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 |
rs3827941 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845912 | taggcacacaccccc[A/T]tgcctggctaatttt | 11060 |
rs3827942 | snp | C/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845911 | AGGCACACACCACCA[C/G/T]GCCTGGCTAATTTTT | 11060 |
rs3842520 | in-del | -/C | 0.335101 | 0.23507 | intron-variant | WWP2 | GRCh38.p7 | 16:69844518 | TCAAGAATTTAGATC[-/C]AAACTTGTTAATAGC | 11060 |
rs3902822 | snp | A/G | 0.110167 | 0.207236 | intron-variant | WWP2 | GRCh38.p7 | 16:69885075 | ACTCCCCCTACACAC[A/G]CACACCACTCTTTTA | 11060 |
rs4078387 | snp | C/T | 0.448836 | 0.15154 | intron-variant | WWP2 | GRCh38.p7 | 16:69780144 | AGTATAAAAGTACGA[C/T]GGGAAGGAACCACAC | 11060 |
rs4146819 | snp | G/T | 0.396546 | 0.202545 | intron-variant | WWP2 | GRCh38.p7 | 16:69889660 | CCGGTTCAGAAGCAT[G/T]CCCTTCCTTTAGGGC | 11060 |
rs4247105 | snp | C/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69812477 | cccCCAACCCCCCCC[C/T]ttttttttttttttt | 11060 |
rs4247109 | snp | A/G | 0.284995 | 0.247539 | intron-variant | WWP2 | GRCh38.p7 | 16:69769540 | TTTCATCTCAAGATC[A/G]GTGTTCACTGGTTTC | 11060 |
rs4275849 | snp | A/G | 0.49931 | 0.0185575 | intron-variant | WWP2 | GRCh38.p7 | 16:69798202 | CTTTAAAAAGTGTTC[A/G]TATCCTTTGGAGGAA | 11060 |
rs4296254 | snp | A/G | 0.360842 | 0.224085 | intron-variant | WWP2 | GRCh38.p7 | 16:69847365 | gctgggattacaggc[A/G]tgagccaccatgccc | 11060 |
rs4341733 | snp | C/T | 0.492287 | 0.0616198 | intron-variant | WWP2 | GRCh38.p7 | 16:69798344 | CTTGTATTGCAGTCA[C/T]TTAAGAGTGACTTAT | 11060 |
rs4464069 | snp | C/T | 0.487754 | 0.114523 | intron-variant | WWP2 | GRCh38.p7 | 16:69782381 | GCTTgaggttgagga[C/T]ggggcaggagccaac | 11060 |
rs4497676 | snp | A/G | 0.467845 | 0.122652 | intron-variant | WWP2 | GRCh38.p7 | 16:69781047 | aaaCAggttggtcct[A/G]tggtagtgggttatc | 11060 |
rs4528563 | snp | C/G | 0.202035 | 0.245356 | intron-variant | WWP2 | GRCh38.p7 | 16:69812523 | tggctctgtggccca[C/G]gctggagtgcagtgg | 11060 |
rs4580150 | snp | A/G | 0.448963 | 0.151372 | intron-variant | WWP2 | GRCh38.p7 | 16:69781050 | CAggttggtcctgtg[A/G]tagtgggttatcaga | 11060 |
rs4608327 | snp | C/G | 0.35894 | 0.225016 | intron-variant | WWP2 | GRCh38.p7 | 16:69816248 | GTATGACTGTAAAAG[C/G]TGTGTAAAATTTCAT | 11060 |
rs4609837 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69784095 | tttctttctttcttt[C/T]ttttttttttttttt | 11060 |
rs4619391 | snp | A/T | 0.289424 | 0.246872 | intron-variant | WWP2 | GRCh38.p7 | 16:69780860 | aataaatacataaat[A/T]aataaaaaaggaaaa | 11060 |
rs4985374 | snp | A/C | 0.491263 | 0.0655142 | intron-variant | WWP2 | GRCh38.p7 | 16:69835822 | TTTTTTTTTTTTTTG[A/C]GACAGAGTCTTGCTC | 11060 |
rs4985375 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69851261 | ggactcaagtgatcc[A/G]cgtgccttggccctc | 11060 |
rs4985376 | snp | A/G | 0.460925 | 0.134204 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910432 | tttttttttttagac[A/G]gagtctcgctctgtt | 11060 |
rs4985377 | snp | A/C | 0.284471 | 0.247612 | intron-variant | WWP2 | GRCh38.p7 | 16:69914594 | gagacactatctctt[A/C]gaaaaacaaaaaatt | 11060 |
rs4985378 | snp | A/G | 0.284733 | 0.247575 | intron-variant | WWP2 | GRCh38.p7 | 16:69915046 | TCAAGGACACAGAGC[A/G]GGTGTGAGATGGACA | 11060 |
rs4985379 | snp | C/T | 0.283947 | 0.247685 | intron-variant | WWP2 | GRCh38.p7 | 16:69915293 | tgaatattgatttaa[C/T]ggtgagtttccatat | 11060 |
rs4985380 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69919170 | ttcttttcttttctt[A/T]tttcttttttttaag | 11060 |
rs4985381 | snp | A/G | 0.241627 | 0.24986 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932072 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 11060 |
rs4985418 | snp | C/T | 0.487809 | 0.0771174 | intron-variant | WWP2 | GRCh38.p7 | 16:69803562 | TTCTATCTCTGAGGC[C/T]CCCCACTTCCACCCT | 11060 |
rs4985445 | snp | A/G | 0.49263 | 0.0602539 | intron-variant | WWP2 | GRCh38.p7 | 16:69833932 | CTCATGCTAGGGAGG[A/G]GGCCAGGGTAGAATC | 11060 |
rs4985446 | snp | C/T | 0.495671 | 0.0463237 | intron-variant | WWP2 | GRCh38.p7 | 16:69846390 | aagccaaacaataca[C/T]gttgtatggatacct | 11060 |
rs4985447 | snp | A/G | 0.465473 | 0.126772 | intron-variant | WWP2 | GRCh38.p7 | 16:69851263 | actcaagtgatccac[A/G]tgccttggccctcac | 11060 |
rs4985448 | snp | A/G | 0.362523 | 0.223246 | intron-variant | WWP2 | GRCh38.p7 | 16:69865492 | tctataaatttagaa[A/G]agagagcttcatttc | 11060 |
rs4985449 | snp | C/G | 0.371177 | 0.218669 | intron-variant | WWP2 | GRCh38.p7 | 16:69866957 | attcttctgcctcag[C/G]ctcctgagtagctgg | 11060 |
rs4985450 | snp | A/T | 0.448195 | 0.152377 | intron-variant | WWP2 | GRCh38.p7 | 16:69867203 | AATTACTCCACATGA[A/T]CTGTTGCAAAGGTGA | 11060 |
rs4985451 | snp | C/T | 0.302184 | 0.244493 | intron-variant | WWP2 | GRCh38.p7 | 16:69911189 | TCACTTAATCATGGC[C/T]GTCCCTGCATAGGAA | 11060 |
rs4985452 | snp | C/T | 0.301681 | 0.2446 | intron-variant | WWP2 | GRCh38.p7 | 16:69911238 | TGAGAATGGGTCCTT[C/T]TATCCGGGAGCAATA | 11060 |
rs4985453 | snp | A/G | 0.29789 | 0.24537 | intron-variant | WWP2 | GRCh38.p7 | 16:69911358 | GATCACTGTGAAACA[A/G]GAGGATTGAGGAGGC | 11060 |
rs4985454 | snp | C/T | 0.284995 | 0.247539 | intron-variant | WWP2 | GRCh38.p7 | 16:69914284 | aaacagctcaccaca[C/T]gcctagcccagagga | 11060 |
rs4985455 | snp | A/G | 0.283158 | 0.247791 | intron-variant | WWP2 | GRCh38.p7 | 16:69915055 | CAGAGCGGGTGTGAG[A/G]TGGACACACAACTGT | 11060 |
rs4985456 | snp | C/T | 0.398174 | 0.201356 | intron-variant | WWP2 | GRCh38.p7 | 16:69918754 | AGAGCAGTCTTCAAA[C/T]GTTACTGTCATTGCA | 11060 |
rs4985457 | snp | C/T | 0.444444 | 0.157135 | intron-variant | WWP2 | GRCh38.p7 | 16:69919139 | atgagccaccatccc[C/T]gaccACATTTAAAtt | 11060 |
rs4985458 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69919195 | tttaagatggagttt[C/T]gctcttgttgcccaa | 11060 |
rs4985459 | snp | A/G | 0.286564 | 0.247312 | intron-variant | WWP2 | GRCh38.p7 | 16:69919605 | ATTAGAGGGTCCACA[A/G]TGAGCTGGAGGTGGG | 11060 |
