206 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875609 | AGGTGTTAGCCACCA[C/T]GGCCGGCCAGATGTA | 4734 |
rs536572292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906332 | AAAGACACATGGACA[C/T]GTATGTTTATTGCAG | 4734 |
rs536594647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973661 | AATGGAAATTAAACA[A/G]TATGCTCCTGAATGA | 4734 |
rs536600551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875168 | TGACGCAGATCATGG[A/G]ATAAGCAGACAAGGA | 4734 |
rs536635159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921388 | GGAATGCAATGGTGT[A/G]ATCTCAGCTCACTGC | 4734 |
rs536636291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983078 | AGTGAACCGAGATTG[A/C]GCCATTGCACTTCAG | 4734 |
rs536657983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884071 | TTTTAGCAGAGATTG[C/G]GTTTCACCATGTTGG | 4734 |
rs536671334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970463 | AAGCCTTAGGCAAAA[A/T]CCAGTACTGTGTTGG | 4734 |
rs536673995 | in-del | -/T | 0.0768403 | 0.180321 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976797 | CACACCTGGCTAATT[-/T]TTTTTTTTTGTATTT | 4734 |
rs536696712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831571 | AGAGGCTATCAAGTC[C/T]AATTAGGCAAAGAAT | 4734 |
rs536719568 | in-del | -/CAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883694 | ACACACACACACACA[-/CAA]ACACACACACACACA | 4734 |
rs536781009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891234 | TGAAATGATCCCAAA[C/T]AGCTGTATTTCCAAT | 4734 |
rs536796143 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959277 | GATTATTTAGAAGTA[C/T]ACTAATTAAATTCCA | 4734 |
rs536797869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966754 | AAAGATAAGCAAAAA[C/T]TTGAGTCAACTTATT | 4734 |
rs536823762 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906687 | ACTTAATGTAAATGA[C/T]GAGTTAATGGGTGCA | 4734 |
rs536828797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981606 | CAGAATTCTTCAAGA[A/G]TTTTTGACAGTAATA | 4734 |
rs536838979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974995 | CCTCCCAGGTTCAAA[C/T]GATTCTCCTGCCTCA | 4734 |
rs536840838 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907597 | CATTTGCTTTGAAGA[C/T]GACTTGAGTTTCCAG | 4734 |
rs536849115 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988442 | AACTAACCTGCGCAA[C/T]GTGCACATGTACACT | 4734 |
rs536868404 | snp | A/G | 8.42993e-05 | 0.00649173 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55951558 | GAACTCCATTCATTG[A/G]GTCATATAACGTCAC | 4734 |
rs536873356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861073 | GGTACTCAAAAATAT[C/T]TGTTGAATGAATAAA | 4734 |
rs536878702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945455 | AAAGTGAGAATACAA[C/G]TTTAGAGAAAAAAGA | 4734 |
rs536883510 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995332 | TGCCCTTCTATTTTG[C/G]GAATATTTCCCTCAT | 4734 |
rs536916117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986891 | TGAGCCACCGCGCCC[A/G]GCCAAGGCCTGTCCT | 4734 |
rs536916616 | snp | C/G | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906643 | GTTGTGGGGTGGGGG[C/G]CTGGGGGAGGGATAG | 4734 |
rs536919785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981107 | GCAGTGGTATGATCT[C/T]GGCTCACTGCTCGCA | 4734 |
rs536923073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862496 | GTTTAACGTAATACC[C/T]TTATTATTGAGTCCT | 4734 |
rs536956952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986556 | CAAAATGAGAAACAT[A/C]GTAGGATGTAAGGCC | 4734 |
rs536960103 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994562 | TAAAAGAGTCTGGGG[A/G]GAATTATGAACACCC | 4734 |
rs536990452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957432 | TACTGGGTTTTTTCA[C/T]AGATACCCCTGATGA | 4734 |
rs537008945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935075 | GTTTCACCATGTTGG[A/C]CAGACTGGTTTTGAA | 4734 |
rs537010399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942133 | TGTGGATTTGTTTAT[C/T]TATTTAGTTCTGTCA | 4734 |
rs537028919 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835890 | TCTTATTGGTTAATA[G/T]CCTTTAATGCTACCT | 4734 |
rs537033403 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966671 | GAAGAATCTTTTTCA[A/G]TAATTAATTTTATTA | 4734 |
rs537059992 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961204 | ACTTGCCTAAGAATA[A/C]CCATGAAAGGCACAC | 4734 |
rs537073703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941576 | AAATTTCTTTTTTTT[G/T]TTTTTTGAGACAGAG | 4734 |
rs537078976 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863409 | AAACAACAATAAAAC[A/G]GAACTTTAAAACAAA | 4734 |
rs537098199 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916923 | TGCACTGCATCAAAA[C/G]AAAAAATCATTTGTG | 4734 |
rs537115096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902430 | TTATATATGTAAAAG[G/T]CTCCTAACCATCACA | 4734 |
rs537141684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870695 | CACACTGCCATGCCC[A/G]GTTAATTTTTGTATT | 4734 |
rs537158423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989137 | GCTACCCTGGAGGGT[A/G]ATGCAGGAAAATCGC | 4734 |
rs537169232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908013 | TTCATTTAAGAGTGC[C/T]ACTCTTCCACGCAAA | 4734 |
rs537203334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952394 | CACTTCTACAAGGAG[A/C]CATGGAGAAGGAAAT | 4734 |
rs537214071 | snp | A/G | 3.30327e-05 | 0.0040639 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842130 | GAACAGTTGCTCGGC[A/G]AAGTTTCATTTCAAA | 4734 |
rs537229921 | snp | G/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994343 | AACCTGCTTTAGCTG[G/T]GCGTTGATCCGCAGC | 4734 |
rs537245160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855538 | GGAAAACAGAGACAA[A/T]CTCAGTAGTGAGGCT | 4734 |
rs537258134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955599 | CTTATTTCAGTTAGT[A/G]TAATATCCTAATGAT | 4734 |
rs537293092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55915053 | AGCTTAAATCACTTA[C/G]GAAGATTTTTAAAAA | 4734 |
rs537341206 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868272 | GGAGACCTAAGCAGG[A/C]CCTCAGTCAGAGGAG | 4734 |
rs537367580 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891757 | AGAACATAAAAAGAA[A/G]ATCCAAATTGCTGTT | 4734 |
rs537390768 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971391 | GCACTTTGGGAGGCT[C/G]AGGCGAGTGGATCTC | 4734 |
rs537407479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948180 | ACAGAGAGCCAAATC[A/C]TGAGTGAACTCCCAT | 4734 |
rs537444613 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994145 | CTGGGGACCGCCAGG[A/G]AAAGCCTGAGCGTGG | 4734 |
rs537448474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960519 | GTACCTTCAGCCACA[G/T]ACTGAAGGCTGCATT | 4734 |
rs537459892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953820 | CCTCCTCCTGGGTTC[A/G]AGCAATTCTCCTGCC | 4734 |
rs537467031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967769 | CACACACCTATTATC[A/G]CAGCACTTTGGGTGG | 4734 |
rs537534126 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911695 | CCACCATGCCCGGCT[A/G]ATTTTTGTATTTTTA | 4734 |
rs537538028 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832183 | CCACCCCTATCTTGA[-/AA]AAAAAAAAAAAAAAA | 4734 |
rs537548496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930615 | AATGCTTACTGATAT[A/G]GTTTGACTGTGTCCC | 4734 |
rs537576447 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935633 | CAGACGGATCATGAG[A/G]TCAGGAGATCGAGAC | 4734 |
rs537612956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937104 | GGCCATAATTTGCTA[C/T]TGAGCACTAACTTCA | 4734 |
rs537618106 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949278 | ACCAGTTAGAATGGC[A/G]AACATTAAAAAGTCA | 4734 |
rs537646799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896513 | TAAAAATTTACCTGA[C/T]GATACTAAATTGCTA | 4734 |
rs537673719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965863 | ACCATGTTGGTCAGG[C/T]TGGTCTCAAACTCCT | 4734 |
rs537691351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929099 | TGAAGCAGGGATGGA[A/C]GTGATGATGGAGGGC | 4734 |
rs537708229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845566 | GTAATGGCATTGTCT[C/T]CCATCTCCTGCTGCC | 4734 |
rs537742583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948617 | AGAGATACAGACCAA[C/T]GGAACAGAAAAGAGC | 4734 |
rs537771160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839759 | GAGGCAGGCGGATAA[C/T]GAGGTCAAAAGACTG | 4734 |
rs537798836 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876353 | AATATGTGGGTAAAG[-/T]TTTTTTTTTTTAAGG | 4734 |
rs537857539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880631 | GGGAGTGTGCCGTGA[C/T]ATGGAAGATGCAGGG | 4734 |
rs537864091 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871559 | TAAAAGACTAAAAGA[C/G]ATTTACATTCCAGAC | 4734 |
rs537864529 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978507 | GCATAAATGCTGCAA[C/T]TATAGAAAAATCTCT | 4734 |
rs537895965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845605 | ATTAATAATTAGATA[C/G]TACAACATGTTTCAA | 4734 |
rs537976009 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926632 | TTAGCTGGGCATCAT[A/G]GCACATGCCTATAGT | 4734 |
rs537980002 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887803 | CCAAGGGGGATTCAT[C/T]ACAGGGATGCAAGGA | 4734 |
rs537993757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985919 | GAAAATGGCTGATTG[C/T]AGATAGCTGAGCCAA | 4734 |
rs537995052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973063 | TATCCCACTTTCGGC[A/T]CTGGATAGATCATTC | 4734 |
rs537998354 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845160 | CCCTCCTTCTGGGGT[G/T]ACTTCATGTCTTTTA | 4734 |
rs538002556 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897536 | CCACTTTGCCCATTT[C/T]AAAAGGGTCAGTATG | 4734 |
rs538005786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949703 | AACTGTCGCAGGGAC[A/G]AAAAACCAAACACCT | 4734 |
rs538015181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859030 | TCCCATGAAGGCAGG[A/G]GATATTGTTAATTTT | 4734 |
rs538022166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945348 | CTGAAAACCATGGCA[C/T]AAGAACTTTGTGATA | 4734 |
rs538034186 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993257 | TGAAGGAAACTGACA[A/G]GTAAGGCGGCGGCCG | 4734 |
rs538041123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886884 | ATTAAATAGTATGCT[C/T]CTGAATGAATGAACA | 4734 |
rs538042665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837428 | AAGTGACTCACTCCG[C/T]GCTCAAAAAAAAAAA | 4734 |
rs538064231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956033 | TCACCAGGCTGGTCT[C/T]GAACTCCAGGGCTCA | 4734 |
rs538078490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858279 | AATGGGATCGTATGT[A/G]ATTTATCATCAGCAA | 4734 |
rs538110518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984013 | CCCTCTTGGCTATAA[A/C]ATCGGTAAAGTATAT | 4734 |
rs538110767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977969 | CTCTCAAGTGGTAAA[A/G]TATAATTGAAAGTGA | 4734 |
rs538127717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955471 | TTCCATTTCTACTTA[A/C]CCCTCACCCCTCACC | 4734 |
rs538136634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942963 | GAATCTTTTGGGAAC[G/T]GAAATAAAGGTCCCT | 4734 |
rs538167649 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903717 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 4734 |
rs538187462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961246 | ATGTCCAAATTCCTA[C/G]AGTCTCATCAGGGCA | 4734 |
rs538202413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939151 | CCACCACCAACAATA[A/G]TATGGTTTGGCTCTG | 4734 |
rs538211596 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978619 | TTAAACACCTTTTCC[A/G]TAATCAAAACAGGGA | 4734 |
rs538217160 | in-del | -/TT | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955527 | CTTTGATTCTATGAA[-/TT]TGACTATTTTAGATA | 4734 |
rs538246534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976408 | TGATATTAAAATGGG[A/C]AAAAGATCTGAATAG | 4734 |
rs538268002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945080 | CAGAAAAGCTGAAAA[C/T]TCTAAAAACCAGAGC | 4734 |
rs538301727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851012 | TTCAACTAATTCTCA[A/G]GCAGTAAGATGTTAG | 4734 |
rs538314765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841173 | TCCTGGCATTGTGAT[A/C]CACCAGCCTTGGCCT | 4734 |
rs538347865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859888 | ATACCAAACATTTCC[C/T]CATCCTGGCAAATGT | 4734 |
rs538367828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912971 | ACAGTGTCCCAGATA[C/G]AGGTAAAAGTTCTCA | 4734 |
rs538369952 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857969 | TACAAACAATATATA[C/T]CCTGCTCATTCTTTG | 4734 |
rs538376228 | snp | A/T | 1.66499e-05 | 0.00288525 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834209 | ATTTCTGTTTCAACA[A/T]AAAATGTTATGTCTT | 4734 |
rs538379112 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905587 | AAATAGACCAAACCC[A/C/G]AAGTAAAATATTCTC | 4734 |
rs538409720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866644 | AGCAAAAGAATATTT[A/C]TTTTAAAGCTTCTTA | 4734 |
rs538440701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911770 | CCTGACCTCGTGATC[C/T]GCCCGTCTCGGCCTC | 4734 |
rs538445801 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949331 | GATGTGGAGAAATAG[C/G]AATACTTTTACACTG | 4734 |
rs538456300 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962960 | CCCAGCTAATTTTGT[A/G]TATTAGTAGAGATGG | 4734 |
rs538463547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873651 | AGTTTTCTTCTGTGA[C/G]CTTAGGCACTCCTCA | 4734 |
rs538496761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926957 | GGCAGGCACCTGTAA[C/T]CCCAGCTAGTTGGGA | 4734 |
rs538498235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992662 | AGACAATCTCCAAGA[A/T]CACACAGAAGCCACA | 4734 |
rs538501600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911521 | AGCACATCACATATT[A/G]GACTGAAAAAAAATT | 4734 |
rs538510898 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963366 | TGAACCTCTGGGCTC[A/C]AGTTCCTGGCTTTTT | 4734 |
rs538519635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969122 | AGAGAATCTATGCCT[C/T]TGCGGGACGAAGGGC | 4734 |
rs538528719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872964 | AGACTGTGGAGAGCC[A/G]ATTAATATAACTCAC | 4734 |
rs538586522 | in-del | -/A | 0.208169 | 0.246476 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983507 | ACTCAATGGGGTTCT[-/A]TTGCCCCACTCTTCA | 4734 |
rs538595315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881718 | GAATACACTGAACAT[A/C]TGTATGTTTGATGAT | 4734 |
rs538596758 | in-del | -/AGAT | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840192 | GACTGATGGATAGAC[-/AGAT]AGGTATGTGATAAAG | 4734 |
rs538613480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861139 | TTTTGCCATGTTATT[A/G]TAAGAGTAATAGAGT | 4734 |
rs538619387 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931951 | CACTAATCTACTTTC[C/T]GTCTCCATAGATTTG | 4734 |
rs538653321 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950853 | TGCTCTGGTAGGGTT[G/T]CGATTCTGGCAACAG | 4734 |
rs538680802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957915 | CTCATAGGTGGGAAC[A/T]GAACAATAACACCTG | 4734 |
rs538690399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928286 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAGCCATC | 4734 |
rs538711709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957221 | CTTGGGGCTTTCTAC[A/G]TACAAACCATGTTGT | 4734 |
rs538720625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867447 | TAGGGTCCTATGATG[C/T]GTGCATGTGGGCAAA | 4734 |
rs538741185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921059 | AGAGAGCTACAAACG[C/T]GTTAAGTCTACGAAT | 4734 |
rs538746223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964287 | ACAAATCCTCAAGGC[C/T]CTGTTGTTGTTGTTG | 4734 |
rs538757168 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874393 | ACATAATGCAGAGAG[A/C]CTAGAACTTAAGCTG | 4734 |
rs538764974 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963253 | CCTCCAACCTCAGCC[G/T]CCTTTGTAGCTGGGA | 4734 |
rs538777724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956907 | AAATGCCACCCTAAC[A/G]CTATTGAGTCTTCTA | 4734 |
rs538812291 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990646 | AGTAAGTGCACTTAA[C/G]TGGGGAGCCTACTTT | 4734 |
rs538858794 | snp | A/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918403 | GTATATTTAAACCCC[A/T]CACCTAAATTTTATA | 4734 |
rs538876316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933549 | TGGGGGGAGGGGGAA[A/G]GGGGAGGGATAGCAT | 4734 |
rs538893893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971713 | GAAATAATAACAAAG[A/T]ACTTTCTAGGCCTAG | 4734 |
rs538916385 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906131 | AAAAAGTCAGGAAAC[-/A]ACAGGTGCTGGAGAG | 4734 |
rs538918772 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901337 | AAGAAACAAGAGTTC[A/G]TTTTAGAACTACCAA | 4734 |
rs538928195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926268 | ACGGGCAACCAATGA[A/G]GCCAACCTAGTGCCA | 4734 |
rs538938919 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851570 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 4734 |
rs538940085 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889670 | AGGGTAACTTTAGTC[A/C]AAAATAATTTAATTT | 4734 |
rs538948747 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968697 | GGGAGTGTAAATTGA[C/T]GGATCATTCTAAAGA | 4734 |
rs538955282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939989 | TTGAAGGATACATTA[A/G]GAAAATGTGACATAT | 4734 |
rs538985512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958347 | TTAATTTTTTTAATG[C/T]TGAACAAACCTTGCA | 4734 |
rs538992412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869258 | AGTGGAGTCTCCTCA[A/G]AATGTCCATATATTT | 4734 |
rs539002309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981670 | GATTTAGGAGCAAGC[A/C]GTAGTTCTCAAAGTG | 4734 |
rs539003580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922421 | AGGCTGAAGTGCAAT[C/G]GTGTTATCTTGGCTC | 4734 |
rs539008249 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986605 | TTTTTTTTTTTTTTT[-/T]GTGAGACGGAGTCTC | 4734 |
rs539017008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832668 | TGATCTGCCTGCCTC[A/G]GCCTCCTGAAGTGCA | 4734 |
rs539024222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965255 | CCAGGCTGGAGTGCA[A/T]TGGCACAATCTTGTC | 4734 |
rs539028839 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945576 | ATGGAACCAAGGTGG[A/C]AAACACTCTACAGGA | 4734 |
rs539030774 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936393 | GCGTATGTAGGTAAG[C/T]TTTTTCCCCCTATCC | 4734 |
rs539046971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836871 | CCTATGTTGTCCACG[C/T]TGGTCTCGAACTCCT | 4734 |
rs539110362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830064 | ACCACCACAGCAAAC[A/G]GAGCAATGCTGCTAT | 4734 |
rs539123538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971290 | TAAAAGTAACAAAGC[A/G]TGCCTACAGGATCTA | 4734 |
rs539161504 | in-del | -/ACA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952217 | CAGGCACTTTTAGTC[-/ACA]ACTACTCGGGAGGCT | 4734 |
rs539168057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884224 | CCACAGCATTACTGG[A/G]CTTGGAATGTCCCCT | 4734 |
rs539191093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894215 | TGGATTCAATCAATC[C/T]GGGATCAAAAATATT | 4734 |
rs539199804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947394 | ATAAACACCTCTATG[A/C]AAATAAACTAGAAAA | 4734 |
rs539213281 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968072 | TCCACTATGTTTACG[A/T]GTGAAAATATTTAAT | 4734 |
rs539228827 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956866 | ATTTTTATTGGGATT[A/G]TGCCAAATCTAATCA | 4734 |
rs539229143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941651 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 4734 |
rs539237330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982720 | TGCATTTCACTCTTT[A/G]TAAATTTCACTCTTC | 4734 |
rs539250014 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983439 | CCTCTTGTTTTAGCA[C/T]TCCAACCTTCCTGTT | 4734 |
rs539250306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975852 | AAAGAACAAAATGGA[A/G]TCAAATTAATTACTG | 4734 |
rs539260174 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854587 | CTGTAGCAATAGAGA[A/G]CAGATGAGCGGTTGC | 4734 |
rs539272629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982151 | AATGTGCAGCAACTA[C/G]AACTTTCACATATTA | 4734 |
rs539282979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946821 | TCTCTCAGACCACAG[G/T]GCAATCAAACTAGAA | 4734 |
rs539308611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853507 | AAGTAACTTGTTAAG[C/T]GACATGGCTTCTAAG | 4734 |
rs539361380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988271 | TAGGTGGGAATTGAA[C/G]AATGAGATCACTTGG | 4734 |
rs539373213 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853934 | GGCAGAGGTTACAGT[C/G]AGCTGAGATTGCACC | 4734 |
rs539375827 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55850188 | TTCTACCTAGCCTCA[C/T]AAGGTTTTTTTGATA | 4734 |
rs539411108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865071 | GGCATGGTGGCGGGC[A/G]CCTGTAATCCCAGCT | 4734 |
rs539417035 | snp | A/G | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918686 | TTATGGGAATTCATT[A/G]CATTTCATTTGACTA | 4734 |
rs539482392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857471 | GTAGCTGGGATTACA[C/G]ACACACGCCACTGCA | 4734 |
rs539494239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895014 | CTCTAAAAAAGGGAG[A/G]GGCTCATCCCATTGT | 4734 |
rs539503770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903757 | GTGAACCCGGGAGGC[A/G]GAGGTTGCAATGAGC | 4734 |
rs539510189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942288 | GTCTAATTTGGCTAA[C/T]GTTAATACAACCATT | 4734 |
rs539511578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991774 | TTCTGGCCTTTGGCC[C/T]CAGTTCCTTACCGAC | 4734 |
rs539550967 | snp | A/G | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918152 | AGCCCTACCCTAGAG[A/G]TGGAATTACTCACCA | 4734 |
rs539580549 | snp | C/G | 1.65603e-05 | 0.00287747 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856118 | TTGATTGATGGGAGA[C/G]GGTAAAACTCACCAC | 4734 |
rs539600752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990046 | AGAATCTAATGCCTG[A/C]TGATTTGTCACTGTC | 4734 |
rs539620434 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977533 | CATATGGTAAATTAA[C/T]ACAACACAAAAAACT | 4734 |
rs539636119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842436 | CTGTAGTCCAGGCTG[A/G]AGTGCAGTGGCGTGA | 4734 |
rs539641617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909138 | TTCTTCACCAACAGA[C/T]ATCCTCGGGCCTAAC | 4734 |
rs539676096 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994456 | CTCCTGTGGAATAAG[G/T]TTATGGAATAATCAT | 4734 |
rs539702009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842992 | AGAACCTGGTGGGAG[A/G]TGATTGAATTATGGG | 4734 |
rs539728234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870301 | TTTTGGATGACAGAA[G/T]AGTAGAGGGCAAGGC | 4734 |
rs539741344 | snp | C/G | 0.000925008 | 0.021486 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915700 | GTTGGGTGAAATGCA[C/G]TGAAACACAAGAATA | 4734 |
rs539743348 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866938 | TTATTTAATTTCTAA[A/C]CGCAAAGCCAATATG | 4734 |
rs539770979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965937 | GATTACAGGCATGAG[A/C]CACCATGCCTGGCCC | 4734 |
rs539774328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851170 | GGAATTCCTCATACA[A/C]AGAAGTAGATTCAAA | 4734 |
rs539783274 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973838 | GTAGAAAAACTTCAA[A/C]AAAAAAAACAACCTA | 4734 |
rs539784274 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957302 | TTTCTTTGCCATACT[A/G]CATGGCTAAAATATA | 4734 |
rs539793769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943359 | TGGCAGCTCCTCCTA[C/T]CACAGCCCCAGAGGA | 4734 |
rs539799581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943678 | TGCAGGGGCAGAGCC[C/G]TCATGGAGAACTTCT | 4734 |
rs539800643 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828247 | ATACCCCAACAAACT[G/T]AAACCAAGAACCAGA | 4734 |
rs539819689 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871899 | TTACAGCTTAAATTT[-/A]AAATTTTTTTGATAA | 4734 |
rs539822812 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895200 | ATTCACACTTCTGAG[C/T]ACTAATTATGATATT | 4734 |
rs539850184 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952576 | CATTTCCTCATACCA[C/T]GTTACCTCTTAATTG | 4734 |
rs539869649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857846 | TCCAGAGGCTGAGGT[G/T]GGAGAATCCCTTGAG | 4734 |
rs539889905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855637 | CTGAGCAGGAAGCAG[A/G]AGGCCTTAGTAGACT | 4734 |
rs539917896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856793 | TTTCCTGGAAATCTC[A/C]TGTTCTTTCTTTCCT | 4734 |
rs539934815 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955023 | CACTGCACTGCACTG[C/T]ATTCCAGCATTTTTT | 4734 |
rs539939073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55954804 | GCTGGGAATACAGGC[A/G]TGAGCCACCGTGCCT | 4734 |
rs539947471 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849261 | TGGAGTGTCGCTCTT[A/G]TCGCCCAGGCTGGAG | 4734 |
rs539969908 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839175 | CTGGGACTACAGGCG[C/T]GCACCACCACGCCTG | 4734 |
rs539982658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863538 | TATCAAAACATCACA[C/T]TGTCCTCCATAAATA | 4734 |
rs539986946 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937506 | TAGCAGAATTTCTAA[C/T]TGAAACAAATGTGTA | 4734 |
rs540023938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958693 | AAATTCAATTTCTTT[C/T]AATAATAAACATCTA | 4734 |
rs540047523 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959825 | CAACCACATTAGCTT[G/T]GAAGTGAATCCTTCC | 4734 |
rs540081073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924538 | CCAGAGTCTCCATAA[C/G]CACCCCCAAGCCATC | 4734 |
rs540116563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966610 | TAAGACACAATTTTT[A/T]AAAAAATATATATCA | 4734 |
rs540127615 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929352 | TAAAAAAATTTATTT[C/T]AGTTTTGGGAGTACA | 4734 |
rs540143685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930102 | TAAAAAAAGAGGCTG[A/G]GCAAATTATGGCTTG | 4734 |
rs540190560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887124 | CCAAACCCAAAATTA[A/G]TAGAATAAAAGAGAT | 4734 |
rs540197446 | in-del | -/AGTT | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917494 | TGTGTGAATTCAAAC[-/AGTT]AGGTAAATTTGGAAA | 4734 |
rs540226522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852062 | GCACTTTAGGAGGCC[A/G]AGGTGGGTGGATCAC | 4734 |
rs540229902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992725 | GTCGTACAATATTTT[C/T]AATAAGCATAGGCAT | 4734 |
rs540242771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873143 | CTTTTCCTGTTTCCC[C/T]TTGTCTGTCTTCTCT | 4734 |
rs540259753 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837066 | AATTTATATTCTGAA[A/T]AAAATATAGCCACAA | 4734 |
rs540266303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992234 | CTATTGTTTCTGAGG[A/G]ACTATGAGCCGCCAC | 4734 |
rs540275534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962357 | ATATTTATTTTAATC[A/C]ATTAATGTTCCTTGT | 4734 |
rs540285831 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963932 | GTTATTTTATTGTTC[C/T]ATTTTCTCCTGGTCT | 4734 |
rs540285894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968750 | GTTCTAAAATAAAAA[A/C]CCAGGAACTGTATTT | 4734 |
rs540302451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872538 | GCATGTACTTTTCAA[C/G]AATACTCATGAACTA | 4734 |
rs540319341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830305 | CTCAGTTTAGGTGGG[C/T]CTCTCTGATCTTCAG | 4734 |
rs540340664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910300 | CTGGCTTTTAACCCC[A/G]CATTCTCCTGAGCCT | 4734 |
rs540355057 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847724 | CTCTGTTGTCCAGGC[C/T]GGAGTGTGGTGGTAC | 4734 |
rs540370242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974244 | AAAACATAAAAAGAC[C/T]AGTAACAAATAATGA | 4734 |
rs540370365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968197 | AATTCATAGAGAGGA[A/G]TAAAAATGAGTAAAG | 4734 |
rs540371113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863821 | CTGACACATGGAAAA[A/C]ATCATTTGATAAAGG | 4734 |
rs540405244 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917600 | TAGTTACATAAAAAG[G/T]GAAAGCTTAAGGACA | 4734 |
rs540407082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973803 | GAGAAGCTTATAGCT[A/G]TAAGTACCTACATGA | 4734 |
rs540430170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960130 | CCACTGACCCCATAC[A/C]CCCAAAGGACTGCAG | 4734 |
rs540433156 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843887 | ATGGGGAATAAAGGG[A/C]ATAAAAACATAGGGT | 4734 |
rs540436501 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901735 | ATGATTCCATTTGTA[A/C]ATATAAAAAACAATT | 4734 |
rs540454627 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976834 | CAGACGGGGTTTCAC[A/C]GTGTTAGCAAGGATG | 4734 |
rs540494551 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984072 | CCACGTGCCTGATAC[-/AT]AGTGTTCATCAAATA | 4734 |
rs540537290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979823 | ATCACATACTATCTT[G/T]TATCTGAGGCAATAA | 4734 |
rs540560844 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868585 | CTTGCCTGCCACCAT[A/G]TAAGCTGTGCCTTTG | 4734 |
rs540565500 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992820 | CTAGTTTTCAAAGGG[-/A]ACAGATGTGGTAACT | 4734 |
rs540568576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878650 | TCCTCTAAAATACTT[A/C]TTCAAGAATGTTCAC | 4734 |
rs540579513 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843625 | AGGTTAGCTCTAAGG[-/A]AAAAAAAATCAATTT | 4734 |
rs540597333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927205 | TGAAAGTTGGGAAGA[A/G]TTTAAATGAGAAGGT | 4734 |
rs540605048 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923657 | TCTCAAAAAAAAAAA[A/T]AAATATATATATATA | 4734 |
rs540614966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920319 | TACAACTGCTAAACG[G/T]GAGAAGCACAGGGTC | 4734 |
rs540628661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891581 | CAAATTTGCATTTGG[C/T]ATAATATAAGTAATT | 4734 |
rs540632661 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957346 | GATAGAACATGAAAG[C/G]AGACAACTTTGCCTT | 4734 |
rs540636641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911026 | TTCTGGCAGATCACC[A/G]CCTCCCACATCCCCA | 4734 |
rs540641074 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922850 | TAAGCTGAGTAACGT[A/G]TATACATATTTGTCT | 4734 |
rs540677640 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919780 | TTACTGATCATCTAC[A/T]TGGAAAATAATGTGA | 4734 |
rs540677689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926344 | AGAGATGTCCCTTTT[A/G]CCCCTTGCATTTATC | 4734 |
rs540692496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890604 | CATTTGGGTTGTTTC[A/C]ACTGTTTGGCTATTA | 4734 |
rs540707816 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933206 | AAGGATTATAAATCA[C/T]GCTGCTATAAAGACA | 4734 |
rs540728879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932187 | AGTTGTAATAAGATC[C/T]GATGGCTTTACCTGC | 4734 |
rs540737825 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975101 | TTTCACCACGTTAGC[C/T]AGGCTGGTCTCAAAC | 4734 |
rs540738656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925960 | ATACTGTATCATACA[A/G]TATGTATATGTAAAA | 4734 |
rs540776736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929754 | CCAGAGATCACGAAC[A/G]TACAAATTAGAAAAA | 4734 |
rs540778364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981238 | AGTAGAGACATATGT[A/G]GGATTCTCATATATC | 4734 |
rs540799182 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900359 | GAGAAGAGAAGAGCT[A/C/G]AGTCAGTGAAATTTG | 4734 |
rs540801747 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901688 | TGCATTTCCCATTAC[C/T]TAACTGTTCATGTGG | 4734 |
rs540819902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899292 | TGAAATGAATAGCCT[C/T]TTATTAGTTTTTAAA | 4734 |
rs540822060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986665 | CATGATCTTGACTCA[C/T]TGCAAGCTCTGCCTC | 4734 |
rs540836900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876339 | ACCAGAAAATGGTAA[A/T]TATGTGGGTAAAGTT | 4734 |
rs540862734 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994228 | AAATTCTCTCCCTAG[G/T]ATTTGTAAACAGTGC | 4734 |
rs540880593 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854246 | CCCTAAGGTGGCTTA[A/C]AACATAAAAACCATC | 4734 |
rs540888220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888347 | CAAGAGTAAACAATT[C/T]GTAAAATAAATCAAG | 4734 |
rs540895955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897576 | GAGCAATAATAGTGA[C/G]GGTCGAATGACCTGC | 4734 |
rs540921121 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842624 | CTCTAGCAATCCTCC[C/T]GCCTTGGCCTCCCAA | 4734 |
rs540921129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937636 | ATGGCAGTAGAGTCC[C/T]AATCCTGATTTGTCA | 4734 |
rs540921583 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906012 | AAGACATTTATGCAG[A/C]CAACAGACACATGAA | 4734 |
rs540957400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904955 | AAATTAGCCGGGTAC[A/G]GTGGCACATGCCTGT | 4734 |
rs540985628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941149 | TAAGGCCAGCTGTTG[A/T]ATATCAATTTCATTA | 4734 |
rs540985664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946955 | AGATGTTCTTTGAAA[C/T]CAATGAGAACAAAGA | 4734 |
rs540994842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933654 | CAAACCTGCACGTTG[C/T]GTACGTGTACCCTAG | 4734 |
rs541009048 | snp | A/G | 3.67208e-05 | 0.00428475 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55834274 | GATCCTGTGGTATTA[A/G]TTCAAAGAATCCCTA | 4734 |
rs541010334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969528 | AGCTCCAGGAGGAGA[C/G]GTAAGAGTAGAGGAG | 4734 |
rs541011443 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956586 | ACAGGAGCTGATCAT[A/C]TATATGTGTATATAT | 4734 |
rs541048607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946362 | GGTTACAATCCTAGT[A/C]TCTGATAAAACAGAC | 4734 |
rs541060742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982424 | GAAATACTATTCACC[A/G]AGAAAAAGAATGAGC | 4734 |
rs541090896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981729 | ACATGGAAATTTGTT[A/G]CATATGCAAATGTTG | 4734 |
rs541108202 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844989 | TTTTAATATTCTTTA[C/T]TTCTGTTTTGGTGTT | 4734 |
rs541142401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852766 | AGAGAGAGAGACAGA[A/G]AGAGACAGGGTCTTG | 4734 |
rs541190632 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859025 | GTAAGTCCCATGAAG[G/T]CAGGAGATATTGTTA | 4734 |
rs541204992 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971581 | AGTCAGCAGAGATTG[C/T]GCCACTGCACTCCAG | 4734 |
rs541210356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906328 | CTATAAAGACACATG[C/G]ACACGTATGTTTATT | 4734 |
rs541244344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914421 | GAACGGCCAAATTAC[A/G]TAAAGAACTTTTGGC | 4734 |
rs541247712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944715 | CCCCGTGTAGCCTAA[A/C]TGGGAGACACTTCCC | 4734 |
rs541270536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957496 | AGAGAGTGTCTATTA[C/T]GAATGGGTGTTGAAT | 4734 |
rs541275034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913032 | TGTTGATTACAGTAA[C/G]CTAGAAACTCAATTT | 4734 |
rs541275460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921496 | GGCCTGGCTAAATTT[C/T]GTATTTTTAGTAGAG | 4734 |
rs541300274 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956964 | TTTATGTTGTCTTCG[A/G]CTTCTCTCAGCACTG | 4734 |
rs541335606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927569 | CACAAGAATATTTTT[A/G]CATTAGACACTGGCA | 4734 |
rs541375973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862844 | AATCCATCTGAGACA[C/T]GACTTCAAAATGAAA | 4734 |
rs541379719 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871008 | ATCCTTTTATTCTGT[C/T]TTCAAGAGATTACCT | 4734 |
rs541428728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902015 | CCTCTGCCTAGGAAT[A/G]AGTAAGGTAGCTATC | 4734 |
rs541470144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907858 | TTTTCAGGAAACTTG[A/G]TCTGAGCCTCTATCC | 4734 |
rs541497128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951765 | GTAATTTTTGCATCT[C/T]GTTAAAAACCTGAAG | 4734 |
rs541527879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958843 | TTTTATCTTTTTCAT[C/T]TCCACAGGGTCTATA | 4734 |
rs541548706 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904166 | CATCTCAAAAGAAAA[G/T]AATATATCAAGGTTT | 4734 |
rs541553657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853560 | CAGGTAATCTAACAA[C/T]AGAAATCATGCTTAT | 4734 |
rs541557592 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932421 | CAAGAAACGGGGAAA[A/G]GATTCCCTATTTAAT | 4734 |
rs541561581 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995565 | GATTATAAAGTAAAG[C/T]AAATTGGCCATTTGA | 4734 |
rs541570594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965564 | CCAGAATCCTTACCA[C/G]TGCCATGTTTTCTTC | 4734 |
rs541577460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845848 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 4734 |
rs541587761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868392 | ATGGTTTGGCTGTGT[C/T]CCCACTCAAATCTCA | 4734 |
rs541596017 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995054 | AACAAGACTCCACCT[A/C]AATTGTCGTACTTTA | 4734 |
rs541608777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971470 | TCTCCACTAAAAATA[C/T]AAAAATTAGCCAAGC | 4734 |
rs541646097 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924905 | AACCTCGTCTCTACT[-/A]AAAAATACAAAAATG | 4734 |
rs541646759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846336 | AGGCAAAGGAGGACA[A/G]GATGAGCAAGTAAGA | 4734 |
rs541657116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867855 | GAGGCCAGGAGTTCA[A/G]GACCAGCCTGGCCAA | 4734 |
rs541661174 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952247 | GCTGAGGCAGGAGAA[C/T]GGCATGAACCTGGAA | 4734 |
rs541688147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874910 | ATCCAGGAGGCAGAC[A/G]TTGCAGTGAGCCTGG | 4734 |
rs541709004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840375 | TCCATGTCATTAAAA[A/G]CAAATTCTTCAAAAT | 4734 |
rs541749534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883507 | GACTTTATCTGCTGA[C/T]TGTAGAGCCCTAGGG | 4734 |
rs541789645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868527 | GAATAAGTCTCATGA[A/G]ATCTGATAGTTTTAT | 4734 |
rs541820793 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856438 | CCTTCTCTTGAATGT[G/T]TCACAGAAACCATTC | 4734 |
rs541826499 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845910 | CCTGCCTCAGCCTCC[A/G]GAGTAGCCGGGATTA | 4734 |
rs541826790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888069 | CCTTTCCTCTAACAT[A/C]TGGAACATGACAGGA | 4734 |
rs541836740 | in-del | -/AGTC | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992545 | TACATGTGGCAGCTT[-/AGTC]AGCCAACAAGAAAGC | 4734 |
rs541842989 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962788 | CTTTTCCGACTTTTA[-/T]TTTTTTTTATTTTAT | 4734 |
rs541884142 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850005 | TCACCATGTTAGCCA[A/G]GATGGTCTCGATCTC | 4734 |
rs541885981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835203 | CAACCCACTGCAATC[A/G]GACTTCTACACTACA | 4734 |
rs541946934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896179 | AATGCCATTTTATTC[A/G]CTTTTGTCTTTATTT | 4734 |
rs541947111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836000 | AGCTCCGCAGGCTGA[C/T]TGTTTCCCTCTTGCA | 4734 |
rs541958429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923103 | GCAGGAGAATAGCTT[A/G]AACCTGGGAGGCAGA | 4734 |
rs541976048 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919704 | TAGAATTTCATATTC[C/T]GGAATGAAACAGATA | 4734 |
rs541976109 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893242 | AATAACAACTGTCTT[C/T]ACAGAGCTGTATTAA | 4734 |
rs541980364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928781 | TTTTATTAAAGTTAA[C/T]TTGGCATATGTGTGA | 4734 |
rs542008940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885354 | CAACAGGAAATTATC[C/T]GAAGGTACAAATTTC | 4734 |
rs542044408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843732 | AGCATGATATGAGCA[A/G]TTTCCTATACTGCTT | 4734 |
rs542046957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903782 | ATGAGCCGAGATCGT[A/G]CCACTGCACTCCAGC | 4734 |
rs542049458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991277 | AATGCTTTCTTCCTT[A/T]AACAAAAGGGGTGTT | 4734 |
rs542054469 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941740 | AGCTACTTTTTGTAT[A/C]CTTTTTTTCTTTAGT | 4734 |
rs542066550 | in-del | -/T | 0.00119784 | 0.0244435 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969008 | CTAGTTTCAACATCG[-/T]TATCAAGGAAAGAGG | 4734 |
rs542075260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948333 | GGAAGAACATTCCAT[A/G]CTCATGGATAGGAAG | 4734 |
rs542105746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837158 | AAGTAGGCCGAGCAC[A/G]GTGGCTCACACTGGT | 4734 |
rs542111941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910027 | TTTCACTCATCATAC[C/T]TGCTTATTCTATAGT | 4734 |
rs542113515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894475 | AATACCAAGAGACAC[C/T]GGTACTTGGTTCTTT | 4734 |
rs542172834 | snp | C/T | 5.95681e-05 | 0.00545715 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838170 | CCATTTTTCAGCTCA[C/T]GTTGATGTGTCTAAA | 4734 |
rs542175258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893717 | ATAAGAAACCATATT[C/T]TTCTGCTTGCTGAAT | 4734 |
rs542191516 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938789 | AAAAAAAAAACAAGC[A/G]TCAACAACAACAACA | 4734 |
rs542191520 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962240 | TATCTTTTTGCGTCC[A/G]CTTTCTTTCAAATTA | 4734 |
rs542213253 | snp | G/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879869 | TTCAAATAAGGAAAT[G/T]ACAGGAGAAAATTCA | 4734 |
rs542227749 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960040 | ATGTGGTCAATCCAG[A/G]TAACTACCTTACACA | 4734 |
rs542228647 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974658 | CAACAGAATGGAGGA[C/G]AAAACCCATATGATC | 4734 |
rs542229524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966870 | TATGTACACAAAATC[A/G]AAAGTTCATAACCAT | 4734 |
rs542234909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930305 | AGAAAAAGTTCACTG[A/G]CCCTCGTCCTAGACA | 4734 |
rs542247785 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897706 | TTATTAATTCCCTGC[C/T]CATGTGTCCTCCTGG | 4734 |
rs542265560 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992889 | TAACATCAACGACGA[A/C]CGGTGAAATAAAGCA | 4734 |
rs542275229 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839885 | GGAGGCTGAGGCAGA[G/T]AATTGCTTGAACTTG | 4734 |
rs542277116 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832160 | AAATAGTAGCCTAAT[A/G]AGATTCTCCACCCCT | 4734 |
rs542278713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937315 | AATACATTCAGTTCA[A/T]AACATTCTGGGCTAT | 4734 |
rs542308949 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905040 | GAGGCTGCAGTGAGC[C/T]GAGATCGTGCCATTG | 4734 |
rs542336685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832894 | TTCAAAATCTTAATT[A/C]TTTTTAAAATTAAGC | 4734 |
rs542339340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949456 | CCATTACTGGGTATA[C/T]ACCCAAAGGATTATA | 4734 |
rs542340061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840206 | CAGATAGGTATGTGA[C/T]AAAGTAAATCTAGAA | 4734 |
rs542376650 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865867 | CTGTATAGAAGGTGA[C/T]GAGTAGTGGAGTAGG | 4734 |
rs542386535 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867696 | CAAAAAGTTAATCAA[A/G]TAAGTGAAGAGAGTT | 4734 |
rs542395493 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943061 | ACTTGAAAGAGATGA[C/G/T]TTACGGTATCTGGCA | 4734 |
rs542397174 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862438 | GTCCTTGATCTGTGC[A/G]TGCTGGAAGTTATGT | 4734 |
rs542398023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833445 | GGTGGATCACTTGAG[G/T]TCAGGAGTTTGAGAC | 4734 |
rs542398835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955670 | TGAATAAACACTGTA[C/T]GTATATACATTTCTT | 4734 |
rs542399923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919330 | TCCAGCCGCCACTTT[C/T]AAAGAAATATCAAAA | 4734 |
rs542400519 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828349 | TTATTCCTAAATCAC[A/C]AAGATACCATACTGA | 4734 |
rs542458669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942746 | ATGGGAAGTCAGGCA[C/T]TGCTATACAGATACC | 4734 |
rs542463313 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918432 | TAGCTGGAACTCCAG[C/T]AATAAATATATACTG | 4734 |
rs542533761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871798 | TCCTTTCTCTGCTTT[A/C]GTTTGACCTTTTTGA | 4734 |
rs542541325 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912719 | ACCTTAGCTCCTTAA[C/T]CTGCTTCTTGATTGA | 4734 |
rs542548761 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877781 | ACATTCTAATTTATA[G/T]CATCATAGACTCATT | 4734 |
rs542553656 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953633 | TTTTAGTAGAGACGC[A/G]GTTTTGCCATCTTGG | 4734 |
rs542582535 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927478 | TTTTTAAAAATTTTT[A/G]CAGAGACAAGGTCTC | 4734 |
rs542583408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903685 | AAAAAATTAGCTGGG[C/T]GTGGTGGCAGGTGCC | 4734 |
rs542596644 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942935 | TCCAGGCTGAGGTGG[C/T]CTCGAAGACAAGGAA | 4734 |
rs542607532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845759 | GAAAACAAATTTCCA[C/G]GGAAATTTCGACACA | 4734 |
rs542613285 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901756 | AAAAACAATTATTAC[A/G]TGTTACATATCATGG | 4734 |
rs542621242 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925374 | TTTATTAATCAGTTT[A/C]GAGCCACCCAAAGTG | 4734 |
rs542629211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859594 | CTCAGCTATTCAGGA[A/G]GCTGAGGCATGAGAA | 4734 |
rs542635408 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969234 | ACCCATGGAGGGAGT[A/G]TTTAGACCAGCCTCA | 4734 |
rs542647143 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937983 | ACGGATGAAATAGAT[A/G]GCTCAAAAATAAACC | 4734 |
rs542678180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956603 | ATATGTGTATATATT[C/G]TCTCTCTCGCTCTCT | 4734 |
rs542679967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985301 | TGTCTGTGGAGTGAG[C/G]GTGAATTTCACAGAG | 4734 |
rs542719955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904448 | GCTGGGATTACAGGC[A/G]TGCACCAACACGCCT | 4734 |
rs542796489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857918 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACCC | 4734 |
rs542797797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873227 | TTATCTCTTTCATCA[A/G]GAGAGCCCATTATTC | 4734 |
rs542811855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955098 | CAATCTCGGCTCACT[C/T]GAAACCTCTGCCTCC | 4734 |
rs542820447 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875471 | ATGCACCATGCACTA[A/C]CATGCCTGGCTGATT | 4734 |
rs542836652 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876520 | ATATTGTTGCAAGAC[-/TT]ATATTTTATATAAAG | 4734 |
rs542847665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961493 | TATTATTATTTGAGA[C/T]GCAGTCTCACTCTGT | 4734 |
rs542877484 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980470 | TATGTGAGAATCCCA[C/T]AGTGAAATGGTAGGT | 4734 |
rs542879772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932250 | AGCTGGAGGCATCAT[A/G]CTACCTGACTTCAAA | 4734 |
rs542892825 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846397 | AATGAAACAGATGGC[A/C]AGATGATGAGTTTAG | 4734 |
rs542908869 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960686 | TCTATCCTATTAGTT[A/C]TGTCCCCCTAGAGAA | 4734 |
rs542924788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852096 | AGGTCAGGAGTTTCA[C/G]ATCAGCCTGGCCAAC | 4734 |
rs542951509 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908370 | ATCTCCATCTTTAAC[-/T]TTTTTTTCTGCTGCA | 4734 |
rs542978653 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916559 | GTACCTTGTTGGCTG[C/T]AGTGAAATCTGTAGA | 4734 |
rs542978777 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896474 | CAGGGTGAGGCACCA[C/T]ACCTGGCCACAATGC | 4734 |
rs543015569 | in-del | -/TATGG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913414 | AACACTAGAATCTTC[-/TATGG]TCCATAAAACAAGCC | 4734 |
rs543017905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884463 | AAATAAAGCACCAGG[A/G]ACCTATCCCAGAAAC | 4734 |
rs543033612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830907 | GATGGGGGTCTCACT[A/G]TGTTGCCCAGGCTGG | 4734 |
rs543077959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927607 | TTTGGTTAGTTAGGG[C/T]AGAGCCAGGATGGGG | 4734 |
rs543080844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883656 | ATGCTTGTGTCATCC[C/T]TCCCCTAGTTCCAGG | 4734 |
rs543092903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912370 | TTAAGACATAAGTTT[A/G]TTACAGTTCTACTAT | 4734 |
rs543141717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891712 | CTAGTATTATAATGA[C/T]ATGAATTTCAGTTTC | 4734 |
rs543154966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969291 | AGTTTAAGGCTAAGT[C/T]TGGGCAAGCCTTGCC | 4734 |
rs543215554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851580 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 4734 |
rs543246774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55987067 | CTTCCACAATGGTTG[A/G]ACTAGTTTACAGTCC | 4734 |
rs543266576 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979141 | CTTACTAGTTCACTA[C/T]TAAAATCCTATATCA | 4734 |
rs543276264 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956622 | CTCTCGCTCTCTCAC[A/C]CACACATGCGCATGT | 4734 |
rs543278580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981276 | CACCATGTTGGCCAG[A/G]CTGGTCTGGAACTCC | 4734 |
rs543293771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931817 | AATTCAATGGTTTTT[A/G]ATATATTCAGAGAAT | 4734 |
rs543303195 | snp | C/T | 1.64887e-05 | 0.00287125 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860654 | AGAACTAGGAAACTA[C/T]TTATACCTCGGAAGA | 4734 |
rs543310380 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881148 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTGAGAT | 4734 |
rs543313101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900298 | GCCATGCCTGGGAAT[C/T]CCAGAAATACTGAAG | 4734 |
rs543315583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986715 | CGGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 4734 |
rs543318204 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973853 | AAAAAAAAACAACCT[A/G]GCTATGCATCTTAAA | 4734 |
rs543327393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945206 | AAGGTCGGTAAAAAC[A/G]AACTTCTCCAAGCTA | 4734 |
rs543331750 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835771 | AGATTACTGTAGCAC[A/T]TTCCCAACTCTGCTG | 4734 |
rs543354983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980508 | ATTCTACTGTGAGAG[A/G]CTCCAGTCAACAGTA | 4734 |
rs543371702 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928144 | CCTCCCAAGTAGCTG[G/T]GACTACAGGGGCGTG | 4734 |
rs543376363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906525 | TTCTCAGCAAACTAT[C/T]GCAGGGACAAAAAAC | 4734 |
rs543384797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849774 | AAAATATATTCATCT[A/G]CTGCTAATTTTAAGT | 4734 |
rs543392493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970759 | GCTCACATATGGCTT[C/T]AGTGACCAAAGACTT | 4734 |
rs543410426 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931241 | CACAGTTGGAAATCA[A/C]CTTGGAACATGCATG | 4734 |
rs543421742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853677 | GAAGTCTGGTTATTT[C/T]CAGGCTTACTTAAAA | 4734 |
rs543422908 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974730 | CTCTTCATGATAAAA[-/T]AAAAAAACCCTCAAA | 4734 |
rs543424628 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827077 | TCAAATAGTTTATAA[C/T]CAAAATGAATTGTGT | 4734 |
rs543425869 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941924 | AACTCGGTTTGTGGC[C/G]CAATATGTGGTCTAT | 4734 |
rs543428724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964027 | TATTTTTCTCTTTTT[G/T]TCAAGATTTTTCTCT | 4734 |
rs543451906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903283 | AGGATTCTCCCAGTG[A/C]CCGATGAGAGTCCTT | 4734 |
rs543483229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854106 | CAGTGAGCCGAGATC[A/G]CCTGGGCACTCCAGC | 4734 |
rs543499645 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856756 | CTTCGCAATCTACCC[C/G]CTGGACATTCCAGAC | 4734 |
rs543518769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990311 | CTGGTGCCAAAACAG[C/T]TGGGGACTGCAGTTC | 4734 |
rs543532244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941045 | AGGCATAAAATTAGT[A/T]ACAATATTACCTTTT | 4734 |
rs543532324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933679 | CCCTAGAACTTAAAG[C/T]ATAAAAAAAAAAATC | 4734 |
rs543552261 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874629 | CTGATTTCAGCTGAT[-/G]TTCACCAAAAGGGAA | 4734 |
rs543554540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969123 | GAGAATCTATGCCTT[C/T]GCGGGACGAAGGGCA | 4734 |
rs543580173 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883278 | GCCCTGTGGCAGGAG[C/T]GGCCACGGAGAGACT | 4734 |
rs543592246 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900801 | TGCCAACTAAACATT[C/T]TAATATGAAGATAAA | 4734 |
rs543592607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946425 | AAGCCATTACATAAT[A/G]GTAAAGGGATCAATT | 4734 |
rs543620842 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945678 | CACAAAGATATTCCT[C/T]GAGAAGAGCAACCCC | 4734 |
rs543647160 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988898 | ATGAGAAGAATACTG[C/G]AGCTCTTTGTGTTGT | 4734 |
rs543649998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855851 | TCCTGAATTGTATGC[C/T]GTATGCAGCGGATCA | 4734 |
rs543652915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906897 | GGTCAGAGGTTCAAG[A/G]CCAGCCTGGCCAACA | 4734 |
rs543656596 | snp | C/G | 1.64857e-05 | 0.00287099 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915441 | AGACAGGAAATATTT[C/G]GATAAGCTCCTCCCA | 4734 |
rs543669950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869472 | CATCCAAGTAAATAA[C/T]CTTCATTGCACATGT | 4734 |
rs543686064 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995656 | TTATTCTGTCTTTCC[A/G]AATATGAAATCATGA | 4734 |
rs543692440 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922974 | GTTTAATTTGTTTCC[A/G]TCTAGAAGGGACCAG | 4734 |
rs543700101 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990516 | CAAAGCAAGTTACCA[C/G]ATACTGGAATACTTT | 4734 |
rs543719296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841804 | TCTCGATATCCTGAC[C/T]TTGTGATCCGCCCGC | 4734 |
rs543721738 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994941 | GCGCCTGGAGTCCCA[G/T]CTGCTTGGGTGGCTG | 4734 |
rs543752506 | snp | A/T | 0.031825 | 0.122064 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914212 | GAAGTTTTTTTTTTT[A/T]AAACAATCTTTAATA | 4734 |
rs543805759 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954194 | TTTTAGATACTACTG[A/T]CCATTTTCTCTTTGA | 4734 |
rs543817261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976701 | GTGGTGCAATCTCAC[C/T]TCACTGCAAGCTCTG | 4734 |
rs543873327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947041 | ATAGCACTAAATGCC[C/T]ACAAGAGAAAGCAGG | 4734 |
rs543873994 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851475 | AATATTTTACATTTT[C/T]TTTTCTGTTTTTTTT | 4734 |
rs543900960 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982939 | CCAGCCTGGCCAACA[A/T]GGTGAAACCCCGTCT | 4734 |
rs543966753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929960 | AATTAAAATAGAAGT[A/G]CTTTAAGAAAAATTT | 4734 |
rs543974188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924413 | CAAGAGGTCTTGAGT[A/T]AGACCTTATAATATG | 4734 |
rs543987640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862035 | GAGGTATGCAACAGC[A/G]CAATTCTACAGAATT | 4734 |
rs543994427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841299 | GAAGGACATTCTGAT[A/G]CATACTACAACATGG | 4734 |
rs544006165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844390 | ACAAGAGGCACACTG[A/G]TCAGTTAAAGACCCC | 4734 |
rs544025840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966789 | TGAATAAGAATTTAT[C/T]GCTGCGCTCAAGAAA | 4734 |
rs544040397 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932589 | AAAGCTAGGCAATAC[C/T]ATTCAGGCCATAGGC | 4734 |
rs544048241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861263 | CAGAATGAAAGATGG[G/T]GTAAGAACTTTATAA | 4734 |
rs544074638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868508 | GTGCTGTTCTCATGA[C/T]AGTGAATAAGTCTCA | 4734 |
rs544076941 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871759 | GTTTAAGAAACAAGA[-/C]AAATACTGTTGCTTT | 4734 |
rs544093971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935972 | CAAGAGAATCCCAGA[C/G]AAGCTGGGTCAAGCA | 4734 |
rs544118775 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832500 | GCTCACTGCAACGTC[C/T]GCCTCCTGGGTTCAA | 4734 |
rs544176202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964832 | GGTCTCGGTTGGAGG[G/T]ATTAGGGTCATGGGA | 4734 |
rs544189342 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991337 | TTCAATCCTTCTTTT[A/C]CTTTTGTGATAGACC | 4734 |
rs544195207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836037 | CACCCAGCATACTCA[A/G]CTGCCTGTGGGTACA | 4734 |
rs544207009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880939 | ATGAAACCCCTGCTC[A/C]CCTTTCCCTGGACCA | 4734 |
rs544207351 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956632 | CTCACACACACATGC[A/C/G]CATGTATTTTTACAC | 4734 |
rs544217702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953115 | CTGCCTAAGCCTCCC[A/G]AGTAGCTGGGACTGC | 4734 |
rs544229678 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944752 | GGCCAACAGACACCT[C/T]ATACAGGCAGGTGCC | 4734 |
rs544246715 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925841 | TTTTTGAAAACTGAA[A/G]TACAACACATATTCA | 4734 |
rs544249739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973767 | GCAAACCTATGGAAT[A/G]GAGCAAAAGCAGTAC | 4734 |
rs544256357 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836662 | TCCCGAGTAGCTGGG[A/C]CTGCACGTGCACGCC | 4734 |
rs544265419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843870 | TTGTAGTAGGGCCAA[C/T]GATGGGGAATAAAGG | 4734 |
rs544293859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968133 | TAAATTTAATACTAT[C/T]CCCATTCTCCCTTCA | 4734 |
rs544322031 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871110 | AGTGTATCCTTTCAT[A/G]AGTAGTCAGTGAAAT | 4734 |
rs544324043 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829323 | TAGGTAACACACTTT[A/C]CAAAGTTTTTTCCCA | 4734 |
rs544361993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923841 | CAGACTTTTTTTTAA[A/T]AAAAAAGCTAGTTTC | 4734 |
rs544407794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966173 | GCTTTTTGTATTAAG[C/T]CCAGAGTTTATGGTT | 4734 |
rs544428058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878103 | GTGCTTATTACTTTC[A/G]GGCTCAAGAGATGAA | 4734 |
rs544430920 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868211 | ACATGGGCATGTGAG[A/G]TAGAGCCTAGCCCCT | 4734 |
rs544477000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831169 | AGGTGATCTGCCTGC[C/T]TCAGTCTCCCAAAAT | 4734 |
rs544478251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897028 | GCCCAGACCGGAGTG[C/T]AGTGGCACAATCTTG | 4734 |
rs544555857 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948805 | TACAAAAATTAATTC[A/G]AGATGGATTAAAGGC | 4734 |
rs544556865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977237 | TCCCATAAAATACCA[C/T]ATTTTTACTTTTCCT | 4734 |
rs544570437 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942172 | TTCGTAATTTTAAAG[A/C]TTACTAGGTCCATAC | 4734 |
rs544595449 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906939 | ATCTCTACTAAAAAT[-/A]AAAAAAATTAGCCAG | 4734 |
rs544601170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871830 | AGTAAATCCACACAC[A/G]TTTTCACTAGATTTT | 4734 |
rs544672422 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889967 | ATCGGCCTCCCAAAG[C/T]GCTAGGATTACAGGC | 4734 |
rs544674551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832941 | ATGGAAGCTTGCGGA[C/T]TCGTCAGCCATGAAA | 4734 |
rs544704197 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921326 | GGGATCTATAATAAC[-/T]TTTTTTTTTTTTCGC | 4734 |
rs544708310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930875 | CCTCCCCAGCCATGT[A/G]GAACTGTGAGTCCAT | 4734 |
rs544713096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938968 | TAAAAATGGTGGTGC[A/G]TGATGGTGTGCACCT | 4734 |
rs544724913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905967 | CCATCAACAAGTGGG[C/T]GAAGGATATGAACAG | 4734 |
rs544732491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842322 | AGGTATATTGTCTTG[A/G]TTTCCTCTATGGTAT | 4734 |
rs544735714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899244 | ATTATGTAGTGGCAG[A/G]ATAAAATGTTTTCTA | 4734 |
rs544769654 | snp | A/T | 1.64996e-05 | 0.0028722 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915947 | AATAAACTGGTGTGA[A/T]GTTTGATAGGATCCT | 4734 |
rs544774167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944695 | ACCTCAAGTGGGTCC[A/C]TGACCCCCGTGTAGC | 4734 |
rs544796773 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924982 | CTGAGGCAGGAAAAT[C/T]GCTTCAACCTGGGAG | 4734 |
rs544851934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896335 | TTAGAGACATGCACC[A/G]GTATGCCTGGCTAAT | 4734 |
rs544863579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993494 | AAGCCCGCCCCGCAG[A/C]CCCGCGGTCCCCGCA | 4734 |
rs544866722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943140 | CTAACCATATGCTTA[C/T]ATGCATTCACAGAAA | 4734 |
rs544879290 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904267 | TAGAAGGCTGTTAGG[G/T]TCTCTTCCTCCTTGT | 4734 |
rs544889191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983812 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 4734 |
rs544913309 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908827 | AGAGGATTGCTTTAG[-/C]CCAGGAGTTCAAATC | 4734 |
rs544928391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948477 | TCATATGGAGCCAAG[A/G]AAGAGCCCACATAGC | 4734 |
rs544943315 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854158 | CATCCCCCTCCCCTC[C/T]GAAAAAAAAAAGTCC | 4734 |
rs544947435 | snp | C/T | 9.30969e-05 | 0.00682201 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872506 | TGGGTTTTCAAAATA[C/T]ATCTATAACACCAAA | 4734 |
rs544956430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865697 | TGACAGGCAGTGGAC[A/G]GCTTCCAAGATGGAA | 4734 |
rs544963695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951623 | AAAAGAAAGAAAAAT[C/T]TTAATTATTGCTTAC | 4734 |
rs544977666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906123 | CGATCATTAAAAAGT[C/T]AGGAAACAACAGGTG | 4734 |
rs544978976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919516 | GGTCTGAAATTGCAT[A/G]GGATCTATACTGCTA | 4734 |
rs544987799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899917 | ACTGGCTACTAAACT[A/G]GACAGTGGTGCTGTA | 4734 |
rs545004089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945117 | TCTCCTCCAAAGGAT[A/C]GCAGCCCCTCGCCAG | 4734 |
rs545011672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880065 | TTGGGAGGCCAAGGA[G/T]GGCGGATCATGAGGT | 4734 |
rs545012742 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904049 | CACCAGTAATCCCAG[A/C]TACTTCGGAGGCTGG | 4734 |
rs545026237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951227 | TTTATGTTTTTTATA[A/G]GACAAAATTTCAATT | 4734 |
rs545035812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945748 | GGAAAAAATGTTAAG[A/G]GCGGCCACAGAGAAA | 4734 |
rs545093055 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950045 | AAATAACTCAACAAC[C/T]TGGGAATTTAAAAAC | 4734 |
rs545140116 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855860 | GTATGCCGTATGCAG[C/T]GGATCACCTCTAGCC | 4734 |
rs545145771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859321 | GTGGCTGAAGTGAAA[A/G]TGTCATCTATCTCCT | 4734 |
rs545165135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927474 | TAATTTTTTAAAAAT[C/T]TTTGCAGAGACAAGG | 4734 |
rs545178381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913387 | TGTTGCCACTGCTAT[A/G]TTTAGAAAAAACAAC | 4734 |
rs545183869 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831361 | CAACTCTGGCTCTAT[G/T]TGTGGGATATTTGCC | 4734 |
rs545185665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949889 | ACACCAATATGGCAC[A/G]TGTATACATATGTAA | 4734 |
rs545207476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866133 | TGCCCAGGCTGGTCT[C/T]AAACTCCTGGGCTCA | 4734 |
rs545215321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992888 | TTAACATCAACGACG[A/G]CCGGTGAAATAAAGC | 4734 |
rs545217101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866957 | AAAGCCAATATGTAA[C/T]TGCTCACAATTTAAT | 4734 |
rs545229822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920173 | GAAGTCTTCACTATA[C/T]ATATATTGTGTGGAA | 4734 |
rs545231042 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982408 | GATATATTCATACAA[C/T]GAAATACTATTCACC | 4734 |
rs545239732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920943 | TTTTGCTGGTAAACC[A/G]AGTTTCTCAAGAAAA | 4734 |
rs545245361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949547 | CAAAGACTTGGAACC[A/C]ACCCAAATGTCCATC | 4734 |
rs545247387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956390 | TTTGTGTAACCCAAT[A/G]GAGCAAAGATTTTTT | 4734 |
rs545273218 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827916 | CTTTCTCATCTGTCT[A/G]GAACTTCTGACAATC | 4734 |
rs545282439 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963141 | CTCTTTTTTATTTTT[A/T]TTTTTTTTGAGACAG | 4734 |
rs545289396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933068 | GAAATAGGAACACTT[C/T]TACACTGTTGGTGGG | 4734 |
rs545330057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969454 | AGTGAGACACCAGAC[A/G]GGGCGGCCAAGGGTG | 4734 |
rs545402539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907032 | CCTGGGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA | 4734 |
rs545405273 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860737 | AATGCACGTTGTGCT[C/T]GCAGTTGAATGTTGC | 4734 |
rs545405578 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868668 | TGAGTCCATTAAACC[C/T]GTTTTTAAAGCTTTA | 4734 |
rs545408573 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995405 | AGTCATTTGAATTTA[A/T]GTTAATTCAGTGTCA | 4734 |
rs545445960 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994994 | TGGGAGGAGGAGGTT[A/G]CAGTGAGCCAAGATT | 4734 |
rs545455863 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927656 | AGAGTTAAGACTTGA[C/T]TGGTAGGGGGATCAA | 4734 |
rs545461826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975234 | ATAGTACTGGAAGTC[C/T]TAGCTAGAGAAATCA | 4734 |
rs545466754 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875972 | CACACCATTATTAAA[C/T]GCTGAAAACAAAAGA | 4734 |
rs545477325 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55948078 | AGCCCAAAATCTCCT[C/T]AAGCTGATAAGCAAC | 4734 |
rs545491830 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919259 | TGGTGTCATCACAGT[C/T]ACTCTGAATGCCTAA | 4734 |
rs545524681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922228 | TGATTTTTCAGAATA[C/T]AGAAAATTATGCATC | 4734 |
rs545535531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970989 | GAGATACGTGAACTC[C/T]CAGATAAATCAAAAT | 4734 |
rs545537188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976652 | TTTTTTTTTTTGAGA[C/T]GGAGGCTCGCTCTGT | 4734 |
rs545555279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885312 | TAAAGGGAGTTCTTC[A/C]GTCTGAAAGAAAAGG | 4734 |
rs545574276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976101 | AATCAAACTAGACCC[C/T]TATCTCTTGTCATAT | 4734 |
rs545589916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935120 | TGATCCACCCTCCTC[A/G]GCCTCCCAAAGTAGT | 4734 |
rs545619480 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905102 | GTCTCAAAAAAAAAA[-/G]AAAAGAAAAGAAAAG | 4734 |
rs545620903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856401 | GCTCCCATGCCCCCC[A/G]TGCTGGACTGCCTCC | 4734 |
rs545623751 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852657 | CAAGCAACCACTCAT[C/G]TGCTCTGTTACTACA | 4734 |
rs545625724 | snp | A/C/T | 0.000161268 | 0.00897845 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55873964 | TATACCAACCGGTAA[A/C/T]GGATAAAGTGGAACA | 4734 |
rs545675213 | in-del | -/T | 0.273049 | 0.248935 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979917 | AATTATAATTATTAC[-/T]TTTTTTTTTTTGAGA | 4734 |
rs545737110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891894 | TCCAAAGTAATAAAA[A/T]ATCAGAATTTAAAAA | 4734 |
rs545748287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881945 | ACCCGCCCTCCAGTT[A/G]TAACAACCAAAAACA | 4734 |
rs545774175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940189 | GAGAATAGAATGGTG[A/G]TTTAATACTATATTA | 4734 |
rs545799018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847519 | ATGAATTAGAAAACA[A/G]AATCTGAATAAAATG | 4734 |
rs545799946 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965494 | CAGTGACTGTGATCT[C/G]TGTTCAGATCTTTTG | 4734 |
rs545800748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839888 | GGCTGAGGCAGAGAA[C/T]TGCTTGAACTTGGAA | 4734 |
rs545860976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848236 | CTGAGACTTGGAGTA[C/T]GGGAAATGGGGGAGA | 4734 |
rs545861523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855939 | CATGCAGAGACTTTG[C/G]TTTTAACATGGGAGA | 4734 |
rs545912185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903420 | TTTCTGGGCCTTTCT[A/C]CTTATTTCTAATATG | 4734 |
rs545920581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884731 | GTGAATTTTAAGAAA[C/G]GCTATTTTAAAAAAC | 4734 |
rs545929092 | snp | A/C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55917003 | AGATACCAGATATCA[A/C/T]AGAAAGAAAAAGACG | 4734 |
rs545956934 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938411 | ACTGGATATCCATAC[G/T]CAAAAGAAAGAAATT | 4734 |
rs545962462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849137 | TCATTTCTTTTGCCC[C/T]GCTCTTTAGGAAATG | 4734 |
rs545977843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990511 | ATGTACAAAGCAAGT[C/T]ACCAGATACTGGAAT | 4734 |
rs545980348 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835988 | AGCTGGTCTGTTAGC[C/T]CCGCAGGCTGATTGT | 4734 |
rs546014207 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941125 | AGTACTCTCTCTGTC[G/T]CTCTCATATAAGGCC | 4734 |
rs546032919 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908579 | ATTGGTACGATCTGT[A/T]ATAAATACAGAAATC | 4734 |
rs546046687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982371 | AGTTGGAAACAATCA[A/G]TGTGTCCATCGAAGG | 4734 |
rs546062172 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909506 | GTGTGAGCAATACTT[C/G/T]GGATTATTTCCAGGG | 4734 |
rs546074519 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974593 | AGTGGGATTCATATC[A/G]GGGATGAAAGGATGG | 4734 |
rs546076623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901917 | TGTTTCATAAATTTT[A/G]TATTATATAAATATA | 4734 |
rs546132990 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985469 | GAATAGCAATATTCC[-/CA]CTGGCATCCAAGGAT | 4734 |
rs546137492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900889 | TATGAGGCAAAAACA[C/T]TGATGACAGCTAGAA | 4734 |
rs546138957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838409 | TTACTGGGAAATGAA[C/T]GTAAAAACAGAGCCT | 4734 |
rs546164879 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873188 | ACTCACGTTGACTGA[G/T]GGTCAATGGCTGGCC | 4734 |
rs546175483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886237 | AGAGAGACAGACCCC[A/C]ATACAATTATAGCTT | 4734 |
rs546208443 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990747 | AGGTGCATGGGAAGG[A/G/T]GGTGGGAAGTGATGC | 4734 |
rs546238506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895576 | ATTCAGGCTGAAATT[C/T]AGTGTGTGTTAAAAT | 4734 |
rs546275402 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862360 | TTTATAAATGTATAT[A/G]CAGTCTAATAATAAA | 4734 |
rs546278944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837290 | CAAAAATTAGCCAGG[C/T]GTGGTGGCGGGCACC | 4734 |
rs546351124 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853133 | TGCTTTAAAACAAAT[A/T]ATATTTTATTTTGAA | 4734 |
rs546369557 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835085 | AGCAAAACAAACAAA[A/C]AAACAAACAAAAACT | 4734 |
rs546380580 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947629 | GGGCTTCATCCCTGG[C/G]ATGCAAGGCTGGTTC | 4734 |
rs546406803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887434 | CTATTAAGATTGAGC[C/T]ATGAAGAAATCCAAA | 4734 |
rs546443913 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947131 | ACACATTCAAAAGCT[A/C]GCAGAAGACAAGAAA | 4734 |
rs546448677 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845100 | GGCCTTTTTACTAAT[A/G]TGAGAATTCATATTC | 4734 |
rs546489584 | snp | C/T | 1.67739e-05 | 0.00289597 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863067 | CTGGTTGGTCCAAAA[C/T]AACCCAGCCAGGCTG | 4734 |
rs546498667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924036 | ACAAAATTAGGAAAA[A/G]GATAGGACTTTAAGA | 4734 |
rs546516282 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934432 | CATTGGTGCGCAAGT[G/T]TTCTGTGCATATATT | 4734 |
rs546518926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910674 | AGCCTTGGTCCTGTA[C/T]GTCCAACTGCCCTAC | 4734 |
rs546535741 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827984 | TGACAGATGAAGAAA[C/T]ATGAATCCAGAGAGG | 4734 |
rs546537367 | in-del | -/T | 0.277067 | 0.24853 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963135 | TGGCACTCTTTTTTA[-/T]TTTTTTTTTTTTTTG | 4734 |
rs546548641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959558 | CATGTTCTTTGTGTT[A/C]CTCTCCTCTTAAGCA | 4734 |
rs546566648 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908963 | TAACTTCAGGTATAA[C/G]TATACTTAACTAAGT | 4734 |
rs546567678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886530 | CCAGCACTTTGGGAG[A/G]CCGAGGTGGGTGGAT | 4734 |
rs546626589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851758 | CTGGGATTATAGGCA[G/T]GAGCCACCTTGCCCG | 4734 |
rs546629372 | in-del | -/AATAAAATACATACT | 0.0532492 | 0.154237 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838078 | TACAAAATTATATCC[-/AATAAAATACATACT]AATAAAATACTTACT | 4734 |
rs546638106 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945662 | GAAATACAGATAACA[A/C]CACAAAGATATTCCT | 4734 |
rs546640054 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965927 | AAATTACTAAGATTA[C/T]AGGCATGAGCCACCA | 4734 |
rs546642962 | in-del | -/AATAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923659 | CAAAAAAAAAAAAAA[-/AATAT]ATATATATATATATA | 4734 |
rs546657666 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942888 | GTTGAATGGTTGTGA[A/C]CAAAATGCTGATAGT | 4734 |
rs546674720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895821 | CCATCTAACGCTGGT[C/T]ATATAATTGGGATAC | 4734 |
rs546677135 | in-del | -/TCAAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964443 | CCAACAATTTTAATT[-/TCAAA]TGCTGTATTTTTCAC | 4734 |
rs546694462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983456 | CCAACCTTCCTGTTC[A/G]TCTCCATCCCATCTT | 4734 |
rs546718214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911391 | GAACTCCAGTTTACC[C/T]ATCAAGACTCGGTTC | 4734 |
rs546727389 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864448 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 4734 |
rs546729454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872069 | ATTGGCTTTGTGCAC[A/G]TCGAGTTAGGTAATG | 4734 |
rs546733657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903621 | CGAGGTCAGGAGATC[A/G]AGACCATCCTAGCTA | 4734 |
rs546740020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991388 | TAGTGGAGAGGGCAA[A/C]CTCCACAAGAAAAAA | 4734 |
rs546787925 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918845 | AACATCTTTTTCTTT[C/T]AAATAAGGAGGAGTC | 4734 |
rs546792611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871452 | ACGCTAGAAAGCATG[C/T]GACAAATTGAAAAGC | 4734 |
rs546813958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909150 | AGACATCCTCGGGCC[C/T]AACTAGAAATGCCAT | 4734 |
rs546825797 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871510 | AAACAATTTAGTTAT[C/T]CTTGATATGCAGATG | 4734 |
rs546847531 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921257 | TTTAGGGTTACAAGC[C/T]AATACCCCAAAAGAA | 4734 |
rs546848490 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862428 | AAGTCATTCCGTCCT[G/T]GATCTGTGCGTGCTG | 4734 |
rs546867986 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843440 | ACTAATCTTTTGTAC[A/G]TTCTTTGCTTATGTG | 4734 |
rs546873905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978301 | ACTAGTTATTTTAAA[C/T]GCTAAGATTAATTGA | 4734 |
rs546905644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959003 | TTTTCTACCATTGTC[C/T]ACTTTCTCTTTCACT | 4734 |
rs546929447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843957 | TATATGTGAAAAACA[A/C]GTGTAAATGATGCTA | 4734 |
rs546951073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911655 | CTGCCTCAGCCTCCC[A/G]TGTAGCTGGGACTAC | 4734 |
rs546963892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920696 | ATTTGCTAGGAAAAT[C/G]GTACATTTTAAATTT | 4734 |
rs547006716 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887536 | GCATCCAATGGCTTC[A/C]CTGATGAATTTTACC | 4734 |
rs547027824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926639 | GGCATCATGGCACAT[G/T]CCTATAGTCCCAGCT | 4734 |
rs547036642 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895234 | TTTTTTCTTTTTAGA[A/T]ATGTCTGCCAAGCTA | 4734 |
rs547120380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889993 | CAGGCATGAACCACC[A/T]CACCAAGACTAATTG | 4734 |
rs547164577 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939520 | CAAGCAACAAAGAAC[A/C]TAATTTAAAAAATGA | 4734 |
rs547189477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925316 | ACGCTTATAAATACA[A/G]ATTAGATTTTGACAC | 4734 |
rs547201206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881415 | CAAAGTGCTGGGATT[A/G]CAGGCATGAGCCACA | 4734 |
rs547204999 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975893 | TATACTACAGAGTTA[C/T]AGTATCCAACACAAC | 4734 |
rs547219781 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894055 | ACAATTTAATCTGTG[C/G]TATAAAATCATAGTG | 4734 |
rs547243362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898245 | AAGTCACTATTTAGC[C/T]CATCATTTGGTTGTT | 4734 |
rs547245405 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969037 | GGCACTGAAGAGGGT[A/G]GGAAAGACAGTCTTG | 4734 |
rs547250575 | snp | C/T | 2.6606e-05 | 0.00364723 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55924657 | TTACCAATCGGTTTT[C/T]GTCAAACACTTCAAA | 4734 |
rs547252627 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931009 | AAAACTGTACATACA[A/G]GGCATATAACTGTGA | 4734 |
rs547258518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931601 | AACAACAGAGGAAAA[A/C]AGTTGCCAAAAAATA | 4734 |
rs547261538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840961 | TTGTTTTTGAGATGG[A/G]GTCTTGCTCTCGCCC | 4734 |
rs547268119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889245 | AAGAAAGGAAATCAG[C/T]GTATTGAAAGGATAT | 4734 |
rs547302955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897269 | TGAGCCACTGCGCCC[A/G]GCCGATATGGCATGT | 4734 |
rs547305191 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905360 | AGAAGACACTAACAA[C/T]TGGGGGGTTTCCCAA | 4734 |
rs547309486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980137 | TAGCTTTGCCACGTT[A/G]GCCAGGCTGATCTTG | 4734 |
rs547356766 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853354 | GTTTAACACAGATAA[A/C]GTCATTTACTTCCCA | 4734 |
rs547375305 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909311 | TTCGCTTCAATCTTA[C/G]TGTGGGTAAAATTGC | 4734 |
rs547385977 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884324 | CCTCCCCAAGAAGGA[C/T]GGGTAAAAATAAGCA | 4734 |
rs547395530 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55850368 | CAAAACAATATTAAA[A/G]AGACGCATAAGCATT | 4734 |
rs547403359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940335 | TGGTTTCACAGCTGT[A/G]TGCATATGTTTAAAC | 4734 |
rs547408627 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962734 | CAAGGGTGAGCCACC[A/G]CACCCAGCCTCTTTT | 4734 |
rs547432907 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882055 | AAATGTTCCAACAAA[C/T]GTGCAGAAGTCTCTT | 4734 |
rs547479061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974504 | TCTGATAAACATTGA[C/T]GCAAAAATCCGTAAT | 4734 |
rs547490321 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933446 | AGAAAACCAAACACC[A/G]CATGTTCTCACTCAC | 4734 |
rs547512255 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855938 | GCATGCAGAGACTTT[C/G]CTTTTAACATGGGAG | 4734 |
rs547518062 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849974 | ATTATTTTGTATTTT[G/T]AGTAGAAACGGGGTT | 4734 |
rs547518205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853735 | GGCTCACCCCTGTAA[A/T]CCCAGCACTTTTGGG | 4734 |
rs547524091 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968632 | GCTAAGAAATACATG[A/C]AAAGATAATCTCACC | 4734 |
rs547527275 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945375 | GATACATGCACAAGC[C/T]TCAGTAGCTGATTCA | 4734 |
rs547530722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939070 | ATGATTGTGCCACTG[C/T]GCTCCAACCTGGATA | 4734 |
rs547531131 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55878225 | GACAAATTAGATTTC[A/G]TGATGATGAGTATTA | 4734 |
