SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs904802 | snp | C/T | 0.0595944 | 0.162005 | intron-variant | WWP2 | GRCh38.p7 | 16:69936468 | GTGAGTCTCAGGCGC[C/T]GGGGGCTCCGCTCCA | 11060 |
rs904803 | snp | A/G | 0.261056 | 0.249755 | intron-variant | WWP2 | GRCh38.p7 | 16:69936626 | GAGCTGGGGGAACCA[A/G]AGCCGAGGTCCTTAG | 11060 |
rs904804 | snp | A/G | 0.241627 | 0.24986 | intron-variant | WWP2 | GRCh38.p7 | 16:69926702 | GCGTAAGGGATCCCC[A/G]AGCTGAACATCAACA | 11060 |
rs904805 | snp | C/T | 0.247621 | 0.249989 | intron-variant | WWP2 | GRCh38.p7 | 16:69926589 | TGACTAAGTGGTACC[C/T]TGCAGGTATAACAGG | 11060 |
rs904806 | snp | C/T | 0.247621 | 0.249989 | intron-variant | WWP2 | GRCh38.p7 | 16:69926361 | TTTACCGTCTTCTGC[C/T]GGCCTAACCAATAAA | 11060 |
rs904807 | snp | C/G | 0.247621 | 0.249989 | intron-variant | WWP2 | GRCh38.p7 | 16:69926085 | GAGGCGGCTACCAAG[C/G]GCGAGGAGAAATCTA | 11060 |
rs904808 | snp | A/G | 0.240765 | 0.249829 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924592 | ATTAGAATCCCCCCC[A/G]CACCCCCTCCAGCCA | 11060 |
rs904809 | snp | C/T | 0.414905 | 0.187899 | intron-variant | WWP2 | GRCh38.p7 | 16:69917388 | CAATCTCAGGACATC[C/T]GCTAGCAAATCTAGG | 11060 |
rs904810 | snp | A/G | 0.4087 | 0.193169 | intron-variant | WWP2 | GRCh38.p7 | 16:69916753 | CTCACCTTCATGACC[A/G]GCTGTCACCCTTCAT | 11060 |
rs1000640 | snp | C/G | 0.189639 | 0.242604 | intron-variant | WWP2 | GRCh38.p7 | 16:69871765 | GACAGACATAAGTCA[C/G]TGTGAAAAGGACAGA | 11060 |
rs1052429 | snp | A/G | 0.242201 | 0.249878 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941457 | GCTTGCCACAGCGCA[A/G]CCTCTTCTGTCCCTT | 11060 |
rs1057877 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69930993 | TTGAAGAATAAAAAA[A/G]AAAATCTAGAAAAAA | 11060 |
rs1112183 | snp | C/T | 0.209388 | 0.246679 | intron-variant | WWP2 | GRCh38.p7 | 16:69905070 | CCCAAATAAGGCAGA[C/T]GCCCAGCTGTAGCTG | 11060 |
rs1116544 | snp | C/T | 0.448066 | 0.152544 | intron-variant | WWP2 | GRCh38.p7 | 16:69868948 | GCTGGAGTGCAGTGG[C/T]ACAATCTCGGCTCAC | 11060 |
rs1318651 | snp | A/G | 0.31721 | 0.240796 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838416 | GTACTGGATCTTGGC[A/G]TAATAGAGGAGGGAG | 11060 |
rs1353985 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823801 | ATCACCTTGTCTTCA[A/G]AAGAAACTTTTCTGC | 11060 |
rs1466863 | snp | A/T | 0.472896 | 0.113214 | intron-variant | WWP2 | GRCh38.p7 | 16:69870235 | GTGCCTGGAACATAA[A/T]GTTAGAGTTCAGTGA | 11060 |
rs1500337 | snp | C/T | 0.371177 | 0.218669 | intron-variant | WWP2 | GRCh38.p7 | 16:69867981 | GGGCCAGCTTTTCAT[C/T]ACAATATGATCCCAT | 11060 |
rs1532637 | snp | C/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69858773 | ACTTCAACTCTGCCA[C/G]AAAAGAATGTTACTT | 11060 |
rs1566451 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69929195 | CCTCCCTCCGACCAA[C/T]CAACCAAAGAAGTGC | 11060 |