rs4985460 | snp | A/G | 0.40853 | 0.193309 | intron-variant | WWP2 | GRCh38.p7 | 16:69930471 | caacatagcgagacc[A/G]tgtctccacaacaat | 11060 |
rs4985461 | snp | C/G | 0.367503 | 0.220665 | intron-variant | WWP2 | GRCh38.p7 | 16:69939752 | CCAGTGTGGTGCAAG[C/G]CCTGTGGCCCTGCTG | 11060 |
rs4985523 | snp | A/T | 0.434976 | 0.168179 | intron-variant | WWP2 | GRCh38.p7 | 16:69763289 | TATCTTGACGAACTG[A/T]AACTAGGTAGGGTGC | 11060 |
rs4985527 | snp | C/T | 0.288646 | 0.246995 | intron-variant | WWP2 | GRCh38.p7 | 16:69778655 | TAGTTACGGTTATTT[C/T]TCTTGAGACAGAGTC | 11060 |
rs4985528 | snp | C/T | 0.288386 | 0.247035 | intron-variant | WWP2 | GRCh38.p7 | 16:69778702 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 11060 |
rs4985529 | snp | C/T | 0.288386 | 0.247035 | intron-variant | WWP2 | GRCh38.p7 | 16:69778860 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGCCCTCA | 11060 |
rs4985530 | snp | C/T | 0.206336 | 0.246157 | intron-variant | WWP2 | GRCh38.p7 | 16:69779745 | TCTAAAATATTCTTT[C/T]ATTTTTAAAGTCTGT | 11060 |
rs4985531 | snp | A/G | 0.284733 | 0.247575 | intron-variant | WWP2 | GRCh38.p7 | 16:69785128 | attccagctacccat[A/G]aggctgaggcacgag | 11060 |
rs4985547 | snp | A/G | 0.226188 | 0.248863 | intron-variant | WWP2 | GRCh38.p7 | 16:69795972 | GAGTACTAAATGCCA[A/G]TATGATCCTAGATTG | 11060 |
rs5817674 | in-del | -/AA | 0.303438 | 0.244222 | intron-variant | WWP2 | GRCh38.p7 | 16:69814454 | CTCAACACTATTTAT[-/AA]ATATTTACAAATTCC | 11060 |
rs5817675 | in-del | -/T | 0.481932 | 0.0933148 | intron-variant | WWP2 | GRCh38.p7 | 16:69870299 | TTTATTTATTTATCC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs5817677 | in-del | -/G | 0.303187 | 0.244277 | intron-variant | WWP2 | GRCh38.p7 | 16:69908706 | TCTTCCTTTCTAACA[-/G]GGGCCTATGCCTTTC | 11060 |
rs6499252 | snp | A/G | 0.139903 | 0.224452 | intron-variant | WWP2 | GRCh38.p7 | 16:69768098 | tgcctcagcctccca[A/G]agtgtttggggttac | 11060 |
rs6499253 | snp | C/T | 0.449218 | 0.151037 | intron-variant | WWP2 | GRCh38.p7 | 16:69768769 | TAGCCTGTAATTCCA[C/T]GGGGCTTCCAATAGT | 11060 |
rs6499255 | snp | A/G | 0.488545 | 0.074807 | intron-variant | WWP2 | GRCh38.p7 | 16:69796425 | atcccgcagctaggc[A/G]agatcatctggtgaa | 11060 |
rs6499256 | snp | A/G | 0.123105 | 0.215401 | intron-variant | WWP2 | GRCh38.p7 | 16:69796753 | TTTCTACCCTGGGCC[A/G]TGCCTCAGTACCACA | 11060 |
rs6499257 | snp | G/T | 0.492087 | 0.0623997 | intron-variant | WWP2 | GRCh38.p7 | 16:69799760 | AGTATTACAAATAGT[G/T]CCCTGTGCTTACTCG | 11060 |
rs6499259 | snp | C/G | 0.299411 | 0.245069 | intron-variant | WWP2 | GRCh38.p7 | 16:69829777 | CTGAATTAATTGTAA[C/G]GTTCCTAAAAGCAGG | 11060 |
rs6499260 | snp | A/G | 0.488965 | 0.0734569 | intron-variant | WWP2 | GRCh38.p7 | 16:69830772 | AGCCGAAGAGCCATC[A/G]TAACAGTAAATCCTG | 11060 |
rs6499261 | snp | C/G | 0.0901694 | 0.192235 | intron-variant | WWP2 | GRCh38.p7 | 16:69850152 | agcactttgggaggc[C/G]aaggtgggcagatca | 11060 |
rs6499262 | snp | A/G | 0.107694 | 0.205546 | intron-variant | WWP2 | GRCh38.p7 | 16:69850244 | acaaaaaaattagcc[A/G]ggcgtggtggtgtgc | 11060 |
rs6499263 | snp | C/T | 0.36315 | 0.222928 | intron-variant | WWP2 | GRCh38.p7 | 16:69856246 | atttatataacatcc[C/T]ggaaaaggcaaaatt | 11060 |
rs6499264 | snp | A/G | 0.202035 | 0.245356 | intron-variant | WWP2 | GRCh38.p7 | 16:69856279 | agggacagaaatcca[A/G]tctgaagatgtgggg | 11060 |
rs6499265 | snp | A/G | 0.471958 | 0.115042 | intron-variant | WWP2 | GRCh38.p7 | 16:69864095 | gaggccaggtgtggt[A/G]gctcatgcctgtaat | 11060 |
rs6499268 | snp | A/G | 0.362732 | 0.22314 | intron-variant | WWP2 | GRCh38.p7 | 16:69872626 | TCAGACTAAGGAAAT[A/G]TAGGACTAAGTATTG | 11060 |
rs6499269 | snp | C/T | 0.365232 | 0.22186 | intron-variant | WWP2 | GRCh38.p7 | 16:69875015 | caacagagtgagacc[C/T]tgtgtcaaaaaaaaa | 11060 |
rs6499270 | snp | C/T | 0.396364 | 0.202676 | intron-variant | WWP2 | GRCh38.p7 | 16:69883837 | CCTGGAGGGAACCTT[C/T]CTAACTAGATTTGCA | 11060 |
rs6499272 | snp | A/G | 0.284471 | 0.247612 | intron-variant | WWP2 | GRCh38.p7 | 16:69915347 | gttgagggatggaat[A/G]caatacctatatcct | 11060 |
rs6499273 | snp | A/T | 0.305186 | 0.243833 | intron-variant | WWP2 | GRCh38.p7 | 16:69915884 | tacaaaaattttttt[A/T]aaaaattagttgaat | 11060 |
rs7184392 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | WWP2 | GRCh38.p7 | 16:69890649 | AATGCCTGGAAGGCC[A/G]GCCTCACTCCTGTGT | 11060 |
rs7184994 | snp | C/T | 0.255503 | 0.249939 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942186 | GGTCACGTAAGGGCT[C/T]GCCACCCACTTTTTT | 11060 |
rs7184995 | snp | C/G | 0.361474 | 0.223771 | intron-variant | WWP2 | GRCh38.p7 | 16:69890930 | TAGAACGTGATGAGG[C/G]CCACATGTGGGCCTG | 11060 |
rs7185321 | snp | C/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69896587 | AATTTTTTAAAGTTT[C/T]TTTCTGATCTTATTA | 11060 |
rs7185659 | snp | A/G | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69891565 | GACAGCAGGTCAGGT[A/G]CTGGGTATGGCAGAT | 11060 |
rs7186296 | snp | A/G | 0.474813 | 0.109357 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69775095 | tttgatgaagagtgg[A/G]caatcgtggagaaat | 11060 |
rs7186422 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | WWP2 | GRCh38.p7 | 16:69891142 | GTCTAAGAGGGAGCA[C/T]GGCAGGCTTTTGGTT | 11060 |
rs7188187 | snp | C/T | 0.349013 | 0.229557 | intron-variant | WWP2 | GRCh38.p7 | 16:69830198 | GCGCTCAGGCGATCT[C/T]TCTGCCTTGGCCTCC | 11060 |
rs7188413 | snp | C/G | 0.108755 | 0.206276 | intron-variant | WWP2 | GRCh38.p7 | 16:69830330 | ctggtctcaagccat[C/G]ctcctgcctcggcct | 11060 |
rs7188693 | snp | A/G | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69896764 | CTAACTACAGCTACC[A/G]TGTATTCTAAGTGTT | 11060 |
rs7189022 | snp | C/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69896799 | AGGTGCTGGGGACTG[C/T]CCAGTTTCCTACCTG | 11060 |
rs7189521 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | WWP2 | GRCh38.p7 | 16:69874230 | TATATAACGTCTGCC[C/T]CAAGGGTACAGAACA | 11060 |
