SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs906811 | snp | C/T | 0.0640965 | 0.167152 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937349 | TTTTCCTCTTTGTCA[C/T]TTATATCATCATTTT | 4734 |
rs925257 | snp | G/T | 0.299411 | 0.245069 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937038 | TGGGAGGCCGAGGAG[G/T]GTGGATTGCCTGAGG | 4734 |
rs952532 | snp | A/C/T | 0.443235 | 0.253513 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926068 | ATGTATTTTTACATA[A/C/T]GTATATGTATTTTAC | 4734 |
rs952533 | snp | C/T | 0.303187 | 0.244277 | intron-variant | NEDD4 | GRCh38.p7 | 15:55926027 | TGTATATGATACATA[C/T]GTATATGTATTTTAC | 4734 |
rs967128 | snp | C/T | 0.340333 | 0.233109 | intron-variant | NEDD4 | GRCh38.p7 | 15:55959485 | gatgccacaATATTC[C/T]GGGCCTTGAAACAAT | 4734 |
rs1042471 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827042 | TTAAAATCTTCTGAC[A/C]CAGTAAATATATATA | 4734 |
rs1042472 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55826996 | CAAAATTTATTGCAC[A/C]CTTTAAAGTGTAAAA | 4734 |
rs1042477 | snp | G/T | 0.472709 | 0.11358 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55829688 | ACACAGTTGTTTCAT[G/T]CTGTCTTTAGAGTTA | 4734 |
rs1112535 | snp | A/C | 0.205723 | 0.246048 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989925 | CAGGCAGCAGAGCTC[A/C]GGAGGTAATGTGATC | 4734 |
rs1126740 | snp | A/G | 0 | 0 | stop-gained, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55834042 | TTATACAGTGGTTTT[A/G]GAAGGCTGTTTTAAT | 4734 |
rs1134352 | snp | A/T | 0.323671 | 0.238899 | intron-variant | NEDD4 | GRCh38.p7 | 15:55877035 | tttttgcaatttttt[A/T]aaatctgaaattctt | 4734 |
rs1152723 | snp | A/G | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55986470 | ttggcaggaatcata[A/G]aaatgatgctgtgtt | 4734 |
rs1152724 | snp | C/G | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55986753 | aaaaaaaaaaaatta[C/G]ccgggtgtggtggtg | 4734 |
rs1509406 | snp | C/T | 0.425894 | 0.177655 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55937562 | AATGTTTTAGCTAGT[C/T]ACATTTACCAAATAT | 4734 |
rs1509407 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | NEDD4 | GRCh38.p7 | 15:55990189 | ATATCACAATGTAAT[A/C]ATAATAGAAGTAGAG | 4734 |
rs1509408 | snp | A/C | 0.204496 | 0.245824 | upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55994115 | TAAGGGTGTCATTCC[A/C]ATAAGAAGCTGGACC | 4734 |
rs1553739 | snp | C/T | 0.299411 | 0.245069 | intron-variant | NEDD4 | GRCh38.p7 | 15:55950679 | gagaagcagaaatga[C/T]gagggcagacaactc | 4734 |
rs1605837 | snp | A/G | 0.338523 | 0.233803 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943663 | gggctctgcccctgc[A/G]atatccagacttctg | 4734 |
rs1863757 | snp | C/T | 0.439224 | 0.163383 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858582 | aaagtgctgggatta[C/T]aggcgtgagccacca | 4734 |
rs1863758 | snp | A/G | 0.471483 | 0.115954 | intron-variant | NEDD4 | GRCh38.p7 | 15:55858832 | ATCCAGACAGTAAAT[A/G]CTGGCTGTGGGCCAT | 4734 |
rs1912394 | snp | C/T | 0.495671 | 0.0463237 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866481 | CGTTAAGTTTTTATA[C/T]TTTACTCTTTTGAGA | 4734 |
rs1912395 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866506 | TTGAGAAAATATAAA[C/T]TTAACATTTTTTGGT | 4734 |
rs1912396 | snp | G/T | 0.189261 | 0.242509 | intron-variant | NEDD4 | GRCh38.p7 | 15:55878870 | tcttgtcgcccaggc[G/T]ggggtgcaatggcgc | 4734 |
rs1912397 | snp | G/T | 0.0622301 | 0.165053 | intron-variant | NEDD4 | GRCh38.p7 | 15:55879035 | TACCATGTTGGCCAG[G/T]CTAGTCTCAAACTAC | 4734 |
rs1912398 | snp | G/T | 0.449853 | 0.150196 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866905 | TTTATAAAATAACTT[G/T]CTAAGTATCAATGAA | 4734 |