rs1566452 | snp | A/G | 0.345717 | 0.230951 | synonymous-codon, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929452 | TCATGTGGCAGAGAA[A/G]AGACAGGACAATGGA | 11060 |
rs1566453 | snp | C/T | 0.430136 | 0.173352 | intron-variant | WWP2 | GRCh38.p7 | 16:69865884 | atcagaaaggaatgc[C/T]ggtcagttgctgtgt | 11060 |
rs1566454 | snp | C/T | 0.362523 | 0.223246 | intron-variant | WWP2 | GRCh38.p7 | 16:69866180 | gtattgtggactgtc[C/T]tgtcatttttttgga | 11060 |
rs1566455 | snp | G/T | 0.362523 | 0.223246 | intron-variant | WWP2 | GRCh38.p7 | 16:69866261 | TGCTTTTTAAAAAAA[G/T]GTTTCACATtttatt | 11060 |
rs1566456 | snp | C/G | 0.472803 | 0.113397 | intron-variant | WWP2 | GRCh38.p7 | 16:69866323 | ttatttatttatGga[C/G]acggagtcttcctac | 11060 |
rs1566457 | snp | C/T | 0.448323 | 0.15221 | intron-variant | WWP2 | GRCh38.p7 | 16:69870538 | actcctgggctcaag[C/T]gatcctcccgccttg | 11060 |
rs1875245 | snp | A/G | 0.0744216 | 0.177967 | synonymous-codon, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929500 | CCATAACACTCGCAC[A/G]ACCCAGTGGGAGGAT | 11060 |
rs1983015 | snp | A/G | 0.241627 | 0.24986 | intron-variant | WWP2 | GRCh38.p7 | 16:69927089 | GTGGTCAGAGTCGAT[A/G]CTGTTAATGAACGAT | 11060 |
rs1983016 | snp | A/G | 0.348394 | 0.229823 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936426 | GAGCATCCGGGTCAC[A/G]GAGGAGAACAAGGAA | 11060 |
rs2047597 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | WWP2 | GRCh38.p7 | 16:69873945 | TAGGTACCATTACTT[A/G]TTGTCCTTATCTCTA | 11060 |
rs2088747 | snp | A/G | 0.296873 | 0.245566 | intron-variant | WWP2 | GRCh38.p7 | 16:69834440 | TCCTCTCCCAGCTTA[A/G]CATTCTTCATCCCCC | 11060 |
rs2102066 | snp | A/G | 0.333172 | 0.235759 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933190 | GGCACCCTCTGCGTC[A/G]ACGGACTCCTCGTCT | 11060 |
rs2102067 | snp | A/G | 0.360842 | 0.224085 | intron-variant | WWP2 | GRCh38.p7 | 16:69847209 | cctgtctcatcctcc[A/G]gagtagctgggacta | 11060 |
rs2102068 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917233 | atatcaccaaggaat[G/T]ggcttttctcccatt | 11060 |
rs2133796 | snp | G/T | 0.499801 | 0.00998203 | intron-variant | WWP2 | GRCh38.p7 | 16:69927091 | GGTCAGAGTCGATAC[G/T]GTTAATGAACGATCA | 11060 |
rs2133798 | snp | G/T | 0.237593 | 0.249692 | intron-variant | WWP2 | GRCh38.p7 | 16:69876354 | GGCATGTTTTTTGGG[G/T]TTTTTTTTTTTTTTC | 11060 |
rs2133799 | snp | C/T | 0.473359 | 0.112298 | intron-variant | WWP2 | GRCh38.p7 | 16:69879123 | TTCATAGTATTTGAT[C/T]ATTTGTCCTTCCGAG | 11060 |
rs2173714 | snp | C/G | 0.492727 | 0.0598633 | intron-variant | WWP2 | GRCh38.p7 | 16:69844631 | TGTTGAGAATGACAC[C/G]AGGTCATCGGTGTTG | 11060 |
rs2228705 | snp | A/G | 0.46875 | 0.121031 | intron-variant | WWP2 | GRCh38.p7 | 16:69883554 | aagaaaGTTTGTGCT[A/G]TACCTTGAGTTCAGA | 11060 |
rs2270838 | snp | A/G | 0.499974 | 0.00359416 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925320 | CATTCCCTGCAAAGC[A/G]CTCAAATGTGGAAGC | 11060 |