rs7189829 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69874260 | AGTGTCACCTTTGCC[A/G]TGGGGAGCAGGCAGA | 11060 |
rs7190013 | snp | A/G | 0.409212 | 0.192748 | intron-variant | WWP2 | GRCh38.p7 | 16:69874345 | ACATCTTCATCCCTC[A/G]GGCTGCTGCTGTGAG | 11060 |
rs7190057 | snp | C/T | 0.105214 | 0.203807 | intron-variant | WWP2 | GRCh38.p7 | 16:69918312 | AAAAACCTGCTACTG[C/T]TTTTTGTTAGATCTT | 11060 |
rs7190486 | snp | A/C | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69796604 | gcatatcgctttcgc[A/C]cccctgtaaagtcaa | 11060 |
rs7190665 | snp | A/C | 0.0777841 | 0.181223 | intron-variant | WWP2 | GRCh38.p7 | 16:69891694 | GGCTGCCTCTGGGAT[A/C]TGATGCTAAGTCCAT | 11060 |
rs7191138 | snp | A/C | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69892078 | tcttatttgcctctg[A/C]atgcccagcacctag | 11060 |
rs7191376 | snp | C/T | 0.153665 | 0.230694 | intron-variant | WWP2 | GRCh38.p7 | 16:69884866 | ggaggtttctcttta[C/T]agaagtattgtagct | 11060 |
rs7191954 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767036 | tggaatAGGGGtttt[G/T]tttttttttttttta | 11060 |
rs7192213 | snp | A/G | 0.396546 | 0.202545 | intron-variant | WWP2 | GRCh38.p7 | 16:69892377 | aggccccggtgtgtg[A/G]tgttcccctccctgt | 11060 |
rs7192245 | snp | C/T | 0.288386 | 0.247035 | intron-variant | WWP2 | GRCh38.p7 | 16:69921902 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 11060 |
rs7192483 | snp | A/G | 0.284471 | 0.247612 | intron-variant | WWP2 | GRCh38.p7 | 16:69915337 | ggaggagatagttga[A/G]ggatggaatgcaata | 11060 |
rs7192584 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | WWP2 | GRCh38.p7 | 16:69871102 | accagccttggcaac[A/G]tagcaagaccccatc | 11060 |
rs7192872 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | WWP2 | GRCh38.p7 | 16:69922264 | AAAAAAAAAAAAAAA[C/T]GCCTGCGTTCCACGC | 11060 |
rs7193038 | snp | G/T | 0.396364 | 0.202676 | intron-variant | WWP2 | GRCh38.p7 | 16:69892231 | ttctggggtatatat[G/T]tgcagaatgtgcagt | 11060 |
rs7193149 | snp | C/T | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69871348 | AAGTTGTTTAATGCC[C/T]CTTGACTTTTATTGC | 11060 |
rs7193221 | snp | C/G | 0.498964 | 0.02274 | intron-variant | WWP2 | GRCh38.p7 | 16:69814818 | TGACAGACAGTGTAC[C/G]CATTTATTTTAAAGT | 11060 |
rs7193518 | snp | C/T | 0.284471 | 0.247612 | intron-variant | WWP2 | GRCh38.p7 | 16:69915357 | ggaatgcaataccta[C/T]atcctcatccctcat | 11060 |
rs7194157 | snp | A/G | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69792513 | TCATATCTTTATTTT[A/G]GCCTGTCTTTTAAGA | 11060 |
rs7194806 | snp | A/T | 0.488666 | 0.0744214 | intron-variant | WWP2 | GRCh38.p7 | 16:69830588 | AGCCAGAGTTCTCAT[A/T]ACATTCTGGGTTCTG | 11060 |
rs7195154 | snp | A/G | 0.152667 | 0.230274 | intron-variant | WWP2 | GRCh38.p7 | 16:69859236 | cattcttatctgcat[A/G]cactggggaagaatt | 11060 |
rs7195843 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69818784 | cttccccagtctgca[A/G]acatgggggtgctcc | 11060 |
rs7195995 | snp | A/G | 0.125874 | 0.217008 | intron-variant | WWP2 | GRCh38.p7 | 16:69810124 | ATTCTCCTCTTCCAC[A/G]GACAGAATTCGTTCT | 11060 |
rs7196525 | snp | A/G | 0.290201 | 0.246747 | intron-variant | WWP2 | GRCh38.p7 | 16:69913933 | aaaaattagccaggc[A/G]tggtggtgcttgcct | 11060 |
rs7196842 | snp | C/T | 0.345037 | 0.231231 | intron-variant | WWP2 | GRCh38.p7 | 16:69889430 | GGTGAGTGGAgatta[C/T]aagcatggacctgtg | 11060 |
rs7196917 | snp | A/G | 0.498693 | 0.0255257 | intron-variant | WWP2 | GRCh38.p7 | 16:69862624 | CTGAATCTGGGGTCA[A/G]TGAACCTCCCTTTCA | 11060 |
rs7197699 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69813656 | gtatttttgtagaga[C/T]agggtttcaccatgt | 11060 |
rs7197706 | snp | G/T | 0.0887219 | 0.191022 | intron-variant | WWP2 | GRCh38.p7 | 16:69915724 | tgcagtcctgtttat[G/T]tttcaaaactatata | 11060 |
rs7197774 | snp | G/T | 0.163892 | 0.234703 | intron-variant | WWP2 | GRCh38.p7 | 16:69877197 | gccaaccccgtcaat[G/T]atcttagctagatct | 11060 |
rs7198532 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | WWP2 | GRCh38.p7 | 16:69884322 | ggatggggacaattt[G/T]aggatcaaaaagaat | 11060 |
rs7198858 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886198 | agtgattctccctca[A/G]tctcctgagtagctg | 11060 |
rs7199853 | snp | C/T | 0.16846 | 0.236329 | intron-variant | WWP2 | GRCh38.p7 | 16:69863332 | catacagccaggtag[C/T]cactatcataatcaa | 11060 |
rs7199881 | snp | A/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69895401 | TATTGTGAATCCTTT[A/T]ATtctatactctgtt | 11060 |
rs7200005 | snp | A/G | 0.498693 | 0.0255257 | intron-variant | WWP2 | GRCh38.p7 | 16:69895234 | AGTTATAAACCAGGC[A/G]CTGCCATTGAATTTC | 11060 |
rs7200168 | snp | G/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69895312 | TTTTAACACTGAGCT[G/T]CTCAAAACTATTTGT | 11060 |
rs7200242 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | WWP2 | GRCh38.p7 | 16:69895512 | gctcatgcctgtaat[C/T]tagcactttgggagg | 11060 |
rs7200258 | snp | G/T | 0.41424 | 0.191714 | intron-variant | WWP2 | GRCh38.p7 | 16:69863566 | attgcttgaacctgg[G/T]gggggcagaggttgt | 11060 |
rs7202223 | snp | A/G | 0.488846 | 0.0738428 | intron-variant | WWP2 | GRCh38.p7 | 16:69841288 | AAACCACAGGGTGCT[A/G]TGAGATTCCTGTACT | 11060 |
rs7202233 | snp | A/G | 0.472896 | 0.113214 | intron-variant | WWP2 | GRCh38.p7 | 16:69860529 | AGATTTGGCCTAGGA[A/G]TTTGGCCACCTGGGT | 11060 |
rs7203292 | snp | C/T | 0.172028 | 0.23753 | intron-variant | WWP2 | GRCh38.p7 | 16:69869421 | AAACAAGGTCTCACT[C/T]TTTTGCCACGctctc | 11060 |
rs7203612 | snp | G/T | 0.356169 | 0.226336 | intron-variant | WWP2 | GRCh38.p7 | 16:69869403 | TAATTTTTTTTTTTT[G/T]TTAAACAAGGTCTCA | 11060 |
rs7204326 | snp | C/T | 0.16846 | 0.236329 | intron-variant | WWP2 | GRCh38.p7 | 16:69869278 | ACAGTTCAGTCGTAC[C/T]CTGTCTCCATTGCCA | 11060 |
rs7204615 | snp | A/G | 0.366885 | 0.220993 | intron-variant | WWP2 | GRCh38.p7 | 16:69769184 | TAGTCAGGCGTGGTG[A/G]CAGGCACCTGTAATC | 11060 |
rs7204759 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | WWP2 | GRCh38.p7 | 16:69887183 | TCTGTCTCATTGTCT[A/G]TTATCTCAGAGAGAA | 11060 |