rs547543316 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834851 | GAGGCAATTATGCAC[A/C]ATGGAACTCCCTCAA | 4734 |
rs547553692 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875250 | GTCATAATGAATGAA[A/C]AGATGGGGAACCTCA | 4734 |
rs547564373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980623 | ATTCAACACAGAAAA[A/G]AGATCGAGTGAATTC | 4734 |
rs547599835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981488 | TAAATTTATTTGAAA[C/T]GATCTATAAAAATAT | 4734 |
rs547604124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991056 | CAGACACTGACTCAG[C/T]GACTATTCACTATAT | 4734 |
rs547676521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832441 | TTTTTTTGAGACAGG[A/G]TCTCAGTCTGTCACC | 4734 |
rs547695820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920976 | TGTATTTCCCACTCA[C/T]AGAAGAGCATCTAAC | 4734 |
rs547699322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944260 | GTGATAAACTGTACC[C/T]GGAAAAACAGGACAC | 4734 |
rs547704356 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831491 | CCTGCCTTCATTTTT[C/T]GCTACTAACTTGTTA | 4734 |
rs547720174 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858840 | AGTAAATACTGGCTG[G/T]GGGCCATATGGTTGC | 4734 |
rs547722251 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933939 | CAGGCAGGTCACCTG[A/T]GGTCAGGAGTTCGAG | 4734 |
rs547738187 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842776 | CCGTTCTGTGACCTG[C/T]AGGATAGCCACTGCC | 4734 |
rs547749722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859750 | ATAACTGGGAGAGAG[A/T]AAAGCAGTCCCTAAC | 4734 |
rs547754374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943878 | ACTAGCCTGTGAAAG[C/T]AGCTGAAGGGATTGT | 4734 |
rs547783092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852252 | GTGAGCCACGATCAC[A/G]CCATTGGACTCCAGC | 4734 |
rs547800229 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55892063 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGTC | 4734 |
rs547807791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982029 | TTTTTATACACAAAG[C/T]ATCACTGGAAGGATA | 4734 |
rs547820836 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926134 | TGTATCAAACCCAGA[A/T]AAAGATATTGAATAC | 4734 |
rs547825072 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865750 | GCTAGACCTGAAAAC[A/C/G]AGGCCTCAGGGAAAA | 4734 |
rs547828578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989034 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 4734 |
rs547862623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891083 | TGTTCATTGGTTGTC[C/T]TTGGGAACAAAAGAA | 4734 |
rs547862631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901111 | CATTTATGGGGTACA[G/T]GAGATGTTTTGATAC | 4734 |
rs547886135 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849255 | CTGAGGTGGAGTGTC[A/G]CTCTTGTCGCCCAGG | 4734 |
rs547892106 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859243 | TAGCTATGAAGTTCT[C/T]ATCGTGGAAGCATAT | 4734 |
rs547912145 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866396 | TGATAATACAGGATC[C/T]AGCATACCTAAAATT | 4734 |
rs547920470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868858 | CTGGAAGAAACCCTC[A/G]AGGTCATCTGATGCC | 4734 |
rs547924030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900445 | AACTCAGATTAAATG[C/G]AGTAAACAGATTTGA | 4734 |
rs547930127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988024 | GAAAGTCATTGCACA[C/T]GTATGTTTATTGCGG | 4734 |
rs547948861 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863787 | AAGCACCTTGCTTAC[A/G]GTAGAAATCAATAAC | 4734 |
rs547949245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906636 | GGGGCCTGTTGTGGG[A/G]TGGGGGGCTGGGGGA | 4734 |
rs547974132 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950748 | ACTCAACAGCTAAAG[C/G]GGAATATGGGGTCAA | 4734 |
rs547976297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928120 | GTTCAAGCGATTCTC[C/T]TGCCTCGACCTCCCA | 4734 |
rs548009210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913626 | AATCTGCACAAAGTT[A/G]TACATTTGATTGTCA | 4734 |
rs548014067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839943 | TCACGCCACTGCACT[C/T]CAGCTTGGCAACAGA | 4734 |
rs548024439 | snp | A/G | 3.35942e-05 | 0.00409829 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860379 | ATATAAACTACTGAA[A/G]CCGTAACAAAATCTA | 4734 |
rs548033773 | snp | C/T | 1.65315e-05 | 0.00287498 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832992 | ATTTTTTTAATGATC[C/T]ATGGAAAATCCTTAC | 4734 |
rs548037965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957174 | TGTTAAATTCATTTA[C/T]TAGTTCTTCCAGTAG | 4734 |
rs548046954 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894749 | TTCATTCATGATTTA[C/T]TGTGAGGATTTAAAA | 4734 |
rs548054564 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994458 | CCTGTGGAATAAGGT[C/T]ATGGAATAATCATGC | 4734 |
rs548075041 | in-del | -/AT | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926082 | CGTATGTAAAAATAC[-/AT]ATACATACTGTACAT | 4734 |
rs548084361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876115 | ATATCTATAAGTGCT[A/G]AAATGGAAAATGTAC | 4734 |
rs548084963 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867113 | TCTATTATAGCCATA[C/T]TTTACTACAGAATAC | 4734 |
rs548093084 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993927 | GGTTGACGGGCCCGC[C/T]GGGGAGCCAGGGAGC | 4734 |
rs548120698 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928220 | TTTCACCGTGTTGGC[A/C]AGGCTGGTCTCGAAC | 4734 |
rs548139435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963210 | AATCATGGCTCATTG[A/G]AGCCTTGACCTCCTG | 4734 |
rs548146162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902378 | TTAGAATTAATGTTG[C/T]TTTTACCATTAATTT | 4734 |
rs548149145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866484 | TAAGTTTTTATATTT[C/T]ACTCTTTTGAGAAAA | 4734 |
rs548174429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834519 | TTCCTGTGGCCAGAC[A/G]CAGTGGCTCATTCTG | 4734 |
rs548202440 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975519 | ATCAAGAATGTAACT[C/G]CCAGTTACAATCCCT | 4734 |
rs548206605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907987 | TTGGCATTCACCCCA[A/G]GGACAAGGTATTCAT | 4734 |
rs548213372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946698 | CCCCAAATCAACAGA[A/G]TATACATCCTTCTCA | 4734 |
rs548265557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923596 | AGGTTGCAGTGAGTT[C/G]AGACTGAGCCACTGT | 4734 |
rs548286834 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951596 | TAAGGATCACTGTTA[-/A]AAAAAAAAAAAAAAA | 4734 |
rs548292234 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881084 | ATAATTTTTGAAATG[G/T]GTAAGTTAGCTTTTA | 4734 |
rs548362029 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828793 | AACAGTATTTTAAAA[A/G]GCATAAGAAATAGTA | 4734 |
rs548366962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914755 | ACACATGTATTTGAG[A/G]TATAGTTTCTCTATG | 4734 |
rs548369268 | snp | A/G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891523 | CATTTCTTTGCAAGA[A/G/T]TTATTTCCTATATTT | 4734 |
rs548402716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972164 | AAGGATATTAATAAG[C/T]GATAAGAAATCATCT | 4734 |
rs548425822 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894724 | AGTTTATCTTTACAT[G/T]CTCTAAAGTTTCATT | 4734 |
rs548430274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921967 | CAACATGCAAATAAC[A/G]CAAATAAAATAGTTC | 4734 |
rs548432759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875156 | CCAGCCACAAGATGA[C/T]GCAGATCATGGAATA | 4734 |
rs548485971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894024 | TATATGTCAATGAGG[A/C]AATGGAGTTAGATAA | 4734 |
rs548493809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983071 | AGGTTGCAGTGAACC[A/G]AGATTGCGCCATTGC | 4734 |
rs548581837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937783 | AATGTTACACTCACC[A/G]AAATTCCAATGGTAC | 4734 |
rs548591345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959724 | GAGCTGCTGAATGGC[A/C]AGAAGCTGAGACGGC | 4734 |
rs548623235 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826706 | TTTTTATCTTCTGGC[C/T]ATTTCACTAACAACC | 4734 |
rs548632816 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886936 | GAAGGATATTGAAAA[G/T]TTTCTTGAAACAAAT | 4734 |
rs548648922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943729 | AAATGTGGGACTGGA[A/G]TCCCCACACAGGGTT | 4734 |
rs548649462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856016 | CACCTGGAGCCTACA[C/T]TCTGTGCTGTATTGG | 4734 |
rs548651669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931040 | AATTTTAAAACACGG[G/T]CGTAAAGATAATTAT | 4734 |
rs548701005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973398 | ACAAAAAAACAACAA[A/C]AAAAAAACAGGCAGA | 4734 |
rs548711294 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965815 | CAAGCGATTTCTGGA[A/T]AATTTTTGTATTTTT | 4734 |
rs548712927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929092 | AGACAGATGAAGCAG[A/G]GATGGAAGTGATGAT | 4734 |
rs548787273 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928564 | GAAACTCACTACTAA[C/T]TGCTTCTTGCATTTT | 4734 |
rs548797843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976855 | AGCAAGGATGGTCTC[A/G]ATCTCCTGACCTCCT | 4734 |
rs548848774 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855466 | AGGAGAAGGGTAGGC[G/T]GAAGAGGCTGGGAGC | 4734 |
rs548866009 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917754 | AGAACAGTCTTTAAA[C/T]GATGCCATTTATATT | 4734 |
rs548879100 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942102 | ATCAGTTACTAGAAG[G/T]GGTAAAATCAACTAT | 4734 |
rs548890757 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55860141 | GAAATGAATAATAAA[C/T]CCAACTTGTTCAATG | 4734 |
rs548893860 | in-del | -/TTTT | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893586 | TTATAAGACATTTAA[-/TTTT]TTTTTATTTGAACAC | 4734 |
rs548904159 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966119 | ACTCCCCACCAGAAT[C/G]TGCCTGCTCTGTTCA | 4734 |
rs548943561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947301 | GAAGAATCAAATAGA[C/T]GCAATAAAAAATGAT | 4734 |
rs548955045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880101 | GTTCGAGACCAGCCT[A/G]ACCTACATGGTGAAA | 4734 |
rs548955640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910428 | CCTCTATGCCTCCAC[A/G]CCTCCATGCTCTCCA | 4734 |
rs548986556 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928337 | TTTTAATCTATCTTT[C/T]GTACTGTAATCGGAC | 4734 |
rs548990245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852315 | AAATAAAAAAAAAAA[A/G]GAAGGTGGTAGAAGT | 4734 |
rs548993073 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985854 | CACCAAGTACCCAAA[C/T]TGTAGCATGTAAAAA | 4734 |
rs549051897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897176 | GATGGGGTTTCACTG[C/T]GTTACCCAGGATGGT | 4734 |
rs549060393 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949136 | CCATCAAGAAGCGGG[C/T]GAAGGATATGAACAG | 4734 |
rs549071559 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871720 | TACTAAGTTCCAAAA[A/G]TACATTTTCAAATGC | 4734 |
rs549084469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978451 | TCACTTTCATGTGTT[C/G]AGATTGTAATCTCTC | 4734 |
rs549091376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956001 | TTCAAAAATTTTTTT[A/G]TAGAGACAGGGTCTT | 4734 |
rs549108019 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858272 | GAAGGGGAATGGGAT[C/T]GTATGTGATTTATCA | 4734 |
rs549109702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865779 | AAGAGTTGGGAAGGA[A/G]AGGAATGTTTTTTGG | 4734 |
rs549121668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984549 | ACTAAAGCATCTTTA[C/T]TGACGGCCATGATTG | 4734 |
rs549159180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905536 | ACCAAAGGGAACCAG[A/T]GACAACATAGGACCT | 4734 |
rs549171285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865111 | GCTGGGGCAGGAGAA[C/T]TGCTTGAGCCCAGGA | 4734 |
rs549171704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949691 | TCATTCTCAGCAAAC[C/T]GTCGCAGGGACAAAA | 4734 |
rs549223412 | snp | G/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948021 | CAAATTGTCCCTGTT[G/T]GCAGATGACATGATT | 4734 |
rs549240498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837386 | AGTGAGCCGAGATCA[C/T]GCCACTGCATTCCAG | 4734 |
rs549257335 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850961 | TTTCCAATAAATTAT[C/T]TTGTAAAACTTTATT | 4734 |
rs549278799 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864011 | CAAAGAAAGATTTTT[A/T]AAAAATGCACTGAGA | 4734 |
rs549291303 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847882 | ACAGGGTTTCACCAC[A/G]TTGGCCGGGCCGGTC | 4734 |
rs549313843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990928 | CTGCACATGCAGCCA[A/G]GGTGATCTCTTACTA | 4734 |
rs549322782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844087 | ATCAAGAAGGCTTTG[A/G]GAGGAAGTCTTTAGA | 4734 |
rs549325911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960183 | CTCTGTGATGGGTAA[C/T]ATTGAGTGTCAACTT | 4734 |
rs549346011 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906111 | CAGTTAGAATGGCGA[A/T]CATTAAAAAGTCAGG | 4734 |
rs549359987 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949952 | ACTTAAAGTATAATT[A/T]AAAAAAAAAAGAAAA | 4734 |
rs549371853 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962887 | TGCCTCCTGGGTTCA[A/G]CTGATTCTCCTGCTT | 4734 |
rs549378072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872169 | GTCTGATAAGTATTA[A/G]GAGAACGAATCTTTC | 4734 |
rs549388612 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993627 | TGGAGGAGGAGGAGG[A/G]GAAGCGGGAGGAGGC | 4734 |
rs549399951 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944364 | TTGGCGGGTACCATG[C/T]CCACAGAGCCTTGCT | 4734 |
rs549402544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925365 | TACTTGCTTTTTATT[A/G]ATCAGTTTAGAGCCA | 4734 |
rs549416253 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961627 | AGGAGCCCACCACCA[A/C]ACCCGGATAATTTTT | 4734 |
rs549439099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880620 | CACCAAAATGAGGGA[G/T]TGTGCCGTGATATGG | 4734 |
rs549441797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850347 | ATGAATATCTCCATC[A/G]TAATCCAAAACAATA | 4734 |
rs549499684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882721 | GAGTGCGTGTGCCAC[A/C]CCTACACCAACCCCA | 4734 |
rs549509083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911718 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 4734 |
rs549529582 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983086 | GAGATTGCGCCATTG[A/C]ACTTCAGCCTGGGCA | 4734 |
rs549552624 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935279 | TTCGTTGTATGAATG[C/T]ATCATAATTTACTTA | 4734 |
rs549558300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872675 | CCGACATCACAACTC[A/T]AATGAAAACTAGCTG | 4734 |
rs549564022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919824 | ATGGATAGGCTCTGG[A/G]TAATCTTAATCATTG | 4734 |
rs549580184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866616 | ATTATAAAAATAGTG[A/C]TAGAAAAATGGTAGC | 4734 |
rs549581215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925985 | GTAAAAATACATATA[C/T]ATATGTATCATATAC | 4734 |
rs549625468 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918970 | ATCAATGAGATCTAA[C/T]TGTTCATGTCTGTGG | 4734 |
rs549625775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844513 | CTGAGTAGTAGACAA[C/G]TGCATGCATTCTGGA | 4734 |
rs549643380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873624 | TATGTTTCCATTGTC[A/G]TAAACTATCTTAGTT | 4734 |
rs549667408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980731 | CAACATAGCAAGAGG[C/T]TGTCTTCAACAAGAA | 4734 |
rs549687702 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889408 | AAAAGGAATGAGATC[C/T]GCTCATTTGCAACAA | 4734 |
rs549754833 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867374 | GGAATTCAAACACTG[A/C]GACATGAGACCGCAA | 4734 |
rs549775289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921002 | CTAACACAGTAGATA[C/T]ACTAAATGGTATATC | 4734 |
rs549791836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957196 | TTCCAGTAGTTTTTT[C/T]TGTAGATTCCTTGGG | 4734 |
rs549839590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941378 | ATAGCTTCATCCCAC[A/G]TTTGGTATGTTATGC | 4734 |
rs549840442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927226 | ATGAGAAGGTATAGA[A/G]AACATGCACAGCAAG | 4734 |
rs549841580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933983 | ACAGGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 4734 |
rs549853101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963242 | GCTCCAGCGATCCTC[C/T]AACCTCAGCCTCCTT | 4734 |
rs549884145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854420 | ATAGATAAATGTAGT[A/G]GATATATCTCTACAG | 4734 |
rs549903141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940468 | AACATCTCTAATTCC[A/G]AAGTAGTCCTTCCTC | 4734 |
rs549927463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850816 | TAGTTAAAAAGGTAA[C/T]TTAACCTGCAAATAG | 4734 |
rs549939209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962916 | TTCAGCCTCCTGAGT[A/G]GCTGGGATTACAGAC | 4734 |
rs549968819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893831 | TAGAAAAAAGGCTCA[C/T]AAAAATCACTGTAAA | 4734 |
rs549972822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970466 | CCTTAGGCAAAATCC[A/C]GTACTGTGTTGGCTT | 4734 |
rs550018381 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932695 | AAACTAAAGAGCTTC[A/T]GTACAGCAAAAGAAA | 4734 |
rs550071939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914535 | TGCCTAGCAATTTAA[A/C]CCAAATTCAAAAATA | 4734 |
rs550072318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899449 | TTTTTACTGAAGACT[A/G]TAACATATCAATGAA | 4734 |
rs550108171 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55878645 | AAATATCCTCTAAAA[C/T]ACTTCTTCAAGAATG | 4734 |
rs550138119 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970589 | AGAGAGAGGGAGAGA[C/T]TCCAATTGGTTGGGG | 4734 |
rs550149513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983373 | CTTAACACGGCATGC[C/T]AGGCTTGCCTGATCA | 4734 |
rs550153733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977044 | AAGCAGTAGCTTGTA[A/T]GCCTTTCTCAGAAGA | 4734 |
rs550193516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875283 | AGTGAAGGGGAAACT[A/G]AAAATGAATCAAATG | 4734 |
rs550225071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986907 | GCCAAGGCCTGTCCT[C/T]CTTAAAACTGTCTAG | 4734 |
rs550256832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884143 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 4734 |
rs550272633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55892166 | AGCTACTCGTGAGGC[A/G]GAGGCATGAGAATCA | 4734 |
rs550295714 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964364 | CAACTGCGTAACAAT[G/T]TCTACTGATCTATCT | 4734 |
rs550308108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947735 | ATGCAGAAAAGGCCT[C/T]TGACAAAATTCAACA | 4734 |
rs550336634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990707 | GGGAAACAGTGTTTA[C/G]TTTTCCCACCTCCAT | 4734 |
rs550351561 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906416 | GACTGGATTAAGAAA[A/G]TGTGGCACATATACA | 4734 |
rs550360769 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869108 | TTGTTAAATTCTACT[A/T]GCCCCACATACAGAA | 4734 |
rs550372715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952457 | CTTTGGACACTTTAC[C/T]TGTCCATTGTTAAAT | 4734 |
rs550380206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988164 | AAATGATGAGTTCAT[A/G]TCCTTTGTAGGGACA | 4734 |
rs550387140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982112 | GAGGAGGGCTTTGGC[C/T]GAAACTTCAAATGTT | 4734 |
rs550391445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833765 | CCCTGCAGGTTATTA[C/T]AAGTTCTTTCAGTCC | 4734 |
rs550414821 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55951424 | CAAACTCTAAAAAAT[A/G]ATAAACATAGTATAA | 4734 |
rs550447384 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986604 | TTTTTTTTTTTTTTT[G/T]TGTGAGACGGAGTCT | 4734 |
rs550466783 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995096 | ATCCATTTCATTCAT[A/G]TAATATGTATCAAAA | 4734 |
rs550476361 | snp | G/T | 3.30781e-05 | 0.00406669 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860810 | AAAAGCCATCATCCA[G/T]GTCTTAAGTAGTTAA | 4734 |
rs550491234 | in-del | -/CTTC | 0.0150606 | 0.0854603 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968470 | ATATTTTAGATACTT[-/CTTC]CTGTAGACATATCTA | 4734 |
rs550504041 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873772 | ACTGGGGTTCATGAA[C/T]GGAAATCTTAAAGAG | 4734 |
rs550533786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894962 | GACTACTAAATATGA[C/G]AAAAAGGTTTTGCAT | 4734 |
rs550537760 | snp | C/T | 9.8925e-05 | 0.00703226 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860430 | ATGCTGGCTGGCTCA[C/T]GGCTGAATTTCCAAA | 4734 |
rs550553995 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935583 | CTGGGCGTGGTGGCT[C/T]ATGCCTGTAATCCTA | 4734 |
rs550559269 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827380 | TTTCTTCCAGACCAC[G/T]AGCCCCTAGTGGGAG | 4734 |
rs550584793 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968288 | AAGTCTAAAAGTGAA[A/G]AGAAATTTTTAAAAG | 4734 |
rs550594177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928815 | CTCCCTACTGAGTTA[C/T]AAACATCACAAATGA | 4734 |
rs550622419 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828551 | TTGTTTTACAAATTC[A/G]TAGACACATTTGCAA | 4734 |
rs550635829 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947328 | TGATAAAGGGGATAT[A/C]ACCACCAATCCCACA | 4734 |
rs550662912 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977478 | TGTATCCGTTGTTAA[C/G]CAATGCATGACTGTA | 4734 |
rs550680802 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877775 | ATTTATACATTCTAA[-/T]TTATATCATCATAGA | 4734 |
rs550684469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837169 | GCACGGTGGCTCACA[A/C]TGGTAACCCCAGCAC | 4734 |
rs550701548 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995441 | GGGCACAATTACAAA[C/T]GTGTAAAAACAGCTT | 4734 |
rs550707806 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864142 | TTTATATGAGAAACC[C/T]CACAAAAGAAAAGGC | 4734 |
rs550729729 | snp | A/G | 2.1664e-05 | 0.00329113 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830027 | AGAGGAAGTGGTTAT[A/G]AAAGACACTGACAAA | 4734 |
rs550729977 | snp | C/G | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917786 | TGACTATTAAAACTG[C/G]CAAGAAATAGCCTAA | 4734 |
rs550750549 | snp | A/G/T | 8.25326e-05 | 0.00642342 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915606 | TTAATATACTCTGAA[A/G/T]CAGAATTAAGCTTAA | 4734 |
rs550759635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861747 | ATATTATTCTAATTA[C/T]TTGCATTTAATATAA | 4734 |
rs550761392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887415 | ATTCCTAGACACATA[C/T]AACCTATTAAGATTG | 4734 |
rs550762257 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916081 | TGTTCCTGCTCACTG[A/G]CAATTTCATAATCTC | 4734 |
rs550765965 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932406 | CAAACCTGACAAAAA[A/C]AAGAAACGGGGAAAG | 4734 |
rs550766985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871383 | GTTCTTTCTACACTT[C/G]CAATAATATTCATTG | 4734 |
rs550776704 | in-del | -/AT | 0.00170895 | 0.0291814 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838204 | AAACACAATAACTTG[-/AT]ATGTTATTTTAGCGA | 4734 |
rs550779899 | snp | A/G | 1.68043e-05 | 0.0028986 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856089 | AAAAAGAGATGCTGA[A/G]TTTTATATTTTTATT | 4734 |
rs550789642 | snp | A/G | 0.000496022 | 0.0157406 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924604 | CTGCTCCACTGAAAT[A/G]TACCCTTACTTCATA | 4734 |
rs550791101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830415 | ATCCATACCTGCCAC[C/T]GACATAACACAGAGG | 4734 |
rs550821525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869136 | GAAGGCTCTTTATTA[G/T]ATCACTTAAATTTTC | 4734 |
rs550826654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978279 | ATTTCCCAACACAAA[A/G]ATCAGAACTAGTTAT | 4734 |
rs550834582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966934 | ACTCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGTG | 4734 |
rs550837475 | in-del | -/CCTCCTGTAGAATAACT | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994406 | TAAAGTGAACTAGGA[-/CCTCCTGTAGAATAACT]CCTCCTGTGGAATAA | 4734 |
rs550843049 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849437 | TCCATGTTGGCCAGG[C/G]TAGTCTCGAACTCCT | 4734 |
rs550844060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922377 | TGGGTTTTTGCTTTT[G/T]TGGAGACAGAGTTTC | 4734 |
rs550873209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972753 | ACAAGAAACACACTT[C/T]ACCTATAAAGACACA | 4734 |
rs550891188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965207 | TCCTGTTTTTGGTTG[G/T]TTGTTTTTTGAGACA | 4734 |
rs550906621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850046 | CCTCGTGATCTCCCC[C/G]CTCGGCCTCCCAAAG | 4734 |
rs550919672 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918577 | TAAAACATATACTCA[C/T]ACTTTGTTAAAAAAA | 4734 |
rs550927547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876274 | GTTCTTCAGGCTGAG[C/G]ATAAGTGGCACCAGA | 4734 |
rs550943849 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894981 | AAGGTTTTGCATTTG[C/T]TTCAACTTTCTTTCC | 4734 |
rs550994575 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931888 | CAAAATGAAACCTTA[C/T]GTCTTTTAACAGACA | 4734 |
rs551017527 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914450 | GCTAAGATTCATAAG[A/G]GTTAAATTACTAATA | 4734 |
rs551018387 | snp | A/C/G | 0.00019778 | 0.00994249 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863006 | TCTTCCCACCCTGGA[A/C/G]GTAGAGGAGAAGGTT | 4734 |
rs551030730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942838 | ATCAGAAGAAGAAAG[A/G]AGGATGATGGAAAGA | 4734 |
rs551067688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968572 | AACTCCTAAAAATCA[A/G]TATGTAAGATATAAT | 4734 |
rs551087156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870733 | AGAGACAGGGTTTTG[C/T]CATGTTGCCCAGGCT | 4734 |
rs551109745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924278 | GGCCACTGTAGTGAG[A/G]AGGCGCAACTGAAGG | 4734 |
rs551119254 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937933 | AAAGCTACAGTAATT[A/C]AAACAGTATGACACA | 4734 |
rs551129903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959796 | GCAGCATGCAAGGAA[C/T]TGAATGCCACCAGCA | 4734 |
rs551209317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904597 | TGTGAGCCACCACAC[A/C]CGGCGTATTTCCATA | 4734 |
rs551213913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929727 | TTTATCACTGTTAAG[C/T]ATGATAGATTACCAG | 4734 |
rs551221774 | snp | G/T | 0.00037237 | 0.0136399 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905241 | GTTGCAGAACTTATA[G/T]AAAGGAATCACCTTC | 4734 |
rs551229793 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983096 | CATTGCACTTCAGCC[C/T]GGGCAACAAGAGTGA | 4734 |
rs551240426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853725 | TGGGCATGATGGCTC[A/T]CCCCTGTAATCCCAG | 4734 |
rs551268966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904077 | TGGGGCAGGAGAATC[A/G]TTTGAACTCTGGAGG | 4734 |
rs551273647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55936265 | TACCTGTTCACACTG[A/G]TCCATACTAGACAGT | 4734 |
rs551316760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984785 | TATCCTCTTAAACTT[C/T]GATACTATTGGCAAG | 4734 |
rs551324284 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836819 | AGGAATGAGCCACCG[C/T]GCCCAAATTTTTAAT | 4734 |
rs551372506 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930788 | TGGGAGTTTCCCTGC[A/G]CACACTCTCTTGCCT | 4734 |
rs551379808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906658 | GCTGGGGGAGGGATA[A/G]CATTAGGTGATATAC | 4734 |
rs551383426 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908764 | GGTAGCCTGTGAGTC[A/G]GACACAGCAGTGCAC | 4734 |
rs551400586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992384 | CCCTTTATAAACAAA[C/G]AACTCTCAAGAGAAG | 4734 |
rs551411165 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952696 | TTGTTTTGAGTCTCA[G/T]CCCCCTTGTTCAGTT | 4734 |
rs551418423 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904847 | CATGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 4734 |
rs551448497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950732 | GGTGAACAGAGAAAC[A/G]ACTCAACAGCTAAAG | 4734 |
rs551461711 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55848154 | ATTCTGACTGTCTGG[A/C]TCACTTGTCCCCTCA | 4734 |
rs551468929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973958 | AAATCAAATTGAAAC[A/G]GAATATAATACAAAG | 4734 |
rs551474569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897998 | TCTATTATTCAAATG[C/T]CATGATATTATAACC | 4734 |
rs551504053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973554 | AAAAGAAAAAAATTT[A/G]AAAAATTAAAATCTT | 4734 |
rs551506615 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875936 | CTGAAGCAGGATAAA[C/G]ATAAAGAAAACATGG | 4734 |
rs551508518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950138 | TTTATTCTGGTTAAA[C/T]AGTAAAAACAGAAAT | 4734 |
rs551513546 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944169 | CACAGAGGGCAAGCC[A/G]AAGCAGGATGGGGCA | 4734 |
rs551569718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956668 | ATTCCACTGAACAAT[A/G]TATCTATTCTCATGC | 4734 |
rs551571309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944946 | ACGGAAAACTAACAA[A/G]CACAAAGGAATAGCA | 4734 |
rs551581880 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924312 | CCCTGGGAAGATTCC[C/T]AGAGCCATGGAGTAG | 4734 |
rs551595228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979536 | TTTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 4734 |
rs551599999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986434 | CAGCATCATGTGTCC[C/T]CTGGTGTGATGCATG | 4734 |
rs551611355 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877246 | TTTAGTAGTCCTGTC[-/TA]TTTAATTTCTTTAAA | 4734 |
rs551627318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844590 | TTGGGCAGGTTACAT[A/G]TCTTTTCTAAGGATT | 4734 |
rs551671808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984061 | CATGCCCTGACCCAC[C/G]TGCCTGATACATAGT | 4734 |
rs551692774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859105 | ATATGTGATCAGCTC[C/T]CATTAAATATTTACT | 4734 |
rs551698499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865054 | AATACAAAAATTAGC[C/T]GGGCATGGTGGCGGG | 4734 |
rs551704500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948632 | TGGAACAGAAAAGAG[C/T]CCTCAGAAATAACAC | 4734 |
rs551736642 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826584 | CTGAATTAACACTCC[A/G]AACTCTTTTTCTCAT | 4734 |
rs551737239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907385 | CATATGGGCAATCAC[A/G]TATCTCAATGTTTAG | 4734 |
rs551740488 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945398 | CTGATTCAATCAAGT[G/T]GAAGAAAGGCTATCA | 4734 |
rs551741301 | in-del | -/T | 0.235273 | 0.249566 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845526 | TTGCTTTTATCATGG[-/T]TTTTTTTTTTGTATT | 4734 |
rs551749255 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955187 | CCACCATGCCTGACT[A/C]ATTGTTGTGTTTTTT | 4734 |
rs551760890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865932 | TCTGGAGGGGAATTT[C/T]TCTCTTTCTTCTCTC | 4734 |
rs551793593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919907 | TTCGATAGGTTATGG[C/T]ACCCACTTGTTTGGT | 4734 |
rs551802807 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995185 | TCAAACATGACTACA[A/G]AATTACAGAATGGTC | 4734 |
rs551816466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851019 | AATTCTCAAGCAGTA[A/T]GATGTTAGTTAACAG | 4734 |
rs551820394 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962007 | TCCAACTATGACGGT[A/G]GGAGTTTTAAAAAGT | 4734 |
rs551843312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906612 | ACAAGAAGGGGAACA[C/T]CACACACCGGGGCCT | 4734 |
rs551886427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851665 | TATTTTTGGTAGAGA[C/T]GGGGTTTCTCCATGT | 4734 |
rs551890085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875067 | ATTGTCCAGCCCACA[A/G]TAAAAAAATTACTAG | 4734 |
rs551895245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958158 | TATTCTATTAATACA[C/G]TGTATTACATCAGTT | 4734 |
rs551897864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859687 | GGTGACAGAGTGAGA[G/T]GTCTCAAAACAAACA | 4734 |
rs551900064 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872406 | TATTATTATTTTATA[G/T]TTACTGACCTTCTTG | 4734 |
rs551900274 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889778 | TGATCTCAGCTCACC[A/G]CAACCTCCACCTTCC | 4734 |
rs551900714 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957815 | GGATGAGTTCATGTC[C/T]TTTGCAGGGACATGG | 4734 |
rs551901360 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855313 | GGTTGGGGAAGAAAA[G/T]GAGAAAGCCATTCCA | 4734 |
rs551911372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906221 | TTGTGGAAGACAGTG[A/T]GGCGATTCCTCACGG | 4734 |
rs551937449 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938839 | TCCCAGGCACAGTGG[C/T]TCATGCCTGTGATCT | 4734 |
rs551946624 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893056 | ATTACAGTAAACTAA[-/C]CTGAGATAGAAACAG | 4734 |
rs551951352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874424 | AAATCTGCACTATTA[C/G]TGGCTTGAGGAGTCA | 4734 |
rs551956901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845169 | TGGGGTGACTTCATG[C/T]CTTTTAACCTTTCTT | 4734 |
rs551973832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911107 | CACATTTCTAGCCTT[C/G]CATATGCTGCTGCTG | 4734 |
rs551981613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920513 | TCACCATAATGAAAC[A/G]ACAATATTTTATAAC | 4734 |
rs551992365 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928024 | ACTACCTCAACTATC[-/TT]TTTTTTTCCCTTCTC | 4734 |
rs552018359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839403 | AAAGAAAAATCTCTT[A/G]ATAAATATAGAGGCT | 4734 |
rs552047960 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911779 | GTGATCCGCCCGTCT[C/G]GGCCTCCCAAAGTGC | 4734 |
rs552059666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975168 | AAAGTGCTGGGATTA[C/G]AGGCGTGTGCCACTG | 4734 |
rs552070837 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914004 | AAATCTGGTTTTAGA[A/G]AAGTTTCCTAAATGG | 4734 |
rs552085446 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883817 | AAGGGAGAAGAACAA[C/G]AGTCTCTGCCTGGTA | 4734 |
rs552092320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968950 | TTATTCTAACAAGAA[A/G]GCACCTACATAAGAA | 4734 |
rs552120907 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839302 | CCAAAGTGCTGGGAT[A/T]ACAGTTGCACACCCC | 4734 |
rs552122930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923371 | TAGATGGCCAGGCTG[A/G]GCATGGCAGCTCATG | 4734 |
rs552139886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872739 | AAGAGAATAAGCAGA[A/G]AAACAGTATAGAGTG | 4734 |
rs552156689 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836210 | CACCTAGCACTTTAT[A/G]CTTGCCTCTGTTCAT | 4734 |
rs552157811 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863563 | TAAATATATACAATT[A/G]TTGTCAATCAAAAAT | 4734 |
rs552161895 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907606 | TGAAGACGACTTGAG[C/T]TTCCAGTAAGCTCTG | 4734 |
rs552187561 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882732 | CCACCCCTACACCAA[C/T]CCCAGGCAGTGCAGC | 4734 |
rs552192691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914579 | TTCAATATTGTTGAA[A/T]GAGTGAGTTACATTT | 4734 |
rs552209354 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55951436 | AATAATAAACATAGT[A/T]TAACTAAATAAGGTT | 4734 |
rs552217748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848052 | CATACACTCTCTGCT[A/C]CTCTCTGATTTGTGG | 4734 |
rs552256203 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921938 | CACAAATGTGAGCTG[C/T]CCCTCCTTGTGGACA | 4734 |
rs552350368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835563 | TTTCACATTTTCCAT[C/T]GTATCGAGTTCACAG | 4734 |
rs552370377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927700 | GGAGAAATGACATAA[C/T]TTAGGTCACATCTGA | 4734 |
rs552403699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935295 | ATCATAATTTACTTA[C/T]TGCTCCACTGATGGG | 4734 |
rs552405347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842642 | CTTGGCCTCCCAAAG[C/T]GCTGAGATTACAGGC | 4734 |
rs552408000 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882845 | CATAGTAGGCTAGGA[A/C]ACTTGCTGACTGAAG | 4734 |
rs552420391 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834421 | CACGGGCTCTTCACT[G/T]AGATCTCAATATTGG | 4734 |
rs552436181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933916 | CCCAGCACTTTGGTA[A/G]GCCGAGGCAGGCAGG | 4734 |
rs552436278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927315 | GACAAAGACGACAAG[A/G]TTCTTTTTTTTTTGA | 4734 |
rs552457805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942053 | TGTTCAAATCATCTA[C/T]ATATTTACTATTTTT | 4734 |
rs552465118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890848 | CTTAGTGGGTGTGAC[A/G]TAGTATACCATCGTG | 4734 |
rs552466833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901339 | GAAACAAGAGTTCGT[C/T]TTAGAACTACCAATT | 4734 |
rs552470150 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832667 | GTGATCTGCCTGCCT[C/T]GGCCTCCTGAAGTGC | 4734 |
rs552524413 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965768 | GTGCAGTGGCACAAT[A/C]TTGGCTCGCTGCAAC | 4734 |
rs552546047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966055 | TGCCCTCAGACCAAT[C/T]CATAGTATCAGGAAC | 4734 |
rs552583280 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971921 | AGCTCCAATACATCT[G/T]GCAGCAGGTTTCTGA | 4734 |
rs552631864 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971996 | GTGCTGAAGGAAAAA[A/G]TTTTTATTGTAGAAT | 4734 |
rs552637247 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928172 | GTGCCACCAGGCCTG[C/G]CTAATTTTTGTATTT | 4734 |
rs552658129 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978545 | TTTTAGAATTCTGAT[A/C]CTGAGCACTATTAAC | 4734 |
rs552668390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876422 | AAAAAAAAAATTGTA[C/T]CGCTATACTATGGGT | 4734 |
rs552676984 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834402 | GTTTCTACCACTACA[A/C/T]AATCACGGGCTCTTC | 4734 |
rs552709224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976752 | CTCCTGCCTCGCCTC[C/T]CTAAGAGCTGGGACT | 4734 |
rs552710857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922110 | GATAGACTCAGACAC[A/G]TACATAGGGAGACAT | 4734 |
rs552711442 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971311 | ACAGGATCTAGAAAA[C/T]AGCCTCAAAAGGGCA | 4734 |
rs552711840 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857162 | ATCATCTACAAATAT[A/C]TGTGTATGCATGCAT | 4734 |
rs552728392 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893951 | CTGTGCTTTATACTA[A/T]AATGGGCTTATTTAA | 4734 |
rs552732883 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834505 | GCTATTTTTAAAACT[C/T]CCTGTGGCCAGACGC | 4734 |
rs552751705 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943928 | GTGGAGACACCCAAG[G/T]CCTTTCGGAACCCAC | 4734 |
rs552757102 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958567 | ATTTTTATTTTTTTT[C/T]CCCTAAATGTCTGAT | 4734 |
rs552757249 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941436 | GTTAATTTCCCTTTT[A/T]TTTTCTTTTTTGATC | 4734 |
rs552813786 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883551 | AGAGGTGGCAGCTAG[C/T]GAGTGGTTACAGCAG | 4734 |
rs552820001 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946830 | CCACAGTGCAATCAA[A/G]CTAGAACTCAGGATT | 4734 |
rs552844421 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985046 | AATATCCTGCTCTGA[C/G]TGATGTTTAATTATG | 4734 |
rs552849616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983198 | GTGAAGAAGCAAGAA[G/T]AAATAAAGAAATAAC | 4734 |
rs552857277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988952 | AAAATAATTTTAAAA[C/T]AGGACGGGCGCGGTG | 4734 |
rs552887028 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946596 | AACATTAGACAGATC[A/G]ATGAGACAGAAAGTT | 4734 |
rs552898255 | in-del | -/TGCACTGCACTGCATTGTATTGCATTGCAC | 0.0479149 | 0.147179 | intron-variant | NEDD4 | GRCh38.p7 | 15:55954975 | ACCTCTACCCTATTT[lengthTooLong]TGCACTGCACTGCAT | 4734 |
rs552915456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850483 | AAAGATTTTAAGGAA[C/G]TATACATAAGAGATG | 4734 |
rs552950279 | snp | A/G | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946124 | TAACCAGTGAACATC[A/G]TAATTACAGGATCAA | 4734 |
rs552964725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929773 | AAATTAGAAAAACTG[C/T]CCTCAAAGGAAAAAG | 4734 |
rs552986006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919270 | CAGTCACTCTGAATG[C/T]CTAATGCTTTCTTTC | 4734 |
rs552990178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904115 | CACAGAGAGCCGAGA[C/T]TGCACAACTGCACTC | 4734 |
rs552998979 | snp | C/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994544 | CACCAAATAAGGCAT[C/T]CATAAAAGAGTCTGG | 4734 |
rs553006557 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868099 | CTATTATTATAGATT[C/T]TCCTGCAAAGCAAAA | 4734 |
rs553026308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929215 | TTAGCCTCCAGATGG[C/T]ACATGTACACACATG | 4734 |
rs553029847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861847 | GAGCTCAGGCTAGTC[A/G]GAAGACCAGTTCTTA | 4734 |
rs553090065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976660 | TTTGAGACGGAGGCT[C/T]GCTCTGTGGCCCAGG | 4734 |
rs553094436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845741 | TCCCAAAGTCTAGAA[A/G]TAGAAAACAAATTTC | 4734 |
rs553121145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991138 | TTTCTCCCTGTTTTA[A/G]TTTCAAATTTAAAAT | 4734 |
rs553138035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970522 | TGATGGTGGCCACAG[C/G]ATTGTGTCACCCTTC | 4734 |
rs553151774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863547 | ATCACATTGTCCTCC[A/T]TAAATATATACAATT | 4734 |
rs553213327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870898 | TTAAGAAATCCTTAC[C/T]TGTCTCAGCTCTCTA | 4734 |
rs553220566 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851197 | CAAATGATGGGCAGA[C/T]AAAATGAATGGCAAA | 4734 |
rs553240453 | in-del | -/TA | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933341 | ACACTGTGGAATACT[-/TA]ACTCATCCATAAAAA | 4734 |
rs553273594 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976127 | CATATACAAAAATCA[A/T]ATCAAAACATTGAGG | 4734 |
rs553285091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954012 | ACTATAGCATACCAC[C/T]TCCTTTTCTTCATTT | 4734 |
rs553289060 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879564 | AAATATTTGGGGAAA[G/T]TTTATAACATGAAAC | 4734 |
rs553326249 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917134 | GCTCAGCTGCAGCAC[A/C]CTGACTCAAACACAG | 4734 |
rs553344076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949409 | GATTCCTCAAGGATC[C/T]AGAACAAGAAATACC | 4734 |
rs553346354 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959829 | CACATTAGCTTGGAA[G/T]TGAATCCTTCCCTAA | 4734 |
rs553353131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844230 | TTATAGGGGAAAAAT[A/G]CAAAAAAGTAGTCTG | 4734 |
rs553385537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867451 | GTCCTATGATGCGTG[C/T]ATGTGGGCAAAACTT | 4734 |
rs553388876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919964 | AAGACATTTAGACAT[G/T]ATTAGCATTTAAATC | 4734 |
rs553407593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943360 | GGCAGCTCCTCCTAT[C/T]ACAGCCCCAGAGGAC | 4734 |
rs553449332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852083 | GGTGGATCACCTGAG[G/T]TCAGGAGTTTCAGAT | 4734 |
rs553453453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904999 | CAGGAGGCTGAGGAA[A/G]GAGAATTGCTTGAAC | 4734 |
rs553457462 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830685 | TCCTACACACACACA[C/G]GGAACTAATCTGGTT | 4734 |
rs553469323 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948708 | AGAAATGGGGAAAGG[A/G]TTCCCTATTTAATAA | 4734 |
rs553471135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943038 | TCTAGAAATCTGTGG[A/C]ACTTTGAACTTGAAA | 4734 |
rs553501205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846018 | TCGTGAACTCCTGAC[C/T]TCAAGTGATCCACCC | 4734 |
rs553532594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948302 | CTCAATGAAATAAAA[A/G]AGGACACAAACAAAT | 4734 |
rs553534994 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983509 | TCAATGGGGTTCTAT[G/T]GCCCCACTCTTCACC | 4734 |
rs553546833 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892704 | GGTGATAGCTGTTTT[A/G]TTTTTGTGCCTATCC | 4734 |
rs553549694 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912167 | ACATTGGTTTATATA[A/G]GTGCTGCTCAAAATA | 4734 |
rs553560676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840232 | TAGAAAAAAAGCAAT[C/T]GTGAGTAGTTGATAT | 4734 |
rs553564727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924984 | GAGGCAGGAAAATCG[C/T]TTCAACCTGGGAGGT | 4734 |
rs553594950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862732 | TTGAATATTATCAAG[C/T]CATTTAAAAAACGAA | 4734 |
rs553602302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961435 | CTGTGAGACAATAAA[C/T]GTACGTTCTTTTAAG | 4734 |
rs553607899 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951296 | ACATCTTCAAATATT[A/G]AAAATGAGAATTTAT | 4734 |
rs553641556 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872109 | AATTCATGTTTGTGA[-/T]TTTTTTAAAGCATAG | 4734 |
rs553655532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878918 | ACCTCCGCCTCCCTC[A/G]TTCAAGCGATTCTTC | 4734 |
rs553692426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911820 | GGCGTGAGCCACCGC[A/G]CCCGGCCTAGACTGA | 4734 |
rs553695725 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832761 | CTGGGCATAGAATTT[G/T]AAGTTAAAGAACGGA | 4734 |
rs553726833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963081 | TGAGCTACCACAACC[A/G]GCCTCCGTTACTTTT | 4734 |
rs553740256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880245 | TGCAGTGAGCCGAGA[C/T]CGCACCATTGCACGC | 4734 |
rs553753641 | snp | A/G | 0.000462519 | 0.0152002 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852533 | GGTAATCCAGATGAA[A/G]TAGGCAAAAGCTAAA | 4734 |
rs553760740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930728 | TTCCCCCATACTGTT[A/C]TCCTGGTAATGAATA | 4734 |
rs553772861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993404 | GCGCCGAGGGAGGAG[A/G]GGCTGACAGCAGAGC | 4734 |
rs553784036 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947296 | AGAGAGAAGAATCAA[A/G]TAGACGCAATAAAAA | 4734 |
rs553784362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962222 | CTTACTGTTTGCATG[A/G]CATATCTTTTTGCGT | 4734 |
rs553785995 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966617 | CAATTTTTTAAAAAA[-/T]ATATATCAAATAAAG | 4734 |
rs553789638 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978883 | TTCTCCACAATTCAT[G/T]AAGACATCTACTAAC | 4734 |
rs553811568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992746 | GCATAGGCATAATCA[A/G]CATTAGTTATTTAGC | 4734 |
rs553866920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865471 | GTATGACACCAAACC[C/T]TGAAGGCATGAAAGA | 4734 |
rs553878045 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55848264 | AGAGGAGAGAACGGC[C/G]AATGTGCTTTCCTCT | 4734 |
rs553920883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880699 | ACAGGGAAAGGAAGT[C/G]TCAGAGTAACAGTTA | 4734 |
rs553947895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830778 | GATTCAAGCTCACTG[C/T]AGCCTCAAGCTCCTG | 4734 |
rs553949389 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872883 | AAGACTGGATTAAAT[A/G]TATTACTGAAAGCTT | 4734 |
rs553955347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931325 | TTAAAAAGTGGGTAG[C/T]AGGAATAGGAGGGAG | 4734 |
rs553957339 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926313 | GAGCTTTTCAGAGGT[-/G]GCTGACTCAGCTGGG | 4734 |
rs553983666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888699 | CATTACCTGACATCA[A/T]ATTACATTACAAAGC | 4734 |
rs553984988 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980394 | CGGCTGCTGTACCCA[C/G]TAAACAGAAGATTGA | 4734 |
rs553985462 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877205 | CTAATTTTAGTCCAG[A/G]GTCCAATTCAGACTC | 4734 |
rs554011413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932202 | TGATGGCTTTACCTG[C/T]ATTGCCAAGACAATC | 4734 |
rs554012304 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944488 | AAAGCAGCCGGGAAG[C/G]TGAAACTAGGCAGAG | 4734 |
rs554035690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974326 | GCTTCACTGCCAAAT[G/T]CTACCAAATATTTAA | 4734 |
rs554044413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967203 | TAATAATTTGTAATA[A/C]CTACTTAGAAAAGGT | 4734 |
rs554059631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979604 | ATGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 4734 |
rs554073197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938868 | CTCAGCACTTTGGGA[C/G]GGCAAGGCAGGAGGA | 4734 |
rs554075501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949825 | GGAAGTGGGGAGGGA[A/T]AGTATTAGGAGATAT | 4734 |
rs554087860 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870736 | GACAGGGTTTTGCCA[C/T]GTTGCCCAGGCTGGT | 4734 |
rs554118130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980396 | GCTGCTGTACCCACT[A/G]AACAGAAGATTGAGC | 4734 |
rs554160382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920794 | TACAATCAGGTCTGT[C/T]ACTCCACCAATGGCT | 4734 |
rs554160394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927369 | AGGCTGGAATGCAGT[C/G]GTGCGATCACAGCTC | 4734 |
rs554182259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901496 | CCTAAGAATACATCC[A/C]ATCAAAATTCGTGAG | 4734 |
rs554192055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982272 | ATTCCATTCCTAGGT[A/T]TTTACACAAGAGAAA | 4734 |
rs554192080 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891653 | GTGATTTTAAACAGG[A/T]CTATCTGCAATGGGC | 4734 |
rs554209726 | in-del | -/AAAGCAAGCA | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894096 | TGGATATCTTTGCAT[-/AAAGCAAGCA]TTCCATGTCTTAAGT | 4734 |
rs554217182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932969 | TAAATGCAAATCAAA[A/T]CGACAATGAGATACC | 4734 |
rs554219725 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837935 | AAACAAAAACTAAAG[A/G]CTAGCTGAGACCAAG | 4734 |
rs554246975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881761 | AGTGCTTAAAAAACA[C/T]AGCTGTGATCAACTG | 4734 |
rs554275911 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839595 | CACAGGAAACAACAC[A/G]GCTACAGTCCGGGGT | 4734 |
rs554280664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939220 | GTGTCAAGGGAGGGA[A/G]CTGGTGGGAGGTGAT | 4734 |
rs554281148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838837 | ATCAATTAATCAATT[A/G]GTGCCTACTTAAAAG | 4734 |
rs554283084 | in-del | -/T/TT | 0.481473 | 0.0944461 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883882 | CCAAAGTGGCACTTC[-/T/TT]TTTTTTTTTTTTTTT | 4734 |
rs554296719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55987042 | GATCCCTGAGGAATC[A/G]CCACACTGACTTCCA | 4734 |
rs554306591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837163 | GGCCGAGCACGGTGG[C/G]TCACACTGGTAACCC | 4734 |
rs554345298 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55861726 | ACACCCTTACCCCAG[C/T]CATTTATATTATTCT | 4734 |
rs554377727 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992179 | CTACAGAATAAAGGT[A/G]CCATTAGCTAGAATG | 4734 |
rs554381551 | snp | A/C | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899707 | TGCAGCTTGAGACCT[A/C]ATGTTCTAGGGGAAC | 4734 |
rs554383578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889544 | GAACTGAGATAGAGA[C/G]TAGAATGATGGTTAC | 4734 |
rs554383637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981734 | GAAATTTGTTACATA[C/T]GCAAATGTTGAGGCC | 4734 |
rs554384574 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994930 | CGTGGTGGCGGGCGC[C/T]TGGAGTCCCAGCTGC | 4734 |
rs554400053 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827785 | TCTCTTAGAAGTCAC[C/T]TTACTTTTAAATGAT | 4734 |
rs554407734 | in-del | -/TTGC | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961138 | CCAGGATATGCAAGT[-/TTGC]TGTGAGAGGGACATC | 4734 |
rs554491523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985990 | GTGTTCAAAGAATGA[C/T]GGGGACTTGTTACGA | 4734 |
rs554493077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900480 | CTTGCTCCAAAATTA[C/T]GGTATCAGTATAATA | 4734 |
rs554511359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975978 | AGAAGTAAATCTATA[C/T]ATCTATAGTGAACTC | 4734 |
rs554533501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946976 | AGAACAAAGACACAA[A/C]ATACCAGAATCTCTG | 4734 |
rs554565915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913076 | ACTGGTAGCTAAACA[C/T]ATAAGAAAAGAAGTT | 4734 |
rs554598222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874604 | GATGGAAGACTGAGA[A/G]GGCTCAGCACTGATT | 4734 |
rs554605898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940801 | TGCTGGTATTATAGG[C/T]ATGAGCCACCATGCC | 4734 |
rs554606795 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888623 | AAATTTATGTGGAAC[C/T]ACAAAATACCCAGAA | 4734 |
rs554617969 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827045 | ATATATTTACTGTGT[A/C]AGAAGATTTTAAAAA | 4734 |
rs554640805 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909299 | CTATCCCAACAGTTC[A/C/G]CTTCAATCTTAGTGT | 4734 |
rs554657118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953236 | CTCAGGTGATCCGCC[C/T]GCCTTGGCTCCCAAA | 4734 |
rs554678413 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835713 | TTACCAATCCTATCT[A/C]AACTCCCTCACCATT | 4734 |
rs554696861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922804 | AGGGATCTAGGGAGG[C/G]TTTCAAAGATTTTGG | 4734 |
rs554726697 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926016 | ATATACAGTATGTAA[A/C]ATACATATACGTATG | 4734 |
rs554727539 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852024 | GCTATGACCAGGCAC[A/G]GTGGCTCATGCCTAT | 4734 |
rs554764412 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847204 | ACTTTAAAATATTTA[A/T]TTTCTCTGTTTAAGA | 4734 |
rs554785546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914157 | AAGAGAGAAAATAAA[C/G]TAGCAATTACTATTT | 4734 |
rs554855435 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876700 | ACTGCACATTCTGAG[A/T]GCTAAATCCAGCCAT | 4734 |
rs554856037 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839186 | GGCGCGCACCACCAC[C/G]CCTGGCTAATTTTTG | 4734 |
rs554884312 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890965 | TCCCTACAGCTTTCA[C/T]CTCCATTGGAGAGGC | 4734 |
rs554902422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971347 | AACAGTTATTGGGCC[A/G]GGCATGGTGGCTCAT | 4734 |
rs554942353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959903 | CAGCTGAAGTGAATT[C/T]CTATAATTTTATGTT | 4734 |
rs554949610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848161 | CTGTCTGGCTCACTT[C/G]TCCCCTCACTGCTAT | 4734 |
rs554954150 | in-del | -/AG | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883731 | CACACACACACAGAA[-/AG]AGAAAGAGAGAGAGA | 4734 |
rs554973664 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968507 | TATCTACAGAAGTAT[C/G]TAAAATATACATCAT | 4734 |
rs554982768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908242 | TCATTGTTCTCTATA[C/G]TAGGGAACTGTATTC | 4734 |
rs554998982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952648 | TTTATCAGAATCCAT[C/T]CTTACCCCTAACCTA | 4734 |
rs555006604 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887829 | AAGGATGGTTCAAGA[C/T]ATGCAAATTAATGAA | 4734 |
rs555052777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959233 | TTTCATTTTCATTCA[A/G]TTCAAAATGTTTTCT | 4734 |
rs555063960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871099 | TTGGCAAATTTAGTG[C/T]ATCCTTTCATGAGTA | 4734 |
rs555068880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861984 | GCCACAGTGAAAGAA[A/C]TGTGATTTTGCTCAT | 4734 |
rs555086117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936580 | ATACACTTGCATATA[C/T]ATACATTACATAAAT | 4734 |
rs555092753 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901120 | GGTACATGAGATGTT[C/T]TGATACGCTATGAAA | 4734 |
rs555103563 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854048 | TCCAGCTACTCGGGA[A/G]GCTGAAGCAGGAGAA | 4734 |
rs555129207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879230 | TGGAAGAGTAGATGA[A/C]AGCAGAGAGATAAGT | 4734 |
rs555132263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869318 | TTTAATGGAGAATAT[A/G]CAGTTTTAGAAAACT | 4734 |
rs555143217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942926 | ACAGGAAAGTCCAGG[C/T]TGAGGTGGTCTCGAA | 4734 |
rs555147373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935813 | GATCGTGCCACTACA[C/T]TCCAGCCTGGCGACA | 4734 |
rs555197994 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955432 | TCCTGCTTGACTCAA[A/G]TTTAATGCCTGTTAA | 4734 |
rs555209156 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55993323 | GCTCCCTCCAGCGAG[C/T]CCCCAGCGCCCGCGC | 4734 |
rs555227584 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851349 | AAAAAGGTGTAGACT[C/T]ACAGGGCCACAACAT | 4734 |
rs555238818 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964648 | GACTGAATTTTGCTG[C/G]TGGTGTGTGTGTGTG | 4734 |
rs555273091 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832795 | TGACTCAAGTCATTT[A/G]ATGTTTCCAGTTTTC | 4734 |
rs555275772 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960240 | GTTCCTAGGTGTGTC[-/TG]TGAGGGTGTTGCCAA | 4734 |
rs555281401 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934178 | ATAATAATGATAATT[A/T]AAAAAAATTACCCAG | 4734 |
rs555283936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841270 | ATAATGGAATATTAT[G/T]CTGCCTTAAAAAGGA | 4734 |
rs555320214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975596 | GAGATCTCTACAATG[A/G]AAACTATAGATGAAA | 4734 |
rs555324854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970628 | GAGAAGAGAACAAGA[C/G]TCTCTGCCTGGTAAT | 4734 |
rs555327872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888799 | GAAACAAATCCATAC[A/C]TCTACAGTGAATTCA | 4734 |
rs555366566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979649 | TGAGCCACCGCGCCC[A/G]GCGAAAGTTTTTACT | 4734 |
rs555376448 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978393 | TGGTTTTAACTTCAT[C/T]TTATGATTTTATTCT | 4734 |
rs555386471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903102 | TTTTTTCACTCAACA[A/G]TGGCCATAAGAAAAC | 4734 |
rs555391073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888078 | TAACATCTGGAACAT[A/G]ACAGGAATGCCACTT | 4734 |
rs555400561 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947499 | ATAGACCAATAACAG[A/G]CTCTGAAATTGAGAC | 4734 |
rs555415484 | in-del | -/AC | 0.0138799 | 0.0821421 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968480 | TACTTCTTCCTGTAG[-/AC]ATATCTAAAATATCT | 4734 |
rs555417687 | snp | A/C | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994752 | ATTACTGGTTTGTTA[A/C]GTAAGATTTTTCTCG | 4734 |
rs555423547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843243 | ATCAGCAGCATGAAA[A/G]CGGACTAAAACAGCC | 4734 |
rs555454337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985043 | TTAAATATCCTGCTC[A/T]GACTGATGTTTAATT | 4734 |
rs555460349 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878065 | TGGAGAATCATATTT[A/C]GATATAAAGATCCGG | 4734 |
rs555482789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929398 | TATAGATAAACTGTG[C/T]GGTATGGGTTTTTTT | 4734 |
rs555524188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886802 | CAAATATCTTCTCTG[A/T]CCACAAAGGAATAAA | 4734 |
rs555525951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971967 | GCAGGAGACAGTGGC[A/G]TGATTTATTTGAAGT | 4734 |
rs555547337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857561 | CTCCTAACCTCATGT[A/G]ATCTGCCTGCCTTGA | 4734 |
rs555562988 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964918 | TCTATTTGTTCCTCT[C/T]GATTTGTCAAAAAGA | 4734 |
rs555590840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896989 | ATTGACATGGCTTTT[C/T]TTGAGATGGAGTCTC | 4734 |
rs555602501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939736 | CTGGAATCCCTGCAC[A/C]TGTTGGTAGCAATGT | 4734 |
rs555608622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864540 | TACAAAATTAGCCAG[A/G]TGTGGTGGCGCATGC | 4734 |
rs555647274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895191 | AAAATAGAGATTCAC[A/T]CTTCTGAGCACTAAT | 4734 |
rs555653714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960450 | AACATCAGACTCCAA[A/G]TTCTTCAGCTTTTGG | 4734 |
rs555654191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904182 | AATATATCAAGGTTT[C/T]CTCCAAGTTAAAAAT | 4734 |
rs555658068 | in-del | -/TTTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895606 | CACCTGATAGGCTAT[-/TTTA]TTAAAGACAGATTGC | 4734 |
rs555670711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948753 | ACTGGCGAGCCATAT[A/G]TAGAAAGCTGAAACT | 4734 |
rs555690047 | snp | A/C/T | 4.95776e-05 | 0.00497863 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848921 | AAAGAACAATACACA[A/C/T]AAATTTTAAAATAAT | 4734 |
rs555714057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983305 | GTGTGTGTGTGCGTG[C/T]GCGCGCGTGCGTGCA | 4734 |
rs555740155 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851506 | TTTCAGATGGAGTTT[C/T]GCTCTTGTTGCCCAG | 4734 |
rs555774593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912960 | ACAGAACACAGACAG[C/T]GTCCCAGATACAGGT | 4734 |
rs555781855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897315 | TGCTGTGTCATCTTC[A/G]TCTTACTTAATCCTT | 4734 |
rs555783167 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988051 | GCGGCACTATTCACA[A/C]TAGCAAAGACTTGGA | 4734 |
rs555801903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938221 | AAAATTAGCTGGGCA[C/T]GGTGGCGTGTGCCTG | 4734 |
rs555821693 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985427 | CTGAGGAGGGGAGGA[C/T]GGCGTTGCACAGGGA | 4734 |
rs555836238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911870 | CATGTCCCTATTACT[A/G]GAATGGGAGCTCCCC | 4734 |
rs555857983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949305 | GTCAGGAAACAACAG[G/T]AGCTGGAGAGGATGT | 4734 |
rs555874417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843502 | CTTATTGTAAATTTT[A/C]CAAAAGATATATCTA | 4734 |
rs555881114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833486 | AACAAGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 4734 |
rs555895329 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920110 | ACTACAATGTAGAAT[A/C]CCTGCCTAAGTTCTC | 4734 |
rs555896573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944622 | CCTATCTGACAGCTC[C/T]GAAGAGAGCAGTGGT | 4734 |
rs555920788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905831 | TGTAGGTTGCCTGTT[C/T]ACTCTGATGGTAGCT | 4734 |
rs555924565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943502 | GGCCCAGATATGTCT[C/G]AGGCCGCTGCTCTAG | 4734 |
rs555939608 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829277 | AGTGAAGAAGTAAAC[A/G]GTTTTTCTGTGAGTT | 4734 |
rs555961881 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993435 | CTCCGGTCGTGGCCG[C/T]CGCCGCTACCTCCCC | 4734 |
rs555963077 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907097 | CAGACTGTCTCAAAA[A/C]TAAAAAAAAATAAAA | 4734 |
rs555968785 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982220 | CTGTTAGGCAGTTTC[C/T]TATAAAGTTAAACAC | 4734 |
rs556031164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841019 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 4734 |
rs556047204 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943249 | AGAAAAGAAAGCCCC[A/G]TTTTGTGGGGAGGAA | 4734 |
rs556061076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954104 | CACTCCTATGAAAAG[C/G]CTGTTGTAAAGTCAT | 4734 |
rs556092130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910044 | GCTTATTCTATAGTT[A/C]CAAGGTGAAAGAACG | 4734 |
rs556095553 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906335 | GACACATGGACACGT[A/G]TGTTTATTGCAGCAC | 4734 |
rs556127835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929379 | TACATGTACAAGTTG[A/G]TTCTATAGATAAACT | 4734 |
rs556134625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950442 | AACATGAAGTACAGA[A/C]GAACGGCTTCTGTTT | 4734 |
rs556134969 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920475 | GAAATGTTCTGTCAT[A/T]ATTGCCACCACTACC | 4734 |
rs556140918 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846202 | TTTGCTAAAAATTTG[G/T]GTGAAACTCTGAGGT | 4734 |
rs556151407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986612 | TTTTTTTTTGTGAGA[C/T]GGAGTCTCGCTCCGT | 4734 |
rs556161342 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993985 | CAGTGTTCCTCAGCA[A/G]CAAGTCTCGCTGAGA | 4734 |
rs556164396 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925780 | TTTTACCTACAGCCA[C/T]GTTCCCAGGCTCATC | 4734 |
rs556203808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840243 | CAATTGTGAGTAGTT[A/G]ATATACAACTGTCCA | 4734 |
rs556239766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921979 | AACGCAAATAAAATA[C/G]TTCACCAATAATACA | 4734 |
rs556255597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866121 | GTCTCGTTATGTTGC[C/T]CAGGCTGGTCTCAAA | 4734 |
rs556260473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964217 | CTCCCCTTTCTGTGT[C/T]AGACTGTAAGATATT | 4734 |
rs556281130 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933535 | GGCCTGTCGTGGGGT[C/G]GGGGGAGGGGGAAGG | 4734 |
rs556320934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872821 | CTGGCTTGGTTAGAG[C/T]ATAGAGATAATTCTA | 4734 |
rs556339454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926113 | TGTATATGATACATA[C/T]GTATATGTATCAAAC | 4734 |
rs556348213 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949739 | TCTCACTCATAGGTG[G/T]GAATTGAACAATGAG | 4734 |
rs556360737 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933007 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 4734 |
rs556386591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968648 | AAAGATAATCTCACC[A/G]GTCAGCAGAAAGAGT | 4734 |
rs556423311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974132 | ATCATTAGAGACTAC[G/T]GCGAACAACTATATG | 4734 |
rs556479056 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846601 | AGTCATAAAAAAATC[C/T]AGACCGTCCTCCAAC | 4734 |
rs556508807 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975014 | TCTCCTGCCTCAGCC[A/T]CCCGACTAGCTGGGA | 4734 |
rs556525905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885198 | CAATAGTATATCTGG[C/T]GAAAATGTCCTTCAA | 4734 |
rs556539719 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921425 | CACCTCCTGGGCTCA[A/C]GCAATTCTCATGCCT | 4734 |
rs556554933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914232 | AATCTTTAATAAACA[A/T]AATGGATGTTACAAA | 4734 |
rs556569107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976590 | AATGCTGGCAAGAAC[A/G]TGGCAAAAGGGGTAC | 4734 |
rs556578573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874818 | ATCTCTACGAAAAAT[A/G]CAAAAATTAGCCAGG | 4734 |
rs556579415 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898709 | GGCACAATCGTAGCT[A/C]AATGCAACTTGGACT | 4734 |
rs556587314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884465 | ATAAAGCACCAGGGA[A/C]CTATCCCAGAAACAG | 4734 |
rs556605548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831632 | CTTTGAGTGGTTACT[C/G]TAGGTAGAGAGGTAG | 4734 |
rs556613010 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970478 | TCCAGTACTGTGTTG[A/G]CTTCAGGTGTGACCC | 4734 |
rs556621493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970006 | AGGGCATTTCTAGAC[C/T]CACTCTGGGCCAGAA | 4734 |
rs556655676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982648 | GAATATTCTGTATCA[C/T]AATTGGGTCATTGGC | 4734 |
rs556665001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832581 | CACCAAGCCCAGCTA[A/G]TATTTGTATTTTTGG | 4734 |
rs556710542 | in-del | -/TTGA | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940307 | GATATGTTTATGACT[-/TTGA]TTGTGGTGATGGTTT | 4734 |
rs556716978 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870603 | CAGTGGCTCAATTAC[A/G]GTTCACTGCAGCCTT | 4734 |
rs556726808 | snp | A/C/T | 0.00279258 | 0.0372817 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894197 | GTCAGCTCTCTCTAT[A/C/T]GGTGGATTCAATCAA | 4734 |
rs556742015 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945602 | CAGGATAATATCAAG[A/G]AGAACTTCCCCAACC | 4734 |
rs556743061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926283 | AGCCAACCTAGTGCC[A/G]GTCACTCCTCAGGAG | 4734 |
rs556754063 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867136 | CAGAATACAAACTAC[C/G]TAAGAGTGAGCTTCA | 4734 |
rs556783309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882438 | GGAAAGCAACACCAG[A/G]CAGAACTCAGCCATG | 4734 |
rs556808945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861091 | TTGAATGAATAAATA[C/T]CAGAGCGCTTCATAG | 4734 |
rs556822136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981616 | CAAGAGTTTTTGACA[C/G]TAATAACCATAATAA | 4734 |
rs556826795 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946770 | AAGTAAAGCACTCCT[C/G]AGCAAATGTAAAAGA | 4734 |
rs556830829 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989142 | CCTGGAGGGTGATGC[A/C]GGAAAATCGCTGGAA | 4734 |
rs556840627 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890433 | CTATTCTGGATATTT[C/T]ATATAAGTGGAATTA | 4734 |
rs556907060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903741 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 4734 |
rs556914268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981122 | CGGCTCACTGCTCGC[A/C]ATGTCTACCTCCCAG | 4734 |
rs556919926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836394 | AGACAAAGTTTCACT[C/T]TGTAGCCCAGACTGG | 4734 |
rs556964478 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854118 | ATCGCCTGGGCACTC[C/G]AGCCTGGACAACAGA | 4734 |
rs556997746 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827868 | AGCACAAAGCACCTT[C/T]TGATTGTATAACACT | 4734 |
rs557008641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868287 | CCCTCAGTCAGAGGA[C/G]AAAGTGTTAAGCAAG | 4734 |
rs557016231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935083 | ATGTTGGCCAGACTG[C/G]TTTTGAACTCCTGGC | 4734 |
rs557027698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854745 | CATGGGTGGATTTTA[C/T]GGTATGTAAATTATA | 4734 |
rs557041839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909422 | AAATTACTGTATCTC[C/T]AAGTATCTGTCTTCA | 4734 |
rs557058930 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828941 | AATCTGTAAACATGA[C/T]AAACCCTGTAAACAT | 4734 |
rs557075263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934371 | CAGTTGATGGACATT[A/T]GTGCTGTTTCTAATT | 4734 |
rs557087246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855592 | AGGGTTAAGGTCCAA[C/G]CTGCCATCCAGGCTG | 4734 |
rs557088247 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948235 | AATACCTAGGAATCC[A/T]ACTTACAAGGGATGT | 4734 |
rs557100255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869978 | TGGCCTTTGAGTTGG[G/T]GTTAGAAGACTGGGG | 4734 |
rs557116586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991023 | CTACATTTTAGCATA[C/T]TTCAGTGCTAATATG | 4734 |
rs557130046 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951750 | AGGTAAGCAATTAAA[G/T]TAATTTTTGCATCTC | 4734 |
rs557131483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946210 | AAGACACAGACTGGC[A/G]AATTAGATAAAGAGT | 4734 |
rs557150628 | snp | G/T | 1.6483e-05 | 0.00287076 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848782 | ATAGCCAAGTTAGAT[G/T]GGTTAGCATTTCTAT | 4734 |
rs557159961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988669 | GATTGAATGGCATTG[C/T]TGTATCAGTGTCCAT | 4734 |
rs557164698 | snp | A/C | 3.30721e-05 | 0.00406632 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915891 | AGAAATCCTTTAGCA[A/C]TAGTGCCATCCTCAT | 4734 |
rs557166084 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832198 | AAAAAAAAAAAAAAA[-/AA]GATTTCATGATCAAA | 4734 |
rs557193377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877921 | TGCATTTCTGATATC[G/T]TCTCAATTTTTTTGT | 4734 |
rs557220599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856365 | CTCTCAGCCCCCTAC[A/G]TGGACACCTTCACAC | 4734 |
rs557241574 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916529 | TAAGACATTGCTAGA[C/T]TGAAGATATCCACTG | 4734 |
rs557270197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870186 | AAATCAGACAACTTC[A/C]GACTTTATTTTGCAT | 4734 |
rs557283615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849816 | TTTTTTTTTTGAGAT[A/G]GAGTCTCGCTCTGTT | 4734 |
rs557287937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55915102 | GTAAAATAACAAATA[C/G]AGTAAAAAACTATAC | 4734 |
rs557294952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895295 | GGTGGACGCTAACAT[A/T]CTCTGGAGAATTATC | 4734 |
rs557310867 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55861941 | TTCCCCCTAAATATA[C/T]GATTTTGGCTACCTG | 4734 |
rs557324385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955015 | TTGCACTGCACTGCA[A/C]TGCACTGCATTCCAG | 4734 |
rs557331232 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942630 | CTTCCTGTACAGCCT[C/G]TGGAACTGTGAGTCA | 4734 |
rs557336145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965895 | ACCCTCAACTGATCC[A/G]CCTGCCTCGGCCTCC | 4734 |
rs557385465 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971845 | GCCAGAGATAAAGAA[A/T]GGATCTTAGACGCAG | 4734 |
rs557397344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863499 | TTAATTAGCCTGATT[C/T]AATCATTTTGCATTG | 4734 |
rs557400029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856744 | AGCCACTTCCCACTT[C/T]GCAATCTACCCCCTG | 4734 |
rs557411653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990478 | CTACCACCACTACTT[C/T]GGTGACTTCCTATCA | 4734 |
rs557420771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852060 | CAGCACTTTAGGAGG[C/G]CGAGGTGGGTGGATC | 4734 |
rs557450019 | snp | C/T | | | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848842 | GGAAGTATCAAGTGA[C/T]GTCTTTCCTCTCAGA | 4734 |
rs557459987 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964352 | TCTCTCATCTTCCAA[C/T]TGCGTAACAATTTCT | 4734 |
rs557462827 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891924 | AACAGTTAAGTTAAA[A/G]TGTCACAACTTTGAA | 4734 |
rs557463309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953861 | GAGTAGCTGGGACTA[C/T]AGGCGCCTGCCACCA | 4734 |
rs557471673 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950734 | TGAACAGAGAAACGA[C/T]TCAACAGCTAAAGGG | 4734 |
rs557482206 | snp | A/G | 0.000332242 | 0.0128845 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852396 | GTTTAAATCCTGTAA[A/G]AAAGCAAGTTGATAG | 4734 |
rs557482247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844786 | TAAAGACAGTGCACG[C/G]CTTTCAAGCACCGGT | 4734 |
rs557483122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848198 | GGGTAAGGATAATGA[C/T]GTTATAGAATCTTTT | 4734 |
rs557501079 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918212 | AGTGGACTGTTTGTC[A/C]TTTTAGAGGTTGTGA | 4734 |
rs557522623 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953378 | ACACAGCTAGAAAGC[A/G]GACAGCCAGGATTGA | 4734 |
rs557549956 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841840 | CCTCCCAAAGTGCTG[G/T]GATTACAGGCATGAG | 4734 |
rs557550990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937185 | TTTTTGAACTTCATG[C/T]TTTCTCAAAGATATA | 4734 |
rs557551033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930012 | AAATAAAAAACTAAG[C/T]TGAAGGGAAATGAGT | 4734 |
rs557573792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967113 | TGGTCTCGAACTCCT[C/G]ACCTCAGGTGATCTG | 4734 |
rs557592702 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914858 | TACTCTATTTCATAA[C/T]GATTAAGAAGAGGAG | 4734 |
rs557592925 | snp | A/T | 8.79933e-05 | 0.00663241 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869552 | TTAAAATTTTTTTAG[A/T]TTAACCAAATATTTA | 4734 |
rs557627627 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923036 | TAAAAATACAAAAAT[A/T]AGCTGGGCAAGGAGG | 4734 |
rs557635683 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971372 | GCTCATGCCTGTAAT[-/C]CCAGCACTTTGGGAG | 4734 |
rs557646381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958615 | TCATGTGGGCCTGGA[A/G]TTTTCTTTGTGGGAA | 4734 |
rs557709249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992215 | TTTAGCTGTAACACA[G/T]TGACTATTGTTTCTG | 4734 |
rs557720707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881746 | GATTTGTGACCCTGC[A/G]GTGCTTAAAAAACAT | 4734 |
rs557752987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910925 | TCAAATAAAGACCTC[C/T]ATTGCCCAACTACTT | 4734 |
rs557766162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925472 | TACTATATAAAGTAC[A/G]TAGCAGTCAAAAGTA | 4734 |
rs557796429 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992492 | TATAAATTAGGTTGA[C/T]GGATTTTCAGTTAAC | 4734 |
rs557808144 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876611 | AGTTAAAATGGAATA[C/T]TGGAAATATCTGACT | 4734 |
rs557851479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980283 | AAACAGAATACTTGG[C/T]GCACAGTAGGGGCTG | 4734 |
rs557869643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830239 | TCTCTGCCACTTCAG[C/T]CTCCAAGATGGAATG | 4734 |
rs557873069 | in-del | -/AGGA | 0.0138799 | 0.0821421 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968498 | ATCTAAAATATCTAC[-/AGGA]AGAAGTATCTAAAAT | 4734 |
rs557910125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871183 | CATACTGAAGGAGAT[A/G]TGAACATTCTGACTT | 4734 |
rs557910222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880156 | AATCAGCAGGGCATA[A/G]TGGTACATGCCTTTA | 4734 |
rs557925140 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926885 | GTCTGAAACCAGCCT[-/G]GCCAACAGGGTGAAA | 4734 |
rs557933992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830649 | CCAGGCATATCAAAA[C/G]TTTTTCTAGTGTACA | 4734 |
rs557952229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898064 | ACACATCCATGAGAG[A/G]TGAAATCCACAACTC | 4734 |
rs557960932 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949303 | AAGTCAGGAAACAAC[A/C]GGAGCTGGAGAGGAT | 4734 |
rs557969369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879482 | CCACTAGTCAGTAGA[C/T]GCCCATGAACAAAAC | 4734 |
rs557987170 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895718 | ATCTGGCCAGCAATA[C/T]ACCTTGAGAAACATG | 4734 |
rs558008003 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839760 | AGGCAGGCGGATAAC[A/G]AGGTCAAAAGACTGA | 4734 |
rs558018229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843871 | TGTAGTAGGGCCAAC[A/G]ATGGGGAATAAAGGG | 4734 |
rs558018648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943300 | TGAATGTTCATAGCC[A/C]AGACAATGGGGAAGA | 4734 |
rs558054871 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870606 | TGGCTCAATTACGGT[A/T]CACTGCAGCCTTGAC | 4734 |
rs558075560 | snp | A/C/G | 0.00438556 | 0.0466571 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944040 | ATGGCCAAATAGGAA[A/C/G]AGCTCCTGTCTGCAG | 4734 |
rs558126305 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896889 | TAAGACCTAAAGATA[A/C]ATTCTAAATTATTAA | 4734 |
rs558137586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850377 | ATTAAAAAGACGCAT[A/T]AGCATTCTCCTGAAT | 4734 |
rs558138160 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870545 | TTTTTTTTTTTTTTT[-/TT]GTTTTGAGACAGCAT | 4734 |
rs558141748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932913 | CAGCCAAAAGACACA[G/T]GAAAAAATGCTCATC | 4734 |
rs558171041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906711 | GGGTGCAGCACACCA[A/G]CATGGCACATGTATA | 4734 |
rs558202201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857761 | GAAACAATACTATAC[C/T]AAGTCTTTACAAAAA | 4734 |
rs558205040 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919323 | AAGTTGATCCAGCCG[C/T]CACTTTTAAAGAAAT | 4734 |
rs558207207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932123 | CCTGGTGGGAGGTAA[C/T]TGAATCATGGGGGCG | 4734 |
rs558210663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844184 | GGGCACAGAAGGAGA[A/G]GAAGGGAGAGGAAGG | 4734 |
rs558217743 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994783 | TACTTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 4734 |
rs558234142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906350 | ATGTTTATTGCAGCA[C/T]TATTCACAATAGCAA | 4734 |
rs558247778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898531 | ATCCTTCTTTAATAA[C/T]TTCAAAACATCTTAT | 4734 |
rs558272844 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949940 | GGTACCCTAGAACTT[-/A]AAAGTATAATTAAAA | 4734 |
rs558276051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944431 | TCTGCAGACTGGTGG[G/T]GTAAGGGGTGTCCAC | 4734 |
rs558290429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985921 | AAATGGCTGATTGTA[C/G]ATAGCTGAGCCAAGC | 4734 |
rs558305741 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994143 | ACCTGGGGACCGCCA[A/G]GGAAAGCCTGAGCGT | 4734 |
rs558336305 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826858 | TGTGAGGAACTAGAC[C/T]AGAAGACATCACCCA | 4734 |
rs558340800 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989712 | ATAGGAAACAGAAAT[C/T]ATTCTAGATGCTTTA | 4734 |
rs558351396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986629 | GAGTCTCGCTCCGTC[A/G]CCGAGGCTGGAGTGC | 4734 |
rs558373280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914062 | AATTTGAAATCTGAT[C/T]TTTTTTTATCCTTAG | 4734 |
rs558388010 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882636 | GTCCTAGTTCGTACT[A/G]GGCTTGGATTGGAAC | 4734 |
rs558388101 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909908 | AGAGGGGACTGAGAA[A/G]GTTAGACTAATGCTG | 4734 |