rs1912399 | snp | A/G | 0.479824 | 0.098392 | intron-variant | NEDD4 | GRCh38.p7 | 15:55884045 | ccaccatgtctggct[A/G]atgtttgtattttta | 4734 |
rs1912401 | snp | A/G | 0.16618 | 0.23553 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869411 | GGCCATTCCTTCTAC[A/G]GAAATATCCTTAGAG | 4734 |
rs1912402 | snp | C/T | 0.459059 | 0.137093 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869721 | ATAAAACTTTAACAC[C/T]GGGAGAAAAGTATTC | 4734 |
rs1912403 | snp | C/T | 0.136828 | 0.222917 | missense, intron-variant, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55916735 | GTCTTTTGAAGCACA[C/T]GTGAACATGGCTATC | 4734 |
rs1912404 | snp | A/G | 0.336245 | 0.234652 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920391 | TGTGTACAGGTGTAT[A/G]TCTTAGACTGGTGAC | 4734 |
rs1912405 | snp | G/T | 0.439363 | 0.163222 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871094 | TGGATTTGGCAAATT[G/T]AGTGTATCCTTTCAT | 4734 |
rs1912406 | snp | C/T | 0.439363 | 0.163222 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871139 | ATCCTGATGCTTATT[C/T]CCAAGGCCGCTAATG | 4734 |
rs1912407 | snp | C/T | 0.434543 | 0.168653 | intron-variant | NEDD4 | GRCh38.p7 | 15:55872678 | ACATCACAACTCAAA[C/T]GAAAACTAGCTGAGC | 4734 |
rs1912408 | snp | A/G | 0.121022 | 0.21416 | intron-variant | NEDD4 | GRCh38.p7 | 15:55873442 | TCCTCACTTTTCTAC[A/G]AGAGACGCCACTCTT | 4734 |
rs1912409 | snp | C/T | 0.495745 | 0.0459295 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866297 | TGCCCAAATTTCATT[C/T]TCTTCTTTCCTTATA | 4734 |
rs1973571 | snp | A/G | 0.299158 | 0.245119 | intron-variant | NEDD4 | GRCh38.p7 | 15:55949897 | atggcacgtgtatac[A/G]tatgtaacaaacctg | 4734 |
rs1983192 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55985249 | TGACTGCTCTGCGCC[A/C]GGAACAGAAAAGGAG | 4734 |
rs1991404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55862168 | GAACAGAAAATATCT[A/G]TAAAAGTGCTTGGCA | 4734 |
rs2036742 | snp | A/G | 0.403684 | 0.197183 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985203 | CTTTTATAGGTAATT[A/G]GGAATTCATATATCA | 4734 |
rs2036743 | snp | A/G | 0.401215 | 0.199083 | intron-variant | NEDD4 | GRCh38.p7 | 15:55984265 | TCCTGCTACTAATAC[A/G]CAAATAAAATAATTT | 4734 |
rs2089634 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960568 | gcaaggaagccagtc[A/C]gagtcccaaaacctc | 4734 |
rs2089635 | snp | C/T | 0.424814 | 0.178718 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944390 | gatctcagactgctg[C/T]gctagcagtgagcaa | 4734 |
rs2089636 | snp | A/G | 0.424814 | 0.178718 | intron-variant | NEDD4 | GRCh38.p7 | 15:55944116 | gtccaaatgagatga[A/G]ccaggcacctcaggt | 4734 |
rs2102465 | snp | A/G | 0.422158 | 0.181278 | intron-variant | NEDD4 | GRCh38.p7 | 15:55960411 | ggaagcatccagcac[A/G]agagaaagatgaagg | 4734 |
rs2136385 | snp | G/T | 0.489665 | 0.0711382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943047 | aatcatctctttcaa[G/T]ttcaaagttccacag | 4734 |
rs2136386 | snp | A/C/G | 0.126564 | 0.217402 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936790 | AAAAAAAAAAGAAAA[A/C/G]AAATAGCAAATTATA | 4734 |
rs2175104 | snp | C/T | 0.126219 | 0.217206 | intron-variant, upstream-variant-2KB | NEDD4 | GRCh38.p7 | 15:55936478 | GCCATAATTTCATCT[C/T]GATAAACCACCACTG | 4734 |
rs2175236 | snp | G/T | 0.439224 | 0.163383 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871265 | AAAGTTTCTCTACAA[G/T]TGTATGTTTCATGTC | 4734 |
rs2175237 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | NEDD4 | GRCh38.p7 | 15:55871328 | ACTTAATGGGGCTCA[A/C]ACAAATTTAGGAATG | 4734 |