rs7205289 | snp | A/C | | | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933102 | TCTCTCTGTGTCCTG[A/C]CAGTGGTTTTACCCT | 11060 |
rs7205972 | snp | C/T | 0.176219 | 0.238865 | intron-variant | WWP2 | GRCh38.p7 | 16:69926245 | GATGATGAGACTTAG[C/T]GCATTTGATAGAGCT | 11060 |
rs7206222 | snp | A/G | 0.247905 | 0.249991 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933413 | AAGTGCAAGAGTGTT[A/G]CATAGCTGGTGGGCA | 11060 |
rs7206524 | snp | G/T | 0.498611 | 0.0263212 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941993 | CCTCTGCCTCCGCCT[G/T]CTGGACCCGGGGGTC | 11060 |
rs7206585 | snp | A/G | 0.490943 | 0.0666801 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838501 | GATTGCATAGTTTCA[A/G]GGGGCTAGATTTGGC | 11060 |
rs8043646 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69934992 | GTTCTGGGGAGGGGC[A/G]TCCCAGCGTCTGTAT | 11060 |
rs8043768 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935322 | TCTGGAAATGGGCAC[A/G]TTCTTCCCAGGTCTA | 11060 |
rs8043835 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69935131 | GGGAGGCACAGCGCG[A/G]GAGCCACATGCATAG | 11060 |
rs8043925 | snp | C/T | 0.499954 | 0.00479211 | intron-variant | WWP2 | GRCh38.p7 | 16:69905287 | CAACCAAGAGTTGTC[C/T]GCTTTGGGGGGTGTG | 11060 |
rs8043950 | snp | A/C | 0.187369 | 0.242028 | intron-variant | WWP2 | GRCh38.p7 | 16:69921039 | AATTAAACACTAAAA[A/C]ATTCTTCTTTCTGAG | 11060 |
rs8044095 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935504 | CACCTGCAGCTGTTC[A/T]GAGCAAGCCTTTTCT | 11060 |
rs8044202 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935362 | CTGGCCCAGCAGCCA[A/G]CAGGACAGACCGGTA | 11060 |
rs8044238 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935495 | CAGGGCTGCCACCTG[C/G]AGCTGTTCAGAGCAA | 11060 |
rs8044373 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935423 | CCAGCTCTCGCTGTC[A/G]GCGGTGTCTGCATTA | 11060 |
rs8044577 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935567 | AGCCAGCCGGCCAGC[A/G]TGCGGGGCAGATGCG | 11060 |
rs8044876 | snp | C/T | 0.396182 | 0.202807 | intron-variant | WWP2 | GRCh38.p7 | 16:69882201 | cctcaggtgattcac[C/T]tgcctcggcctccca | 11060 |
rs8044920 | snp | C/T | 0.487746 | 0.0773096 | intron-variant | WWP2 | GRCh38.p7 | 16:69804773 | CATATGTAAAGTTAA[C/T]GTAATGGGGAATTTT | 11060 |
rs8045428 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | WWP2 | GRCh38.p7 | 16:69782278 | acagagcgagactcc[A/G]tctcaaacaaacaaa | 11060 |
rs8045482 | snp | C/T | 0.109108 | 0.206518 | intron-variant | WWP2 | GRCh38.p7 | 16:69833269 | ctccttgcagtgtgt[C/T]gttgaagaaactgga | 11060 |
rs8046469 | snp | A/C | 0.0955749 | 0.196603 | intron-variant | WWP2 | GRCh38.p7 | 16:69799624 | GAAACTGTCAAATAC[A/C]TCTAGCCTAAATCAT | 11060 |
rs8047010 | snp | G/T | 0.0930568 | 0.194599 | intron-variant | WWP2 | GRCh38.p7 | 16:69821448 | AGAGGCTGCCTTGTG[G/T]AGCCTCACCTGAAGA | 11060 |
rs8047194 | snp | G/T | 0.473266 | 0.112482 | intron-variant | WWP2 | GRCh38.p7 | 16:69857607 | ATGTCTATATTTTGG[G/T]TCTACTTTGTGTGTT | 11060 |
rs8047388 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | WWP2 | GRCh38.p7 | 16:69849486 | atttatttatttatt[C/T]attcattcattcatt | 11060 |
rs8047570 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857792 | tcagtctcccaggta[A/G]ctgagactacaggtg | 11060 |
rs8047682 | snp | A/G | 0.406986 | 0.194565 | intron-variant | WWP2 | GRCh38.p7 | 16:69879543 | CATGTTGTAGCGTGT[A/G]TCAGAATTTCCTTCC | 11060 |
rs8047730 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69903942 | TTGTGCCACAAAACT[A/T]CCCAAAGAACTGTTT | 11060 |
rs8047818 | snp | A/G | 0.297636 | 0.24542 | intron-variant | WWP2 | GRCh38.p7 | 16:69933829 | CATATAGGTTAGCCC[A/G]GGTGCTTGTCACAGG | 11060 |
rs8047888 | snp | C/T | 0.0249661 | 0.108902 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69934066 | CCTGCAGATCAACCC[C/T]GCCTCCTCCATCAAC | 11060 |
rs8048550 | snp | G/T | 0.362523 | 0.223246 | intron-variant | WWP2 | GRCh38.p7 | 16:69857856 | TTTTTGTAGTGACAG[G/T]GTCTTCCTGTGTTGC | 11060 |
rs8048563 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935591 | AGATGCGGGCCCGGA[C/T]GTGGGTTCCCGCACC | 11060 |
rs8048590 | snp | C/T | 0.262159 | 0.249704 | intron-variant | WWP2 | GRCh38.p7 | 16:69934464 | CCATGTTGCTTTGTA[C/T]AGGACTTGTCAAGAG | 11060 |
rs8048678 | snp | A/G | 0.265453 | 0.249522 | intron-variant | WWP2 | GRCh38.p7 | 16:69934298 | AGGAGGCAGCGTGGC[A/G]TGAACGGCAGCCCCC | 11060 |
rs8048838 | snp | G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69934434 | AGTGGCTGCCCTGTA[G/T]GTAGTGAAGAGTTTC | 11060 |
rs8049004 | snp | G/T | 0.247621 | 0.249989 | intron-variant | WWP2 | GRCh38.p7 | 16:69934493 | AGGGAGCCCAGGGTC[G/T]CTGGGCCACAGACTT | 11060 |
rs8049373 | snp | G/T | 0.407845 | 0.193868 | intron-variant | WWP2 | GRCh38.p7 | 16:69905802 | TCATCTTCCTTTTCT[G/T]CCCATTCTTCCTTTC | 11060 |
rs8050175 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | WWP2 | GRCh38.p7 | 16:69904545 | gactatttaaaaaaa[A/T]ttttttatagagatg | 11060 |
rs8050295 | snp | C/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826963 | aaaaaaaGGGGGGGG[C/G/T]GCGGAGAGAATAATG | 11060 |
rs8050369 | snp | A/G | 0.283947 | 0.247685 | intron-variant | WWP2 | GRCh38.p7 | 16:69782708 | ATCTTTTTGGAAACT[A/G]GATATATCACATAAG | 11060 |
rs8050414 | snp | A/T | 0.36315 | 0.222928 | intron-variant | WWP2 | GRCh38.p7 | 16:69852910 | gttagaacagagatc[A/T]tatggtcagcaaaac | 11060 |
rs8050516 | snp | C/T | 0.472803 | 0.113397 | intron-variant | WWP2 | GRCh38.p7 | 16:69862106 | ctttcgctcttgttg[C/T]cccggctggagtgca | 11060 |
rs8050892 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | WWP2 | GRCh38.p7 | 16:69861630 | CGGTTCACTTCTCCT[A/T]TTACCCGCCCTCTCC | 11060 |
rs8051025 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931097 | GGCTGACAAAGACAA[A/G]TTGTTCATTTTCTGA | 11060 |
rs8051168 | snp | A/T | 0.363359 | 0.222822 | intron-variant | WWP2 | GRCh38.p7 | 16:69853371 | AACCGCTTTATGTAT[A/T]TGAAGTGGGTGTGCA | 11060 |