rs558391976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873652 | GTTTTCTTCTGTGAG[C/G]TTAGGCACTCCTCAT | 4734 |
rs558401597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957233 | TACGTACAAACCATG[C/T]TGTCTGCAAATAAAG | 4734 |
rs558407969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834882 | GCTTCTCCATCCCTG[C/T]GTCCCAACCATCACC | 4734 |
rs558410163 | in-del | -/CA | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959988 | CTTAGTCACCCTTAG[-/CA]CAGTTTCCAGTTCTC | 4734 |
rs558464519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865276 | TGGCAAAATACGCAG[A/G]TTACTTAGAAAATGG | 4734 |
rs558484868 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981714 | AGCAGTATGAACATC[A/T]CATGGAAATTTGTTA | 4734 |
rs558493164 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842815 | GTTGTGCCTGTCTGT[G/T]CAGGCTTTTCCCTAC | 4734 |
rs558532520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945523 | ACTATGTGAAAAGAC[A/C]AACTCTATGTTTGGT | 4734 |
rs558533270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866187 | CCAAAGTGCTGGGAT[A/T]ACCAGCGTGAGCCAC | 4734 |
rs558538019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847117 | GTTGTATTTTATGAA[C/T]GTAAGGGCATTAAAA | 4734 |
rs558538783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841174 | CCTGGCATTGTGATC[A/C]ACCAGCCTTGGCCTC | 4734 |
rs558564094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922462 | CCACCTCCTGGGTTC[A/G]GGCAAGTCTCCCAAC | 4734 |
rs558570887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920279 | ACAATCTATTGTTTC[C/T]GTTTCTCTGGAGAAC | 4734 |
rs558655949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859929 | TCTACTTTGCTAATC[A/T]TAGCTTTAGCCTCAC | 4734 |
rs558657037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950901 | AATAGGTACAAGGAG[A/G]CACTGTCAGTCTGAG | 4734 |
rs558665804 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835183 | TCACCTCCCATCTAA[A/C]CCCTCAACCCACTGC | 4734 |
rs558672860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958384 | GGAAAAATCCTAAGT[A/G]GTGATATATTGCTAC | 4734 |
rs558686859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833182 | GAAACATAAGCTATC[A/G]GAATTTAGAATATTA | 4734 |
rs558720043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950486 | CAAGTATGGTACCAC[A/C]GAAGCCTCCAGAGAG | 4734 |
rs558748291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927499 | ACAAGGTCTCACTGT[A/G]TTGCCTAGGCTGATC | 4734 |
rs558751737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965289 | CTGCAGCAGCCTCAA[A/C]CACCCAGACTCAAGC | 4734 |
rs558773754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962962 | CAGCTAATTTTGTAT[A/G]TTAGTAGAGATGGGA | 4734 |
rs558810851 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933550 | GGGGGGAGGGGGAAG[A/G]GGGAGGGATAGCATT | 4734 |
rs558844070 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863711 | TAGGCTGTTCTCTAA[A/G]TTATCAACTGAATGA | 4734 |
rs558900415 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955064 | CTTGCAACGTTGCCC[A/G]GGCTGGAGTGCAGTG | 4734 |
rs558903680 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868900 | CTGCAAACAAGATCC[C/T]GAGGTTCGGAAAAGT | 4734 |
rs558939149 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55892638 | ATCAAAAAGAAAATG[A/C]AACAGTTTCTACCCT | 4734 |
rs558940630 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866299 | CCCAAATTTCATTCT[C/T]TTCTTTCCTTATATC | 4734 |
rs558956311 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907728 | TCTGAGAATCCCAGC[C/T]CTTACAATAAAGTCT | 4734 |
rs558965980 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957957 | GGGAACATCACACAC[C/G]AGGGCCTGTCGTGGA | 4734 |
rs558973560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940702 | CTTGTGAAGAGGGTC[A/G]TTTTTTTTTGGTAGA | 4734 |
rs558974997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877056 | ATTGCAAAAATACTG[C/T]GAGAGAATCCTCATA | 4734 |
rs558994362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869274 | AATGTCCATATATTT[A/G]ACTTCAAAATACTAA | 4734 |
rs559057751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868338 | AGAGCAATTTGGTGC[C/T]ATACGCTGTGTGCTT | 4734 |
rs559099145 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969613 | CAGAGTCCTGAAGCC[C/T]CCATTCTAGGTCATA | 4734 |
rs559119789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965496 | GTGACTGTGATCTCT[G/T]TTCAGATCTTTTGTC | 4734 |
rs559120002 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855972 | CGGTTCTCCATGTTT[G/T]GTCTTTAAGCCCCTT | 4734 |
rs559122281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875474 | CACCATGCACTACCA[C/T]GCCTGGCTGATTTTT | 4734 |
rs559171053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976168 | GAACACTGGTCTAGG[A/C]AAAACTTTCTTGAGT | 4734 |
rs559190067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970535 | AGGATTGTGTCACCC[G/T]TCTGCCAACTCCAGG | 4734 |
rs559209613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975623 | GAAAGAGATAGAAGA[C/T]GACACCAAAAAAAAA | 4734 |
rs559227085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970063 | ACCCAGGCCTGGCAG[G/T]ACTCACCATCTACTG | 4734 |
rs559228958 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968106 | ATTATCTTTTTTCTC[C/T]AAAGTAATCTATAAA | 4734 |
rs559229027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975953 | ACCAATGGAACAGAA[C/T]AGAGAACCCAGAAGT | 4734 |
rs559247869 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851991 | ACATCAGTGTCAGAA[C/T]ATAAATAATTAGAAG | 4734 |
rs559250155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939995 | GATACATTAAGAAAA[C/T]GTGACATATACATAC | 4734 |
rs559266004 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983492 | CATGTGGTTCTATTT[A/C]CTCAATGGGGTTCTA | 4734 |
rs559273293 | snp | A/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55917124 | TTTAAGCTGAGCTCA[A/G]CTGCAGCACACTGAC | 4734 |
rs559282208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846230 | GGTGGCCCACCCACC[A/G]TCTTGAATATTTGTG | 4734 |
rs559282401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853984 | AACTGAGCAAAACTC[C/T]GACTCAAAATAACAG | 4734 |
rs559285739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847554 | AAGCAGCTATAAAAA[A/G]GGATAATTTTCCTAT | 4734 |
rs559292924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861627 | TATGCCTTGCATGCC[C/T]GTATCAAAACCTCTC | 4734 |
rs559339691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958215 | TATTTTATGTTAGTT[G/T]GCTGAGAGGTTTTAT | 4734 |
rs559344144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841544 | GCACAACAATGTGAA[A/T]GTATGTAATGACTCT | 4734 |
rs559345933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848246 | GAGTATGGGAAATGG[A/G]GGAGAGGAGAGAACG | 4734 |
rs559351348 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941137 | GTCTCTCTCATATAA[A/G]GCCAGCTGTTGTATA | 4734 |
rs559373890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836683 | CGTGCACGCCACCAC[A/G]TCCGGCTAATTTTTT | 4734 |
rs559375576 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982377 | AAACAATCAATGTGT[C/G]CATCGAAGGAGAATG | 4734 |
rs559397659 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856406 | CATGCCCCCCGTGCT[A/G]GACTGCCTCCTGGAC | 4734 |
rs559420456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964967 | TTGCTTCCACTCTTG[C/T]TATGTGATTTCTTTG | 4734 |
rs559423071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895592 | AGTGTGTGTTAAAAT[C/T]ACCTGATAGGCTATT | 4734 |
rs559433542 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829745 | TTAAAAATAAGTTGT[C/T]GTACTATTTCTTCAA | 4734 |
rs559454732 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876513 | CAAATCTATATTGTT[A/G]CAAGACTTATATTTT | 4734 |
rs559466498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878668 | CAAGAATGTTCACAG[A/C]ATTTCATTCATAATA | 4734 |
rs559476866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928618 | TAAGGTCTATCCACT[C/T]GCAACACCTTCTCCA | 4734 |
rs559484042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903434 | TACTTATTTCTAATA[C/T]GGAGATATAATCACT | 4734 |
rs559489117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849163 | AAATGTGTCACTATA[C/T]AGGGCTTTTCTCTAT | 4734 |
rs559527467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886247 | ACCCCAATACAATTA[C/T]AGCTTGAGAATTCAA | 4734 |
rs559529232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990518 | AAGCAAGTTACCAGA[C/T]ACTGGAATACTTTCG | 4734 |
rs559540422 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872900 | ATTACTGAAAGCTTA[C/T]GGTCCTGCACCCTGT | 4734 |
rs559542752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883929 | CTGTTGCCCAGGCTG[C/G]AGTACAGTGGCATGA | 4734 |
rs559564244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933919 | AGCACTTTGGTAGGC[C/T]GAGGCAGGCAGGTCA | 4734 |
rs559570001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937002 | TTCACCATATTGGCC[A/G]GGCTGGTCTTGAACT | 4734 |
rs559577610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977381 | CCTAGGTGTGTAGTA[A/G]GCTATACTTTCTAGG | 4734 |
rs559626658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940268 | AAAAAAGGGGGTGAT[A/G]GGAGGAAACTTTTGG | 4734 |
rs559647119 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837101 | AGGCAGCTATATGTC[A/G]TCACATGTAAATATC | 4734 |
rs559663936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983318 | TGCGCGCGCGTGCGT[A/G]CATTTGATTTCCATG | 4734 |
rs559735709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838386 | TTCTTGCTCAGAGAC[A/G]GCTTTTGTTACTGGG | 4734 |
rs559739575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844879 | GTGGCATGATTATAG[C/T]CCAGTGCAGCTTTGA | 4734 |
rs559748225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978136 | AAAACCATCCATGTT[A/G]GCCTCGACTGAAACA | 4734 |
rs559766468 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949108 | CAAACAAATTTACAA[A/G]AAAAAAACAACCCCA | 4734 |
rs559783686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834441 | CTCAATATTGGCCAG[A/C]AAATGTACATGTGCA | 4734 |
rs559784050 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908602 | CAGAAATCTCAGGCC[C/G]CCATTCTGAGACCTA | 4734 |
rs559802371 | snp | A/G | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839244 | ATGTTGGCCAGGCTG[A/G]TCTCAAACTCCTGAC | 4734 |
rs559822636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862090 | CTGTACGTCACTCTA[C/T]GAAGACTGAAGCTTC | 4734 |
rs559828915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948573 | ACAAGGCTACAGTAA[C/T]CAAAACAGCATGGTA | 4734 |
rs559846530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979403 | CCAGGCCGGACTGCG[G/T]ACTGCAGTGGCGCAA | 4734 |
rs559906374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983055 | TGAACCCAGAAGGCA[A/G]AGGTTGCAGTGAACC | 4734 |
rs559928072 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862369 | GTATATACAGTCTAA[C/T]AATAAAAAAAATCAC | 4734 |
rs559950969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953624 | TTTTTGTATTTTTAG[C/T]AGAGACGCGGTTTTG | 4734 |
rs559972876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831214 | CATGAGCTACCGCAC[C/T]CAGCCGCCTTAACAT | 4734 |
rs559975541 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828160 | ATGCTGTGGTGTTTG[C/G]AAAGTAGAAAGTGGT | 4734 |
rs559990121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924539 | CAGAGTCTCCATAAC[C/G]ACCCCCAAGCCATCA | 4734 |
rs560099999 | in-del | -/A | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828284 | TTTTACAGTTCTCAC[-/A]GGGTGTGTATATATA | 4734 |
rs560130443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904430 | GTCATAGCCTCCTGA[A/G]TAGCTGGGATTACAG | 4734 |
rs560152737 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962368 | AATCCATTAATGTTC[C/T]TTGTAATTATTGATA | 4734 |
rs560164555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897159 | TTTTGTATTTTTGTA[C/G]AGATGGGGTTTCACT | 4734 |
rs560178127 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982733 | TTGTAAATTTCACTC[G/T]TCCCCACCCCCATTC | 4734 |
rs560186651 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945163 | GGAAGGAGAATGACT[C/T]TGATGAGTTGACAGA | 4734 |
rs560208140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955051 | TTTGAGACAGAGTCT[C/T]GCAACGTTGCCCAGG | 4734 |
rs560213461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961758 | ACAGATGTGAGCCAC[C/T]GCGCCTGGCCAGTTT | 4734 |
rs560223377 | in-del | -/T | 0.318174 | 0.240525 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851374 | AACATCAATGCAAAG[-/T]TTTTTTTTTTATCAA | 4734 |
rs560266109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966060 | TCAGACCAATTCATA[A/G]TATCAGGAACTCACT | 4734 |
rs560271746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960609 | GCAGATGGCCAATAG[C/T]GGGACATCACTTTGT | 4734 |
rs560307478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911656 | TGCCTCAGCCTCCCG[C/T]GTAGCTGGGACTACA | 4734 |
rs560327403 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849409 | TTTGTATATTTAATA[A/G]AGACGGGGTTTCTCC | 4734 |
rs560348684 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901921 | TCATAAATTTTATAT[C/T]ATATAAATATAAAAA | 4734 |
rs560380342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863933 | TCATTCTCATTCCCT[C/T]GTCTGATTTCTCTCT | 4734 |
rs560414157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879670 | ACCGTAATATTCCCA[C/G]AGATAAGAGGAGATG | 4734 |
rs560417299 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955578 | TATCTGTCTTTCTGT[G/T]ACTGTCTTATTTCAG | 4734 |
rs560438464 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930113 | GCTGGGCAAATTATG[G/T]CTTGTGTGCTAAATC | 4734 |
rs560439551 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871534 | GCAGATGTCACAATC[A/C]GTCTAAAATTAAAAG | 4734 |
rs560443925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871267 | AGTTTCTCTACAATT[A/G]TATGTTTCATGTCTT | 4734 |
rs560469520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870579 | CCCTCTGTCGCCCAG[A/G]ATGAAGCACAGTGGC | 4734 |
rs560471263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966798 | ATTTATCGCTGCGCT[C/G]AAGAAAATCTAAAGC | 4734 |
rs560494111 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920325 | TGCTAAACGTGAGAA[A/G]CACAGGGTCTCCACC | 4734 |
rs560499383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912278 | TATATTTAAAACATC[C/T]ATTTTAGGAAGAACA | 4734 |
rs560513933 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956588 | AGGAGCTGATCATAT[A/G]TATGTGTATATATTC | 4734 |
rs560536378 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925152 | ATTTTAAAATTACAT[G/T]AAATAAGAGCAGACT | 4734 |
rs560538906 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982592 | AGTAGACGGGCAGAA[C/T]TGACTGGAAGAGGGC | 4734 |
rs560546974 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926427 | GACCATGGAGTAACT[A/G]AGGATAGACATGCCA | 4734 |
rs560548512 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844139 | GGAGGAACAGCATAC[A/G]TGAGAGGTCTGATAT | 4734 |
rs560554890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850871 | CTCTAAATATTTGAG[C/G]CTCATTTTCAAATGT | 4734 |
rs560565754 | in-del | -/TAAAACA | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885721 | TTAAAAGACAGAAAT[-/TAAAACA]TACCACCAGATAAAA | 4734 |
rs560587276 | snp | A/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936511 | ATTTTCATTTCTCTT[A/T]ATTAAAAAAACTATC | 4734 |
rs560608724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925967 | ATCATACAGTATGTA[C/T]ATGTAAAAATACATA | 4734 |
rs560612053 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935213 | ATAATCTGAAATGAA[C/T]TATCTATAACAACAT | 4734 |
rs560627011 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980156 | AGGCTGATCTTGAAC[A/G]CCTGACCTCAGGTGA | 4734 |
rs560651508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872546 | TTTTCAAGAATACTC[A/C]TGAACTATCACCTAA | 4734 |
rs560660869 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890662 | TAAAAGCTTTTGTAC[A/G]AACATATGTTTTCAT | 4734 |
rs560664558 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842674 | TAAGCCATGGCACCC[A/G]GCCTAAAGAAGCAAT | 4734 |
rs560705606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883530 | CCCTAGGGCCTTGGA[A/G]CAAACAGAGGTGGCA | 4734 |
rs560722264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900158 | GGACAAGAACTCATC[A/G]TAAGGAAAGGAGGAG | 4734 |
rs560724126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890168 | ATATATACCTACTAT[C/G]TACCCACAAAAATTA | 4734 |
rs560734084 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826496 | GGCTGGCTTGAGTGG[A/G]TGGGAGTGGATTCCC | 4734 |
rs560739124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931778 | ATAATTCACATAGCA[C/T]ACACTCATCCCTTTG | 4734 |
rs560748555 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835602 | CACTTAAGCAGATGA[A/T]CCCCAAATCCATACA | 4734 |
rs560749361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975473 | ATCAGTAGCATTTTT[A/G]TATGCCAACAGTGAA | 4734 |
rs560770188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897667 | CAGTTTGACAGCCTG[A/G]TAAGGTTTGGGCTCC | 4734 |
rs560785324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899354 | TTACAATTTGATTAC[C/T]TGGTTATCTGATCAA | 4734 |
rs560816474 | in-del | -/T/TTT | 0.554138 | 0.200642 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914200 | TTACTTATCCAGAAG[-/T/TTT]TTTTTTTTTTTAAAA | 4734 |
rs560824716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979854 | ACTTTATGCCTTTCT[C/T]CACTTTTAAAACTGA | 4734 |
rs560836608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851553 | ATAATCTTGGCTCAC[C/T]GCAACCTCCGCCTCC | 4734 |
rs560856550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970126 | AGCAGTAGCCAGACT[A/G]TAGTAGCCACAGGTC | 4734 |
rs560877919 | in-del | -/TGAA | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986497 | CAAGAGAGCGTGACC[-/TGAA]TGAACATGGTCATCA | 4734 |
rs560937300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941285 | GAACTTAAGGTGGAA[A/G]CTTAGATCATTGATT | 4734 |
rs560962029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853480 | TCTTAGCCAAAAGGC[C/T]GAGAGTAATGGAAGT | 4734 |
rs560975876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911036 | TCACCGCCTCCCACA[A/T]CCCCAGGCTACCCTA | 4734 |
rs560995687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939468 | AATTACCCAGTCTCA[C/G]GTAGTATCTTTATCA | 4734 |
rs560999234 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946381 | GATAAAACAGACTTT[A/C]AACCAACAAAGACCA | 4734 |
rs561021037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848286 | CTTTCCTCTCAATGC[C/G]TGTAGGGTTATGCCC | 4734 |
rs561051855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975118 | GGCTGGTCTCAAACT[C/T]CTGACCTCAGGCAAT | 4734 |
rs561055564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939071 | TGATTGTGCCACTGC[A/G]CTCCAACCTGGATAA | 4734 |
rs561061906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946061 | AACCATGCCAAATTA[C/T]AAAGATCATCGATGC | 4734 |
rs561111546 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950924 | AGTCTGAGGGCCTTG[A/C]TGAGGAATTGGAAAT | 4734 |
rs561177377 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907773 | TTATAAAACAACGAT[A/C]AACTGAAAGAAAGCT | 4734 |
rs561217938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982908 | AGGTGGATCACCTGA[A/G]GTCAGGAGTTCGAGA | 4734 |
rs561224454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907878 | AGCCTCTATCCAGAC[A/G]CCCAGTTATACGGTA | 4734 |
rs561251702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949915 | TGTAACAAACCTGCA[C/T]GTTGTGCACAGGTAC | 4734 |
rs561300187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958066 | TGGCATATGTATACA[C/T]GTGTAACAAACCTGC | 4734 |
rs561311091 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990686 | CCATTAATTTCAATG[C/G]AGTGTGGGAAACAGT | 4734 |
rs561315249 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856462 | ACCATTCTCAAATAC[A/C]CTCCCTCTCCACTTT | 4734 |
rs561322641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984923 | CAGCTCTGGAGTAGA[C/T]AACCATGATAGATTG | 4734 |
rs561347962 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904298 | TCTATTTCCATACAC[C/T]TTTTATTTTATTTCA | 4734 |
rs561367000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852821 | GTGGTATGATCTCGG[C/T]TCACTGCAACCTCTG | 4734 |
rs561404247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862178 | TATCTGTAAAAGTGC[C/T]TGGCATATATCAGGC | 4734 |
rs561425202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839951 | CTGCACTCCAGCTTG[A/G]CAACAGAGTGACACT | 4734 |
rs561428362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845849 | GGAGTGCAGTGGCGC[A/G]ATCTTGGCTCACTGC | 4734 |
rs561435323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988034 | GCACACGTATGTTTA[C/T]TGCGGCACTATTCAC | 4734 |
rs561461131 | snp | A/G | 3.30131e-05 | 0.00406269 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860781 | TGTTAGGTTGTCCCT[A/G]TATTGGAAGTATAAA | 4734 |
rs561466518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927581 | TTTGCATTAGACACT[A/G]GCAAGAAAAGTTTGG | 4734 |
rs561470056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958850 | TTTTTCATTTCCACA[C/G]GGTCTATAGCAATGC | 4734 |
rs561483389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909658 | ACAAAGCCTCTTGTC[A/C]TGGCTTCTCCTGGTC | 4734 |
rs561521481 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906338 | ACATGGACACGTATG[C/T]TTATTGCAGCACTAT | 4734 |
rs561523824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867919 | AAATTAGCCAGGCAT[A/G]GTAGCACATGCCTGT | 4734 |
rs561531528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951369 | GTAAAATAAAATATA[C/T]ACTTACTCTGAATAA | 4734 |
rs561534825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965568 | AATCCTTACCACTGC[C/T]ATGTTTTCTTCAGAT | 4734 |
rs561539890 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952290 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCAAG | 4734 |
rs561547934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833663 | GAGACTCCATCTCAA[A/G]AAACACATTATATTA | 4734 |
rs561558833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850022 | ATGGTCTCGATCTCC[A/G]TCTCCTGACCTCGTG | 4734 |
rs561565932 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929726 | TTTTATCACTGTTAA[C/G]TATGATAGATTACCA | 4734 |
rs561579216 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950040 | TAAATAAATAACTCA[A/G]CAACTTGGGAATTTA | 4734 |
rs561613471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954685 | ATGCATCACCACACC[C/T]GGCTAATTTTGTATT | 4734 |
rs561620464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843364 | TAAAACTGAAGAAGA[C/T]GACTTAAGAAAGTCT | 4734 |
rs561672282 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861796 | AATTTTGTTCAAATA[-/T]TTAATAATAAAATTA | 4734 |
rs561683117 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916654 | TTTCCTTTATTAACG[G/T]AGCTAGTGCAGTCTG | 4734 |
rs561694439 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930673 | ATCCAAATGTGTCAA[C/T]GGCAGGGCTAGGTGG | 4734 |
rs561744855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909008 | ATTTAAAGACATTGT[C/T]TACTATATCATCAAT | 4734 |
rs561746863 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871033 | TTACCTACCCCCACT[C/T]CCAAGCCTCCCCTAA | 4734 |
rs561759932 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995269 | TTTAAGTTGTCACAT[A/G]TCTGTGGGATTTGTG | 4734 |
rs561760854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971489 | AATTAGCCAAGCATG[A/G]CAGCGTGCACCTGTA | 4734 |
rs561767935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842476 | ACTGCAGCCTCGACC[C/T]CATGGGCTCAAGTGA | 4734 |
rs561783720 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898501 | CTTGATGCTTACAAT[A/G]ATTTCAACACTCTGA | 4734 |
rs561808758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923119 | AACCTGGGAGGCAGA[A/G]GTTGCAGTGAGCTGA | 4734 |
rs561814496 | snp | C/G | 1.6504e-05 | 0.00287258 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850524 | TTATAAATTTAAATG[C/G]AAAAGTATCAAAGTT | 4734 |
rs561848400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976699 | CAGTGGTGCAATCTC[A/G]CTTCACTGCAAGCTC | 4734 |
rs561852276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887344 | CAGAAATCAAAGGAT[A/C]ATTAGAGATTATGAC | 4734 |
rs561860618 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992925 | TTCTCACACTAGACA[C/T]TTGTTGCTAAAGAGG | 4734 |
rs561876595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843739 | TATGAGCAGTTTCCT[A/G]TACTGCTTATGTCAT | 4734 |
rs561900234 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919764 | CATTCAGAGCTGTTG[A/G]TTACTGATCATCTAC | 4734 |
rs561901655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978186 | AAATGTAACAAGCAT[C/T]AATCAAAAACAATTC | 4734 |
rs561916056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896309 | GCCTCAGCCTCCCCA[A/G]GTACCTGGGATTAGA | 4734 |
rs561948068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830396 | CAACTCCTTCTTACC[C/G]ATAATCCATACCTGC | 4734 |
rs561962809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876154 | CTGTATCTAGCAAAA[A/T]CTATCCATAAAAAAG | 4734 |
rs561964220 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938979 | GTGCGTGATGGTGTG[A/C]ACCTGTGTTTGCAGC | 4734 |
rs561977781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895637 | TGGGCTCTACCCCTA[C/G]AATTTCTGATTCTGC | 4734 |
rs561985464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879897 | TCAAAAGTCAACATC[A/G]AAATAATAGGCATTC | 4734 |
rs561988139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983770 | TATATGCTACCATGC[C/G]TGGCTAATTTTTGTA | 4734 |
rs562007994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930306 | GAAAAAGTTCACTGA[A/C]CCTCGTCCTAGACAA | 4734 |
rs562009047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830964 | CACTCTGTCACCCAG[C/G]CTGAAGTAAAATGGC | 4734 |
rs562024998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983365 | TCCAAATCCTTAACA[C/T]GGCATGCCAGGCTTG | 4734 |
rs562044962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934536 | AATAGAAAGTATTCC[A/G]GCATTTTAATTTAAA | 4734 |
rs562049311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856039 | TGTATTGGCTCCCTG[A/T]AAGGCAAACGTTCAC | 4734 |
rs562148118 | in-del | -/GA | 0.0111196 | 0.0737302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852274 | GACTCCAGCCTGGGC[-/GA]CAATACTGAGACTCC | 4734 |
rs562152260 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938410 | AACTGGATATCCATA[C/T]GCAAAAGAAAGAAAT | 4734 |
rs562162165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832255 | TTTCTTCTAACAGTA[A/C]AGGTTCTACAGAAGT | 4734 |
rs562182972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975430 | AAAATCAGTAGCATT[C/T]ATTTTAATTTAAGAA | 4734 |
rs562195880 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889400 | CCAGCCATAAAAGGA[A/G]TGAGATCCGCTCATT | 4734 |
rs562240076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903550 | TATACTGGGGCCGGG[C/T]AAGGTGGCTCACGCC | 4734 |
rs562241136 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902294 | CAAGTCAAAAGAGAT[A/G]TATCCATCTTGAATT | 4734 |
rs562243154 | snp | C/T | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838564 | AATTCTGTTGGGTCA[C/T]TTTCAAGAATCCATC | 4734 |
rs562278529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947712 | AAACCATATGATTAT[C/T]TCAATAGATGCAGAA | 4734 |
rs562279835 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943752 | ACAGGGTTCCCACTG[G/T]GACACTGCCTAGTGG | 4734 |
rs562299793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911598 | GCAGTGGCGCGATCT[C/T]GACTCACTGCAAGCT | 4734 |
rs562340083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903836 | TCTCAAAAAAAAAAA[A/C]AAAACACACATATAT | 4734 |
rs562341558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942821 | TGAAACAGTTTGGAG[A/G]GATCAGAAGAAGAAA | 4734 |
rs562361835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911061 | ACCCTATGCTTGAGC[A/C]CCACTGGACTATTTA | 4734 |
rs562375961 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935363 | TTATTCAAATATTGG[A/G]TGACTATGTCTGTCA | 4734 |
rs562382819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991290 | TTTAACAAAAGGGGT[A/G]TTTGGGGGTGGGGAG | 4734 |
rs562408086 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957968 | ACACCAGGGCCTGTC[A/G]TGGAGTGGGGGAAGG | 4734 |
rs562423390 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918496 | TCCGTTGTTTATACC[A/G]CATGCTACTACACCC | 4734 |
rs562424841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980534 | CAGTACCCGCCCCTC[A/G]TACAGAGGATGTAAG | 4734 |
rs562437417 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889062 | CTTCAGTAATACTCC[A/T]TAAGCACAGACAACC | 4734 |
rs562486596 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917759 | AGTCTTTAAATGATG[C/T]CATTTATATTTTGAC | 4734 |
rs562500612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904529 | GCCTGTCTCAAAGTC[C/T]TGACCTCAAGTGATC | 4734 |
rs562541558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949133 | ACCCCATCAAGAAGC[A/G]GGCGAAGGATATGAA | 4734 |
rs562550672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985344 | CATGCTCGCCAGCAC[A/G]GGGCACTGAGGGGAG | 4734 |
rs562576374 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944157 | GTGGGTGCAGCCCAC[A/C]GAGGGCAAGCCGAAG | 4734 |
rs562598467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905102 | CGTCTCAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 4734 |
rs562603311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859596 | CAGCTATTCAGGAGG[C/T]TGAGGCATGAGAATC | 4734 |
rs562603385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957085 | AAATTGTATTTTCCA[A/G]TGGCCCAATGATAGG | 4734 |
rs562608736 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925674 | GGTGTACATGTCAAA[A/T]CTATTGATAGAAAAA | 4734 |
rs562621984 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831202 | TGAGATTACAGGCAT[A/G]AGCTACCGCACCCAG | 4734 |
rs562640379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984572 | CATGATTGTTTGTTC[A/G]TATTACTCTCTTCAT | 4734 |
rs562643841 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947366 | AAACTACAAACTACC[A/G]TCAGAGAATACTATA | 4734 |
rs562665024 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888737 | ACCAAAATGGCATGG[G/T]ACTGGTATAAAAACA | 4734 |
rs562669086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857957 | AAAAACAAAAGGTAC[A/C]AACAATATATATCCT | 4734 |
rs562684196 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956780 | AAATTGTTTTGGCTA[C/T]TCTATGTGCCTTGAC | 4734 |
rs562684872 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979363 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 4734 |
rs562725624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962434 | TCCATTGTCACTGCC[C/T]TTTACGTTGTTTTTT | 4734 |
rs562732402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955118 | CCTCTGCCTCCCGGG[C/G]TCAAGCAATCCTCCC | 4734 |
rs562762985 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877790 | TTTATATCATCATAG[A/T]CTCATTGATATTTGT | 4734 |
rs562783542 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945270 | AAAAACCTTGAAAAA[A/T]GGTTAGCCCAATGGC | 4734 |
rs562792682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864133 | GTTAATGCTTTTATA[A/T]GAGAAACCTCACAAA | 4734 |
rs562793022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960726 | TGATTTCTCAGACAC[A/C]GCATGACTCCATGAA | 4734 |
rs562798224 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950109 | ATCAAAACCAGACAT[G/T]ATCAAGTCTGGAATT | 4734 |
rs562821763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871803 | TCTCTGCTTTAGTTT[A/G]ACCTTTTTGACAGTA | 4734 |
rs562826928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932324 | ACCAAAACAGAGATA[C/T]AGACCAATGGAACAG | 4734 |
rs562827854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906552 | AAACCAAACACCCCA[C/T]GTTCTCACTCATAGG | 4734 |
rs562838849 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993633 | AGGAGGAGGAGAAGC[A/G]GGAGGAGGCGGGGAA | 4734 |
rs562867013 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986725 | CTCCCGAGTAGCTGG[C/G]ACTACAGGCACCCAC | 4734 |
rs562889740 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913150 | AGTGATTTAATTTCA[A/C]GGCTGCTCAGTACAG | 4734 |
rs562898626 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914570 | AACTTAGAATTCAAT[A/T]TTGTTGAAAGAGTGA | 4734 |
rs562903696 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994403 | AAATAAAGTGAACTA[A/G]GACCTCCTGTAGAAT | 4734 |
rs562907447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851605 | CCTCAGCCTCCTAAG[C/T]AGATGGGATTACAGG | 4734 |
rs562931429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875864 | GGGGAAAAAAACAGC[C/G]AAAATATTCACACAT | 4734 |
rs562941586 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893970 | GGGCTTATTTAAAAC[A/G]TTTTCCTAGAAGTTC | 4734 |
rs562968705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844535 | CATTCTGGAATCTGG[A/T]CCTGTGTTATTGACT | 4734 |
rs563012288 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931589 | ATAAATGCATAAAAC[A/G]ACAGAGGAAAAAAGT | 4734 |
rs563015140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913440 | AAGCCTTTGATTTAT[C/T]AATTAGATCTATTTA | 4734 |
rs563056399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968450 | AAAATGAAAAAAACA[A/G]GGGGATATTTTAGAT | 4734 |
rs563084226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873308 | CCCTTTTCCCTACCT[A/G]GCTGATTTTTATCTC | 4734 |
rs563094523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922187 | AATATCTATTAAGGA[C/G]GTTAAATACATAAAT | 4734 |
rs563104935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852141 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCAGGT | 4734 |
rs563115707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882823 | ACAACCTGGATACCA[A/G]CTCAGCCATAGTAGG | 4734 |
rs563118966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881627 | GGTTTAGGCTTAATC[A/G]GATTAAAAAAAACAA | 4734 |
rs563124195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881923 | TCTACCCACTTGTGT[C/T]AGTAGTACCCGCCCT | 4734 |
rs563126345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968896 | GCTCATTAGAACCCT[A/C]CAGTGAGAGTCCCCA | 4734 |
rs563155817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928183 | CCTGGCTAATTTTTG[C/T]ATTTTTTTAGTAGAG | 4734 |
rs563183161 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889714 | GTTTTGTTTTGTTTT[G/T]TTTGGAGACAGAGTC | 4734 |
rs563184943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981880 | AACTGCTGCAGTTAA[C/T]GTGGTTATGGAAGTA | 4734 |
rs563186829 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935283 | TTGTATGAATGTATC[A/G]TAATTTACTTACTGC | 4734 |
rs563187232 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881210 | GCAATGGCGTGATCT[C/T]GGCTCACTGCAACCT | 4734 |
rs563265222 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988619 | AAAAAGAGAAATTAT[C/T]AGTAACATTTATCAA | 4734 |
rs563281390 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868085 | AAAGGTCTTTCCTTC[C/T]ATTATTATAGATTCT | 4734 |
rs563316609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921804 | ACACAGTAAATGCTT[A/G]AGGAATGTTAATTCA | 4734 |
rs563371237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900809 | AAACATTTTAATATG[A/C]AGATAAATTGGCACA | 4734 |
rs563374356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855310 | GATGGTTGGGGAAGA[A/T]AATGAGAAAGCCATT | 4734 |
rs563380122 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927639 | CACTGACATCCAGAA[A/G]AAGAGTTAAGACTTG | 4734 |
rs563411067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945707 | CCAAGACACATAATT[A/G]TCAGATTCACCAACG | 4734 |
rs563413216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55987093 | AGTCCCACCAACAGT[A/G]TAAAAGTGTTCCTAT | 4734 |
rs563438216 | snp | A/G | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848388 | GGTCCAGTTATTGCT[A/G]CATTCTCCAACCGAG | 4734 |
rs563438225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855861 | TATGCCGTATGCAGC[A/G]GATCACCTCTAGCCA | 4734 |
rs563441523 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904384 | CTCGGCTCACTGCAA[A/C]CTCCGCCTCCCAGGT | 4734 |
rs563451178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969130 | TATGCCTTTGCGGGA[C/T]GAAGGGCAAAGTGAT | 4734 |
rs563481498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933253 | TATTGCAGCACTATT[C/T]ACAATAGCAAAGACT | 4734 |
rs563486845 | in-del | -/CTAT | 0.00676609 | 0.0577691 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928019 | GATTCACTACCTCAA[-/CTAT]CTTTTTTTTTCCCTT | 4734 |
rs563524386 | snp | C/T | 3.85929e-05 | 0.0043926 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842211 | ATCAGTTCAACATAA[C/T]AACAAACCCATCTCT | 4734 |
rs563532630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890790 | AGATTTCAATTCCTC[C/T]CCTTTCTTACCAACA | 4734 |
rs563552758 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973240 | ATGTTAGCCACAAAA[G/T]AAGTCTTTAAAAATT | 4734 |
rs563635356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902727 | GAACTTAAGGATGAA[A/G]TTCATAAACAATGTT | 4734 |
rs563657640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971582 | GTCAGCAGAGATTGC[A/G]CCACTGCACTCCAGC | 4734 |
rs563717728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927946 | AGATGTTTAATGAAT[A/G]TTGCTAAGAAACTAA | 4734 |
rs563719192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976715 | CTTCACTGCAAGCTC[C/T]GCCTCCTGGGCTCAC | 4734 |
rs563727943 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894521 | CTACTTGAAATTCTA[C/T]GGCCCTTAGAAACCC | 4734 |
rs563730617 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846618 | GACCGTCCTCCAACA[A/C]AGTCAAAGACTAGGC | 4734 |
rs563736101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948514 | AATCCTAAGCAAAAA[C/G]AACAAAGCTGGAGGC | 4734 |
rs563756177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983014 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGGAG | 4734 |
rs563770681 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927947 | GATGTTTAATGAATA[C/T]TGCTAAGAAACTAAT | 4734 |
rs563795093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954235 | TCATTTTGCTTCTAC[A/G]ACACATCTCTTCTAG | 4734 |
rs563796085 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840534 | TTGCAAAAAACCAAA[C/T]ACATTTAGGATGATT | 4734 |
rs563828706 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833842 | TTACTACCTTCTGAA[C/G]ATTTTACTTACCTAG | 4734 |
rs563837448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941386 | ATCCCACATTTGGTA[C/T]GTTATGCTTTAACAA | 4734 |
rs563868145 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952722 | CAGTTCTCTGAACTT[C/T]GGAGCCTTGCGTCAT | 4734 |
rs563895770 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983861 | AGTGATCCACCCATC[G/T]CAGCCTCCGAAAGTG | 4734 |
rs563900417 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946458 | ACAAGAAGAGCTAAC[A/T]ATCCTAAATATATAT | 4734 |
rs563906687 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908073 | CATCACAGTCATCAC[G/T]CAAATATCCTAGTTT | 4734 |
rs563916794 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988905 | GAATACTGGAGCTCT[C/T]TGTGTTGTACTTTCA | 4734 |
rs563921974 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959503 | ATATTGTGGCATCCA[C/G]ACACTAGGGCAGCTC | 4734 |
rs563931307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952095 | GTACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAT | 4734 |
rs563937784 | snp | A/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991360 | GATAGACCAGAAAAT[A/T]AATGGCAAATGATAG | 4734 |
rs563943393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906479 | GAGTTCATGTCCTCT[A/G]TAGGGACATGGATGA | 4734 |
rs563947765 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826566 | AGGAAAAGACACTTC[A/G]TTCTGAATTAACACT | 4734 |
rs563969168 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846484 | AGCATAAGGAGACAA[A/G]TCACAAGAGCACAGT | 4734 |
rs563976128 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930639 | GTGTCCCTACCCAAA[C/T]TTCACCTGAATTGTA | 4734 |
rs564008359 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907890 | GACACCCAGTTATAC[A/G]GTACCAGTTAGTGGA | 4734 |
rs564010979 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827087 | TATAATCAAAATGAA[C/T]TGTGTTTAACTTGAT | 4734 |
rs564015857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837178 | CTCACACTGGTAACC[C/T]CAGCACTTTGGGAGG | 4734 |
rs564032650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860927 | TTCAACATGCAAAGA[C/T]TCAATCATGGGTAGG | 4734 |
rs564037547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903887 | ACATTGGCTGGGCAC[A/G]GTGGCTCATGCCTGT | 4734 |
rs564084129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55936027 | ACCAACCTTCTTCTA[C/T]GCTTCTTATGATTAA | 4734 |
rs564085223 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916750 | TGTGAACATGGCTAT[C/T]CAAGTCATCTCCGGA | 4734 |
rs564092114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911299 | GATAGCCCCCACTAC[A/G]AAAGTGTCCAGCCCA | 4734 |
rs564129162 | snp | A/T | 9.31316e-05 | 0.00682328 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872507 | GGGTTTTCAAAATAT[A/T]TCTATAACACCAAAA | 4734 |
rs564140159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962712 | GCCTCCCAAAGTGTC[A/G]GGATTACAAGGGTGA | 4734 |
rs564147044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923949 | GTTTCTATACTTACC[G/T]GTTCAAATCTTACAG | 4734 |
rs564157260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966266 | TGTATCTTGTGACTA[C/T]TGCTATCATTTGTAC | 4734 |
rs564157773 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828595 | CAGGACTCAGCTTCT[C/G]TGAAGCTGACAACTC | 4734 |
rs564162149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909692 | CTTGTTTCCCTGTCA[C/T]CTGTGATGTAAAGGG | 4734 |
rs564166375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947745 | GGCCTTTGACAAAAT[C/T]CAACAGCCCTTCATG | 4734 |
rs564166628 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873730 | GTTTTCACAATGCCA[A/G]CAAACATCAGAAATT | 4734 |
rs564194025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881012 | CGGTTGGAGTCTAAG[G/T]CCTAACAAATTAGCT | 4734 |
rs564194078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872027 | CTGAAATACTAAGTA[G/T]GCAAAATATAGTTAG | 4734 |
rs564201516 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831702 | CTTGGCAAGCTGACC[A/C]GATTTGCCATGGAGA | 4734 |
rs564205033 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917471 | GACTGTTAATTTTTT[C/T]TTTTTAATGTGTGAA | 4734 |
rs564217136 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829593 | AGGACAAAATTCACT[A/G]TTTAAGTCATACAGG | 4734 |
rs564226445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960101 | ACAACCAGATTCAAC[C/G]TACTTGACTTGCTCC | 4734 |
rs564257004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838318 | AGAAAACTTAAAATA[C/T]TAGTTTTACTAAAAT | 4734 |
rs564286640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831172 | TGATCTGCCTGCCTC[A/G]GTCTCCCAAAATGTT | 4734 |
rs564297197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973301 | TCCAACACTTTGGGA[C/T]GCCAAGATGGGAGGA | 4734 |
rs564306715 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899232 | GCACAAGACTACATT[A/T]TGTAGTGGCAGAATA | 4734 |
rs564310676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865066 | AGCCGGGCATGGTGG[C/T]GGGCGCCTGTAATCC | 4734 |
rs564376704 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856559 | CAATATCCTAAGAGG[C/T]TTCCCCGTTGCAAGT | 4734 |
rs564385465 | in-del | -/TTTTTTTTT | 0.497641 | 0.0342639 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934861 | TATACAATGTTCTGC[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 4734 |
rs564386261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877389 | ATGCATTTTTTGCAA[A/G]AATACCATAAAGGTG | 4734 |
rs564386484 | snp | G/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994838 | AGGCGGTGAATCACC[G/T]TAGGTCAGGAGTTCG | 4734 |
rs564387263 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55936005 | ACTTCTTTCACCTGC[A/T]GCAATGACCAACCTT | 4734 |
rs564391707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923314 | GTAACTAACCATATC[C/T]GATAATCAAATCAGC | 4734 |
rs564395203 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962405 | GATTTAGTCTACAGG[C/T]TTATTGTTTGTTTTC | 4734 |
rs564412192 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944857 | CCTCCACTGGTGATA[C/T]CCAAGCAAACAGGGT | 4734 |
rs564441764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850059 | CCCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 4734 |
rs564455085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955205 | TGTTGTGTTTTTTTG[C/T]AGAAACAGGGTTTCA | 4734 |
rs564485988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961594 | TCCTGCCTCAGCCTC[C/T]CGAGCAGCTGGGACT | 4734 |
rs564495065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925857 | TACAACACATATTCA[A/G]TGAAGTATAAAGTAT | 4734 |
rs564500701 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853820 | ATGGTGAAAACTTGT[C/T]TCTACTAAAAGTACA | 4734 |
rs564523900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836674 | GGGACTGCACGTGCA[C/T]GCCACCACGTCCGGC | 4734 |
rs564549393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932416 | AAAAACAAGAAACGG[A/G]GAAAGGATTCCCTAT | 4734 |
rs564608602 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954509 | TGAACAATACACAGA[C/T]ACTGTGTTCAAGAGT | 4734 |
rs564620249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930987 | AGGCCAAACACAATG[A/G]ATTTTAAAAACTGTA | 4734 |
rs564643162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899272 | CTATAAAAAGTTTTA[C/T]TTTTTGAAATGAATA | 4734 |
rs564659744 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943160 | ATTCACAGAAATGAT[C/G]TGAAACTGGAACTTA | 4734 |
rs564679093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930358 | TTTCTCTCATGTATC[C/T]AGAATGGTACTGGTT | 4734 |
rs564684198 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842346 | ATGGTATGAGACAGT[C/T]TCTGCATTTTCTTTA | 4734 |
rs564720052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907535 | GGAAGAATATTTGCC[A/C]CTTATGGCAGGCACA | 4734 |
rs564737802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939371 | TGTGGAGAAGGTGCC[C/T]GCTTCCTGTTCATCT | 4734 |
rs564742868 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897042 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAAGCT | 4734 |
rs564765681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905225 | ACCTGGAATTCACTC[A/C]GTTGCAGAACTTATA | 4734 |
rs564771522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943657 | TCCACACAGAAGTCT[G/T]GATATTGCAGGGGCA | 4734 |
rs564827354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975055 | GCGATACCACACCCG[G/T]GTAATTTTTGTATTT | 4734 |
rs564828953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968973 | CATAAGAACCAAAAA[C/T]CAGGTGACTGATCAC | 4734 |
rs564831882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992942 | TGTTGCTAAAGAGGA[A/G]GAGGAAAATTTATGT | 4734 |
rs564846332 | snp | A/G | 0.00359349 | 0.0422354 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873928 | TAAAAAAATAAGCCC[A/G]AAAGGAAAATCATGG | 4734 |
rs564874433 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881968 | CAAAAACATTTTCTG[G/T]CTTTGTCAAATATCC | 4734 |
rs564919580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974458 | AACCAGACAAAGATC[C/T]ATTGAAAAAAGAAAA | 4734 |
rs564922865 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944188 | CAGGATGGGGCATTG[C/T]CTCACCTCGGAAGTG | 4734 |
rs564928489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945782 | GAGGTTACCCACTAA[C/G]AGAAACCCATTAGAC | 4734 |
rs564929298 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932960 | GAGTTTGCATAAATG[C/T]AAATCAAAACGACAA | 4734 |
rs564932688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859448 | CCTGTAATCCCAGCA[C/G]TTTGGGAGTCTGAGG | 4734 |
rs564937633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889968 | TCGGCCTCCCAAAGC[A/G]CTAGGATTACAGGCA | 4734 |
rs564945036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985471 | ATAGCAATATTCCCA[C/T]TGGCATCCAAGGATG | 4734 |
rs564950045 | in-del | -/TATTTTAT | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914168 | TAAACTAGCAATTAC[-/TATTTTAT]TCACCTAAAGTTACT | 4734 |
rs564955500 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906189 | ACTGTTGGTGGGACT[C/G]TAAACTAGTTCAACC | 4734 |
rs564961307 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912062 | TTCCTCAGTTCTAAG[A/T]AATATACATGTACAA | 4734 |
rs564965203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939048 | AAGGTTGAGGCTGCA[A/G]TAAGCCATGATTGTG | 4734 |
rs564976494 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985846 | AATGAGCACACCAAG[C/T]ACCCAAATTGTAGCA | 4734 |
rs564993282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945339 | CTGATGGAGCTGAAA[A/G]CCATGGCACAAGAAC | 4734 |
rs565031723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854162 | CCCCTCCCCTCCGAA[A/T]AAAAAAAGTCCTAAA | 4734 |
rs565060595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986138 | TCTATGCTGATATAA[A/T]TAAATGACAGGAAAA | 4734 |
rs565104390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988744 | CTTGTTTTAGAAAAA[C/T]ACACACTAGAGTATT | 4734 |
rs565114757 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55850050 | GTGATCTCCCCCCTC[A/G]GCCTCCCAAAGTGCT | 4734 |
rs565123522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853726 | GGGCATGATGGCTCA[A/C]CCCTGTAATCCCAGC | 4734 |
rs565130754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949559 | ACCAACCCAAATGTC[C/T]ATCAATAATAGACTG | 4734 |
rs565150175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858728 | CAGGCGGATTTACTG[A/G]CAGATATTCATATTC | 4734 |
rs565175805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911649 | ATTCTCCTGCCTCAG[C/T]CTCCCGTGTAGCTGG | 4734 |
rs565198460 | snp | G/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860744 | GTTGTGCTTGCAGTT[G/T]AATGTTGCCATTCTC | 4734 |
rs565210661 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865703 | GCAGTGGACGGCTTC[C/T]AAGATGGAAGAGAAT | 4734 |
rs565224502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914377 | AATTTAAAAAATCTA[A/T]TTCAGTTCAAACCAT | 4734 |
rs565225577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927122 | AGAAAAAGAAAAACA[G/T]TGTAAGATGATTTTT | 4734 |
rs565253352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957439 | TTTTTTCATAGATAC[C/T]CCTGATGAGGTTTAG | 4734 |
rs565286462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926626 | CAAAAATTAGCTGGG[A/C]ATCATGGCACATGCC | 4734 |
rs565288790 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974001 | GAAATGTTGGTGTTT[G/T]GAAAAGATAAACAAA | 4734 |
rs565296413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921472 | CGGGACTACAGGTGC[A/G]CACCATCAGGCCTGG | 4734 |
rs565296854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901374 | GATATTCAATGTGGG[G/T]CTTGTGGCCCACATA | 4734 |
rs565307818 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907052 | GTGAGCCAAGATCAC[A/G]GCACTGCACTCCAGC | 4734 |
rs565367140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906620 | GGGAACATCACACAC[C/T]GGGGCCTGTTGTGGG | 4734 |
rs565373209 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995012 | GTGAGCCAAGATTGC[A/G]CCGTTGCACTCCAGC | 4734 |
rs565377580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852241 | GCAGAGGTGCAGTGA[C/G]CCACGATCACGCCAT | 4734 |
rs565410750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948534 | AAGCTGGAGGCATCA[C/T]GCTACCTGACTTCAA | 4734 |
rs565412258 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994448 | AATAACTCCTCCTGT[A/G]GAATAAGGTTATGGA | 4734 |
rs565417967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964114 | TATTATCCTGCTTGG[C/T]GTTTTTAAATACTAT | 4734 |
rs565424033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906804 | TAAATAAATAAAAAA[A/T]AAAATTTTAGGCTGG | 4734 |
rs565426602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920589 | CTTTATTGAAAGCAA[A/G]TATCACTTACATTAC | 4734 |
rs565441561 | snp | A/T | 0.266 | 0.249487 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852709 | TATATATATATATAT[A/T]TATATATATATATAT | 4734 |
rs565452650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882569 | AGCACTCTGGGGTTC[C/T]AAATAAACTTGAAAG | 4734 |
rs565468130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867007 | AAGAAAGCATTCAGA[G/T]GTACAACCAACATTT | 4734 |
rs565498620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920963 | TCTCAAGAAAAGCTG[G/T]ATTTCCCACTCATAG | 4734 |
rs565527019 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55861633 | TTGCATGCCTGTATC[-/A]AAACCTCTCATGTAC | 4734 |
rs565528482 | snp | A/G | 8.78156e-05 | 0.00662571 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874042 | AAAATATAATTAGTA[A/G]TACGCTCAATTCCTT | 4734 |
rs565550082 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967031 | AGCTGAGATTACAGG[C/G/T]ATGCGCCACCATGCC | 4734 |
rs565563004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907439 | ATATAAACATTATTA[C/T]ATATTATACTATATT | 4734 |
rs565584740 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965841 | TTTTTAGTAGAGACA[A/G]GGTTTCACCATGTTG | 4734 |
rs565591044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873365 | CATTTTCTTTGTTTC[C/T]TATCAAAACTCTGTT | 4734 |
rs565629338 | snp | C/T | | | intron-variant, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55991993 | TGAGAAATCTGCAAT[C/T]AGCAGGGCCTACCTG | 4734 |
rs565636048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982198 | ATGGTACAATCGTGT[C/T]GGGAGACTGTTAGGC | 4734 |
rs565641139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873696 | CAGAATATTTTCAAA[C/T]TAATCTTTTTTACAC | 4734 |
rs565642194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855350 | GAAATGGAATGCACA[C/T]AGACTCAGAAGCGGG | 4734 |
rs565650731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848085 | GACTGTCATCATTCT[C/T]GTTCAGACAGTGGGA | 4734 |
rs565654057 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984487 | TTCAGTTAAAGGCAG[C/T]TGCTATTTATTTAGG | 4734 |
rs565654942 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946128 | CAGTGAACATCATAA[A/T]TACAGGATCAAATTC | 4734 |
rs565669392 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835967 | TTCACACACAGGCCC[C/T]GTATAAGCTGGTCTG | 4734 |
rs565698645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835568 | CATTTTCCATTGTAT[C/T]GAGTTCACAGCTTCA | 4734 |
rs565702065 | in-del | -/AAG | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897467 | ATGCTGCAATATCAA[-/AAG]AAGATGGTATCAGAT | 4734 |
rs565739274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923422 | GGAGTCAGAGGCAGG[C/T]GGATCACGAGATCAG | 4734 |
rs565779244 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842293 | TACGTAATATACTCA[A/G]GGAAAACACAACTAG | 4734 |
rs565783428 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856766 | TACCCCCTGGACATT[C/T]CAGACTACTTGTTTC | 4734 |
rs565787783 | in-del | -/AC/AT | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979070 | TCTATTTTTAAAAAT[-/AC/AT]ATATATATATACCCC | 4734 |
rs565794655 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989812 | TAGGCTGGACTTCTA[C/G]AGCAGGGGTCCCCAA | 4734 |
rs565801089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922520 | GGTGCCCACCATCAC[A/G]CCTAACTAATTTTTG | 4734 |
rs565816815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914120 | GGCATTGGTAACAAT[C/T]ATTATATTTACCAGA | 4734 |
rs565892112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836216 | GCACTTTATGCTTGC[C/G]TCTGTTCATTTCACT | 4734 |
rs565898878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959068 | TACTTATTTTAGAAT[G/T]CATTCGCTCTTCTTT | 4734 |
rs565961021 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991656 | ATGGAACTGACAGCC[A/G]GAACTCCCAGAATGT | 4734 |
rs565962963 | in-del | -/ATAAATAAATAAATAAATAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892304 | TAAATAAATAAATAA[-/ATAAATAAATAAATAAATAA]TAAATATGAATTATA | 4734 |
rs565964542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833962 | TGTAATCCACCAGTA[C/T]AGTTAATCAAGAGTT | 4734 |
rs565968602 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866682 | CTCTCTTAAATGTCT[C/G]CTTAATGTATTTATA | 4734 |
rs566008363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927036 | AACCAAGATCGTGCC[A/G]CCGCACTGTCCAGCC | 4734 |
rs566025688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833315 | TTTTAGAATGGGATT[A/G]TAACCTAGTGAAGTA | 4734 |
rs566102093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986886 | AGGCGTGAGCCACCG[C/T]GCCCGGCCAAGGCCT | 4734 |
rs566121962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869288 | TAACTTCAAAATACT[A/G]AATTGTGTTCTTACT | 4734 |
rs566126138 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956806 | TTGACTTTCCATACA[A/C]ATATTGAAATCAGCT | 4734 |
rs566131020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934917 | TCTATTGCCCAGGCT[A/G]GAGTGCAGTGGCACA | 4734 |
rs566153531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976488 | TGCTCAAATCACTGA[G/T]CATCAGGGAAGTGCA | 4734 |
rs566160100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857253 | TCAGTATCATTTATT[C/T]TTTAGGTCTTTGACC | 4734 |
rs566164934 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55971633 | CTGTCTCAAAAAAAA[A/C]AAAAAGACTTATTAG | 4734 |
rs566165089 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955265 | CAGGCTCAAGTGATC[C/T]ACCTGCCTCAGCCTC | 4734 |
rs566168595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885618 | AATCAGTGTTAAGTT[G/T]TCATCAGTTTAAAAC | 4734 |
rs566169434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972469 | CAGTTTAAAATAATG[C/T]ATTGTAAGATGTTAA | 4734 |
rs566201509 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971171 | TTAAAGAATGCATCA[C/G]AATCTCTCAATGGCA | 4734 |
rs566211250 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826613 | ATAGAAATGATGTTG[C/T]AAATAGTGGTTGGCT | 4734 |
rs566243165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942894 | TGGTTGTGACCAAAA[C/T]GCTGATAGTGATATG | 4734 |
rs566306827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947893 | TTGAAAACTGGCACA[A/C]GACAGGGATGCCCTC | 4734 |
rs566318207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934083 | GCTTGAACCCAGGAG[A/G]TGGAGGTTGCAGTGA | 4734 |
rs566337370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929778 | AGAAAAACTGTCCTC[A/G]AAGGAAAAAGAGATA | 4734 |
rs566359322 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985195 | CTCCTATGTGATATA[C/T]GAATTCCTAATTACC | 4734 |
rs566360951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893052 | AAAGATTACAGTAAA[C/G]TAACCTGAGATAGAA | 4734 |
rs566379576 | snp | C/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995019 | AAGATTGCGCCGTTG[C/G]ACTCCAGCCTGGGCG | 4734 |
rs566380603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886532 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 4734 |
rs566389328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946604 | ACAGATCAATGAGAC[A/G]GAAAGTTAACAAGGA | 4734 |
rs566394709 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924489 | AGTAGGACCAGGAGG[-/A]AGAAAACAAATTCTA | 4734 |
rs566400927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936447 | ACACATAGGAAATCC[C/G]AGAAAAGCATATTAT | 4734 |
rs566483106 | snp | A/G/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55830569 | GTTCAACTGTAAATG[A/G/T]CTGTGGTCCATTTGA | 4734 |
rs566501416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55978405 | CATTTTATGATTTTA[C/T]TCTAGAGAATTGTCA | 4734 |
rs566508356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896422 | CTCCTGGCCTCAAGG[G/T]ATGCACCTGCCTTGG | 4734 |
rs566512157 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983487 | TTGCACATGTGGTTC[C/T]ATTTACTCAATGGGG | 4734 |
rs566512478 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948879 | CAGGCAGTACCATTC[A/T]GGACATAGGCATGGG | 4734 |
rs566572656 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910478 | CCTCTGTGTGGTTCC[C/T]CCTTAGTCTCTTCTT | 4734 |
rs566613699 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979515 | CCCGCCACCGCGCCC[A/G]GCTAATTTTTTGTAT | 4734 |
rs566634027 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903641 | CATCCTAGCTAAACA[C/T]GGTGAAACCTCAGCT | 4734 |
rs566642149 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865099 | GCTACTCGAGAGGCT[G/T]GGGCAGGAGAATTGC | 4734 |
rs566651902 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856626 | GCAGGCTCAGAGCAT[A/C]CTGCAATGCACAGCC | 4734 |
rs566655362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953186 | GTACAGACAGGGCTT[C/T]ACCATGTTGGCCAGG | 4734 |
rs566676679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990867 | AATCTGGTATAAATT[A/T]TACTACACTTCCTCC | 4734 |
rs566679563 | snp | A/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995715 | AACTAGAGTAATTAT[A/T]GTATCCCGGTCAACA | 4734 |
rs566693662 | snp | A/G | 0.000197958 | 0.00994684 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916291 | TGACACTGTTAGTAT[A/G]TGAACCTCCACTTGT | 4734 |
rs566716384 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979609 | CCACCCGCCTCGGCC[A/T]CCCAAAGTGCTGGGA | 4734 |
rs566749392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967650 | AACATGTATATTTTT[A/T]AAAAAATTCACAAGT | 4734 |
rs566755954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843467 | TGTGACAAATGTACA[A/C]AACTATGCTTTAGGC | 4734 |
rs566765070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990150 | AATTCTACATTACGG[C/T]GAGCTGTATAATTAC | 4734 |
rs566765846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851773 | TGAGCCACCTTGCCC[A/G]GCCCAGCATAAACTT | 4734 |
rs566774337 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939594 | GGCCCACTCTTTATG[-/T]TAAAAAGGTGCTCAA | 4734 |
rs566792791 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886565 | AGGTCAGAGATCGAG[A/T]CCATCCTGCCAACAT | 4734 |
rs566809525 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960943 | ATGCTGCCCTCTTCT[C/G]TCTGGCATCTGTAAG | 4734 |
rs566819342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836906 | TCAAGCAATCCTCCC[A/G]CCTCAGCCTCCTCAA | 4734 |
rs566848851 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943904 | ATTGTACCTTGCAGA[C/G]ACACAGGGGTGGAGA | 4734 |
rs566859069 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939189 | CCCAAATCTCATCTC[A/G]ATCCGTAATCCCCAC | 4734 |
rs566862849 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870327 | AAGGCCTGATCAGTG[A/T]CTGAAACCTGCTACA | 4734 |
rs566872503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857494 | CCACTGCACTCGGCT[A/G]ATTTTTGTATTAGAG | 4734 |
rs566882248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904708 | AAAGTTGAGAAATAC[A/G]TTAAGGAAACCACAT | 4734 |
rs566884291 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896985 | GATTATTGACATGGC[-/T]TTTTTTGAGATGGAG | 4734 |
rs566912794 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858249 | TTAAGTAAAAAAAAT[A/G]CCAGGAAGAAGGGGA | 4734 |
rs566940874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911402 | TACCTATCAAGACTC[A/G]GTTCAAATGTCACCT | 4734 |
rs566972666 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958159 | ATTCTATTAATACAG[C/T]GTATTACATCAGTTA | 4734 |
rs566990162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919991 | AATCAGTAGACTCTG[A/C]GTAGAGCACATTACC | 4734 |
rs567002708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960393 | ACTTGCTGAGTCTTC[C/T]GGCCTTCATCTTTCT | 4734 |
rs567017382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961065 | TCTCCTAGAGAGTGG[C/T]TATCTGCTATTTTGG | 4734 |
rs567025638 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850301 | AAGCATTTATGGCTA[A/G]TGAGCTAAAAACTGG | 4734 |
rs567053466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926101 | ACATACTGTACATGT[A/G]TATGATACATACGTA | 4734 |
rs567074940 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925320 | TTATAAATACAGATT[A/C]GATTTTGACACCTTA | 4734 |
rs567129206 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937685 | TCAAGACAAAAATAA[A/C]TGGAAAGACATCCTG | 4734 |
rs567136091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924789 | ATGCTGCCATTTGGT[C/G]GGGCATGGTGGCTCA | 4734 |
rs567162960 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931608 | AGGAAAAAAGTTGCC[-/A]AAAAAATATCCAGTT | 4734 |
rs567176356 | in-del | -/AGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975421 | AATACACAAAAAATC[-/AGT]AGCATTTATTTTAAT | 4734 |
rs567184249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930471 | GAAGAACAGAAAATC[A/C]CTCTAGGTGACCTTC | 4734 |
rs567201577 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929254 | CGCACGCACACACAC[C/T]CTCTTATTAGAGATT | 4734 |
rs567214215 | snp | C/T | 6.59196e-05 | 0.00574068 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834094 | CATTTTTATACTTTG[C/T]ATGTTCCCTCCAGTC | 4734 |
rs567215725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926649 | CACATGCCTATAGTC[C/G]CAGCTACTCAGGAGG | 4734 |
rs567223600 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909601 | CTGACCTCAACACAT[C/T]GCCTGGCCTCACCCA | 4734 |
rs567241422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956758 | CTTCCAATTTTGTTC[C/T]TTTTTGAAATTGTTT | 4734 |
rs567253287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866578 | ATTTATTAATAAAAT[A/G]GTTCTCACTACTGCT | 4734 |
rs567256232 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853737 | CTCACCCCTGTAATC[C/T]CAGCACTTTTGGGGG | 4734 |
rs567296886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853334 | CAATAACAAGCACGT[C/G]TCCTGTTTAACACAG | 4734 |
rs567304687 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855046 | ACAGTGAGTGAGAGT[A/T]AGGCTAGCGATGATA | 4734 |
rs567318831 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962743 | GCCACCGCACCCAGC[C/T]TCTTTTACTTTTTTT | 4734 |
rs567375959 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940361 | TAAACCTATCAAACT[G/T]TATGAATTAAATATG | 4734 |
rs567379571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962223 | TTACTGTTTGCATGG[C/T]ATATCTTTTTGCGTC | 4734 |
rs567413305 | in-del | -/T | 0.150333 | 0.229274 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954530 | TTCAAGAGTTTTGCC[-/T]TTTTTTTTTTTGAGA | 4734 |
rs567424284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881465 | CTTTATTCCTGTTTT[C/T]ATCACAAGTAGATGT | 4734 |
rs567444759 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931965 | CTGTCTCCATAGATT[A/T]GCCTATTCTGGACAT | 4734 |
rs567455538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939813 | CAGTATAAAGGTTCC[A/C]CAAAAAATTAAAAAG | 4734 |
rs567464910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938087 | AAATGGTGGCCAGGC[A/G]CAGTGGCTCACACCT | 4734 |
rs567493128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974091 | AAAAAGGAGACATTA[C/G]AACTGACACCACAGA | 4734 |
rs567516809 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945396 | AGCTGATTCAATCAA[A/G]TGGAAGAAAGGCTAT | 4734 |
rs567518485 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55848301 | CTGTAGGGTTATGCC[C/T]GTGACTATCTGCTCT | 4734 |
rs567526460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980140 | CTTTGCCACGTTGGC[A/C]AGGCTGATCTTGAAC | 4734 |
rs567578940 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947272 | CTACCAAGACTAATA[-/AAG]AAGAAAAGAGAGAAG | 4734 |
rs567581233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944319 | GGTCTTATCAACTGG[C/T]AGACCAGGAGATTCT | 4734 |
rs567592181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975678 | TCATGGATTGGAACA[A/G]TCAATATTGTTAAAA | 4734 |
rs567613636 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827708 | AAGATCCATATACAG[A/G]TATACACATGTGTAT | 4734 |
rs567633203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884050 | ATGTCTGGCTAATGT[A/T]TGTATTTTTAGCAGA | 4734 |
rs567634952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844651 | ATAATGATAGCTACC[C/T]ACATGGAGTTGTTTC | 4734 |
rs567659049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927374 | GGAATGCAGTGGTGC[A/G]ATCACAGCTCAGTGC | 4734 |
rs567667064 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829385 | TCTACAAAATAATAA[A/G]TAGCTGCGAGTAGCA | 4734 |
rs567676562 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55894107 | GCATAAAGCAAGCAT[C/T]CCATGTCTTAAGTTT | 4734 |
rs567685146 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982242 | GTTAAACACATATAA[C/T]CCTATGACCCAGAAA | 4734 |
rs567688322 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883090 | CAAGCCTCTTGGGGT[C/T]CTTGATGCCAAGGCT | 4734 |
rs567692493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969865 | CAGGGAGACTCCTGC[C/T]TAAGGAAAGGAGAGG | 4734 |
rs567695713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845467 | TAACATATGTAAACT[C/T]CTAAGAAGAACGCCT | 4734 |
rs567721696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982606 | ATTGACTGGAAGAGG[A/G]CCCAAGGGAGCATTC | 4734 |
rs567738349 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982061 | AGATGGAGCTGATAA[A/C]CTAGGTTACTAGAGA | 4734 |
rs567756659 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891195 | CCAATGATCTGAAAT[G/T]AGTTTCTTCACTTCT | 4734 |
rs567783842 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906638 | GGCCTGTTGTGGGGT[A/C/G]GGGGGCTGGGGGAGG | 4734 |
rs567805243 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989052 | ACCAGCCTGGCCAAC[A/G]TGGTAAAACCCCATC | 4734 |
rs567822844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950759 | AAAGGGGAATATGGG[A/G]TCAAGGAAGAACATT | 4734 |
rs567827354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981555 | ATTAGAAGTGTCCTT[A/G]TAAAGCTGGAGTCTA | 4734 |
rs567838843 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961628 | GGAGCCCACCACCAC[A/C]CCCGGATAATTTTTT | 4734 |
rs567853122 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994540 | CCTCCACCAAATAAG[C/G]CATCCATAAAAGAGT | 4734 |
rs567860055 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986890 | GTGAGCCACCGCGCC[C/T]GGCCAAGGCCTGTCC | 4734 |
rs567898708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861039 | GTCACTATGTCTAGG[A/G]TAATGTCCAACACAT | 4734 |
rs567900627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958315 | CTTTACTGTATTAAT[A/G]CAGTGAATTGCATTA | 4734 |
rs567900675 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911533 | ATTAGACTGAAAAAA[A/T]ATTTTTTTTTTTTTG | 4734 |
rs567913621 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839753 | GACGCTGAGGCAGGC[A/G]GATAACGAGGTCAAA | 4734 |
rs567915810 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923519 | AGGTGTGGTGGTGAG[-/C]GCCTGTGGTCCCAGC | 4734 |
rs567923597 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902789 | AATAAAAGTAATCAG[-/A]AAAAAAACAAAGTAA | 4734 |
rs567932839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842342 | CTCTATGGTATGAGA[C/T]AGTTTCTGCATTTTC | 4734 |
rs567948568 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926258 | CCTTGTACCTACGGG[C/T]AACCAATGAAGCCAA | 4734 |
rs567950032 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864162 | AAAGAAAAGGCAGTA[G/T]GTCAAAGATTCTATT | 4734 |
rs567960528 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943298 | GCTGAATGTTCATAG[C/T]CAAGACAATGGGGAA | 4734 |
rs567961971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957837 | GGGACATGGGTGAAG[C/G]TGGAAACCATCATTC | 4734 |
rs567970958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950350 | CAACAGCTTCCTTGC[C/T]CTTAATGTCAGCAAT | 4734 |
rs567975040 | snp | C/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993945 | GGAGCCAGGGAGCGC[C/G]GGGAAGCGCCGGGAA | 4734 |
rs567979659 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859822 | AAATCAAGACCACTC[A/T]GTAATCGTGGCTGAA | 4734 |
rs567984351 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902382 | AATTAATGTTGCTTT[C/T]ACCATTAATTTTGTC | 4734 |
rs568008870 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920977 | GTATTTCCCACTCAT[A/T]GAAGAGCATCTAACA | 4734 |
rs568013972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976554 | TTAAAATGGCTCTTA[A/T]CCAAAAGATGGGCAA | 4734 |
rs568017598 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849264 | AGTGTCGCTCTTGTC[A/G]CCCAGGCTGGAGTAC | 4734 |
rs568026822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946739 | ACACTTATTCCAAAA[C/T]TGACCACATAGTTGG | 4734 |
rs568026891 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955684 | ATGTATATACATTTC[-/T]TTTTTTTTTCTTTTC | 4734 |
rs568029674 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964181 | TATTTCTTCAAAAAA[C/T]ATTGTGCCTTCTTCT | 4734 |
rs568044439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907988 | TGGCATTCACCCCAG[G/T]GACAAGGTATTCATT | 4734 |
rs568062162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941521 | CGTGTGTTACTGAAT[A/T]GTAACTTAAATCTGC | 4734 |
rs568071718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834541 | CTCATTCTGTAATCC[C/T]AGCACTTTGGGAGGC | 4734 |
rs568076168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842801 | ACTGCCTGCTAGCTG[C/T]TGTGCCTGTCTGTTC | 4734 |
rs568093033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835726 | CTCAACTCCCTCACC[A/G]TTCCCTTAATTCCTC | 4734 |
rs568125282 | in-del | -/AGC | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854586 | ACTGTAGCAATAGAG[-/AGC]AGATGAGCGGTTGCT | 4734 |
rs568175830 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974347 | AAATATTTAAAGAAG[A/G]ATTAATACCAATCCT | 4734 |
rs568188975 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889440 | TGGATAAAACTGAAG[G/T]TCATTATGTTAAGTG | 4734 |
rs568192251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907540 | AATATTTGCCACTTA[C/T]GGCAGGCACATATTC | 4734 |
rs568199003 | snp | C/T | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916407 | CAAATGGCTGGACTG[C/T]TTACAAGGTGACCAT | 4734 |
rs568209514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868256 | GCTTCACTGTTCTTA[A/T]GGAGACCTAAGCAGG | 4734 |
rs568260485 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995289 | TGGGATTTGTGGGTT[A/T]AGAATAAAATAATCT | 4734 |
rs568271338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875165 | AGATGACGCAGATCA[C/T]GGAATAAGCAGACAA | 4734 |
rs568329291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921970 | CATGCAAATAACGCA[A/G]ATAAAATAGTTCACC | 4734 |
rs568346391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953800 | ATCTCGGCTCACTGC[A/G]ACCTCCTCCTCCTGG | 4734 |
rs568352828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885795 | AAGGAAGAAAAAACT[A/G]TAAAACAACCAGAAA | 4734 |
rs568353787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888657 | CCAGAGGCATCCTAA[A/G]CAAAAAGAACAAAAC | 4734 |
rs568412065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885180 | AAAAAAAGTTTTACC[C/T]TACAATAGTATATCT | 4734 |
rs568450280 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863402 | CATCTCAAAACAACA[A/G]TAAAACAGAACTTTA | 4734 |
rs568469263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831252 | ATTGGCTATCTAATA[C/T]TGTAATTTTAACATT | 4734 |
rs568490531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870694 | ACACACTGCCATGCC[C/T]GGTTAATTTTTGTAT | 4734 |
rs568509360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959301 | AATTCCAAATATCTG[C/T]AGTTTTTCTAGATCT | 4734 |
rs568513547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959730 | CTGAATGGCAAGAAG[A/C]TGAGACGGCCTCCAG | 4734 |
rs568516206 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972353 | ATAATAAGACAAAAA[C/T]AGAAACAATAAAAAG | 4734 |
rs568523409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924128 | TTGCTTTTTGCTTCT[C/G]TAAGAGCTGGCCATC | 4734 |
rs568553665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878798 | TAACATATATAAATC[C/T]CAAAGAAAAGTGGTT | 4734 |
rs568568954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929093 | GACAGATGAAGCAGG[G/T]ATGGAAGTGATGATG | 4734 |
rs568586479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929660 | AATTGTAACATATAA[C/T]TGTTAAATGTTTATG | 4734 |
rs568594784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972189 | TCATCTGAAGGTACA[A/G]AATTCACATGTAAAA | 4734 |
rs568623887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55955510 | GCAACCAGCATTCCA[A/C]TCTTTGATTCTATGA | 4734 |
rs568641640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976870 | GATCTCCTGACCTCC[C/T]GATCCACCCGCCTTG | 4734 |
rs568642813 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937076 | GGGAAAACAGGCATG[A/T]GCCACCGTGCCTGGC | 4734 |
rs568664056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848722 | TAATAACATTAATTA[C/T]AGATGATAAAGAAAT | 4734 |
rs568692072 | in-del | -/A/AA/AAAA | 0.495671 | 0.0463237 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995519 | CTAAAACTGGTAATT[-/A/AA/AAAA]AAAAAAAAAAAAATC | 4734 |
rs568693203 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836522 | TATGCACATGCCATG[A/G]CACCAGGCTAATTTT | 4734 |
rs568710910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943256 | AAAGCCCCATTTTGT[A/G]GGGAGGAATTCAAGC | 4734 |
rs568730350 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55860164 | GTTCAATGACAAATG[C/T]GTCCCTAGTGATTTT | 4734 |
rs568730379 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834708 | GAGGTATTCCAGCCT[C/T]GGCAAAAAGTGAGAT | 4734 |
rs568751441 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852344 | GTATCCAGTGTATCC[G/T]ACAAAGTGATGTAAT | 4734 |
rs568767990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942939 | GGCTGAGGTGGTCTC[A/G]AAGACAAGGAATCTT | 4734 |
rs568791336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967764 | GCCGGCACACACCTA[G/T]TATCACAGCACTTTG | 4734 |
rs568803110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934996 | GCCTCAGCCTCCCAA[C/G]TAGCTGTAATTAGAG | 4734 |
rs568804060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967073 | TCTATTTTTAGTAGA[A/G]ACAGGGTTTCACCAT | 4734 |
rs568841865 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979991 | TCTCGGCTCACTGCA[A/G]CCTCTGCCTCCTAGG | 4734 |
rs568843683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880627 | ATGAGGGAGTGTGCC[A/G]TGATATGGAAGATGC | 4734 |
rs568878859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889409 | AAAGGAATGAGATCC[A/G]CTCATTTGCAACAAC | 4734 |
rs568904169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888449 | CAAACACTGATGAAA[A/G]AAATCAAAGAGGACA | 4734 |
rs568944155 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881231 | ACTGCAACCTCTACC[C/T]CCCGGGTTCCGGCAA | 4734 |
rs568951132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979514 | GCCCGCCACCGCGCC[C/T]GGCTAATTTTTTGTA | 4734 |
rs568969466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887751 | AAATACTAGCAAACC[A/G]AATTCAACAACCTAT | 4734 |
rs568986926 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966194 | GTTTATGGTTGTTAT[C/G]TGCTAAAGGATTAGT | 4734 |
rs569048687 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964938 | TGTCAAAAAGAGGCT[A/G]GCACACCTCCCCCTT | 4734 |
rs569054002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904052 | CAGTAATCCCAGCTA[C/T]TTCGGAGGCTGGGGC | 4734 |
rs569077072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948042 | TGACATGATTGTATA[C/T]TTAGAAAACCCCACC | 4734 |
rs569092220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956031 | TATCACCAGGCTGGT[C/T]TCGAACTCCAGGGCT | 4734 |
rs569095808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858273 | AAGGGGAATGGGATC[A/G]TATGTGATTTATCAT | 4734 |
rs569104863 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842269 | CCTGTGTCCAAGTCT[C/T]TTTTTCCTTACGTAA | 4734 |
rs569123571 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991508 | CAAACAGTAAATGAA[C/T]GTCTGTTGAATGAAT | 4734 |
rs569126431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974134 | CATTAGAGACTACTG[C/T]GAACAACTATATGCC | 4734 |
rs569138849 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837426 | CAAAGTGACTCACTC[A/C]GCGCTCAAAAAAAAA | 4734 |
rs569152536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944919 | TGTGCAGCTGAGGGA[A/G]CTGAGTGTTAGACGG | 4734 |
rs569153425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961818 | AATACAGCCCATGTG[C/T]GGTCTATGCTAGTGA | 4734 |
rs569155091 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921348 | TTTTTTCGCCGAGAC[A/G]GAGTCTCACTCTGTT | 4734 |
rs569156358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954588 | GGAATGCAATGGCGC[A/G]ATCTCGGCTCACCGC | 4734 |
rs569178048 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894582 | GATTGGGGTGAGGTG[A/G]AAGTCAGGAGAAACT | 4734 |
rs569187460 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943435 | GCCCTACACAACCTT[A/G]GGACACTGCTCTCTG | 4734 |
rs569196363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850363 | TAATCCAAAACAATA[C/T]TAAAAAGACGCATAA | 4734 |
rs569196813 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856669 | CTGGAGCTGAAGTCA[A/G]TGACAACACAGAAAA | 4734 |
rs569215193 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890787 | GTAAGATTTCAATTC[C/T]TCCCCTTTCTTACCA | 4734 |
rs569215361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961194 | GCATGAGGGCACTTG[C/G]CTAAGAATACCCATG | 4734 |
rs569225157 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933566 | GGGAGGGATAGCATT[A/T]GGAGATGTACCTAAT | 4734 |
rs569226302 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939791 | ATAGTATAGCCTCTA[C/T]AGAAAACAGTATAAA | 4734 |
rs569261817 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898497 | CAGCCTTGATGCTTA[A/C]AATAATTTCAACACT | 4734 |
rs569264212 | snp | A/G | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906667 | GGGATAGCATTAGGT[A/G]ATATACTTAATGTAA | 4734 |
rs569267537 | in-del | -/TTTG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871927 | TAAACATCAAGTAAC[-/TTTG]TTTGGGAAAATGGAA | 4734 |
rs569268975 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946368 | ATCCTAGTCTCTGAT[-/A]AAAACAGACTTTCAA | 4734 |
rs569274653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938686 | ACCGTACAAAATGGG[A/G]AAAATATTTGCAGAC | 4734 |
rs569274749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845577 | GTCTCCCATCTCCTG[C/G]TGCCTGGAAGACATT | 4734 |
rs569304767 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900147 | AGGATGCTTCTGGAC[A/G]AGAACTCATCGTAAG | 4734 |
rs569337442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850992 | TTTACAGTAATTTAT[A/G]ATTTTTCAACTAATT | 4734 |
rs569342629 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918064 | GCTGTTTGATATCTA[C/T]AAAGAAATACAAACC | 4734 |
rs569369496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993140 | GCTGCGACCGTCTCC[C/G]AACGCCTGGGAGCTC | 4734 |