rs2270839 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69929993 | CTCACGACTTGGGTC[A/G]TGCTTCTTGGGTGCA | 11060 |
rs2270840 | snp | A/T | 0.343622 | 0.231808 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931121 | TTTCTGAGAAATCGC[A/T]TGAACCCCTGAACAT | 11060 |
rs2270841 | snp | C/T | 0.34753 | 0.230191 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69933994 | TTTCCTCCTGTCTCA[C/T]GAGGTGCTCAACCCT | 11060 |
rs2270842 | snp | G/T | 0.240478 | 0.249819 | intron-variant | WWP2 | GRCh38.p7 | 16:69936097 | GGCCCCTGAGCTCTT[G/T]TCCAGCCTCTATAAG | 11060 |
rs2270843 | snp | A/G | 0.298398 | 0.245271 | intron-variant | WWP2 | GRCh38.p7 | 16:69939224 | ACGTCAGTGGGATGG[A/G]GAAGAGCTGTGGCCT | 11060 |
rs2270844 | snp | C/T | 0.129451 | 0.219016 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939394 | GGCAAGGAAACCTGG[C/T]TGCCCAGAAGCCACA | 11060 |
rs2291959 | snp | G/T | 0.457916 | 0.138962 | intron-variant | WWP2 | GRCh38.p7 | 16:69840089 | ACTTGGGGTGCATTC[G/T]CTTTAGCCCATCCAT | 11060 |
rs2291960 | snp | C/T | 0.246037 | 0.249969 | intron-variant | WWP2 | GRCh38.p7 | 16:69840295 | TCCTCAGGACTGTGC[C/T]GGGACAGGGTGGGGC | 11060 |
rs2291961 | snp | A/G | 0.241627 | 0.24986 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931689 | ACTTTCCAGGGCGTG[A/G]GTCTTGGTGACTGTG | 11060 |
rs2362636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69849096 | CTCTAAATAGATCAT[C/T]AACTGTGTCTGCAGA | 11060 |
rs2362637 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868688 | acacacacacacaca[C/G]acacagacatacaca | 11060 |
rs2362638 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868698 | acacacacacagaca[C/T]acacacacagatata | 11060 |
rs2362641 | snp | A/T | 0.396727 | 0.202413 | intron-variant | WWP2 | GRCh38.p7 | 16:69881858 | caccacacccagcta[A/T]ttttttctattttta | 11060 |
rs2362642 | snp | A/G | 0.348354 | 0.22984 | intron-variant | WWP2 | GRCh38.p7 | 16:69897555 | AAACTGCTATACGGT[A/G]TTCTGTTACATGAAC | 11060 |
rs2362643 | snp | A/G | 0.301177 | 0.244706 | intron-variant | WWP2 | GRCh38.p7 | 16:69911629 | CAGTCACTGTTCTGT[A/G]CAAGATTTCAACTGA | 11060 |
rs2362644 | snp | A/C | 0.302435 | 0.244439 | intron-variant | WWP2 | GRCh38.p7 | 16:69912301 | catctcaaaaaaaaa[A/C]aaaacaaaaCCTCAT | 11060 |
rs2885566 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868692 | acacacacacacaca[C/T]agacatacacacaca | 11060 |
rs2885567 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868694 | acacacacacacaca[C/G]acatacacacacaga | 11060 |
rs2937120 | snp | G/T | 0.315758 | 0.241197 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839207 | ACGGGGTCCGTCCAC[G/T]CCACACCTTACAAAA | 11060 |
rs2937121 | snp | A/C | 0.367913 | 0.220446 | intron-variant | WWP2 | GRCh38.p7 | 16:69836506 | AGACCTCTGGCTGTC[A/C]CCATGATAACCAAGT | 11060 |