rs8051533 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931334 | TGTGTCTTAGGCGGG[C/G]GCAAGACACTTGTCT | 11060 |
rs8051544 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931404 | CCTAGGGCACATGCT[A/G]TTGCCTCCTGGCCCA | 11060 |
rs8051682 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931396 | TTTTCATTCCTAGGG[C/G/T]ACATGCTATTGCCTC | 11060 |
rs8052225 | snp | A/G | 0.360842 | 0.224085 | intron-variant | WWP2 | GRCh38.p7 | 16:69849750 | GAGTTTGAGGCTGCA[A/G]TGAGTTATGATCGTG | 11060 |
rs8052369 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931149 | CATCTTTGCTCTTCC[C/T]AGGACGAAGCAAGGT | 11060 |
rs8052428 | snp | C/T | 0.465052 | 0.127485 | intron-variant | WWP2 | GRCh38.p7 | 16:69880093 | TATCAAAATAAATAT[C/T]CCATTAGAATTTATA | 11060 |
rs8052558 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931268 | TGGCAGTTGGGGTTA[C/T]TGAGTTATTTCAGTG | 11060 |
rs8052727 | snp | G/T | 0.246769 | 0.249979 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931378 | CTGTCTCTAGGAAGC[G/T]AGTTTTCATTCCTAG | 11060 |
rs8052959 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | WWP2 | GRCh38.p7 | 16:69815521 | GGGCAGGggctgggc[A/G]cggtgcctgtaatct | 11060 |
rs8053447 | snp | C/T | 0.174932 | 0.238463 | intron-variant | WWP2 | GRCh38.p7 | 16:69919258 | gtaacctccactgcc[C/T]gggttcaagcaattc | 11060 |
rs8056426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931686 | CAGACTTTCCAGGGC[A/G]TGAGTCTTGGTGACT | 11060 |
rs8056578 | snp | A/C/G | 4.98255e-05 | 0.00499106 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931784 | GTGGCAGGCTGGCCC[A/C/G]ATGCTCTGTCTTCCC | 11060 |
rs8056707 | snp | A/G | 0.193966 | 0.243639 | intron-variant | WWP2 | GRCh38.p7 | 16:69901730 | ATACAAGCTGATAAT[A/G]CTCTTACCAAGACTG | 11060 |
rs8057106 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | WWP2 | GRCh38.p7 | 16:69777030 | ATTTTATATCTTAAA[A/G]CAgtatatgtgtgtg | 11060 |
rs8057620 | snp | A/T | 0.487809 | 0.0771174 | intron-variant | WWP2 | GRCh38.p7 | 16:69850716 | ATAAAAGTCATTTAG[A/T]AATGTTGACATGTAA | 11060 |
rs8057650 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | WWP2 | GRCh38.p7 | 16:69807324 | acaggcgtgagccac[C/T]gtgcctggccTATCC | 11060 |
rs8057938 | snp | G/T | 0.284733 | 0.247575 | intron-variant | WWP2 | GRCh38.p7 | 16:69777206 | caatatacatatgga[G/T]atatcatatatgcac | 11060 |
rs8058029 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | WWP2 | GRCh38.p7 | 16:69777447 | ctgggattacaggca[C/T]ctgccaccacgacca | 11060 |
rs8058594 | snp | G/T | 0.301681 | 0.2446 | intron-variant | WWP2 | GRCh38.p7 | 16:69807124 | acctctgcctcctgg[G/T]ttcaagtgattctcc | 11060 |
rs8058669 | snp | C/G | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69771673 | atcagcttgtcaatt[C/G]ctgaaaaacaaTTCT | 11060 |
rs8059162 | snp | A/C/G | 0.0930568 | 0.194599 | intron-variant | WWP2 | GRCh38.p7 | 16:69810640 | gtttcactgtgttag[A/C/G]cagatagtctcaatc | 11060 |
rs8059345 | snp | A/G | 0.459004 | 0.137176 | intron-variant | WWP2 | GRCh38.p7 | 16:69765051 | tctacaaaaaataca[A/G]aaattagccaggtgc | 11060 |
rs8059645 | snp | G/T | 0.488666 | 0.0744214 | intron-variant | WWP2 | GRCh38.p7 | 16:69840806 | AAATTATTTCATGAA[G/T]TCCGAGGTCTGAAAT | 11060 |
rs8059816 | snp | A/G | 0.148996 | 0.228688 | intron-variant | WWP2 | GRCh38.p7 | 16:69810811 | ccagactggagtgca[A/G]tggcacaatctccgc | 11060 |
rs8060478 | snp | A/G | 0.370974 | 0.218781 | intron-variant | WWP2 | GRCh38.p7 | 16:69868967 | ATCTCGGCTCACTGC[A/G]ACCTCCACCTCCCGG | 11060 |
rs8060916 | snp | G/T | 0.0966517 | 0.197444 | intron-variant | WWP2 | GRCh38.p7 | 16:69810900 | ggtgggattacaggt[G/T]cacaccaccacgccc | 11060 |
rs8062076 | snp | C/T | 0.281577 | 0.247998 | intron-variant | WWP2 | GRCh38.p7 | 16:69789913 | ccaaaactttactaa[C/T]agcctgctgttgact | 11060 |
rs8062334 | snp | A/G | 0.120326 | 0.21374 | intron-variant | WWP2 | GRCh38.p7 | 16:69799067 | TGTGGGTGTCTGCCT[A/G]TTTTGGTTCCCCCTC | 11060 |
rs8062543 | snp | A/G | 0.0273479 | 0.113693 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69799183 | TTTCAGGAATGTCAC[A/G]GCACAGAGTCATTTA | 11060 |
rs8062596 | snp | A/G | 0.123105 | 0.215401 | intron-variant | WWP2 | GRCh38.p7 | 16:69799397 | AGGACTAGGGGCTGC[A/G]GTACCTCTGTTCTCC | 11060 |
rs8062707 | snp | A/C | 0 | 0 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837942 | TAAAATGAATGAAGG[A/C]TAgggcgcggtggct | 11060 |
rs8062809 | snp | A/G | 0.143284 | 0.226079 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837836 | GGACAGTTTGTCTGC[A/G]TGATGGGTCTGTGGC | 11060 |
rs8063027 | snp | A/G | 0.123105 | 0.215401 | intron-variant | WWP2 | GRCh38.p7 | 16:69799436 | TGTCTTTGGAGTTTT[A/G]GGAAGGCTGAGGGCT | 11060 |
rs8063219 | snp | G/T | 0.49931 | 0.0185575 | intron-variant | WWP2 | GRCh38.p7 | 16:69799009 | GAGCGTTCATTATTA[G/T]CTAGAGGGTTACAGG | 11060 |
rs8063226 | snp | A/G | 0.472429 | 0.114129 | intron-variant | WWP2 | GRCh38.p7 | 16:69864581 | gggagacagagtctc[A/G]ctctgtcacccaggc | 11060 |
rs9302605 | snp | A/T | 0.221439 | 0.248363 | intron-variant | WWP2 | GRCh38.p7 | 16:69938583 | GGACCGTGCCACTGC[A/T]CTGCAGTGAGCTGGA | 11060 |
rs9630631 | snp | C/T | 0.489024 | 0.0732638 | intron-variant | WWP2 | GRCh38.p7 | 16:69832824 | ctgggattacaggtg[C/T]gaaccactgtgcctg | 11060 |
rs9673566 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69938094 | AAATAGCGATTACAG[A/G]TATTCTTAGTACATG | 11060 |
rs9746247 | snp | C/G | 0.486266 | 0.0817214 | intron-variant | WWP2 | GRCh38.p7 | 16:69922057 | CACTCCAGCCAGAGA[C/G]ACAGAGTGAGACTCC | 11060 |
rs9888980 | snp | C/G | 0.323434 | 0.238972 | intron-variant | WWP2 | GRCh38.p7 | 16:69848678 | AAGCTATATATAGAG[C/G]CTTCAACAATTTATT | 11060 |
rs9888981 | snp | A/G | 0.323434 | 0.238972 | intron-variant | WWP2 | GRCh38.p7 | 16:69848752 | AATGCATGTGAACGC[A/G]CATGAGAGAGTGTGT | 11060 |
rs9921205 | snp | G/T | 0.046775 | 0.145601 | intron-variant | WWP2 | GRCh38.p7 | 16:69887861 | ATTTCCTTTGGACAG[G/T]CATTAATGACTTGCT | 11060 |