rs569399410 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925969 | CATACAGTATGTATA[C/T]GTAAAAATACATATA | 4734 |
rs569400150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844090 | AAGAAGGCTTTGAGA[C/G]GAAGTCTTTAGACAG | 4734 |
rs569429145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911730 | AGACGGGGTTTCACC[G/T]TGTTAGCCAGGATGG | 4734 |
rs569483550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865173 | ACTGCATACCAGCCT[C/G]GGCGATAGAGCAAGA | 4734 |
rs569489947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911516 | TATTTAGCACATCAC[A/G]TATTAGACTGAAAAA | 4734 |
rs569541334 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834722 | TCGGCAAAAAGTGAG[A/G]TCCTGTCTCAAAACA | 4734 |
rs569543674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872170 | TCTGATAAGTATTAG[C/G]AGAACGAATCTTTCC | 4734 |
rs569554819 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918979 | ATCTAATTGTTCATG[C/T]CTGTGGCCTAAAACT | 4734 |
rs569555449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882207 | CACCTTCATAAGAAC[C/T]AAAAATCAGGTGAGC | 4734 |
rs569580481 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925434 | CCTTTTATTATTGAC[G/T]TAATAAAATTACATG | 4734 |
rs569584914 | snp | C/G/T | 1.6528e-05 | 0.00287467 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860800 | TGGAAGTATAAAAAG[C/G/T]CATCATCCATGTCTT | 4734 |
rs569606996 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826736 | CAGACTTATGCAATA[C/T]GACCTTTTTGTAAAG | 4734 |
rs569617115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881693 | TAAATAGCCTTGTCC[C/T]GAGTAAACAGAATAC | 4734 |
rs569619167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890305 | CAATCAATTTTAGAA[C/T]ATTTTCATCACCCAA | 4734 |
rs569619826 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887492 | AGATTGAAGCTGTAA[A/T]AAAATGTCTATCACC | 4734 |
rs569645072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853914 | AAGAACTGCTTGAAC[C/T]GGGAGGCAGAGGTTA | 4734 |
rs569652135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950832 | CCTAAAATGCATCTC[C/T]ACCACTGCTCTGGTA | 4734 |
rs569656194 | snp | A/G | 8.24436e-05 | 0.00641989 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860431 | TGCTGGCTGGCTCAC[A/G]GCTGAATTTCCAAAA | 4734 |
rs569657335 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963252 | TCCTCCAACCTCAGC[A/C]TCCTTTGTAGCTGGG | 4734 |
rs569664446 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836820 | GGAATGAGCCACCGC[A/G]CCCAAATTTTTAATT | 4734 |
rs569672028 | snp | A/G | 3.32629e-05 | 0.00407803 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55847030 | TCCCTGGAGTAGGGC[A/G]CTGCCTTTAGTTGGA | 4734 |
rs569707293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55969667 | TCCTGGGCCAGAGGG[A/G]AACCTGCCACCCTGA | 4734 |
rs569712935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957201 | GTAGTTTTTTCTGTA[C/G]ATTCCTTGGGGCTTT | 4734 |
rs569718814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859850 | GAATATAGACAAAAC[A/G]TGAACATTGTCCAAG | 4734 |
rs569740802 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885399 | GAACACAGAAAAGCA[C/T]AGAATATGATAATAC | 4734 |
rs569746938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866620 | TAAAAATAGTGCTAG[A/G]AAAATGGTAGCAAAA | 4734 |
rs569779763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920757 | GAATGACATTTATAA[C/T]GACACAGGTCATTTG | 4734 |
rs569810371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873646 | ATCTTAGTTTTCTTC[C/T]GTGAGCTTAGGCACT | 4734 |
rs569835642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962934 | TGGGATTACAGACAC[A/G]CGCCACCATACCCAG | 4734 |
rs569842802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926942 | TTAGCTGGGTGTGGC[A/G]GCAGGCACCTGTAAC | 4734 |
rs569859815 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955090 | CAGTGCTGCAATCTC[A/G]GCTCACTCGAAACCT | 4734 |
rs569860046 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841720 | GGGACTACAGGCGCC[C/T]GCCACCACGCCTGGG | 4734 |
rs569902847 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862495 | CGTTTAACGTAATAC[C/G]CTTATTATTGAGTCC | 4734 |
rs569916477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845918 | AGCCTCCGGAGTAGC[C/T]GGGATTAAAGGTGTG | 4734 |
rs569921886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835450 | TTTTTCCCATGCCCT[A/G]AACTGTCCATTTATA | 4734 |
rs569974613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939974 | TAATCTAAATACCCA[C/T]TGAAGGATACATTAA | 4734 |
rs569976143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840141 | TGTTTAATGTTATCT[A/G]TAACTTACTCTGAAA | 4734 |
rs569996125 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839740 | CCCAGCACTTTGGGA[C/G]GCTGAGGCAGGCGGA | 4734 |
rs569997333 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970693 | CAAGTTGGTGCCTCT[A/T]TGAGACTACAAGAGT | 4734 |
rs570003151 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939135 | CAACAAACAAAAAAA[A/C]CCACCACCAACAATA | 4734 |
rs570011177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868311 | AAGCAAGGCAACAAA[C/T]AAGAACCCTCCAGAG | 4734 |
rs570043506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922002 | ATAATACACTCAATG[A/G]TCAGGCAAAATTCAC | 4734 |
rs570076880 | snp | G/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953002 | TTTTTTTTTTTCTTT[G/T]TTTTTGAGACAGAGT | 4734 |
rs570083902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977544 | TTAACACAACACAAA[A/C]AACTCTGACTGGAGA | 4734 |
rs570118617 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969340 | CCAAGATCCTAAATA[A/C]ACTTAAAAGGCAGTC | 4734 |
rs570118836 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55892486 | TTTAAAGAGTAAAAA[A/T]AAATTTTATACCTGA | 4734 |
rs570123898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977085 | GGAGAAAATATGCAT[A/T]TCATAGATTATTTAT | 4734 |
rs570147812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940601 | TCACTATGTTGCCCA[C/T]GGTATCCTCGAATTC | 4734 |
rs570164261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884159 | TGCTGGGATTACAGG[C/T]ATGAGCCACCATGCC | 4734 |
rs570187768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881036 | ATTAGCTTAGTTTAA[C/T]GCCATATTCCTATTC | 4734 |
rs570212100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946101 | ACTCCATCAATTAAC[A/G]AGCAAAATAACCAGT | 4734 |
rs570252756 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988241 | AAAAAACCAAACACC[A/G]CATATTCTCACTCAT | 4734 |
rs570260059 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829443 | TAAAGTATTTCTTTT[C/T]CCAAATTTCAGTTTT | 4734 |
rs570262484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891294 | AAAAGTCAATATGCA[C/T]AGTCTCAGAAGAAGA | 4734 |
rs570312414 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836468 | ACTTCCCAGGCTCAA[A/G]TGATCCTCCAGCCTC | 4734 |
rs570314497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886011 | AAAGGGATGGAAAAA[G/T]GTACTTCATTAAAAC | 4734 |
rs570321590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900536 | GCTAATATTTATAAA[C/T]AACATGCCAGGGTCA | 4734 |
rs570348703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945506 | CCTCCAAGAAATATG[C/G]GACTATGTGAAAAGA | 4734 |
rs570356996 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952459 | TTGGACACTTTACTT[G/T]TCCATTGTTAAATTT | 4734 |
rs570357059 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958950 | TTAAAACTTTAATTG[A/T]TGTCTTCAAATAACA | 4734 |
rs570358048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981635 | TAACCATAATAAAGA[A/C]GAAATATCCAGAATC | 4734 |
rs570364715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986918 | TCCTTCTTAAAACTG[C/T]CTAGGATAAGAAAAA | 4734 |
rs570383900 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55951425 | AAACTCTAAAAAATA[A/T]TAAACATAGTATAAC | 4734 |
rs570391652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843421 | AATGGAGCTACATTG[C/T]CTCACTAATCTTTTG | 4734 |
rs570395438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55895699 | TCTTGGGTGATACTA[A/G]TGCATCTGGCCAGCA | 4734 |
rs570404890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55942191 | CTAGGTCCATACACA[C/T]TTCAGATTGTATGTC | 4734 |
rs570419383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55958337 | ATTGCATTAATTAAT[C/T]TTTTTAATGTTGAAC | 4734 |
rs570419707 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885168 | AAGTGCTGAAGTAAA[A/C]AAAGTTTTACCCTAC | 4734 |
rs570452666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55935587 | GCGTGGTGGCTCATG[C/T]CTGTAATCCTAGCAC | 4734 |
rs570456123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836870 | CCCTATGTTGTCCAC[A/G]TTGGTCTCGAACTCC | 4734 |
rs570463854 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904089 | ATCGTTTGAACTCTG[C/G]AGGCGGAGGTCACAG | 4734 |
rs570468159 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827472 | ATCATGTTCTATGAG[A/T]CACAGAATCATCCAA | 4734 |
rs570506136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964375 | CAATTTCTACTGATC[C/T]ATCTTTAAGTTCAGT | 4734 |
rs570525013 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910583 | GTATACCTTCCCTAA[C/T]GTGTTCATCCTTATC | 4734 |
rs570542293 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865070 | GGGCATGGTGGCGGG[C/T]GCCTGTAATCCCAGC | 4734 |
rs570582289 | snp | A/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995578 | AGCAAATTGGCCATT[A/T]GATGTATCCAATAGG | 4734 |
rs570588571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909884 | GTCTCGTCTTATTTT[C/T]GGTGGTAGAGAGGGG | 4734 |
rs570625355 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871411 | TTGCAGACAGAAGAA[A/C]CAAATTGTATTTTTT | 4734 |
rs570659116 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869866 | AGGCAAACATATATA[A/T]ATAAATAAATAAATA | 4734 |
rs570668785 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869249 | TTCCTAATCAGTGGA[C/G]TCTCCTCAAAATGTC | 4734 |
rs570668792 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981881 | ACTGCTGCAGTTAAC[A/G]TGGTTATGGAAGTAT | 4734 |
rs570675925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908024 | GTGCCACTCTTCCAC[A/G]CAAAGGATGAAGCAT | 4734 |
rs570748410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849445 | GGCCAGGCTAGTCTC[A/G]AACTCCTGACCTCAG | 4734 |
rs570759303 | snp | G/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994432 | ATAACTCCTCCTGTG[G/T]AATAACTCCTCCTGT | 4734 |
rs570793058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972294 | ACTAAAAGATGAACC[C/T]ATCAAAAATAATAAC | 4734 |
rs570809063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856753 | CCACTTCGCAATCTA[C/T]CCCCTGGACATTCCA | 4734 |
rs570814100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55857453 | CTTGCCTCAGCCTAC[C/T]GAGTAGCTGGGATTA | 4734 |
rs570829924 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991738 | GCAAGTTCAGGAAAT[C/T]CACATTTCAAAGGGT | 4734 |
rs570840910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948658 | AACACCACACATCTA[A/C]AACCATCTGATCTTT | 4734 |
rs570864101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937412 | AGAAGATATTTCACC[A/G]TATGTTTTCAGTTTT | 4734 |
rs570872262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863521 | TTTGCATTGTAAGTA[C/T]ATATCAAAACATCAC | 4734 |
rs570876916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864246 | ACTTTAAAATGCTCC[C/T]AAAAGGACACAAAAG | 4734 |
rs570893294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939439 | GTGAGTCAGTTAAAC[A/C]TCCTTTGTTTATAAA | 4734 |
rs570905189 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55917059 | AAAATGTCTTGAATC[C/G]CTTGTAGTCAAAATG | 4734 |
rs570928170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960307 | GCAGACACACCCTCA[A/G]TCTGGGTGGGCACCA | 4734 |
rs570961245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953972 | TGACCCTCCTGCCTC[A/G]GCCTCCCAGCCTATA | 4734 |
rs570968301 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924321 | GATTCCCAGAGCCAT[G/T]GAGTAGGAACCAGGG | 4734 |
rs570973961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925496 | AAAAGTATACACTGC[A/G]TTTTCACTTAAGGTT | 4734 |
rs570974164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55931897 | ACCTTATGTCTTTTA[A/G]CAGACACTCCCCATT | 4734 |
rs570974819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924635 | TTTCATATAAGCACA[A/G]TATAACTTACCAATC | 4734 |
rs570983126 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966990 | CCTCCCGGTTCAAGC[A/G]ATTCTCATGCCTCAA | 4734 |
rs571001121 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958674 | TTCAATTTCTTTTAA[C/T]AACAAATTCAATTTC | 4734 |
rs571003188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966607 | AACTAAGACACAATT[G/T]TTTAAAAAATATATA | 4734 |
rs571063108 | in-del | -/GAG | 0.00220656 | 0.0331423 | cds-indel, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863010 | CCCACCCTGGAGGTA[-/GAG]GAGAAGGTTCTTGTT | 4734 |
rs571079150 | in-del | -/GTATGTAT | 0.407957 | 0.193777 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965661 | CTATTTGGTATGTAT[-/GTATGTAT]GTATGTATGTATGTA | 4734 |
rs571082128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853200 | TACATTTTAGTGAAA[A/T]AAACCACATTTTAAA | 4734 |
rs571082378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845591 | GCTGCCTGGAAGACA[C/T]TAATAATTAGATACT | 4734 |
rs571129434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886504 | AGGCGTGGTTGCTCA[C/T]GCCTCTAATCCCAGC | 4734 |
rs571136257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865325 | CTTCACTTGAATTCC[C/T]ACCTCATGCCTTATA | 4734 |
rs571143215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845974 | TATTTTTAGTAGAGA[C/T]GGGGGTTTCACCACG | 4734 |
rs571175595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909723 | AGAGTGGACACAAAC[A/G]GGTGAGGCCTCACAA | 4734 |
rs571182987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961425 | ACCACAGAAACTGTG[A/T]GACAATAAATGTACG | 4734 |
rs571187284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962021 | TGGGAGTTTTAAAAA[G/T]TTCCCCTTTAATTCC | 4734 |
rs571197835 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929197 | AATGTCTCAAATACC[A/T]CCTTAGCCTCCAGAT | 4734 |
rs571206301 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846712 | ACAGGGATACACCAG[A/G]TTAGAGCTCTGGAAA | 4734 |
rs571225203 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988978 | CGGTGCCTCACGCCT[A/G]TAATCCCAGCACTTT | 4734 |
rs571226783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930820 | CTACCATGTATGATA[C/T]GCCTTTGCTTCTCCT | 4734 |
rs571243632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872750 | CAGAAAAACAGTATA[C/G]AGTGGTTAGTATGTT | 4734 |
rs571255856 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881372 | TCTTGAACTCCTGAC[C/G]TCCAGTAATCTACCC | 4734 |
rs571277587 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966644 | AAAGTAATTAGGATA[C/T]TAAAATTAATTGAAG | 4734 |
rs571305872 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872234 | ATGTTTTGCAATGTG[A/C]ATACAGTACTTTTAA | 4734 |
rs571319532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974669 | AGGACAAAACCCATA[C/T]GATCATTTCAACTGA | 4734 |
rs571329777 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904904 | TTGAGACTAGCCTGA[A/C]CAACATGGAGAAACC | 4734 |
rs571350248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973967 | TGAAACAGAATATAA[A/T]ACAAAGAATCAACAA | 4734 |
rs571379018 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991507 | GCAAACAGTAAATGA[A/G]TGTCTGTTGAATGAA | 4734 |
rs571379576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55887971 | TACAAAAAATGGTAT[C/T]GAAGAAATATAGCTC | 4734 |
rs571384598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888680 | AACAAAACTGGAGAA[A/T]TCACATTACCTGACA | 4734 |
rs571445477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897224 | GTGATCCGCCCGCCT[C/G]GGCCTCCCAAAGTGC | 4734 |
rs571467990 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951015 | TGTCAATGACGTGTG[A/G]ATAAAAAGAAATGCA | 4734 |
rs571479386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55979574 | TAGCCAGGATGGTCT[C/G]GATCTCCTGACCTCA | 4734 |
rs571488177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950181 | TTCTTCATTTGACGA[C/T]CCAATTGATTCAATA | 4734 |
rs571515707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890882 | TTTTGCATTTCCCTG[A/G]CAGCCAATGAGATTG | 4734 |
rs571579093 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937383 | AGGACCACACATAAT[-/A]ATGTCCTTTGCACAG | 4734 |
rs571580690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949219 | TCATCATCACTGGCC[A/G]TCAGAGAAATGCAAA | 4734 |
rs571584041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55882311 | TGCTGACACCCACCC[C/G]CTCCATCCCCTGGCA | 4734 |
rs571596361 | snp | A/G | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826836 | CACTGAAAATTTAAC[A/G]TGCTGCTGTGAGGAA | 4734 |
rs571605266 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845847 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 4734 |
rs571612086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956129 | CACATTTCTTTTTTT[A/T]ATGTTTTTAATTTTT | 4734 |
rs571641371 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851065 | TCTGACTGAAGGAGC[A/G]AGGTCTGCAAGCTCA | 4734 |
rs571642286 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890338 | AGAACACCCTTACCA[A/G]TCAGCATTCACTGCC | 4734 |
rs571647994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837718 | TTTCTCAGATGTGAT[A/G]AGGCCTAATATTTGA | 4734 |
rs571655847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932943 | CATCACTGGCCATCA[A/G]AGAGTTTGCATAAAT | 4734 |
rs571705195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851689 | TCCATGTTGGTCAGG[A/C]TGATCTTGAACTCCC | 4734 |
rs571707029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844199 | AGAAGGGAGAGGAAG[A/G]GAAAGAAGGCAGGGA | 4734 |
rs571748086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986450 | CTGGTGTGATGCATG[C/T]GAAGAACACAGCATC | 4734 |
rs571759321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899590 | AAATAAAGCCATTGG[A/G]ATGGGGCTCCACTCC | 4734 |
rs571760944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912868 | TGCCAGTCACTGTTA[C/T]GTTGTTTGCTATGCC | 4734 |
rs571769271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985941 | CTGAGCCAAGCAAAA[C/T]ACAAGAGAAGCCTGG | 4734 |
rs571796459 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900012 | TCTGAGATTCAGACA[C/T]GTCCTCAAAGCTGAA | 4734 |
rs571799816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866467 | TCAATCCCAAAACAC[A/G]TTAAGTTTTTATATT | 4734 |
rs571803230 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971248 | ATTTGAAAATATACC[A/G]TCAGAGGTGTAAAAA | 4734 |
rs571822520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898576 | TTCCTTGCCTAGACT[G/T]CCCTATCAGAAGTTG | 4734 |
rs571852313 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990639 | AATCTCAAGTAAGTG[C/G]ACTTAACTGGGGAGC | 4734 |
rs571856911 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906360 | CAGCACTATTCACAA[C/T]AGCAAAGACTTGGAA | 4734 |
rs571883496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905679 | AAACAAGAAAGAACT[C/T]TAAAAATAAAATTTT | 4734 |
rs571884735 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911801 | CCAAAGTGCTGGGAT[A/T]ACAGGCGTGAGCCAC | 4734 |
rs571891617 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993802 | CGGGGCTCGGGGAGT[G/T]GGGAGGGCGTGCGGC | 4734 |
rs571907579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55891580 | ACAAATTTGCATTTG[A/G]TATAATATAAGTAAT | 4734 |
rs571917113 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945531 | AAAAGACCAACTCTA[C/T]GTTTGGTGTAGCTGA | 4734 |
rs571920775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906001 | CTTCTCAAAAGAAGA[C/T]ATTTATGCAGCCAAC | 4734 |
rs571925376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865949 | CTCTTTCTTCTCTCT[A/C]TCAACAGGGTCTCAT | 4734 |
rs571926227 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940013 | GACATATACATACAA[A/T]AGAATATTATTCAGC | 4734 |
rs571927078 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994192 | CTGGAGGGATCGCAG[C/T]AGTCTTGGACTCGGG | 4734 |
rs571953435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866705 | TATTTATATTATCTG[A/G]GTAAATTCAGGAAGA | 4734 |
rs571974262 | snp | C/G | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856145 | CCACAGGAAGTGTAG[C/G]TTGTTCCTCAAAAGT | 4734 |
rs571978471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833594 | TGAACATGGGAGGTG[A/G]AGGTGGCAGTGAGCT | 4734 |
rs571986685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933123 | GGAAGACAGTGTGGC[A/G]ATTCCTCAAGGATCT | 4734 |
rs572008946 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882670 | TGGACTTGGGGGGCA[C/G]GTGATCTAGTGAGAC | 4734 |
rs572013084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866193 | TGCTGGGATTACCAG[C/T]GTGAGCCACTGTGCC | 4734 |
rs572031584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890570 | CCACATTTTATTTAT[C/G]CATTTTTCAGTTGAT | 4734 |
rs572073589 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975095 | ACAGGGTTTCACCAC[A/G]TTAGCCAGGCTGGTC | 4734 |
rs572093923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946314 | AGGGATGGAGGAAGA[A/T]CTATCAAGCAAATGG | 4734 |
rs572095542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981193 | GACTACAGGTGCCCA[C/T]CACCACACACAGCTA | 4734 |
rs572110769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945575 | AATGGAACCAAGGTG[A/G]AAAACACTCTACAGG | 4734 |
rs572127737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859934 | TTTGCTAATCATAGC[C/T]TTAGCCTCACTACAG | 4734 |
rs572131566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986631 | GTCTCGCTCCGTCGC[C/T]GAGGCTGGAGTGCAG | 4734 |
rs572156637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55913021 | CATTAATAAGCTGTT[G/T]ATTACAGTAAGCTAG | 4734 |
rs572156803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951754 | AAGCAATTAAAGTAA[C/T]TTTTGCATCTCGTTA | 4734 |
rs572168037 | snp | G/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827025 | TGATACATCAATCTT[G/T]ATATATATATTTACT | 4734 |
rs572183472 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906232 | AGTGTGGCGATTCCT[C/T]ACGGATCTAGAACTA | 4734 |
rs572184932 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896053 | TCCTTGGCATGGAAT[C/T]CTAGTTTGTTTTTTC | 4734 |
rs572211460 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920772 | TGACACAGGTCATTT[A/C/G]TTGCTATACAATCAG | 4734 |
rs572235983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963014 | GGTCTCAAACTCCTG[C/T]CCTCAGGTGATCCAC | 4734 |
rs572236527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922062 | CAGTAATACCATGAT[A/C]TAGCAATTCAACTCT | 4734 |
rs572269005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854962 | AGGACATTATAACGT[A/G]CAGAGGGAAAAACAC | 4734 |
rs572297056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949896 | TATGGCACGTGTATA[C/T]ATATGTAACAAACCT | 4734 |
rs572332846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920318 | ATACAACTGCTAAAC[C/G]TGAGAAGCACAGGGT | 4734 |
rs572392727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861216 | TTGGTCTTAAGCCAG[G/T]AGTAGAGTACTCCAT | 4734 |
rs572458227 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966676 | ATCTTTTTCAATAAT[C/G/T]AATTTTATTAAAAGT | 4734 |
rs572460800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957967 | CACACCAGGGCCTGT[C/T]GTGGAGTGGGGGAAG | 4734 |
rs572477001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870339 | GTGTCTGAAACCTGC[C/T]ACATCTCTTTGGCAG | 4734 |
rs572510041 | snp | A/T | 9.89348e-05 | 0.00703261 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860763 | GTTGCCATTCTCAGC[A/T]TCTGTTAGGTTGTCC | 4734 |
rs572522142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852744 | CTTTTCTGAGAGAGT[A/G]AGAGAGAGAGAGAGA | 4734 |
rs572526624 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929610 | CTGTTCCTGTAAGCA[G/T]CAGTTTTAATATATA | 4734 |
rs572580007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868347 | TGGTGCCATACGCTG[C/T]GTGCTTTGCTTTCAG | 4734 |
rs572580665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965549 | TCAGCTCTCTCTCTT[A/C]CAGAATCCTTACCAC | 4734 |
rs572596726 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953350 | CTATTCCTTTCTTTA[C/T]TTCATACAGATCACA | 4734 |
rs572618006 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973067 | CCACTTTCGGCACTG[A/G]ATAGATCATTCAGAC | 4734 |
rs572623285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964389 | CTATCTTTAAGTTCA[A/G]TTAATCTTTCCTCTT | 4734 |
rs572623448 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55952239 | CTCGGGAGGCTGAGG[C/T]AGGAGAATGGCATGA | 4734 |
rs572635688 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983628 | CTTTTTTTTTTTTTT[-/TT]GAGACAGAGTGTTCT | 4734 |
rs572636309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963790 | TTCAGCTGAAAGGAC[A/T]TTAAGATATCTTACA | 4734 |
rs572644154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853989 | AGCAAAACTCCGACT[C/T]AAAATAACAGAAATT | 4734 |
rs572645535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883423 | GCCCTGACTTCTAGA[C/T]GGCATCTCTGAATGC | 4734 |
rs572646799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867800 | GTGGCTCACGCCTGT[A/T]GTCCCAGCACTTTGG | 4734 |
rs572647157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55875523 | GGGTTTCACCATGTT[A/G]ACCAGTCTGGTCTCA | 4734 |
rs572677678 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983494 | TGTGGTTCTATTTAC[C/T]CAATGGGGTTCTATT | 4734 |
rs572711937 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874905 | CTTAAATCCAGGAGG[A/C]AGACGTTGCAGTGAG | 4734 |
rs572716078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970567 | AGCTCAGAACAGAGA[C/G]AGAGACAGAGAGAGG | 4734 |
rs572721978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846245 | ATCTTGAATATTTGT[A/G]AAAGCCAGCTTCTGG | 4734 |
rs572722852 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959443 | TCTTGATTAACGTAC[A/C]ATGTGCATTTCAAAA | 4734 |
rs572752315 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941993 | ACTTGGGTATTAGCT[C/G]TAGTGTACTATACAT | 4734 |
rs572815124 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874390 | TCCACATAATGCAGA[C/G]AGCCTAGAACTTAAG | 4734 |
rs572846025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877115 | AACATCTTAAATAAC[A/C]ATATTATGATGATCA | 4734 |
rs572849282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929282 | ATTTTCTCTTTATGT[C/T]TGATTTCAGGAGGAG | 4734 |
rs572858824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888029 | CCCATAGTGAATATC[A/G]TACTGAATAGGGAAA | 4734 |
rs572869010 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923800 | TTGAGGGCAAAAAAA[A/C]CATGAATGTAGTTTA | 4734 |
rs572874483 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919614 | AAAACAGGAGTGTTA[A/C]TCCTAACCTTAAGTG | 4734 |
rs572892510 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886038 | AAACGGAAATCAAAA[A/C]AGGGCATGAGTAGCT | 4734 |
rs572901080 | in-del | -/GAC | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830270 | TCTAGCCTGTCTTGG[-/GAC]GACAGCCCATCACTC | 4734 |
rs572908588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885353 | GCAACAGGAAATTAT[C/T]TGAAGGTACAAATTT | 4734 |
rs572908664 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872489 | TGTCTAGAATAAAAT[A/G]GTGGGTTTTCAAAAT | 4734 |
rs572983138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896134 | GATCCTATATTTTGC[C/T]CTCTCAAGCTCACTC | 4734 |
rs572993929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941742 | CTACTTTTTGTATAC[C/T]TTTTTTCTTTAGTAG | 4734 |
rs572996248 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851235 | CACAGAAATGGATAA[C/T]TGAAATGCAATATAT | 4734 |
rs573025729 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55991792 | GTTCCTTACCGACCA[A/C]CCATTAACTGCCACA | 4734 |
rs573026952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941710 | CTGGTATTACAGGTG[C/T]GCACCATCACACCCA | 4734 |
rs573041218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982840 | TAAAATAAATTCTAG[A/G]GCTGGGGGTGGTGGC | 4734 |
rs573072736 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843133 | TTGCTCCTCCTTGCC[A/T]TCTGCCATGATTGTG | 4734 |
rs573117449 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976150 | CATTGAGGAAACTCT[C/T]CAGAACACTGGTCTA | 4734 |
rs573118131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843726 | AATATAAGCATGATA[C/T]GAGCAGTTTCCTATA | 4734 |
rs573153730 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990560 | GATGTTTACATGACT[A/G]TGCTTATCAGCAGAA | 4734 |
rs573156887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893646 | ATATTCGCACATGAG[C/T]GTCTCAGAAAAATAA | 4734 |
rs573158456 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973222 | TTCTCAAGGATAAAC[C/T]ACATGTTAGCCACAA | 4734 |
rs573159423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972659 | TAATAACAATGAATG[C/T]AAGTGAACTAAACTC | 4734 |
rs573179558 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844318 | CCACACGGTCAGATT[G/T]CTGGGTTCTCAGAAG | 4734 |
rs573181000 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841781 | TTTCACCGTGTTAGC[C/T]AGGATGGTCTCGATA | 4734 |
rs573205864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989245 | CGTCTCAAAAGTAAA[C/T]ACATAATTTAAAAAT | 4734 |
rs573215136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936865 | TGGTGTGAACTCGGC[C/T]CACTGCAACCTCTGC | 4734 |
rs573288865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944107 | TACATTTCCACCTGA[A/G]GTGCCTGGTTCATCT | 4734 |
rs573300098 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920005 | GAGTAGAGCACATTA[C/T]CCTCCACAATGTGTG | 4734 |
rs573329098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835991 | TGGTCTGTTAGCTCC[A/G]CAGGCTGATTGTTTC | 4734 |
rs573334047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903768 | AGGCGGAGGTTGCAA[G/T]GAGCCGAGATCGTGC | 4734 |
rs573334624 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943381 | CCCAGAGGACTAGAA[C/G]GGAAGAATGATTTCA | 4734 |
rs573338925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865657 | CTGTTCTAGGCCTGG[A/G]GATCAGCAGTAAATG | 4734 |
rs573386793 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893043 | TGTAACAATAAAGAT[A/T]ACAGTAAACTAACCT | 4734 |
rs573392163 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828333 | TAACATATATTTACA[A/T]TTATTCCTAAATCAC | 4734 |
rs573393438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909990 | TTTTCTGTTTCCTTC[A/T]TTTGATATTGCTGAA | 4734 |
rs573417972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55836549 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTT | 4734 |
rs573426051 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879587 | CATGAAACACACAGA[C/G]CTAAATGAAAGACGG | 4734 |
rs573427820 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874487 | GAAAAAGAGGAGAAA[C/G]GTCCCAGAAAAAAAG | 4734 |
rs573428604 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909638 | CTGCCAAGCCCCTTC[A/G]GCCTACAAAGCCTCT | 4734 |
rs573433206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55919326 | TTGATCCAGCCGCCA[C/G]TTTTAAAGAAATATC | 4734 |
rs573460316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948329 | AAATGGAAGAACATT[C/T]CATACTCATGGATAG | 4734 |
rs573467779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953632 | TTTTTAGTAGAGACG[C/T]GGTTTTGCCATCTTG | 4734 |
rs573467981 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840234 | GAAAAAAAGCAATTG[C/T]GAGTAGTTGATATAC | 4734 |
rs573479639 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829160 | CAGGCAAGAGAAAGG[C/T]TTTAATACTTTTTAC | 4734 |
rs573492982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959835 | AGCTTGGAAGTGAAT[A/C]CTTCCCTAAGCAAGC | 4734 |
rs573494001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55925699 | GAAAAAAGTCCTATG[C/T]TTGTGACAAAGATAT | 4734 |
rs573526016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55888927 | ACTAGACTCCTATTT[C/T]TCACCTTATACAAAA | 4734 |
rs573527738 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947676 | AAACGTAATCCAGCA[C/G/T]ATAAACAGAACCAAA | 4734 |
rs573534228 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902293 | GCAAGTCAAAAGAGA[-/T]GTATCCATCTTGAAT | 4734 |
rs573560296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844893 | GCCCAGTGCAGCTTT[C/G]AACTCCTGAGCTCAA | 4734 |
rs573563727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911824 | TGAGCCACCGCGCCC[A/G]GCCTAGACTGAAAAT | 4734 |
rs573576306 | snp | C/T | 0.00100826 | 0.0224302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993495 | AGCCCGCCCCGCAGC[C/T]CCGCGGTCCCCGCAC | 4734 |
rs573589687 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976904 | TCCCGAAGTGCTGGG[A/G]TTACAGGTGTGAGCC | 4734 |
rs573594410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900627 | CAGTAAAGGGAGAGA[G/T]AGCTATAAGAGAGCT | 4734 |
rs573625338 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963421 | TTAAAATTTCTACTG[-/T]TTTTTTATCTATAAT | 4734 |
rs573631003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949448 | CAGCAATCCCATTAC[C/T]GGGTATATACCCAAA | 4734 |
rs573649609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911556 | TTTTTTTGAGACGGG[A/G]TTTCGCTCTGTGGCC | 4734 |
rs573651071 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949607 | ACATATACACCATGG[A/C]ATACTATGCAGCCAT | 4734 |
rs573662353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55859234 | TTAGACAGCTAGCTA[C/T]GAAGTTCTCATCGTG | 4734 |
rs573664840 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879604 | TAAATGAAAGACGGG[A/G]GTCTGATGAATAAGA | 4734 |
rs573693216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993416 | GAGGGGCTGACAGCA[A/G]AGCCTCCGGTCGTGG | 4734 |
rs573715605 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830966 | CTCTGTCACCCAGGC[C/T]GAAGTAAAATGGCAT | 4734 |
rs573724207 | snp | A/G | 9.67165e-05 | 0.00695334 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872375 | GTGTAATGAAGAGAT[A/G]AAAAATTTAATATGC | 4734 |
rs573754191 | snp | A/T | | | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852523 | CCAACCTGGTGGTAA[A/T]CCAGATGAAGTAGGC | 4734 |
rs573775236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949694 | TTCTCAGCAAACTGT[C/T]GCAGGGACAAAAAAC | 4734 |
rs573788045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865477 | CACCAAACCTTGAAG[A/G]CATGAAAGAGAAGAT | 4734 |
rs573815322 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871677 | TTACAAACAGTAATT[A/T]AAAAAATCATTTTTA | 4734 |
rs573853358 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55961449 | ATGTACGTTCTTTTA[A/G]GCAACTAAGTTTGTG | 4734 |
rs573853415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864676 | AACAAGAGTGAAACT[C/G]TGTCTCATAAGAAAA | 4734 |
rs573854986 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951805 | AGTGAAAGACACAAA[C/G]AACTAGAAAGAAAAC | 4734 |
rs573859002 | in-del | -/T | 0.355311 | 0.226737 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900068 | GAATCATGACTCCAC[-/T]TTTTTTTTTTTTTAA | 4734 |
rs573906266 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995663 | GTCTTTCCGAATATG[A/T]AATCATGAAGAATTA | 4734 |
rs573911741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930734 | CATACTGTTCTCCTG[A/G]TAATGAATAAGTCTC | 4734 |
rs573922057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967993 | GGGTGACAGAGCAAG[A/G]CCTTATTTTAAAAAA | 4734 |
rs573962813 | in-del | -/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827314 | CCGCAGTAGAATGCA[-/T]TTTGAGACACTTTTC | 4734 |
rs573967661 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844249 | AAAAGTAGTCTGGGG[C/T]CAGAGGGTGGACAGT | 4734 |
rs573988188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873907 | ATATGTAAGTATTTA[C/T]TAAATTAAAAAAATA | 4734 |
rs574018064 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944580 | GCTGAACAAAATGCA[C/G]CAGAAACTTCTACAG | 4734 |
rs574045834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831521 | AAAGTAGAGAAGATG[C/G]AGGAAGGGGAGTCAG | 4734 |
rs574051335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55912907 | ACATTATTATGGAGA[C/T]AGACTACAAAGTCTC | 4734 |
rs574055222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884356 | AGACTGTGAAGACTA[C/T]AATAAATACCTAACT | 4734 |
rs574084545 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932992 | GAGATACCATCTCAC[A/C]CCAGTTAGAATGGCG | 4734 |
rs574089784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920825 | ATAGGTTCTATAACA[C/T]CTCAGGTCATCTCTA | 4734 |
rs574110828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926478 | GGGGAGGGAAAAATA[A/G]TGTTAAGACGGCCGG | 4734 |
rs574116792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55883548 | AACAGAGGTGGCAGC[A/T]AGCGAGTGGTTACAG | 4734 |
rs574118166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974955 | TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG | 4734 |
rs574138909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55881894 | TTGAAGGATATTTAC[A/C]AACATTCCTGGCCTC | 4734 |
rs574146889 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923322 | CCATATCTGATAATC[A/C]AATCAGCAACATCTG | 4734 |
rs574171820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55932249 | AAGCTGGAGGCATCA[C/T]GCTACCTGACTTCAA | 4734 |
rs574185348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982279 | TCCTAGGTATTTACA[C/G]AAGAGAAATAAAAAT | 4734 |
rs574222209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981794 | AGTCTGTATTTTAAC[A/C]ACTCTTCAGATGATT | 4734 |
rs574296245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905750 | GTAAATTTGTTTGAG[A/T]TCTTTGTAGATTCTG | 4734 |
rs574305140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55889600 | AGGGAGAAGTAGAGA[C/T]AAGTAATGGCTACAC | 4734 |
rs574313959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55987046 | CCTGAGGAATCGCCA[C/T]ACTGACTTCCACAAT | 4734 |
rs574315479 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903596 | TTGGGAGGCCGAGGT[A/G]GGTGGATCACGAGGT | 4734 |
rs574329996 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837265 | TGAAACCATGTCTCT[A/G]CTAAAAATACAAAAA | 4734 |
rs574338594 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860643 | GTCTTTCAAGGAGAA[C/T]TAGGAAACTACTTAT | 4734 |
rs574352495 | in-del | -/AAG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843370 | TGAAGAAGACGACTT[-/AAG]AAAGTCTTAGCTCCT | 4734 |
rs574353336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975991 | TACATCTATAGTGAA[C/G]TCCTTTTTGACAAAG | 4734 |
rs574359742 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835636 | CTATCCTTTAAGTCT[C/G]CCTTTTTGAATGCCA | 4734 |
rs574372443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55898675 | AAGGTCTTACTTTGT[C/T]GCCCAGGCTAAATAC | 4734 |
rs574375634 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827049 | ATTTACTGTGTCAGA[A/T]GATTTTAAAAAGTCA | 4734 |
rs574400205 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858570 | TCCCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 4734 |
rs574402220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860021 | GTAGAGCAAAGTCCT[A/G]CTTCCTAAAACCCTC | 4734 |
rs574415903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986004 | ATGGGGACTTGTTAC[A/G]AAGACCTAGGAACCT | 4734 |
rs574431801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933675 | TGTACCCTAGAACTT[A/G]AAGTATAAAAAAAAA | 4734 |
rs574454812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835030 | TGGCTCACTCTGTAC[A/G]CATTTAAATGTGCTC | 4734 |
rs574458287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901635 | CCCAGATTCGTGGTC[C/T]GTGTATTTTTACTTG | 4734 |
rs574462743 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827796 | TCACTTTACTTTTAA[A/G]TGATTCTTTGGGAGT | 4734 |
rs574467172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975476 | AGTAGCATTTTTATA[G/T]GCCAACAGTGAACAA | 4734 |
rs574469024 | in-del | -/GATT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959262 | CTTCTTTGACATATA[-/GATT]ATTTAGAAGTATACT | 4734 |
rs574477899 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957506 | TATTATGAATGGGTG[C/T]TGAATTTTGTCAGTT | 4734 |
rs574492570 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845775 | GGAAATTTCGACACA[A/C]AGTTATTCTTTTTTT | 4734 |
rs574499915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946190 | GGGCTAAATGCCCCC[A/G]TTAAAAGACACAGAC | 4734 |
rs574534049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839316 | TTACAGTTGCACACC[C/G]CTGTGTCCGGCACTA | 4734 |
rs574542209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55940991 | AGTATATTTTGGCTT[A/G]TAAGAATTTATCCAT | 4734 |
rs574590446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950982 | GTAAATGAGGCAGAT[C/G]GGGTGGAAAGGCAGC | 4734 |
rs574597856 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842788 | CTGTAGGATAGCCAC[C/T]GCCTGCTAGCTGTTG | 4734 |
rs574603347 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868101 | ATTATTATAGATTCT[C/T]CTGCAAAGCAAAATC | 4734 |
rs574604834 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994938 | CGGGCGCCTGGAGTC[A/C]CAGCTGCTTGGGTGG | 4734 |
rs574637810 | snp | A/G | 3.31554e-05 | 0.00407144 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915853 | TTGTTTTAGATAACC[A/G]AAGTCCATTGACAGC | 4734 |
rs574655852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906507 | TGAAGCTGGAAACCA[C/T]CATTCTCAGCAAACT | 4734 |
rs574655858 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919818 | CATGGTATGGATAGG[A/C]TCTGGGTAATCTTAA | 4734 |
rs574659236 | snp | A/G | 1.65477e-05 | 0.00287638 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848935 | ACAAATTTTAAAATA[A/G]TCAAAGTCAGTCTGT | 4734 |
rs574666996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945669 | AGATAACACCACAAA[A/G]ATATTCCTCGAGAAG | 4734 |
rs574687503 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990260 | CTGGACCGCATCCCC[A/G]GTCCATGGAAAAACT | 4734 |
rs574696977 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915413 | TTTAGAACAATTGTG[C/T]TTAAGGCTGGATAGA | 4734 |
rs574722720 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994308 | ACCAGTAACAATCCA[A/G]TCTCCAGGCTGACCC | 4734 |
rs574737851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855846 | AGTGATCCTGAATTG[A/T]ATGCCGTATGCAGCG | 4734 |
rs574757459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947543 | CTACCAACCAAAAAA[A/G]GTCCAGGACCAGACG | 4734 |
rs574766038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55914180 | TACTATTTTATTCAC[C/G]TAAAGTTACTTATCC | 4734 |
rs574783677 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55947040 | TATAGCACTAAATGC[C/T]CACAAGAGAAAGCAG | 4734 |
rs574785610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886015 | GGATGGAAAAAGGTA[C/T]TTCATTAAAACGGAA | 4734 |
rs574798940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856302 | GGCAGAAGAGAGAAG[C/G]CTGGCTAGGATGCAA | 4734 |
rs574820187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55988803 | CTTGCTCTCAAGTGG[C/T]TCAGAAAAAGATTAA | 4734 |
rs574829745 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853655 | GTTTGTTACAAATGA[A/C]TAAAGAGAAGTCTGG | 4734 |
rs574830297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921347 | TTTTTTTCGCCGAGA[C/T]GGAGTCTCACTCTGT | 4734 |
rs574842076 | snp | A/C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891060 | TGTTTTTATTGCTCT[A/C/G]TATTTGTTGTTCATT | 4734 |
rs574845482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952667 | ACCCCTAACCTAGTG[A/C]GTCAGGAGTCCTCTT | 4734 |
rs574862356 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960507 | CTAGGGGCTCTTGTA[C/T]CTTCAGCCACAGACT | 4734 |
rs574897448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907942 | CTCCACTGTGGAAAC[C/T]AATCCTTGAGTCACG | 4734 |
rs574906369 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982920 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 4734 |
rs574928554 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922658 | ATAAGCAACCATGCC[C/T]GGCCAACAATGTGTT | 4734 |
rs574970164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55868476 | AGGTAACTGAATCAT[C/G]AGAGTGAGTTTTTCC | 4734 |
rs574985044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55922900 | ATTATGTGGGCTTTT[C/T]TGTATGTATATTTCA | 4734 |
rs575008875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851444 | GTTGCAAAATTAGAA[A/G]CACAGGCATATAAAC | 4734 |
rs575012681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876796 | TAACCATATGTTGCC[C/T]ATAAAAGACATCTAT | 4734 |
rs575066517 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55957276 | CTTCCTTTTTGACTG[-/T]GTGATTTTTTTTTCT | 4734 |
rs575151081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863702 | GTGTAATCTTAGGCT[G/T]TTCTCTAAATTATCA | 4734 |
rs575199053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880917 | ATTTAAAATACTGGC[A/G]TATATAATGAAACCC | 4734 |
rs575199694 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850587 | AAAGAAAGGCCTCCC[A/G]TTTGGTGCATGCCGG | 4734 |
rs575215376 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841801 | TGGTCTCGATATCCT[C/G]ACCTTGTGATCCGCC | 4734 |
rs575250499 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898569 | CTTTGTCTTCCTTGC[C/T]TAGACTGCCCTATCA | 4734 |
rs575280546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966757 | GATAAGCAAAAACTT[A/G]AGTCAACTTATTACA | 4734 |
rs575280754 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901218 | TAACTATTGAGAGCT[C/T]TGTGAATTCTTTAGT | 4734 |
rs575316881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927071 | CAACAGAGTGAGACT[A/G]CGTCTCAAAAAAAAA | 4734 |
rs575321409 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917277 | ATGAACATTTAACTA[C/T]GTGAATCACAGTGCC | 4734 |
rs575333410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55929936 | TGCTGGAATGAAAAA[C/T]GACTGTTGAATTAAA | 4734 |
rs575366819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972493 | ATGTTAATTGCAACC[C/T]TCATGTAACATCAAG | 4734 |
rs575371371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844340 | TCTCAGAAGCTGACG[A/G]GACAGGGTGTAAAGG | 4734 |
rs575402579 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829289 | AACAGTTTTTCTGTG[A/G]GTTAGTTGGCTAGAA | 4734 |
rs575436482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838244 | TAAAAAGTATACATA[C/T]TGTAGTTATACGAGA | 4734 |
rs575450278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839060 | TTGAGACAGGGTCTC[A/G]CTCTGTCCCTTAGGT | 4734 |
rs575453321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984420 | ATAATGTTGTGATGA[A/T]TACAGCTAAAGTATG | 4734 |
rs575475989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886875 | AACATCGAAATTAAA[C/T]AGTATGCTCCTGAAT | 4734 |
rs575489158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952943 | CTTATATAGCAATTA[C/T]TCAGTGCCAGACACC | 4734 |
rs575510753 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955114 | GAAACCTCTGCCTCC[C/T]GGGCTCAAGCAATCC | 4734 |
rs575518740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977933 | TCTCTTCTGTGATGA[C/T]TTAATTAACAAGTAC | 4734 |
rs575525367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842489 | CCTCATGGGCTCAAG[G/T]GATCCTCTTGCTTCC | 4734 |
rs575538767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55886130 | TAATAACAAATGGGT[C/T]AATTCAATAATAGGA | 4734 |
rs575541197 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893735 | CTGCTTGCTGAATAT[A/C]ATAAAAACTATTATT | 4734 |
rs575601525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973743 | AAATAATAATGGAAA[C/T]ACAACATAGCAAACC | 4734 |
rs575606077 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974541 | CTAGCAAACCAAATT[A/T]GACAACACATTGAAA | 4734 |
rs575609426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55938967 | ATAAAAATGGTGGTG[C/T]GTGATGGTGTGCACC | 4734 |
rs575612317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831028 | GGTTCAAATGATTCT[C/T]ATGCCTCAGCCCTCC | 4734 |
rs575622245 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871563 | AGACTAAAAGAGATT[G/T]ACATTCCAGACATCT | 4734 |
rs575643015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983307 | GTGTGTGTGCGTGCG[C/T]GCGCGTGCGTGCATT | 4734 |
rs575643335 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897326 | CTTCGTCTTACTTAA[C/T]CCTTCCTTTGTAAAC | 4734 |
rs575646271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55906342 | GGACACGTATGTTTA[C/T]TGCAGCACTATTCAC | 4734 |
rs575670032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944011 | TTGGAGCTTTAAGAT[A/G]TAATGATTGGAAGAT | 4734 |
rs575708130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905872 | TGCAGAAGCTCTTTA[A/G]TTTAATTAGATCCCA | 4734 |
rs575750623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897006 | TGAGATGGAGTCTCA[C/T]TCTGTTGCCCAGACC | 4734 |
rs575768716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55930859 | CGCCATGATTGTGAG[A/G]CCTCCCCAGCCATGT | 4734 |
rs575769523 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985519 | AGAGGAGATGTCTGC[A/G]TGGTCAGGAAGTTAG | 4734 |
rs575771844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911949 | AGTGCCTGGCACTCA[A/C]ATGTGTACTGGATGA | 4734 |
rs575778794 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842280 | GTCTCTTTTTCCTTA[C/T]GTAATATACTCAGGG | 4734 |
rs575796844 | snp | C/T | 1.65348e-05 | 0.00287526 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834188 | AAGGAAAATAATGGG[C/T]TCACAATTTCTGTTT | 4734 |
rs575810756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904233 | CTAGTGACAGTGAAC[A/T]TCCAATATTAAACTC | 4734 |
rs575828262 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55903838 | TCAAAAAAAAAAAAA[A/C]AACACACATATATAT | 4734 |
rs575830432 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893757 | ACTATTATTTTAAAT[A/G]AACATCCTTCCTCTC | 4734 |
rs575841256 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948767 | TGTAGAAAGCTGAAA[A/C]TAGATCCCTTCCTTA | 4734 |
rs575850467 | in-del | -/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918084 | AAATACAAACCAAGC[-/T]GCACATTTCTTTATA | 4734 |
rs575855662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55992091 | GCACTGGGCAGTCTA[C/T]GTAGCAAGCAGGGAA | 4734 |
rs575856974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948466 | TACTTTAAAGTTCAT[A/G]TGGAGCCAAGAAAGA | 4734 |
rs575859153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55864542 | CAAAATTAGCCAGGT[A/G]TGGTGGCGCATGCCT | 4734 |
rs575886963 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979821 | TTATCACATACTATC[-/T]TGTATCTGAGGCAAT | 4734 |
rs575903442 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55899915 | CTACTGGCTACTAAA[A/C]TGGACAGTGGTGCTG | 4734 |
rs575931736 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945096 | TCTAAAAACCAGAGC[A/G]CATCTTCTCCTCCAA | 4734 |
rs575965659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839903 | TTGCTTGAACTTGGA[A/T]AGCAGAGGTTGCAGT | 4734 |
rs575986370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55910802 | ATCTTAGTTCATAAC[A/G]TCACTGTTAACCCAG | 4734 |
rs575994861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840276 | GTAAAATTCTTCCAA[C/T]TTTATTATATGTTAG | 4734 |
rs575996235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951136 | TGCTCAACTGGAGTA[A/G]GACTACTGTACAGTC | 4734 |
rs576011500 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994055 | TCCGTGAGCTTAATC[C/T]CCGCTTAAATCCCAA | 4734 |
rs576016225 | in-del | -/TG | 0.0103295 | 0.0711199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55981783 | CACTGTGGGGTAGTC[-/TG]TATTTTAACAACTCT | 4734 |
rs576073214 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929385 | TACAAGTTGGTTCTA[C/T]AGATAAACTGTGTGG | 4734 |
rs576130150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55980537 | TACCCGCCCCTCGTA[C/T]AGAGGATGTAAGCCA | 4734 |
rs576131375 | snp | C/T | 1.75081e-05 | 0.00295867 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993483 | AACCCGAAGGGAAGC[C/T]CGCCCCGCAGCCCCG | 4734 |
rs576132685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866132 | TTGCCCAGGCTGGTC[A/T]CAAACTCCTGGGCTC | 4734 |
rs576167304 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920131 | CTAAGTTCTCAGCTT[C/T]CTGGCCTGCCCTGCA | 4734 |
rs576197836 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872937 | AAAAAAAAAAAAGAT[C/T]ATGCTCTGGAAAGAC | 4734 |
rs576224107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55865693 | TGTGTGACAGGCAGT[A/G]GACGGCTTCCAAGAT | 4734 |
rs576225717 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933536 | GCCTGTCGTGGGGTG[A/G]GGGGAGGGGGAAGGG | 4734 |
rs576230022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926161 | ATACTCTGTTCTATT[C/G]TATATATTGTTTTTT | 4734 |
rs576272051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55956384 | GTAAACTTTGTGTAA[C/T]CCAATAGAGCAAAGA | 4734 |
rs576288991 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55933062 | TATGGAGAAATAGGA[A/C]CACTTTTACACTGTT | 4734 |
rs576306016 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929234 | TGTACACACATGCAC[A/G]AGCACGCACGCACAC | 4734 |
rs576336169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55962239 | ATATCTTTTTGCGTC[C/T]GCTTTCTTTCAAATT | 4734 |
rs576349854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55939353 | TTCTGTCTCCTACCA[C/T]CTTGTGGAGAAGGTG | 4734 |
rs576398096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55876907 | ATGGAGTCTTGCCAT[A/C]TTACGCAGGATGGTC | 4734 |
rs576398860 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55867762 | TGATTTGAAGAAAAA[A/T]GGTTCTTTCCTGGCT | 4734 |
rs576420122 | in-del | -/AACAAAAAAACAAC | 0.0189856 | 0.0955633 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973382 | TATCTCTTAAAAACA[-/AACAAAAAAACAAC]AACAAAAAAACAGGC | 4734 |
rs576441581 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952186 | ACAAAAAAAAAAAAT[C/T]AGCCAGGCGTGGTGG | 4734 |
rs576461023 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55885240 | AAATAAAGACTTTCA[C/T]AGACAAACAAAACCT | 4734 |
rs576474513 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55964691 | TGTGAATTTTGCTGC[-/T]GGTGTGTGTGTGTGT | 4734 |
rs576482427 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967974 | CACCACTGCACTCCA[A/G]CCTGGGTGACAGAGC | 4734 |
rs576496975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927468 | CTCGGCTAATTTTTT[A/T]AAAATTTTTGCAGAG | 4734 |
rs576503306 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949802 | ACTGGGGCCTGTCAT[G/T]GGGTGGGGGAAGTGG | 4734 |
rs576529199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976642 | ATTTTTTTTTTTTTT[C/T]TTTTTGAGACGGAGG | 4734 |
rs576531560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970019 | ACCCACTCTGGGCCA[C/G]AAGGAAACCCACTGC | 4734 |
rs576577248 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | NEDD4 | GRCh38.p7 | 15:55927096 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 4734 |
rs576612150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55874828 | AAAATACAAAAATTA[G/T]CCAGGTGTGGTGGCA | 4734 |
rs576617510 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861422 | TAAATCAGATTGGAC[A/G]GTTAATGAGTATTAA | 4734 |
rs576633280 | snp | C/T | 0.000131885 | 0.00811942 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848771 | AAATATTTGAGATAG[C/T]CAAGTTAGATGGGTT | 4734 |
rs576657280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55890437 | TCTGGATATTTCATA[A/T]AAGTGGAATTATATA | 4734 |
rs576671434 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876192 | AAATAAAGATACTTT[C/T]GGATAAAGTAGAGAT | 4734 |
rs576685125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55845773 | AGGGAAATTTCGACA[C/T]AAAGTTATTCTTTTT | 4734 |
rs576719090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55975343 | TTTGGAAAAGCTAAA[C/G]ACTCCACCCAAAAGC | 4734 |
rs576732522 | snp | A/G | 0.00156343 | 0.0279154 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951613 | AAAAAAAAAAAAAAG[A/G]AAGAAAAATTTTAAT | 4734 |
rs576736896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55965481 | CCCGTTTCTTAGGCA[A/G]TGACTGTGATCTCTG | 4734 |
rs576801899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55936094 | TTGCTACTTCAAGTC[C/T]ATAACTTGAAGCTAA | 4734 |
rs576868551 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55970943 | ACCAAACAAACTAAA[A/T]AGGGCACCAGTGACC | 4734 |
rs576875793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55854750 | GTGGATTTTATGGTA[C/T]GTAAATTATACTCCA | 4734 |
rs576887900 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938403 | TTGGGAAAACTGGAT[A/G]TCCATACGCAAAAGA | 4734 |
rs576888184 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55941641 | ACAATTTCAGCTCAC[G/T]GCAACCTCCGCCTCC | 4734 |
rs576908717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55982709 | TTTATAATCTGTGCA[C/T]TTCACTCTTTGTAAA | 4734 |
rs576936028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848200 | GTAAGGATAATGACG[A/T]TATAGAATCTTTTCA | 4734 |
rs576961955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55909429 | TGTATCTCTAAGTAT[C/G]TGTCTTCATCTGACC | 4734 |
rs576962593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928191 | ATTTTTGTATTTTTT[C/T]AGTAGAGACAGGGTT | 4734 |
rs576977636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55901847 | GCTACTCTTTATTGA[C/G]CATCAAGTATTTGCC | 4734 |
rs576993843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843061 | GGTCTCACGACATCT[A/C]ATGGTTTCTATGCAC | 4734 |
rs577005699 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55946215 | ACAGACTGGCGAATT[A/T]GATAAAGAGTCAAGA | 4734 |
rs577022610 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839849 | AGTGTGGTGGTGCGC[A/G]CCTGTAGTCCCAGCT | 4734 |
rs577034566 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855914 | CCCAGATACCACCCA[A/C]AGTCACCAGCATGCA | 4734 |
rs577035838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55908463 | ACAATAATGGCATTG[C/T]AGGGACTCAATGGAT | 4734 |
rs577045117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55900845 | ATATATTTCCCATTG[C/T]AAATGTATTAATAAT | 4734 |
rs577071951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55945724 | CAGATTCACCAACGT[C/T]GAAATGAAGGAAAAA | 4734 |
rs577074391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55843317 | ATAACAACACTATGC[A/G]AAAGCTACTATTATT | 4734 |
rs577074455 | in-del | -/AAA | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967419 | AATAACTTAGCAAAT[-/AAA]AAACTGAACATAACT | 4734 |
rs577081729 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55861092 | TGAATGAATAAATAT[C/T]AGAGCGCTTCATAGA | 4734 |
rs577097629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856378 | ACGTGGACACCTTCA[A/C]ACATCCAGCTCCCAT | 4734 |
rs577122675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55896064 | GAATTCTAGTTTGTT[C/T]TTTCCAATCTACCTT | 4734 |
rs577157487 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849878 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAT | 4734 |
rs577187289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907641 | TGTTTAAGAGGGTTC[A/C]GTCTTTCAGCCTTGT | 4734 |
rs577190924 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983539 | CTGCTAACTCCTATT[C/G]ATCCTTAGTTTCAAT | 4734 |
rs577201825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55851502 | TTTTTTTCAGATGGA[A/G]TTTCGCTCTTGTTGC | 4734 |
rs577220154 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850462 | AGGTTATACTAATAC[A/G]TACTTAAAGATTTTA | 4734 |
rs577228504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55983315 | GCGTGCGCGCGCGTG[C/T]GTGCATTTGATTTCC | 4734 |
rs577246935 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992564 | AGCCAACAAGAAAGC[-/A]AAAAACTTGATTTTT | 4734 |
rs577255040 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995404 | AAGTCATTTGAATTT[A/C]AGTTAATTCAGTGTC | 4734 |
rs577283609 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990721 | AGTTTTCCCACCTCC[A/G]TATCACAGGGAGGTG | 4734 |
rs577303539 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900646 | TATAAGAGAGCTTTA[A/T]AAAAGCCCTATCAGA | 4734 |
rs577326468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844799 | CGGCTTTCAAGCACC[A/G]GTTTTCAATTTTTTT | 4734 |
rs577332886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977263 | TTCCTTTTCTATGTT[C/T]TGGTACACAATATTT | 4734 |
rs577346105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862682 | TATTAAAATTAAGAC[A/G]CAATTAAAAGGGTAG | 4734 |
rs577353857 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55948244 | GAATCCAACTTACAA[C/G]GGATGTGAAGGACCT | 4734 |
rs577400214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835075 | TTTAAAACAAAGCAA[A/G]ACAAACAAACAAACA | 4734 |
rs577401983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842419 | TGTTTTTGGAGACAG[C/T]TCTGTAGTCCAGGCT | 4734 |
rs577412162 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935717 | CCAAGCGTGGTGGCA[C/T]GCGCCTGTAGTCCCA | 4734 |
rs577439870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923763 | TGGCAATATCTTTAG[C/T]TGCCAGTATAATTAC | 4734 |
rs577451098 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55934423 | TGCTACGAACATTGG[C/T]GCGCAAGTTTTCTGT | 4734 |
rs577461544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862205 | AGGCACAAAATATCA[C/T]AGCCAAAAATTAGGA | 4734 |
rs577462380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835903 | TAGCCTTTAATGCTA[C/T]CTTCCTTCTCCCTCA | 4734 |
rs577471569 | snp | A/C | 8.39384e-05 | 0.00647782 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869560 | TTTTTAGTTTAACCA[A/C]ATATTTATAAAATCT | 4734 |
rs577480970 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953465 | TTTTTTTTTTGAGAT[A/G]AAGTCTCACTCTGTA | 4734 |
rs577493340 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NEDD4 | GRCh38.p7 | 15:55923056 | GGGCAAGGAGGCGGG[G/T]GCCTGTAATCCCAGC | 4734 |
rs577540735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952732 | AACTTTGGAGCCTTG[C/T]GTCATCTGTTCTCAC | 4734 |
rs577555443 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828239 | ATCATGTTATACCCC[A/C]ACAAACTTAAACCAA | 4734 |
rs577583013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873059 | CTTCTCTGATGTTCT[A/G]CATTGTTAACTACCC | 4734 |
rs577592275 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849242 | TCTTTCTTTTTTTCT[A/G]AGGTGGAGTGTCGCT | 4734 |
rs577607521 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827185 | TGATGAAATGCATTT[G/T]TAATACAATTTTGTT | 4734 |
rs577631266 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918289 | TTCAGTTTACTAGGC[A/G]ATCAAAATTTAATAT | 4734 |
rs577655966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960567 | TGAGGTTTTGGGACT[C/T]TGACTGGCTTCCTTG | 4734 |
rs577678460 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | NEDD4 | GRCh38.p7 | 15:55976006 | TCCTTTTTGACAAAG[-/A]GTGCCATGAACACAC | 4734 |
rs577691544 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917543 | ATGAATTAAAACTTT[A/G]GCACTACATCAAATA | 4734 |
rs577691969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55968149 | CCCATTCTCCCTTCA[A/C]ATTTTTTCATGGATC | 4734 |
rs577714240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960125 | TTGCTCCACTGACCC[A/C]ATACCCCCAAAGGAC | 4734 |
rs577714979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD4 | GRCh38.p7 | 15:55974210 | TACAACCTTCCAAGA[C/T]TGAACCATGAAGAAA | 4734 |
rs577737864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55839114 | GCTCACTGCAGCCTC[A/G]ACCTCCTTGACTCAA | 4734 |
rs577740135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55967121 | AACTCCTGACCTCAG[A/G]TGATCTGCCTGCCTC | 4734 |
rs577780314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973788 | AAAGCAGTACTAAAA[C/G]AGAAGCTTATAGCTA | 4734 |
rs577799879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55831816 | GACTTGTAGTCCCCA[A/G]GTCAATCCTAATCTT | 4734 |
rs577812785 | snp | A/G | 0.000162813 | 0.0090211 | missense, intron-variant, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55873959 | ACACCTATACCAACC[A/G]GTAATGGATAAAGTG | 4734 |
rs577814717 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903133 | ACTTGATCTGGACTA[C/T]ACATTCTTCAGAGTG | 4734 |
rs577836645 | snp | G/T | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826643 | TACAAGAATGGCTTC[G/T]TTGATGAGCAGCAAG | 4734 |
rs577855104 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925053 | AGCCTGGGCGACATA[C/G]AGAGACTCCATCTCA | 4734 |
rs577863904 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979644 | AGGCGTGAGCCACCG[C/T]GCCCGGCGAAAGTTT | 4734 |
rs577878182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871209 | GACTTGTGGCTATAA[A/G]AGATGGATACAGAAA | 4734 |
rs577883266 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898104 | TAGATTCAGATAAAA[C/G]TACCCCACTTAATAG | 4734 |
rs577919592 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944928 | GAGGGAACTGAGTGT[C/T]AGACGGAAAACTAAC | 4734 |
rs577921243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55973095 | GACAGAAAACCAACA[A/C]AGAAATGTTGGACTT | 4734 |
rs578025651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55977999 | ACAACAGCAAATAAT[A/G]TTACTTATCTTATTT | 4734 |
rs578081996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830707 | AATCTGGTTTATTTA[C/T]TTATATTTTAGAGAT | 4734 |
rs578094895 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942317 | TTAACATATTTTTTC[G/T]GGTGTTTGTATGGTA | 4734 |
rs578132735 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945722 | GTCAGATTCACCAAC[A/G]TTGAAATGAAGGAAA | 4734 |
rs578147010 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870698 | ACTGCCATGCCCGGT[A/T]AATTTTTGTATTTTT | 4734 |
rs578161748 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868475 | GAGGTAACTGAATCA[C/T]GAGAGTGAGTTTTTC | 4734 |
rs578189090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985238 | TATAGTTCCTTCTCC[C/T]TTTCTGTTCCTGGCG | 4734 |
rs578200057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858376 | CAATGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 4734 |
rs578246148 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55897056 | TTGGCTCACTGCAAG[C/G]TCCACCTCCCAGGTT | 4734 |
rs578246709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904949 | AATACAAAATTAGCC[A/G]GGTACGGTGGCACAT | 4734 |
rs578255007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55907769 | CATTTTATAAAACAA[C/T]GATAAACTGAAAGAA | 4734 |
rs578262288 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55904295 | TGTTCTATTTCCATA[A/C]ACCTTTTATTTTATT | 4734 |
rs578262647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55911550 | TTTTTTTTTTTTTGA[C/G]ACGGGGTTTCGCTCT | 4734 |
rs745372399 | snp | A/G | 3.29625e-05 | 0.00405958 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852463 | AGTCGTTCTGGAATT[A/G]TGATCTACATAATAT | 4734 |
rs745396767 | snp | A/G | 1.6517e-05 | 0.00287372 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840507 | CTTGTAAAATGGGCG[A/G]ATGAAAAAACCTTGC | 4734 |
rs745400493 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940772 | TTTAGGGGGCCCACC[C/T]TGGCCTCTCGAAGTG | 4734 |
rs745418424 | snp | A/G | 0.000247609 | 0.011124 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915930 | ATTTCACTAGGAGAA[A/G]TAATAAACTGGTGTG | 4734 |
rs745420125 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55848480 | TCACACATAAAATTT[A/T]TTACAAAAAATAACA | 4734 |
rs745427234 | snp | C/G | 1.799e-05 | 0.00299911 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863091 | CAGGCTGAAAAACAG[C/G]ATGGCAGCAATTAAG | 4734 |
rs745449263 | snp | A/G | 1.67548e-05 | 0.00289432 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852559 | CTAAAGTGAAGAATA[A/G]CAGAAGAATTAAATA | 4734 |
rs745470209 | snp | A/T | 3.29592e-05 | 0.00405938 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916486 | CATCCTTCAAGATAC[A/T]AGTAAACGAAGCATC | 4734 |
rs745494394 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921513 | TATTTTTAGTAGAGA[C/T]GCAGTTTCACCATGC | 4734 |
rs745520583 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920935 | GCTCTTTGTTTTGCT[A/G]GTAAACCGAGTTTCT | 4734 |
rs745525670 | snp | A/G | 1.73688e-05 | 0.00294688 | utr-variant-5-prime, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993605 | CCCCGCCCAGGGCAG[A/G]CAACTGTGGAGGAGG | 4734 |
rs745553291 | snp | A/G | 4.95323e-05 | 0.00497631 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833009 | TGGAAAATCCTTACC[A/G]TATAGTTCAGCAAAT | 4734 |
rs745560873 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55848914 | AGTAAATAAAGAACA[A/C]TACACACAAATTTTA | 4734 |
rs745570649 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855900 | CTTCAACTGACAAGC[C/G]CAGATACCACCCACA | 4734 |
rs745572371 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990479 | TACCACCACTACTTC[A/G]GTGACTTCCTATCAA | 4734 |
rs745604129 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951672 | AGACTATAAAATTCA[C/G]AGTTTTCCTTGTTAG | 4734 |
rs745624523 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851507 | TTCAGATGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 4734 |
rs745633810 | snp | C/T | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860558 | GTGGCTTCATCTTCT[C/T]TTATAATTTCCCAGT | 4734 |
rs745633827 | snp | C/T | 1.66905e-05 | 0.00288876 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848572 | TTCTCTCTTCCCATC[C/T]TGGCTATAATTAAAA | 4734 |
rs745638113 | in-del | -/A | 2.00519e-05 | 0.00316632 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834290 | TCAAAGAATCCCTAG[-/A]AAAAAAGATGTATTT | 4734 |
rs745665000 | snp | G/T | 1.76393e-05 | 0.00296974 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55834261 | AAAATTTTGATGAGA[G/T]CCTGTGGTATTAGTT | 4734 |
rs745677910 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864447 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 4734 |
rs745684734 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866338 | TTGTCTGCCCATCCA[C/T]GTTGATCTTCCTTCT | 4734 |
rs745697145 | snp | C/T | 4.94417e-05 | 0.00497176 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916493 | CAAGATACAAGTAAA[C/T]GAAGCATCATCACTA | 4734 |
rs745697625 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880923 | AATACTGGCGTATAT[A/G]ATGAAACCCCTGCTC | 4734 |
rs745716311 | snp | G/T | 1.66032e-05 | 0.0028812 | stop-gained, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916781 | GGTTTCTGACAAAGG[G/T]TAAGTATTGCTTCTT | 4734 |
rs745754852 | snp | C/T | 6.62789e-05 | 0.00575631 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915861 | GATAACCGAAGTCCA[C/T]TGACAGCTGTTGAAA | 4734 |
rs745785188 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969602 | AAAGCAGCAACCAGA[A/G]TCCTGAAGCCCCCAT | 4734 |
rs745803675 | in-del | -/CACACACT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836367 | ACACACACACACACA[-/CACACACT]TTAGAGACAAAGTTT | 4734 |
rs745808674 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939188 | ACCCAAATCTCATCT[C/T]GATCCGTAATCCCCA | 4734 |
rs745857869 | snp | A/C | 6.23655e-05 | 0.0055838 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838650 | TGTATCTATAACACA[A/C]CTGAAATTGCAAAAA | 4734 |
rs745873813 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955149 | ACCTCAGCCTCCCAA[A/G]TAGCGGGGACTACAG | 4734 |
rs745876987 | in-del | -/TTCTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870526 | TTCTTCTTCTTCTTC[-/TTCTT]TTCTTTTTTTTTTTT | 4734 |
rs745898213 | in-del | -/TTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898632 | TTTCACAAAAAGAAC[-/TTT]TTTTTTTTTTTTTTT | 4734 |
rs745898704 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977088 | GAAAATATGCATATC[A/G]TAGATTATTTATTTT | 4734 |
rs745899632 | snp | C/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995722 | GTAATTATTGTATCC[C/G]GGTCAACAGCTAGGA | 4734 |
rs745900526 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830016 | TGAAAGAACAGAGAG[A/G]AAGTGGTTATGAAAG | 4734 |
rs745912672 | snp | C/T | 9.89103e-05 | 0.00703174 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860506 | ATCCAAGTTACTTGA[C/T]GGTGGAGGTGATGGG | 4734 |
rs745928639 | snp | A/C | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850599 | CCCATTTGGTGCATG[A/C]CGGACTTCCCAGCCT | 4734 |
rs745936862 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912568 | AGGGTACTGAAATCT[C/T]TGAGCATCCTAACAA | 4734 |
rs745955300 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994656 | CAAAATCTAATTTTT[A/G]TTTTCCTCAATGATT | 4734 |
rs745967171 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875895 | TTAGAAAAACACAAG[A/C]TGAGACAGTCAATAA | 4734 |
rs745978190 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828900 | TGATACTAAAAATAT[A/T]AAAATGCGACTACAG | 4734 |
rs745982774 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860736 | AAATGCACGTTGTGC[C/T]TGCAGTTGAATGTTG | 4734 |
rs746001353 | in-del | -/GGAAAATCAT | 3.6064e-05 | 0.00424626 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873932 | AAAATAAGCCCAAAA[-/GGAAAATCAT]GGACACCTATACCAA | 4734 |
rs746019744 | in-del | -/T | 1.65168e-05 | 0.00287369 | frameshift-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852426 | ATTACAGGATACCTG[-/T]TACAGTGGGCTTTGT | 4734 |
rs746036747 | snp | A/T | 9.66324e-05 | 0.00695031 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872380 | ATGAAGAGATAAAAA[A/T]TTTAATATGCTATTA | 4734 |
rs746045907 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874934 | AGCCTGGACCATGCC[A/G]CTGCACTCCAGCTTG | 4734 |
rs746082002 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908623 | CTGAGACCTACTGAA[-/C]CAGAACCAGAATCTG | 4734 |
rs746091972 | snp | A/G | 1.64991e-05 | 0.00287215 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916048 | CTAAGGAGGAGTAAC[A/G]TTTTAGTGGAATTTT | 4734 |
rs746103211 | snp | A/C/G | 5.27369e-05 | 0.0051348 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993472 | GGCTGCTGAATAACC[A/C/G]GAAGGGAAGCCCGCC | 4734 |
rs746113797 | snp | C/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936729 | TGCATTGCACCTAAT[C/G]TGTTGCACTTTTTTC | 4734 |
rs746126578 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975882 | GGACTTCAAATTATA[C/T]TACAGAGTTATAGTA | 4734 |
rs746165007 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943823 | GGGAGATTGACTAAC[C/G]GCTTGCACTGTTTGC | 4734 |
rs746175321 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961376 | CCAAGACCCTGTAGC[A/C]GAGGACCCAGTTAAA | 4734 |
rs746188336 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885796 | AGGAAGAAAAAACTA[G/T]AAAACAACCAGAAAA | 4734 |
rs746203139 | snp | A/G | 3.36956e-05 | 0.00410447 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55837826 | TTCTGGATTCGGTTT[A/G]CAAATCGCCATTGTA | 4734 |
rs746207089 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869915 | ATGACACAAAGAAGA[C/T]GCTAAGGAAGTTTAA | 4734 |
rs746211690 | snp | C/T | 8.29442e-05 | 0.00643935 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55847024 | TTGTAATCCCTGGAG[C/T]AGGGCACTGCCTTTA | 4734 |
rs746236564 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915535 | CTCCATTGATATTTA[C/T]TTGACAATCTACATT | 4734 |
rs746243360 | snp | A/C | 3.3998e-05 | 0.00412284 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846944 | TATTGATGACTCTTA[A/C]GTATTTATTATAAAC | 4734 |
rs746245731 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922430 | TGCAATGGTGTTATC[-/T]TGGCTCACTGCAACC | 4734 |
rs746263158 | snp | A/G | 1.65353e-05 | 0.00287531 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856125 | ATGGGAGAGGGTAAA[A/G]CTCACCACAGGAAGT | 4734 |
rs746266205 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953114 | CCTGCCTAAGCCTCC[C/T]GAGTAGCTGGGACTG | 4734 |
rs746270852 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884258 | ACACATATGGCTGCA[A/G]CAACCAAAACTCAGA | 4734 |
rs746289497 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916560 | TACCTTGTTGGCTGT[A/G]GTGAAATCTGTAGAC | 4734 |
rs746298752 | snp | C/T | 6.60851e-05 | 0.00574789 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915684 | AATGTAGCTGCTTTT[C/T]GTTGGGTGAAATGCA | 4734 |
rs746318868 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860662 | GAAACTACTTATACC[C/T]CGGAAGACTCTCGGT | 4734 |
rs746320213 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898075 | AGAGGTGAAATCCAC[A/G]ACTCAAGTGGACTTA | 4734 |
rs746337323 | in-del | -/CA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867412 | TGAAGCAGTTCTCTC[-/CA]CAGAAACTCAACTGT | 4734 |
rs746348276 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942468 | CTCTGGTGATAGTAA[C/G]CGACTTCTTATGAGA | 4734 |
rs746367461 | in-del | -/GTGTGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964695 | AATTTTGCTGCTGGT[-/GTGTGT]GTGTGTGTGTGTGTG | 4734 |
rs746401342 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941991 | ACACTTGGGTATTAG[C/T]TGTAGTGTACTATAC | 4734 |
rs746412090 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956193 | TACATGAGATTACCC[A/C]TTCATTTGACAATGG | 4734 |
rs746435891 | snp | A/G | 5.66685e-05 | 0.00532269 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838079 | ACAAAATTATATCCA[A/G]TAAAATACATACTAA | 4734 |
rs746440429 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952550 | ATCCAAACTATCCTT[-/C]CCCCCAACTCCATTT | 4734 |
rs746463086 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950161 | ACAGAAATTTAGCTT[C/G]ATTTTTCTTCATTTG | 4734 |
rs746503117 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877292 | TAGTCTTTCTTTGTC[-/T]TTCATAATCTTGACA | 4734 |
rs746512029 | in-del | -/ATAAG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900970 | AGTGGTTTTTACAAA[-/ATAAG]ATGTTTATTTTAATG | 4734 |
rs746514808 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872812 | GTCTGCAGGCTGGCT[C/T]GGTTAGAGCATAGAG | 4734 |
rs746520548 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900149 | GATGCTTCTGGACAA[G/T]AACTCATCGTAAGGA | 4734 |
rs746526226 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989298 | TATTTATTCACTTCT[G/T]TAGTCCCTGCTCCAT | 4734 |
rs746528761 | snp | C/G | 3.29995e-05 | 0.00406185 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833020 | TACCGTATAGTTCAG[C/G]AAATCCATTCATAGG | 4734 |
rs746549611 | snp | G/T | 1.70217e-05 | 0.00291729 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852577 | GAAGAATTAAATACA[G/T]CAAGTTTAAGAATCC | 4734 |
rs746557945 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904447 | AGCTGGGATTACAGG[C/T]GTGCACCAACACGCC | 4734 |
rs746580869 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867889 | AGTAAAACTCTGTCT[C/G]TACTAAAAATACAAA | 4734 |
rs746613093 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919299 | TCAGGATTTTTCTTG[C/T]TGTTGTTGAAGTTGA | 4734 |
rs746614127 | snp | A/G | 1.64765e-05 | 0.00287019 | stop-gained, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916669 | GAGCTAGTGCAGTCT[A/G]TCTGGGAGTCAGCTT | 4734 |
rs746641654 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55936202 | TTACTCTCCGGTATC[-/A]TTGTTTTCCCTTCCA | 4734 |
rs746661355 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961255 | TTCCTAGAGTCTCAT[C/T]AGGGCAGGGCTAGAG | 4734 |
rs746670918 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960368 | AGCAGGCAGAACGTG[A/G]AAGGACTTGACTTGC | 4734 |
rs746729704 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925810 | CACACTGCACACCTC[-/TT]GAGGAAACCACTAAT | 4734 |
rs746737998 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844808 | AGCACCGGTTTTCAA[-/TT]TTTTTTTTTTTTTTT | 4734 |
rs746739678 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956456 | CTCATACTAATTTTC[G/T]GTATGATGTGTGGTA | 4734 |
rs746751419 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968616 | GATACCATATAGAAT[A/G]GCTAAGAAATACATG | 4734 |
rs746765217 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913295 | CTGTTTATTTATAAG[A/T]GAGTTACAATATACC | 4734 |
rs746765330 | snp | C/T | 1.65075e-05 | 0.00287289 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840552 | ATTTAGGATGATTAC[C/T]AAGTGAAAGAAAACA | 4734 |
rs746769078 | snp | G/T | 1.64942e-05 | 0.00287173 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848893 | TGGATCTTCCTTTTT[G/T]GGTAGAGTAAATAAA | 4734 |
rs746773197 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862207 | GCACAAAATATCATA[G/T]CCAAAAATTAGGAGG | 4734 |
rs746784217 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879820 | AAAAAAATTCTCAGA[A/G]AGTAGAACTAAAAGA | 4734 |
rs746789440 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843206 | TTCCTTTTGTAAATT[A/G]CCTGGTCTCAGGTAT | 4734 |
rs746832193 | snp | C/T | 6.47815e-05 | 0.00569092 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55951377 | AAATATATACTTACT[C/T]TGAATAATATTTCTT | 4734 |
rs746852384 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891075 | ATATTTGTTGTTCAT[G/T]GGTTGTCTTTGGGAA | 4734 |
rs746859157 | in-del | -/G | 1.71405e-05 | 0.00292745 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848607 | ATTTCAATTATTTTA[-/G]GAGAGGGGCGTAGAT | 4734 |
rs746905814 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967213 | TAATAACTACTTAGA[A/G]AAGGTTATTTTTTTA | 4734 |
rs746916447 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938227 | AGCTGGGCATGGTGG[C/T]GTGTGCCTGTAGTCC | 4734 |
rs746944423 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951045 | ATTCACTTGATAGGC[C/T]CTAATCTGTTTAATA | 4734 |
rs746961160 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977329 | GTATCATGCTGTAAA[G/T]GTTTGTAGACTAGGA | 4734 |
rs746975011 | snp | A/T | 3.29739e-05 | 0.00406028 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830609 | GAAGAATTTATTTGG[A/T]TTCATTTACTCTCTA | 4734 |
rs746976966 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855400 | CAGTCTGCTTGGAAG[-/A]AAAAAGCATAGACAG | 4734 |
rs746998179 | snp | A/G | 0.000248425 | 0.0111423 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840682 | AGAGAGGTGATCTTC[A/G]TTACACAATCCAGAG | 4734 |
rs747018660 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994246 | TTGTAAACAGTGCCA[A/G]TTCCTAAGCTATTTG | 4734 |
rs747032435 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874852 | GGTGGCACATGCCTG[C/T]AATCCCAGCTACTTG | 4734 |
rs747043017 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827737 | ATCCATATTATTTAT[A/C]TATTTAATATCAGAA | 4734 |
rs747060102 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841984 | AAACATTTCCTTTGA[C/G]ATCAGGAAGAACCAT | 4734 |
rs747077580 | snp | A/C | 1.71179e-05 | 0.00292552 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850736 | GCTGACTGGTCTCCA[A/C]TGTGGCCTAGCACAT | 4734 |
rs747085371 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888651 | GAATAGCCAGAGGCA[C/T]CCTAAGCAAAAAGAA | 4734 |
rs747104209 | snp | A/C | 3.30126e-05 | 0.00406266 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916260 | GGTGGAAAAGTATAA[A/C]TACTACTGTCACTGA | 4734 |