rs2271288 | snp | A/T | 0.303688 | 0.244167 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924554 | CACCCCCAAGCCATC[A/T]CTCAAATCCCAGACT | 4734 |
rs2271289 | snp | C/T | 0.440057 | 0.162414 | intron-variant | NEDD4 | GRCh38.p7 | 15:55924595 | TTCCCCTGGCTGCTC[C/T]ACTGAAATGTACCCT | 4734 |
rs2288344 | snp | G/T | 0.453818 | 0.144769 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830149 | AGTAAGACGTAGGAC[G/T]GGGTTCTGGGCATGG | 4734 |
rs2288345 | snp | C/T | 0.472709 | 0.11358 | intron-variant | NEDD4 | GRCh38.p7 | 15:55830263 | TGGAATGTTCTAGCC[C/T]GTCTTGGGACAGCCC | 4734 |
rs2288346 | snp | C/T | 0.186315 | 0.241757 | intron-variant | NEDD4 | GRCh38.p7 | 15:55846955 | CTTAAGTATTTATTA[C/T]AAACATGACTAACCT | 4734 |
rs2303579 | snp | C/T | 0.383349 | 0.211467 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860531 | GATGGGAAGGCCTGG[C/T]TGCTATACATGGTGG | 4734 |
rs2303580 | snp | C/T | 0.383548 | 0.211363 | missense, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55860674 | ACCTCGGAAGACTCT[C/T]GGTTGTCAACACTTT | 4734 |
rs2414444 | snp | C/T | 0.477175 | 0.104362 | intron-variant | NEDD4 | GRCh38.p7 | 15:55835919 | CTTCCTTCTCCCTCA[C/T]TGAAATTCAGAGAAA | 4734 |
rs2414445 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849797 | TTTTAAGTAAttttt[C/T]tttttttttttttga | 4734 |
rs2414446 | snp | C/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55849815 | tttttttttttgaga[C/T]ggagtctcgctctgt | 4734 |
rs2414447 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | NEDD4 | GRCh38.p7 | 15:55866261 | TTTATAAGAATTGTT[A/C]TCTCTATTTTTTCTT | 4734 |
rs2414448 | snp | A/G | 0.439363 | 0.163222 | intron-variant | NEDD4 | GRCh38.p7 | 15:55870268 | ATGTGCTTTAGGGAT[A/G]CTAATCTGGCCATAT | 4734 |
rs2414449 | snp | C/T | 0.427727 | 0.175821 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880041 | atgcctgtaatcaat[C/T]ccagcactttgggag | 4734 |
rs2414450 | snp | C/T | 0.492137 | 0.0622048 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880246 | gcagtgagccgagat[C/T]gcaccattgcacgct | 4734 |
rs2414451 | snp | G/T | 0.189576 | 0.242588 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880454 | tacacaaacctgaaa[G/T]ataagagagtacttc | 4734 |
rs2414452 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883695 | cacacacacacacac[A/C]aacacacacacacac | 4734 |
rs2414453 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883697 | cacacacacacacaa[A/C]cacacacacacacac | 4734 |
rs2414454 | snp | A/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883698 | ACACACACACACAAA[A/C]ACACACACACACACA | 4734 |
rs2438128 | snp | A/G | 0.43978 | 0.162738 | intron-variant | NEDD4 | GRCh38.p7 | 15:55855654 | GGCCTTAGTAGACTG[A/G]TGGATGTGATATTGC | 4734 |
rs2438129 | snp | C/T | 0.493293 | 0.0575177 | intron-variant | NEDD4 | GRCh38.p7 | 15:55844339 | CTTTACACCCTGTCC[C/T]GTCAGCTTCTGAGAA | 4734 |
rs2556570 | snp | C/G | | | | | GRCh38.p7 | 15:55892405 | ATAATTTCTTCACAG[C/G]CAGAGGCCAACAAGA | 4734 |
rs2899593 | snp | C/T | 0.0685596 | 0.171987 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55828523 | GCCTTATTCTGCTTA[C/T]GCCTACTTTTGATTG | 4734 |
rs2899594 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NEDD4 | GRCh38.p7 | 15:55869889 | AATAAATAAATAAAT[A/C]AATAATTGTTATGAC | 4734 |
rs3049220 | in-del | -/C | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883694 | ACACACACACACACA[-/C]AAACACACACACACA | 4734 |
rs3049242 | in-del | -/ACAC | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883721 | cacacacacacacac[-/ACAC]acagaaagagaaaga | 4734 |
rs3049244 | in-del | -/CA | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55883727 | acacacacacacaca[-/CA]gaaagagaaagagag | 4734 |