rs9921747 | snp | A/G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69852677 | aaaatctggttgttc[A/G/T]tgttcttattgttga | 11060 |
rs9922223 | snp | C/T | 0.319856 | 0.240042 | intron-variant | WWP2 | GRCh38.p7 | 16:69853107 | GTAAGGCTATTTCTG[C/T]GGTAAATTATTCAGG | 11060 |
rs9922239 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853217 | agcagaaaaggattt[A/T]atatggggaattaga | 11060 |
rs9922240 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853218 | gcagaaaaggattta[A/T]tatggggaattagat | 11060 |
rs9922342 | snp | A/G | 0.319376 | 0.240181 | intron-variant | WWP2 | GRCh38.p7 | 16:69853369 | GCAACCGCTTTATGT[A/G]TTTGAAGTGGGTGTG | 11060 |
rs9922603 | snp | A/G/T | 0.0178098 | 0.0926698 | intron-variant | WWP2 | GRCh38.p7 | 16:69853407 | TGAGGCATGGTGTCT[A/G/T]CTGGAGCCCCTGCCA | 11060 |
rs9922964 | snp | C/T | 0.396182 | 0.202807 | intron-variant | WWP2 | GRCh38.p7 | 16:69921917 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 11060 |
rs9923038 | snp | G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69813092 | tatgcgtgtgtgtag[G/T]tatgtattatcagct | 11060 |
rs9923471 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69862379 | cCttgttttgttttt[C/T]tgagatggagtctcg | 11060 |
rs9924630 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69883625 | caggtttgttacatc[A/G]gttaaacatgcgcca | 11060 |
rs9925155 | snp | A/G | 0.100944 | 0.200705 | intron-variant | WWP2 | GRCh38.p7 | 16:69884216 | GTTCTGCACTTTTTC[A/G]TTTAGTAGTTATCTT | 11060 |
rs9927105 | snp | C/T | 0.303688 | 0.244167 | intron-variant | WWP2 | GRCh38.p7 | 16:69793330 | gcactccagcctggg[C/T]gacagagcaagactc | 11060 |
rs9927269 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | WWP2 | GRCh38.p7 | 16:69860260 | TGCAAAGTACTGGAG[A/G]TTACAGGCCCAAGAG | 11060 |
rs9927967 | snp | C/T | 0.473451 | 0.112115 | intron-variant | WWP2 | GRCh38.p7 | 16:69878094 | attacaggtgtgagc[C/T]accgtgcccagccca | 11060 |
rs9928560 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69865687 | aggggacacacatgc[A/G]tgtgtcataaactaa | 11060 |
rs9928613 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69777597 | tgagccaccgtgctc[A/G]gcctatattttcttt | 11060 |
rs9928815 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69807898 | tgggagatagaggct[A/G]cagtaagctgtaatc | 11060 |
rs9929073 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | WWP2 | GRCh38.p7 | 16:69903571 | cagaagatcgagacc[A/G]tcctggccaacatgg | 11060 |
rs9929123 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | WWP2 | GRCh38.p7 | 16:69857024 | TCTCGTGATTCTTGA[C/T]ATCTTTAGAGTTGTT | 11060 |
rs9930692 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69791148 | AGCAGAAGTTGGCCT[A/G]TTGGACCTGGTAACA | 11060 |
rs9930991 | snp | C/T | 0.0158469 | 0.0875917 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761347 | ggaggccaaggtggg[C/T]ggatcatttgaagtc | 11060 |
rs9931243 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69879538 | tcatccatgttgtag[C/T]gtgtgtcagaatttc | 11060 |
rs9931479 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69778752 | gttcaagcaattctc[C/T]tgcctcagcctcccg | 11060 |
rs9932486 | snp | A/T | 0.319616 | 0.240112 | intron-variant | WWP2 | GRCh38.p7 | 16:69852598 | gagagtcttttcata[A/T]gcttatattccatct | 11060 |
rs9933606 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909811 | tatagagagaataat[A/G]ttacaaacccccaca | 11060 |
rs9933646 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | WWP2 | GRCh38.p7 | 16:69805794 | ctttttttttttttt[C/T]agagatggtatctca | 11060 |
rs9933681 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813093 | atgcgtgtgtgtagg[C/T]atgtattatcagctt | 11060 |
rs9933745 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69822318 | TGATTTATCAGCTTT[C/T]GTGCAGTAAGCACCT | 11060 |
rs9934685 | snp | A/G | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69898177 | ggattacaggcatct[A/G]ccaccatgcttggct | 11060 |
rs9934743 | snp | A/C | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69898142 | aagtgattctcctgc[A/C]tcagcctcccaagta | 11060 |
rs9934928 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69868353 | CTCCATGCTGACCAC[A/G/T]TGCCCTTTCTGGGAA | 11060 |
rs9934983 | snp | C/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69898396 | gaagatcttcaactt[C/T]agtaggtattatcaa | 11060 |
rs9935008 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | WWP2 | GRCh38.p7 | 16:69898529 | gggcatgaatggtac[A/G]tctttgaggattcag | 11060 |
rs9935492 | snp | A/G | 0.089084 | 0.191327 | intron-variant | WWP2 | GRCh38.p7 | 16:69862773 | tgcccaggatagagt[A/G]tagtggtgtgagtgt | 11060 |
rs9935643 | snp | C/T | 0.17138 | 0.237316 | intron-variant | WWP2 | GRCh38.p7 | 16:69884062 | CCTTCAGTTTCCTCC[C/T]CCAAGGCCCACTGTT | 11060 |
rs9935697 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69828249 | CTAAGGGCAGATGCC[C/T]CATCCATGCTTAGAG | 11060 |
rs9935973 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69886133 | tgtcacctaggctgg[A/G]ttgcagtggtgcaat | 11060 |
rs9936451 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69762984 | TGGGTAGGGTTTCCA[C/G]TTCTTGGGAGCCTAG | 11060 |
rs9936589 | snp | C/T | 0.467234 | 0.12373 | intron-variant | WWP2 | GRCh38.p7 | 16:69850914 | CCACTATCAACATCC[C/T]CCACCAGAGTGGTAC | 11060 |
rs9936723 | snp | A/G | 0.467946 | 0.122472 | intron-variant | WWP2 | GRCh38.p7 | 16:69850951 | tagaatgatgagcct[A/G]cattgacacatcatt | 11060 |
rs9936761 | snp | A/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69816336 | gcttgtaatttcagc[A/T]ctttggagactgagg | 11060 |
rs9938610 | snp | C/T | 0.123452 | 0.215605 | intron-variant | WWP2 | GRCh38.p7 | 16:69907966 | TGACTTTAagccggg[C/T]gcggtggctcactcc | 11060 |
rs9939065 | snp | C/G | 0.046775 | 0.145601 | intron-variant | WWP2 | GRCh38.p7 | 16:69887533 | gcctcagcctcccaa[C/G]tagctgggattatag | 11060 |
rs9940008 | snp | C/T | 0.320096 | 0.239972 | intron-variant | WWP2 | GRCh38.p7 | 16:69852568 | catgagctgccttgc[C/T]cggcctatgatatgg | 11060 |
rs9940315 | snp | A/G | 0.367708 | 0.220556 | intron-variant | WWP2 | GRCh38.p7 | 16:69842261 | GACTCAGTAGTTAAG[A/G]AAGCTAATAGAGGAG | 11060 |