rs747111533 | snp | A/C | 1.64841e-05 | 0.00287085 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916361 | GTAAGACCCATTATC[A/C]CTGGTTGAAAAGTTA | 4734 |
rs747130212 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873278 | TGGACAGTGATAACA[C/T]TCAATCCTTCCAGTC | 4734 |
rs747143959 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839570 | ACATTGTGTGAGGCT[-/G]ATTCAGCAGCACAGG | 4734 |
rs747150036 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936587 | TGCATATATATACAT[C/T]ACATAAATCTAATAT | 4734 |
rs747191355 | in-del | -/AAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951595 | GTAAGGATCACTGTT[-/AAA]AAAAAAAAAAAAAAG | 4734 |
rs747201464 | snp | G/T | 3.49926e-05 | 0.00418271 | stop-gained, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915311 | AGACAGTTCATTTGT[G/T]CAATCTCTGTTGCTG | 4734 |
rs747204245 | in-del | -/A | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826553 | CTGAGAGGAAGGAGG[-/A]AAAAGACACTTCGTT | 4734 |
rs747220690 | in-del | -/A | 1.64906e-05 | 0.00287142 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915558 | CTACATTTTGGGAGG[-/A]ATGGCAAACATGCAG | 4734 |
rs747242532 | in-del | -/TTTTTTTTTTTTTTTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974907 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTT]TTTTTGAGATGGAGT | 4734 |
rs747272366 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839170 | AGTAGCTGGGACTAC[-/A]GGCGCGCACCACCAC | 4734 |
rs747281511 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944481 | GGTAAACAAAGCAGC[C/T]GGGAAGCTGAAACTA | 4734 |
rs747317636 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970953 | CTAAATAGGGCACCA[A/G]TGACCAATTCCAGAG | 4734 |
rs747317721 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983023 | GCTACTCGGGAGGCT[A/G]AGGGAGGAGAATCAC | 4734 |
rs747321821 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846604 | CATAAAAAAATCCAG[A/C]CCGTCCTCCAACACA | 4734 |
rs747333110 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985788 | ACACACACACACACA[C/T]GCTTAACTGTTCAGA | 4734 |
rs747348587 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55833698 | GATTGAATGGCATAC[A/G]TATTTCTCTATGAGA | 4734 |
rs747356914 | snp | G/T | 1.66696e-05 | 0.00288696 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838212 | TAACTTGATATGTTA[G/T]TTTAGCGAGAAAAAT | 4734 |
rs747383393 | snp | C/G/T | 3.29696e-05 | 0.00406001 | missense, synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860742 | ACGTTGTGCTTGCAG[C/G/T]TGAATGTTGCCATTC | 4734 |
rs747404246 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941944 | ATGTGGTCTATCTTG[A/G]TAAATGTTCCATGGG | 4734 |
rs747412275 | snp | C/G | 3.29473e-05 | 0.00405864 | splice-donor-variant | NEDD4 | GRCh38.p7 | 15:55848371 | TGGCAGAGAGACTTA[C/G]TGGTCCAGTTATTGC | 4734 |
rs747423211 | snp | A/G | 3.30437e-05 | 0.00406457 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915694 | CTTTTCGTTGGGTGA[A/G]ATGCACTGAAACACA | 4734 |
rs747425566 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853310 | AACAACCCTAATAAA[A/C]CATACCAACAATAAC | 4734 |
rs747425648 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883573 | TTACAGCAGGCCTTG[A/G]GCGAGACTCAGTGCT | 4734 |
rs747463586 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984357 | TGAACAAATCAGAAT[C/T]TCATATTCCTTATCT | 4734 |
rs747476638 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855448 | GGCTTCTGTTGGGGG[-/A]TAAGGAGAAGGGTAG | 4734 |
rs747478841 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929653 | TAACTAAAATTGTAA[C/T]ATATAATTGTTAAAT | 4734 |
rs747496892 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955067 | GCAACGTTGCCCAGG[A/C]TGGAGTGCAGTGCTG | 4734 |
rs747564480 | snp | C/T | 2.00058e-05 | 0.00316267 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829876 | ATGGCAGTAAAAACA[C/T]TACAGATTGTTATTT | 4734 |
rs747566313 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828819 | TAGTAATAAATTTAA[C/T]ACAAATTATGCATTA | 4734 |
rs747569297 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859016 | CACTAGAATGTAAGT[C/T]CCATGAAGGCAGGAG | 4734 |
rs747606258 | in-del | -/C | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938071 | GGACAGTCTCTTCAA[-/C]AAATGGTGGCCAGGC | 4734 |
rs747608721 | snp | C/T | 0.000165046 | 0.00908273 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916762 | TATCCAAGTCATCTC[C/T]GGAGGTTTCTGACAA | 4734 |
rs747619627 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834675 | TGTGAACCTGTGGTC[C/T]CAGCTACTGGGGAGG | 4734 |
rs747636872 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848381 | ACTTACTGGTCCAGT[C/T]ATTGCTACATTCTCC | 4734 |
rs747661064 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867825 | CTTTGGGAAGCCGAG[A/G]CGGATGGACGGCTTG | 4734 |
rs747672661 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955309 | ATTATAGGTTATAGG[C/T]ATCAGCCACCATACC | 4734 |
rs747677757 | snp | A/T | 1.74854e-05 | 0.00295676 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847076 | AAGAAGTTTAGGTTG[A/T]TTTTATTCTGGAACA | 4734 |
rs747678021 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897817 | CAAGTTGTCTTCCTT[-/A]ACGAAGGGGTGATCC | 4734 |
rs747682970 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903334 | GGTGCTTTAAAATAC[A/G]TAATGGAGTTGCGTT | 4734 |
rs747688203 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872340 | TTTAAACCCTGAATT[C/T]CTAATAAGGCTACTG | 4734 |
rs747688279 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881346 | GGGTTTCACCATGTT[A/G]GCCAGGCTGGTCTTG | 4734 |
rs747699916 | snp | C/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917871 | GATAGTTTGAACACA[C/T]AGGATATTTTATTCC | 4734 |
rs747725847 | snp | A/G | 1.68744e-05 | 0.00290463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860370 | ATATGCATAATATAA[A/G]CTACTGAAGCCGTAA | 4734 |
rs747744115 | snp | A/T | 1.64757e-05 | 0.00287012 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916680 | GTCTGTCTGGGAGTC[A/T]GCTTCATTTGAACAA | 4734 |
rs747754930 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929509 | ACCCTCAAGCAGGCC[A/G]CGGTGTCTATTGTTC | 4734 |
rs747765939 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940955 | ATATCCATATTTTCT[A/G]TTTCTACTTATATTG | 4734 |
rs747826064 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970848 | AGACTGTGAAGATTA[G/T]AATAAATACCTAACT | 4734 |
rs747864089 | in-del | -/CTCTCTCTGC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940538 | TCTCTCTCTCTCTCT[-/CTCTCTCTGC]CTCTCTGCCTCTCTC | 4734 |
rs747872562 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956680 | ATATATCTATTCTCA[-/T]TGCCACTGCCACTCT | 4734 |
rs747882191 | snp | A/G | 9.67258e-05 | 0.00695367 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872368 | CTGTAAGGTGTAATG[A/G]AGAGATAAAAAATTT | 4734 |
rs747893773 | snp | C/G | 1.7348e-05 | 0.00294512 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842175 | CATTCTGAAAATCCA[C/G]AGGAGAGACGTACTG | 4734 |
rs747918878 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850579 | TGGTCAATAAAGAAA[G/T]GCCTCCCATTTGGTG | 4734 |
rs747921966 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977232 | GGTGGTCCCATAAAA[C/T]ACCACATTTTTACTT | 4734 |
rs747943707 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855518 | CAAAAACAAGTAGGG[C/T]TTCTGGAAAACAGAG | 4734 |
rs747945706 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841171 | ACTCCTGGCATTGTG[A/T]TCCACCAGCCTTGGC | 4734 |
rs747968382 | snp | G/T | 1.65132e-05 | 0.00287339 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856148 | CAGGAAGTGTAGGTT[G/T]TTCCTCAAAAGTATA | 4734 |
rs747969745 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890692 | TTTCTCTTGGATATA[C/T]ACTCAGGAACAGAAT | 4734 |
rs747992988 | snp | C/G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904252 | AATATTAAACTCTAC[C/G/T]AGAAGGCTGTTAGGG | 4734 |
rs748010103 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937294 | TCAACAGACATTTTT[A/G]TGGCGAATACATTCA | 4734 |
rs748026671 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845690 | CATTAACAATGAAAA[C/T]ATTTAGCAGAACAAT | 4734 |
rs748059797 | snp | C/T | 9.48542e-05 | 0.00688608 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872526 | ATAACACCAAAAGCA[C/T]GTACTTTTCAAGAAT | 4734 |
rs748067047 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950021 | AATAAAACAAAAGTA[C/T]AAATAAATAAATAAC | 4734 |
rs748067066 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936773 | AAAGTGTAGATTTTA[A/G]TTATAATTTGCTATT | 4734 |
rs748086871 | snp | A/G | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55919066 | GTATTTGGTCAGATA[A/G]ATGTCTTCTCTTTGG | 4734 |
rs748091255 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869093 | TGTCATCCATGAAAA[C/T]TGTTAAATTCTACTT | 4734 |
rs748114231 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945752 | AAAATGTTAAGGGCG[G/T]CCACAGAGAAAGGTG | 4734 |
rs748121665 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965328 | TGACTCAGTCACCCA[C/T]GTAGCCAGGAGTACA | 4734 |
rs748130098 | snp | C/T | | | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838121 | CTAAATATATTCCTT[C/T]TTGTTCTTATTGGTG | 4734 |
rs748172651 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966330 | TACCAAGAGATTTAG[C/T]AAACCACCAACTGGT | 4734 |
rs748183523 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973576 | TAAAATCTTAAAAGT[A/G]TCTTCTCTGACTACA | 4734 |
rs748199134 | snp | C/G | 1.78966e-05 | 0.00299132 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55834267 | TTGATGAGATCCTGT[C/G]GTATTAGTTCAAAGA | 4734 |
rs748219295 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887587 | CCAATCCTACTCAAA[A/C]AATTCTGAAAAACAG | 4734 |
rs748223474 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859205 | TTCTACTCAATCTCC[C/T]TTGATGATACATATT | 4734 |
rs748230421 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934265 | AGTATAATGATTTCA[A/G]GGTTCATCCAAGTTG | 4734 |
rs748245247 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851220 | ATGGCAAATATCTAC[C/T]ACAGAAATGGATAAT | 4734 |
rs748247615 | snp | G/T | 4.94539e-05 | 0.00497238 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915425 | GTGCTTAAGGCTGGA[G/T]AGACAGGAAATATTT | 4734 |
rs748261860 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951103 | ATTTGCATCATCTTT[A/G]TGAGAAAACACTGAA | 4734 |
rs748268494 | snp | C/T | 4.94556e-05 | 0.00497246 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916461 | TCGACCACAGCACTA[C/T]TGTAAATACCATCCT | 4734 |
rs748275293 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916328 | TGCACATGACCCAAA[A/G]TCACTACCGTTGCTG | 4734 |
rs748276596 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862600 | CAAACTACAAGAATT[A/C]TCCAAGACTTCTAAT | 4734 |
rs748358091 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900267 | CAGGACTGGATTTGT[A/T]TTAGAGCGCATGGGA | 4734 |
rs748364228 | snp | C/T | 3.49071e-05 | 0.0041776 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924625 | TTACTTCATATTTCA[C/T]ATAAGCACAATATAA | 4734 |
rs748379995 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973059 | TCAATATCCCACTTT[C/T]GGCACTGGATAGATC | 4734 |
rs748388934 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942783 | TGTGGAAGCAAGTTT[A/T]GAAGTGGGTAATGGA | 4734 |
rs748389427 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957303 | TTCTTTGCCATACTA[C/T]ATGGCTAAAATATAT | 4734 |
rs748389990 | in-del | -/AATAAATAAATA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892275 | CCAACTCAATAAATA[-/AATAAATAAATA]AATAAATAAATAAAT | 4734 |
rs748443339 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849414 | ATATTTAATAGAGAC[A/G]GGGTTTCTCCATGTT | 4734 |
rs748443347 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863925 | TGGAAAAGTCATTCT[C/G]ATTCCCTTGTCTGAT | 4734 |
rs748449851 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973393 | AACAAACAAAAAAAC[A/C]ACAACAAAAAAACAG | 4734 |
rs748456020 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984028 | AATCGGTAAAGTATA[A/T]TCTATATCATTATAC | 4734 |
rs748464479 | snp | C/T | 1.69341e-05 | 0.00290977 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55837794 | AAATGAATACCTCTT[C/T]AAAAGCAGCCATTTG | 4734 |
rs748471042 | in-del | -/ATCTAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958704 | CTTTCAATAATAAAC[-/ATCTAT]TAAAGTTTTGTATTT | 4734 |
rs748476451 | in-del | -/TATCTATCC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960668 | TCCCCTTCATATATA[-/TATCTATCC]TATCTATCCTATTAG | 4734 |
rs748479398 | snp | A/G | 1.73682e-05 | 0.00294683 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829912 | CTAATCAACTCCATC[A/G]AAGCCCTGGGTGTTT | 4734 |
rs748518114 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992680 | CACAGAAGCCACATA[C/T]CATTTACGACGGAAC | 4734 |
rs748521566 | snp | A/G | 1.85927e-05 | 0.00304894 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850746 | CTCCACTGTGGCCTA[A/G]CACATTAATGAAATC | 4734 |
rs748526558 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953871 | GACTACAGGCGCCTG[C/T]CACCACGCTTGGCTA | 4734 |
rs748528734 | in-del | -/AAAA | 0.000721848 | 0.0189843 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951595 | GTAAGGATCACTGTT[-/AAAA]AAAAAAAAAAAAAGA | 4734 |
rs748545652 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55878906 | CGACTCACTGCAACC[C/T]CCGCCTCCCTCGTTC | 4734 |
rs748553716 | snp | C/G | 3.40785e-05 | 0.00412772 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862882 | GTTAAAGTGTTTCCA[C/G]ATTAAAATTGTGAAA | 4734 |
rs748593765 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873074 | GCATTGTTAACTACC[C/G]AGTCTGCCTTGAAAC | 4734 |
rs748609751 | snp | C/G/T | 3.29702e-05 | 0.00406008 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916375 | CACTGGTTGAAAAGT[C/G/T]ACTAAGGCTACCACT | 4734 |
rs748629301 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908570 | ATTACCAGCATTGGT[A/G]CGATCTGTTATAAAT | 4734 |
rs748658998 | snp | C/T | 1.70333e-05 | 0.00291828 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993545 | AACACCTCCACCGCG[C/T]AAGTTGCCATTTCCG | 4734 |
rs748664857 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952975 | CTGTAATCACGTTTC[A/G]TGTATTAATTCTTTT | 4734 |
rs748674876 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827387 | CAGACCACGAGCCCC[C/T]AGTGGGAGATGAAGG | 4734 |
rs748703164 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839174 | GCTGGGACTACAGGC[A/G]CGCACCACCACGCCT | 4734 |
rs748705432 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935477 | ATGGGGTAGGAAATA[G/T]GCACATTACACAATT | 4734 |
rs748710051 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991712 | AACTTCCTAGAAGTA[C/T]AAATCCTTCAGCAAG | 4734 |
rs748729687 | snp | A/C | 3.29734e-05 | 0.00406025 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852445 | AGTGGGCTTTGTCCA[A/C]GTAGTCGTTCTGGAA | 4734 |
rs748736517 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898633 | TTCACAAAAAGAACT[-/TT]TTTTTTTTTTTTTTT | 4734 |
rs748752737 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842039 | AATCCCTTTTCACCA[C/T]CAAACTCAATCCACA | 4734 |
rs748758314 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845032 | ATTCTAAGTGTTCTG[A/C]TCTTTTGCTATGATG | 4734 |
rs748762298 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832477 | TGAACTACAGTGGTG[C/G]GATCTTGGCTCACTG | 4734 |
rs748765362 | snp | A/G | 1.84568e-05 | 0.00303777 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838623 | GATGGGAAAAATTAC[A/G]TATTTAAAATTTGTA | 4734 |
rs748813292 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844211 | AAGGGAAAGAAGGCA[A/G]GGATTATAGGGGAAA | 4734 |
rs748821658 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968528 | TATACATCATTGAGA[A/C]AAATGATAATTATCC | 4734 |
rs748832479 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920207 | TATATATTCATATAT[G/T]ATACATAATTTCATA | 4734 |
rs748835437 | snp | C/G | 1.66266e-05 | 0.00288323 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863058 | AAGCAGCATCTGGTT[C/G]GTCCAAAACAACCCA | 4734 |
rs748844962 | snp | C/T | 3.56652e-05 | 0.00422272 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916854 | CATTTCCAAACATGT[C/T]AAGGGCTGAAAGTCA | 4734 |
rs748853445 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832541 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 4734 |
rs748854523 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894852 | GTTGTGTCCGTATCA[A/C]ATATAAATAGGATTT | 4734 |
rs748855054 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940602 | CACTATGTTGCCCAC[A/G]GTATCCTCGAATTCC | 4734 |
rs748855662 | snp | C/T | 5.10782e-05 | 0.00505336 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993552 | CCACCGCGCAAGTTG[C/T]CATTTCCGAACGCTT | 4734 |
rs748856558 | snp | A/C | 1.65214e-05 | 0.0028741 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848514 | TGAAAAATCGCACTG[A/C]ACATACTGTGATTTA | 4734 |
rs748859082 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55946556 | CCCACACAATAATAA[C/T]GGGAGACTTTAACAC | 4734 |
rs748884997 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909513 | CAATACTTTGGATTA[C/T]TTCCAGGGTATGCTG | 4734 |
rs748887166 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928516 | CCCCCTGCCCAACCA[A/C]ATATGCATCTACCCT | 4734 |
rs748906357 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939310 | GATCTGACAGTTTTA[C/T]AAAGGGTTCCTCCCC | 4734 |
rs748977171 | in-del | -/TTATG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867022 | GGTACAACCAACATT[-/TTATG]TTAATTTTGTAAAAT | 4734 |
rs748986966 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970044 | CACTGCCCTAAAGGG[A/C]GAGACCCAGGCCTGG | 4734 |
rs749000205 | snp | C/T | 1.65263e-05 | 0.00287452 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840493 | TTGTGAAGCATCATC[C/T]TGTAAAATGGGCGGA | 4734 |
rs749025176 | snp | C/T | 3.35672e-05 | 0.00409664 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860381 | ATAAACTACTGAAGC[C/T]GTAACAAAATCTAAG | 4734 |
rs749030952 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975133 | CCTGACCTCAGGCAA[C/T]CCACCCACCTCGGCC | 4734 |
rs749048064 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841965 | ACAACCCATAATAAG[A/G]GTTAAACATTTCCTT | 4734 |
rs749075110 | snp | C/T | 1.79835e-05 | 0.00299857 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915286 | AAAGGAAACTTACCT[C/T]GCAAGAATTAGACAG | 4734 |
rs749092252 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870234 | AGAATTTGGGGGATA[A/G]AGAAAGGTATCCTCA | 4734 |
rs749092459 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927100 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAAAGA | 4734 |
rs749106039 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935727 | TGGCATGCGCCTGTA[A/G]TCCCAGCTACTCGGG | 4734 |
rs749111892 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867737 | CAAACCAGGGGCTAT[A/C]TATACTCTGTGATTT | 4734 |
rs749121566 | snp | A/T | 1.67871e-05 | 0.00289711 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834013 | TATCAAAAAGTAAGT[A/T]ATGAAAATAGAAGTT | 4734 |
rs749128962 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978305 | GTTATTTTAAATGCT[-/AA]GATTAATTGATAAGC | 4734 |
rs749133184 | snp | C/T | 5.22534e-05 | 0.00511116 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873951 | AATCATGGACACCTA[C/T]ACCAACCGGTAATGG | 4734 |
rs749142744 | snp | A/G | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917564 | ACATCAAATAGATAC[A/G]TATTTTAGCTTCCAA | 4734 |
rs749145366 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903183 | TGTAGTCAGCCCAAA[C/T]GGAATTTTTCCTTTA | 4734 |
rs749161403 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944563 | TCTGTGAGCAGGGCA[C/T]AGCTGAACAAAATGC | 4734 |
rs749184478 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860464 | GGTGAGTCTGGCATT[C/T]AATTCTTCTGCAAGA | 4734 |
rs749185001 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929451 | GTAATAAGCATAGTA[C/T]CCAACAGGCAGCTTT | 4734 |
rs749212387 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960190 | ATGGGTAATATTGAG[C/T]GTCAACTTCATTAGA | 4734 |
rs749273671 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959055 | TATTTCTTCCCTCTA[C/T]TTATTTTAGAATTCA | 4734 |
rs749283319 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907950 | TGGAAACTAATCCTT[C/G]AGTCACGATCATAAT | 4734 |
rs749305584 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849089 | AATATCAAAAGGAAT[A/C]ACGATCAGTTCTCAG | 4734 |
rs749312195 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965893 | TGACCCTCAACTGAT[-/C]CGCCTGCCTCGGCCT | 4734 |
rs749313575 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55987413 | AAAATTTTCTCCCAT[G/T]TTGTAGGTTGCCTGT | 4734 |
rs749329005 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983948 | CACTGTTTTCCTTAA[C/T]AACACTTATAAAATA | 4734 |
rs749334756 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910531 | CCAAAGTTGGTGGTC[A/C]CCAAAATTATAATTT | 4734 |
rs749380111 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914271 | TTAAGGTTTTTTCCC[C/T]CCAAAACTATGATGT | 4734 |
rs749394295 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942597 | ATTGTTAAGTTTCCT[A/G]AGGCCCCCTCATCCA | 4734 |
rs749409580 | snp | A/G | 3.29783e-05 | 0.00406055 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915528 | TCCAATTCTCCATTG[A/G]TATTTATTTGACAAT | 4734 |
rs749411345 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862191 | GCTTGGCATATATCA[C/G]GCACAAAATATCATA | 4734 |
rs749411472 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860603 | AATAAGCTTGAGCCA[C/T]ACATACTTTATTGCT | 4734 |
rs749421973 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898323 | GAATCTAAAAGTTAC[A/G]AACTACTGAACTTCA | 4734 |
rs749432890 | in-del | -/CACACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836367 | ACACACACACACACA[-/CACACAC]TTTAGAGACAAAGTT | 4734 |
rs749445280 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956374 | TACTGTTCACGTAAA[C/T]TTTGTGTAACCCAAT | 4734 |
rs749459699 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830994 | CATGATCTCGGCTCA[A/G]TGCAACCTCTGGCTC | 4734 |
rs749464387 | snp | G/T | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860565 | CATCTTCTCTTATAA[G/T]TTCCCAGTTCTAAAA | 4734 |
rs749479659 | snp | A/C/T | 4.95138e-05 | 0.00497543 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915966 | TGATAGGATCCTTTG[A/C/T]TCAGAAGAGTACACA | 4734 |
rs749488080 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912864 | CATATGCCAGTCACT[A/G]TTATGTTGTTTGCTA | 4734 |
rs749545515 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963455 | TTGCATTATTTTTTA[C/T]TGGTTTCTCTGGATA | 4734 |
rs749584280 | snp | A/C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872771 | TTAGTATGTTAACAT[A/C/T]CCAAAAGAACACGGA | 4734 |
rs749606856 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908363 | TTGCCATATCTCCAT[C/G]TTTAACTTTTTTTTC | 4734 |
rs749633708 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857223 | TATGTATGCATGTGA[C/T]TTATCACCAGCAAAT | 4734 |
rs749651566 | snp | A/G | 1.67047e-05 | 0.00288999 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852555 | AAAGCTAAAGTGAAG[A/G]ATAACAGAAGAATTA | 4734 |
rs749656595 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835108 | CAAAAACTAATGACT[A/C]TCTTTTTCCCTTCAC | 4734 |
rs749657138 | snp | C/T | 1.64787e-05 | 0.00287038 | splice-acceptor-variant | NEDD4 | GRCh38.p7 | 15:55830588 | TGGTCCATTTGAACC[C/T]ATAAGGAAGAATTTA | 4734 |
rs749676885 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837880 | ATTTCATTTTCATGT[G/T]AACCAAGACAAAATT | 4734 |
rs749687699 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896127 | TGCAATGATCCTATA[-/T]TTTTGCCCTCTCAAG | 4734 |
rs749707107 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916552 | ATCCACTGTACCTTG[C/T]TGGCTGTAGTGAAAT | 4734 |
rs749712759 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921737 | AACTGTTAATATCAA[A/C]GGCAATACTTTTTTC | 4734 |
rs749793244 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962489 | ACTCTTGTCATGCAG[C/G]CTGAAGTGCAGTGGC | 4734 |
rs749838184 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972971 | TCCAACACTGAAATA[C/G]CCAGTTATATAAAGC | 4734 |
rs749845519 | in-del | -/CTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983505 | TTACTCAATGGGGTT[-/CTA]TTGCCCCACTCTTCA | 4734 |
rs749871279 | snp | C/T | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826655 | TTCTTTGATGAGCAG[C/T]AAGGTGCCTGAAATC | 4734 |
rs749876652 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55850831 | CTTAACCTGCAAATA[C/G]AATACACACCCTCCA | 4734 |
rs749878041 | snp | C/G | 1.71205e-05 | 0.00292574 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846936 | CATCTATATATTGAT[C/G]ACTCTTAAGTATTTA | 4734 |
rs749896315 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904443 | GAGTAGCTGGGATTA[C/T]AGGCGTGCACCAACA | 4734 |
rs749898040 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909448 | CTTCATCTGACCATG[C/G]TCTCCCAATTTTACA | 4734 |
rs749904706 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874149 | CAATGGAAAATAAAA[A/T]GTAATGTGGTACAAC | 4734 |
rs749912748 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850548 | CAAAGTTACCCAGGT[A/G]GTGGTTTTAGTGTTG | 4734 |
rs749912840 | in-del | -/GGTGTGTG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964650 | CTGAATTTTGCTGCT[-/GGTGTGTG]TGTGTGTGTGTGTGT | 4734 |
rs749926103 | snp | A/G | 1.6495e-05 | 0.0028718 | stop-gained, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916003 | TTGGAGAAGTCGGTC[A/G]GGTAGTTGAAGGACT | 4734 |
rs749933715 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924203 | ACAGATTTCCTCTGT[A/G]GAAGAGTGGGGATGA | 4734 |
rs749938704 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961441 | GACAATAAATGTACG[A/T]TCTTTTAAGCAACTA | 4734 |
rs749964316 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860699 | CACTTTCTGTTTCCT[C/T]GGATATCTGCCGCCT | 4734 |
rs749967991 | in-del | -/TAGT | 5.14112e-05 | 0.00506981 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862865 | CAAAATGAAAATTCG[-/TAGT]TAAAGTGTTTCCAGA | 4734 |
rs750006882 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906694 | GTAAATGACGAGTTA[A/G]TGGGTGCAGCACACC | 4734 |
rs750007782 | snp | C/T | 1.71396e-05 | 0.00292737 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869675 | ACCTTTAACTCTTGA[C/T]TTGTGACTGTAGAAA | 4734 |
rs750015988 | snp | C/T | 1.65302e-05 | 0.00287486 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916135 | GGACAAAAGGATCTG[C/T]ACTTGTACTTCTTGA | 4734 |
rs750018604 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974383 | AACTATTTCAAAAAA[C/T]AGAGGAGGAGGAATA | 4734 |
rs750064400 | in-del | -/A | 1.64781e-05 | 0.00287033 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848442 | ATATCTGAAGGGAAG[-/A]AAAAGAAAAAAGATG | 4734 |
rs750092706 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890496 | TTACTTAGTATGTTT[-/C]CAAGATTCATCCATA | 4734 |
rs750104896 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944156 | AGTGGGTGCAGCCCA[C/G]AGAGGGCAAGCCGAA | 4734 |
rs750104966 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933969 | GACCATTCTGGCCAA[A/C]AGGGTGAAACCTCGT | 4734 |
rs750130339 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852171 | TGTGGTGGCGGGCAC[C/T]TGTAATCCCATCTAC | 4734 |
rs750134492 | snp | A/G | 1.6943e-05 | 0.00291053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840763 | AAATACTTCATTTGA[A/G]AAACTTTAATATGAC | 4734 |
rs750150433 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886677 | GCAGGAGAACTGCTT[C/G]AACCCAGGAGACAGA | 4734 |
rs750165932 | snp | A/C | 1.72359e-05 | 0.00293558 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837776 | GGAAGAGCAAATAAA[A/C]GAAAATGAATACCTC | 4734 |
rs750179860 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930387 | TTAAGACTAGCCTTG[A/G]AAGATGTGAGAAAAA | 4734 |
rs750182050 | snp | C/T | 1.6531e-05 | 0.00287493 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55846969 | ATAAACATGACTAAC[C/T]TGCTTCTTCAACTTT | 4734 |
rs750194156 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854409 | CAGCTGGTGAATAGA[-/TT]TAAATGTAGTGGATA | 4734 |
rs750203732 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919919 | TGGTACCCACTTGTT[G/T]GGTCAAACATCAGTA | 4734 |
rs750212142 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915492 | ATACCATGGTTTTTG[C/T]TCATCTGTGAATGTG | 4734 |
rs750229915 | snp | C/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917452 | TCAAGTTAGTTAATA[C/T]AGGGACTGTTAATTT | 4734 |
rs750232895 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941712 | GGTATTACAGGTGCG[C/G]ACCATCACACCCAGC | 4734 |
rs750248588 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844918 | GCTCAAGTAATTCTC[C/G]TGCCTCAGCCTCCCA | 4734 |
rs750287785 | in-del | -/TTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870532 | CTTCTTCTTCTTCTT[-/TTT]TTTTTTTTTTTTGTT | 4734 |
rs750310571 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940306 | GGATATGTTTATGAC[-/TT]TGATTGTGGTGATGG | 4734 |
rs750323623 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897380 | GTACTCTAGGACGTG[C/G]AGGGAATTTTCCAAG | 4734 |
rs750324121 | snp | A/C | 3.24512e-05 | 0.00402797 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924730 | TCTTTATTTAAAAAC[A/C]AGTAAACATCAACCC | 4734 |
rs750332686 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940360 | TTAAACCTATCAAAC[C/T]GTATGAATTAAATAT | 4734 |
rs750370488 | snp | C/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953423 | GCTCCAGAGGCCATA[C/G]TCTTCTTTTTTTATC | 4734 |
rs750384477 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828421 | ATTCCAATATAAGGA[G/T]GAAACAATATAAGTA | 4734 |
rs750413150 | snp | C/G | 1.73724e-05 | 0.00294719 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837857 | TTACAAGACTAAAAA[C/G]AAACAACATTTCATT | 4734 |
rs750425849 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980544 | CCCTCGTACAGAGGA[A/T]GTAAGCCACCAAACA | 4734 |
rs750434638 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971496 | CAAGCATGGCAGCGT[A/G]CACCTGTAATCCCAG | 4734 |
rs750439811 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978400 | AACTTCATTTTATGA[C/T]TTTATTCTAGAGAAT | 4734 |
rs750452795 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858595 | TACAGGCGTGAGCCA[C/G]CACGCCTGGCCTAAT | 4734 |
rs750455014 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966959 | GTGGTGTGATCCTGG[A/C]TCACTGTAACCTCTG | 4734 |
rs750467917 | in-del | -/G | 5.12256e-05 | 0.00506065 | utr-variant-5-prime, frameshift-variant | NEDD4 | GRCh38.p7 | 15:55951580 | TAACGTCACTCTCAC[-/G]TAAGGATCACTGTTA | 4734 |
rs750476489 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842816 | TTGTGCCTGTCTGTT[C/G]AGGCTTTTCCCTACC | 4734 |
rs750477308 | snp | A/G | 1.65195e-05 | 0.00287393 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838531 | AAAAGTTCTTCATCT[A/G]TGATAAACCTGAGGT | 4734 |
rs750483763 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842076 | CCTTCAGGAAGTCTG[C/T]TCTCTTGACACCCAT | 4734 |
rs750494685 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927238 | AGAGAACATGCACAG[C/G]AAGGTCACATGAGAA | 4734 |
rs750495106 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877578 | TTTGAGGTTATGTAA[A/G]TAGCCCATTTCTCAT | 4734 |
rs750498328 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957614 | TGACCCAGCGATCCC[A/C]TTACTGGGTATATAC | 4734 |
rs750516948 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856392 | ACACATCCAGCTCCC[A/G]TGCCCCCCGTGCTGG | 4734 |
rs750520231 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871439 | TTTAAAGATAAAGAC[A/G]CTAGAAAGCATGTGA | 4734 |
rs750521430 | snp | A/G | 4.94629e-05 | 0.00497283 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848459 | AAAGAAAAAAGATGT[A/G]CTTTCTCACACATAA | 4734 |
rs750534490 | snp | A/G | 3.37382e-05 | 0.00410706 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838196 | CTAAAATTAAACACA[A/G]TAACTTGATATGTTA | 4734 |
rs750535713 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907834 | AAGATCTTTGTCCAT[C/T]CAATCTTCTTTTCAG | 4734 |
rs750543991 | snp | G/T | 1.65641e-05 | 0.00287781 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915753 | ACAGTCTGTCTGGGA[G/T]TATTATTCGAAAGAA | 4734 |
rs750558430 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870741 | GGTTTTGCCATGTTG[-/C]CCAGGCTGGTCTGGA | 4734 |
rs750564541 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937632 | GGAAATGGCAGTAGA[A/G]TCCTAATCCTGATTT | 4734 |
rs750564907 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890476 | TCCTTTATGACTGAC[C/T]TATTTTACTTAGTAT | 4734 |
rs750592843 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970284 | CCTAAAGTCCCTAAT[-/C]CCAGGCCCCAACTCC | 4734 |
rs750596034 | in-del | -/CTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986905 | CGGCCAAGGCCTGTC[-/CTT]CTTAAAACTGTCTAG | 4734 |
rs750615384 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950750 | TCAACAGCTAAAGGG[C/G]AATATGGGGTCAAGG | 4734 |
rs750633389 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991021 | ATCTACATTTTAGCA[C/T]ACTTCAGTGCTAATA | 4734 |
rs750657099 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830499 | TGTTCTATCAAGGTC[C/T]AAACAACTGCTTACC | 4734 |
rs750674743 | snp | A/G | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862951 | TGTTCTTCTAGATTC[A/G]TGGTTTACATAATAG | 4734 |
rs750681803 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989952 | CCTGTCAGATCAGCA[A/G]CGGCATTAGATTCTC | 4734 |
rs750707428 | snp | A/G | | | stop-gained, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850691 | TGGAGGCTTGTGATT[A/G]AGGGCCTGCAGAACT | 4734 |
rs750712799 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855423 | ATAGACAGGAATGAA[A/G]GCAGCAGGAGGCTTC | 4734 |
rs750719936 | snp | A/G | 1.67209e-05 | 0.00289139 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856234 | GAAGAATACCTTGAT[A/G]TTTGTGATTTGCCTT | 4734 |
rs750746395 | snp | C/T | 3.29565e-05 | 0.00405921 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916652 | GTTTTCCTTTATTAA[C/T]GGAGCTAGTGCAGTC | 4734 |
rs750758667 | snp | A/G | 1.68335e-05 | 0.00290111 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862898 | ATTAAAATTGTGAAA[A/G]CCATCAGCACATACT | 4734 |
rs750779188 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899812 | CATGTAGCTATGGAG[C/T]ACAGGAAATGTGTCT | 4734 |
rs750812606 | snp | A/G | 2.31624e-05 | 0.00340303 | missense, utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55872466 | GGTCTCTCCAATCTT[A/G]GATTTTCTGTCTAGA | 4734 |
rs750833367 | in-del | -/AC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985762 | GTAGAGTACACATAC[-/AC]ACACACACACACACA | 4734 |
rs750852044 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888923 | CAAACTAGACTCCTA[-/T]TTTCTCACCTTATAC | 4734 |
rs750859004 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891018 | GAAAGAAAACTCATC[A/C]CATCCCATCTCCCTA | 4734 |
rs750865943 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914097 | GTAGTGGCTTATATT[A/C]ACATCTGGGCATTGG | 4734 |
rs750887251 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983783 | GCCTGGCTAATTTTT[C/G]TATTTTTGGTAGAGA | 4734 |
rs750889690 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831803 | AGGCAGCAGTCCCGA[C/T]TTGTAGTCCCCAGGT | 4734 |
rs750945918 | in-del | -/AAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832182 | TCCACCCCTATCTTG[-/AAA]AAAAAAAAAAAAAAA | 4734 |
rs751018467 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921457 | AGTCTCCAGAGTAGC[C/T]GGGACTACAGGTGCG | 4734 |
rs751022805 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55993265 | ACTGACAAGTAAGGC[G/T]GCGGCCGCTCCGGGA | 4734 |
rs751024124 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879383 | GAACAACTAAGCAAC[C/G]CAATGAGACAGACTT | 4734 |
rs751045333 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850656 | AGATGGCTGGGTCAC[C/G]TGCTGGCCTGAATCA | 4734 |
rs751063547 | snp | A/C | 1.65364e-05 | 0.0028754 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916187 | ATTCCTGTTTGGCAC[A/C]CTTCTATTGGAGGTG | 4734 |
rs751076478 | in-del | -/AAATAAATAAATA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892306 | AATAAATAAATAAAT[-/AAATAAATAAATA]AATAATAAATATGAA | 4734 |
rs751077272 | in-del | -/AG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973958 | AAATCAAATTGAAAC[-/AG]AATATAATACAAAGA | 4734 |
rs751078385 | snp | A/G | 1.65127e-05 | 0.00287334 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841936 | TAAAGGTACTTACGT[A/G]GCAGAATATTCAAAC | 4734 |
rs751095109 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870779 | GGCTCAAGCAATCCA[A/C]CCACCTAAGCCTCCC | 4734 |
rs751095119 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886525 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGGTGGG | 4734 |
rs751131569 | snp | A/C | 8.54168e-05 | 0.00653461 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841885 | CGACTCTTACTTTTA[A/C]AACAGTGATTTTTCT | 4734 |
rs751167440 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899641 | ACAGCAGCTTTAGGC[A/G]TTTTCCTCAATACAC | 4734 |
rs751173711 | in-del | -/T | 3.29658e-05 | 0.00405978 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916346 | CTACCGTTGCTGCTG[-/T]TAAGACCCATTATCA | 4734 |
rs751185832 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931988 | CTGGACATTTCATGT[A/T]AGTGGAATCATACAA | 4734 |
rs751197762 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55850094 | TGAGCCACTGCACCC[A/G]GCCTTTAGGTAATTT | 4734 |
rs751217726 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943020 | GCAGCATTGTGCCCC[C/T]GCTCTAGAAATCTGT | 4734 |
rs751253832 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980380 | GGGTCTGAGAACAGC[A/G]GCTGCTGTACCCACT | 4734 |
rs751256217 | snp | C/T | 1.69258e-05 | 0.00290905 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55834230 | GTTATGTCTTACCTC[C/T]AGTTCATTTTCATCA | 4734 |
rs751270415 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858526 | TTGCCCAGGCTGGTC[G/T]TGAACTCCTGACTTC | 4734 |
rs751277402 | snp | A/G | 1.68929e-05 | 0.00290623 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860361 | AATAGTATAATATGC[A/G]TAATATAAACTACTG | 4734 |
rs751282387 | in-del | -/TTG | 4.94866e-05 | 0.00497402 | cds-indel, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863023 | TAGAGGAGAAGGTTC[-/TTG]TTGTTGCTGCAAATG | 4734 |
rs751285904 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959590 | GGGACAGATCTATAT[A/T]TTCTAACCAACAGAT | 4734 |
rs751309311 | snp | G/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834091 | AGCCATTTTTATACT[G/T]TGTATGTTCCCTCCA | 4734 |
rs751326578 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894562 | AAAGGGGCTTTTACC[C/T]CACAGATTGGGGTGA | 4734 |
rs751331662 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942225 | TTGTTGAATTCACTC[C/T]TTATAATCATGAAAT | 4734 |
rs751347463 | snp | C/T | 3.29609e-05 | 0.00405948 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860706 | TGTTTCCTCGGATAT[C/T]TGCCGCCTGGTGGTA | 4734 |
rs751380022 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857645 | TTATTTTATATACCT[A/G]AATACAATCTCAATT | 4734 |
rs751385882 | snp | C/T | 1.65078e-05 | 0.00287291 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915607 | TAATATACTCTGAAT[C/T]AGAATTAAGCTTAAT | 4734 |
rs751409029 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829642 | GAACTCTAAAGCCAG[A/G]TGTGGTGGTGCCTGG | 4734 |
rs751430528 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907972 | GATCATAATATTCCA[C/T]TGGCATTCACCCCAG | 4734 |
rs751452956 | in-del | -/GC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854112 | GCCGAGATCGCCTGG[-/GC]ACTCCAGCCTGGACA | 4734 |
rs751461020 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938753 | AATTACATACAAAAG[A/G]AACTCCCATAACCCA | 4734 |
rs751473286 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919480 | TTCTAGGGAGGCTGA[A/G]CAATTTGCATTGCTG | 4734 |
rs751514775 | snp | A/C | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826487 | ACCTTCCCAGGCTGG[A/C]TTGAGTGGGTGGGAG | 4734 |
rs751536376 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992195 | CCATTAGCTAGAATG[A/G]TATCTTTAGCTGTAA | 4734 |
rs751560652 | snp | C/T | 4.23729e-05 | 0.00460268 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863113 | GCAATTAAGTTTACG[C/T]ATGATTTTTTTAACT | 4734 |
rs751567069 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968010 | CTTATTTTAAAAAAT[G/T]TATAAAATATTGAAG | 4734 |
rs751583068 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850560 | GGTGGTGGTTTTAGT[A/G]TTGTGGTCAATAAAG | 4734 |
rs751626019 | snp | C/G | 1.65723e-05 | 0.00287852 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852411 | GAAAGCAAGTTGATA[C/G]ATTACAGGATACCTG | 4734 |
rs751635687 | snp | C/G | 0.000102659 | 0.00716372 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993581 | TTCCAGCAAACCGGA[C/G]GCGCTCGCCCCCGCC | 4734 |
rs751645022 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842236 | ATCTCTCATAAAGTT[A/G]TAACATTCCCTCTAC | 4734 |
rs751645124 | snp | G/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55830542 | TTGGCAGCTTTTCAG[G/T]AGTACCCCACTGTTC | 4734 |
rs751666722 | snp | G/T | 1.6617e-05 | 0.00288239 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840451 | AAAAGACATACCACA[G/T]ATTCCATATCATGAA | 4734 |
rs751674720 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868694 | CTTTATAAATTACCC[A/G]GTCTCTGATATTTCT | 4734 |
rs751677362 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916442 | CACAGCATTCAATTC[A/G]TTATCGACCACAGCA | 4734 |
rs751680876 | snp | C/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863000 | TGCCTCTCTTCCCAC[C/G]CTGGAGGTAGAGGAG | 4734 |
rs751712978 | snp | A/G | 1.65326e-05 | 0.00287507 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915893 | AAATCCTTTAGCACT[A/G]GTGCCATCCTCATTA | 4734 |
rs751726940 | in-del | -/TAAAGA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896881 | TATCTATTTAAGACC[-/TAAAGA]TAAATTCTAAATTAT | 4734 |
rs751755080 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960025 | CCTCTCAGCTCCTCA[A/G]TGTGGTCAATCCAGA | 4734 |
rs751779057 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960586 | CTGGCTTCCTTGCTC[C/T]GCAGCTTGCAGATGG | 4734 |
rs751785586 | snp | A/C | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852512 | TGTTTTTCTTCCCAA[A/C]CTGGTGGTAATCCAG | 4734 |
rs751818357 | in-del | -/GGTG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964650 | CTGAATTTTGCTGCT[-/GGTG]TGTGTGTGTGTGTGT | 4734 |
rs751833836 | snp | C/T | 3.30186e-05 | 0.00406303 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842126 | TCAAGAACAGTTGCT[C/T]GGCGAAGTTTCATTT | 4734 |
rs751849794 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971222 | AGAATTAGCGAGCTT[A/G]AAGATAGGTTATTTG | 4734 |
rs751870709 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55861885 | GTAGCTAAAGAAAAC[A/T]TAATTTTGATACATG | 4734 |
rs751876183 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877263 | TTTAATTTCTTTAAA[A/T]CTGGAAAGTACCTTA | 4734 |
rs751905718 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879051 | CTAGTCTCAAACTAC[C/T]GACCCCAGGTGATCC | 4734 |
rs751908504 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830791 | TGTAGCCTCAAGCTC[C/T]TGGGCTCAAGTGATC | 4734 |
rs751917149 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912202 | TAACCAAATCTCTCT[A/C]AATATTCTGCTAAAT | 4734 |
rs751934031 | snp | C/T | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860418 | TTACTGAGCTCGATG[C/T]TGGCTGGCTCACGGC | 4734 |
rs751948838 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913919 | TAGCATACTATTAAC[A/G]TTTCTTCTCAGTGCC | 4734 |
rs751961286 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963188 | CTAGGCTGGAGTGCA[G/T]TGGCAAAATCATGGC | 4734 |
rs752011962 | in-del | -/GTGTGTGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964693 | TGAATTTTGCTGCTG[-/GTGTGTGT]GTGTGTGTGTGTGTG | 4734 |
rs752012536 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937451 | CATAATGAATTAGCA[C/T]TGATCCACACAAATT | 4734 |
rs752014000 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925656 | GTGATATCTTAAAAC[A/G]TTGGTGTACATGTCA | 4734 |
rs752015758 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844873 | AGTGCAGTGGCATGA[C/T]TATAGCCCAGTGCAG | 4734 |
rs752041093 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955884 | AAGGTGGCACAAACA[C/T]GGCTCACTGTAGCCT | 4734 |
rs752047492 | snp | C/G | 1.65946e-05 | 0.00288046 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915816 | AGCGGCCGTATGTCT[C/G]TTACTTCTCCGGGGG | 4734 |
rs752060829 | in-del | -/TC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886793 | AAATAATATCAAATA[-/TC]TTCTCTGACCACAAA | 4734 |
rs752066364 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964628 | TATAAATGTTAAGTT[G/T]TGGAGACTGAATTTT | 4734 |
rs752104770 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829749 | AAATAAGTTGTCGTA[C/G]TATTTCTTCAAATGC | 4734 |
rs752113504 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55948317 | GAGGACACAAACAAA[C/T]GGAAGAACATTCCAT | 4734 |
rs752143750 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966006 | ATGTTCCCAGGCCAT[C/G]AAGACTACAATTTTT | 4734 |
rs752154317 | snp | A/G | 8.24151e-05 | 0.00641878 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842100 | CACCCATAATTCTCC[A/G]GTAAGAGTCTTCAAG | 4734 |
rs752167231 | snp | A/G | 5.23684e-05 | 0.00511678 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848617 | TTTTAGGAGAGGGGC[A/G]TAGATGAATGGATAG | 4734 |
rs752169073 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875723 | AAGTATGAACTTGAA[A/G]ATATAGAGACAGAAT | 4734 |
rs752178791 | snp | A/T | 1.87117e-05 | 0.00305868 | intron-variant | NEDD4 | GRCh38.p7 | 15:55915240 | ATATTTCATTAAGTT[A/T]TTCTCATATAAATTA | 4734 |
rs752206844 | snp | C/T | 1.70043e-05 | 0.0029158 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55834237 | CTTACCTCTAGTTCA[C/T]TTTCATCAAAAATTT | 4734 |
rs752209528 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942372 | TCTGCCAAAATCTCA[C/T]GTCAAATTGTAATCC | 4734 |
rs752215187 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864681 | GAGTGAAACTCTGTC[A/T]CATAAGAAAAAAAAA | 4734 |
rs752223012 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899389 | AAGTTTAGCTGATCT[A/G]TAAACAGTTTTTAAG | 4734 |
rs752228130 | snp | A/G | 1.65553e-05 | 0.00287705 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915362 | TTTACCTTCATTTCC[A/G]GATGCAAACTTTATG | 4734 |
rs752267269 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846407 | ATGGCCAGATGATGA[G/T]TTTAGTTCCAAACAT | 4734 |
rs752276612 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897578 | GCAATAATAGTGAGG[A/G]TCGAATGACCTGCTC | 4734 |
rs752277175 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950232 | AATTTCCAAACCGAT[C/T]TAAAAGGTTGTTTTT | 4734 |
rs752320526 | in-del | -/GA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832181 | CTCCACCCCTATCTT[-/GA]AAAAAAAAAAAAAAA | 4734 |
rs752329478 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912047 | GTCTGAAATTAACAA[C/T]TCCTCAGTTCTAAGA | 4734 |
rs752338683 | snp | C/T | 1.74592e-05 | 0.00295454 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916829 | TCGTAAGCTTTGTGC[C/T]ATTTGTTCTCATTTC | 4734 |
rs752352790 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941820 | TCAAGTGATATGCCT[C/G]CATCGGCTTCCCAAA | 4734 |
rs752389426 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871572 | GAGATTTACATTCCA[C/G]ACATCTACAGAAATT | 4734 |
rs752415511 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988462 | ACATGTACACTAAAA[C/T]TTAGAGTATAATAAA | 4734 |
rs752530438 | in-del | -/A/AA/AAAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935845 | GTGAGACTCTGTTTC[-/A/AA/AAAA]AAAAAAAAAAAAAAA | 4734 |
rs752533683 | snp | C/T | 3.44554e-05 | 0.00415049 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993505 | GCAGCCCCGCGGTCC[C/T]CGCACCTCGTCCTCC | 4734 |
rs752535318 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921343 | TTTTTTTTTTTCGCC[A/G]AGACGGAGTCTCACT | 4734 |
rs752574813 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937867 | CCCTGCATCTTGAGA[-/AAG]AAGAACAAAGCTAGA | 4734 |
rs752584655 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933774 | GAGGGATGTGTTTGC[A/T]TCCCCTTCTATCATG | 4734 |
rs752586740 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920524 | AAACGACAATATTTT[A/G]TAACACTCAAGTCTT | 4734 |
rs752623801 | snp | A/G | 0.000164867 | 0.00907779 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916320 | GTGATACTTGCACAT[A/G]ACCCAAAATCACTAC | 4734 |
rs752631416 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981041 | ATGCATATTTTTTCC[-/T]TTTTTTTTTTTTTTG | 4734 |
rs752636723 | snp | A/T | 1.66424e-05 | 0.0028846 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852374 | TAGTTTACATAGGGA[A/T]GTGACAGTTTAAATC | 4734 |
rs752639358 | in-del | -/AAAT | 0.000161212 | 0.00897665 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869694 | TGACTGTAGAAAAGA[-/AAAT]AAATATTCATAAAAC | 4734 |
rs752681851 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851579 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 4734 |
rs752720324 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865978 | ATTCTGACACCCAGG[A/T]TGGAGTGCAGTGGTG | 4734 |
rs752739252 | snp | A/G | 0.000148421 | 0.00861326 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841950 | TAGCAGAATATTCAA[A/G]CAACCCATAATAAGG | 4734 |
rs752762351 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916543 | ACTGAAGATATCCAC[G/T]GTACCTTGTTGGCTG | 4734 |
rs752793601 | snp | C/T | 1.66949e-05 | 0.00288915 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856103 | AGTTTTATATTTTTA[C/T]TGATTGATGGGAGAG | 4734 |
rs752794416 | snp | A/G | 5.15548e-05 | 0.00507688 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846922 | TTCCCATTACTTTCC[A/G]TCTATATATTGATGA | 4734 |
rs752794465 | in-del | -/CTT | | | cds-indel, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916791 | AAAGGGTAAGTATTG[-/CTT]CTTCTGGCTGCAAAG | 4734 |
rs752820047 | snp | C/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918483 | AAGGTAAAATAGTTC[C/T]GTTGTTTATACCACA | 4734 |
rs752843909 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959584 | AAGCATGGGACAGAT[C/T]TATATATTCTAACCA | 4734 |
rs752848556 | snp | C/T | 0.000278404 | 0.0117951 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869633 | GCCACTGGTTTTAGG[C/T]AAATAAGTCATTTTT | 4734 |
rs752848604 | snp | C/G | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852527 | CCTGGTGGTAATCCA[C/G]ATGAAGTAGGCAAAA | 4734 |
rs752867699 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940025 | CAATAGAATATTATT[C/T]AGCCTTCAAAAAGGA | 4734 |
rs752869942 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891889 | AGAATCCAAAGTAAT[-/A]AAAAAATCAGAATTT | 4734 |
rs752894002 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969480 | GGGTGTGCTTGTGTC[A/T]CCCCTCCTCCAACTT | 4734 |
rs752895149 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958669 | ACAAATTCAATTTCT[C/T]TTAACAACAAATTCA | 4734 |
rs752910465 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844653 | AATGATAGCTACCCA[C/T]ATGGAGTTGTTTCAA | 4734 |
rs752916621 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952703 | GAGTCTCATCCCCCT[C/T]GTTCAGTTCTCTGAA | 4734 |
rs752920324 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929095 | CAGATGAAGCAGGGA[C/T]GGAAGTGATGATGGA | 4734 |
rs752924716 | snp | A/G | 1.65403e-05 | 0.00287574 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55847001 | TTCGGAAGAACTCAT[A/G]CTTTCTTTTGTAATC | 4734 |
rs752964760 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832095 | TAACTATTCTGAAAA[C/T]CAAGAGATATGTAGT | 4734 |
rs752975150 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895549 | GTGCCCAACCTAATC[C/T]AGAGTTTCAAGATTC | 4734 |
rs752977790 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929750 | ATTACCAGAGATCAC[A/G]AACGTACAAATTAGA | 4734 |
rs752979424 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939369 | CTTGTGGAGAAGGTG[-/C]CCGCTTCCTGTTCAT | 4734 |
rs752983491 | in-del | -/TTAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843400 | CCTGAGTCTGTGCTC[-/TTAA]TTAATGGAGCTACAT | 4734 |
rs752992830 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981119 | TCTCGGCTCACTGCT[C/T]GCAATGTCTACCTCC | 4734 |
rs753011718 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994212 | TTGGACTCGGGATCT[A/G]AAATTCTCTCCCTAG | 4734 |
rs753021735 | snp | C/T | 1.65408e-05 | 0.00287578 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840479 | GAAGGGTTATTGGTT[C/T]GTGAAGCATCATCTT | 4734 |
rs753032958 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889078 | TAAGCACAGACAACC[A/C]AATCAAAATGGACAA | 4734 |
rs753041400 | snp | A/G | 2.73205e-05 | 0.00369588 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55924696 | GGTGCTGCTGAGGAT[A/G]AACCTAAGAAAAACA | 4734 |
rs753055474 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924346 | CCAGGGGTCATGGGC[A/G]AGTGAGAGGGAAGGC | 4734 |
rs753078904 | snp | A/C | 3.52398e-05 | 0.00419746 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848624 | AGAGGGGCGTAGATG[A/C]ATGGATAGAAAAATA | 4734 |
rs753086375 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903633 | ATCGAGACCATCCTA[A/G]CTAAACACGGTGAAA | 4734 |
rs753125408 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932288 | ACAAGGATACAGTAA[C/T]CAAAACAGCATGGTA | 4734 |
rs753137897 | snp | A/G | 3.31906e-05 | 0.0040736 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915827 | GTCTCTTACTTCTCC[A/G]GGGGTACAAATTGTT | 4734 |
rs753140628 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888376 | AGAAGGCAATCCTAT[C/T]TACAATAACTACAAA | 4734 |
rs753152833 | in-del | -/T | 1.89611e-05 | 0.00307899 | frameshift-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829994 | GGCAAGTCCAGGCGA[-/T]TAAAACTGAAAGAAC | 4734 |
rs753178185 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989107 | TGGGCGTGGTGGTGC[A/G]TGCCTATAATCCCAG | 4734 |
rs753189798 | snp | G/T | 0.000540833 | 0.0164354 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869543 | AATAAGAAATTAAAA[G/T]TTTTTTAGTTTAACC | 4734 |
rs753207079 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978477 | CTCTCACATGTTTGA[A/G]AAGGAGGGAAAGCAG | 4734 |
rs753211882 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974891 | CATTTCTTTTCCTTT[-/C]TTTTTTTTTTTTTTT | 4734 |
rs753234924 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975666 | AATATTCCATGTTCA[C/T]GGATTGGAACAATCA | 4734 |
rs753241422 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859732 | CAAAAAACCAACTTC[A/G]GCATAACTGGGAGAG | 4734 |
rs753244222 | snp | A/G/T | 6.65816e-05 | 0.00576949 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832967 | TGAAAAAGACAATAC[A/G/T]CATTATTCCATTTTT | 4734 |
rs753252785 | snp | A/C | 3.30022e-05 | 0.00406202 | splice-donor-variant | NEDD4 | GRCh38.p7 | 15:55840605 | TATACTTAATACTAA[A/C]CATCCAACAGTTTGC | 4734 |
rs753258172 | snp | C/T | 4.94564e-05 | 0.0049725 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848772 | AATATTTGAGATAGC[C/T]AAGTTAGATGGGTTA | 4734 |
rs753262259 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962936 | GGATTACAGACACGC[A/G]CCACCATACCCAGCT | 4734 |
rs753280416 | in-del | -/GAG | 1.7219e-05 | 0.00293414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842175 | CATTCTGAAAATCCA[-/GAG]GAGAGACGTACTGTT | 4734 |
rs753288799 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875441 | TTAGCCACACAGGTA[C/G]CTGGGATTACAGGCA | 4734 |
rs753311890 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961629 | GAGCCCACCACCACA[C/T]CCGGATAATTTTTTG | 4734 |
rs753315030 | snp | A/C | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860539 | GGCCTGGTTGCTATA[A/C]ATGGTGGCTTCATCT | 4734 |
rs753329330 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855117 | TGACCAGAGCAATGA[C/T]GCATAGGTGGGCGAC | 4734 |
rs753341428 | snp | C/T | 1.65625e-05 | 0.00287766 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924712 | AACCTAAGAAAAACA[C/T]AATCTTTATTTAAAA | 4734 |
rs753345861 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55954794 | CTCCCAAAGTGCTGG[C/G]AATACAGGCGTGAGC | 4734 |
rs753380308 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944606 | TACAGACTTAAATGT[-/C]CCTATCTGACAGCTC | 4734 |
rs753381661 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909599 | TCCTGACCTCAACAC[A/G]TCGCCTGGCCTCACC | 4734 |
rs753393630 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858811 | TAGCACACATTTCCT[A/G]TTAAGATCCAGACAG | 4734 |
rs753399586 | in-del | -/AAC | 0.00148407 | 0.0271999 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834170 | AAATGTCAAATTATA[-/AAC]AAGGAAAATAATGGG | 4734 |
rs753424601 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910580 | ACTGTATACCTTCCC[A/T]AACGTGTTCATCCTT | 4734 |
rs753425801 | snp | C/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994068 | TCCCCGCTTAAATCC[C/T]AAACGGAAAATCATA | 4734 |
rs753435329 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922169 | AATACTGGAAATAAC[A/C]CTAATATCTATTAAG | 4734 |
rs753469187 | snp | A/G | 1.65113e-05 | 0.00287322 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915924 | TGTGCAATTTCACTA[A/G]GAGAAATAATAAACT | 4734 |
rs753537723 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827229 | AAGAGATTGTAGGCT[A/G]AAGTTATATGCTTGT | 4734 |
rs753569525 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975538 | GTTACAATCCCTACA[A/G]ATAAAATTAAACAAC | 4734 |
rs753575101 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920220 | ATTATACATAATTTC[A/G]TATATAAAATATATG | 4734 |
rs753582483 | snp | A/C | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848837 | TCATTGGAAGTATCA[A/C]GTGATGTCTTTCCTC | 4734 |
rs753589023 | snp | C/G/T | 3.29991e-05 | 0.00406185 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842121 | AGTCTTCAAGAACAG[C/G/T]TGCTCGGCGAAGTTT | 4734 |
rs753589459 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971569 | GCAGAGGCTGCAGTC[-/A]AGCAGAGATTGCGCC | 4734 |
rs753622616 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835767 | ACCAAGATTACTGTA[C/G]CACTTTCCCAACTCT | 4734 |
rs753628215 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899675 | ATCATTGTGAAAGTA[C/T]AGGGGTATCAATGTC | 4734 |
rs753645702 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836168 | CCTTCCTTTGCCCCT[C/T]CCTGGTTTGTACTTC | 4734 |
rs753659942 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882277 | GGCACTGAAGAGGGT[A/G]GGAAAGACAGTCTTC | 4734 |
rs753663347 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897570 | AACTTGGAGCAATAA[C/T]AGTGAGGGTCGAATG | 4734 |
rs753669632 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931718 | TCTGCCAGTGGTTGT[C/G]GGAACAAACAATACA | 4734 |
rs753670752 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916417 | GACTGCTTACAAGGT[A/G]ACCATCATTCACAGC | 4734 |
rs753713408 | snp | C/T | 1.75474e-05 | 0.00296199 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837760 | TATACTGTGACATTA[C/T]GGAAGAGCAAATAAA | 4734 |
rs753723019 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942226 | TGTTGAATTCACTCT[A/T]TATAATCATGAAATG | 4734 |
rs753757380 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930665 | TTGTAATAATCCAAA[C/T]GTGTCAACGGCAGGG | 4734 |
rs753758689 | snp | A/C/T | 4.94705e-05 | 0.00497325 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915393 | AGTAACTGAGATGGT[A/C/T]CCCCTTTAGAACAAT | 4734 |
rs753767487 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901596 | CTTTGATCTTTGCTT[C/T]GGTTTCTTATGAAGA | 4734 |
rs753776003 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941761 | TTTCTTTAGTAGAGG[C/T]GGGGTTTCATCATAT | 4734 |
rs753801260 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863044 | TTGCTGCAAATGGCA[A/G]GCAGCATCTGGTTGG | 4734 |
rs753814269 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834569 | GGCTGGGTGGGCAGA[C/T]TGCTTGAGCCAAGGA | 4734 |
rs753821189 | snp | A/G | 1.75606e-05 | 0.00296311 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842180 | TGAAAATCCAGAGGA[A/G]AGACGTACTGTTTAA | 4734 |
rs753844653 | snp | A/T | 1.64795e-05 | 0.00287045 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916734 | GGTCTTTTGAAGCAC[A/T]TGTGAACATGGCTAT | 4734 |
rs753884753 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990372 | CATCCAGGAAGCTAC[-/T]ACCTCTCCCAGTCAG | 4734 |
rs753887239 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831898 | TTTATTCTTGGATTC[A/T]TGGTTTCCTTAAAAG | 4734 |
rs753897393 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966995 | CGGTTCAAGCGATTC[C/T]CATGCCTCAACCTCC | 4734 |
rs753900700 | snp | C/T | 4.95577e-05 | 0.00497759 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915642 | GACATTTCTGGTTTA[C/T]AATCACCATTTGTTG | 4734 |
rs753911811 | in-del | -/ATAATT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980921 | AAAAATGTGAAATAA[-/ATAATT]ATAAACATAATATAG | 4734 |
rs753918767 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864684 | TGAAACTCTGTCTCA[-/T]AAGAAAAAAAAAAAA | 4734 |
rs753929150 | in-del | -/AC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883683 | CAGGCATCTCAACAC[-/AC]ACACACACACAAACA | 4734 |
rs753931145 | snp | A/G | 4.94214e-05 | 0.00497074 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848357 | CCATCAGAGCACACT[A/G]GCAGAGAGACTTACT | 4734 |
rs753937911 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916035 | CTAGGAAAAATGACT[A/G]AGGAGGAGTAACGTT | 4734 |
rs753947823 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863611 | AATAGAAAAAAAGGA[C/T]AAAAAATCGTTTAAA | 4734 |
rs753979414 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894470 | CTGCAAATACCAAGA[C/G]ACACCGGTACTTGGT | 4734 |
rs753982347 | snp | A/G | 1.65781e-05 | 0.00287902 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55847022 | TTTTGTAATCCCTGG[A/G]GTAGGGCACTGCCTT | 4734 |
rs753984411 | snp | A/G | 3.31961e-05 | 0.00407394 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856204 | GAATGATTCTTGTGA[A/G]AAAACAAGACAACAG | 4734 |
rs753987125 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969192 | CCTGTCGCAGTGGAA[A/G]GCAACAGAGGGCAGA | 4734 |
rs753990240 | snp | C/T | 1.65578e-05 | 0.00287726 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915746 | TTCACAGACAGTCTG[C/T]CTGGGAGTATTATTC | 4734 |
rs753990774 | snp | C/T | 3.29598e-05 | 0.00405941 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916636 | TTTCTTGAGACTGAA[C/T]GTTTTCCTTTATTAA | 4734 |
rs753995622 | snp | A/G | 9.8894e-05 | 0.00703116 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860725 | CGCCTGGTGGTAAAT[A/G]CACGTTGTGCTTGCA | 4734 |
rs754001446 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879574 | GGAAAGTTTATAACA[C/T]GAAACACACAGACCT | 4734 |
rs754030104 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847176 | TAGAAGAAAAACAAA[C/T]ACAAAACTTTAAACT | 4734 |
rs754034730 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976623 | TTATCCAATCTGGGC[-/AA]AAATTTTTTTTTTTT | 4734 |
rs754044729 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843799 | ACTTTAGACTGGATA[C/T]TAGGCAGCTGGTGCA | 4734 |
rs754058098 | snp | C/T | 6.05822e-05 | 0.0055034 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838176 | TTCAGCTCATGTTGA[C/T]GTGTCTAAAATTAAA | 4734 |
rs754076962 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938630 | CTACATTTAACTAAA[A/C]AGCTATATGACAAAA | 4734 |
rs754083442 | snp | A/T | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826506 | AGTGGGTGGGAGTGG[A/T]TTCCCTTCTAACTGG | 4734 |
rs754102165 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843043 | TTCTCATGATAGTGA[A/T]TGGGTCTCACGACAT | 4734 |
rs754122518 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983312 | TGTGCGTGCGCGCGC[A/G]TGCGTGCATTTGATT | 4734 |
rs754128182 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952533 | GAAGTACCCTCCAAA[C/G]TAATCCAAACTATCC | 4734 |
rs754133817 | snp | C/T | 6.14723e-05 | 0.00554368 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869658 | ATTTTTAGTCTCAGA[C/T]AACCTTTAACTCTTG | 4734 |
rs754136536 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828962 | CTGTAAACATACATT[A/T]ACTACATAATTGTAC | 4734 |
rs754153011 | snp | C/T | 1.65414e-05 | 0.00287583 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832987 | ATTCCATTTTTTTAA[C/T]GATCTATGGAAAATC | 4734 |
rs754159489 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906249 | CGGATCTAGAACTAG[-/A]AATACCATTTGACCC | 4734 |
rs754166280 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974525 | AATCCGTAATAAAAT[A/G]CTAGCAAACCAAATT | 4734 |
rs754169868 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888210 | ATCCTTGTTTGTAGA[C/T]GATATGATCTTATAT | 4734 |
rs754172339 | snp | A/C | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55830514 | CAAACAACTGCTTAC[A/C]AGGTATGAGCTCTTG | 4734 |
rs754182996 | snp | A/G | 8.24831e-05 | 0.00642143 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915999 | CTTGTTGGAGAAGTC[A/G]GTCGGGTAGTTGAAG | 4734 |
rs754194504 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853736 | GCTCACCCCTGTAAT[C/T]CCAGCACTTTTGGGG | 4734 |
rs754199332 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935345 | GCTAAAAGAATTATA[A/G]TTTTATTCAAATATT | 4734 |
rs754204571 | snp | C/T | 3.29973e-05 | 0.00406172 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840620 | CCATCCAACAGTTTG[C/T]CATGATAAACTGCCA | 4734 |
rs754229717 | snp | G/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55917025 | AAAAAGACGACCCAT[G/T]CCAGAGACTGACGTT | 4734 |
rs754241259 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865272 | TCTGTGGCAAAATAC[A/G]CAGATTACTTAGAAA | 4734 |
rs754258493 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944268 | CTGTACCTGGAAAAA[C/T]AGGACACTTCTGGCC | 4734 |
rs754262310 | snp | G/T | 0.000173837 | 0.0093214 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869554 | AAAATTTTTTTAGTT[G/T]AACCAAATATTTATA | 4734 |
rs754323847 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832868 | ACTCCAGTGTCCCTA[A/C]TGGTATCACTTTCAA | 4734 |
rs754353756 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958420 | GTTTAATTTCATTTT[C/T]GCATCTATGTTGACA | 4734 |
rs754382041 | snp | A/G | 6.6119e-05 | 0.00574936 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833091 | CTTTTTTCTGAATCC[A/G]TCATTAAAACAGCCT | 4734 |
rs754387659 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986184 | CATAGAATGCCAACT[A/C]ACAGAGATGGAAATA | 4734 |
rs754419904 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982698 | CAAATTATACATTTA[C/T]AATCTGTGCATTTCA | 4734 |
rs754422888 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944665 | GGATTTGAGCTCTGA[G/T]AACAAGAGACTGCCA | 4734 |
rs754423250 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941774 | GGCGGGGTTTCATCA[C/T]ATTGGTCAGGCTTGT | 4734 |
rs754424940 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929458 | GCATAGTACCCAACA[A/G]GCAGCTTTTCTATCC | 4734 |
rs754439148 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984668 | GGCTACAGACATATT[A/T]ACTCAACTTTCAGAA | 4734 |
rs754465396 | snp | A/G | 1.65688e-05 | 0.00287821 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856116 | TATTGATTGATGGGA[A/G]AGGGTAAAACTCACC | 4734 |
rs754483113 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970707 | TATGAGACTACAAGA[A/G]TCATATCATTACTGG | 4734 |
rs754534988 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846255 | TTTGTGAAAGCCAGC[G/T]TCTGGCTTAGAATGC | 4734 |
rs754541469 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832546 | CAGCCTCCCAAGTAG[C/T]TGGGACTACAGGTGT | 4734 |
rs754568256 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859818 | GACAAAATCAAGACC[A/G]CTCTGTAATCGTGGC | 4734 |
rs754574732 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848374 | CAGAGAGACTTACTG[A/G]TCCAGTTATTGCTAC | 4734 |
rs754579935 | snp | G/T | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841940 | GGTACTTACGTAGCA[G/T]AATATTCAAACAACC | 4734 |
rs754580275 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986520 | GGTCATCAAGAAACA[C/T]TAAACAGACCCAAAC | 4734 |
rs754584115 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864674 | ACAACAAGAGTGAAA[A/C]TCTGTCTCATAAGAA | 4734 |
rs754586873 | snp | G/T | 1.6489e-05 | 0.00287128 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860419 | TACTGAGCTCGATGC[G/T]GGCTGGCTCACGGCT | 4734 |
rs754588199 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845099 | GGGCCTTTTTACTAA[C/T]GTGAGAATTCATATT | 4734 |
rs754599908 | snp | G/T | 0.000372024 | 0.0136335 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905267 | CCTTCACTCCTGATT[G/T]GTCACTAACCATGGC | 4734 |
rs754613922 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922170 | ATACTGGAAATAACA[C/T]TAATATCTATTAAGG | 4734 |
rs754629879 | snp | C/T | 1.68892e-05 | 0.00290591 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860365 | GTATAATATGCATAA[C/T]ATAAACTACTGAAGC | 4734 |
rs754634802 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953794 | GGCACGATCTCGGCT[C/T]ACTGCAACCTCCTCC | 4734 |
rs754654057 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55954823 | GCCACCGTGCCTAGC[C/T]GAGTTTTGCCATTTT | 4734 |
rs754681502 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871960 | ATTATAAGCATGCTA[-/T]TTGGGTTTTAAATTC | 4734 |
rs754708734 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971675 | AGGTAGCAAGAGAGA[C/T]TGGGGTAAAAAGTTT | 4734 |
rs754712643 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909634 | GACTCTGCCAAGCCC[A/C]TTCAGCCTACAAAGC | 4734 |
rs754742233 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975931 | TGGCATAAAAACAGA[C/T]GTACAAACCAATGGA | 4734 |
rs754752070 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899710 | AGCTTGAGACCTAAT[A/G]TTCTAGGGGAACCCT | 4734 |
rs754756622 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855474 | GGTAGGCTGAAGAGG[C/T]TGGGAGCCTGGGAGT | 4734 |
rs754757704 | snp | A/G | 0.00450692 | 0.0472562 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951607 | GTTAAAAAAAAAAAA[A/G]AAAAGAAAGAAAAAT | 4734 |
rs754778510 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989972 | ATTAGATTCTCATAA[A/G]AGCATGAACCCTATT | 4734 |
rs754787878 | snp | C/T | 6.59228e-05 | 0.00574083 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860710 | TCCTCGGATATCTGC[C/T]GCCTGGTGGTAAATG | 4734 |
rs754805860 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868908 | AAGATCCTGAGGTTC[A/G]GAAAAGTTCAATGAC | 4734 |
rs754821381 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961011 | GCCTCCCGTGTCTCA[C/T]CTGACTGATACACTC | 4734 |
rs754822624 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883358 | TTGTGTGTCCACTCA[C/G]CTGCAGCAGAATAGT | 4734 |
rs754850090 | snp | A/T | 8.25266e-05 | 0.00642312 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848905 | TTTTGGTAGAGTAAA[A/T]AAAGAACAATACACA | 4734 |
rs754850145 | in-del | -/T | 4.41911e-05 | 0.00470038 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863117 | TAAGTTTACGCATGA[-/T]TTTTTTTAACTTTCT | 4734 |
rs754864520 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920366 | GTGGCTCCTAAAACC[A/G]GTGGCTGAATGTGTA | 4734 |
rs754869604 | in-del | -/C | 1.64803e-05 | 0.00287052 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848794 | GATGGGTTAGCATTT[-/C]TATACACTTACAGGT | 4734 |
rs754877786 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850561 | GTGGTGGTTTTAGTG[C/T]TGTGGTCAATAAAGA | 4734 |
rs754883599 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931734 | GGAACAAACAATACA[G/T]ATACATCTTTAAAAT | 4734 |
rs754905603 | in-del | -/TTTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963128 | CCTTTTCTGGCACTC[-/TTTTT]TTTTTTATTTTTTTT | 4734 |
rs754915551 | snp | C/T | 1.65384e-05 | 0.00287557 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916194 | TTTGGCACACTTCTA[C/T]TGGAGGTGCTGTCAG | 4734 |
rs754941419 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935428 | AATTTTGATTCCTCT[-/A]AGCCTTAGGGTAACA | 4734 |
rs754960543 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943443 | CAACCTTGGGACACT[A/G]CTCTCTGAGTCCCAG | 4734 |
rs754976889 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912684 | GAATAGCAATCATTG[-/T]TTGTAACTGTATACA | 4734 |
rs754984817 | snp | A/G | 3.42994e-05 | 0.00414108 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993584 | CAGCAAACCGGACGC[A/G]CTCGCCCCCGCCCAG | 4734 |
rs754991678 | snp | A/G | 9.11203e-05 | 0.00674921 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966557 | TTTTCCTAAAATACA[A/G]AAATTTAGATTTCAT | 4734 |
rs755048693 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880593 | TTCAGGGAGGTAATG[A/G]AGGATATACTTCACC | 4734 |
rs755056123 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969215 | AGGGCAGAAGTCAGC[G/T]TGCACCCATGGAGGG | 4734 |
rs755061013 | snp | A/G | 6.60229e-05 | 0.00574518 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852430 | ACAGGATACCTGTAC[A/G]GTGGGCTTTGTCCAA | 4734 |
rs755066212 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889319 | AGCCAAGATTTGAAA[A/G]CAACCAAAGTATCCA | 4734 |
rs755070924 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965180 | TCATCCTGTTTGGAC[A/G]AGAGCCACAAATCCT | 4734 |
rs755080037 | snp | A/G | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852515 | TTTTCTTCCCAACCT[A/G]GTGGTAATCCAGATG | 4734 |
rs755080475 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831924 | AAAAGCAAGTAAATA[G/T]CATTCCAATAAACAG | 4734 |
rs755087896 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847242 | GTATTCAGCAATTCC[C/T]ATGGCTGTAATTTTC | 4734 |
rs755090079 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984685 | CTCAACTTTCAGAAA[A/T]GCCTTATCAAAATGC | 4734 |
rs755102490 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914910 | AATAGGAATAAAGTA[C/T]TGAGCTACACAAAAG | 4734 |
rs755108294 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922938 | AAAACAAAACACACA[-/C]AAAAACTCCACCAAT | 4734 |
rs755131702 | snp | C/T | 3.53619e-05 | 0.00420473 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55834263 | AATTTTGATGAGATC[C/T]TGTGGTATTAGTTCA | 4734 |
rs755133015 | in-del | -/CAAAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883694 | ACACACACACACACA[-/CAAAC]ACACACACACACACA | 4734 |
rs755140857 | snp | C/G | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826665 | AGCAGCAAGGTGCCT[C/G]AAATCCAGTCCATTT | 4734 |
rs755151423 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863744 | GGCAAGGATTATTTC[C/T]TATTGGTCATTGTCT | 4734 |
rs755176207 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879766 | TAGAAATAAAAAATA[C/T]AACTCAAAAACTTCA | 4734 |
rs755198991 | snp | C/T | 3.29701e-05 | 0.00406005 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915408 | CCCCCTTTAGAACAA[C/T]TGTGCTTAAGGCTGG | 4734 |
rs755219359 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914296 | TGATGTACTGTCATG[G/T]AAAATTGCTTTAGTT | 4734 |
rs755229270 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892850 | TGGTTGTATGGTATG[C/G]TATTATATGGTACAG | 4734 |
rs755255109 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964774 | TGTATCCTTCAAACC[A/G]CATGTTGAAATTTGA | 4734 |
rs755294202 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938683 | GGCACCGTACAAAAT[A/G]GGAAAAATATTTGCA | 4734 |
rs755341176 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923012 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 4734 |
rs755368523 | snp | C/T | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838562 | CCAATTCTGTTGGGT[C/T]ATTTTCAAGAATCCA | 4734 |
rs755380658 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963495 | ACATCATTAATCTTT[G/T]ATTCAACTTATACTT | 4734 |
rs755386033 | snp | A/G | 1.65671e-05 | 0.00287807 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840464 | CAGATTCCATATCAT[A/G]AAGGGTTATTGGTTT | 4734 |
rs755407982 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898631 | TTTCACAAAAAGAAC[-/T]TTTTTTTTTTTTTTT | 4734 |
rs755437949 | snp | C/T | 1.72021e-05 | 0.0029327 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916821 | AAGTGCAATCGTAAG[C/T]TTTGTGCCATTTGTT | 4734 |
rs755463962 | snp | A/G | 1.65704e-05 | 0.00287836 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915770 | ATTATTCGAAAGAAC[A/G]ATTTTCTTCTGTAAC | 4734 |
rs755465246 | snp | C/G | 1.70886e-05 | 0.00292301 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993528 | CGTCCTCCAGGAGCC[C/G]GAACACCTCCACCGC | 4734 |
rs755478346 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852245 | AGGTGCAGTGAGCCA[C/T]GATCACGCCATTGGA | 4734 |
rs755507240 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901760 | ACAATTATTACATGT[C/T]ACATATCATGGCACT | 4734 |
rs755520697 | snp | A/G | 1.65723e-05 | 0.00287852 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860826 | GTCTTAAGTAGTTAA[A/G]ATGATTGTCAAAGAT | 4734 |
rs755547350 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944353 | CCATGCCTGGATTGG[C/T]GGGTACCATGCCCAC | 4734 |
rs755557199 | snp | C/T | 1.65946e-05 | 0.00288046 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915817 | GCGGCCGTATGTCTC[C/T]TACTTCTCCGGGGGT | 4734 |
rs755586118 | snp | A/G | 1.65209e-05 | 0.00287405 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916766 | CAAGTCATCTCCGGA[A/G]GTTTCTGACAAAGGG | 4734 |
rs755612509 | snp | A/C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973528 | TGGTCAACAGAGTAG[A/C/T]CCTGTCTTGAAAAAG | 4734 |
rs755664485 | in-del | -/C/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974891 | ATTTCTTTTCCTTTC[-/C/TT]TTTTTTTTTTTTTTT | 4734 |
rs755672466 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858714 | GGGCAGGAGGCAGGC[A/G]GGCGGATTTACTGGC | 4734 |
rs755678813 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844130 | GGGAAGGACGGAGGA[A/C]CAGCATACATGAGAG | 4734 |
rs755681412 | snp | C/T | 1.70388e-05 | 0.00291875 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55834239 | TACCTCTAGTTCATT[C/T]TCATCAAAAATTTTG | 4734 |
rs755681520 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992423 | GTTTGACGACACCAA[A/G]GTACTAAGAGAAGGA | 4734 |
rs755689919 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874248 | AAATACTAAAAGAGC[C/T]ATTTGAAAGTACAAC | 4734 |
rs755700341 | snp | A/G | 1.6593e-05 | 0.00288031 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915828 | TCTCTTACTTCTCCG[A/G]GGGTACAAATTGTTT | 4734 |
rs755709822 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838905 | AGATTTTATCATCCA[C/G]TTAAAGGAATGAATA | 4734 |
rs755712125 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909462 | GGTCTCCCAATTTTA[C/T]ACAAGGAACAGAGGA | 4734 |
rs755718014 | snp | C/T | 9.97987e-05 | 0.00706324 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838588 | ATCCATCTTAGGGAA[C/T]TGTAATATTCACTAT | 4734 |
rs755718052 | snp | A/C | 1.64893e-05 | 0.0028713 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848758 | ACCCGAAAATGCAAA[A/C]TATTTGAGATAGCCA | 4734 |
rs755729257 | snp | A/T | 1.64846e-05 | 0.0028709 | stop-gained, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860536 | GAAGGCCTGGTTGCT[A/T]TACATGGTGGCTTCA | 4734 |
rs755733777 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857776 | CAAGTCTTTACAAAA[A/T]TTTTTTAAAAAAATT | 4734 |
rs755737234 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886789 | ATTGAAATAATATCA[A/T]ATATCTTCTCTGACC | 4734 |
rs755768814 | snp | A/G | 3.30382e-05 | 0.00406423 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848508 | ACATAATGAAAAATC[A/G]CACTGCACATACTGT | 4734 |
rs755771950 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920092 | CAGCAATTCTGCCTC[-/A]AGACTACAATGTAGA | 4734 |
rs755799304 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922461 | TCCACCTCCTGGGTT[C/T]GGGCAAGTCTCCCAA | 4734 |
rs755822161 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983501 | CTATTTACTCAATGG[C/G]GTTCTATTGCCCCAC | 4734 |
rs755854909 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921593 | GGAACACCTCCTGAT[C/T]CACCCGCCTCAGCCT | 4734 |
rs755858068 | snp | C/G | 1.64885e-05 | 0.00287123 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841954 | AGAATATTCAAACAA[C/G]CCATAATAAGGGTTA | 4734 |
rs755868939 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930478 | AGAAAATCACTCTAG[A/G]TGACCTTCCATTCAA | 4734 |
rs755886792 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956416 | TTTTTCCTATGTGTT[-/C]CCTATAGAAGTTTTA | 4734 |
rs755889932 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867601 | CTGGTACACCAAAAA[G/T]CCAGGTAGAGAAACT | 4734 |
rs755902039 | snp | C/T | 3.43389e-05 | 0.00414346 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993513 | GCGGTCCCCGCACCT[C/T]GTCCTCCAGGAGCCC | 4734 |
rs755903951 | snp | A/G | 1.6516e-05 | 0.00287362 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916235 | TCCACCCAAAAAAGT[A/G]TCATCACTTGGTGGA | 4734 |
rs755910875 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834355 | ATGCCTCAGCTTCTG[A/G]ATGCTACTGGAGGAA | 4734 |
rs755916131 | snp | A/C | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917498 | TGAATTCAAACAGTT[A/C]GGTAAATTTGGAAAT | 4734 |
rs755927576 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950771 | GGGGTCAAGGAAGAA[C/T]ATTTTAGGGATGATA | 4734 |
rs755955417 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850686 | ACTGGTGGAGGCTTG[C/T]GATTGAGGGCCTGCA | 4734 |
rs755958857 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895714 | ATGCATCTGGCCAGC[A/G]ATACACCTTGAGAAA | 4734 |
rs755983012 | in-del | -/TTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870531 | TCTTCTTCTTCTTCT[-/TTTT]TTTTTTTTTTTTGTT | 4734 |
rs755986829 | snp | C/T | 1.69896e-05 | 0.00291454 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841894 | CTTTTAAAACAGTGA[C/T]TTTTCTTTTTCTGCC | 4734 |
rs755998430 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880997 | CCAAGAAAAGGAGTA[C/T]GGTTGGAGTCTAAGG | 4734 |
rs756009608 | in-del | -/A | 9.42551e-05 | 0.00686431 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872519 | TATATCTATAACACC[-/A]AAAGCATGTACTTTT | 4734 |
rs756011926 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55946143 | TTACAGGATCAAATT[C/T]ACACATAACAATATT | 4734 |