rs2937123 | snp | A/G | 0.316243 | 0.241064 | intron-variant | WWP2 | GRCh38.p7 | 16:69832602 | tgagctgagatccat[A/G]tcactgcactccgga | 11060 |
rs2937124 | snp | A/G | 0.343701 | 0.231776 | intron-variant | WWP2 | GRCh38.p7 | 16:69828206 | AAAGGAAGGTGGATT[A/G]GGCACTCATGTCCTC | 11060 |
rs2937125 | snp | A/T | 0.231775 | 0.249335 | intron-variant | WWP2 | GRCh38.p7 | 16:69827670 | CCTCTCTCAGTTGCC[A/T]GGTATCAAAGCCATG | 11060 |
rs2937126 | snp | G/T | 0.300926 | 0.244758 | intron-variant | WWP2 | GRCh38.p7 | 16:69821408 | CTCAGTGACACAGGG[G/T]GCAGGATTGTTGGAA | 11060 |
rs2937127 | snp | A/G | 0.359364 | 0.22481 | intron-variant | WWP2 | GRCh38.p7 | 16:69821358 | GTGTTTACTTTTTGA[A/G]ACTTGTGGCTAAAAG | 11060 |
rs2965755 | snp | C/T | 0.226484 | 0.248892 | intron-variant | WWP2 | GRCh38.p7 | 16:69824833 | TGCAGTACAGTGGTG[C/T]GATCTTGGCTCACTG | 11060 |
rs2965756 | snp | A/G | 0.316 | 0.241131 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839267 | TGGTAATTATTAAAC[A/G]GCCCTGAACTGAAGG | 11060 |
rs2965758 | snp | C/T | 0.184521 | 0.241273 | intron-variant | WWP2 | GRCh38.p7 | 16:69835652 | CAATTTACCTTCAAA[C/T]GGCTCAGGAAAAAAA | 11060 |
rs2965759 | snp | C/T | 0.29432 | 0.24604 | intron-variant | WWP2 | GRCh38.p7 | 16:69835100 | TAGGTTTAGTGAGTC[C/T]ATTTCCATAACTGGA | 11060 |
rs2965760 | snp | A/G | 0.315758 | 0.241197 | intron-variant | WWP2 | GRCh38.p7 | 16:69834230 | cagctggagtggagc[A/G]agggaagagaggagc | 11060 |
rs2965761 | snp | A/C | 0.315516 | 0.241263 | intron-variant | WWP2 | GRCh38.p7 | 16:69834156 | ggacaaggtccttgg[A/C]aattgctcaacatgg | 11060 |
rs2965762 | snp | C/T | 0.348354 | 0.22984 | intron-variant | WWP2 | GRCh38.p7 | 16:69830655 | AATGCTGACTCTGCT[C/T]ACTCCACCTCCCCGC | 11060 |
rs2965763 | snp | C/T | 0.302435 | 0.244439 | intron-variant | WWP2 | GRCh38.p7 | 16:69830408 | TGTTTCTTGTTCATT[C/T]ATTCAGGAAACATTT | 11060 |
rs2965764 | snp | A/T | 0.349671 | 0.229272 | intron-variant | WWP2 | GRCh38.p7 | 16:69830157 | GACCCACCTAGGCAA[A/T]GTGGTGAAACCCCAT | 11060 |
rs3051438 | in-del | -/AC/CA/CACA/CACT | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69885141 | ACACACACACACACA[-/AC/CA/CACA/CACT]TTCTTCTTCTTTAGA | 11060 |
rs3051446 | in-del | -/ACACAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912401 | cacacacacacacac[-/ACACAC]acacaGCCTCATGAC | 11060 |
rs3086443 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838461 | AAAAAAAAAAAAAAA[-/AAA]GCCCACaataatcaa | 11060 |
rs3180763 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909114 | CCGCCGTACCCTATG[C/T]CCAGCCTGTCCCTAA | 11060 |
rs3192882 | snp | A/T | 0.293037 | 0.246268 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941728 | TCTTGTGCAATAAAC[A/T]ATCAGCAGCTGTGGG | 11060 |
rs3215101 | in-del | -/CT/TC | 0.42 | 0.183303 | intron-variant | WWP2 | GRCh38.p7 | 16:69917945 | TGCGAATGTGCAGCC[-/CT/TC]ACGTGTTCTCTGTTG | 11060 |