rs9940805 | snp | A/G | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69900292 | TTCTTGATAGTAACT[A/G]TCCCTATACTGCCAA | 11060 |
rs10048088 | snp | A/G | 0.241627 | 0.24986 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932414 | GGCCTGGGGTGCCCC[A/G]CTGGGCTGGACATTA | 11060 |
rs10048090 | snp | A/G | 0.248471 | 0.249995 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932459 | GGGTCATGAGGCGAC[A/G]GAGGACTCCTGGGAG | 11060 |
rs10048129 | snp | C/T | 0.241627 | 0.24986 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932247 | GGCGGGAGAATCGCT[C/T]GAACCTGGGAGGCAG | 11060 |
rs10400955 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | WWP2 | GRCh38.p7 | 16:69802669 | gcagtggcgcgatct[C/T]ggctcactgcaaccc | 11060 |
rs10400956 | snp | A/G | 0.307176 | 0.243374 | intron-variant | WWP2 | GRCh38.p7 | 16:69802765 | CCTGCCACCATGCCC[A/G]GCTAATTTTTTTATT | 11060 |
rs10445022 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812744 | gaacacccaggagtg[A/T]ctttgtgtccttctc | 11060 |
rs10525822 | in-del | -/TATTTATT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866801 | TTGCTTTCAGTTCCG[-/TATTTATT]TATTTATTTATTTAT | 11060 |
rs10532241 | in-del | -/TTAT | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69778943 | GTCACACCTGGCCGG[-/TTAT]TTATTTATTTATTTA | 11060 |
rs10578834 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795260 | AAAAAAAATGCGGAT[-/AC]ACACACACACACACA | 11060 |
rs10605057 | in-del | -/TT | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69901165 | CAGAAGAAATAAATC[-/TT]ATGGTTCTCCCCGGA | 11060 |
rs10607599 | in-del | -/AA | 0 | 0 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838462 | AAAAAAAAAAAAAAA[-/AA]GCCCACAATAATCAA | 11060 |
rs10628008 | in-del | -/AATT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849861 | ATACATTGGTTTATT[-/AATT]TTGCATCAATTAAAA | 11060 |
rs10632935 | in-del | -/ATTC/ATTCATTC/ATTCATTCATTC | 0.490881 | 0.207915 | intron-variant | WWP2 | GRCh38.p7 | 16:69849482 | TTTATTTATTTATTT[-/ATTC/ATTCATTC/ATTCATTCATTC]ATTCATTCATTCATT | 11060 |
rs10633789 | in-del | -/ATTA | 0.360842 | 0.224085 | intron-variant | WWP2 | GRCh38.p7 | 16:69849858 | TTTATACATTGGTTT[-/ATTA]TATTTTGCATCAATT | 11060 |
rs10668229 | in-del | -/CT | 0.286564 | 0.247312 | intron-variant | WWP2 | GRCh38.p7 | 16:69785222 | CTTAGGTGTGTGAGA[-/CT]CTGTCTCAAAAAAAA | 11060 |
rs10671857 | in-del | -/A/AA/AAA | 0.494315 | 0.0530107 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761572 | AAAAAAAAAAAAAAA[-/A/AA/AAA]TATCATCTATCTATC | 11060 |
rs10708547 | in-del | -/C | 0.123105 | 0.215401 | intron-variant | WWP2 | GRCh38.p7 | 16:69803376 | TTTACATAAAAAAAA[-/C]ATTATCTTACACAAT | 11060 |
rs10712484 | in-del | -/C | 0.256619 | 0.249912 | intron-variant | WWP2 | GRCh38.p7 | 16:69939720 | TGAAGGCCTGACTGG[-/C]AGCCCCTGAGCCCTA | 11060 |
rs10852459 | snp | G/T | 0.230896 | 0.249269 | intron-variant | WWP2 | GRCh38.p7 | 16:69802300 | tttttaggtgtatag[G/T]ttagtggtgttaagt | 11060 |
rs10852460 | snp | A/G | 0.467845 | 0.122652 | intron-variant | WWP2 | GRCh38.p7 | 16:69851116 | cccaggttcaagtga[A/G]tctcatgcctcagcc | 11060 |
rs10852461 | snp | C/T | 0.405776 | 0.195535 | intron-variant | WWP2 | GRCh38.p7 | 16:69894943 | GGACTGCCGACTTAC[C/T]TCAGCTCTGCCATTT | 11060 |
rs11075734 | snp | G/T | 0.434543 | 0.168653 | intron-variant | WWP2 | GRCh38.p7 | 16:69767494 | GTGAGTTGCTTTTGA[G/T]CGACTTTGAGTCCCT | 11060 |
rs11075736 | snp | G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69776852 | aaaaataaaaaaaaT[G/T]ATAATAAACTGATGA | 11060 |
rs11075738 | snp | C/T | 0.499265 | 0.0191552 | intron-variant | WWP2 | GRCh38.p7 | 16:69802222 | atgagccaccgtgcc[C/T]ggccTATATTTAttt | 11060 |
rs11075739 | snp | C/T | 0.488905 | 0.0736498 | intron-variant | WWP2 | GRCh38.p7 | 16:69830331 | TGGTCTCAAGCCATC[C/T]TCCTGCCTCGGCCTC | 11060 |
rs11075740 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848448 | agagcaaagctccat[C/T]tcaaaaaaaaaaaac | 11060 |
rs11075742 | snp | A/G | 0.471863 | 0.115225 | intron-variant | WWP2 | GRCh38.p7 | 16:69865031 | attttccctctgtag[A/G]tcttctttggtgatg | 11060 |
rs11075743 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | WWP2 | GRCh38.p7 | 16:69869900 | GACTCCCAGCAGGGT[C/T]GTTCTGCTGGAGGTG | 11060 |
rs11075744 | snp | A/G | 0.446771 | 0.154211 | intron-variant | WWP2 | GRCh38.p7 | 16:69875212 | tttacactatactat[A/G]gtccataaaaggtac | 11060 |
rs11075745 | snp | C/T | 0.499087 | 0.0213463 | intron-variant | WWP2 | GRCh38.p7 | 16:69900769 | CCTCAGGTGATCTGC[C/T]CGCCTTGGCCTCCCA | 11060 |
rs11075746 | snp | A/G | 0.364609 | 0.222182 | intron-variant | WWP2 | GRCh38.p7 | 16:69906452 | CAGTTTAAATAAGAA[A/G]TGGCAGTGAGTACAG | 11060 |
rs11075747 | snp | A/G | 0.495745 | 0.0459295 | intron-variant | WWP2 | GRCh38.p7 | 16:69906458 | AAATAAGAAGTGGCA[A/G]TGAGTACAGGTAATA | 11060 |
rs11287046 | in-del | -/T | 0.46845 | 0.121572 | intron-variant | WWP2 | GRCh38.p7 | 16:69867141 | ACACCTGGCCAAGGC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs11308765 | in-del | -/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69800569 | AGTTATTGTTTTTTC[-/T]TTTTTTTTTTTTTGA | 11060 |
rs11337802 | in-del | -/A | 0.495174 | 0.0488838 | intron-variant | WWP2 | GRCh38.p7 | 16:69916037 | GAGTGAGACCCTGTC[-/A]AAAAAAAAAAAAAAT | 11060 |
rs11343848 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897105 | CCGTCTTTTTTTTTT[-/T]GTTTGTGTGTTTTGT | 11060 |
rs11353651 | in-del | -/T | 0.191147 | 0.242974 | intron-variant | WWP2 | GRCh38.p7 | 16:69833405 | GACTGACCTTGGTTC[-/T]TTTTTTTTCTCTGGT | 11060 |
rs11370872 | in-del | -/A/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803098 | TTGTAAAAAAAAAAA[-/A/AA]GCCTTTTTTTTTCCT | 11060 |
rs11375021 | in-del | -/T | 0.0777841 | 0.181223 | intron-variant | WWP2 | GRCh38.p7 | 16:69892161 | AACAATGATTCTCTC[-/T]TTTTTTTTAATTTAA | 11060 |
rs11390043 | in-del | -/T | 0.477768 | 0.103061 | intron-variant | WWP2 | GRCh38.p7 | 16:69861645 | TTTTTTTTTTTTTTT[-/T]CTAATCCACATTTGA | 11060 |