rs3049245 | snp | C/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55965691 | atgtatgtatgtatg[C/T]atgcatgtttgtatg | 4734 |
rs3049246 | in-del | -/AC/ACAC | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55985788 | CACACACACACACAC[-/AC/ACAC]GCTTAACTGTTCAGA | 4734 |
rs3088077 | snp | C/T | 0.331179 | 0.236453 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827379 | GTTTCTTCCAGACCA[C/T]GAGCCCCTAGTGGGA | 4734 |
rs3217300 | in-del | -/ACT | 0.0222698 | 0.103145 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860650 | GAGAACTAGGAAACT[-/ACT]TATACCTCGGAAGAC | 4734 |
rs3759865 | snp | A/G | 0.315273 | 0.241329 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848189 | TATTGCGTAGGGTAA[A/G]GATAATGACGTTATA | 4734 |
rs3759866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD4 | GRCh38.p7 | 15:55848282 | TGTGCTTTCCTCTCA[A/G]TGCCTGTAGGGTTAT | 4734 |
rs3833005 | in-del | -/ACTTT | 0.333261 | 0.235728 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827783 | TGTCTCTTAGAAGTC[-/ACTTT]ACTTTTAAATGATTC | 4734 |
rs4144243 | snp | C/T | 0.206947 | 0.246265 | intron-variant | NEDD4 | GRCh38.p7 | 15:55989550 | GCCCTTCTTACCCTG[C/T]TACTTATGCACTGTT | 4734 |
rs4145115 | snp | C/G | 0.0926964 | 0.194308 | utr-variant-3-prime, nc-transcript-variant | NEDD4 | GRCh38.p7 | 15:55827361 | CTGTGTTGCTTGATA[C/G]ATGTTTCTTCCAGAC | 4734 |
rs4296197 | snp | A/C | 0.0640965 | 0.167152 | intron-variant | NEDD4 | GRCh38.p7 | 15:55928605 | CTTCTGAGCATGTTA[A/C]GGTCTATCCACTTGC | 4734 |
rs4340270 | snp | A/T | | | intron-variant | NEDD4 | GRCh38.p7 | 15:55904896 | TTGGGAGTTTGAGAC[A/T]AGCCTGACCAACATG | 4734 |
rs4461012 | snp | A/T | 0.137527 | 0.223271 | intron-variant | NEDD4 | GRCh38.p7 | 15:55841178 | gcattgtgatccacc[A/T]gccttggcctcccaa | 4734 |
rs4480735 | snp | G/T | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55880022 | tggctgggcatggtg[G/T]ctcatgcctgtaatc | 4734 |
rs4492984 | snp | A/C | 0.321053 | 0.23969 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972079 | ctggacaaacaaaag[A/C]tgagggatttaatca | 4734 |
rs4509960 | snp | A/C | 0 | 0 | intron-variant | NEDD4 | GRCh38.p7 | 15:55943352 | atctttgtggcagct[A/C]ctcctatcacagccc | 4734 |
rs4609780 | snp | C/T | 0.321053 | 0.23969 | intron-variant | NEDD4 | GRCh38.p7 | 15:55972129 | agaaatgctaaaggg[C/T]gtcccacagtctaaa | 4734 |
rs4640119 | snp | C/T | 0.499087 | 0.0213463 | intron-variant | NEDD4 | GRCh38.p7 | 15:55902993 | GTGACAGAGCGAGAC[C/T]CCATCTCAAATAAAA | 4734 |
rs4774228 | snp | A/G | 0.0143543 | 0.0834931 | intron-variant | NEDD4 | GRCh38.p7 | 15:55860400 | ACAAAATCTAAGAGC[A/G]TCTTACTGAGCTCGA | 4734 |
rs4774229 | snp | A/G | 0.35445 | 0.227135 | intron-variant | NEDD4 | GRCh38.p7 | 15:55893210 | CTTACATTTGTATTA[A/G]TATCTTAATCATTGT | 4734 |
rs4774831 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD4 | GRCh38.p7 | 15:55853881 | ctgtaatcccagcta[C/T]tcaggaggctgagac | 4734 |
rs4774833 | snp | A/G | 0.316968 | 0.240864 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55917970 | ACATCAAATAAACAT[A/G]TCTCAATGCCAATTC | 4734 |
rs4774834 | snp | A/G | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant | NEDD4 | GRCh38.p7 | 15:55918105 | TTTCTTTATATAAAC[A/G]AAGTACATACTTGTT | 4734 |
rs4774835 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NEDD4 | GRCh38.p7 | 15:55920769 | TAATGACACAGGTCA[C/T]TTGTTGCTATACAAT | 4734 |
rs4774836 | snp | A/T | 0.160938 | 0.233598 | intron-variant | NEDD4 | GRCh38.p7 | 15:55921089 | TGTTAAATGACATTT[A/T]ATATTTGTATCATGA | 4734 |
rs4774837 | snp | G/T | 0.148326 | 0.228391 | intron-variant | NEDD4 | GRCh38.p7 | 15:55963576 | CTTTATGTTATAGTT[G/T]TTTTATGTATTCCAT | 4734 |