rs756027334 | in-del | -/CTT | 2.58689e-05 | 0.00359635 | cds-indel | NEDD4 | GRCh38.p7 | 15:55924666 | GGTTTTCGTCAAACA[-/CTT]CAAAAAGAAGCCGGT | 4734 |
rs756044542 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940372 | AACTGTATGAATTAA[A/T]TATGTGCAGGCTTTT | 4734 |
rs756045985 | snp | C/T | 1.86426e-05 | 0.00305303 | intron-variant | NEDD4 | GRCh38.p7 | 15:55915249 | TAAGTTATTCTCATA[C/T]AAATTAACATTTACC | 4734 |
rs756050948 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844984 | GGTGTTTTTAATATT[C/T]TTTATTTCTGTTTTG | 4734 |
rs756080748 | in-del | -/GT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983286 | ATGATGACGACAATG[-/GT]GTGTGTGTGTGTGCG | 4734 |
rs756116600 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830984 | AGTAAAATGGCATGA[C/T]CTCGGCTCAATGCAA | 4734 |
rs756142113 | snp | C/G | 1.64879e-05 | 0.00287118 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916324 | TACTTGCACATGACC[C/G]AAAATCACTACCGTT | 4734 |
rs756142343 | in-del | -/CACACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836365 | ACACACACACACACA[-/CACACAC]ACTTTAGAGACAAAG | 4734 |
rs756147004 | snp | C/T | 1.68009e-05 | 0.00289831 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55837807 | TTTAAAAGCAGCCAT[C/T]TGCTTCTGGATTCGG | 4734 |
rs756194851 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966982 | AACCTCTGCCTCCCG[A/G]TTCAAGCGATTCTCA | 4734 |
rs756200498 | snp | A/G | 1.71572e-05 | 0.00292888 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846928 | TTACTTTCCATCTAT[A/G]TATTGATGACTCTTA | 4734 |
rs756206420 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979216 | ATAACAGAATAATTA[C/T]ATTAATTGAAAAAAT | 4734 |
rs756214199 | snp | C/T | 1.65441e-05 | 0.00287607 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55847005 | GAAGAACTCATACTT[C/T]CTTTTGTAATCCCTG | 4734 |
rs756229892 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843599 | TCAATATTCTGTCAC[C/T]TCCAAAAAAGAAGGT | 4734 |
rs756242319 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873762 | TCTATTTCTCACTGG[A/G]GTTCATGAACGGAAA | 4734 |
rs756244571 | snp | A/C/G | 4.15035e-05 | 0.00455525 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830019 | AAGAACAGAGAGGAA[A/C/G]TGGTTATGAAAGACA | 4734 |
rs756273814 | snp | C/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937825 | ATAGAACACATAATC[C/G]TAAAATTCATACAGA | 4734 |
rs756283154 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845370 | TGATCACATTACCTA[G/T]TCTCTCTGTGCCTCA | 4734 |
rs756287206 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933065 | GGAGAAATAGGAACA[-/C]TTTTACACTGTTGGT | 4734 |
rs756293781 | snp | A/G | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842090 | GCTCTCTTGACACCC[A/G]TAATTCTCCGGTAAG | 4734 |
rs756303866 | snp | A/G | 7.80001e-05 | 0.00624451 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838059 | GAGTCTTTCTGGAAT[A/G]AAGTACAAAATTATA | 4734 |
rs756318586 | snp | G/T | 1.66568e-05 | 0.00288585 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860652 | GGAGAACTAGGAAAC[G/T]ACTTATACCTCGGAA | 4734 |
rs756328026 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892144 | GGTGGTGGCCACCTA[A/G]AATCCCAGCTACTCG | 4734 |
rs756328189 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877737 | ATTATTCTGCTTAAG[C/T]AAAGAATTTTCCCCT | 4734 |
rs756376024 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944185 | AAGCAGGATGGGGCA[C/T]TGCCTCACCTCGGAA | 4734 |
rs756381085 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890539 | TTTTTTATTGTTGTT[A/T]CATTATATGGATATA | 4734 |
rs756398201 | snp | A/C | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937288 | GTTATCTCAACAGAC[A/C]TTTTTATGGCGAATA | 4734 |
rs756398817 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973438 | CCAGCTCATCAGGAG[G/T]CTGAGGTGGGAGGAT | 4734 |
rs756399062 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977200 | TATTTTGGCCAATGA[C/T]GGACAGCATATATGA | 4734 |
rs756401975 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887261 | TTTAGCCAGACTAAG[-/A]AAAAAAAGAGAGAAA | 4734 |
rs756425772 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888934 | TCCTATTTCTCACCT[C/T]ATACAAAAATCAAAT | 4734 |
rs756431300 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852178 | GCGGGCACCTGTAAT[C/T]CCATCTACTCAGGAG | 4734 |
rs756455566 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858569 | ATCCCAGCCTCCCAA[A/G]GTGCTGGGATTACAG | 4734 |
rs756470609 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837247 | CCAGCCCGACCAACA[C/T]GGTGAAACCATGTCT | 4734 |
rs756489868 | snp | A/C | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55830577 | GTAAATGACTGTGGT[A/C]CATTTGAACCTATAA | 4734 |
rs756511532 | snp | A/G | 1.65381e-05 | 0.00287555 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840482 | GGGTTATTGGTTTGT[A/G]AAGCATCATCTTGTA | 4734 |
rs756520692 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972686 | ACTCTCCAATCAAAA[G/T]ACATAGAGTGGTTGA | 4734 |
rs756540218 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901287 | TTACATTTATGAAAT[C/T]GTCTCCATAAGTCAA | 4734 |
rs756565933 | snp | G/T | 3.30371e-05 | 0.00406417 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915911 | GCCATCCTCATTATG[G/T]GCAATTTCACTAGGA | 4734 |
rs756569578 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885801 | GAAAAAACTATAAAA[C/G]AACCAGAAAACAAAT | 4734 |
rs756591358 | snp | A/C | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916470 | GCACTACTGTAAATA[A/C]CATCCTTCAAGATAC | 4734 |
rs756592764 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862113 | GAAGCTTCTGTGCCA[C/T]GAAGTACTTGAATTG | 4734 |
rs756595183 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899822 | TGGAGCACAGGAAAT[A/G]TGTCTAGTGCAAATG | 4734 |
rs756614123 | snp | C/G | 1.65113e-05 | 0.00287322 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55863035 | TTCTTGTTGTTGCTG[C/G]AAATGGCAAGCAGCA | 4734 |
rs756642213 | in-del | -/CT | 6.59685e-05 | 0.00574281 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830618 | ATTTGGTTTCATTTA[-/CT]CTCTACAAGGATCTC | 4734 |
rs756680432 | snp | C/G | 1.72119e-05 | 0.00293354 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993593 | GGACGCGCTCGCCCC[C/G]GCCCAGGGCAGGCAA | 4734 |
rs756702165 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879434 | GTCTTCCAATAAAAT[C/G]ACTAATTCTCTCTGC | 4734 |
rs756704044 | snp | A/G | 1.77644e-05 | 0.00298025 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869550 | AATTAAAATTTTTTT[A/G]GTTTAACCAAATATT | 4734 |
rs756714809 | snp | A/C | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848855 | GATGTCTTTCCTCTC[A/C]GATGGGCTGGAATTT | 4734 |
rs756719823 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963225 | GAGCCTTGACCTCCT[C/G]GGCTCCAGCGATCCT | 4734 |
rs756768859 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838840 | AATTAATCAATTGGT[A/G]CCTACTTAAAAGTTT | 4734 |
rs756769099 | in-del | -/ACAG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923276 | TAAACAAGCAAAAAC[-/ACAG]ACAGAAAACAAATAG | 4734 |
rs756770606 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973368 | ACACAGTCAGGCCCT[A/C]TCTCTTAAAAACAAA | 4734 |
rs756775068 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919377 | AAGAAAGAATGACGT[C/T]TGAAAAATTTACAGA | 4734 |
rs756785614 | snp | A/T | 1.6522e-05 | 0.00287414 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840497 | GAAGCATCATCTTGT[A/T]AAATGGGCGGATGAA | 4734 |
rs756789093 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837073 | ATTCTGAATAAAATA[C/T]AGCCACAAAGAAAGG | 4734 |
rs756798613 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836053 | CTGCCTGTGGGTACA[A/G]CCTACCTTATTGCCA | 4734 |
rs756800664 | snp | G/T | 1.65037e-05 | 0.00287256 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840631 | TTTGCCATGATAAAC[G/T]GCCATTCCAGCTACC | 4734 |
rs756808261 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991375 | AAATGGCAAATGATA[C/G]TGGAGAGGGCAACCT | 4734 |
rs756842900 | in-del | -/A | 8.48702e-05 | 0.00651367 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846947 | TGATGACTCTTAAGT[-/A]TTTATTATAAACATG | 4734 |
rs756843694 | in-del | -/A | 6.6206e-05 | 0.00575314 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834193 | AAATAATGGGTTCAC[-/A]ATTTCTGTTTCAACA | 4734 |
rs756857980 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959764 | ACAGCTAGTAAGAAA[C/T]GGAAACGCTCAGACT | 4734 |
rs756868539 | snp | C/G/T | 4.9504e-05 | 0.00497493 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916002 | GTTGGAGAAGTCGGT[C/G/T]GGGTAGTTGAAGGAC | 4734 |
rs756869916 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870909 | TTACTTGTCTCAGCT[C/G]TCTATATAGATTTTT | 4734 |
rs756923683 | snp | A/G | 1.65121e-05 | 0.00287329 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915925 | GTGCAATTTCACTAG[A/G]AGAAATAATAAACTG | 4734 |
rs756981784 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876552 | TGGTATGATTGACAT[-/A]AGTTAATCATTAATT | 4734 |
rs756988583 | snp | G/T | 1.7361e-05 | 0.00294621 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55834254 | TTCATCAAAAATTTT[G/T]ATGAGATCCTGTGGT | 4734 |
rs757011759 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832297 | CCATTTAACTTTGTT[G/T]AGTCCAGCATTTCCT | 4734 |
rs757020583 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940049 | AAAAGGAAACCCTGC[C/T]ATTTCCAACAAAATG | 4734 |
rs757025432 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844074 | TTCAAATGAGGCAAT[A/C]AAGAAGGCTTTGAGA | 4734 |
rs757026354 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852338 | GTAGAAGTATCCAGT[A/G]TATCCTACAAAGTGA | 4734 |
rs757033711 | in-del | -/ACACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883679 | GTTCCAGGCATCTCA[-/ACACAC]ACACACACACAAACA | 4734 |
rs757064359 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916422 | CTTACAAGGTGACCA[C/T]CATTCACAGCATTCA | 4734 |
rs757070537 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879846 | AAAGACAATACACTA[C/T]AGGATTCTTCAAATA | 4734 |
rs757074528 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857649 | TTTATATACCTAAAT[A/G]CAATCTCAATTTGTA | 4734 |
rs757138920 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980499 | GTTCAGATCATTCTA[C/T]TGTGAGAGGCTCCAG | 4734 |
rs757149557 | snp | A/C/G | 3.48762e-05 | 0.00417577 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837767 | TGACATTATGGAAGA[A/C/G]CAAATAAAAGAAAAT | 4734 |
rs757161265 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893119 | AATACTTTTCTGAGT[A/G]AGCCAAGAAGCACAG | 4734 |
rs757166937 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909370 | CTTCCCAAAACATCT[C/T]ATTGAACTGGGACAG | 4734 |
rs757173186 | snp | A/G | 1.78892e-05 | 0.0029907 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916856 | TTTCCAAACATGTTA[A/G]GGGCTGAAAGTCATA | 4734 |
rs757181958 | snp | C/T | 1.79641e-05 | 0.00299696 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915288 | AGGAAACTTACCTTG[C/T]AAGAATTAGACAGTT | 4734 |
rs757195154 | snp | C/T | | | intron-variant, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55952620 | GCACCAGAACACTCG[C/T]AACATACTGGTATTT | 4734 |
rs757216126 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907994 | TCACCCCAGGGACAA[A/G]GTATTCATTTAAGAG | 4734 |
rs757216876 | snp | C/G | 6.59381e-05 | 0.00574149 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860542 | CTGGTTGCTATACAT[C/G]GTGGCTTCATCTTCT | 4734 |
rs757254601 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966019 | ATGAAGACTACAATT[G/T]TTCCAGGTTCTGATT | 4734 |
rs757262352 | in-del | -/AA/AAAT | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995533 | TAAAAAAAAAAAAAT[-/AA/AAAT]CAGTAAATCCCCAAG | 4734 |
rs757278017 | snp | G/T | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860471 | CTGGCATTCAATTCT[G/T]CTGCAAGATGAGTTG | 4734 |
rs757281341 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841859 | TACAGGCATGAGCCA[C/T]TGCACCCGGCCGACT | 4734 |
rs757328601 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895327 | TGCAGTTTAAATGAG[-/A]AAATGAAATCAGCAG | 4734 |
rs757331187 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855415 | GAAAAAGCATAGACA[A/G]GAATGAAGGCAGCAG | 4734 |
rs757332495 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978823 | AATGTGTTATCTATG[C/T]GGGCAGCGTCAATAA | 4734 |
rs757339423 | in-del | -/GCT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891236 | AAATGATCCCAAATA[-/GCT]GTATTTCCAATATTT | 4734 |
rs757350233 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889343 | GTATCCATCAACAGA[C/T]ATATAAAGAAAATAC | 4734 |
rs757365505 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897096 | CTCCTGCCTCAGCCT[A/C]CCGAGTAGCTGGGAC | 4734 |
rs757378456 | snp | C/T | 1.67942e-05 | 0.00289772 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840741 | CCCTGTAAAGACAAC[C/T]CCATTTAAATACTTC | 4734 |
rs757391564 | snp | C/G | 1.65209e-05 | 0.00287405 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915667 | TTGTTGTTTCACAGT[C/G]TAATGTAGCTGCTTT | 4734 |
rs757398278 | snp | A/G | 3.04261e-05 | 0.00390027 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838177 | TCAGCTCATGTTGAT[A/G]TGTCTAAAATTAAAC | 4734 |
rs757403709 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989166 | GCTGGAACCTGGTAG[A/G]CAGAGGGTGCAGTGA | 4734 |
rs757403852 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868768 | GATACTTCTTTTTGA[C/T]GATAATGTGCTTTCA | 4734 |
rs757431859 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854195 | TGGCCTTCCTGTTGT[C/G]ATTTTGAACCAGATA | 4734 |
rs757434225 | snp | A/G | 1.65239e-05 | 0.00287431 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860799 | TTGGAAGTATAAAAA[A/G]CCATCATCCATGTCT | 4734 |
rs757449463 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848358 | CATCAGAGCACACTG[A/G]CAGAGAGACTTACTG | 4734 |
rs757453375 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838077 | GTACAAAATTATATC[A/C]AATAAAATACATACT | 4734 |
rs757464727 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850586 | TAAAGAAAGGCCTCC[C/T]ATTTGGTGCATGCCG | 4734 |
rs757474060 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960869 | TGCCCTGTTCCCCAC[C/T]CACTAGTTGACTGTG | 4734 |
rs757484432 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983615 | ATTTTTAGATATACT[-/T]TTTTTTTTTTTTTTG | 4734 |
rs757487344 | snp | A/G | 3.29658e-05 | 0.00405978 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860727 | CCTGGTGGTAAATGC[A/G]CGTTGTGCTTGCAGT | 4734 |
rs757509770 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934905 | ATGGAGTCTCACTCT[A/T]TTGCCCAGGCTGGAG | 4734 |
rs757511660 | snp | G/T | 1.65614e-05 | 0.00287757 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915749 | ACAGACAGTCTGTCT[G/T]GGAGTATTATTCGAA | 4734 |
rs757531507 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903972 | TGAGACCAGCCTGGC[C/T]AACACGGTGAAACCC | 4734 |
rs757551038 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945452 | AATAAAGTGAGAATA[A/C]AAGTTTAGAGAAAAA | 4734 |
rs757586745 | snp | C/G | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918895 | AATGACTTCAGCGTT[C/G]TTTCTGGGATTAAGT | 4734 |
rs757589590 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883755 | GAGAGAGAGAGACTC[C/T]ATTTGTGTGTGAGAG | 4734 |
rs757594249 | snp | A/G | 1.65389e-05 | 0.00287562 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833094 | TTTTCTGAATCCATC[A/G]TTAAAACAGCCTGAA | 4734 |
rs757622518 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883695 | CACACACACACACAC[-/AA]ACACACACACACACA | 4734 |
rs757639345 | in-del | -/AT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907341 | TTTTAAAATGGGCAC[-/AT]GTTTTACCTTGATAA | 4734 |
rs757650831 | in-del | -/GT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964653 | AATTTTGCTGCTGGT[-/GT]GTGTGTGTGTGTGTG | 4734 |
rs757666020 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55861895 | AAAACATAATTTTGA[C/T]ACATGGCTCTAAGGG | 4734 |
rs757680293 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843794 | CAGCAACTTTAGACT[A/G]GATACTAGGCAGCTG | 4734 |
rs757700176 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897875 | CTTCCACATCCGGTT[A/C]CTGACCTTTCCTGCC | 4734 |
rs757702188 | snp | A/T | 6.33774e-05 | 0.00562891 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869667 | CTCAGATAACCTTTA[A/T]CTCTTGATTTGTGAC | 4734 |
rs757721935 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875759 | TAATATGAAAAATAA[A/T]GGGAACTTGTGGAAA | 4734 |
rs757731785 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830829 | TTTAGTCTCCTGAGT[A/G]GCCAGGACTACAGGT | 4734 |
rs757737565 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926809 | GGGTGGGCATGGTGG[C/T]TCACGCCTGTAATCC | 4734 |
rs757737588 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915531 | AATTCTCCATTGATA[C/T]TTATTTGACAATCTA | 4734 |
rs757753009 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912299 | AGGAAGAACAATAAA[A/C]TAAGAAAATATTGAA | 4734 |
rs757784736 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829830 | AGTAGTTCCCCGGAA[A/T]ATTTTAAGTCAAGAT | 4734 |
rs757792589 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925714 | CTTGTGACAAAGATA[C/T]CTAGATACCTAACTC | 4734 |
rs757807694 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972479 | TAATGCATTGTAAGA[C/T]GTTAATTGCAACCCT | 4734 |
rs757812783 | snp | C/T | 3.29538e-05 | 0.00405904 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916556 | ACTGTACCTTGTTGG[C/T]TGTAGTGAAATCTGT | 4734 |
rs757828987 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55948374 | GTGAAAATGGCCATA[A/C]TGCCCAAGATAATTT | 4734 |
rs757885884 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961056 | TGTCAGGATTCTCCT[A/G]GAGAGTGGCTATCTG | 4734 |
rs757894111 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835999 | TAGCTCCGCAGGCTG[A/G]TTGTTTCCCTCTTGC | 4734 |
rs757908792 | snp | A/C | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833011 | GAAAATCCTTACCGT[A/C]TAGTTCAGCAAATCC | 4734 |
rs757911431 | in-del | -/CAAACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883694 | ACACACACACACACA[-/CAAACAC]ACACACACACACACA | 4734 |
rs757917244 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900047 | GCCCCACACCACACT[-/G]TGTTCAGAATCATGA | 4734 |
rs757920180 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846436 | ATATTGCATTTGTGG[C/T]GATGGGAAAAAGTGT | 4734 |
rs757943058 | snp | C/T | 1.65312e-05 | 0.00287495 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856128 | GGAGAGGGTAAAACT[C/T]ACCACAGGAAGTGTA | 4734 |
rs757959167 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972994 | TATAAAGCAAATATT[A/G]TTAAAGTCAAAGAGT | 4734 |
rs757961850 | snp | A/G | 3.31005e-05 | 0.00406807 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840673 | CTTGAAGTAAGAGAG[A/G]TGATCTTCGTTACAC | 4734 |
rs757974612 | snp | A/C/G | 3.29866e-05 | 0.00406108 | synonymous-codon, missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916016 | TCGGGTAGTTGAAGG[A/C/G]CTCCTAGGAAAAATG | 4734 |
rs757982258 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971728 | AACTTTCTAGGCCTA[A/G]AAAAAGATATCAATA | 4734 |
rs758001445 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836382 | ACACACTTTAGAGAC[-/A]AAAGTTTCACTCTGT | 4734 |
rs758020217 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850555 | ACCCAGGTGGTGGTT[C/T]TAGTGTTGTGGTCAA | 4734 |
rs758038723 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941864 | AGGCGTGAGCCATTG[C/T]GCCCAGCCAATCCTG | 4734 |
rs758046027 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930954 | AGCAGCATCAGAATG[C/G]ACTAATTCACTTACC | 4734 |
rs758056330 | snp | A/G | 1.92989e-05 | 0.00310629 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869698 | TGTAGAAAAGAAAAT[A/G]AATATTCATAAAACT | 4734 |
rs758069845 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942390 | CAAATTGTAATCCCT[A/C]ATGTTGGAGGAGGGG | 4734 |
rs758111664 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874726 | CACCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 4734 |
rs758113655 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982850 | TCTAGGGCTGGGGGT[A/G]GTGGCTCACACCTGT | 4734 |
rs758132315 | in-del | -/A | 4.95299e-05 | 0.00497619 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848484 | CATAAAATTTATTAC[-/A]AAAAAATAACATAAT | 4734 |
rs758147886 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959543 | CCACCTCCTAATATT[-/C]ATGTTCTTTGTGTTC | 4734 |
rs758155069 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896085 | AATCTACCTTGCAGC[C/G]TTCTATTAACAAAAG | 4734 |
rs758187870 | snp | A/T | 1.64866e-05 | 0.00287106 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915503 | TTTGTTCATCTGTGA[A/T]TGTGGTCTTTCCAAT | 4734 |
rs758203163 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857549 | GCTGGTCTCGAACTC[C/G]TAACCTCATGTGATC | 4734 |
rs758208348 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851673 | GTAGAGATGGGGTTT[C/T]TCCATGTTGGTCAGG | 4734 |
rs758217633 | snp | A/G | 5.14814e-05 | 0.00507327 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837780 | GAGCAAATAAAAGAA[A/G]ATGAATACCTCTTTA | 4734 |
rs758222467 | in-del | -/T | 8.84791e-05 | 0.00665069 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837743 | TTTGAAACTTATAGG[-/T]TTATACTGTGACATT | 4734 |
rs758224781 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870670 | TCCTAAATAACTGGG[A/T]CTACAGGCACACACT | 4734 |
rs758235639 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991273 | CTGCAATGCTTTCTT[C/T]CTTTAACAAAAGGGG | 4734 |
rs758293018 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827033 | CAATCTTGATATATA[C/T]ATTTACTGTGTCAGA | 4734 |
rs758313710 | snp | A/G | 1.65081e-05 | 0.00287293 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915932 | TTCACTAGGAGAAAT[A/G]ATAAACTGGTGTGAA | 4734 |
rs758319670 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855609 | TGCCATCCAGGCTGT[G/T]GCTGGGACAGCACTG | 4734 |
rs758322702 | snp | A/G | 1.64928e-05 | 0.00287161 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860561 | GCTTCATCTTCTCTT[A/G]TAATTTCCCAGTTCT | 4734 |
rs758346608 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893135 | AGCCAAGAAGCACAG[A/G]TAAGTTTAAATACCT | 4734 |
rs758359897 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891993 | ATTATAGGCTGGGCA[C/T]GGTGGCTCATGCCTG | 4734 |
rs758361528 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848864 | CCTCTCAGATGGGCT[A/G]GAATTTTCAATCTTG | 4734 |
rs758366409 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869146 | TATTAGATCACTTAA[A/G]TTTTCCTTGCTCCCT | 4734 |
rs758399068 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829421 | TATATTGTAGTTTAC[G/T]CAATAGTAAAGTATT | 4734 |
rs758401367 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982717 | CTGTGCATTTCACTC[-/TT]TGTAAATTTCACTCT | 4734 |
rs758413042 | snp | A/G | 1.64928e-05 | 0.00287161 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860624 | CTTTATTGCTATAGC[A/G]TGTGTCTTTCAAGGA | 4734 |
rs758413665 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959649 | TTACATTACATAAGA[C/T]TGTAATCCATCTTGC | 4734 |
rs758426758 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951595 | GTAAGGATCACTGTT[-/AA]AAAAAAAAAAAAAAA | 4734 |
rs758454377 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867450 | GGTCCTATGATGCGT[A/G]CATGTGGGCAAAACT | 4734 |
rs758457855 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950108 | AATCAAAACCAGACA[A/T]TATCAAGTCTGGAAT | 4734 |
rs758462436 | snp | A/C/T | 3.30618e-05 | 0.00406571 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860804 | AGTATAAAAAGCCAT[A/C/T]ATCCATGTCTTAAGT | 4734 |
rs758464508 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902972 | TGCTATTGCATTCCA[G/T]CCTGGGTGACAGAGC | 4734 |
rs758481278 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989125 | CCTATAATCCCAGCT[A/G]CCCTGGAGGGTGATG | 4734 |
rs758527272 | snp | A/G | 2.03287e-05 | 0.00318809 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830013 | AACTGAAAGAACAGA[A/G]AGGAAGTGGTTATGA | 4734 |
rs758531796 | in-del | -/TGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964291 | TCCTCAAGGCTCTGT[-/TGT]TGTTGTTGTTGTTGT | 4734 |
rs758543908 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853822 | GGTGAAAACTTGTCT[C/T]TACTAAAAGTACAAA | 4734 |
rs758547640 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839277 | CAAGTGATCCACCTG[C/T]CTCAGCTTCCCAAAG | 4734 |
rs758563504 | snp | A/G | 1.65935e-05 | 0.00288036 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852404 | CCTGTAAGAAAGCAA[A/G]TTGATAGATTACAGG | 4734 |
rs758565837 | snp | G/T | 3.29592e-05 | 0.00405938 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841966 | CAACCCATAATAAGG[G/T]TTAAACATTTCCTTT | 4734 |
rs758575554 | snp | C/T | 2.18067e-05 | 0.00330195 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829847 | TTTTAAGTCAAGATT[C/T]TGGTTATAAAACTAT | 4734 |
rs758577603 | snp | A/T | 1.65176e-05 | 0.00287376 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838534 | AGTTCTTCATCTATG[A/T]TAAACCTGAGGTCCA | 4734 |
rs758594687 | in-del | -/C | 1.73199e-05 | 0.00294273 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916828 | ATCGTAAGCTTTGTG[-/C]CATTTGTTCTCATTT | 4734 |
rs758602765 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866023 | TGCAGCCTTGACCTC[C/T]TGAGCTCAAGCAATC | 4734 |
rs758621928 | snp | C/G | 1.66161e-05 | 0.00288232 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850719 | ACTCTGGCTTGAGGT[C/G]AGCTGACTGGTCTCC | 4734 |
rs758625505 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925302 | TTAAATGTTTGCAAA[C/T]GCTTATAAATACAGA | 4734 |
rs758640977 | snp | C/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994022 | CCAGAGTTCGGCCTC[C/T]GACTAGACGCCTGGG | 4734 |
rs758652000 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55954901 | ATATATAGGGGGTTA[A/G]TGGCCTTCTTCAGAT | 4734 |
rs758737877 | snp | A/G | 1.66095e-05 | 0.00288175 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55847027 | TAATCCCTGGAGTAG[A/G]GCACTGCCTTTAGTT | 4734 |
rs758740674 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981845 | CAACCACAGGTACAG[A/T]ACATGGGGGTAGGAA | 4734 |
rs758743902 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976623 | TTATCCAATCTGGGC[-/A]AAAATTTTTTTTTTT | 4734 |
rs758744483 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995311 | AAATAATCTGAAAAT[A/G]TTGTGTGCCCTTCTA | 4734 |
rs758744671 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55860058 | ATCACCTAACAGGAG[C/G]CCAAATCCCTGAAGT | 4734 |
rs758797806 | snp | C/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994274 | TTGTTGTCCTATGGT[C/G]TGTCCATCTTTAAAT | 4734 |
rs758821192 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828778 | ATTGTCTTCATAGTA[A/C]ACAGTATTTTAAAAG | 4734 |
rs758831835 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888439 | ATATCTCTATCAAAC[A/G]CTGATGAAAGAAATC | 4734 |
rs758843604 | snp | C/T | 8.36141e-05 | 0.0064653 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856236 | AGAATACCTTGATAT[C/T]TGTGATTTGCCTTTG | 4734 |
rs758847267 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965903 | CTGATCCGCCTGCCT[C/T]GGCCTCCCAAATTAC | 4734 |
rs758891485 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889083 | ACAGACAACCAAATC[A/G]AAATGGACAAATGGG | 4734 |
rs758913476 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838203 | TAAACACAATAACTT[G/T]ATATGTTATTTTAGC | 4734 |
rs758947192 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936452 | TAGGAAATCCCAGAA[A/G]AGCATATTATCAGTG | 4734 |
rs758968501 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55861341 | CTGTTTTTCGTAATA[C/T]ACAGTCATGGGCCTG | 4734 |
rs758968622 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842585 | GTCTTGCCATCTTGC[C/T]CAGGCTGGTCTCAAA | 4734 |
rs758980770 | snp | C/T | 0.000164905 | 0.00907884 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830481 | TCTCACTCTCTGAGG[C/T]TTTGTTCTATCAAGG | 4734 |
rs759000153 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864573 | GTAAATCCCAGTTAT[C/T]CGGGAGGCTGAGGCA | 4734 |
rs759010689 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975670 | TTCCATGTTCATGGA[C/T]TGGAACAATCAATAT | 4734 |
rs759011453 | snp | A/T | 2.34261e-05 | 0.00342235 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850771 | GAAATCATATTGTAA[A/T]ATTTTATAGAGAGAA | 4734 |
rs759031516 | in-del | -/AC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830675 | TACACTAGTTCCTAC[-/AC]ACACACACAGGGAAC | 4734 |
rs759046864 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55878571 | CTTATAAAGTTAAAC[A/G]TATACCAGTATATGA | 4734 |
rs759069643 | snp | C/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995057 | AAGACTCCACCTCAA[C/T]TGTCGTACTTTATGA | 4734 |
rs759090171 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943800 | CACTATCGTCCAGAC[C/T]CCAGAATGGGAGATT | 4734 |
rs759090539 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829562 | CTGGCAGATACTATA[C/T]AAGAGGTAAATGTTA | 4734 |
rs759092946 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937357 | GATATAAATGACAAA[A/G]AGGAAAATAGAGGAC | 4734 |
rs759103902 | snp | C/T | 8.23974e-05 | 0.00641809 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842091 | CTCTCTTGACACCCA[C/T]AATTCTCCGGTAAGA | 4734 |
rs759140273 | in-del | -/GT | 1.64772e-05 | 0.00287025 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916561 | ACCTTGTTGGCTGTA[-/GT]GAAATCTGTAGACAG | 4734 |
rs759171663 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947691 | TATAAACAGAACCAA[A/G]GACAAAAACCATATG | 4734 |
rs759173178 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911872 | TGTCCCTATTACTAG[A/G]ATGGGAGCTCCCCTA | 4734 |
rs759181317 | snp | C/T | 1.70327e-05 | 0.00291823 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993565 | TGCCATTTCCGAACG[C/T]TTCCAGCAAACCGGA | 4734 |
rs759188409 | snp | A/C/T | 0.000115975 | 0.00761424 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915360 | ACTTTACCTTCATTT[A/C/T]CAGATGCAAACTTTA | 4734 |
rs759196457 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888938 | ATTTCTCACCTTATA[C/T]AAAAATCAAATAAAA | 4734 |
rs759198988 | snp | C/T | 3.39489e-05 | 0.00411987 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55834233 | ATGTCTTACCTCTAG[C/T]TCATTTTCATCAAAA | 4734 |
rs759199057 | snp | C/G | 3.32419e-05 | 0.00407675 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842149 | TTTCATTTCAAATTT[C/G]TTTGGAATGTCATTC | 4734 |
rs759234630 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886250 | CCAATACAATTATAG[C/T]TTGAGAATTCAACAT | 4734 |
rs759238280 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916402 | CACTACAAATGGCTG[A/G]ACTGCTTACAAGGTG | 4734 |
rs759245796 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925144 | TGGAATGCATTTTAA[A/C]ATTACATGAAATAAG | 4734 |
rs759254962 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984071 | CCCACGTGCCTGATA[A/C]ATAGTGTTCATCAAA | 4734 |
rs759283591 | snp | C/G | 2.97827e-05 | 0.00385882 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838171 | CATTTTTCAGCTCAT[C/G]TTGATGTGTCTAAAA | 4734 |
rs759345224 | snp | C/T | 4.96915e-05 | 0.0049843 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862920 | GCACATACTGAGGGG[C/T]TGGTCTTTTCCACTG | 4734 |
rs759354364 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962180 | TATTTTACCAGATAC[A/G]AATATATCCACTTCA | 4734 |
rs759356317 | in-del | -/AC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830674 | TGTACACTAGTTCCT[-/AC]ACACACACAGGGAAC | 4734 |
rs759381027 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836860 | GATAAGGTCTCCCTA[C/T]GTTGTCCACGTTGGT | 4734 |
rs759382318 | snp | A/T | 1.6554e-05 | 0.00287693 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915738 | GATGACTTTTCACAG[A/T]CAGTCTGTCTGGGAG | 4734 |
rs759397152 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864604 | GGAGAATCACTTGAA[C/T]CCGAGAGGCGGAGGT | 4734 |
rs759447335 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877182 | CTCAAAATTCACCAA[A/C]TGTCTGCCTAATTTT | 4734 |
rs759459758 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942847 | AGAAAGGAGGATGAT[A/G]GAAAGATAGAATTTC | 4734 |
rs759469131 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898967 | TTTAAAAAGCAAAAT[A/C]TGTTTGTTAGATTTT | 4734 |
rs759469427 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850678 | CCTGAATCACTGGTG[A/G]AGGCTTGTGATTGAG | 4734 |
rs759472034 | snp | A/C | 1.65886e-05 | 0.00287993 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915790 | TCTTCTGTAACGAGC[A/C]CTTCCTGTGAAGCGG | 4734 |
rs759498673 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942266 | TCTCTGGCAATACTG[C/T]CCTGAAGTCTAATTT | 4734 |
rs759512639 | snp | G/T | 1.6679e-05 | 0.00288777 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840723 | TCTGTAGGGTATAAT[G/T]GTCCCTGTAAAGACA | 4734 |
rs759517734 | snp | C/G | 1.72507e-05 | 0.00293685 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993503 | CCGCAGCCCCGCGGT[C/G]CCCGCACCTCGTCCT | 4734 |
rs759524146 | snp | C/T | 4.95111e-05 | 0.00497525 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860778 | ATCTGTTAGGTTGTC[C/T]CTATATTGGAAGTAT | 4734 |
rs759537479 | snp | C/T | 1.78538e-05 | 0.00298774 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829969 | TAATTCTTCAAATGA[C/T]TCATAAGGTGGCAAG | 4734 |
rs759550238 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913267 | ACTGGAGTCATGGGA[A/C]ATATTTTGGGAGCTG | 4734 |
rs759590614 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845678 | CCAGCGTATTCTCAT[A/T]AACAATGAAAATATT | 4734 |
rs759606769 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853604 | AGTTACTCCTGCCTT[A/G]TTTCTCTAAAAGCTA | 4734 |
rs759622214 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941506 | TTTGTGATATACATA[C/T]GTGTGTTACTGAATT | 4734 |
rs759629375 | snp | A/T | 1.67685e-05 | 0.00289551 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856096 | GATGCTGAGTTTTAT[A/T]TTTTTATTGATTGAT | 4734 |
rs759639756 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844551 | CCTGTGTTATTGACT[C/T]CACCATTCACTAGGA | 4734 |
rs759641106 | snp | C/G | 1.66585e-05 | 0.00288599 | intron-variant | NEDD4 | GRCh38.p7 | 15:55832959 | GTCAGCCATGAAAAA[C/G]ACAATACGCATTATT | 4734 |
rs759651234 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881933 | TGTGTCAGTAGTACC[C/T]GCCCTCCAGTTATAA | 4734 |
rs759667461 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981014 | TTCAACAAAAAAAAA[C/T]TGCTAGGGAGGGATG | 4734 |
rs759691858 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859216 | CTCCCTTGATGATAC[A/G]TATTAGACAGCTAGC | 4734 |
rs759699949 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895336 | AAATGAGAAATGAAA[C/T]CAGCAGACGACTGCT | 4734 |
rs759705181 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910084 | AACCTTTATTTTTTT[A/C]TCCAGGAAAAAGAGA | 4734 |
rs759736921 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980313 | GACAAATTCTGGATT[A/C]ACAAGAAACCTTTCT | 4734 |
rs759739298 | snp | C/T | 2.47197e-05 | 0.00351557 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863124 | TACGCATGATTTTTT[C/T]AACTTTCTAAATTAT | 4734 |
rs759753985 | in-del | -/TGATA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877796 | TCATCATAGACTCAT[-/TGATA]TTTGTTTTATATTAT | 4734 |
rs759756445 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909298 | TCTATCCCAACAGTT[C/T]GCTTCAATCTTAGTG | 4734 |
rs759768492 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923298 | GAAAACAAATAGCTC[G/T]GTAACTAACCATATC | 4734 |
rs759776625 | in-del | -/A | 3.54742e-05 | 0.00421139 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838613 | ACTATCCTAGATGGG[-/A]AAAAATTACATATTT | 4734 |
rs759793936 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954091 | TTCCCTTTAGATCCA[C/T]TCCTATGAAAAGGCT | 4734 |
rs759843153 | snp | A/G | 1.66593e-05 | 0.00288607 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869631 | GAGCCACTGGTTTTA[A/G]GTAAATAAGTCATTT | 4734 |
rs759866026 | snp | A/G | 3.29734e-05 | 0.00406025 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915446 | GGAAATATTTGGATA[A/G]GCTCCTCCCAATGAA | 4734 |
rs759874076 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827979 | TCATTTGACAGATGA[A/T]GAAATATGAATCCAG | 4734 |
rs759896714 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882786 | TCCTTTTGCTTAAGA[A/G]GAGTAAAGAGGACTT | 4734 |
rs759924879 | in-del | -/GCCTCTCTGC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940546 | TCTCTCTCTCTCTCT[-/GCCTCTCTGC]CTCTCTCTGTCTCTT | 4734 |
rs759942614 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860521 | CGGTGGAGGTGATGG[A/G]AAGGCCTGGTTGCTA | 4734 |
rs759943605 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854830 | GCATGGAAACAACTT[C/T]TCTGGTACTAAAATA | 4734 |
rs759976445 | snp | A/G | 2.58228e-05 | 0.00359315 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55924681 | CTTCAAAAAGAAGCC[A/G]GTGCTGCTGAGGATG | 4734 |
rs759977936 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831048 | CTCAGCCCTCCCAAG[A/C]AGCTGAGATTCCAGG | 4734 |
rs759992698 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989026 | GGATCATCTGAGGTC[A/T]GGAGTTCGAGACCAG | 4734 |
rs759998558 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853763 | GGGGGCTGAGGTGGG[C/T]GGATCACCTGAGTTC | 4734 |
rs760002547 | snp | C/G | 2.28809e-05 | 0.0033823 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834311 | AGATGTATTTAAAAA[C/G]TTGATGGGCAGGGCC | 4734 |
rs760009305 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971163 | TTGGCAAATTAAAGA[A/C]TGCATCAGAATCTCT | 4734 |
rs760013095 | in-del | -/TCTC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939334 | CCTCCCCCTTCACTT[-/TCTC]TTCTGTCTCCTACCA | 4734 |
rs760032310 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960434 | ATGCTTCCTGCCCTC[A/G]AACATCAGACTCCAA | 4734 |
rs760049613 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866947 | TTCTAACCGCAAAGC[C/T]AATATGTAATTGCTC | 4734 |
rs760055301 | snp | A/C | 8.90274e-05 | 0.00667126 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951472 | TTATAAAAATAAAAC[A/C]AAGTACATTAAAAAC | 4734 |
rs760071562 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953791 | AATGGCACGATCTCG[A/G]CTCACTGCAACCTCC | 4734 |
rs760080515 | snp | A/C | 1.6531e-05 | 0.00287493 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915897 | CCTTTAGCACTAGTG[A/C]CATCCTCATTATGTG | 4734 |
rs760085639 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959544 | CACCTCCTAATATTC[A/G]TGTTCTTTGTGTTCC | 4734 |
rs760088905 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875170 | ACGCAGATCATGGAA[C/T]AAGCAGACAAGGAAA | 4734 |
rs760099564 | snp | A/T | 1.65581e-05 | 0.00287728 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834035 | ATAGAAGTTTCAAAT[A/T]ACCTTCCAAAACCAC | 4734 |
rs760142230 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888896 | AAAACTGGATATCCA[C/T]ATGCAAAAGAAACAA | 4734 |
rs760143712 | snp | A/C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929737 | TTAAGTATGATAGAT[A/C/T]ACCAGAGATCACGAA | 4734 |
rs760157254 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828460 | AAATACAGTCTTGGC[A/C]CACTTTATCTTTGCA | 4734 |
rs760158990 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841248 | AAACAAAGCATTATA[A/T]GCAAAAATAATGGAA | 4734 |
rs760221723 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945945 | AAATAAAACCCTTTA[G/T]AGACAAGCTGAGAGA | 4734 |
rs760244937 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837567 | AAAGTGAAGAGAATG[A/G]AATAGGGAAAAGGCT | 4734 |
rs760261724 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913311 | GAGTTACAATATACC[-/A]CTATAATTAGATTAA | 4734 |
rs760267527 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903546 | AGAATATACTGGGGC[C/G]GGGCAAGGTGGCTCA | 4734 |
rs760268554 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909290 | GCTCTTGTTCTATCC[C/T]AACAGTTCGCTTCAA | 4734 |
rs760317333 | snp | A/C/G | 3.29567e-05 | 0.00405924 | synonymous-codon, missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916505 | AAACGAAGCATCATC[A/C/G]CTATCAGCTAAGACA | 4734 |
rs760325038 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888141 | CCTAGCTACAGCAAT[C/T]AGGCAAGAAAAAGAA | 4734 |
rs760325545 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924236 | GAGTGGATAGGATGT[C/T]CATTGGATACAGGTA | 4734 |
rs760325601 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936854 | CTGGAGCACAATGGT[A/G]TGAACTCGGCTCACT | 4734 |
rs760331066 | snp | C/T | 1.64936e-05 | 0.00287168 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860610 | TTGAGCCACACATAC[C/T]TTATTGCTATAGCAT | 4734 |
rs760350454 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983420 | CTCATCTGCTGACGT[C/T]GTGCCTCTTGTTTTA | 4734 |
rs760391997 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942159 | TGTCAATTTTGACTT[C/T]GTAATTTTAAAGATT | 4734 |
rs760406672 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945065 | GGGGAGAAACCAGAG[C/T]AGAAAAGCTGAAAAT | 4734 |
rs760407940 | snp | A/G | 1.90871e-05 | 0.0030892 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829996 | CAAGTCCAGGCGATT[A/G]AAACTGAAAGAACAG | 4734 |
rs760461560 | snp | A/G | 1.66241e-05 | 0.00288302 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852392 | GACAGTTTAAATCCT[A/G]TAAGAAAGCAAGTTG | 4734 |
rs760494424 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55833909 | TAAAATCAAAGATAA[-/T]TTTTTTCTGGTCTGT | 4734 |
rs760503227 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971230 | CGAGCTTGAAGATAG[A/G]TTATTTGAAAATATA | 4734 |
rs760516800 | snp | A/C | 3.30175e-05 | 0.00406296 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862933 | GGTTGGTCTTTTCCA[A/C]TGTGTTCTTCTAGAT | 4734 |
rs760545433 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852485 | ACATAATATGATCTT[C/T]CTCTTTCATCTTGTT | 4734 |
rs760550047 | in-del | -/GCCT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940541 | TCTCTCTCTCTCTCT[-/GCCT]CTCTGCCTCTCTGCC | 4734 |
rs760564947 | snp | C/T | 1.73339e-05 | 0.00294392 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840415 | GCTTGTTAAATTATA[C/T]TTCGTCTATACTATA | 4734 |
rs760570616 | snp | A/C | 1.65499e-05 | 0.00287657 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915878 | GACAGCTGTTGAAAG[A/C]AATCCTTTAGCACTA | 4734 |
rs760583857 | in-del | -/AT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966777 | AACTTATTACACTGA[-/AT]AAGAATTTATCGCTG | 4734 |
rs760592874 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876320 | AAAGAGAGTAATAAA[C/G]AGCACCAGAAAATGG | 4734 |
rs760597776 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899625 | GCCATAACCACCTAG[C/T]ACAGCAGCTTTAGGC | 4734 |
rs760615558 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911305 | CCCCACTACAAAAGT[G/T]TCCAGCCCAATATAA | 4734 |
rs760624130 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859628 | CCTGAAGCTGGAGAC[A/G]GAGTTTGCAGTAAGC | 4734 |
rs760654682 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990828 | CATGTTATTCTCTAC[G/T]GTGAATCTCAAGTGA | 4734 |
rs760673890 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829459 | CCAAATTTCAGTTTT[C/G]CATCTCAAAATGCAT | 4734 |
rs760698013 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925072 | GACTCCATCTCAAGA[A/T]AAACAAAACAAAACA | 4734 |
rs760709058 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980090 | TGGGATTACAGGCGC[A/G]TGCCACTATGCCCAG | 4734 |
rs760710470 | in-del | -/TAGATAAAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972535 | ACAACAGACATACAA[-/TAGATAAAC]CAAGAAATTAAAGCA | 4734 |
rs760712995 | snp | C/T | 1.66043e-05 | 0.00288129 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834029 | ATGAAAATAGAAGTT[C/T]CAAATTACCTTCCAA | 4734 |
rs760739018 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938555 | GGTCTTGACAATGAC[A/G]ATGATTTTTTGGGTG | 4734 |
rs760740828 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957882 | CACGGACAGAAAACC[A/G]AACACCGCATGTTCT | 4734 |
rs760741466 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837157 | AAAGTAGGCCGAGCA[C/T]GGTGGCTCACACTGG | 4734 |
rs760766144 | snp | C/T | 3.3024e-05 | 0.00406336 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833077 | GAAGTAATCTTATTC[C/T]TTTTTCTGAATCCAT | 4734 |
rs760770287 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857378 | CTGATGCCCAGGCTG[C/G]AGTATGGTGGTGCGA | 4734 |
rs760783196 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907859 | TTTCAGGAAACTTGA[G/T]CTGAGCCTCTATCCA | 4734 |
rs760788124 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901567 | TAGAAATCCTGTATT[C/T]CTTTGAAAACAGACT | 4734 |
rs760822826 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991786 | GCCCCAGTTCCTTAC[A/C]GACCACCCATTAACT | 4734 |
rs760834218 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921230 | GTATTTTTAGAAGGA[C/T]TGAATAATTTGTTTA | 4734 |
rs760834802 | snp | A/T | 0.000281064 | 0.0118513 | stop-gained, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856171 | AAAGTATAGGCTTGT[A/T]AGCTGCCTCTTCTGC | 4734 |
rs760855804 | snp | A/C | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916708 | CAACGTTAGACGTTG[A/C]AATCCGTGTTGGTCT | 4734 |
rs760868740 | in-del | -/ACACACACTTTAGAGACAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836366 | CACACACACACACAC[-/ACACACACTTTAGAGACAA]AGTTTCACTCTGTAG | 4734 |
rs760871923 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908865 | TGTAACATAATGAGA[C/T]CTCATCATAAAAAAA | 4734 |
rs760883663 | snp | G/T | 6.55143e-05 | 0.00572301 | missense, utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55872439 | TGAAGAACAAAATCC[G/T]TAAATGTATATGGTC | 4734 |
rs760907153 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916625 | AACAGATGATCTTTC[C/T]TGAGACTGAACGTTT | 4734 |
rs760912463 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846846 | AGCATCCTTTCTCTA[A/G]GAAAAACTGTTCACT | 4734 |
rs760926456 | snp | A/T | 1.66029e-05 | 0.00288117 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860397 | GTAACAAAATCTAAG[A/T]GCATCTTACTGAGCT | 4734 |
rs760948834 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862221 | AGCCAAAAATTAGGA[-/G]GCTAATGAACACATT | 4734 |
rs760950613 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832802 | AGTCATTTGATGTTT[C/T]CAGTTTTCCCCTTTA | 4734 |
rs761017202 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962879 | GCAACCTCTGCCTCC[A/T]GGGTTCAACTGATTC | 4734 |
rs761017280 | snp | A/C | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840611 | TAATACTAACCATCC[A/C]ACAGTTTGCCATGAT | 4734 |
rs761024849 | in-del | -/CTATAAAAAAGGATAATTTTCCTATCAATC | 1.70242e-05 | 0.0029175 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841890 | TTACTTTTAAAACAG[lengthTooLong]TGATTTTTCTTTTTC | 4734 |
rs761032036 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891058 | CCTGTTTTTATTGCT[C/G]TATATTTGTTGTTCA | 4734 |
rs761043755 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838361 | AGTCAAATGTTAAAG[A/G]AAGTACAAATTCTTG | 4734 |
rs761082736 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916811 | TCTGGCTGCAAAGTG[C/T]AATCGTAAGCTTTGT | 4734 |
rs761092597 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985949 | AGCAAAATACAAGAG[A/C]AGCCTGGAACAACTT | 4734 |
rs761093380 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952019 | AAACTGCTTTCACTT[-/A]AAAAAAAAAAAAACA | 4734 |
rs761098352 | snp | A/T | 3.30011e-05 | 0.00406195 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915988 | GAGTACACAGACTTG[A/T]TGGAGAAGTCGGTCG | 4734 |
rs761101504 | snp | G/T | 1.6743e-05 | 0.0028933 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840735 | AATTGTCCCTGTAAA[G/T]ACAACCCCATTTAAA | 4734 |
rs761106311 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939622 | CAAAAATCACTAATC[A/G]TCAGGGAAATGCAAA | 4734 |
rs761116919 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849946 | TACAGGCACCCGCCA[C/T]CATGCCTGACTAATT | 4734 |
rs761144804 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848828 | GGCCCTAGATCATTG[G/T]AAGTATCAAGTGATG | 4734 |
rs761165236 | in-del | -/TGCTGGCTGGC | 1.64904e-05 | 0.00287139 | frameshift-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860416 | TCTTACTGAGCTCGA[-/TGCTGGCTGGC]TCACGGCTGAATTTC | 4734 |
rs761183187 | snp | A/G | 1.95173e-05 | 0.00312383 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966465 | ATAATCCAAATAGAT[A/G]TACTTACCTAGCTCC | 4734 |
rs761200090 | snp | C/T | 3.30235e-05 | 0.00406333 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916088 | GCTCACTGGCAATTT[C/T]ATAATCTCTAATCCA | 4734 |
rs761219465 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895152 | GCTCTTCCTTTCCAA[A/T]AGAAAAGTATTCACT | 4734 |
rs761225711 | snp | C/G | 5.7612e-05 | 0.00536681 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869640 | GTTTTAGGTAAATAA[C/G]TCATTTTTAGTCTCA | 4734 |
rs761230140 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894449 | GGGGTCCTGGAACCA[C/T]TCCCCCTGCAAATAC | 4734 |
rs761247525 | snp | A/C | 1.71749e-05 | 0.00293038 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55837847 | CGCCATTGTATTACA[A/C]GACTAAAAAGAAACA | 4734 |
rs761273887 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902599 | GGTTCACTGCAATAT[C/T]CTTTCTACTTTTGTG | 4734 |
rs761276720 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894460 | ACCATTCCCCCTGCA[A/C]ATACCAAGAGACACC | 4734 |
rs761304271 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865077 | GTGGCGGGCGCCTGT[A/T]ATCCCAGCTACTCGA | 4734 |
rs761313241 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952264 | GCATGAACCTGGAAG[A/G]TGGAGCTTGCAGTGA | 4734 |
rs761336467 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851958 | TATTAGAGATTCATA[C/G]GAAAAGGTAGACACT | 4734 |
rs761351364 | snp | A/G | 4.06645e-05 | 0.00450894 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838114 | ATACTTACTAAATAT[A/G]TTCCTTTTTGTTCTT | 4734 |
rs761399958 | snp | C/T | 0.000230711 | 0.0107379 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860677 | TCGGAAGACTCTCGG[C/T]TGTCAACACTTTCTG | 4734 |
rs761422461 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931769 | TTACTAGCTATAATT[C/G]ACATAGCATACACTC | 4734 |
rs761447669 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962401 | ATTGGATTTAGTCTA[C/T]AGGTTTATTGTTTGT | 4734 |
rs761461190 | snp | G/T | 4.94956e-05 | 0.00497447 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915589 | ATGTCCTATGCATGA[G/T]CTTAATATACTCTGA | 4734 |
rs761463411 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865352 | TATATCAGGATAAGT[C/T]ACAGACTGAATAATA | 4734 |
rs761464749 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928661 | ACACTGTGCTCATCA[C/T]TCAAGCCCAGCTCAA | 4734 |
rs761467505 | snp | A/T | 1.64925e-05 | 0.00287158 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850530 | ATTTAAATGGAAAAG[A/T]ATCAAAGTTACCCAG | 4734 |
rs761478509 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900543 | TTTATAAATAACATG[A/C]CAGGGTCATACCCAA | 4734 |
rs761526494 | in-del | -/TCTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870528 | TCTTCTTCTTCTTCT[-/TCTTT]TTTTTTTTTTTTTTG | 4734 |
rs761533140 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915782 | AACAATTTTCTTCTG[C/T]AACGAGCCCTTCCTG | 4734 |
rs761576018 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961166 | GACATCTGGTCATAG[C/G]TCAGACACTTAGGCA | 4734 |
rs761581913 | snp | C/T | 1.71531e-05 | 0.00292852 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852582 | ATTAAATACATCAAG[C/T]TTAAGAATCCTTCTA | 4734 |
rs761592561 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984476 | CAGAGTGGGTATTCA[C/G]TTAAAGGCAGTTGCT | 4734 |
rs761594337 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906645 | TGTGGGGTGGGGGGC[G/T]GGGGGAGGGATAGCA | 4734 |
rs761603531 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964322 | TGTTTTTCTCCAATC[-/TT]TGTCTCTCTCATCTC | 4734 |
rs761621232 | in-del | -/TGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973100 | AAACCAACAAAGAAA[-/TGT]TGTTGGACTTAATCT | 4734 |
rs761625916 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832723 | CCCGGCCAAGGTAAT[A/G]CTTTTTCTGTAACGG | 4734 |
rs761630496 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854529 | ACACGTAAGCCCACA[C/G]CCTACGAGTCCCTTT | 4734 |
rs761634969 | snp | A/G | 4.94556e-05 | 0.00497246 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852493 | TGATCTTCCTCTTTC[A/G]TCTTGTTTTTCTTCC | 4734 |
rs761643808 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944349 | TCTCCCATGCCTGGA[C/T]TGGCGGGTACCATGC | 4734 |
rs761665381 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910413 | CACCTTTCACCCATG[A/C]CTCTATGCCTCCACG | 4734 |
rs761668982 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859485 | GATCACTTGAGGCCA[C/G]GAGTTCAAGACTAGC | 4734 |
rs761669415 | snp | G/T | 1.65375e-05 | 0.0028755 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846962 | ATTTATTATAAACAT[G/T]ACTAACCTGCTTCTT | 4734 |
rs761676033 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828369 | TACCATACTGAGAAA[C/T]AGGTTTAATCTTTTT | 4734 |
rs761681946 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857122 | TTACCAAAAAGTATG[-/T]TTTAAGATGATCTCA | 4734 |
rs761690439 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858539 | TCTTGAACTCCTGAC[G/T]TCAACCCATCTATAA | 4734 |
rs761706901 | snp | C/T | 0.000109878 | 0.00741127 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869611 | GTTCTGCATTATCAT[C/T]TTCTGAGCCACTGGT | 4734 |
rs761719734 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899680 | GTGAAAGTACAGGGG[-/T]TATCAATGTCTTGCA | 4734 |
rs761745692 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888821 | GTGAATTCATATTGG[A/G]TAAAGGTGCCGAGAA | 4734 |
rs761800390 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839880 | ACACAGGAGGCTGAG[A/G]CAGAGAATTGCTTGA | 4734 |
rs761809197 | snp | A/C | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953306 | TATATTAATTCTTTG[A/C]ATCTCTATAACCACC | 4734 |
rs761825528 | snp | G/T | 6.59076e-05 | 0.00574016 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916522 | TATCAGCTAAGACAT[G/T]GCTAGACTGAAGATA | 4734 |
rs761829834 | in-del | -/ATGGGATTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944646 | AGTGGTTCTCCCAGC[-/ATGGGATTT]ATGGGATTTGAGCTC | 4734 |
rs761831803 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935846 | GTGAGACTCTGTTTC[A/C]AAAAAAAAAAAAAAA | 4734 |
rs761890335 | snp | A/C | 1.6628e-05 | 0.00288335 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834207 | CAATTTCTGTTTCAA[A/C]ATAAAATGTTATGTC | 4734 |
rs761892691 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950700 | CAGACAACTCTCCCA[C/T]GAATGTTCCTTATTC | 4734 |
rs761892891 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953435 | TACTCTTCTTTTTTT[-/A]ATCTTCTTTTTTGTT | 4734 |
rs761900326 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989846 | TAGGAACCAGCCACA[C/G]AGCAGGAGGTGAGTG | 4734 |
rs761921031 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835458 | ATGCCCTAAACTGTC[C/T]ATTTATAAACCATCC | 4734 |
rs761921788 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920069 | GCAAACACAGGTTGT[A/G]TAAGAAGCAGCAATT | 4734 |
rs761936568 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923678 | TATATATATATAGCA[A/G]GTCAGTGATAGTCTT | 4734 |
rs761948091 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856363 | CGCTCTCAGCCCCCT[A/G]CGTGGACACCTTCAC | 4734 |
rs761958374 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836817 | ACAGGAATGAGCCAC[C/T]GCGCCCAAATTTTTA | 4734 |
rs761992122 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899484 | GGAAAAACGGGGATG[C/T]GGGTTACTGTTGCTT | 4734 |
rs762055260 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905248 | AACTTATATAAAGGA[A/C]TCACCTTCACTCCTG | 4734 |
rs762055544 | snp | A/C/G | 3.38766e-05 | 0.00411551 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848590 | GCTATAATTAAAAAT[A/C/G]TATTTCAATTATTTT | 4734 |
rs762058810 | snp | A/G | 1.65682e-05 | 0.00287817 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841922 | GCCGATAATCATTGT[A/G]AAGGTACTTACGTAG | 4734 |
rs762059589 | snp | C/G | 1.65919e-05 | 0.00288022 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838502 | TAACTGATCAAAATT[C/G]ACAAACCTGTCCAAA | 4734 |
rs762060364 | snp | C/G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932970 | AAATGCAAATCAAAA[C/G/T]GACAATGAGATACCA | 4734 |
rs762093480 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967878 | ATAAGCCAGGCATGA[C/T]AACTTGTGTCTGTAA | 4734 |
rs762134452 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879172 | GAGTACATGCTGTCC[A/G]ATTTAATTTACATGA | 4734 |
rs762158266 | in-del | -/TTTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870530 | TTCTTCTTCTTCTTC[-/TTTTT]TTTTTTTTTTTTGTT | 4734 |
rs762171127 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857301 | GAGCATATATTAGTG[A/G]TAAGATAGAAGGTTT | 4734 |
rs762173624 | snp | A/G | 3.32127e-05 | 0.00407495 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856205 | AATGATTCTTGTGAA[A/G]AAACAAGACAACAGA | 4734 |
rs762178218 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972029 | TATATCCGGTGAAAA[C/T]ACCCTTCAAACATAA | 4734 |
rs762203928 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938490 | GACACAAACAAGACC[C/T]GACACTGTAAAACCC | 4734 |
rs762222852 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957035 | TGTATTTATTTCTAA[A/C]TATTTAACTTTTATA | 4734 |
rs762226166 | snp | C/T | 1.65274e-05 | 0.00287462 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916132 | CCTGGACAAAAGGAT[C/T]TGTACTTGTACTTCT | 4734 |
rs762230212 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927971 | AACTAATCTGCTGTC[C/T]TGGTTCAGACTGTAA | 4734 |
rs762239127 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876032 | ATACATTACACACAG[A/G]AGAATAAGAATACAA | 4734 |
rs762249582 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831719 | ATTTGCCATGGAGAA[G/T]AAAGGTTTAGCTATC | 4734 |
rs762253276 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952054 | CTAGGTGTGGCCGCG[C/T]ACGGTGGCTCATGCC | 4734 |
rs762263111 | in-del | -/T | 1.66932e-05 | 0.002889 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860651 | GGAGAACTAGGAAAC[-/T]TACTTATACCTCGGA | 4734 |
rs762268530 | snp | G/T | 1.68818e-05 | 0.00290527 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840754 | ACCCCATTTAAATAC[G/T]TCATTTGAAAAACTT | 4734 |
rs762306764 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894214 | GTGGATTCAATCAAT[C/T]CGGGATCAAAAATAT | 4734 |
rs762314172 | snp | C/T | 1.65015e-05 | 0.00287237 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916267 | AAGTATAACTACTAC[C/T]GTCACTGATGACACT | 4734 |
rs762325483 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842773 | ACACCGTTCTGTGAC[A/C]TGTAGGATAGCCACT | 4734 |
rs762327682 | in-del | -/T | 1.65935e-05 | 0.00288036 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915808 | CCTGTGAAGCGGCCG[-/T]TATGTCTCTTACTTC | 4734 |
rs762331039 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950380 | TTTCTTCCCTTCAAA[-/T]TCACTTTATTAAAAT | 4734 |
rs762335961 | snp | A/G | 0.000159834 | 0.0089382 | missense, intron-variant, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55873972 | CCGGTAATGGATAAA[A/G]TGGAACATCCACTTG | 4734 |
rs762336622 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937483 | ATCTAGTTATCCTTA[C/T]AATAAAATAGCAGAA | 4734 |
rs762349443 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890786 | TGTAAGATTTCAATT[A/C]CTCCCCTTTCTTACC | 4734 |
rs762365547 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828738 | AGCATTTTGCCTACA[A/G]AATTCTGGATTTGTA | 4734 |
rs762371324 | snp | G/T | 3.29728e-05 | 0.00406021 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834060 | AACCACTGTATAACC[G/T]GATGATTTGCACTGT | 4734 |
rs762372035 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892028 | CCTAACACTCTGGGA[G/T]GCCAAGGCAGGTGGA | 4734 |
rs762409150 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981882 | CTGCTGCAGTTAACG[A/T]GGTTATGGAAGTATT | 4734 |
rs762410353 | snp | C/G | 3.29924e-05 | 0.00406142 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860772 | CTCAGCATCTGTTAG[C/G]TTGTCCCTATATTGG | 4734 |
rs762420380 | snp | C/T | 3.44869e-05 | 0.00415238 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829936 | GGTGTTTTCAATTGC[C/T]ATCTGAAGTTTATCC | 4734 |
rs762425487 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907792 | TGAAAGAAAGCTAGT[C/T]AAATGGCTTTTGTCT | 4734 |
rs762438200 | in-del | -/CT | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994681 | ATGATTTCAGAATAA[-/CT]CTGATTTATTTTTAA | 4734 |
rs762438964 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915601 | TGAGCTTAATATACT[C/T]TGAATCAGAATTAAG | 4734 |
rs762465154 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983540 | TGCTAACTCCTATTC[A/T]TCCTTAGTTTCAATT | 4734 |
rs762473426 | snp | C/G | 1.68917e-05 | 0.00290613 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838481 | CTCACAATTTATGTG[C/G]CATTTTAACTGATCA | 4734 |
rs762498929 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957572 | AGTGTGGCGATTCCT[C/T]AAGGATCTAGAACTA | 4734 |
rs762563507 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55993162 | TGGGAGCTCCGCACA[A/C]CCGGCGGGGGTGGCA | 4734 |
rs762594441 | in-del | -/AGG | 1.65373e-05 | 0.00287548 | cds-indel, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916163 | TGAAAAAATTTCACA[-/AGG]AGTAGTATTCCTGTT | 4734 |
rs762608202 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931533 | AAAAATAAAAATATC[A/G]GTGACAGACTTATTG | 4734 |
rs762611288 | snp | C/T | 1.65343e-05 | 0.00287521 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916157 | ACTTCTTGAAAAAAT[C/T]TCACAAGGAGTAGTA | 4734 |
rs762616952 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899488 | AAACGGGGATGTGGG[C/T]TACTGTTGCTTAAGA | 4734 |
rs762627706 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851482 | ACATTTTCTTTTCTG[-/T]TTTTTTTTTTTCAGA | 4734 |
rs762639314 | snp | C/T | 2.24384e-05 | 0.00334943 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850765 | ATTAATGAAATCATA[C/T]TGTAATATTTTATAG | 4734 |
rs762639567 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866658 | TCTTTTAAAGCTTCT[G/T]AGAGATTTCTCTCTT | 4734 |
rs762644362 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913788 | CACAACAAACTATAA[C/T]TATTACCACAAAATA | 4734 |
rs762655162 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873441 | TTCCTCACTTTTCTA[C/T]AAGAGACGCCACTCT | 4734 |
rs762682153 | in-del | -/C | 1.64773e-05 | 0.00287026 | frameshift-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862982 | TCCTTCCAAGGATAT[-/C]CCTGCCTCTCTTCCC | 4734 |
rs762683629 | snp | C/T | 1.72988e-05 | 0.00294093 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993499 | CGCCCCGCAGCCCCG[C/T]GGTCCCCGCACCTCG | 4734 |
rs762700060 | snp | A/C | 1.65334e-05 | 0.00287514 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55846978 | ACTAACCTGCTTCTT[A/C]AACTTTCTTCGGAAG | 4734 |
rs762703934 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829775 | AATGCTTTTTATATG[A/T]TTTTCTTCAAGATCT | 4734 |
rs762713421 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903929 | CTTTGTGAGGGCGAG[A/G]TGGGAGGATCACCTG | 4734 |
rs762727730 | snp | A/G | 1.80059e-05 | 0.00300043 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837878 | ACATTTCATTTTCAT[A/G]TGAACCAAGACAAAA | 4734 |
rs762730598 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830695 | ACACAGGGAACTAAT[A/C]TGGTTTATTTATTTA | 4734 |
rs762739922 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973904 | AACCAACTCCAAAAT[C/T]AGTAGAAGAAAAGAA | 4734 |
rs762751325 | snp | C/T | 1.65378e-05 | 0.00287552 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915719 | AACACAAGAATATCC[C/T]TCAGATGACTTTTCA | 4734 |
rs762784711 | snp | C/T | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826419 | CATGGCCTAGGTCCC[C/T]AAAATTAAAAGCTAT | 4734 |
rs762788714 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952561 | TCCTTCCCCCAACTC[C/T]ATTTCCTCATACCAC | 4734 |
rs762789944 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961003 | GTTGAGTTGCCTCCC[A/G]TGTCTCACCTGACTG | 4734 |
rs762813565 | snp | C/T | 5.98193e-05 | 0.00546865 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838144 | TATTGGTGACAACTA[C/T]TTCTGATCCACCATT | 4734 |
rs762826342 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55840042 | ATATATATATATATA[-/T]ACATTCATCATAAAA | 4734 |
rs762847291 | snp | C/T | 1.65252e-05 | 0.00287443 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856168 | TCAAAAGTATAGGCT[C/T]GTAAGCTGCCTCTTC | 4734 |
rs762859480 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871607 | GTGACTTCCTTTATA[G/T]AGAGTAAATATTAAC | 4734 |
rs762883853 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916695 | AGCTTCATTTGAACA[A/G]CGTTAGACGTTGAAA | 4734 |
rs762927340 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934716 | CACCCCCAGAGCAAA[C/T]ACAGTAAACAGTTTC | 4734 |
rs762934900 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985551 | TACACTGAACACATA[A/G]GTCAATGAACAAATA | 4734 |
rs762944607 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902400 | CATTAATTTTGTCAC[G/T]ACTGCATGGTGGCTT | 4734 |
rs762982574 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936795 | TTGCTATTTCTTTTC[-/T]TTTTTTTTTTTTTTG | 4734 |
rs763004953 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851754 | AGTGCTGGGATTATA[C/G]GCATGAGCCACCTTG | 4734 |
rs763018546 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884822 | GAAAATAGCCTCAAA[C/T]GGGCAAATCGAAGAG | 4734 |
rs763021767 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942079 | TTTTTTTTTTGTCTA[G/T]TTGTTGTATCAGTTA | 4734 |
rs763043484 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960559 | CCTATTTTTGAGGTT[G/T]TGGGACTCTGACTGG | 4734 |
rs763048731 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882012 | ATCATTCCTCATTAA[C/G]AACCACTGCTACAGA | 4734 |
rs763055630 | in-del | -/TTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870999 | AGAGTCCTAATCCTT[-/TTA]TTCTGTCTTCAAGAG | 4734 |
rs763061214 | snp | A/C | 8.55103e-05 | 0.00653818 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993577 | ACGCTTCCAGCAAAC[A/C]GGACGCGCTCGCCCC | 4734 |
rs763061906 | in-del | -/CA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854104 | GCAGTGAGCCGAGAT[-/CA]CGCCTGGGCACTCCA | 4734 |
rs763081690 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988464 | TGTACACTAAAACTT[-/A]AGAGTATAATAAAAA | 4734 |
rs763092733 | snp | A/G | 1.654e-05 | 0.00287571 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915888 | GAAAGAAATCCTTTA[A/G]CACTAGTGCCATCCT | 4734 |
rs763096130 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971204 | ATTGATCACGCAGAA[A/G]AAAGAATTAGCGAGC | 4734 |
rs763118026 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941634 | CAGCAGCACAATTTC[A/G]GCTCACTGCAACCTC | 4734 |
rs763122986 | snp | G/T | 3.46087e-05 | 0.0041597 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848614 | TTATTTTAGGAGAGG[G/T]GCGTAGATGAATGGA | 4734 |
rs763129818 | in-del | -/TAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921183 | GATAGGCAGGGCAAA[-/TAT]TGTTGTCCTCATTTT | 4734 |
rs763143227 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883048 | TTACAGTTTAGGTAC[C/T]AGCTTGGCCACAGTA | 4734 |
rs763153587 | snp | A/C/T | 3.31819e-05 | 0.00407309 | missense, synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915809 | CCTGTGAAGCGGCCG[A/C/T]ATGTCTCTTACTTCT | 4734 |
rs763176423 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895598 | TGTTAAAATCACCTG[A/C]TAGGCTATTTAAAGA | 4734 |
rs763178611 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911218 | TGTCACACTGGGAGA[A/T]AGGGGTGTTACTAGC | 4734 |
rs763183333 | snp | A/G | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918484 | AGGTAAAATAGTTCC[A/G]TTGTTTATACCACAT | 4734 |
rs763191558 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931529 | GAAAAAAAATAAAAA[C/T]ATCAGTGACAGACTT | 4734 |
rs763208413 | snp | A/G | 3.35222e-05 | 0.00409389 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834220 | AACATAAAATGTTAT[A/G]TCTTACCTCTAGTTC | 4734 |
rs763210880 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942082 | TTTTTTTGTCTAGTT[G/T]TTGTATCAGTTACTA | 4734 |
rs763221753 | snp | A/G | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860414 | CATCTTACTGAGCTC[A/G]ATGCTGGCTGGCTCA | 4734 |
rs763238896 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937441 | TTTTTCTAAGCATAA[C/T]GAATTAGCATTGATC | 4734 |
rs763245648 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930017 | AAAAACTAAGTTGAA[A/G]GGAAATGAGTGAAAA | 4734 |
rs763250387 | in-del | -/AA/AAAA | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995518 | CCTAAAACTGGTAAT[-/AA/AAAA]TAAAAAAAAAAAAAT | 4734 |
rs763277370 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916387 | AGTTACTAAGGCTAC[C/T]ACTACAAATGGCTGG | 4734 |
rs763293851 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877085 | TATACTTTTCACCCA[G/T]ATCCACCAAATGTTA | 4734 |
rs763303790 | snp | C/G | 1.68091e-05 | 0.00289901 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915343 | CTCTTGATAAATTAT[C/G]CACTTTACCTTCATT | 4734 |
rs763310737 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848461 | AGAAAAAAGATGTAC[C/T]TTCTCACACATAAAA | 4734 |
rs763321294 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904948 | AAATACAAAATTAGC[C/T]GGGTACGGTGGCACA | 4734 |
rs763321473 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982544 | CTAGAACAGACAAAA[C/G]TAATCCATGGTGACA | 4734 |
rs763329852 | snp | A/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55830520 | ACTGCTTACCAGGTA[A/T]GAGCTCTTGGCAGCT | 4734 |
rs763335092 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977909 | AAACTGAATTCTGCC[A/G]ATTAAAAATCTCTTC | 4734 |
rs763343097 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898903 | AATCTCAGTCTCCTA[A/T]GTGCTGGGCTTACAG | 4734 |
rs763386221 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934447 | TTTCTGTGCATATAT[A/T]TTAATAACACTGTAA | 4734 |
rs763388292 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990694 | TTCAATGGAGTGTGG[C/G]AAACAGTGTTTAGTT | 4734 |
rs763394158 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872977 | CCAATTAATATAACT[A/C]ACAAGACTGAAAAAG | 4734 |
rs763410519 | snp | G/T | 3.2963e-05 | 0.00405961 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834082 | TTGCACTGTAGCCAT[G/T]TTTATACTTTGTATG | 4734 |
rs763435575 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989639 | CCGATAGCGGAGACT[C/G]TGAACTCTTTCCTCT | 4734 |
rs763440937 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841729 | GGCGCCCGCCACCAC[A/G]CCTGGGTAAGTTTTT | 4734 |
rs763441769 | in-del | -/GAG | 1.68067e-05 | 0.00289881 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833148 | AACAGCACTGGGAAA[-/GAG]GTAAACAAATTATCC | 4734 |
rs763442523 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856079 | TCCAAAAAATAAAAA[C/G]AGATGCTGAGTTTTA | 4734 |
rs763513769 | in-del | -/CCAAAG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841190 | ACCAGCCTTGGCCTC[-/CCAAAG]TGGTGGGATTACAGG | 4734 |
rs763526606 | snp | A/G | 5.11505e-05 | 0.00505694 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916813 | TGGCTGCAAAGTGCA[A/G]TCGTAAGCTTTGTGC | 4734 |
rs763596432 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864916 | CTTTATAGGAATTCC[A/G]GCCAGGCACAGTGGT | 4734 |
rs763606586 | snp | C/T | 3.2969e-05 | 0.00405998 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860537 | AAGGCCTGGTTGCTA[C/T]ACATGGTGGCTTCAT | 4734 |
rs763616699 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973920 | AGTAGAAGAAAAGAA[A/G]TAATAAAGATCAGAG | 4734 |
rs763622501 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929401 | AGATAAACTGTGTGG[C/T]ATGGGTTTTTTTGGT | 4734 |
rs763634833 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848831 | CCTAGATCATTGGAA[A/G]TATCAAGTGATGTCT | 4734 |
rs763655302 | snp | A/G | 1.70197e-05 | 0.00291711 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55837841 | ACAAATCGCCATTGT[A/G]TTACAAGACTAAAAA | 4734 |
rs763682985 | in-del | -/GA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852745 | TTTCTGAGAGAGTGA[-/GA]GAGAGAGAGAGAGAG | 4734 |
rs763689860 | snp | C/T | 3.2987e-05 | 0.00406108 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860612 | GAGCCACACATACTT[C/T]ATTGCTATAGCATGT | 4734 |
rs763695150 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983542 | CTAACTCCTATTCAT[C/T]CTTAGTTTCAATTTC | 4734 |
rs763711668 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862681 | CTATTAAAATTAAGA[C/T]GCAATTAAAAGGGTA | 4734 |
rs763755519 | snp | C/G/T | 6.82342e-05 | 0.00584064 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993572 | TCCGAACGCTTCCAG[C/G/T]AAACCGGACGCGCTC | 4734 |
rs763793327 | snp | A/C | 8.31198e-05 | 0.00644616 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924702 | GCTGAGGATGAACCT[A/C]AGAAAAACACAATCT | 4734 |
rs763807276 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880120 | TACATGGTGAAACCC[A/C]ATCTCTACTAAAAAT | 4734 |
rs763807279 | snp | A/C | 1.66172e-05 | 0.00288242 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852394 | CAGTTTAAATCCTGT[A/C]AGAAAGCAAGTTGAT | 4734 |
rs763822172 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975192 | GCCACTGTGCCCGGC[C/T]GCCCACTTTTACCAC | 4734 |
rs763839983 | snp | A/C | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826483 | CAGCACCTTCCCAGG[A/C]TGGCTTGAGTGGGTG | 4734 |
rs763850109 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857576 | GATCTGCCTGCCTTG[A/G]CCTCTCAAAGTGCTG | 4734 |
rs763864428 | in-del | -/TGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964289 | AAATCCTCAAGGCTC[-/TGT]TGTTGTTGTTGTTGT | 4734 |
rs763889354 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922233 | TTTCAGAATATAGAA[A/C]ATTATGCATCATTGA | 4734 |
rs763907119 | snp | A/G | 1.70799e-05 | 0.00292227 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55834242 | CTCTAGTTCATTTTC[A/G]TCAAAAATTTTGATG | 4734 |
rs763928504 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953274 | GATTACCCACGTGAG[C/T]CATAGCGCTGAGCCC | 4734 |
rs763959293 | snp | C/G | 1.71349e-05 | 0.00292697 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993519 | CCCGCACCTCGTCCT[C/G]CAGGAGCCCGAACAC | 4734 |
rs763963842 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938722 | ATAAGATAAAGAGTT[A/G]ATCTCCAAACTTCAA | 4734 |
rs763982088 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964249 | TATAATGATATCCAT[A/G]TTAGACTTTTATATA | 4734 |
rs763996980 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934970 | GCCTCCCAGACTCAA[A/G]TGATTCTCCTGCCTC | 4734 |
rs764027205 | snp | C/G | 1.64849e-05 | 0.00287092 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830498 | TTGTTCTATCAAGGT[C/G]CAAACAACTGCTTAC | 4734 |
rs764028608 | in-del | -/AATT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983591 | CTCCACACCATATAA[-/AATT]AATTAATTTTTAGAT | 4734 |
rs764054329 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944305 | GTGCTTTTCCCATGG[-/T]TCTTATCAACTGGCA | 4734 |
rs764071283 | in-del | -/AT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854108 | TGAGCCGAGATCGCC[-/AT]TGGGCACTCCAGCCT | 4734 |
rs764083234 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931597 | ATAAAACAACAGAGG[A/G]AAAAAGTTGCCAAAA | 4734 |
rs764083603 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921452 | GCCTCAGTCTCCAGA[A/G]TAGCCGGGACTACAG | 4734 |
rs764136731 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989150 | GTGATGCAGGAAAAT[C/T]GCTGGAACCTGGTAG | 4734 |
rs764138904 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868584 | TCTTGCCTGCCACCA[C/T]ATAAGCTGTGCCTTT | 4734 |
rs764158172 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919298 | TTCAGGATTTTTCTT[A/G]TTGTTGTTGAAGTTG | 4734 |
rs764203196 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55847017 | CTTTCTTTTGTAATC[C/T]CTGGAGTAGGGCACT | 4734 |
rs764207192 | snp | C/T | 1.65446e-05 | 0.00287612 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856180 | GCTTGTAAGCTGCCT[C/T]TTCTGCTGGAATGAT | 4734 |
rs764209389 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921705 | ATTTTGTCATATTTA[C/T]CCATCTATAAATATC | 4734 |
rs764231471 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920003 | CTGAGTAGAGCACAT[C/T]ACCCTCCACAATGTG | 4734 |
rs764246267 | in-del | -/ATAAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851405 | GCAGCACCTCATTCT[-/ATAAA]ATAAAATGAGTGTTC | 4734 |
rs764270071 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883083 | AGAGCACCAAGCCTC[C/T]TGGGGTCCTTGATGC | 4734 |
rs764294623 | snp | A/T | 1.65534e-05 | 0.00287688 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915740 | TGACTTTTCACAGAC[A/T]GTCTGTCTGGGAGTA | 4734 |
rs764302261 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873215 | GGCCCTCCGTTCTTA[C/T]CTCTTTCATCAGGAG | 4734 |
rs764322380 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959976 | CCAGAAGCAGGTCTT[A/T]GTCACCCTTAGCACA | 4734 |
rs764323329 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882040 | AGAAGGTATAAGACC[A/T]AATGTTCCAACAAAC | 4734 |
rs764326630 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926488 | AAATAGTGTTAAGAC[A/G]GCCGGATGTGCTGGT | 4734 |
rs764346727 | snp | C/T | 6.00096e-05 | 0.00547734 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838172 | ATTTTTCAGCTCATG[C/T]TGATGTGTCTAAAAT | 4734 |
rs764369330 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896652 | AGTGACTAGCTTCTA[C/G]AGTCAGGCTCCAGGT | 4734 |
rs764396996 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843461 | TGCTTATGTGACAAA[G/T]GTACACAACTATGCT | 4734 |
rs764408798 | in-del | -/TG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980963 | AGATGTGAATAATAC[-/TG]TATTTATATAGGGTA | 4734 |
rs764424614 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916713 | TTAGACGTTGAAATC[A/C]GTGTTGGTCTTTTGA | 4734 |
rs764435885 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848334 | AAGAGACAGGTGAGC[A/G]GACAGTCCCATCAGA | 4734 |
rs764443528 | snp | A/T | 8.44559e-05 | 0.00649775 | utr-variant-5-prime, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55951547 | CACACTTGTAAGAAC[A/T]CCATTCATTGGGTCA | 4734 |
rs764457924 | snp | G/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937446 | CTAAGCATAATGAAT[G/T]AGCATTGATCCACAC | 4734 |
rs764467343 | snp | C/T | 1.65023e-05 | 0.00287244 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915998 | ACTTGTTGGAGAAGT[C/T]GGTCGGGTAGTTGAA | 4734 |
rs764492205 | snp | A/G | 2.17782e-05 | 0.00329979 | missense, utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55872442 | AGAACAAAATCCTTA[A/G]ATGTATATGGTCTCT | 4734 |
rs764511146 | snp | C/G | 0.000131974 | 0.00812217 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840613 | ATACTAACCATCCAA[C/G]AGTTTGCCATGATAA | 4734 |
rs764512935 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855127 | AATGATGCATAGGTG[A/G]GCGACCTCTCATTCC | 4734 |
rs764544014 | snp | G/T | 3.30256e-05 | 0.00406346 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833079 | AGTAATCTTATTCTT[G/T]TTTCTGAATCCATCA | 4734 |
rs764547361 | snp | A/T | 0.000115606 | 0.00760195 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916107 | ATCTCTAATCCATGT[A/T]CCAAGTCATCCTGGA | 4734 |
rs764591435 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842725 | CCATGAAGGCATTTC[A/G]TTAACAGTCCTTTTC | 4734 |
rs764595494 | snp | A/C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966869 | ATATGTACACAAAAT[A/C/T]GAAAGTTCATAACCA | 4734 |
rs764596867 | snp | A/C | 1.67652e-05 | 0.00289522 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840737 | TTGTCCCTGTAAAGA[A/C]AACCCCATTTAAATA | 4734 |
rs764612309 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856113 | TTTTATTGATTGATG[A/G]GAGAGGGTAAAACTC | 4734 |
rs764646441 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841747 | TGGGTAAGTTTTTGT[A/G]TTTTTAGTAGAGACG | 4734 |
rs764649575 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983495 | GTGGTTCTATTTACT[C/G]AATGGGGTTCTATTG | 4734 |
rs764658970 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980483 | CACAGTGAAATGGTA[A/G]GTTCAGATCATTCTA | 4734 |
rs764663279 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890366 | GCCCATTTCCCCACC[A/C]CTCCTTCAGTCCTAG | 4734 |
rs764665783 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989705 | CTTTCTTATAGGAAA[C/G]AGAAATCATTCTAGA | 4734 |
rs764677924 | in-del | -/C | 1.65337e-05 | 0.00287517 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846959 | AGTATTTATTATAAA[-/C]ATGACTAACCTGCTT | 4734 |
rs764689415 | snp | C/T | 3.31901e-05 | 0.00407356 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856111 | ATTTTTATTGATTGA[C/T]GGGAGAGGGTAAAAC | 4734 |
rs764705242 | snp | C/T | 5.75027e-05 | 0.00536172 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869641 | TTTTAGGTAAATAAG[C/T]CATTTTTAGTCTCAG | 4734 |
rs764717569 | in-del | -/ACTCAAGAGTAGTACA | 1.70194e-05 | 0.00291709 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841892 | ACTTTTAAAACAGTG[-/ACTCAAGAGTAGTACA]ATTTTTCTTTTTCTG | 4734 |
rs764734101 | snp | A/G | 3.29598e-05 | 0.00405941 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848859 | TCTTTCCTCTCAGAT[A/G]GGCTGGAATTTTCAA | 4734 |
rs764746938 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905152 | ACTGCAAATGAATTA[A/C]ATTATCATCAGCATG | 4734 |
rs764755629 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829564 | GGCAGATACTATACA[A/G]GAGGTAAATGTTAAG | 4734 |
rs764761760 | snp | C/T | 1.69286e-05 | 0.0029093 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840759 | ATTTAAATACTTCAT[C/T]TGAAAAACTTTAATA | 4734 |
rs764771485 | snp | A/C | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860686 | TCTCGGTTGTCAACA[A/C]TTTCTGTTTCCTCGG | 4734 |
rs764771832 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949913 | TATGTAACAAACCTG[C/T]ACGTTGTGCACAGGT | 4734 |
rs764777367 | in-del | -/CATCT | 3.30554e-05 | 0.00406529 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860800 | GGAAGTATAAAAAGC[-/CATCT]CATCATCCATGTCTT | 4734 |