rs3748386 | snp | C/T | 0.49621 | 0.0433651 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940756 | TCCTGAGAGGCGTGG[C/T]TGTTTGGGAAACTCT | 11060 |
rs3748387 | snp | C/T | 0.495135 | 0.0490805 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940643 | AAAAACCTGCAACCC[C/T]ACAACACAACCACTT | 11060 |
rs3748388 | snp | G/T | 0.242201 | 0.249878 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940545 | AGACAAACCTTCATT[G/T]GCTGAGAATGAATTA | 11060 |
rs3748389 | snp | C/T | 0.490146 | 0.0694958 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939922 | CTCCTGTCCAAAGCC[C/T]TCGGTCTCCTCAATG | 11060 |
rs3762177 | snp | C/T | 0.24019 | 0.249807 | intron-variant | WWP2 | GRCh38.p7 | 16:69938062 | TTTTTGTATGCTGTA[C/T]TTCATAACGACAACA | 11060 |
rs3762178 | snp | A/G | 0.231482 | 0.249313 | intron-variant | WWP2 | GRCh38.p7 | 16:69927861 | CAGCCTGGGCAACAC[A/G]GCGAGACTTCATCTC | 11060 |
rs3790075 | snp | C/T | 0.409212 | 0.192748 | intron-variant | WWP2 | GRCh38.p7 | 16:69873908 | AATGTAGGGGAAATA[C/T]AGCTCTATTGAAATG | 11060 |
rs3790076 | snp | A/C | 0.409552 | 0.192466 | intron-variant | WWP2 | GRCh38.p7 | 16:69873542 | CCGGATGTTCCAGCA[A/C]AAGGATACAGTGGGT | 11060 |
rs3790078 | snp | A/G | 0.362732 | 0.22314 | intron-variant | WWP2 | GRCh38.p7 | 16:69872279 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 11060 |
rs3790079 | snp | C/G | 0.192715 | 0.243348 | intron-variant | WWP2 | GRCh38.p7 | 16:69871310 | ATGCATATGTTGACA[C/G]TTTTTGTTGTTGTCA | 11060 |
rs3790080 | snp | C/T | 0.362523 | 0.223246 | intron-variant | WWP2 | GRCh38.p7 | 16:69868236 | TAGGGGCAGCTGGGA[C/T]CACTTTGCATGAACT | 11060 |
rs3790082 | snp | C/T | 0.472896 | 0.113214 | intron-variant | WWP2 | GRCh38.p7 | 16:69862851 | gtgatcccagctatg[C/T]gggaggctgaggtgg | 11060 |
rs3790083 | snp | C/T | 0.471863 | 0.115225 | intron-variant | WWP2 | GRCh38.p7 | 16:69861383 | AGGTGGCAATTTCAT[C/T]AGACTAAAAAAACTC | 11060 |
rs3790084 | snp | A/G | 0.31503 | 0.241394 | intron-variant | WWP2 | GRCh38.p7 | 16:69853892 | GCCGACCACCATGGG[A/G]GATGTGGTTTTAAAG | 11060 |
rs3790085 | snp | C/T | 0.489024 | 0.0732638 | intron-variant | WWP2 | GRCh38.p7 | 16:69853817 | TGAATGACAGCACAG[C/T]AGAGGAATCTGGGAG | 11060 |
rs3790086 | snp | C/G | 0.498369 | 0.0285077 | intron-variant | WWP2 | GRCh38.p7 | 16:69853804 | AGTAGAGGAATCTGG[C/G]AGTACCCCCCTCCCT | 11060 |
rs3790087 | snp | C/T | 0.319376 | 0.240181 | intron-variant | WWP2 | GRCh38.p7 | 16:69853611 | TGGTCTCAGCCCCAC[C/T]GTATCAGACATTCCC | 11060 |
rs3790088 | snp | C/T | 0.300421 | 0.244863 | intron-variant | WWP2 | GRCh38.p7 | 16:69844258 | CCCATCATGGCTTTG[C/T]TGACACAAGATTTGC | 11060 |
rs3827939 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845915 | TTATAGGCACACACC[A/G]CCATGCCTGGCTAAT | 11060 |
rs3827940 | snp | C/G | 0.277778 | 0.248452 | intron-variant | WWP2 | GRCh38.p7 | 16:69845913 | ATAGGCACACACCAC[C/G]ATGCCTGGCTAATTT | 11060 |