rs764809394 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926313 | GAGCTTTTCAGAGGT[G/T]GCTGACTCAGCTGGG | 4734 |
rs764835696 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955545 | GACTATTTTAGATAT[A/T]TAAATGTAAACATGC | 4734 |
rs764842375 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876980 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACTG | 4734 |
rs764851476 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836238 | CATTTCACTCTTTAC[A/G]TCATACATACCTTAA | 4734 |
rs764864542 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947695 | AACAGAACCAAAGAC[A/G]AAAACCATATGATTA | 4734 |
rs764868716 | snp | A/G | 1.65312e-05 | 0.00287495 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916134 | TGGACAAAAGGATCT[A/G]TACTTGTACTTCTTG | 4734 |
rs764880045 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870532 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTG | 4734 |
rs764887416 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875519 | GACAGGGTTTCACCA[C/T]GTTGACCAGTCTGGT | 4734 |
rs764889374 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890252 | AGTGTACAATTCAAT[C/G]TTTTTTAGTATTTTC | 4734 |
rs764896460 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916526 | AGCTAAGACATTGCT[A/G]GACTGAAGATATCCA | 4734 |
rs764920077 | snp | A/G | 8.76924e-05 | 0.00662106 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55966501 | TATCCTTCTTGGCAA[A/G]GCCTATTCCGGCTAT | 4734 |
rs764925186 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55972919 | GATAAAGGCATCATT[G/T]CAACAAGAAGATACA | 4734 |
rs764997630 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932241 | AAAGAACAAAGCTGG[A/G]GGCATCATGCTACCT | 4734 |
rs765004130 | snp | A/G | 3.29652e-05 | 0.00405974 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850537 | TGGAAAAGTATCAAA[A/G]TTACCCAGGTGGTGG | 4734 |
rs765007269 | snp | A/C | 5.35509e-05 | 0.00517422 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852591 | ATCAAGTTTAAGAAT[A/C]CTTCTATCACCCCCA | 4734 |
rs765022255 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886380 | AGAACACTTCATTCA[A/G]CTGCTTCAGATTACA | 4734 |
rs765033232 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933740 | TTCTTGACACTTCTA[A/C]TTGCTGCTGCCATGT | 4734 |
rs765057213 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962894 | TGGGTTCAACTGATT[C/G]TCCTGCTTCAGCCTC | 4734 |
rs765080476 | snp | A/G | 3.54994e-05 | 0.00421289 | intron-variant | NEDD4 | GRCh38.p7 | 15:55842185 | ATCCAGAGGAGAGAC[A/G]TACTGTTTAAATCAG | 4734 |
rs765087838 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916429 | GGTGACCATCATTCA[C/T]AGCATTCAATTCATT | 4734 |
rs765102231 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950829 | ATTCCTAAAATGCAT[A/C]TCTACCACTGCTCTG | 4734 |
rs765115367 | snp | A/G | 1.73351e-05 | 0.00294402 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837856 | ATTACAAGACTAAAA[A/G]GAAACAACATTTCAT | 4734 |
rs765130145 | snp | G/T | 1.64866e-05 | 0.00287106 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915489 | AAAATACCATGGTTT[G/T]TGTTCATCTGTGAAT | 4734 |
rs765153528 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962194 | CGAATATATCCACTT[C/G]AGTCTTTTTATGCTT | 4734 |
rs765158446 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942864 | AAAGATAGAATTTCC[C/T]AGAGACTTGTTGAAT | 4734 |
rs765170414 | snp | A/G | 3.30639e-05 | 0.00406581 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846966 | ATTATAAACATGACT[A/G]ACCTGCTTCTTCAAC | 4734 |
rs765177148 | snp | A/G | 1.6563e-05 | 0.00287771 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915750 | CAGACAGTCTGTCTG[A/G]GAGTATTATTCGAAA | 4734 |
rs765180994 | snp | A/C | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917170 | CTTGTTTCAATTATA[A/C]CTTCTCCAATTTGCA | 4734 |
rs765214505 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877204 | CCTAATTTTAGTCCA[A/G]GGTCCAATTCAGACT | 4734 |
rs765222491 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847976 | TGAGCCTGGCTTGAT[C/T]TCTATAAAAAAATTT | 4734 |
rs765229573 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931767 | CTTTACTAGCTATAA[G/T]TCACATAGCATACAC | 4734 |
rs765234110 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916736 | TCTTTTGAAGCACAT[A/G]TGAACATGGCTATCC | 4734 |
rs765251433 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860622 | TACTTTATTGCTATA[A/G]CATGTGTCTTTCAAG | 4734 |
rs765272939 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970137 | GACTATAGTAGCCAC[A/G]GGTCTGGGGCAGTGG | 4734 |
rs765274228 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960934 | CTGGGAGGCATGCTG[C/T]CCTCTTCTCTCTGGC | 4734 |
rs765283014 | snp | A/C | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834079 | GATTTGCACTGTAGC[A/C]ATTTTTATACTTTGT | 4734 |
rs765288815 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959581 | CTTAAGCATGGGACA[A/G]ATCTATATATTCTAA | 4734 |
rs765313212 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899384 | AATGTAAGTTTAGCT[A/G]ATCTATAAACAGTTT | 4734 |
rs765318990 | in-del | -/GT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983287 | GATGACGACAATGGT[-/GT]GTGTGTGTGTGTGCG | 4734 |
rs765361408 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865014 | ACCAGCCTGGCCAAC[-/A]TGGTGAAACCCCATC | 4734 |
rs765395062 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844617 | GATTAGTTTCCTCAT[C/T]TATAAAATAGGGATA | 4734 |
rs765403235 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984838 | CTAAAGAAGAAGTAA[C/T]ATCAATTGCCACAGA | 4734 |
rs765422737 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928927 | TTAAAAATTAAAAAT[A/G]CTAATTAAAACATGA | 4734 |
rs765427939 | snp | C/T | 1.65048e-05 | 0.00287265 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862934 | GTTGGTCTTTTCCAC[C/T]GTGTTCTTCTAGATT | 4734 |
rs765475202 | snp | A/T | 1.64838e-05 | 0.00287083 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848455 | AGAAAAAGAAAAAAG[A/T]TGTACTTTCTCACAC | 4734 |
rs765488485 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880652 | AGATGCAGGGGATTC[A/G]AGATAGGAGAGCATA | 4734 |
rs765491039 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936972 | TGATTTTTGTATTTT[C/T]AGCAGAGATGAGGTT | 4734 |
rs765498434 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858514 | GGTTTCGCCATGTTG[C/T]CCAGGCTGGTCTTGA | 4734 |
rs765516304 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888956 | AAATCAAATAAAAAT[A/G]GATTAAACACTTACA | 4734 |
rs765569019 | snp | A/C | 1.65389e-05 | 0.00287562 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838518 | ACAAACCTGTCCAAA[A/C]AGTTCTTCATCTATG | 4734 |
rs765576540 | snp | A/C | 1.66001e-05 | 0.00288094 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833108 | CATTAAAACAGCCTG[A/C]ATAAGATAAAAACAT | 4734 |
rs765582532 | snp | C/T | 9.09546e-05 | 0.00674307 | synonymous-codon, utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55872456 | AAATGTATATGGTCT[C/T]TCCAATCTTGGATTT | 4734 |
rs765636644 | snp | A/G | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860408 | TAAGAGCATCTTACT[A/G]AGCTCGATGCTGGCT | 4734 |
rs765644471 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932259 | CATCATGCTACCTGA[C/T]TTCAAACTATACTAC | 4734 |
rs765658554 | snp | A/C | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936379 | CGCCAAATTTGTGTG[A/C]GTATGTAGGTAAGTT | 4734 |
rs765667604 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945127 | AGGATCGCAGCCCCT[C/T]GCCAGCAACAGAACA | 4734 |
rs765667696 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960481 | ACTCTTGGACTTACA[C/G]CAGTGATATGCTAGG | 4734 |
rs765688982 | snp | G/T | 1.65509e-05 | 0.00287666 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841926 | ATAATCATTGTAAAG[G/T]TACTTACGTAGCAGA | 4734 |
rs765690175 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926583 | ACCAGCCTGGGCATC[-/A]ATAGGGAGACCATCT | 4734 |
rs765718588 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55870944 | GATGATTTTTTACAG[A/G]TATCAGATATGTAGC | 4734 |
rs765737626 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975649 | AAAAAACAAAAGGGA[A/T]AAATATTCCATGTTC | 4734 |
rs765758833 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903627 | CAGGAGATCGAGACC[A/C]TCCTAGCTAAACACG | 4734 |
rs765767638 | snp | C/T | 8.00929e-05 | 0.00632772 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55873991 | AACATCCACTTGACC[C/T]AGGAAATCATCTCTT | 4734 |
rs765774868 | snp | G/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834067 | GTATAACCTGATGAT[G/T]TGCACTGTAGCCATT | 4734 |
rs765784329 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843080 | GTTTCTATGCACAAG[A/C]TCTCTCTTTGCCTGC | 4734 |
rs765799699 | snp | A/G | 1.67022e-05 | 0.00288978 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856232 | CAGAAGAATACCTTG[A/G]TATTTGTGATTTGCC | 4734 |
rs765813423 | snp | A/C | 1.64741e-05 | 0.00286998 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848359 | ATCAGAGCACACTGG[A/C]AGAGAGACTTACTGG | 4734 |
rs765815150 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853776 | GGCGGATCACCTGAG[A/T]TCAGGAAGTCGAGGC | 4734 |
rs765858702 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883024 | AGGAAGAGTAAAGAG[A/G]ACTTTGTATTACAGT | 4734 |
rs765861113 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829489 | TCAAACTTTTCACAC[A/G]TGACACGTATCACAA | 4734 |
rs765864949 | snp | C/T | 1.65392e-05 | 0.00287564 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916180 | GAGTAGTATTCCTGT[C/T]TGGCACACTTCTATT | 4734 |
rs765872178 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867280 | ATAAGCACAGATTCA[A/T]GTGTTTGAATTCCTA | 4734 |
rs765878404 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55906822 | AATTTTAGGCTGGGC[A/G]CAGTGGCTCACGCCC | 4734 |
rs765883456 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974726 | ACATCTCTTCATGAT[-/AA]AAAAAAAAAAACCCT | 4734 |
rs765911232 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962909 | CTCCTGCTTCAGCCT[C/G]CTGAGTAGCTGGGAT | 4734 |
rs765913670 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828495 | TGCTGGAACCTAGAA[C/T]ACTTTCCCTTTTGCC | 4734 |
rs765920290 | snp | C/T | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834089 | GTAGCCATTTTTATA[C/T]TTTGTATGTTCCCTC | 4734 |
rs765922680 | snp | C/G | 8.79159e-05 | 0.0066295 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55966525 | CGGCTATAACTCTTA[C/G]TCTCACAATTCGTGA | 4734 |
rs765942609 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874310 | GATGTCAATCCTTCA[A/G]AGAAGGAACTACACT | 4734 |
rs765951355 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841302 | GGACATTCTGATACA[C/T]ACTACAACATGGATG | 4734 |
rs765954779 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853671 | TAAAGAGAAGTCTGG[A/T]TATTTCCAGGCTTAC | 4734 |
rs765964661 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964319 | TGTTGTTTTTCTCCA[A/G]TCTTTGTCTCTCTCA | 4734 |
rs765970535 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944558 | CAACCTCTGTGAGCA[A/G]GGCATAGCTGAACAA | 4734 |
rs765987672 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916296 | CTGTTAGTATATGAA[C/T]CTCCACTTGTGATAC | 4734 |
rs765988461 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924282 | ACTGTAGTGAGGAGG[C/T]GCAACTGAAGGATAC | 4734 |
rs765995523 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888143 | TAGCTACAGCAATCA[A/G]GCAAGAAAAAGAAAT | 4734 |
rs766004722 | snp | G/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936887 | AACCTCTGCCTCCCA[G/T]GTTCAAGTGATTCTC | 4734 |
rs766066486 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903598 | GGGAGGCCGAGGTGG[C/G]TGGATCACGAGGTCA | 4734 |
rs766098313 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930575 | AATTTCCAGAGTTGA[A/G]GAGAAACAGTATTCA | 4734 |
rs766102020 | snp | A/C | 3.29571e-05 | 0.00405924 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842087 | TCTGCTCTCTTGACA[A/C]CCATAATTCTCCGGT | 4734 |
rs766109912 | in-del | -/C | 1.64942e-05 | 0.00287173 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916299 | TTAGTATATGAACCT[-/C]CACTTGTGATACTTG | 4734 |
rs766127640 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898716 | TCGTAGCTCAATGCA[A/G]CTTGGACTCCTGGGC | 4734 |
rs766155164 | snp | A/G | 1.65201e-05 | 0.00287398 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841934 | TGTAAAGGTACTTAC[A/G]TAGCAGAATATTCAA | 4734 |
rs766155386 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834400 | AAGTTTCTACCACTA[C/T]ACAATCACGGGCTCT | 4734 |
rs766155913 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931643 | AAAAAGAACAAAGGT[G/T]TTGGTAAGTATATGA | 4734 |
rs766171415 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942166 | TTTGACTTCGTAATT[G/T]TAAAGATTACTAGGT | 4734 |
rs766190670 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55936181 | AGTGATCCCCCAACC[C/T]TGTATTTACTCTCCG | 4734 |
rs766201754 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836042 | AGCATACTCAACTGC[C/T]TGTGGGTACAGCCTA | 4734 |
rs766208589 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55861104 | TATCAGAGCGCTTCA[C/T]AGATTATTTCATTGT | 4734 |
rs766225139 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55987765 | TTTTCTCAGGTTTGT[C/G]AAAGATCAGATAGTT | 4734 |
rs766230903 | snp | A/C | 1.82327e-05 | 0.00301927 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837884 | CATTTTCATGTGAAC[A/C]AAGACAAAATTCTGA | 4734 |
rs766233380 | snp | A/G | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994970 | TGAGGCAAGGGAATC[A/G]CTTGAGCTTGGGAGG | 4734 |
rs766239309 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957904 | GCATGTTCTCACTCA[C/T]AGGTGGGAACTGAAC | 4734 |
rs766240559 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983451 | GCACTCCAACCTTCC[A/T]GTTCGTCTCCATCCC | 4734 |
rs766247623 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901577 | TATTCCTTTGAAAAC[-/A]AGACTTTGATCTTTG | 4734 |
rs766257808 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860702 | TTTCTGTTTCCTCGG[A/G]TATCTGCCGCCTGGT | 4734 |
rs766260285 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960872 | CCTGTTCCCCACCCA[C/T]TAGTTGACTGTGCAT | 4734 |
rs766289489 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944668 | TTGAGCTCTGATAAC[-/A]AAGAGACTGCCACCT | 4734 |
rs766298720 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894468 | CCCTGCAAATACCAA[C/G]AGACACCGGTACTTG | 4734 |
rs766308956 | snp | C/T | 3.29538e-05 | 0.00405904 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862990 | AAGGATATCCTGCCT[C/T]TCTTCCCACCCTGGA | 4734 |
rs766320630 | snp | A/C/T | 2.90913e-05 | 0.00381377 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838156 | CTATTTCTGATCCAC[A/C/T]ATTTTTCAGCTCATG | 4734 |
rs766325357 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928167 | GGGGCGTGCCACCAG[A/G]CCTGGCTAATTTTTG | 4734 |
rs766326491 | snp | C/T | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860773 | TCAGCATCTGTTAGG[C/T]TGTCCCTATATTGGA | 4734 |
rs766369913 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955420 | AGAGCTTATTCTTCC[C/T]GCTTGACTCAAGTTT | 4734 |
rs766369922 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941741 | GCTACTTTTTGTATA[C/G]TTTTTTTCTTTAGTA | 4734 |
rs766373273 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859644 | GAGTTTGCAGTAAGC[C/T]GAGATAGCACCACTG | 4734 |
rs766379331 | snp | A/G | 1.65427e-05 | 0.00287595 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915727 | AATATCCTTCAGATG[A/G]CTTTTCACAGACAGT | 4734 |
rs766391594 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895841 | AATTGGGATACATTT[G/T]GTTAAACCAAGCTCA | 4734 |
rs766395218 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850556 | CCCAGGTGGTGGTTT[C/T]AGTGTTGTGGTCAAT | 4734 |
rs766435242 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969160 | TTGTGGGACTTTGCA[G/T]TGGAACTCAGTGCTG | 4734 |
rs766439621 | snp | A/G | 1.66208e-05 | 0.00288273 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840450 | AAAAAGACATACCAC[A/G]GATTCCATATCATGA | 4734 |
rs766451523 | in-del | -/GGAG/GGTTG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881189 | CTTTTTGCCCAGGCT[-/GGAG/GGTTG]GGAGTGCAATGGCGT | 4734 |
rs766468144 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991808 | CCATTAACTGCCACA[A/G]TTAGTTTTATTTCAG | 4734 |
rs766482726 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968243 | TTCAATCACTATCTT[A/C]TACTAAAACATAAAA | 4734 |
rs766495588 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909040 | TCTTGCTTGGGTAAT[A/G]TATTTTTCTACTAAG | 4734 |
rs766498441 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879462 | TGCTCACCCCAAAGT[A/G]AAGTCCACTAGTCAG | 4734 |
rs766515384 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843721 | TAAGCAATATAAGCA[C/T]GATATGAGCAGTTTC | 4734 |
rs766604445 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939239 | GTGGGAGGTGATTGG[A/G]TCACGGGGGCAGTTT | 4734 |
rs766610272 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892158 | AGAATCCCAGCTACT[C/T]GTGAGGCAGAGGCAT | 4734 |
rs766620184 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945095 | TTCTAAAAACCAGAG[C/T]GCATCTTCTCCTCCA | 4734 |
rs766621708 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856432 | TGGACACCTTCTCTT[C/G]AATGTTTCACAGAAA | 4734 |
rs766659697 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907868 | ACTTGATCTGAGCCT[C/T]TATCCAGACACCCAG | 4734 |
rs766662782 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860416 | TCTTACTGAGCTCGA[C/T]GCTGGCTGGCTCACG | 4734 |
rs766672292 | snp | A/G | 1.65105e-05 | 0.00287315 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830636 | TCTACAAGGATCTCC[A/G]GGCATATCAAAACTT | 4734 |
rs766672918 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891151 | TACCTACATTTTAAA[C/T]ATTTCTTGCAACAGT | 4734 |
rs766683978 | snp | C/G | 0.000102608 | 0.00716194 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993578 | CGCTTCCAGCAAACC[C/G]GACGCGCTCGCCCCC | 4734 |
rs766725469 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841866 | ATGAGCCACTGCACC[C/T]GGCCGACTCTTACTT | 4734 |
rs766725546 | snp | C/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55830530 | AGGTATGAGCTCTTG[C/G]CAGCTTTTCAGGAGT | 4734 |
rs766745563 | in-del | -/TAG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841752 | AAGTTTTTGTATTTT[-/TAG]TAGAGACGGGGTTTC | 4734 |
rs766757049 | in-del | -/TTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847677 | TCTTTTTCTTTTTCC[-/TTT]TTTTTTTTTTTTTTT | 4734 |
rs766772453 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952292 | TGAGCCAAGATCACG[C/T]CACTGCACTCAAGCC | 4734 |
rs766775624 | snp | A/G | 1.73288e-05 | 0.00294348 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848615 | TATTTTAGGAGAGGG[A/G]CGTAGATGAATGGAT | 4734 |
rs766775926 | snp | C/G | 1.76524e-05 | 0.00297084 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916845 | ATTTGTTCTCATTTC[C/G]AAACATGTTAAGGGC | 4734 |
rs766784326 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944197 | GCATTGCCTCACCTC[A/G]GAAGTGCAAGGGGTC | 4734 |
rs766793732 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865263 | CATTTGAAATCTGTG[A/G]CAAAATACGCAGATT | 4734 |
rs766810376 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831892 | AAAAGATTTATTCTT[C/G]GATTCTTGGTTTCCT | 4734 |
rs766827149 | snp | A/C | 5.0653e-05 | 0.00503229 | stop-gained, intron-variant | NEDD4 | GRCh38.p7 | 15:55834229 | TGTTATGTCTTACCT[A/C]TAGTTCATTTTCATC | 4734 |
rs766841338 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958401 | TGATATATTGCTACA[C/T]AATGTTTAATTTCAT | 4734 |
rs766867841 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832829 | TTTATTATCTGATTA[G/T]AAGGTGTAAATATAT | 4734 |
rs766876077 | snp | C/G/T | 3.30553e-05 | 0.00406531 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838559 | GGTCCAATTCTGTTG[C/G/T]GTCATTTTCAAGAAT | 4734 |
rs766893416 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860507 | TCCAAGTTACTTGAC[A/G]GTGGAGGTGATGGGA | 4734 |
rs766915892 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916011 | GTCGGTCGGGTAGTT[A/G]AAGGACTCCTAGGAA | 4734 |
rs766931136 | snp | C/T | 3.29864e-05 | 0.00406105 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848465 | AAAAGATGTACTTTC[C/T]CACACATAAAATTTA | 4734 |
rs766959451 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881835 | GCACTACTGACAATT[C/T]GAGCCAGATAATTTT | 4734 |
rs766996104 | snp | A/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953771 | CTGTCGCCAGGCTGG[A/T]GTGCAATGGCACGAT | 4734 |
rs767002985 | snp | C/G | 0.000186029 | 0.00964261 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905290 | ACCATGGCTGTAAAA[C/G]ATAACTGGCAATCAT | 4734 |
rs767004068 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964355 | CTCATCTTCCAACTG[C/T]GTAACAATTTCTACT | 4734 |
rs767033414 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911361 | CCTAGAATCTCTTTG[-/A]TTTCTCTGCCTGATG | 4734 |
rs767043853 | snp | G/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55995238 | TCGAAAAAGCCATGA[G/T]AGCATTAATTTGTTT | 4734 |
rs767047105 | snp | A/T | 1.7086e-05 | 0.00292279 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916814 | GGCTGCAAAGTGCAA[A/T]CGTAAGCTTTGTGCC | 4734 |
rs767072824 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886556 | TGGATCACGAGGTCA[A/G]AGATCGAGACCATCC | 4734 |
rs767083781 | snp | C/T | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838603 | TTGTAATATTCACTA[C/T]CCTAGATGGGAAAAA | 4734 |
rs767094508 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55936071 | GCTTATTGTGAAGGC[A/G]GTTTTCATTGCTACT | 4734 |
rs767104239 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973372 | AGTCAGGCCCTATCT[C/T]TTAAAAACAAACAAA | 4734 |
rs767107740 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865650 | AGAGCTTCTGTTCTA[C/G]GCCTGGAGATCAGCA | 4734 |
rs767108293 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961218 | ACCCATGAAAGGCAC[A/G]CTGTAAACATCTATG | 4734 |
rs767137062 | snp | C/G/T | 3.40763e-05 | 0.00412762 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993568 | CATTTCCGAACGCTT[C/G/T]CAGCAAACCGGACGC | 4734 |
rs767159349 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881484 | ACAAGTAGATGTTAT[A/G]CTTCATTAAGTCTGA | 4734 |
rs767189924 | snp | A/G | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850598 | TCCCATTTGGTGCAT[A/G]CCGGACTTCCCAGCC | 4734 |
rs767239410 | snp | A/G | 1.65061e-05 | 0.00287277 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834317 | ATTTAAAAACTTGAT[A/G]GGCAGGGCCAATGGC | 4734 |
rs767240510 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940199 | TGGTGGTTTAATACT[A/G]TATTATACACCAAAA | 4734 |
rs767276601 | in-del | -/GTCT | 1.6476e-05 | 0.00287014 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916665 | AACGGAGCTAGTGCA[-/GTCT]GTCTGGGAGTCAGCT | 4734 |
rs767318805 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954296 | GGTGGCTTACTTAGG[C/T]ACCTCTTCTACTATC | 4734 |
rs767320329 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828398 | TTAAGAGCATTTTCT[A/G]TATAATCATTCCAAT | 4734 |
rs767344747 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910452 | CTCTCCATGCCTCCA[A/T]GCTCTCTTGGCCTCT | 4734 |
rs767359526 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55947706 | AGACAAAAACCATAT[-/G]ATTATCTCAATAGAT | 4734 |
rs767360937 | snp | G/T | 1.79703e-05 | 0.00299747 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829973 | TCTTCAAATGATTCA[G/T]AAGGTGGCAAGTCCA | 4734 |
rs767371889 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965357 | CAGGCATGCGCCACC[A/G]TGCCCAGCTGATTTT | 4734 |
rs767382776 | snp | A/G | 9.25969e-05 | 0.00680367 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966579 | AGATTTCATTTTCAT[A/G]TACTTATAAGTTAAC | 4734 |
rs767389819 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850681 | GAATCACTGGTGGAG[A/G]CTTGTGATTGAGGGC | 4734 |
rs767401981 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924059 | CTTTAAGAGAGTCTT[C/T]AGGAATTCAGAAATC | 4734 |
rs767427909 | in-del | -/ACACACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836334 | GAAAAAGTATGTGAC[-/ACACACAC]ACACACACACACACA | 4734 |
rs767437074 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831987 | TCTACATCAGAAATG[A/G]CACTTTTAAACAAAA | 4734 |
rs767438924 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852519 | CTTCCCAACCTGGTG[A/G]TAATCCAGATGAAGT | 4734 |
rs767468393 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981267 | TCACCTCACCACCAT[A/G]TTGGCCAGGCTGGTC | 4734 |
rs767471114 | snp | A/G | 2.61537e-05 | 0.0036161 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850781 | TGTAATATTTTATAG[A/G]GAGAACTCACAAATA | 4734 |
rs767478725 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859523 | ACAGGGTGAAACTCC[C/T]CCATCTCTACTAAAA | 4734 |
rs767492305 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55833559 | CCAGCTACTCGGGAA[A/G]CTGAGGCAAGAGAAT | 4734 |
rs767505820 | snp | C/T | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826590 | TAACACTCCGAACTC[C/T]TTTTCTCATAGAAAT | 4734 |
rs767530398 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909381 | ATCTCATTGAACTGG[A/G]ACAGATCTGCTCATC | 4734 |
rs767553203 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856380 | GTGGACACCTTCACA[C/G]ATCCAGCTCCCATGC | 4734 |
rs767561342 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956411 | AAGATTTTTTTCCTA[C/T]GTGTTCCTATAGAAG | 4734 |
rs767572597 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992381 | CCACCCTTTATAAAC[A/G]AAGAACTCTCAAGAG | 4734 |
rs767588001 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842249 | TTATAACATTCCCTC[-/T]ACACCCTGTGTCCAA | 4734 |
rs767617759 | snp | C/T | 3.44703e-05 | 0.00415138 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993504 | CGCAGCCCCGCGGTC[C/T]CCGCACCTCGTCCTC | 4734 |
rs767629239 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977036 | CCACTGGCAAGCAGT[A/G]GCTTGTATGCCTTTC | 4734 |
rs767640063 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890471 | CGTGGTCCTTTATGA[A/C]TGACTTATTTTACTT | 4734 |
rs767641934 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55907815 | TTTTGTCTGAATACC[C/T]TTAAAGATCTTTGTC | 4734 |
rs767648342 | snp | G/T | 1.66624e-05 | 0.00288633 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869632 | AGCCACTGGTTTTAG[G/T]TAAATAAGTCATTTT | 4734 |
rs767709872 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949894 | AATATGGCACGTGTA[C/T]ACATATGTAACAAAC | 4734 |
rs767748064 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868800 | AGGGAACCTCAACGA[C/G]CAGGTGTTTTTTTGA | 4734 |
rs767775757 | in-del | -/GGG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892194 | TCACTTGAACCTGGA[-/GGG]GCAGAGGCTGCAGTG | 4734 |
rs767776448 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916538 | GCTAGACTGAAGATA[C/T]CCACTGTACCTTGTT | 4734 |
rs767778293 | snp | G/T | 1.72794e-05 | 0.00293928 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916822 | AGTGCAATCGTAAGC[G/T]TTGTGCCATTTGTTC | 4734 |
rs767779001 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961865 | TGAAAAGAATGTACA[C/T]TTGAAAAGAAAGTTG | 4734 |
rs767785731 | snp | G/T | 1.64944e-05 | 0.00287175 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833054 | CCGAGATGTGCCAGT[G/T]ACAAACTGAAGTAAT | 4734 |
rs767803159 | snp | C/T | 5.24856e-05 | 0.00512251 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848622 | GGAGAGGGGCGTAGA[C/T]GAATGGATAGAAAAA | 4734 |
rs767806836 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969087 | CCCACATGCCCTGGC[A/T]GTGCAGTGTGGTGGC | 4734 |
rs767814306 | snp | C/T | 1.67562e-05 | 0.00289444 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856097 | ATGCTGAGTTTTATA[C/T]TTTTATTGATTGATG | 4734 |
rs767818508 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845208 | TTATCCCCTTACATA[C/T]CTTTGTTGCATTCTG | 4734 |
rs767824444 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920136 | TTCTCAGCTTCCTGG[C/G]CTGCCCTGCAGATTT | 4734 |
rs767827841 | in-del | -/CA | 3.33117e-05 | 0.00408102 | frameshift-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840447 | GTGAAAAAGACATAC[-/CA]CAGATTCCATATCAT | 4734 |
rs767843006 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905384 | TTCCCAACAGTGAAA[C/T]CCACCAGTTGAAAAG | 4734 |
rs767870879 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928056 | ACTCTGTCACCCTGG[C/G]TGGAGTACAGTGGTG | 4734 |
rs767874914 | in-del | -/AAAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923645 | GCGAGACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 4734 |
rs767876259 | snp | C/T | 2.70537e-05 | 0.00367779 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55924695 | CGGTGCTGCTGAGGA[C/T]GAACCTAAGAAAAAC | 4734 |
rs767931142 | in-del | -/AATC | 8.27219e-05 | 0.00643072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848934 | CACAAATTTTAAAAT[-/AATC]AAAGTCAGTCTGTTA | 4734 |
rs767935791 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55860958 | CAGACTGGTATATTT[A/G]GAGTACCTTACGGAG | 4734 |
rs767959847 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957063 | ATACAATTGTAAACA[C/T]GTTTTTAAATTGTAT | 4734 |
rs767981566 | snp | C/T | 1.65064e-05 | 0.00287279 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840590 | ATATTGTAAAAAGTT[C/T]ATACTTAATACTAAC | 4734 |
rs767985180 | snp | A/G | 1.64781e-05 | 0.00287033 | stop-gained, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916633 | ATCTTTCTTGAGACT[A/G]AACGTTTTCCTTTAT | 4734 |
rs767985817 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980713 | AACAGTCCAGATGGA[A/T]TGCAACATAGCAAGA | 4734 |
rs768020075 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857309 | ATTAGTGGTAAGATA[A/G]AAGGTTTAATTTTTA | 4734 |
rs768023523 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843576 | AACCAGTAAGAGAAA[A/G]CATGCCATCAATATT | 4734 |
rs768035021 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831740 | TTTAGCTATCCCATC[A/T]TATGGTCAGCTTCTA | 4734 |
rs768037809 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879219 | AAAAGGGAGACTGGA[A/G]GAGTAGATGACAGCA | 4734 |
rs768060899 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966839 | CAACTAATAGGAATT[C/T]CCAATTATTGCTATA | 4734 |
rs768074501 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950387 | CCTTCAAATTCACTT[C/T]ATTAAAATTGAACAA | 4734 |
rs768088377 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965755 | TGCCCAGGCTAGAGT[C/G]CAGTGGCACAATCTT | 4734 |
rs768091963 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920338 | AAGCACAGGGTCTCC[A/C]CCCAGAATATAGGTG | 4734 |
rs768095018 | snp | C/T | 6.61802e-05 | 0.00575202 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840473 | TATCATGAAGGGTTA[C/T]TGGTTTGTGAAGCAT | 4734 |
rs768095099 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890946 | CTAAAATCTCTTACA[A/T]TCTTCCCTACAGCTT | 4734 |
rs768109505 | snp | A/G | 1.65326e-05 | 0.00287507 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846960 | GTATTTATTATAAAC[A/G]TGACTAACCTGCTTC | 4734 |
rs768119682 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881303 | CACGCCACCACTCCC[A/G]CCTAATTTTGTATTT | 4734 |
rs768123923 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980648 | GAATTCTCACAATGA[C/T]GGCAAATGGAAGCCC | 4734 |
rs768133386 | snp | C/G | 3.30017e-05 | 0.00406199 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915984 | AGAAGAGTACACAGA[C/G]TTGTTGGAGAAGTCG | 4734 |
rs768135005 | snp | A/C | 9.00779e-05 | 0.0067105 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869541 | AAAATAAGAAATTAA[A/C]ATTTTTTTAGTTTAA | 4734 |
rs768136784 | in-del | -/ATAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926038 | ATACGTATGTATCAT[-/ATAC]ATATACAGTATGTAA | 4734 |
rs768150868 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985650 | GGTATTAGGTTTGAA[A/T]TGGAAAAAATCAGTA | 4734 |
rs768157015 | in-del | -/TC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940520 | CCCTCCTCCCCCTTC[-/TC]TCTCTCTCTCTCTCT | 4734 |
rs768163650 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892039 | GGGAGGCCAAGGCAG[A/G]TGGATCACCTGAGGT | 4734 |
rs768212499 | snp | A/G | 1.65184e-05 | 0.00287384 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856141 | CTCACCACAGGAAGT[A/G]TAGGTTGTTCCTCAA | 4734 |
rs768220736 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865277 | GGCAAAATACGCAGA[C/T]TACTTAGAAAATGGG | 4734 |
rs768227070 | snp | G/T | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916570 | GCTGTAGTGAAATCT[G/T]TAGACAGCTGCTCTT | 4734 |
rs768285347 | snp | C/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936744 | GTGTTGCACTTTTTT[C/G]CCTCTAAGCATGTAA | 4734 |
rs768326328 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55840958 | CGTTTGTTTTTGAGA[C/T]GGAGTCTTGCTCTCG | 4734 |
rs768342269 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895970 | AATGGGGTAGGTTTT[A/G]TACGAGGCATCTTAC | 4734 |
rs768345353 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927948 | ATGTTTAATGAATAT[G/T]GCTAAGAAACTAATC | 4734 |
rs768347119 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939325 | CAAAGGGTTCCTCCC[C/T]CTTCACTTTCTCTTC | 4734 |
rs768360144 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968943 | TAAACAATTATTCTA[A/C]CAAGAAAGCACCTAC | 4734 |
rs768369918 | snp | C/G | 0.000200385 | 0.0100076 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863106 | GATGGCAGCAATTAA[C/G]TTTACGCATGATTTT | 4734 |
rs768386421 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831517 | TGTTAAAGTAGAGAA[C/G]ATGGAGGAAGGGGAG | 4734 |
rs768400983 | snp | G/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953719 | AGTGCTGGGATTACA[G/T]GCATGAGCCAACATG | 4734 |
rs768403992 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977441 | ACAATGATGAAATTG[C/T]CTAATGACACATTTC | 4734 |
rs768434224 | snp | C/T | 4.95029e-05 | 0.00497484 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915960 | GAAGTTTGATAGGAT[C/T]CTTTGCTCAGAAGAG | 4734 |
rs768443762 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855054 | TGAGAGTAAGGCTAG[C/T]GATGATAGTCTTTCA | 4734 |
rs768455354 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962354 | CTCATATTTATTTTA[A/T]TCCATTAATGTTCCT | 4734 |
rs768458263 | snp | A/C | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916671 | GCTAGTGCAGTCTGT[A/C]TGGGAGTCAGCTTCA | 4734 |
rs768458391 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915580 | AACATGCAGATGTCC[C/T]ATGCATGAGCTTAAT | 4734 |
rs768482150 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854544 | CCCTACGAGTCCCTT[C/T]ACACGAGATTTCTAG | 4734 |
rs768501604 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935771 | AGACTCATTTGAATC[C/T]GGGAGGCAGAGGTTG | 4734 |
rs768521498 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973954 | AAATAAATCAAATTG[A/T]AACAGAATATAATAC | 4734 |
rs768529438 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841817 | ACCTTGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 4734 |
rs768533683 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853175 | TATTATAATAAAAAT[G/T]GGTAAATTATACATT | 4734 |
rs768546091 | snp | A/C | 0.000102492 | 0.00715791 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852580 | GAATTAAATACATCA[A/C]GTTTAAGAATCCTTC | 4734 |
rs768555128 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916364 | AGACCCATTATCACT[A/G]GTTGAAAAGTTACTA | 4734 |
rs768572306 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945679 | ACAAAGATATTCCTC[A/G]AGAAGAGCAACCCCA | 4734 |
rs768601149 | snp | C/T | 5.85223e-05 | 0.00540904 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869598 | AATTCCTCAGCCTGT[C/T]CTGCATTATCATCTT | 4734 |
rs768610143 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903260 | TTTTCCAAGCAGCTT[C/T]ATCCTGTAGGATTCT | 4734 |
rs768619065 | snp | A/G | 1.65113e-05 | 0.00287322 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840564 | TACCAAGTGAAAGAA[A/G]ACAGGTAATTATATT | 4734 |
rs768633915 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885488 | ATCAAAAATAGTACC[C/T]ATAACAACTTTTTAA | 4734 |
rs768652808 | in-del | -/TACT | 1.68513e-05 | 0.00290265 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838100 | TACATACTAATAAAA[-/TACT]TACTAAATATATTCC | 4734 |
rs768662607 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900016 | AGATTCAGACATGTC[C/G]TCAAAGCTGAATGAT | 4734 |
rs768670122 | snp | C/T | 6.59848e-05 | 0.00574352 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833032 | CAGCAAATCCATTCA[C/T]AGGCACCCGAGATGT | 4734 |
rs768671283 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963786 | TTTCTTCAGCTGAAA[C/G]GACTTTAAGATATCT | 4734 |
rs768693970 | snp | A/C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944648 | GTGGTTCTCCCAGCA[A/C/T]GGGATTTGAGCTCTG | 4734 |
rs768712526 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847479 | ATAGTAATAAAAAAC[A/G]GTATCTTCAGTTTTA | 4734 |
rs768716607 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990107 | TGGGACCATCTAGTT[C/G]CAGGAAAACAAGCTC | 4734 |
rs768721578 | snp | C/T | 1.65712e-05 | 0.00287843 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840686 | AGGTGATCTTCGTTA[C/T]ACAATCCAGAGTTTG | 4734 |
rs768730883 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949137 | CATCAAGAAGCGGGC[A/G]AAGGATATGAACAGA | 4734 |
rs768753371 | snp | A/G | 1.66167e-05 | 0.00288237 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916783 | TTTCTGACAAAGGGT[A/G]AGTATTGCTTCTTCT | 4734 |
rs768767603 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836650 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTG | 4734 |
rs768768800 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842006 | AAGAACCATTCTCTG[C/G]CAACTCCTCCATAAT | 4734 |
rs768778156 | in-del | -/A | 0.32 | 0.24 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951594 | GTAAGGATCACTGTT[-/A]AAAAAAAAAAAAAAA | 4734 |
rs768783283 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884831 | CTCAAATGGGCAAAT[C/T]GAAGAGGTATTGTCT | 4734 |
rs768786409 | snp | C/T | 1.74821e-05 | 0.00295647 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915312 | GACAGTTCATTTGTG[C/T]AATCTCTGTTGCTGT | 4734 |
rs768822375 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849091 | TATCAAAAGGAATAA[C/T]GATCAGTTCTCAGGG | 4734 |
rs768838098 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973024 | TCAGCTAGACTTCAA[C/T]ATAGTAATAGTTGGA | 4734 |
rs768884562 | snp | C/T | 1.90794e-05 | 0.00308858 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829883 | TAAAAACACTACAGA[C/T]TGTTATTTGTAATCT | 4734 |
rs768920282 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956423 | CTATGTGTTCCTATA[A/G]AAGTTTTATCATTTT | 4734 |
rs768930665 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992342 | TTCTCAAAATATCCT[A/G]AAATAACTGCATTAA | 4734 |
rs768939431 | snp | G/T | 3.96377e-05 | 0.00445166 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838214 | ACTTGATATGTTATT[G/T]TAGCGAGAAAAATTT | 4734 |
rs768945438 | in-del | -/ACAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883692 | AACACACACACACAC[-/ACAA]ACAAACACACACACA | 4734 |
rs768952367 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862200 | ATATCAGGCACAAAA[C/T]ATCATAGCCAAAAAT | 4734 |
rs768959008 | snp | A/G | 1.89921e-05 | 0.00308151 | utr-variant-5-prime, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55966475 | TAGATATACTTACCT[A/G]GCTCCCAATATATCC | 4734 |
rs768964537 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860483 | TCTTCTGCAAGATGA[A/G]TTGGAACATCCAAGT | 4734 |
rs768967114 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938435 | AGAAATTGACCCTTA[A/T]CTTAAAACAAACACA | 4734 |
rs769019548 | snp | C/G | 1.6599e-05 | 0.00288084 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860398 | TAACAAAATCTAAGA[C/G]CATCTTACTGAGCTC | 4734 |
rs769021326 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871236 | GAAAATGTGCTCAGA[C/T]AATGTTTTGTTGAAA | 4734 |
rs769025252 | in-del | -/T | 6.59544e-05 | 0.0057422 | frameshift-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860434 | TGGCTGGCTCACGGC[-/T]GAATTTCCAAAAATG | 4734 |
rs769027125 | in-del | -/ACAG | 1.65488e-05 | 0.00287647 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915734 | TTCAGATGACTTTTC[-/ACAG]ACAGTCTGTCTGGGA | 4734 |
rs769052109 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850612 | TGCCGGACTTCCCAG[A/C]CTTTAGGAAGGAATC | 4734 |
rs769080760 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934102 | AGGTTGCAGTGAGCC[A/G]AAATTGCGCCACTGC | 4734 |
rs769089076 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908421 | TATTATTGATATGTT[G/T]TTAATGAATTACTCG | 4734 |
rs769104408 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991684 | TGTGAATGGGATAGG[C/T]CACAGTCCATGAAAC | 4734 |
rs769112300 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838444 | ATGTATTAAGTGTAC[A/G]TATTAACATCTAAAC | 4734 |
rs769121315 | snp | C/G/T | 9.91775e-05 | 0.0070413 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915711 | TGCACTGAAACACAA[C/G/T]AATATCCTTCAGATG | 4734 |
rs769136195 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880380 | CACATCACCGTGACA[-/T]TTTCAGAGCACCAGA | 4734 |
rs769143978 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55848647 | GAAAAATAGCACTGG[C/T]TGTATGGTTAATTTA | 4734 |
rs769165881 | snp | G/T | 1.74509e-05 | 0.00295384 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850740 | ACTGGTCTCCACTGT[G/T]GCCTAGCACATTAAT | 4734 |
rs769189850 | snp | C/G | 1.7501e-05 | 0.00295807 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993484 | ACCCGAAGGGAAGCC[C/G]GCCCCGCAGCCCCGC | 4734 |
rs769209073 | in-del | -/ACTGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956707 | CTCTGTCTTATTATA[-/ACTGT]GTAGCAAGTCTTGAA | 4734 |
rs769224426 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953731 | ACAGGCATGAGCCAA[C/T]ATGCCCGGCTTAAAC | 4734 |
rs769285379 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921868 | ATTAAGAAAGAGTCA[C/T]GCAAATACTAAAGTT | 4734 |
rs769301626 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981683 | GCAGTAGTTCTCAAA[A/G]TGGATTCCATGGACT | 4734 |
rs769353336 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848382 | CTTACTGGTCCAGTT[A/G]TTGCTACATTCTCCA | 4734 |
rs769353739 | in-del | -/GATAAT | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938137 | AGGCTGAGGTGGGCA[-/GATAAT]GAAGTCAAGAGATGG | 4734 |
rs769355502 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893429 | ATCAAGAAATACTTC[A/G]GAGATCACAAAAGAC | 4734 |
rs769355533 | snp | C/T | 3.74118e-05 | 0.00432487 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838122 | TAAATATATTCCTTT[C/T]TGTTCTTATTGGTGA | 4734 |
rs769408709 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891548 | ATATTTGAACTGCAT[A/G]CAGCCTACTTCATAA | 4734 |
rs769440233 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944502 | GCTGAAACTAGGCAG[A/G]GCCCACCTCAGCTCA | 4734 |
rs769441946 | snp | C/T | 5.17219e-05 | 0.0050851 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829919 | ACTCCATCAAAGCCC[C/T]GGGTGTTTTCAATTG | 4734 |
rs769519197 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928919 | AATACTAATTAAAAA[G/T]TAAAAATACTAATTA | 4734 |
rs769530889 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856987 | GTGAAATGCCTTAAG[G/T]GTTACTTGTACAATG | 4734 |
rs769539190 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850648 | TCAATTTCAGATGGC[C/T]GGGTCACCTGCTGGC | 4734 |
rs769566354 | snp | A/G | 9.67258e-05 | 0.00695367 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872370 | GTAAGGTGTAATGAA[A/G]AGATAAAAAATTTAA | 4734 |
rs769582411 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856025 | CCTACATTCTGTGCT[G/T]TATTGGCTCCCTGTA | 4734 |
rs769587920 | snp | A/G | 0.000134807 | 0.00820886 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860376 | ATAATATAAACTACT[A/G]AAGCCGTAACAAAAT | 4734 |
rs769606361 | snp | C/T | 4.94271e-05 | 0.00497102 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916687 | TGGGAGTCAGCTTCA[C/T]TTGAACAACGTTAGA | 4734 |
rs769648436 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943935 | CACCCAAGGCCTTTC[A/G]GAACCCACCCCTTGC | 4734 |
rs769676477 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866442 | TGAATCAGACTGTAT[A/G]TTTCTGGTTTCAATC | 4734 |
rs769691511 | snp | G/T | 0.000126513 | 0.00795237 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847085 | AGGTTGTTTTTATTC[G/T]GGAACAATTTTTATT | 4734 |
rs769709350 | snp | C/G | 1.68866e-05 | 0.00290569 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834001 | TATGATTCAATCTAT[C/G]AAAAAGTAAGTTATG | 4734 |
rs769712382 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931089 | AGAAGGAAAGAGGGA[C/G]AAAAAAGGAACAAGT | 4734 |
rs769720658 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864452 | TTTGGGAGGCCGAGG[A/C]GGGCAGATCACTTGA | 4734 |
rs769748140 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983215 | AATAAAGAAATAACT[A/G]GCAAACAAATGTTAA | 4734 |
rs769763188 | snp | A/G | 1.64931e-05 | 0.00287163 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833048 | AGGCACCCGAGATGT[A/G]CCAGTGACAAACTGA | 4734 |
rs769770919 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905771 | GTAGATTCTGGATAT[C/T]AGCTCTTTGTCAGAT | 4734 |
rs769774443 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884679 | TAATGCATCAGAGTC[C/T]GTTAATATCAGAATT | 4734 |
rs769794405 | snp | A/G | 1.65141e-05 | 0.00287346 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856156 | GTAGGTTGTTCCTCA[A/G]AAGTATAGGCTTGTA | 4734 |
rs769814730 | snp | A/G | 3.2956e-05 | 0.00405918 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916603 | TATTAACATTTTCAG[A/G]TGAGGGAACAGATGA | 4734 |
rs769837468 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957554 | TAAGATGACTGTCTT[C/T]TCAGTGTGGCGATTC | 4734 |
rs769844414 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962478 | GATGGAGTTTCACTC[-/TT]GTCATGCAGGCTGAA | 4734 |
rs769855705 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896525 | TGATGATACTAAATT[A/G]CTAATTTCCTCCTCT | 4734 |
rs769858173 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859254 | TTCTCATCGTGGAAG[C/G]ATATGCTGGGATACT | 4734 |
rs769899171 | snp | C/T | 1.65452e-05 | 0.00287616 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915884 | TGTTGAAAGAAATCC[C/T]TTAGCACTAGTGCCA | 4734 |
rs769902852 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846834 | ACTCAAAAAATGAGC[A/G]TCCTTTCTCTAGGAA | 4734 |
rs769921631 | snp | A/G | 3.29848e-05 | 0.00406095 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860571 | CTCTTATAATTTCCC[A/G]GTTCTAAAATGAACA | 4734 |
rs769927265 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854100 | AGGTTGCAGTGAGCC[A/G]AGATCGCCTGGGCAC | 4734 |
rs769928568 | snp | G/T | 1.64849e-05 | 0.00287092 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915432 | AGGCTGGATAGACAG[G/T]AAATATTTGGATAAG | 4734 |
rs769933397 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955153 | CAGCCTCCCAAGTAG[C/T]GGGGACTACAGGCGC | 4734 |
rs769952940 | snp | A/G | 3.15582e-05 | 0.00397217 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924637 | TCATATAAGCACAAT[A/G]TAACTTACCAATCGG | 4734 |
rs769957259 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941996 | TGGGTATTAGCTGTA[C/G]TGTACTATACATGTC | 4734 |
rs769970212 | snp | C/T | 1.82271e-05 | 0.00301881 | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55834272 | GAGATCCTGTGGTAT[C/T]AGTTCAAAGAATCCC | 4734 |
rs769982355 | snp | A/T | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860499 | TTGGAACATCCAAGT[A/T]ACTTGACGGTGGAGG | 4734 |
rs769999889 | snp | C/T | 1.70266e-05 | 0.00291771 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993549 | CCTCCACCGCGCAAG[C/T]TGCCATTTCCGAACG | 4734 |
rs770001452 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911136 | TGCCACCTACAGCAG[A/T]GACTCTCAACAGGGG | 4734 |
rs770016629 | in-del | -/CACACACACT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836365 | ACACACACACACACA[-/CACACACACT]TTAGAGACAAAGTTT | 4734 |
rs770021177 | in-del | -/AT/GA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880453 | TACACAAACCTGAAA[-/AT/GA]TATAAGAGAGTACTT | 4734 |
rs770093146 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875918 | GTCAATAAAGTCAGT[A/G]AACTGAAGCAGGATA | 4734 |
rs770098376 | snp | C/T | 2.40654e-05 | 0.00346873 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830050 | CTGACAAAGCAAGTA[C/T]CACCACAGCAAACAG | 4734 |
rs770098397 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989457 | TGTGTAGTACATAAA[G/T]GTTTGGGAAGTTTGT | 4734 |
rs770116262 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962384 | TTGTAATTATTGATA[C/T]GATTGGATTTAGTCT | 4734 |
rs770116565 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950658 | AGTGGGTTAACGAGC[A/G]TCCCGGAGAAGCAGA | 4734 |
rs770123726 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966320 | GTAATTCAGATACCA[A/G]GAGATTTAGTAAACC | 4734 |
rs770129583 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922551 | ATTTTTATTACAGAC[-/A]AGAGTTTCACCACGT | 4734 |
rs770132027 | snp | C/T | 0.00022205 | 0.0105345 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55951387 | TTACTCTGAATAATA[C/T]TTCTTCATTCCACTT | 4734 |
rs770146576 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889599 | TAGGGAGAAGTAGAG[A/G]TAAGTAATGGCTACA | 4734 |
rs770180198 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884272 | AGCAACCAAAACTCA[A/G]ATCACAACAACCAGG | 4734 |
rs770204656 | snp | C/T | 6.58979e-05 | 0.00573974 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842057 | AACTCAATCCACAGT[C/T]GAGCCTTCAGGAAGT | 4734 |
rs770241389 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900235 | GTGCGCTGCATATGC[C/G]TGGAAATACTGCTCC | 4734 |
rs770265553 | snp | G/T | 1.72243e-05 | 0.0029346 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915323 | TGTGCAATCTCTGTT[G/T]CTGTCTCTTGATAAA | 4734 |
rs770282305 | snp | A/C | 1.67472e-05 | 0.00289367 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862903 | AATTGTGAAAGCCAT[A/C]AGCACATACTGAGGG | 4734 |
rs770309188 | snp | G/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937341 | GCTATATAAAAATGA[G/T]GATATAAATGACAAA | 4734 |
rs770317727 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898547 | TTCAAAACATCTTAT[A/G]TATGTTCTTTGTCTT | 4734 |
rs770322894 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872855 | GATCAAAAAAGTCAA[A/C]AGCCTGGAAAGTAAG | 4734 |
rs770338840 | snp | C/T | 1.89676e-05 | 0.00307952 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850749 | CACTGTGGCCTAGCA[C/T]ATTAATGAAATCATA | 4734 |
rs770343071 | in-del | -/TGTC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964731 | GTGTGTGTGTGTGTC[-/TGTC]TGCTTATCATTCTAT | 4734 |
rs770359798 | snp | C/T | 3.31625e-05 | 0.00407188 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915852 | ATTGTTTTAGATAAC[C/T]GAAGTCCATTGACAG | 4734 |
rs770362073 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950240 | AACCGATTTAAAAGG[C/T]TGTTTTTATGTCATA | 4734 |
rs770365784 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890197 | TAAAAATAAAAAAAG[C/G]TTTATTAAGATGTAA | 4734 |
rs770380647 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976396 | ACTCCAATAATCTGA[C/T]ATTAAAATGGGCAAA | 4734 |
rs770395702 | in-del | -/AC | 3.4195e-05 | 0.00413477 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993580 | CTTCCAGCAAACCGG[-/AC]GCGCTCGCCCCCGCC | 4734 |
rs770398902 | snp | G/T | 1.85211e-05 | 0.00304306 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838624 | ATGGGAAAAATTACA[G/T]ATTTAAAATTTGTAT | 4734 |
rs770420190 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932101 | TCCCTTTGTGTAGTG[A/G]GAGGGACCTGGTGGG | 4734 |
rs770438914 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852447 | TGGGCTTTGTCCAAG[C/T]AGTCGTTCTGGAATT | 4734 |
rs770441969 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978817 | TGATGTAATGTGTTA[-/T]CTATGCGGGCAGCGT | 4734 |
rs770445486 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846053 | CGACCTCCCAAAGTG[C/G]TGGGATTACAGGCAT | 4734 |
rs770452703 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977364 | TAGGCTATATCACAC[A/G]GCCTAGGTGTGTAGT | 4734 |
rs770471395 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942495 | GAGATTTGGTTGCTT[A/G]AAAGTGTGTAGTACT | 4734 |
rs770473605 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931428 | ATTCTTTCACAAGAT[G/T]TTTTAAATTTATTGA | 4734 |
rs770478294 | snp | G/T | 1.72647e-05 | 0.00293804 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829941 | TTTCAATTGCCATCT[G/T]AAGTTTATCCCATAA | 4734 |
rs770481940 | in-del | -/A | 3.3184e-05 | 0.00407319 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915834 | CTTCTCCGGGGGTAC[-/A]AAATTGTTTTAGATA | 4734 |
rs770482890 | snp | A/C/G | 3.47375e-05 | 0.00416746 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993604 | CCCCCGCCCAGGGCA[A/C/G]GCAACTGTGGAGGAG | 4734 |
rs770496843 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983073 | GTTGCAGTGAACCGA[A/G]ATTGCGCCATTGCAC | 4734 |
rs770499160 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964182 | TTTCTTCAAAAAATA[-/TT]TTGTGCCTTCTTCTT | 4734 |
rs770571362 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854793 | AAAAAAACCCCAATC[A/G]ATGTATTGAGGGAAA | 4734 |
rs770598091 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990317 | CCAAAACAGTTGGGG[A/G]CTGCAGTTCTAGAAG | 4734 |
rs770605800 | snp | A/C | 1.6483e-05 | 0.00287076 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916393 | TAAGGCTACCACTAC[A/C]AATGGCTGGACTGCT | 4734 |
rs770610028 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938258 | CAGCTACTCAGGAAG[C/T]TGAGGCAGGAGAATC | 4734 |
rs770621984 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984041 | TATTCTATATCATTA[A/T]ACCTCATGCCCTGAC | 4734 |
rs770637557 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961257 | CCTAGAGTCTCATCA[C/G]GGCAGGGCTAGAGTT | 4734 |
rs770642362 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864180 | CAAAGATTCTATTAA[A/T]TACTGATTGGTTAGG | 4734 |
rs770659195 | snp | C/T | 3.40547e-05 | 0.00412628 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993553 | CACCGCGCAAGTTGC[C/T]ATTTCCGAACGCTTC | 4734 |
rs770662125 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916697 | CTTCATTTGAACAAC[A/G]TTAGACGTTGAAATC | 4734 |
rs770670209 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942818 | GGTTGAAACAGTTTG[A/G]AGAGATCAGAAGAAG | 4734 |
rs770733863 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831297 | TCCTATAAATACATA[A/G]GAATTTGACTTTGTA | 4734 |
rs770755836 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888418 | GGAATTAACCAAAGA[C/T]GTGAAATATCTCTAT | 4734 |
rs770765491 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976624 | TATCCAATCTGGGCA[-/A]AAATTTTTTTTTTTT | 4734 |
rs770767533 | in-del | -/CGCA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983312 | GTGCGTGCGCGCGCG[-/CGCA]TGCGTGCATTTGATT | 4734 |
rs770799930 | snp | C/T | 1.64893e-05 | 0.0028713 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834151 | ACATAAGAAGCTACA[C/T]AAGAAATGTCAAATT | 4734 |
rs770803502 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876620 | GGAATATTGGAAATA[A/T]CTGACTAACCCAAAA | 4734 |
rs770806512 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889891 | TTTTTTAGTAGAGAT[-/G]GGGGTTTCACTGTGT | 4734 |
rs770828979 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862283 | CTAAAGGAAGACTTT[A/G]TAAGACTATATGGAA | 4734 |
rs770830882 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843209 | CTTTTGTAAATTGCC[G/T]GGTCTCAGGTATGTC | 4734 |
rs770834469 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837484 | CAAAATGTGTAAGGT[A/G]ATCCTATTTAGAAAA | 4734 |
rs770872852 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928637 | ACACCTTCTCCACTC[C/T]ACATGTCTACACTGT | 4734 |
rs770890186 | snp | A/G | 0.000642891 | 0.0179174 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830613 | AATTTATTTGGTTTC[A/G]TTTACTCTCTACAAG | 4734 |
rs770893318 | snp | A/C | 9.94942e-05 | 0.00705246 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916777 | CGGAGGTTTCTGACA[A/C]AGGGTAAGTATTGCT | 4734 |
rs770927989 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931015 | GTACATACAAGGCAT[A/G]TAACTGTGAAATTTT | 4734 |
rs770967684 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967235 | ATTTTTTTAAATCCC[A/G]TTCAACAGACAACAG | 4734 |
rs770976085 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909931 | TAATGCTGTCCAAAA[C/T]GAGGTGTGAATATTC | 4734 |
rs770985172 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980814 | TGTGTGTGTGTGTGT[A/G]TTACATTTTTACCGC | 4734 |
rs770990574 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927683 | TCAAAGCAGTTTTAA[A/G]AGGAGAAATGACATA | 4734 |
rs770992254 | in-del | -/GTTGTTATA | 1.65501e-05 | 0.00287659 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850505 | TAAGAGATGATTATT[-/GTTGTTATA]AATTTAAATGGAAAA | 4734 |
rs771016602 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839572 | CATTGTGTGAGGCTA[A/T]TCAGCAGCACAGGAA | 4734 |
rs771026536 | in-del | -/TATGT | 3.32265e-05 | 0.0040758 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838205 | AACACAATAACTTGA[-/TATGT]TATTTTAGCGAGAAA | 4734 |
rs771032598 | in-del | -/TGC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960581 | TCTGACTGGCTTCCT[-/TGC]TCCGCAGCTTGCAGA | 4734 |
rs771040763 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873309 | CCTTTTCCCTACCTA[A/G]CTGATTTTTATCTCT | 4734 |
rs771062562 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858278 | GAATGGGATCGTATG[G/T]GATTTATCATCAGCA | 4734 |
rs771066024 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965130 | GGAATTCTGTTATAG[A/C]AACACTAAACATAAT | 4734 |
rs771067108 | snp | G/T | 3.29755e-05 | 0.00406038 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860656 | AACTAGGAAACTACT[G/T]ATACCTCGGAAGACT | 4734 |
rs771071589 | snp | C/T | 3.30508e-05 | 0.00406501 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848919 | ATAAAGAACAATACA[C/T]ACAAATTTTAAAATA | 4734 |
rs771086342 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992784 | AAACAGCTTTGCCTT[C/T]TTCAAATCCCAGAGC | 4734 |
rs771092081 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887750 | AAAATACTAGCAAAC[C/T]GAATTCAACAACCTA | 4734 |
rs771093721 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941715 | ATTACAGGTGCGCAC[C/T]ATCACACCCAGCTAC | 4734 |
rs771103342 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954042 | TCCTTAATTCATGTT[A/G]CACTTCAAAACCCTA | 4734 |
rs771112706 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874886 | GGCTGAGGCAGGAGA[C/G]TGGCTTAAATCCAGG | 4734 |
rs771138587 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923245 | GGGAAAAAAAGGAAA[A/G]CATTTTATATTCTTT | 4734 |
rs771141153 | snp | C/G | 3.29641e-05 | 0.00405968 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916481 | AATACCATCCTTCAA[C/G]ATACAAGTAAACGAA | 4734 |
rs771191752 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935663 | CCATCCTGGCTAACA[C/T]AGTGAAACCCTGTCT | 4734 |
rs771199162 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974833 | GTAAATGGGGAGAAA[A/C]TGAAAGCCTTTCCTC | 4734 |
rs771200697 | snp | A/G | 4.95438e-05 | 0.00497689 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840568 | AAGTGAAAGAAAACA[A/G]GTAATTATATTGTAA | 4734 |
rs771218289 | snp | C/T | 1.6659e-05 | 0.00288604 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915351 | AAATTATCCACTTTA[C/T]CTTCATTTCCAGATG | 4734 |
rs771238681 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895002 | TTTCTTTCCACCTCT[-/A]AAAAAAGGGAGGGGC | 4734 |
rs771262990 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971709 | CAGAGAAATAATAAC[A/G]AAGAACTTTCTAGGC | 4734 |
rs771277822 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982058 | TACAGATGGAGCTGA[C/T]AACCTAGGTTACTAG | 4734 |
rs771300129 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892308 | TAAATAAATAAATAA[-/A]TAAATAAATAAATAA | 4734 |
rs771308009 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971065 | GGATCTCAGGATCCT[A/G]TCAAATAAATTTAAC | 4734 |
rs771310380 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896165 | AGCACACCCAGCTCA[A/G]TGCCATTTTATTCAC | 4734 |
rs771311271 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900731 | TCTCAAAGAGTAACT[A/G]TATAAATGTAAAATT | 4734 |
rs771311762 | snp | A/G | 0.000188982 | 0.00971882 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951616 | AAAAAAAAAAAGAAA[A/G]AAAAATTTTAATTAT | 4734 |
rs771313629 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962115 | ATATATTCCTGATTG[A/G]CTTTATTCTTTATCA | 4734 |
rs771347618 | snp | A/G | 2.02263e-05 | 0.00318006 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834293 | AAAGAATCCCTAGAA[A/G]AAAGATGTATTTAAA | 4734 |
rs771371063 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853332 | AACAATAACAAGCAC[A/G]TGTCCTGTTTAACAC | 4734 |
rs771406040 | snp | A/C | 0.000181418 | 0.0095224 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860604 | ATAAGCTTGAGCCAC[A/C]CATACTTTATTGCTA | 4734 |
rs771414736 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903376 | ATGACATTTGCTAGA[C/T]TTGTGATTTTCAGCA | 4734 |
rs771426339 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941958 | GGTAAATGTTCCATG[C/G]GCATATAAAAAGAAT | 4734 |
rs771433009 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923830 | ACACTAAAAACAGAC[-/T]TTTTTTTTAAAAAAA | 4734 |
rs771459099 | snp | C/G | 1.6486e-05 | 0.00287102 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915442 | GACAGGAAATATTTG[C/G]ATAAGCTCCTCCCAA | 4734 |
rs771473948 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975351 | AGCTAAAGACTCCAC[C/T]CAAAAGCTATTAGAA | 4734 |
rs771475435 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896056 | TTGGCATGGAATTCT[A/G]GTTTGTTTTTTCCAA | 4734 |
rs771481184 | snp | A/G | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842145 | GAAGTTTCATTTCAA[A/G]TTTGTTTGGAATGTC | 4734 |
rs771488181 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842473 | CTTACTGCAGCCTCG[A/T]CCTCATGGGCTCAAG | 4734 |
rs771500186 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919284 | GCCTAATGCTTTCTT[C/T]CAGGATTTTTCTTGT | 4734 |
rs771520967 | snp | C/T | 0.00021429 | 0.0103489 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830604 | ATAAGGAAGAATTTA[C/T]TTGGTTTCATTTACT | 4734 |
rs771545841 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867835 | CCGAGGCGGATGGAC[A/G]GCTTGAGGCCAGGAG | 4734 |
rs771549185 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852300 | GACTCCATCTCAAAA[A/C]AATAAAAAAAAAAAA | 4734 |
rs771551293 | in-del | -/ATTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983977 | TATTGATGTGTGATA[-/ATTT]ATTTAATGTTTCTCT | 4734 |
rs771570983 | snp | A/T | 5.10634e-05 | 0.00505263 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846942 | TATATTGATGACTCT[A/T]AAGTATTTATTATAA | 4734 |
rs771586536 | in-del | -/TTG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919296 | CTTTCAGGATTTTTC[-/TTG]TTGTTGTTGAAGTTG | 4734 |
rs771601341 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989267 | TTTAAAAATAAATTA[C/T]TTTAAAAATACACTA | 4734 |
rs771626635 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941250 | TTCCACTCTTATTTC[C/T]TTCCTTCTTTTTCTT | 4734 |
rs771639455 | snp | C/T | 1.66286e-05 | 0.0028834 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842151 | TCATTTCAAATTTGT[C/T]TGGAATGTCATTCTG | 4734 |
rs771667503 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945823 | TCTCTCAGCAGAAAC[C/T]TTACAAGCCAGAAGA | 4734 |
rs771690817 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970883 | AATGTTCAGACATTA[A/G]TGAACATCCACAAGC | 4734 |
rs771713739 | snp | C/T | 1.69192e-05 | 0.00290849 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846950 | TGACTCTTAAGTATT[C/T]ATTATAAACATGACT | 4734 |
rs771736063 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866636 | AAAATGGTAGCAAAA[G/T]AATATTTCTTTTAAA | 4734 |
rs771740195 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915447 | GAAATATTTGGATAA[A/G]CTCCTCCCAATGAAA | 4734 |
rs771752256 | in-del | AGCGAGACTCCATCTC/CTCCATCTCAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923630 | CCCACCTGGCGACAA[AGCGAGACTCCATCTC/CTCCATCTCAA]AAAAAAAAAAAAAAA | 4734 |
rs771766911 | snp | G/T | 1.68459e-05 | 0.00290219 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852565 | TGAAGAATAACAGAA[G/T]AATTAAATACATCAA | 4734 |
rs771785560 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881620 | TAACTTAGGTTTAGG[C/T]TTAATCAGATTAAAA | 4734 |
rs771794513 | snp | C/T | 3.31906e-05 | 0.0040736 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915803 | GCCCTTCCTGTGAAG[C/T]GGCCGTATGTCTCTT | 4734 |
rs771824617 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882488 | AGATCAGCCAGAGCC[A/G]GTGGAGAATTGTCCA | 4734 |
rs771836315 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911235 | GGGGTGTTACTAGCA[C/T]TTAGTGGGTGGAGGC | 4734 |
rs771877576 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935623 | GAGGCTGAGGCAGAC[G/T]GATCATGAGGTCAGG | 4734 |
rs771887913 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916487 | ATCCTTCAAGATACA[A/G]GTAAACGAAGCATCA | 4734 |
rs771972289 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965332 | TCAGTCACCCATGTA[A/G]CCAGGAGTACAGGCA | 4734 |
rs771978574 | snp | C/T | 1.8281e-05 | 0.00302327 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863093 | GGCTGAAAAACAGGA[C/T]GGCAGCAATTAAGTT | 4734 |
rs771984974 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951205 | TTTACCTCTCCATTA[C/T]CTTACATTTATGTTT | 4734 |
rs772014148 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889668 | ATAGGGTAACTTTAG[A/T]CAAAAATAATTTAAT | 4734 |
rs772038857 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55924866 | TGATGTCAGGAGTTC[G/T]AGACGAGCCTGGCCA | 4734 |
rs772047463 | snp | G/T | 1.67318e-05 | 0.00289234 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848574 | CTCTCTTCCCATCCT[G/T]GCTATAATTAAAAAT | 4734 |
rs772049635 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875968 | TAGGCACACCATTAT[C/T]AAACGCTGAAAACAA | 4734 |
rs772051090 | snp | C/G/T | 3.47356e-05 | 0.00416735 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840410 | AAGCTGCTTGTTAAA[C/G/T]TATACTTCGTCTATA | 4734 |
rs772081456 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949767 | GAGAACACTTGGACA[A/C]AGGAAGGGGTACGTC | 4734 |
rs772132686 | snp | A/G | 1.65023e-05 | 0.00287244 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916056 | GAGTAACGTTTTAGT[A/G]GAATTTTTGTGTTCC | 4734 |
rs772147104 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922023 | CAAAATTCACATCGG[C/T]ATCAGTGGCAACAGG | 4734 |
rs772154052 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837055 | AGTAACTTTTTAATT[G/T]ATATTCTGAATAAAA | 4734 |
rs772163003 | snp | G/T | 0.0039176 | 0.0440846 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856169 | CAAAAGTATAGGCTT[G/T]TAAGCTGCCTCTTCT | 4734 |
rs772187620 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958834 | ATGTTTTCTTTTTAT[C/G]TTTTTCATTTCCACA | 4734 |
rs772193409 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863984 | AGGCATTTTATCAAG[A/T]CATAAAACAGCCAAA | 4734 |
rs772197507 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867073 | AAAGTTGCAAATGGT[A/G]CAAAAATCAAATGTT | 4734 |
rs772199349 | snp | A/G | 3.34169e-05 | 0.00408746 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840730 | GGTATAATTGTCCCT[A/G]TAAAGACAACCCCAT | 4734 |
rs772201886 | snp | A/C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900275 | GATTTGTTTTAGAGC[A/C/G]CATGGGAGCCATGCC | 4734 |
rs772202070 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934304 | ATCAATACTTCATTC[A/C]TTTTTATTGATGAAT | 4734 |
rs772211814 | snp | C/G | 1.65089e-05 | 0.00287301 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916254 | TCACTTGGTGGAAAA[C/G]TATAACTACTACTGT | 4734 |
rs772247359 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887657 | GTATTACTCAGAGAC[C/G]AAAACCAAACAGACA | 4734 |
rs772255151 | snp | C/G | 1.64906e-05 | 0.00287142 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915553 | GACAATCTACATTTT[C/G]GGAGGATGGCAAACA | 4734 |
rs772274889 | in-del | -/A | 0.000142318 | 0.00843439 | intron-variant | NEDD4 | GRCh38.p7 | 15:55905238 | TCAGTTGCAGAACTT[-/A]TATAAAGGAATCACC | 4734 |
rs772291120 | in-del | -/AGA | 1.6777e-05 | 0.00289624 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852561 | AAAGTGAAGAATAAC[-/AGA]AGAATTAAATACATC | 4734 |
rs772325475 | snp | C/T | | | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838166 | TCCACCATTTTTCAG[C/T]TCATGTTGATGTGTC | 4734 |
rs772367099 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844411 | TAAAGACCCCTGGAA[A/T]AGCTGAGTGAGAGAA | 4734 |
rs772370699 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928702 | CTCCCTAGAGCCTGA[C/T]CTCCCCATTCACTAC | 4734 |
rs772399424 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827542 | TCATGCTTAGATAGT[G/T]CACAAACATAATATT | 4734 |
rs772431036 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940962 | TATTTTCTGTTTCTA[A/C]TTATATTGGTTTTAG | 4734 |
rs772453109 | snp | A/G | 0.000188271 | 0.00970051 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872405 | CTATTATTATTTTAT[A/G]TTTACTGACCTTCTT | 4734 |
rs772463791 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969811 | CAGTATTATGCTGAC[G/T]TCGGGTGTGATCCAA | 4734 |
rs772468745 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858941 | GCTGTATTCCAATGG[C/T]AATTATTCATAACAG | 4734 |
rs772473224 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876419 | TACAAAAAAAAAATT[-/G]TATCGCTATACTATG | 4734 |
rs772473649 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845312 | AGGAACATGGGATCT[A/G]GAGCTAGACCACTTA | 4734 |
rs772488115 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953956 | CAATCTCTTGACCTC[A/G]TGACCCTCCTGCCTC | 4734 |
rs772506022 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895110 | CCAGGAAATACTCAC[A/C]GCTAGGTAACTGCTA | 4734 |
rs772511001 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992745 | AGCATAGGCATAATC[A/G]GCATTAGTTATTTAG | 4734 |
rs772513285 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953135 | GCTGGGACTGCAGGC[A/G]CACACCACCACGCCC | 4734 |
rs772521280 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858031 | TTCCTGTTTAGTCCT[C/T]GAGTAAATTATACAC | 4734 |
rs772521597 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852959 | TTCACCATATTGGCC[A/C]GGCTGGTCTCGAACT | 4734 |
rs772539392 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941683 | GATTCTCGTGCCCAG[C/T]CTCCCAAGTAGCTGG | 4734 |
rs772558933 | snp | A/G | 7.503e-05 | 0.00612449 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838081 | AAAATTATATCCAAT[A/G]AAATACATACTAATA | 4734 |
rs772567083 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941509 | TGATATACATACGTG[-/T]TGTTACTGAATTGTA | 4734 |
rs772570084 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873128 | TTATTTTACTTGGCT[C/G]TTTTCCTGTTTCCCC | 4734 |
rs772579513 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847678 | CTTTTTCTTTTTCCT[-/TT]TTTTTTTTTTTTTTT | 4734 |
rs772614059 | snp | C/T | 3.38089e-05 | 0.00411136 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55837832 | ATTCGGTTTACAAAT[C/T]GCCATTGTATTACAA | 4734 |
rs772624777 | snp | A/G | 4.04424e-05 | 0.00449662 | intron-variant | NEDD4 | GRCh38.p7 | 15:55966457 | TTAAAATTATAATCC[A/G]AATAGATATACTTAC | 4734 |
rs772655831 | snp | C/T | 1.70586e-05 | 0.00292045 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838459 | GTATTAACATCTAAA[C/T]ATTTGTCTCACAATT | 4734 |
rs772666184 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876407 | CAAATTGTTGTATAC[-/AA]AAAAAAAATTGTATC | 4734 |
rs772673092 | snp | A/G | 5.19215e-05 | 0.00509491 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993498 | CCGCCCCGCAGCCCC[A/G]CGGTCCCCGCACCTC | 4734 |
rs772700187 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894221 | CAATCAATCCGGGAT[A/C]AAAAATATTTGAAAA | 4734 |
rs772713130 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55978231 | ATAACACAGCTATCC[C/T]AGATACATTTAACTT | 4734 |
rs772730140 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853530 | CTTCTAAGGAATGGA[A/G]CTGAGATTTGAACCC | 4734 |
rs772734015 | snp | A/G | 4.96151e-05 | 0.00498047 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841928 | AATCATTGTAAAGGT[A/G]CTTACGTAGCAGAAT | 4734 |
rs772737847 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903395 | TGATTTTCAGCAAGT[C/G]ATTTAAAAATTTCTG | 4734 |
rs772751341 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908681 | ACATGCACATGAGAA[C/T]TTAAAAATCACTGGC | 4734 |
rs772769173 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55833591 | GCTTGAACATGGGAG[A/G]TGGAGGTGGCAGTGA | 4734 |
rs772808224 | snp | C/G | 3.29815e-05 | 0.00406075 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860765 | TGCCATTCTCAGCAT[C/G]TGTTAGGTTGTCCCT | 4734 |
rs772810502 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979339 | GAAAGTTTTTACCTC[-/T]TTTTTTTTTTTTTTT | 4734 |
rs772817232 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945873 | ACATTCTTAAAGAAA[A/G]TAATTTTGAATGCAG | 4734 |
rs772844670 | snp | A/G | 1.65214e-05 | 0.0028741 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856161 | TTGTTCCTCAAAAGT[A/G]TAGGCTTGTAAGCTG | 4734 |
rs772845093 | in-del | -/C | 1.65315e-05 | 0.00287498 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916141 | AGGATCTGTACTTGT[-/C]ACTTCTTGAAAAAAT | 4734 |
rs772870156 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960365 | TAAAGCAGGCAGAAC[A/G]TGGAAGGACTTGACT | 4734 |
rs772886831 | in-del | -/AG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857012 | ACAATGGAATATGCC[-/AG]AGTTTAATGACTGTT | 4734 |
rs772893795 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876084 | AAAACAATGGAAGCC[A/G]GAAGACAACTGAATG | 4734 |
rs772903842 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867880 | GGCCAACATAGTAAA[A/C]CTCTGTCTCTACTAA | 4734 |
rs772915790 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911295 | ACAGGATAGCCCCCA[C/T]TACAAAAGTGTCCAG | 4734 |
rs772935075 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55987686 | AGTTTCAGCTTTCTA[C/T]ATATGGCTAGCCAGT | 4734 |
rs772950066 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945022 | GTCACGAACGTCAAA[C/G]ATGAAAGGTAGATAA | 4734 |
rs772962284 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909145 | CCAACAGACATCCTC[A/G]GGCCTAACTAGAAAT | 4734 |
rs772971947 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896861 | TTTATAGTTTTAACA[C/T]AATTTATCTATTTAA | 4734 |
rs772986257 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956449 | ATTTTAGCTCATACT[A/G]ATTTTCTGTATGATG | 4734 |
rs772993001 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973835 | AAAGTAGAAAAACTT[-/C]AAAAAAAAAAACAAC | 4734 |
rs773010759 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965333 | CAGTCACCCATGTAG[A/C]CAGGAGTACAGGCAT | 4734 |
rs773037105 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955308 | GATTATAGGTTATAG[C/G]CATCAGCCACCATAC | 4734 |
rs773049730 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830214 | CACCACATCTTCCAA[A/C]TGTCTGAGTTCTCTG | 4734 |
rs773055195 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942117 | TGGTAAAATCAACTA[C/T]TGTGGATTTGTTTAT | 4734 |
rs773070050 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949811 | TGTCATGGGGTGGGG[A/G]AAGTGGGGAGGGATA | 4734 |
rs773090541 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954329 | CCAGTTAAATACTGA[C/T]ATTCCCTAAGTATTG | 4734 |
rs773091428 | snp | A/G | 3.30126e-05 | 0.00406266 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915605 | CTTAATATACTCTGA[A/G]TCAGAATTAAGCTTA | 4734 |
rs773102704 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829349 | TCCCAAAAATCTAGG[C/T]AGTAAGGTGCATAAG | 4734 |
rs773116025 | snp | G/T | 1.71752e-05 | 0.00293041 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848608 | TTTCAATTATTTTAG[G/T]AGAGGGGCGTAGATG | 4734 |
rs773130308 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908768 | GCCTGTGAGTCGGAC[A/C]CAGCAGTGCACCTGT | 4734 |
rs773133450 | snp | A/C/G | 0.000109755 | 0.00740714 | missense, synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838124 | AATATATTCCTTTTT[A/C/G]TTCTTATTGGTGACA | 4734 |
rs773138943 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923819 | GAATGTAGTTTAACA[C/T]TAAAAACAGACTTTT | 4734 |
rs773154358 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859627 | GCCTGAAGCTGGAGA[C/T]GGAGTTTGCAGTAAG | 4734 |
rs773154676 | in-del | -/T | 3.37382e-05 | 0.00410706 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838196 | TAAAATTAAACACAA[-/T]TAACTTGATATGTTA | 4734 |
rs773167275 | snp | A/G | 4.94507e-05 | 0.00497221 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860500 | TGGAACATCCAAGTT[A/G]CTTGACGGTGGAGGT | 4734 |
rs773175432 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887719 | TCTGACAAGCATTGA[C/T]ACAAAAATCCTCAAC | 4734 |
rs773186343 | snp | A/G | 9.03922e-05 | 0.0067222 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847086 | GGTTGTTTTTATTCT[A/G]GAACAATTTTTATTT | 4734 |
rs773188785 | in-del | -/TTTCTGGTTTTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899959 | TTAGTAAAACAGTAC[-/TTTCTGGTTTTA]AGATCTTAGTTTTAG | 4734 |
rs773233305 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873251 | ATTATTCTCAGAGAT[C/T]CTGCTGTTATCTGGA | 4734 |
rs773268794 | snp | C/T | 4.94271e-05 | 0.00497102 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916688 | GGGAGTCAGCTTCAT[C/T]TGAACAACGTTAGAC | 4734 |
rs773290603 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871446 | ATAAAGACGCTAGAA[A/G]GCATGTGACAAATTG | 4734 |
rs773307919 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910482 | GTGTGGTTCCTCCTT[-/A]AGTCTCTTCTTTATC | 4734 |
rs773321836 | in-del | -/TCTATAAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963537 | ATTCTACCAAATAGG[-/TCTATAAC]TTATACCTGCTCCAT | 4734 |
rs773417584 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884208 | CTGTAAGTTCAAGAG[-/C]CCACAGCATTACTGG | 4734 |
rs773418683 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953150 | GCACACCACCACGCC[C/T]GGCTAATTTTTGTAT | 4734 |
rs773473742 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55963670 | TATTTTAAAAAGGTA[G/T]GATGAGAAAAGCAAA | 4734 |
rs773492455 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941071 | CTTTTAAAAAGTATC[C/T]GTAGGTTCCCTCCTC | 4734 |
rs773495358 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55846649 | CAGAAGATAATTTCC[G/T]GACCCACTCTTGCTC | 4734 |
rs773518743 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876453 | TTAAAATATATGTAG[A/C]TGTAATAAAAATGAC | 4734 |
rs773521634 | snp | A/T | 3.29544e-05 | 0.00405908 | splice-donor-variant | NEDD4 | GRCh38.p7 | 15:55848804 | CATTTCTATACACTT[A/T]CAGGTAAAGGCCCTA | 4734 |
rs773535194 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838209 | CAATAACTTGATATG[A/T]TATTTTAGCGAGAAA | 4734 |
rs773536264 | snp | C/G | 1.64844e-05 | 0.00287087 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916386 | AAGTTACTAAGGCTA[C/G]CACTACAAATGGCTG | 4734 |
rs773536658 | snp | A/G | 8.04408e-05 | 0.00634145 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55873994 | ATCCACTTGACCTAG[A/G]AAATCATCTCTTGTC | 4734 |
rs773546321 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886233 | AAAGAGAGAGACAGA[A/C]CCCAATACAATTATA | 4734 |
rs773552466 | snp | C/T | 8.27123e-05 | 0.00643034 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915886 | TTGAAAGAAATCCTT[C/T]AGCACTAGTGCCATC | 4734 |
rs773568856 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832770 | GAATTTGAAGTTAAA[A/G]AACGGAAAGTGACTC | 4734 |
rs773573925 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879747 | GAGGACAAGAAATAT[C/T]TCTTAGAAATAAAAA | 4734 |
rs773579050 | snp | A/G | 3.29511e-05 | 0.00405887 | stop-gained, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842058 | ACTCAATCCACAGTC[A/G]AGCCTTCAGGAAGTC | 4734 |
rs773588134 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851477 | TATTTTACATTTTCT[C/T]TTCTGTTTTTTTTTT | 4734 |
rs773588338 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836824 | TGAGCCACCGCGCCC[A/G]AATTTTTAATTTTTT | 4734 |
rs773593500 | snp | A/C | 1.64974e-05 | 0.00287201 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916286 | ACTGATGACACTGTT[A/C]GTATATGAACCTCCA | 4734 |
rs773652373 | snp | A/G | 1.70301e-05 | 0.00291801 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993551 | TCCACCGCGCAAGTT[A/G]CCATTTCCGAACGCT | 4734 |
rs773661694 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881726 | TGAACATCTGTATGT[C/T]TGATGATTTGTGACC | 4734 |
rs773697003 | snp | A/G | 1.72779e-05 | 0.00293916 | intron-variant | NEDD4 | GRCh38.p7 | 15:55863082 | CAACCCAGCCAGGCT[A/G]AAAAACAGGATGGCA | 4734 |
rs773714743 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880338 | ATTAGGCAAAGTGCA[A/T]GAAAGGGGAAAAAGA | 4734 |
rs773716753 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895112 | AGGAAATACTCACAG[C/G]TAGGTAACTGCTAAA | 4734 |
rs773718755 | snp | A/T | 2.04857e-05 | 0.00320038 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850757 | CCTAGCACATTAATG[A/T]AATCATATTGTAATA | 4734 |
rs773761455 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858111 | ACACACTGTTCTGTA[A/C]CTTGCTGTTTTTCAT | 4734 |
rs773768809 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844414 | AGACCCCTGGAATAG[C/G]TGAGTGAGAGAAGAC | 4734 |
rs773782038 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851922 | ACTTGTTTTATATAA[C/T]AACAAGTGGTAATTC | 4734 |
rs773783208 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894107 | CATAAAGCAAGCATT[-/C]CCATGTCTTAAGTTT | 4734 |
rs773791473 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992755 | TAATCAGCATTAGTT[A/C]TTTAGCTGAAAAGAA | 4734 |
rs773799857 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830616 | TTATTTGGTTTCATT[C/T]ACTCTCTACAAGGAT | 4734 |
rs773807279 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916396 | GGCTACCACTACAAA[C/T]GGCTGGACTGCTTAC | 4734 |
rs773811252 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931716 | ATTCTGCCAGTGGTT[G/T]TGGGAACAAACAATA | 4734 |
rs773812177 | snp | C/T | 1.67396e-05 | 0.00289301 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834219 | CAACATAAAATGTTA[C/T]GTCTTACCTCTAGTT | 4734 |
rs773897474 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844261 | GGGCCAGAGGGTGGA[A/C]AGTGTGAATGCAGTT | 4734 |
rs773906689 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830384 | GTTGGGTGTCACCAA[C/T]TCCTTCTTACCCATA | 4734 |
rs773906995 | in-del | -/CGCCCC | 1.71443e-05 | 0.00292777 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993586 | CAAACCGGACGCGCT[-/CGCCCC]CGCCCCCGCCCAGGG | 4734 |
rs773913090 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894297 | CAGCACAAGTATTTA[A/C]ATAGTGTTTACACTG | 4734 |
rs773924638 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55928634 | GCAACACCTTCTCCA[C/T]TCTACATGTCTACAC | 4734 |
rs773928074 | snp | A/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852462 | TAGTCGTTCTGGAAT[A/T]GTGATCTACATAATA | 4734 |
rs773928258 | snp | A/T | 1.66582e-05 | 0.00288597 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862909 | GAAAGCCATCAGCAC[A/T]TACTGAGGGGTTGGT | 4734 |
rs773946670 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916653 | TTTTCCTTTATTAAC[A/G]GAGCTAGTGCAGTCT | 4734 |
rs773964525 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828173 | TGGAAAGTAGAAAGT[A/G]GTTTTGCTACTGTCA | 4734 |
rs773979838 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55865299 | GAAAATGGGCACCCA[A/T]TTGGAAAAAACTTCA | 4734 |
rs773982650 | snp | C/T | 1.70304e-05 | 0.00291803 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993558 | CGCAAGTTGCCATTT[C/T]CGAACGCTTCCAGCA | 4734 |
rs774019309 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55969734 | CTGACTAAAGAGCTC[C/T]TGGGCCTTGAATAAA | 4734 |
rs774049666 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959198 | TTTAGCTGCATTCCA[C/G]AATTGTGATATTGCT | 4734 |
rs774055676 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944082 | ATTGACGCAGAAGAC[A/G]GGTGATTTCTACATT | 4734 |
rs774110123 | snp | A/G | 3.32049e-05 | 0.00407448 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916780 | AGGTTTCTGACAAAG[A/G]GTAAGTATTGCTTCT | 4734 |
rs774110266 | snp | C/T | 1.65444e-05 | 0.00287609 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915730 | ATCCTTCAGATGACT[C/T]TTCACAGACAGTCTG | 4734 |
rs774143569 | snp | C/T | 1.66183e-05 | 0.00288251 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842148 | GTTTCATTTCAAATT[C/T]GTTTGGAATGTCATT | 4734 |
rs774168189 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841851 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 4734 |
rs774174005 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831592 | GGCAAAGAATGACTG[A/C]ATTGGTTACTGGCAA | 4734 |
rs774194036 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965241 | TCTCACTTTGTCACC[C/T]AGGCTGGAGTGCATT | 4734 |
rs774197694 | snp | A/T | 3.36644e-05 | 0.00410257 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838484 | ACAATTTATGTGCCA[A/T]TTTAACTGATCAAAA | 4734 |
rs774200630 | snp | A/C | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842089 | TGCTCTCTTGACACC[A/C]ATAATTCTCCGGTAA | 4734 |
rs774201273 | snp | C/G | 1.64768e-05 | 0.00287021 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848327 | GCTCTTGAAGAGACA[C/G]GTGAGCGGACAGTCC | 4734 |
rs774219600 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962387 | TAATTATTGATATGA[C/T]TGGATTTAGTCTACA | 4734 |
rs774221893 | snp | A/T | 3.29995e-05 | 0.00406185 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860776 | GCATCTGTTAGGTTG[A/T]CCCTATATTGGAAGT | 4734 |
rs774221904 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914356 | GTAAAACATTCCAAA[-/T]ACAGAAATTTAAAAA | 4734 |
rs774224689 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903286 | ATTCTCCCAGTGCCC[G/T]ATGAGAGTCCTTTTG | 4734 |
rs774227720 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55993085 | CGTAAAGTTAAGTCG[A/G]CCCGGCCTCCGCCAG | 4734 |
rs774233300 | snp | C/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936766 | AGCATGTAAAGTGTA[C/G]ATTTTAATTATAATT | 4734 |
rs774238615 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836790 | ACCTCGGACTCCCAA[A/C]GTGCTGGGATCACAG | 4734 |
rs774241908 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908337 | CTAGTGAATTTACAT[G/T]TGCCTACCTATTGCC | 4734 |
rs774243254 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964260 | CCATGTTAGACTTTT[A/G]TATATTAGCTAACAA | 4734 |
rs774259565 | snp | C/T | 3.53176e-05 | 0.00420209 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829962 | TATCCCATAATTCTT[C/T]AAATGATTCATAAGG | 4734 |
rs774259650 | in-del | -/C | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954432 | TATTAAATATAAATA[-/C]AAAATGTAAATGTAA | 4734 |
rs774278333 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944196 | GGCATTGCCTCACCT[C/T]GGAAGTGCAAGGGGT | 4734 |
rs774297333 | snp | G/T | 1.66128e-05 | 0.00288204 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860396 | CGTAACAAAATCTAA[G/T]AGCATCTTACTGAGC | 4734 |
rs774303393 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888794 | ACCCAGAAACAAATC[C/T]ATACATCTACAGTGA | 4734 |
rs774323015 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853229 | AATATCTTAAAATGT[A/G]CAAGATAAAGTGTAC | 4734 |
rs774325685 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934860 | TATACAATGTTCTGC[-/T]TTTTTTTTTTTTTTT | 4734 |
rs774333668 | snp | C/T | 2.03689e-05 | 0.00319124 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838648 | TTTGTATCTATAACA[C/T]ACCTGAAATTGCAAA | 4734 |
rs774337431 | snp | C/T | 3.31785e-05 | 0.00407286 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915789 | TTCTTCTGTAACGAG[C/T]CCTTCCTGTGAAGCG | 4734 |
rs774348989 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961760 | AGATGTGAGCCACCG[C/T]GCCTGGCCAGTTTGT | 4734 |
rs774417212 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884841 | CAAATCGAAGAGGTA[C/T]TGTCTTTAAAGAAGT | 4734 |
rs774423759 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941567 | ACCCTGTTAAATTTC[-/T]TTTTTTTTTTTTTTT | 4734 |
rs774445458 | in-del | -/TGT | 1.65233e-05 | 0.00287426 | cds-indel, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852425 | AGATTACAGGATACC[-/TGT]ACAGTGGGCTTTGTC | 4734 |
rs774463137 | in-del | -/GAG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830427 | CACCGACATAACACA[-/GAG]GAGACTAGCCCTGCT | 4734 |
rs774465410 | in-del | -/AAAG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55886099 | ACTATAAAAAAAGAC[-/AAAG]AAGGTCATTATATAA | 4734 |
rs774497829 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888003 | ACATAACAAAAGTCA[C/T]ACATGACAGACCCAT | 4734 |
rs774525206 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990147 | ACTAATTCTACATTA[C/T]GGTGAGCTGTATAAT | 4734 |
rs774542665 | snp | A/G | 1.65012e-05 | 0.00287234 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915969 | TAGGATCCTTTGCTC[A/G]GAAGAGTACACAGAC | 4734 |
rs774544678 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921009 | AGTAGATATACTAAA[C/T]GGTATATCTTAGCTA | 4734 |
rs774601282 | snp | C/T | 1.66438e-05 | 0.00288472 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915352 | AATTATCCACTTTAC[C/T]TTCATTTCCAGATGC | 4734 |
rs774604266 | in-del | -/AATT | 1.69928e-05 | 0.00291481 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838471 | AAACATTTGTCTCAC[-/AATT]TATGTGCCATTTTAA | 4734 |
rs774608938 | in-del | -/ATTTCCTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835388 | TGTCTGCCTCTGTTA[-/ATTTCCTT]ATTTCCTTTGCAGTC | 4734 |
rs774633402 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835542 | GGCCATCCGCTTTCA[C/T]AGCCCTTTCACATTT | 4734 |
rs774656454 | in-del | -/TGAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858625 | TGTAGTTTAGGTCTT[-/TGAC]TGACCTGTCCCACTC | 4734 |
rs774667888 | snp | C/G | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860511 | AGTTACTTGACGGTG[C/G]AGGTGATGGGAAGGC | 4734 |
rs774674685 | snp | A/T | 1.65996e-05 | 0.00288089 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840699 | TACACAATCCAGAGT[A/T]TGGATTTATCTGTAG | 4734 |
rs774687847 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971981 | CATGATTTATTTGAA[C/G]TGCTGAAGGAAAAAA | 4734 |
rs774714288 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849249 | TTTTTTCTGAGGTGG[A/C]GTGTCGCTCTTGTCG | 4734 |
rs774737408 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55938489 | AGACACAAACAAGAC[C/T]CGACACTGTAAAACC | 4734 |
rs774763616 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847568 | AAGGATAATTTTCCT[A/C]TCAATCTGACTCAAG | 4734 |
rs774779717 | snp | C/T | 4.94964e-05 | 0.00497451 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916047 | ACTAAGGAGGAGTAA[C/T]GTTTTAGTGGAATTT | 4734 |
rs774801098 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916483 | TACCATCCTTCAAGA[C/T]ACAAGTAAACGAAGC | 4734 |
rs774815261 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991710 | GAAACTTCCTAGAAG[C/T]ACAAATCCTTCAGCA | 4734 |
rs774844482 | in-del | -/ATATATAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852699 | TCTAGAAATATATAT[-/ATATATAT]ATATATATATATATA | 4734 |
rs774863320 | snp | A/C/G/T | 6.59113e-05 | 0.00574038 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848825 | AAAGGCCCTAGATCA[A/C/G/T]TGGAAGTATCAAGTG | 4734 |
rs774868751 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951934 | TTCAATGATTCTGAC[A/G]CTGGTTTTGTAAGAC | 4734 |
rs774898763 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860605 | TAAGCTTGAGCCACA[C/T]ATACTTTATTGCTAT | 4734 |
rs774922061 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962659 | ATGTTGCCCAGGCTA[C/G]TCTCGAACTCCTGAC | 4734 |
rs774933057 | snp | C/T | 2.57895e-05 | 0.00359083 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55924680 | ACTTCAAAAAGAAGC[C/T]GGTGCTGCTGAGGAT | 4734 |
rs774940657 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55952204 | CCAGGCGTGGTGGCA[A/G]GCACTTTTAGTCACA | 4734 |
rs774941927 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880034 | GTGTCTCATGCCTGT[A/G]ATCAATCCCAGCACT | 4734 |
rs774949048 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55926432 | TGGAGTAACTGAGGA[C/T]AGACATGCCAAACAT | 4734 |
rs774965844 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988475 | AACTTAGAGTATAAT[-/A]AAAAAAAAAATTAAA | 4734 |
rs775013997 | snp | A/G | 3.33823e-05 | 0.00408534 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842156 | TCAAATTTGTTTGGA[A/G]TGTCATTCTGAAAAT | 4734 |
rs775017557 | in-del | -/ATTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985143 | TGCTCACCCTAAATG[-/ATTT]ATTTACAAGGTCTCT | 4734 |
rs775029344 | snp | C/G | 1.68202e-05 | 0.00289996 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55837822 | TTGCTTCTGGATTCG[C/G]TTTACAAATCGCCAT | 4734 |
rs775055909 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981718 | GTATGAACATCACAT[A/G]GAAATTTGTTACATA | 4734 |
rs775067047 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852472 | GGAATTGTGATCTAC[A/G]TAATATGATCTTCCT | 4734 |
rs775085836 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838387 | TCTTGCTCAGAGACA[A/G]CTTTTGTTACTGGGA | 4734 |
rs775097388 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927857 | GAGTAGGGAGGGAGA[C/G]AGGGCTATAGAAACC | 4734 |
rs775108095 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890669 | TTTTGTACGAACATA[C/T]GTTTTCATTTCTCTT | 4734 |
rs775120312 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831455 | AAGAGAGGCCAGAGA[C/T]GGAAAGGGGCATTTG | 4734 |
rs775132802 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929080 | CAGTTACCTAGCAGA[C/G]AGATGAAGCAGGGAT | 4734 |
rs775140652 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55831762 | AGCTTCTATTTGCAC[-/A]AAAAAATTCAGCTTA | 4734 |
rs775162262 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967035 | GAGATTACAGGCATG[C/T]GCCACCATGCCCAGA | 4734 |
rs775167733 | snp | C/T | 3.62549e-05 | 0.00425748 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924618 | TGTACCCTTACTTCA[C/T]ATTTCATATAAGCAC | 4734 |
rs775238194 | snp | C/T | 9.91359e-05 | 0.00703975 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55862929 | GAGGGGTTGGTCTTT[C/T]CCACTGTGTTCTTCT | 4734 |
rs775239449 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864670 | CTGGACAACAAGAGT[A/G]AAACTCTGTCTCATA | 4734 |
rs775243054 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943994 | AGTCAAAGGAGATTA[C/T]TTTGGAGCTTTAAGA | 4734 |
rs775250097 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843427 | GCTACATTGCCTCAC[C/T]AATCTTTTGTACGTT | 4734 |
rs775258810 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922180 | TAACACTAATATCTA[C/T]TAAGGAGGTTAAATA | 4734 |
rs775266689 | snp | A/G | 1.69146e-05 | 0.0029081 | stop-gained, intron-variant | NEDD4 | GRCh38.p7 | 15:55837833 | TTCGGTTTACAAATC[A/G]CCATTGTATTACAAG | 4734 |
rs775267675 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847888 | TTTCACCACGTTGGC[C/T]GGGCCGGTCTCGAAC | 4734 |
rs775281778 | snp | A/G | 3.31824e-05 | 0.00407309 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915804 | CCCTTCCTGTGAAGC[A/G]GCCGTATGTCTCTTA | 4734 |
rs775297163 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957560 | GACTGTCTTCTCAGT[A/G]TGGCGATTCCTCAAG | 4734 |
rs775303594 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842635 | CTCCCGCCTTGGCCT[C/G]CCAAAGTGCTGAGAT | 4734 |
rs775303836 | in-del | -/CA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903784 | GAGCCGAGATCGTGC[-/CA]CTGCACTCCAGCCTG | 4734 |
rs775307079 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964223 | TTTCTGTGTTAGACT[-/G]TAAGATATTATATAA | 4734 |
rs775321774 | snp | A/G | 2.68143e-05 | 0.00366148 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834328 | TGATGGGCAGGGCCA[A/G]TGGCCTTTCCTATGC | 4734 |
rs775355297 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55905936 | TGGTGTTTTAGACAT[A/G]AAGTCCTTGCCCATG | 4734 |
rs775374627 | snp | G/T | 1.65056e-05 | 0.00287272 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833072 | AAACTGAAGTAATCT[G/T]ATTCTTTTTTCTGAA | 4734 |
rs775379141 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887895 | TATAAACAGAATGAT[A/C]ATTTCAATTGATGCT | 4734 |
rs775383547 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985517 | GCAGAGGAGATGTCT[A/G]CGTGGTCAGGAAGTT | 4734 |
rs775386921 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882980 | CTCAGCTGTGTTGGC[C/T]ATAGAGACTCCTGCG | 4734 |
rs775394568 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931488 | ATAGAGTTTATAAGA[C/T]GATATTTTAAGGAAA | 4734 |
rs775432088 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902156 | AAGGCCTCAATTATA[C/T]TGGTAACCCATGCAT | 4734 |
rs775452036 | snp | A/T | 3.30224e-05 | 0.00406326 | stop-gained, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916087 | TGCTCACTGGCAATT[A/T]CATAATCTCTAATCC | 4734 |
rs775453275 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864550 | GCCAGGTGTGGTGGC[A/G]CATGCCTGTAAATCC | 4734 |
rs775470675 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942029 | ACAGGTTAACATGAT[A/T]GGTAGTGTTGTTCAA | 4734 |
rs775486776 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55854101 | GGTTGCAGTGAGCCG[A/C]GATCGCCTGGGCACT | 4734 |
rs775488130 | snp | A/G/T | 1.648e-05 | 0.0028705 | missense, synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834095 | ATTTTTATACTTTGT[A/G/T]TGTTCCCTCCAGTCA | 4734 |
rs775496654 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966193 | AGTTTATGGTTGTTA[-/T]CTGCTAAAGGATTAG | 4734 |
rs775497253 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971195 | AATGGCAGAATTGAT[A/C]ACGCAGAAGAAAGAA | 4734 |
rs775506736 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942898 | TGTGACCAAAATGCT[C/G]ATAGTGATATGAACA | 4734 |
rs775523665 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955167 | GCGGGGACTACAGGC[A/G]CACACCACCATGCCT | 4734 |
rs775549551 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985165 | TACAAGGTCTCTTCC[A/G]GCTCAAAGATTCTAC | 4734 |
rs775551629 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896564 | ACTTCCCTTTGTATC[G/T]GTTTTTAATATCTGT | 4734 |
rs775562536 | snp | C/T | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860532 | ATGGGAAGGCCTGGT[C/T]GCTATACATGGTGGC | 4734 |
rs775624522 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900367 | AAGAGCTAAGTCAGT[A/G]AAATTTGGGTTATAA | 4734 |
rs775650315 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990621 | CCTCATTTCCACTCT[A/G]CAAATCTCAAGTAAG | 4734 |
rs775673727 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908881 | CTCATCATAAAAAAA[-/C]AATTGAGATAAAAAG | 4734 |
rs775677768 | snp | C/T | 0.000274361 | 0.0117092 | missense, utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55872431 | TTCTTGGATGAAGAA[C/T]AAAATCCTTAAATGT | 4734 |
rs775733834 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941552 | TGTGATCAGAGAACA[C/T]ACCCTGTTAAATTTC | 4734 |
rs775734127 | snp | A/C | 1.64953e-05 | 0.00287182 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860609 | CTTGAGCCACACATA[A/C]TTTATTGCTATAGCA | 4734 |
rs775744362 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955759 | TGGCACATCTTACAC[A/C]TGTGCATGGACACCC | 4734 |
rs775749408 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55911175 | GCCCCTAGGGGACAT[C/T]TGGCAATGTCTGGGG | 4734 |
rs775753079 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929958 | TGAATTAAAATAGAA[A/G]TGCTTTAAGAAAAAT | 4734 |
rs775759471 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944090 | AGAAGACGGGTGATT[G/T]CTACATTTCCACCTG | 4734 |
rs775774877 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55845771 | CCAGGGAAATTTCGA[C/T]ACAAAGTTATTCTTT | 4734 |
rs775775742 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983244 | AAGCATATGAGGAAC[A/T]AATATTAACTATGAA | 4734 |
rs775788808 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55954253 | ACATCTCTTCTAGTG[C/T]TCCTCATACCACTCG | 4734 |
rs775790821 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55896551 | CCTCTGTAATTCTAC[C/T]TCCCTTTGTATCTGT | 4734 |
rs775811555 | snp | C/T | 3.33545e-05 | 0.00408364 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834021 | AGTAAGTTATGAAAA[C/T]AGAAGTTTCAAATTA | 4734 |
rs775815623 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829102 | TTCTAACTACACTAA[A/C]ATATGAAAAAGTGAT | 4734 |
rs775816969 | in-del | -/GCTTGTAA | 1.65231e-05 | 0.00287424 | frameshift-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856165 | TCCTCAAAAGTATAG[-/GCTTGTAA]GCTGCCTCTTCTGCT | 4734 |
rs775832765 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55982357 | TCATAATAGCCCAAA[G/T]TTGGAAACAATCAAT | 4734 |
rs775833361 | in-del | -/A | 1.65141e-05 | 0.00287346 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840523 | ATGAAAAAACCTTGC[-/A]AAAAACCAAATACAT | 4734 |
rs775886401 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950662 | GGTTAACGAGCGTCC[C/T]GGAGAAGCAGAAATG | 4734 |
rs775887225 | snp | A/G | 0.000230764 | 0.0107391 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860664 | AACTACTTATACCTC[A/G]GAAGACTCTCGGTTG | 4734 |
rs775903539 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890253 | GTGTACAATTCAATG[A/T]TTTTTAGTATTTTCA | 4734 |
rs775903991 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868258 | TTCACTGTTCTTATG[C/G]AGACCTAAGCAGGCC | 4734 |
rs775908801 | snp | A/G | 8.11326e-05 | 0.00636865 | missense, intron-variant, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55873960 | CACCTATACCAACCG[A/G]TAATGGATAAAGTGG | 4734 |
rs775909553 | snp | C/T | 8.65988e-05 | 0.00657966 | splice-donor-variant | NEDD4 | GRCh38.p7 | 15:55951510 | TATTGCTAAGTCTAA[C/T]CTTTTTAATGGTTTT | 4734 |
rs775916619 | snp | G/T | 1.65288e-05 | 0.00287474 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856170 | AAAAGTATAGGCTTG[G/T]AAGCTGCCTCTTCTG | 4734 |
rs775928815 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55856055 | AAGGCAAACGTTCAC[A/G]CTCAATCTTCCAAAA | 4734 |
rs775933925 | snp | C/G | 1.64912e-05 | 0.00287147 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915557 | ATCTACATTTTGGGA[C/G]GATGGCAAACATGCA | 4734 |
rs775949854 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872884 | AGACTGGATTAAATA[C/T]ATTACTGAAAGCTTA | 4734 |
rs775968460 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850601 | CATTTGGTGCATGCC[A/G]GACTTCCCAGCCTTT | 4734 |
rs775972670 | snp | A/C | 1.67416e-05 | 0.00289318 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840734 | TAATTGTCCCTGTAA[A/C]GACAACCCCATTTAA | 4734 |
rs775997366 | snp | C/T | 1.64996e-05 | 0.0028722 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915986 | AAGAGTACACAGACT[C/T]GTTGGAGAAGTCGGT | 4734 |
rs776001253 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835067 | TACCTACCTTTAAAA[C/T]AAAGCAAAACAAACA | 4734 |
rs776028059 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961512 | GTCTCACTCTGTCAC[C/T]CAGGCTGGAGTGCAG | 4734 |
rs776029426 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920966 | CAAGAAAAGCTGTAT[C/T]TCCCACTCATAGAAG | 4734 |
rs776035801 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844826 | TTTTTTTTTTTTTTT[-/G]AGACAGAGTACTGCT | 4734 |
rs776058373 | snp | C/T | 3.45447e-05 | 0.00415586 | intron-variant | NEDD4 | GRCh38.p7 | 15:55847069 | AAAAATAAAGAAGTT[C/T]AGGTTGTTTTTATTC | 4734 |
rs776062136 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829495 | TTTTCACACATGACA[C/T]GTATCACAAATATTT | 4734 |
rs776068432 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55891287 | CCAAACTAAAAGTCA[A/G]TATGCATAGTCTCAG | 4734 |
rs776094701 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55873700 | TATTTTCAAACTAAT[-/C]CTTTTTTACACAATG | 4734 |
rs776105715 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55884614 | ATTAAAATAATTAAA[A/G]AGAATCAAGCAGAAA | 4734 |
rs776144870 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842568 | TTTTTTAAGTTTTTG[A/G]GGTCTTGCCATCTTG | 4734 |
rs776151175 | snp | A/T | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860480 | AATTCTTCTGCAAGA[A/T]GAGTTGGAACATCCA | 4734 |
rs776154638 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876863 | TTTTTTTTTCACTTT[C/T]TTTTTCTTTTTTCTT | 4734 |
rs776175668 | snp | A/T | 1.67055e-05 | 0.00289006 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838103 | ATACTAATAAAATAC[A/T]TACTAAATATATTCC | 4734 |
rs776230389 | snp | C/G | 3.2956e-05 | 0.00405918 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916583 | CTGTAGACAGCTGCT[C/G]TTTTTATTAACATTT | 4734 |
rs776247859 | snp | C/T | 0.000175065 | 0.00935424 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869599 | ATTCCTCAGCCTGTT[C/T]TGCATTATCATCTTC | 4734 |
rs776268092 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885142 | TTGGAGATAGTGGCA[G/T]GACATTTTAGAAGTG | 4734 |
rs776298176 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950519 | TGGTGTTTCAGGAAT[G/T]ATCTGCCATGTCAAA | 4734 |
rs776325812 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925122 | CCATTTTCTAATTCC[C/G]ATTATTTGGAATGCA | 4734 |
rs776340217 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977409 | AGGTTTGTGTAACTA[C/T]ACTCTATGACATTTG | 4734 |
rs776366501 | snp | C/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852492 | ATGATCTTCCTCTTT[C/G]ATCTTGTTTTTCTTC | 4734 |
rs776372275 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913671 | GTTAGCTTACCTAAG[C/T]ATAAATAAAACCAGT | 4734 |
rs776394404 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976498 | ACTGATCATCAGGGA[A/G]GTGCAAATCAAAACT | 4734 |
rs776398887 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893816 | CATACTAGATATAGA[C/T]AGAAAAAAGGCTCAC | 4734 |
rs776448624 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942841 | AGAAGAAGAAAGGAG[C/G]ATGATGGAAAGATAG | 4734 |
rs776455197 | in-del | -/CT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889017 | AGAAAACTGAAGAAA[-/CT]CTGCAGACATTGGAG | 4734 |
rs776469476 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839594 | GCACAGGAAACAACA[C/T]GGCTACAGTCCGGGG | 4734 |
rs776469632 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55878140 | ATTCAAATATACAGA[C/T]AAATTGAAGATAAAG | 4734 |
rs776488991 | snp | C/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994377 | ACCAGAAGGCAGTGA[C/T]GAAGAGGGAAAAATA | 4734 |
rs776504584 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849525 | CCCTGGACCACATGA[C/T]ATTTCTAAGCCCCAG | 4734 |
rs776505282 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55859195 | AATCTTTGTCTTCTA[C/T]TCAATCTCCCTTGAT | 4734 |
rs776542025 | snp | A/T | 1.6537e-05 | 0.00287545 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846961 | TATTTATTATAAACA[A/T]GACTAACCTGCTTCT | 4734 |
rs776543494 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864449 | CACTTTGGGAGGCCG[A/C]GGCGGGCAGATCACT | 4734 |
rs776548728 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895287 | TTCGAAGAGGTGGAC[A/G]CTAACATTCTCTGGA | 4734 |
rs776557407 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984043 | TTCTATATCATTATA[C/G]CTCATGCCCTGACCC | 4734 |
rs776591678 | snp | A/T | 8.00737e-05 | 0.00632696 | missense, intron-variant, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55873969 | CAACCGGTAATGGAT[A/T]AAGTGGAACATCCAC | 4734 |
rs776597642 | snp | A/G | 1.71246e-05 | 0.00292609 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852581 | AATTAAATACATCAA[A/G]TTTAAGAATCCTTCT | 4734 |
rs776610923 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55838339 | TTACTAAAATAAATA[C/T]GGAACGAGTCAAATG | 4734 |
rs776621928 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844545 | TCTGGTCCTGTGTTA[C/T]TGACTCCACCATTCA | 4734 |
rs776623739 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834192 | AAAATAATGGGTTCA[C/T]AATTTCTGTTTCAAC | 4734 |
rs776641007 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880020 | GCTGGCTGGGCATGG[G/T]GTCTCATGCCTGTAA | 4734 |
rs776643125 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980947 | CATAATATAGTGATT[A/C]AGATGTGAATAATAC | 4734 |
rs776650019 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913089 | CATATAAGAAAAGAA[A/G]TTGTAGACTCTCAGT | 4734 |
rs776679600 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965150 | CTAAACATAATAAGA[C/T]TATCATGCAACTAAT | 4734 |
rs776768906 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923283 | GCAAAAACACAGACA[A/G]AAAACAAATAGCTCT | 4734 |
rs776819207 | in-del | -/CTTG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974922 | TTTTTGAGATGGAGT[-/CTTG]CTTGCTGTCACCCAG | 4734 |
rs776828894 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919409 | AGGGTTTCAGCCAAG[C/G]AAATGTAAGGTAAGA | 4734 |
rs776844594 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961065 | CTCCTAGAGAGTGGC[-/T]TATCTGCTATTTTGG | 4734 |
rs776854835 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909228 | AATCGAGCTACAAGG[C/T]GCACATACACACTAG | 4734 |
rs776868307 | in-del | -/TTC | 3.3151e-05 | 0.00407117 | cds-indel, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915774 | TTCGAAAGAACAATT[-/TTC]TTCTGTAACGAGCCC | 4734 |
rs776903598 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939732 | GAAACTGGAATCCCT[A/G]CACATGTTGGTAGCA | 4734 |
rs776906011 | snp | A/C | 1.66037e-05 | 0.00288125 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838499 | TTTTAACTGATCAAA[A/C]TTCACAAACCTGTCC | 4734 |
rs776941954 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953784 | GGAGTGCAATGGCAC[A/G]ATCTCGGCTCACTGC | 4734 |
rs776946998 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991901 | ATCATGTACCAAGAG[A/G]GAGAAAACAGATGGT | 4734 |
rs776954684 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953240 | GGTGATCCGCCCGCC[C/T]TGGCTCCCAAAGTGC | 4734 |
rs776959005 | snp | C/G/T | 3.29697e-05 | 0.00406005 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860484 | CTTCTGCAAGATGAG[C/G/T]TGGAACATCCAAGTT | 4734 |
rs776959817 | snp | A/G | 1.75019e-05 | 0.00295815 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993485 | CCCGAAGGGAAGCCC[A/G]CCCCGCAGCCCCGCG | 4734 |
rs776985290 | snp | A/G | 1.67506e-05 | 0.00289396 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848575 | TCTCTTCCCATCCTG[A/G]CTATAATTAAAAATG | 4734 |
rs776986816 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842018 | CTGGCAACTCCTCCA[C/T]AATCCAATCCCTTTT | 4734 |
rs776999094 | in-del | -/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994452 | ACTCCTCCTGTGGAA[-/T]AAGGTTATGGAATAA | 4734 |
rs777002049 | snp | A/C | 8.23662e-05 | 0.00641688 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850627 | CCTTTAGGAAGGAAT[A/C]CTTGCTCAATTTCAG | 4734 |
rs777010552 | snp | C/T | 8.79005e-05 | 0.00662892 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55966488 | CTAGCTCCCAATATA[C/T]CCTTCTTGGCAAGGC | 4734 |
rs777028762 | snp | A/G | 1.65255e-05 | 0.00287445 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916130 | ATCCTGGACAAAAGG[A/G]TCTGTACTTGTACTT | 4734 |
rs777034840 | in-del | -/AC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883696 | CACACACACACACAA[-/AC]ACACACACACACACA | 4734 |
rs777035185 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835029 | TTGGCTCACTCTGTA[C/T]GCATTTAAATGTGCT | 4734 |
rs777039303 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960433 | GATGCTTCCTGCCCT[A/C]GAACATCAGACTCCA | 4734 |
rs777040201 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848437 | TTTTTATATCTGAAG[A/G]GAAGAAAAAGAAAAA | 4734 |
rs777069155 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55988962 | TAAAATAGGACGGGC[A/G]CGGTGCCTCACGCCT | 4734 |
rs777072893 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830722 | TTTATATTTTAGAGA[C/T]GGGGTATCCCTCTGT | 4734 |
rs777073695 | snp | G/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918337 | ATGCCATAGACCAAG[G/T]TTGGTATTCTATTTG | 4734 |
rs777093221 | snp | A/C | 6.60807e-05 | 0.0057477 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848510 | ATAATGAAAAATCGC[A/C]CTGCACATACTGTGA | 4734 |
rs777106875 | snp | C/T | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834050 | TACCTTCCAAAACCA[C/T]TGTATAACCTGATGA | 4734 |
rs777115663 | snp | A/G | 6.63471e-05 | 0.00575927 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915786 | ATTTTCTTCTGTAAC[A/G]AGCCCTTCCTGTGAA | 4734 |
rs777132037 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55950155 | GTAAAAACAGAAATT[C/T]AGCTTCATTTTTCTT | 4734 |
rs777136746 | snp | A/G | 3.29679e-05 | 0.00405991 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860745 | TTGTGCTTGCAGTTG[A/G]ATGTTGCCATTCTCA | 4734 |
rs777141100 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929706 | AACAACAGATGATTT[C/T]TCTGTTTTATCACTG | 4734 |
rs777152638 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882712 | TGGTCAAGGGAGTGC[A/G]TGTGCCACCCCTACA | 4734 |
rs777164391 | snp | A/G | 1.65252e-05 | 0.00287443 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916767 | AAGTCATCTCCGGAG[A/G]TTTCTGACAAAGGGT | 4734 |
rs777215497 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55836026 | TTGCATTCTCTCACC[C/G]AGCATACTCAACTGC | 4734 |
rs777228138 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942429 | GAGGTGACCGGATCA[C/T]GGAGGCAGACTTCCC | 4734 |
rs777257673 | snp | C/T | 4.3692e-05 | 0.00467376 | missense, utr-variant-5-prime, intron-variant | NEDD4 | GRCh38.p7 | 15:55872448 | AAATCCTTAAATGTA[C/T]ATGGTCTCTCCAATC | 4734 |
rs777292965 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919290 | TGCTTTCTTTCAGGA[C/T]TTTTCTTGTTGTTGT | 4734 |
rs777333374 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55962292 | TGCATCACGTAGGAC[A/G]GTATATAGTTGGGTC | 4734 |
rs777340830 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55881875 | GTGGGGGCTGTCTTG[A/T]GCATTGAAGGATATT | 4734 |
rs777365036 | snp | G/T | 5.05233e-05 | 0.00502585 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834007 | TCAATCTATCAAAAA[G/T]TAAGTTATGAAAATA | 4734 |
rs777383044 | snp | A/C | 3.30006e-05 | 0.00406192 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830465 | TAGACTAACAGAGGA[A/C]TCTCACTCTCTGAGG | 4734 |
rs777384727 | snp | C/T | 1.65323e-05 | 0.00287505 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840486 | TATTGGTTTGTGAAG[C/T]ATCATCTTGTAAAAT | 4734 |
rs777387578 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892909 | ACAGACAATTAGATT[G/T]TCAATCTAAATTCAG | 4734 |
rs777409655 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970919 | CATCATCCAGGACAA[C/T]ATGATCTCACCAAAC | 4734 |
rs777419742 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931007 | TAAAAACTGTACATA[C/T]AAGGCATATAACTGT | 4734 |
rs777434669 | snp | A/G | 1.70061e-05 | 0.00291595 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838602 | ATTGTAATATTCACT[A/G]TCCTAGATGGGAAAA | 4734 |
rs777459034 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834881 | AGCTTCTCCATCCCT[A/G]CGTCCCAACCATCAC | 4734 |
rs777540474 | snp | A/G | 3.3184e-05 | 0.00407319 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915831 | CTTACTTCTCCGGGG[A/G]TACAAATTGTTTTAG | 4734 |
rs777548552 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889630 | CAAAAAAGAATAAAT[A/G]AGATCTAGTATTTGA | 4734 |
rs777551588 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883989 | GGTTCAAGCAATTCT[A/C]CTGCCTCAGCCTCCC | 4734 |
rs777559208 | snp | C/T | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841955 | GAATATTCAAACAAC[C/T]CATAATAAGGGTTAA | 4734 |
rs777570845 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860438 | TGGCTCACGGCTGAA[C/T]TTCCAAAAATGGTGA | 4734 |
rs777577931 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937969 | TAAGACAGACAGAGA[C/T]GGATGAAATAGATAG | 4734 |
rs777599151 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843175 | GCCATGTAGAACTGT[A/T]GGTCCAATAAACCTC | 4734 |
rs777606847 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897674 | ACAGCCTGGTAAGGT[C/T]TGGGCTCCAGACTGG | 4734 |
rs777667904 | snp | C/G | 6.59381e-05 | 0.00574149 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916332 | CATGACCCAAAATCA[C/G]TACCGTTGCTGCTGT | 4734 |
rs777669514 | snp | C/T | | | synonymous-codon, intron-variant | NEDD4 | GRCh38.p7 | 15:55834284 | TATTAGTTCAAAGAA[C/T]CCCTAGAAAAAAGAT | 4734 |
rs777669892 | snp | C/T | 1.74549e-05 | 0.00295417 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873948 | GAAAATCATGGACAC[C/T]TATACCAACCGGTAA | 4734 |
rs777710359 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951010 | AGCAATGTCAATGAC[A/G]TGTGGATAAAAAGAA | 4734 |
rs777723315 | snp | C/T | 4.95348e-05 | 0.00497644 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916242 | AAAAAAGTATCATCA[C/T]TTGGTGGAAAAGTAT | 4734 |
rs777743830 | snp | A/C | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55938204 | TCTCTACTAAAAATA[A/C]AAAAATTAGCTGGGC | 4734 |
rs777752223 | in-del | -/A | 2.58481e-05 | 0.00359491 | utr-variant-5-prime, frameshift-variant | NEDD4 | GRCh38.p7 | 15:55924670 | TTCGTCAAACACTTC[-/A]AAAAGAAGCCGGTGC | 4734 |
rs777758654 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974892 | ATTTCTTTTCCTTTC[-/TT]TTTTTTTTTTTTTTT | 4734 |
rs777774427 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913090 | ATATAAGAAAAGAAG[-/T]TGTAGACTCTCAGTG | 4734 |
rs777782598 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937299 | AGACATTTTTATGGC[A/C/G]AATACATTCAGTTCA | 4734 |
rs777786758 | in-del | -/GA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990248 | ATCCTGAAACCACTG[-/GA]CCGCATCCCCGGTCC | 4734 |
rs777789935 | snp | C/T | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834137 | ATCTCCCAGTCCACA[C/T]ATAAGAAGCTACATA | 4734 |
rs777790906 | snp | C/T | 4.94654e-05 | 0.00497295 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915525 | CTTTCCAATTCTCCA[C/T]TGATATTTATTTGAC | 4734 |
rs777814906 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991295 | CAAAAGGGGTGTTTG[G/T]GGGTGGGGAGGATGG | 4734 |
rs777845396 | snp | C/T | 3.36264e-05 | 0.00410026 | missense, intron-variant | NEDD4 | GRCh38.p7 | 15:55837820 | ATTTGCTTCTGGATT[C/T]GGTTTACAAATCGCC | 4734 |
rs777850971 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868351 | GCCATACGCTGTGTG[C/T]TTTGCTTTCAGTAAC | 4734 |
rs777854942 | snp | A/T | 9.91326e-05 | 0.00703964 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848915 | GTAAATAAAGAACAA[A/T]ACACACAAATTTTAA | 4734 |
rs777859160 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904858 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 4734 |
rs777861274 | in-del | -/ATATATATAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852697 | TTTCTAGAAATATAT[-/ATATATATAT]ATATATATATATATA | 4734 |
rs777866325 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990251 | CTGAAACCACTGGAC[C/T]GCATCCCCGGTCCAT | 4734 |
rs777867513 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888522 | TTGTTAAAATGCCCA[C/T]ACTACCCAAAGCAAT | 4734 |
rs777874890 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55952901 | AAACCTTTTCAGAGG[C/T]AGTTTTTAATAATAA | 4734 |
rs777875905 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923175 | GGCAACAGAGTGAGA[G/T]TCTGTCAAAAAATAA | 4734 |
rs777877529 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866062 | CAGGCTTTAGGTGTG[C/T]ACTACCATCCCAAGC | 4734 |
rs777881779 | snp | A/G | 7.69793e-05 | 0.00620353 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838072 | ATAAAGTACAAAATT[A/G]TATCCAATAAAATAC | 4734 |
rs777900593 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892447 | TTCTGCTGTAATATC[-/A]AACTTTTTGTTTCAA | 4734 |
rs777906774 | snp | A/G | 1.68482e-05 | 0.00290238 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860653 | GAGAACTAGGAAACT[A/G]CTTATACCTCGGAAG | 4734 |
rs777914403 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944461 | CCATTGCTGAGGCTT[A/G]AGTAGGTAAACAAAG | 4734 |
rs777920052 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902987 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA | 4734 |
rs777922879 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55902058 | ACCCTAAATACAGTG[C/T]GGCAATTAAGGCTTA | 4734 |
rs777958700 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974715 | TGATAAATTTCAACA[C/T]CTCTTCATGATAAAA | 4734 |
rs777961270 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839531 | CTTGGTACTAAGGAA[G/T]ATGCCCTGGAATTCA | 4734 |
rs777966772 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853956 | GATTGCACCATTGCA[C/T]TCTAGCCTGGGCAAC | 4734 |
rs777969350 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860711 | CCTCGGATATCTGCC[A/G]CCTGGTGGTAAATGC | 4734 |
rs777990555 | in-del | -/AATAAATA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892279 | CTCAATAAATAAATA[-/AATAAATA]AATAAATAAATAAAT | 4734 |
rs778017970 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986422 | GTTGGGACAAGTCAG[C/T]ATCATGTGTCCCCTG | 4734 |
rs778058497 | in-del | -/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55893825 | TATAGATAGAAAAAA[-/G]GCTCACAAAAATCAC | 4734 |
rs778115481 | snp | A/C | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994278 | TGTCCTATGGTCTGT[A/C]CATCTTTAAATCCCA | 4734 |
rs778146495 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975676 | GTTCATGGATTGGAA[A/C]AATCAATATTGTTAA | 4734 |
rs778160604 | in-del | -/GCAATATTTGCTGTTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944803 | AGGAAGGATGAGGCA[-/GCAATATTTGCTGTTTT]GCAATATTTGCTGTT | 4734 |
rs778168415 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981875 | AAGAAAACTGCTGCA[C/G]TTAACGTGGTTATGG | 4734 |
rs778187191 | snp | C/G | 1.65244e-05 | 0.00287436 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842133 | CAGTTGCTCGGCGAA[C/G]TTTCATTTCAAATTT | 4734 |
rs778189858 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941899 | ATTTCAATCCTTTTA[A/T]CTGTACTGAAACTCG | 4734 |
rs778208339 | snp | G/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917402 | CATCAAATCAAAGAT[G/T]GAATTTCCAAATAGT | 4734 |
rs778217794 | snp | C/T | 0.000148668 | 0.00862044 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840501 | CATCATCTTGTAAAA[C/T]GGGCGGATGAAAAAA | 4734 |
rs778235387 | snp | A/G | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55852449 | GGCTTTGTCCAAGTA[A/G]TCGTTCTGGAATTGT | 4734 |
rs778252151 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875669 | AAATAAAAAAATTCA[A/G]TAAATGGGTTTAAAA | 4734 |
rs778254406 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55876557 | TGATTGACATAAGTT[-/A]ATCATTAATTGACTG | 4734 |
rs778267009 | snp | A/C | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917698 | GAGAAGCTGTCACTA[A/C]GCATTTTCTCCTGTA | 4734 |
rs778274151 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976626 | TCCAATCTGGGCAAA[A/T]ATTTTTTTTTTTTTT | 4734 |
rs778313132 | snp | G/T | 9.88957e-05 | 0.00703122 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916473 | CTACTGTAAATACCA[G/T]CCTTCAAGATACAAG | 4734 |
rs778338597 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55970824 | AGAAGGATGGGTACA[A/C]ACCAGCCCAGACTGT | 4734 |
rs778350213 | snp | C/G | 1.65119e-05 | 0.00287327 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915927 | GCAATTTCACTAGGA[C/G]AAATAATAAACTGGT | 4734 |
rs778370630 | in-del | -/TG | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967442 | AACATAACTATGCTG[-/TG]TGTGTGTGTGTGTGT | 4734 |
rs778393773 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55981489 | AAATTTATTTGAAAC[A/G]ATCTATAAAAATATA | 4734 |
rs778405220 | snp | A/T | 3.01209e-05 | 0.00388066 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924721 | AAAACACAATCTTTA[A/T]TTAAAAACAAGTAAA | 4734 |
rs778415196 | snp | A/T | 3.42818e-05 | 0.00414001 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846930 | ACTTTCCATCTATAT[A/T]TTGATGACTCTTAAG | 4734 |
rs778425200 | snp | C/T | 8.25389e-05 | 0.0064236 | intron-variant | NEDD4 | GRCh38.p7 | 15:55840578 | AAACAGGTAATTATA[C/T]TGTAAAAAGTTTATA | 4734 |
rs778429399 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965046 | AGGCCCTCACTAGAT[A/G]CAAAGGCCCAGTCTT | 4734 |
rs778430347 | snp | G/T | 6.45099e-05 | 0.00567898 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869669 | CAGATAACCTTTAAC[G/T]CTTGATTTGTGACTG | 4734 |
rs778445589 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855424 | TAGACAGGAATGAAG[A/G]CAGCAGGAGGCTTCT | 4734 |
rs778484050 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971417 | ATCTCTTGAGGTCAG[A/G]AGTTCGAGACTAGTC | 4734 |
rs778503652 | snp | C/T | 3.3024e-05 | 0.00406336 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833008 | ATGGAAAATCCTTAC[C/T]GTATAGTTCAGCAAA | 4734 |
rs778513543 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55897770 | CTGTCTTTCCTGCCT[C/T]AGGGACTGAATTGTG | 4734 |
rs778537469 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55864675 | CAACAAGAGTGAAAC[C/T]CTGTCTCATAAGAAA | 4734 |
rs778541437 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867254 | CTAGTCATTAGCTAC[-/A]CAGAAGGTAAATAAG | 4734 |
rs778546897 | snp | C/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937293 | CTCAACAGACATTTT[C/T]ATGGCGAATACATTC | 4734 |
rs778552253 | snp | G/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994123 | TCATTCCCATAAGAA[G/T]CTGGACCTGGGGACC | 4734 |
rs778559976 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960223 | GAAGGATGCAAAGTA[C/T]TGTTCCTAGGTGTGT | 4734 |
rs778566758 | in-del | -/AGATTCAGACATGTCCTCAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55900001 | TTCTTGCTGTCTCTG[-/AGATTCAGACATGTCCTCAA]AGCTGAATGATGCCC | 4734 |
rs778625309 | snp | C/T | 1.67279e-05 | 0.002892 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852557 | AGCTAAAGTGAAGAA[C/T]AACAGAAGAATTAAA | 4734 |
rs778634581 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990013 | CATGCAAGCGATCTA[A/G]GTTGTGTACCCCTTA | 4734 |
rs778639844 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955254 | TCTCAAATTTGCAGG[C/T]TCAAGTGATCCACCT | 4734 |
rs778643623 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980661 | GATGGCAAATGGAAG[C/T]CCACAGATGATGGCT | 4734 |
rs778649489 | snp | A/G | 1.65124e-05 | 0.00287331 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840648 | CCATTCCAGCTACCC[A/G]ACCAATAAACTTGAA | 4734 |
rs778651817 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858843 | AAATACTGGCTGTGG[A/G]CCATATGGTTGCTGC | 4734 |
rs778670174 | in-del | -/TC | 1.65674e-05 | 0.00287809 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834197 | AATGGGTTCACAATT[-/TC]TGTTTCAACATAAAA | 4734 |
rs778680099 | snp | C/T | 0.000327976 | 0.0128016 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869564 | TAGTTTAACCAAATA[C/T]TTATAAAATCTCACC | 4734 |
rs778699970 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848780 | AGATAGCCAAGTTAG[A/G]TGGGTTAGCATTTCT | 4734 |
rs778734474 | snp | A/G | | | | | GRCh38.p7 | 15:55975932 | GGCATAAAAACAGAC[A/G]TACAAACCAATGGAA | 4734 |
rs778744413 | snp | A/C | 1.76232e-05 | 0.00296838 | | | GRCh38.p7 | 15:55834260 | AAAAATTTTGATGAG[A/C]TCCTGTGGTATTAGT | 4734 |
rs778763540 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55867793 | GGGTGCCGTGGCTCA[C/G]GCCTGTAGTCCCAGC | 4734 |
rs778770682 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910711 | ACAGCACTATCAGGG[A/C]AGCCTCTGATACACA | 4734 |
rs778805451 | snp | G/T | 3.29728e-05 | 0.00406021 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860473 | GGCATTCAATTCTTC[G/T]GCAAGATGAGTTGGA | 4734 |
rs778805639 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915395 | TAACTGAGATGGTCC[C/T]CCTTTAGAACAATTG | 4734 |
rs778819470 | in-del | -/CAT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992257 | CCGCCACCATTTGTC[-/CAT]CATCATCACTTTATT | 4734 |
rs778852331 | snp | A/G | 1.77735e-05 | 0.00298101 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915298 | CCTTGCAAGAATTAG[A/G]CAGTTCATTTGTGCA | 4734 |
rs778855272 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55853862 | TAGGCATGGTGGTGG[A/G]CACCTGTAATCCCAG | 4734 |
rs778876397 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989231 | ACAGAGCAAGACTCC[A/G]TCTCAAAAGTAAATA | 4734 |
rs778882927 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55949963 | AATTAAAAAAAAAAA[G/T]AAAATACATATGTTT | 4734 |
rs778885462 | snp | A/G | 3.60497e-05 | 0.00424541 | utr-variant-5-prime, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916869 | TAAGGGCTGAAAGTC[A/G]TAACAAAGATCTCTG | 4734 |
rs778887429 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958083 | TGTAACAAACCTGCA[A/C]ATTGTGCACATGTAC | 4734 |
rs778903120 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868911 | ATCCTGAGGTTCGGA[A/G]AAGTTCAATGACTCA | 4734 |
rs778908477 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55966131 | AATCTGCCTGCTCTG[C/T]TCACTCTCCACTGCC | 4734 |
rs778917449 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912879 | GTTATGTTGTTTGCT[A/G]TGCCTGAAATCAACA | 4734 |
rs778928932 | in-del | -/ATAAATAA/ATAAATAAATAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869862 | AAAAGGCAAACATAT[-/ATAAATAA/ATAAATAAATAA]ATAAATAAATAAATA | 4734 |
rs778934431 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55961028 | TGACTGATACACTCG[A/G]CCCTAACTTGTTTGT | 4734 |
rs778950396 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937847 | TCATACAGAACTACA[A/G]AAGACCCTGCATCTT | 4734 |
rs778958024 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883430 | CTTCTAGACGGCATC[C/T]CTGAATGCACTCTGG | 4734 |
rs778969654 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860657 | ACTAGGAAACTACTT[A/G]TACCTCGGAAGACTC | 4734 |
rs778990384 | snp | C/T | 5.06274e-05 | 0.00503102 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841904 | AGTGATTTTTCTTTT[C/T]CTGCCGATAATCATT | 4734 |
rs779024425 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889375 | GTACATATACACAAT[A/G]GAGTACTATCCAGCC | 4734 |
rs779030150 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860551 | ATACATGGTGGCTTC[A/G]TCTTCTCTTATAATT | 4734 |
rs779049525 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879798 | GATAGAGTTAGAAGA[C/T]AGAGTTAAAAAAATT | 4734 |
rs779052346 | snp | A/G | 1.65209e-05 | 0.00287405 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915678 | CAGTCTAATGTAGCT[A/G]CTTTTCGTTGGGTGA | 4734 |
rs779057855 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914405 | CATTTTAAATACTTT[A/G]GAACGGCCAAATTAC | 4734 |
rs779067969 | snp | C/T | 5.2732e-05 | 0.00513451 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993471 | CGGCTGCTGAATAAC[C/T]CGAAGGGAAGCCCGC | 4734 |
rs779081139 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851190 | GTAGATTCAAATGAT[A/G]GGCAGACAAAATGAA | 4734 |
rs779082267 | snp | A/G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857919 | CACTCCAGCCTGGGC[A/G/T]ACAGAGTGAGACCCT | 4734 |
rs779086352 | snp | A/G | 8.27219e-05 | 0.00643072 | intron-variant | NEDD4 | GRCh38.p7 | 15:55856122 | TTGATGGGAGAGGGT[A/G]AAACTCACCACAGGA | 4734 |
rs779087617 | in-del | -/CA | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826912 | TATTTTATAATGAAC[-/CA]CAGTTTTGTTTTGTT | 4734 |
rs779098016 | snp | A/G | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850694 | AGGCTTGTGATTGAG[A/G]GCCTGCAGAACTCTG | 4734 |
rs779135670 | in-del | -/ATA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898126 | CTTAATAGTTTAAGT[-/ATA]ATAATCTAAGAATGT | 4734 |
rs779139073 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55920948 | TGGTAAACCGAGTTT[-/C]CTCAAGAAAAGCTGT | 4734 |
rs779178547 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874570 | GTTTTACTCTGAACT[A/G]AACAAGTGAAAATCA | 4734 |
rs779192589 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839336 | GTCCGGCACTAAGTG[G/T]GAAATGTTTAAGTAG | 4734 |
rs779196060 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984950 | ATTGAGAAGCAATTG[C/T]GTTCAACTGGTTCCT | 4734 |
rs779199715 | snp | C/G | 3.30836e-05 | 0.00406702 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838194 | GTCTAAAATTAAACA[C/G]AATAACTTGATATGT | 4734 |
rs779219957 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976284 | AATCAACAAAGTTAG[A/G]AGACAGACCACAGAA | 4734 |
rs779220536 | in-del | -/AC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883699 | CACACACACACAAAC[-/AC]ACACACACACACACA | 4734 |
rs779222883 | in-del | -/ATTTTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55976627 | CCAATCTGGGCAAAA[-/ATTTTT]TTTTTTTTTTTTTTT | 4734 |
rs779224148 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935410 | CCTCTCTCCCAGGGG[C/T]TGAATTTTGATTCCT | 4734 |
rs779248914 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55984023 | TATAAAATCGGTAAA[C/G]TATATTCTATATCAT | 4734 |
rs779264609 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55839173 | AGCTGGGACTACAGG[C/T]GCGCACCACCACGCC | 4734 |
rs779310069 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844809 | GCACCGGTTTTCAAT[-/T]TTTTTTTTTTTTTTT | 4734 |
rs779319408 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992587 | TGATTTTTTTCACTC[A/G]GAACCAGTCACTGTT | 4734 |
rs779323018 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55953838 | CAATTCTCCTGCCTC[A/G]GCCTCCTGAGTAGCT | 4734 |
rs779344599 | snp | A/T | 1.6489e-05 | 0.00287128 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915532 | ATTCTCCATTGATAT[A/T]TATTTGACAATCTAC | 4734 |
rs779363644 | snp | A/G | 3.40153e-05 | 0.0041239 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846943 | ATATTGATGACTCTT[A/G]AGTATTTATTATAAA | 4734 |
rs779374108 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964872 | TCCTGAATAGATTAA[C/T]GCCCTCCCTCGGAAG | 4734 |
rs779376560 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888316 | ACATACAAATATCAG[C/T]AGCATTTCTCAATGC | 4734 |
rs779488449 | snp | A/T | 2.0403e-05 | 0.00319391 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869708 | AAAATAAATATTCAT[A/T]AAACTTTAACACCGG | 4734 |
rs779494037 | snp | G/T | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55833019 | TTACCGTATAGTTCA[G/T]CAAATCCATTCATAG | 4734 |
rs779527355 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941015 | TATCCATTTAAACTG[A/G]GTTGTTAAAATTACA | 4734 |
rs779528586 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916648 | GAACGTTTTCCTTTA[C/T]TAACGGAGCTAGTGC | 4734 |
rs779539984 | snp | C/T | 1.66452e-05 | 0.00288484 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55869590 | TCACCTCTAATTCCT[C/T]AGCCTGTTCTGCATT | 4734 |
rs779540155 | snp | A/G | 5.678e-05 | 0.00532792 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838078 | TACAAAATTATATCC[A/G]ATAAAATACATACTA | 4734 |
rs779541215 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992464 | TTAAATATTACAATA[C/G]TTAAGCAAGCAGTAT | 4734 |
rs779570817 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55973562 | AAAATTTAAAAAATT[A/C]AAATCTTAAAAGTAT | 4734 |
rs779581982 | in-del | -/GGAAATAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922160 | TAAGAGCAAAATACT[-/GGAAATAA]CACTAATATCTATTA | 4734 |
rs779635684 | snp | C/T | | | downstream-variant-500B | NEDD4 | GRCh38.p7 | 15:55826835 | GCACTGAAAATTTAA[C/T]GTGCTGCTGTGAGGA | 4734 |
rs779655180 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858803 | GCAGAGGTTAGCACA[C/G]ATTTCCTGTTAAGAT | 4734 |
rs779666792 | snp | C/T | 3.38066e-05 | 0.00411122 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860356 | TGTTGAATAGTATAA[C/T]ATGCATAATATAAAC | 4734 |
rs779668357 | snp | A/G | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918913 | TCTGGGATTAAGTGT[A/G]GGGTCTAATAACTCA | 4734 |
rs779701657 | in-del | -/TAATC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55992801 | TCAAATCCCAGAGCT[-/TAATC]TAGTTTTCAAAGGGA | 4734 |
rs779703191 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945636 | CAAGGCATGACAACA[C/T]TCAAATTCAGGAAAT | 4734 |
rs779774357 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991617 | GTGGACAAAATAGAG[C/T]GGGGACAGAAGCAAA | 4734 |
rs779804986 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55872719 | TGGAGCCAAAGGGAG[A/G]GCAGAAGAGAATAAG | 4734 |
rs779823515 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908330 | ATCAATTCTAGTGAA[C/T]TTACATTTGCCTACC | 4734 |
rs779839507 | snp | C/T | 3.29843e-05 | 0.00406092 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860625 | TTTATTGCTATAGCA[C/T]GTGTCTTTCAAGGAG | 4734 |
rs779849426 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55857884 | ATTTGAGGTTGCAGT[G/T]GGCTATGATCATGCT | 4734 |
rs779870409 | snp | C/T | 0.000118956 | 0.00771127 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951349 | AACTTACTTTTTCCA[C/T]TTTAGTAAAATAAAA | 4734 |
rs779889900 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986499 | AAGAGAGCGTGACCT[A/G]AACATGGTCATCAAG | 4734 |
rs779891166 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55832340 | ACCATGACTCTGTTT[G/T]TATTTTTTTAAAAAT | 4734 |
rs779905090 | snp | C/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917526 | AATACCAAAACTTTA[C/T]AATGAATTAAAACTT | 4734 |
rs779917841 | snp | A/G | 7.89193e-05 | 0.0062812 | utr-variant-5-prime, synonymous-codon | NEDD4 | GRCh38.p7 | 15:55951580 | TAACGTCACTCTCAC[A/G]TAAGGATCACTGTTA | 4734 |
rs779922852 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922668 | ATGCCCGGCCAACAA[C/T]GTGTTTTTTGGGGAT | 4734 |
rs779923961 | in-del | -/CTCTCTGC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940540 | TCTCTCTCTCTCTCT[-/CTCTCTGC]CTCTCTGCCTCTCTC | 4734 |
rs779937442 | in-del | -/A | 1.68527e-05 | 0.00290277 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848584 | ATCCTGGCTATAATT[-/A]AAAATGTATTTCAAT | 4734 |
rs779942138 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944527 | AGCTCATCAAGGCCT[A/C]CTGCCTATATAGACT | 4734 |
rs779945635 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903126 | AGAAAACACTTGATC[A/T]GGACTATACATTCTT | 4734 |
rs779963523 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55882233 | TGAGCAATCACAGTA[C/T]CTAGTTTTAACTTCA | 4734 |
rs779981198 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55957129 | ACTGATTTTGGGTTA[C/T]ACAAACACTGACTTT | 4734 |
rs780001127 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55956558 | CTTGAATTACCTCAG[C/T]ATTTTTTGTTAAACA | 4734 |
rs780029490 | in-del | -/A | 3.68949e-05 | 0.00429489 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837890 | CATGTGAACCAAGAC[-/A]AAATTCTGAGGCACA | 4734 |
rs780048646 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980804 | TAGGGGTGTGTGTGT[A/G]TGTGTGTGTGTTACA | 4734 |
rs780052584 | in-del | -/TTCC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909983 | CTTATAATTTTCTGT[-/TTCC]TTCATTTGATATTGC | 4734 |
rs780104360 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929415 | GTATGGGTTTTTTTG[A/G]TACATATTATTTCAT | 4734 |
rs780111388 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55871530 | ATATGCAGATGTCAC[A/C]ATCAGTCTAAAATTA | 4734 |
rs780115152 | snp | C/T | 4.95806e-05 | 0.00497874 | intron-variant | NEDD4 | GRCh38.p7 | 15:55834172 | ATGTCAAATTATAAA[C/T]AAGGAAAATAATGGG | 4734 |
rs780115488 | snp | C/T | 3.31186e-05 | 0.00406918 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55840681 | AAGAGAGGTGATCTT[C/T]GTTACACAATCCAGA | 4734 |
rs780117307 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830056 | AAGCAAGTACCACCA[C/G]AGCAAACAGAGCAAT | 4734 |
rs780147205 | snp | A/G | 1.65078e-05 | 0.00287291 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916256 | ACTTGGTGGAAAAGT[A/G]TAACTACTACTGTCA | 4734 |
rs780166457 | snp | A/G | 1.6574e-05 | 0.00287867 | intron-variant | NEDD4 | GRCh38.p7 | 15:55852410 | AGAAAGCAAGTTGAT[A/G]GATTACAGGATACCT | 4734 |
rs780167806 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942564 | GATGAGCCTGCTTCC[C/T]CTTCACCTTCTGTCA | 4734 |
rs780170872 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848879 | GGAATTTTCAATCTT[A/G]GATCTTCCTTTTTTG | 4734 |
rs780175372 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910510 | ATCCCCTCTTCTACC[A/G]CCTCACCAAAGTTGG | 4734 |
rs780192237 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55927309 | GAGACAGACAAAGAC[A/G]ACAAGATTCTTTTTT | 4734 |
rs780195861 | snp | A/C | 1.64836e-05 | 0.0028708 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916353 | TTGCTGCTGTAAGAC[A/C]CATTATCACTGGTTG | 4734 |
rs780204545 | snp | A/G | 8.76755e-05 | 0.00662043 | intron-variant | NEDD4 | GRCh38.p7 | 15:55993478 | TGAATAACCCGAAGG[A/G]AAGCCCGCCCCGCAG | 4734 |
rs780216259 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971944 | GTTTCTGAGTGGACA[-/C]CTAATAGGCAGGAGA | 4734 |
rs780216275 | snp | G/T | 3.29468e-05 | 0.00405861 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848369 | ACTGGCAGAGAGACT[G/T]ACTGGTCCAGTTATT | 4734 |
rs780221501 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835420 | CAGTCTCCTGTTCTG[-/T]TTTTTTTTTTTTTTT | 4734 |
rs780226262 | snp | G/T | 0.000148531 | 0.00861646 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55842123 | TCTTCAAGAACAGTT[G/T]CTCGGCGAAGTTTCA | 4734 |
rs780235915 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55843010 | ATTGAATTATGGGGG[C/T]GGATCTTTCCTGCAC | 4734 |
rs780237552 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55887317 | AAAATGGAGACATTA[C/T]AACTGATACCACAGA | 4734 |
rs780249375 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55830988 | AAATGGCATGATCTC[A/G]GCTCAATGCAACCTC | 4734 |
rs780284935 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55841980 | GGTTAAACATTTCCT[C/T]TGAGATCAGGAAGAA | 4734 |
rs780289104 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889210 | TAATCCAGCAATCTC[A/C]CTACTAGGTATATGC | 4734 |
rs780291170 | in-del | -/TAAGAAT | 1.79777e-05 | 0.00299809 | frameshift-variant, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915287 | AGGAAACTTACCTTG[-/TAAGAAT]CAAGAATTAGACAGT | 4734 |
rs780357566 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55943270 | TGGGGAGGAATTCAA[C/G]CCAGCTGCTGGAGCT | 4734 |
rs780364789 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55861808 | ATATTTAATAATAAA[A/C]TTACTGTTTATTTAA | 4734 |
rs780386429 | snp | A/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937929 | TCACAAAGCTACAGT[A/T]ATTAAAACAGTATGA | 4734 |
rs780410040 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55877745 | GCTTAAGCAAAGAAT[C/T]TTCCCCTTCCTCCCA | 4734 |
rs780436576 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55948685 | CTTTGACAAACCTGA[C/G]AAAAACAAGAAATGG | 4734 |
rs780443357 | snp | C/T | 3.60835e-05 | 0.0042474 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838207 | CACAATAACTTGATA[C/T]GTTATTTTAGCGAGA | 4734 |
rs780458685 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837737 | CCTAATATTTGAAAC[C/T]TATAGGTTATACTGT | 4734 |
rs780462955 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55890575 | TTTTATTTATCCATT[A/T]TTCAGTTGATTGACA | 4734 |
rs780471573 | snp | A/G | 3.29679e-05 | 0.00405991 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860740 | GCACGTTGTGCTTGC[A/G]GTTGAATGTTGCCAT | 4734 |
rs780473336 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875921 | AATAAAGTCAGTGAA[C/G]TGAAGCAGGATAAAC | 4734 |
rs780541241 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916672 | CTAGTGCAGTCTGTC[C/T]GGGAGTCAGCTTCAT | 4734 |
rs780585986 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55934069 | GAGACAGGAGAACAG[C/T]TTGAACCCAGGAGGT | 4734 |
rs780629163 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55878299 | TCATAAAATATTACT[A/G]TAAGTCAATAATATG | 4734 |
rs780635736 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55848998 | AATATTCTCTTGTAA[A/G]AGTCAATTTATACTT | 4734 |
rs780687878 | snp | A/G | 4.29424e-05 | 0.0046335 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829863 | TGGTTATAAAACTAT[A/G]GCAGTAAAAACACTA | 4734 |
rs780721990 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55960038 | CAATGTGGTCAATCC[A/C]GATAACTACCTTACA | 4734 |
rs780730934 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55863175 | AGAGATTTATTATAT[C/T]AAGTTTTAGAAATTA | 4734 |
rs780744114 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55952660 | CATCCTTACCCCTAA[C/G]CTAGTGAGTCAGGAG | 4734 |
rs780759541 | snp | A/C/G | 0.00016567 | 0.0091001 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915762 | CTGGGAGTATTATTC[A/C/G]AAAGAACAATTTTCT | 4734 |
rs780794378 | in-del | -/TT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989691 | TTGCTTCAGTCAGCC[-/TT]TCTTATAGGAAACAG | 4734 |
rs780803819 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55837152 | AGAAGAAAGTAGGCC[A/G]AGCACGGTGGCTCAC | 4734 |
rs780845740 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983649 | CAGAGTGTTCTTCTG[C/T]TGCCCAGACTGGAGT | 4734 |
rs780863285 | snp | A/G | 3.29761e-05 | 0.00406041 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860425 | GCTCGATGCTGGCTG[A/G]CTCACGGCTGAATTT | 4734 |
rs780865270 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848375 | AGAGAGACTTACTGG[C/T]CCAGTTATTGCTACA | 4734 |
rs780868423 | in-del | -/ATAA | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828443 | ATATAAGTATGAAAT[-/ATAA]ATACAGTCTTGGCAC | 4734 |
rs780868503 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945175 | ACTTTGATGAGTTGA[C/G]AGAAGTAGGCTTCAG | 4734 |
rs780870147 | in-del | -/AGAAA | 7.48923e-05 | 0.00611887 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869686 | TTGATTTGTGACTGT[-/AGAAA]AGAAAATAAATATTC | 4734 |
rs780870805 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880456 | ACAAACCTGAAATAT[-/AA]AAGAGAGTACTTCCT | 4734 |
rs780887324 | snp | C/T | 0.000127467 | 0.00798231 | intron-variant | NEDD4 | GRCh38.p7 | 15:55838218 | GATATGTTATTTTAG[C/T]GAGAAAAATTTAAAA | 4734 |
rs780900256 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880807 | GATAATCATATCGAC[G/T]AGTAGGGTTTGGTGA | 4734 |
rs780901296 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968110 | TCTTTTTTCTCCAAA[A/G]TAATCTATAAATTTA | 4734 |
rs780914759 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55991434 | TCCCTCAGTCCGAGG[C/T]TGAGACTGTCTTTTT | 4734 |
rs780917405 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55919837 | GGGTAATCTTAATCA[C/T]TGACTGAACTTTGAA | 4734 |
rs780956620 | snp | C/G | 1.64988e-05 | 0.00287213 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916759 | GGCTATCCAAGTCAT[C/G]TCCGGAGGTTTCTGA | 4734 |
rs780962091 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55990459 | TCTTGACGTCTGGAA[A/G]CCACTACCACCACTA | 4734 |
rs780971078 | in-del | -/GA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55852744 | CTTTTCTGAGAGAGT[-/GA]GAGAGAGAGAGAGAG | 4734 |
rs780983420 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55850575 | GTTGTGGTCAATAAA[G/T]AAAGGCCTCCCATTT | 4734 |
rs781042067 | snp | C/G | 1.65312e-05 | 0.00287495 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916207 | TATTGGAGGTGCTGT[C/G]AGAAGGTAAGTTTCC | 4734 |
rs781057759 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55933952 | TGAGGTCAGGAGTTC[A/G]AGACCATTCTGGCCA | 4734 |
rs781100521 | snp | C/T | 1.65143e-05 | 0.00287348 | synonymous-codon, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55856146 | CACAGGAAGTGTAGG[C/T]TGTTCCTCAAAAGTA | 4734 |
rs781104769 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929244 | TGCACGAGCACGCAC[A/G]CACACACACCCTCTT | 4734 |
rs781144844 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55968642 | ACATGAAAAGATAAT[C/T]TCACCGGTCAGCAGA | 4734 |
rs781151845 | snp | A/G | 0.000103956 | 0.00720881 | intron-variant | NEDD4 | GRCh38.p7 | 15:55951612 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAATTTTAA | 4734 |
rs781165950 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55844104 | AGGAAGTCTTTAGAC[A/G]GAGAAAGGGAGGGAA | 4734 |
rs781180124 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55879872 | AAATAAGGAAATTAC[A/T]GGAGAAAATTCAAAA | 4734 |
rs781187379 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55892257 | AGGCAAAAGAGCAAA[A/C]CTCCAACTCAATAAA | 4734 |
rs781206081 | snp | G/T | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936664 | AGGAAATGGGGTGAG[G/T]CTTTTTCAGATGCCC | 4734 |
rs781217262 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55925737 | CCTAACTCAGTGTCT[A/G]CTTTTCCCTCTGAGA | 4734 |
rs781231263 | in-del | -/A | 3.29989e-05 | 0.00406182 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848902 | CTTTTTTGGTAGAGT[-/A]AATAAAGAACAATAC | 4734 |
rs781236065 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980533 | ACAGTACCCGCCCCT[C/T]GTACAGAGGATGTAA | 4734 |
rs781239115 | snp | A/T | 9.53062e-05 | 0.00690246 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869730 | TAACACCGGGAGAAA[A/T]GTATTCAATTAATAA | 4734 |
rs781246887 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55840794 | AAATAATTACAAATA[A/G]TCTTCCTCCTTTAAG | 4734 |
rs781256672 | snp | A/G | 5.05702e-05 | 0.00502817 | intron-variant | NEDD4 | GRCh38.p7 | 15:55833151 | AGCACTGGGAAAGAG[A/G]TAAACAAATTATCCT | 4734 |
rs781261933 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55841479 | TTACTGGGTATAGGG[C/T]TTCATTTTGGGAAGA | 4734 |
rs781264160 | snp | C/T | 1.71885e-05 | 0.00293154 | utr-variant-5-prime | NEDD4 | GRCh38.p7 | 15:55993590 | ACCGGACGCGCTCGC[C/T]CCCGCCCAGGGCAGG | 4734 |
rs781265318 | snp | C/G/T | 3.29887e-05 | 0.00406122 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860568 | CTTCTCTTATAATTT[C/G/T]CCAGTTCTAAAATGA | 4734 |
rs781266666 | snp | C/T | 3.2969e-05 | 0.00405998 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916366 | ACCCATTATCACTGG[C/T]TGAAAAGTTACTAAG | 4734 |
rs781267857 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55875760 | AATATGAAAAATAAA[A/G]GGAACTTGTGGAAAA | 4734 |
rs781283624 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975054 | TGCGATACCACACCC[A/G]GGTAATTTTTGTATT | 4734 |
rs781313588 | snp | A/C/G | 5.10711e-05 | 0.00505306 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841890 | CTTACTTTTAAAACA[A/C/G]TGATTTTTCTTTTTC | 4734 |
rs781314476 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55932668 | GCCAAAATTGACAAA[C/T]TGGAGCTAATTAAAC | 4734 |
rs781320921 | snp | A/G | 4.94499e-05 | 0.00497217 | synonymous-codon, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915416 | AGAACAATTGTGCTT[A/G]AGGCTGGATAGACAG | 4734 |
rs781347537 | snp | C/T | 4.96151e-05 | 0.00498047 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55838568 | CTGTTGGGTCATTTT[C/T]AAGAATCCATCTTAG | 4734 |
rs781352785 | snp | A/G | | | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937045 | CAATCCACCCTCCTC[A/G]GCCTCCCAAAGCACT | 4734 |
rs781373794 | snp | C/T | 1.71314e-05 | 0.00292667 | intron-variant | NEDD4 | GRCh38.p7 | 15:55837782 | GCAAATAAAAGAAAA[C/T]GAATACCTCTTTAAA | 4734 |
rs781402169 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989175 | TGGTAGGCAGAGGGT[A/G]CAGTGAGCTGAGATC | 4734 |
rs781412371 | snp | A/G | 1.78391e-05 | 0.00298651 | stop-gained, intron-variant | NEDD4 | GRCh38.p7 | 15:55834265 | TTTTGATGAGATCCT[A/G]TGGTATTAGTTCAAA | 4734 |
rs781421572 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955112 | TCGAAACCTCTGCCT[A/C]CCGGGCTCAAGCAAT | 4734 |
rs781432511 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975863 | TGGAGTCAAATTAAT[C/T]ACTGGACTTCAAATT | 4734 |
rs781444970 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55855419 | AAGCATAGACAGGAA[C/T]GAAGGCAGCAGGAGG | 4734 |
rs781460082 | in-del | -/TGTC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964728 | GTGTGTGTGTGTGTG[-/TGTC]TGCTTATCATTCTAT | 4734 |
rs781473504 | snp | A/T | 1.64874e-05 | 0.00287113 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915504 | TTGTTCATCTGTGAA[A/T]GTGGTCTTTCCAATT | 4734 |
rs781474188 | in-del | -/GTC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55958133 | AAAAAAAAGATGACT[-/GTC]GTCTTCTTTTATTCT | 4734 |
rs781500897 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55948458 | GAAAAAACTACTTTA[A/G]AGTTCATATGGAGCC | 4734 |
rs781501486 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979151 | CACTATTAAAATCCT[A/G]TATCATCTAGGCAGA | 4734 |
rs781548761 | in-del | -/GTGTGC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983295 | CAATGGTGTGTGTGT[-/GTGTGC]GTGTGCGTGCGCGCG | 4734 |
rs781551517 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914043 | ATTCTAAATTATAGA[C/T]CAGAATTTGAAATCT | 4734 |
rs781552363 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889421 | TCCGCTCATTTGCAA[A/C]AACTGGATAAAACTG | 4734 |
rs781576378 | snp | A/G | 2.1613e-05 | 0.00328725 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830029 | AGGAAGTGGTTATGA[A/G]AGACACTGACAAAGC | 4734 |
rs781579854 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899682 | TGAAAGTACAGGGGT[A/T]TCAATGTCTTGCAGC | 4734 |
rs781589067 | snp | A/C | 1.82115e-05 | 0.00301751 | intron-variant | NEDD4 | GRCh38.p7 | 15:55850745 | TCTCCACTGTGGCCT[A/C]GCACATTAATGAAAT | 4734 |
rs781592465 | snp | C/T | | | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55848422 | CTTCCCATTGTGTTC[C/T]TTTTATATCTGAAGG | 4734 |
rs781608139 | in-del | -/AAAAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55951595 | GTAAGGATCACTGTT[-/AAAAA]AAAAAAAAAAAAGAA | 4734 |
rs781610714 | in-del | -/GTGT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55964697 | TTTTGCTGCTGGTGT[-/GTGT]GTGTGTGTGTGTGTG | 4734 |
rs781620286 | in-del | -/GTGTA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55989443 | CTTCTCCTCCTTTGT[-/GTGTA]GTACATAAAGGTTTG | 4734 |
rs781647345 | snp | C/G | 1.71205e-05 | 0.00292574 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862867 | AAATGAAAATTCGTA[C/G]TTAAAGTGTTTCCAG | 4734 |
rs781647757 | in-del | -/AAAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945337 | ACCTGATGGAGCTGA[-/AAAC]CATGGCACAAGAACT | 4734 |
rs781648726 | snp | C/T | 4.97913e-05 | 0.00498931 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915826 | TGTCTCTTACTTCTC[C/T]GGGGGTACAAATTGT | 4734 |
rs781694615 | snp | C/T | 1.65817e-05 | 0.00287933 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55915780 | AGAACAATTTTCTTC[C/T]GTAACGAGCCCTTCC | 4734 |
rs781704268 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55830544 | GGCAGCTTTTCAGGA[A/G]TACCCCACTGTTCAA | 4734 |
rs781714033 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912395 | TACTATACTAGGCTT[A/C]AGCAATTTACCTATT | 4734 |
rs781714238 | snp | A/G | 1.70435e-05 | 0.00291915 | utr-variant-5-prime, missense | NEDD4 | GRCh38.p7 | 15:55993542 | CCGAACACCTCCACC[A/G]CGCAAGTTGCCATTT | 4734 |
rs781714784 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55942464 | GCTGCTCTGGTGATA[A/G]TAAGCGACTTCTTAT | 4734 |
rs781741834 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941964 | TGTTCCATGGGCATA[C/T]AAAAAGAATATACAC | 4734 |
rs781762476 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55858520 | GCCATGTTGCCCAGG[C/T]TGGTCTTGAACTCCT | 4734 |
rs796067596 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55910145 | CTTATACATCTTATA[C/T]CCACTTCACATATGC | 4734 |
rs796079035 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55929833 | TTTAAAAACTATAAG[A/G]AGTATCCTTAGAAAC | 4734 |
rs796096294 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55939461 | GTTTATAAATTACCC[A/T]GTCTCAGGTAGTATC | 4734 |
rs796131264 | snp | G/T | | | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55993941 | CCGGGGAGCCAGGGA[G/T]CGCCGGGAAGCGCCG | 4734 |
rs796153521 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55885117 | ACTTTTCAGTGGAAA[C/T]CTTATTACCTTGGAG | 4734 |
rs796170075 | in-del | -/TCTCTCTCTCTCTC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55940519 | TTCCCTCCTCCCCCT[-/TCTCTCTCTCTCTC]TCTCTCTCTCTCTGC | 4734 |
rs796180037 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866327 | ATCCTCTTACTTTGT[A/C]TGCCCATCCATGTTG | 4734 |
rs796197736 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986756 | ACCACACCCGGCTAA[-/T]TTTTTTTTTTTTGTA | 4734 |
rs796223860 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55908311 | TCTCCAGAATACTTC[C/T]CTAATCAATTCTAGT | 4734 |
rs796238846 | in-del | -/AA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55912788 | ATTTATTTTCAGATC[-/AA]AAGTCATTATATAGC | 4734 |
rs796254653 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55914239 | AATAAACATAATGGA[A/T]GTTACAAAAACACAG | 4734 |
rs796257571 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977515 | CTACTAATTCTAAAA[-/A]TCCATATGGTAAATT | 4734 |
rs796279036 | in-del | -/TC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55923014 | CATGGTGAAACCCCG[-/TC]TCTACTAAAAATACA | 4734 |
rs796348285 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55974425 | GATTCTATAAGGCCA[A/G]TATTACTCTGATATC | 4734 |
rs796356422 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971893 | CAAAACAAAACAAAA[C/G]AAAAAACAAAGCAGC | 4734 |
rs796358993 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55993189 | GGCAGGAAGGGGCTG[C/G]CGCGGTGATGTGGGT | 4734 |
rs796359984 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55931330 | AAGTGGGTAGCAGGA[A/G]TAGGAGGGAGGACAG | 4734 |
rs796363587 | in-del | -/TTT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55959251 | CAAAATGTTTTCTTC[-/TTT]GACATATAGATTATT | 4734 |
rs796391142 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55894193 | TATAGTCAGCTCTCT[C/T]TATCGGTGGATTCAA | 4734 |
rs796437180 | in-del | -/AT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979069 | AGTCTATTTTTAAAA[-/AT]ATATATATATACCCC | 4734 |
rs796443132 | in-del | -/T | | | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917476 | TTAATTTTTTTTTTT[-/T]AATGTGTGAATTCAA | 4734 |
rs796451329 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55869885 | AATAAATAAATAAAT[A/C]AATAAATAATTGTTA | 4734 |
rs796457111 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55979606 | GATCCACCCGCCTCG[G/T]CCTCCCAAAGTGCTG | 4734 |
rs796466065 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55944018 | TTTAAGATGTAATGA[C/T]TGGAAGATGGCCAAA | 4734 |
rs796477535 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55889653 | GTATTTGATAGCAGA[A/G]TAGGGTAACTTTAGT | 4734 |
rs796478869 | in-del | AGG/GA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874989 | AAAGAAAAAAAAAAA[AGG/GA]AATCAACTCTCCTCA | 4734 |
rs796481842 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849396 | TGCCTAGCTAATTTT[C/T]GTATATTTAATAGAG | 4734 |
rs796493084 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851483 | ACATTTTCTTTTCTG[-/T]TTTTTTTTTTCAGAT | 4734 |
rs796500771 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55868659 | ATGTGGAACTGAGTC[C/G]ATTAAACCTGTTTTT | 4734 |
rs796532349 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980598 | AAACAAGAAATTAAA[C/G]AAACAGTAGATTCAA | 4734 |
rs796538464 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55930357 | ATTTCTCTCATGTAT[C/T]TAGAATGGTACTGGT | 4734 |
rs796555889 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55842781 | CTGTGACCTGTAGGA[C/T]AGCCACTGCCTGCTA | 4734 |
rs796559792 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55903780 | CAATGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 4734 |
rs796574549 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55862145 | TGATTTGTTTTGGAA[C/G]GATTTGAGAACAGAA | 4734 |
rs796577796 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55835625 | TCCATACATCTCTAT[A/C]CTTTAAGTCTCCCTT | 4734 |
rs796582007 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880305 | TCCAAAAAAAAAGAA[C/T]AAAAAGGCCCACTGA | 4734 |
rs796609402 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55834363 | GCTTCTGGATGCTAC[C/T]GGAGGAATCCCACAT | 4734 |
rs796613527 | in-del | -/ACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985761 | GTGTAGAGTACACAT[-/ACAC]ACACACACACACACA | 4734 |
rs796620920 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55946462 | GAAGAGCTAACTATC[C/G]TAAATATATATGCAC | 4734 |
rs796624342 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55980439 | CCAAGGGAAAAAAAA[-/A]TGCTATAAATCCTGA | 4734 |
rs796628542 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55913280 | GAAATATTTTGGGAG[C/T]TGTTTATTTATAAGT | 4734 |
rs796631890 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904460 | GGCGTGCACCAACAC[A/G]CCTGGCTAATTTTTC | 4734 |
rs796633385 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55945721 | TGTCAGATTCACCAA[A/C]GTTGAAATGAAGGAA | 4734 |
rs796659347 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55922847 | TCTTAAGCTGAGTAA[C/T]GTGTATACATATTTG | 4734 |
rs796693447 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55888536 | ATACTACCCAAAGCA[A/G]TCTACAGATTTGATG | 4734 |
rs796704745 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955988 | CCTGGCTAATTTTTC[-/A]AAAAATTTTTTTGTA | 4734 |
rs796718511 | in-del | -/AT | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55880453 | ATACACAAACCTGAA[-/AT]ATAAGAGAGTACTTC | 4734 |
rs796727030 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55901199 | TTTATCCTTTGTGAT[A/T]TCTTAACTATTGAGA | 4734 |
rs796734348 | in-del | -/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977748 | TCTTGTTTTTTTTTT[-/T]AATTTAAAAAGATTA | 4734 |
rs796736680 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55975639 | GACACCAAAAAAAAA[-/A]CAAAAGGGAAAAATA | 4734 |
rs796739620 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847378 | GATTTCTCCATTAAA[A/G]GGACAATGTGAAAAG | 4734 |
rs796752084 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55909915 | ACTGAGAAAGTTAGA[C/G]TAATGCTGTCCAAAA | 4734 |
rs796755482 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55847509 | ATTTATTTTTATGAA[C/T]TAGAAAACAAAATCT | 4734 |
rs796795622 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55874794 | GCCTGACCAACACGG[A/T]GAAACCTCATCTCTA | 4734 |
rs796801253 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55849121 | GATCACCACTAACTG[A/G]TCATTTCTTTTGCCC | 4734 |
rs796801803 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55866431 | CTTGCATATATTGAA[C/T]CAGACTGTATGTTTC | 4734 |
rs796808415 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828524 | CCTTATTCTGCTTAC[A/G]CCTACTTTTGATTGT | 4734 |
rs796819438 | in-del | -/GTG | | | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829643 | ACTCTAAAGCCAGGT[-/GTG]GTGGTGGTGCCTGGC | 4734 |
rs796821818 | snp | G/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55899303 | GCCTTTTATTAGTTT[G/T]TAAAAATGTATTTCA | 4734 |
rs796840370 | in-del | -/ACACAA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883691 | TCAACACACACACAC[-/ACACAA]ACACACACACACACA | 4734 |
rs796851614 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55971638 | TCAAAAAAAAAAAAA[-/A]GACTTATTAGCTTTA | 4734 |
rs796861391 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55921454 | CTCAGTCTCCAGAGT[A/G]GCCGGGACTACAGGT | 4734 |
rs796865161 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55851350 | AAAAGGTGTAGACTT[-/A]CAGGGCCACAACATC | 4734 |
rs796868395 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55955993 | GCTAATTTTTCAAAA[A/T]TTTTTTTGTAGAGAC | 4734 |
rs796886453 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55935387 | TCTGTCAGGGATAGA[C/G]AGCAACTCCTCTCTC | 4734 |
rs796915775 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55983735 | CCTGCCTCAGCCTCT[C/T]AAGTACCTGAGACTA | 4734 |
rs796923105 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977480 | TATCCGTTGTTAAGC[A/C]ATGCATGACTGTAAA | 4734 |
rs796923153 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55977638 | GAAAGAAGGGAAATC[-/C]TCAGGTATCAGAAAT | 4734 |
rs796924051 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55941587 | TTTTTTTTTTGAGAC[-/A]AGAGTCTCACTCTGT | 4734 |
rs796924533 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55898058 | TAAAACACACATCCA[C/T]GAGAGGTGAAATCCA | 4734 |
rs796939323 | in-del | -/A | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967706 | ATTAATAAGAAATAT[-/A]AAAAAAACTTCATAG | 4734 |
rs796977079 | snp | A/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55895114 | GAAATACTCACAGCT[A/G]GGTAACTGCTAAAAT | 4734 |
rs796992314 | in-del | -/TA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55967475 | GTGTGTGTGTGTGTG[-/TA]TGTGTGTGTATACAA | 4734 |