rs11392322 | in-del | -/A | 0.0948562 | 0.196037 | intron-variant | WWP2 | GRCh38.p7 | 16:69871128 | CATCTCCCCAAAAAT[-/A]AAAAAAATGAGCCAG | 11060 |
rs11449005 | in-del | -/A | 0.457504 | 0.139435 | intron-variant | WWP2 | GRCh38.p7 | 16:69875021 | GTGAGACCTTGTGTC[-/A]AAAAAAAAAAAAATT | 11060 |
rs11462005 | in-del | -/T | 0.457037 | 0.140127 | intron-variant | WWP2 | GRCh38.p7 | 16:69829957 | TTTTTTTTTTTTTTT[-/T]CAGATAGAGTCTAAC | 11060 |
rs11464525 | in-del | -/A | 0.455621 | 0.142197 | intron-variant | WWP2 | GRCh38.p7 | 16:69860840 | TTAAAAAAAAAAAAA[-/A]GGAAAGAAAGAACAC | 11060 |
rs11510266 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | WWP2 | GRCh38.p7 | 16:69882062 | TGGCTTCAAATGATC[C/T]ACCTGCTTTGGCCTC | 11060 |
rs11639891 | snp | A/C | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69912923 | ccagtctctacaaaa[A/C]aaaaaaaaaaaaaaa | 11060 |
rs11640490 | snp | C/T | 0.202035 | 0.245356 | intron-variant | WWP2 | GRCh38.p7 | 16:69813223 | gctggagtgcaatgg[C/T]gcgatcttcgctcac | 11060 |
rs11641521 | snp | C/G | 0.449853 | 0.150196 | intron-variant | WWP2 | GRCh38.p7 | 16:69789178 | ttctcctgtctcagc[C/G]ttccaagtagctggg | 11060 |
rs11641899 | snp | A/G | 0.488905 | 0.0736498 | intron-variant | WWP2 | GRCh38.p7 | 16:69844027 | TGGGCTTATGAGGTT[A/G]TGGTGACTGGCAAGT | 11060 |
rs11642008 | snp | A/G | 0.470618 | 0.117591 | intron-variant | WWP2 | GRCh38.p7 | 16:69894736 | CTGTTTTTTCTCAGC[A/G]CTCAGCCCACTTTGG | 11060 |
rs11642095 | snp | A/G | 0.00472811 | 0.0483911 | intron-variant | WWP2 | GRCh38.p7 | 16:69844429 | AGTAACTACATCTTA[A/G]TCTTTTAGCTGAGTT | 11060 |
rs11643398 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895785 | aaaaaaaGTTTCTAA[A/G]TGCTTAGAAACTTCA | 11060 |
rs11643817 | snp | G/T | 0.487746 | 0.0773096 | intron-variant | WWP2 | GRCh38.p7 | 16:69802902 | AAACCACCGCATCTG[G/T]CCCAAGATATCTTAT | 11060 |
rs11643926 | snp | A/G | 0.450231 | 0.149691 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773379 | agattgggtttcact[A/G]tgttggccgggctga | 11060 |
rs11644247 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848661 | aaaaaaaaaaaaaAA[A/G]GAAGCTATATATAGA | 11060 |
rs11644838 | snp | C/G | 0.449218 | 0.151037 | intron-variant | WWP2 | GRCh38.p7 | 16:69778802 | GCGCCACCACTCCTC[C/G]CTAATTTTTGTATTT | 11060 |
rs11644914 | snp | A/G | 0.448963 | 0.151372 | intron-variant | WWP2 | GRCh38.p7 | 16:69779077 | GCCTCAGCCTCCCAA[A/G]CAGCTGGGATTACAG | 11060 |
rs11645064 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897313 | ttgccgtgttgctca[A/G]gctggtcttgaactc | 11060 |
rs11645233 | snp | C/T | 0.284733 | 0.247575 | intron-variant | WWP2 | GRCh38.p7 | 16:69912865 | ggtgggaggatcgct[C/T]gagtccaggagttcg | 11060 |
rs11645326 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WWP2 | GRCh38.p7 | 16:69766894 | gagtagctgggatta[C/T]aggcatctgccacta | 11060 |
rs11645565 | snp | A/G | 0.499121 | 0.020948 | intron-variant | WWP2 | GRCh38.p7 | 16:69862345 | GCTGGGATTACAGGC[A/G]TGAGCTACCGCGCCT | 11060 |
rs11646929 | snp | C/T | 0.201418 | 0.245234 | intron-variant | WWP2 | GRCh38.p7 | 16:69768153 | AGGGCTCTGGAATTT[C/T]TGAAAGATGGGAACA | 11060 |
rs11647767 | snp | A/T | 0.397633 | 0.201754 | intron-variant | WWP2 | GRCh38.p7 | 16:69919991 | GTAGAGATGGGGTTT[A/T]GCCATGTTGCCCAGG | 11060 |
rs11648348 | snp | A/G | 0.472147 | 0.114677 | intron-variant | WWP2 | GRCh38.p7 | 16:69856819 | ACAACAACAAAACCC[A/G]TTTGGTGTGACGTTA | 11060 |
rs11859017 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887783 | AACCACAGTATGTTA[A/G]AAAAACTTGATAAAG | 11060 |
rs11859635 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69846292 | tatggtggaatctta[A/G]aaacataatgttgaa | 11060 |
rs11859668 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69906576 | CCTAAAAGTCAGCAC[A/G]TGATGCAAAATTATG | 11060 |
rs11860910 | snp | A/C | 0.0966517 | 0.197444 | intron-variant | WWP2 | GRCh38.p7 | 16:69814234 | ggtgtgatcataggt[A/C]actgtagcctcgaac | 11060 |
rs11862482 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69765594 | ttttggaggctgaga[C/T]gggcggatcacttga | 11060 |
rs11862697 | snp | C/T | 0.337386 | 0.23423 | intron-variant | WWP2 | GRCh38.p7 | 16:69844935 | TGTCTCTTTGCCTCC[C/T]TAAAAGCCCCCTTTC | 11060 |
rs11863500 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69927257 | CCCAGGGCTCACCGA[C/G]AATGAACAGGAAGAA | 11060 |
rs11864225 | snp | A/T | 0.0930568 | 0.194599 | intron-variant | WWP2 | GRCh38.p7 | 16:69836162 | atttcaaacatcatc[A/T]aatattcagtttgta | 11060 |
rs11864678 | snp | C/T | 0.241627 | 0.24986 | intron-variant | WWP2 | GRCh38.p7 | 16:69928578 | GCCCCACTCCATGAA[C/T]ATTCCCCTGTCTCAA | 11060 |
rs12019048 | snp | A/C | 0.305186 | 0.243833 | intron-variant | WWP2 | GRCh38.p7 | 16:69854182 | ACAAGTTTAGAGAGA[A/C]GCCAATAAAAAGAGT | 11060 |
rs12102498 | snp | A/T | 0.100944 | 0.200705 | intron-variant | WWP2 | GRCh38.p7 | 16:69907300 | AAGTCTTCTGTGTTC[A/T]TCTAGTGTTTCTCAC | 11060 |
rs12149320 | snp | C/G | 0.385359 | 0.210185 | intron-variant | WWP2 | GRCh38.p7 | 16:69925918 | TTTCTTTGCAGCTGA[C/G]ATGTTGGAGGACTTT | 11060 |
rs12149920 | snp | A/G | 0.284733 | 0.247575 | intron-variant | WWP2 | GRCh38.p7 | 16:69782130 | tttactaaaaataca[A/G]aaattagctgggcgt | 11060 |
rs12164965 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69771269 | TAtttttctttttga[A/G]atgaaatcttgctgt | 11060 |
rs12444607 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69819128 | atatattctgggatc[C/T]gaccatctgtcactg | 11060 |
rs12444699 | snp | A/G | 0.108048 | 0.20579 | intron-variant | WWP2 | GRCh38.p7 | 16:69789540 | gccTCCTATAGTTCA[A/G]AATTCTTTCCTGCAG | 11060 |
rs12444927 | snp | A/G | 0.129664 | 0.219133 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932235 | TGGGGAGGCTGAGGC[A/G]GGAGAATCGCTTGAA | 11060 |
rs12445239 | snp | A/G | 0.107341 | 0.205301 | intron-variant | WWP2 | GRCh38.p7 | 16:69772189 | tggtctcgaactccc[A/G]aacttgggtgatccg | 11060 |
rs12445435 | snp | A/G | 0.109108 | 0.206518 | intron-variant | WWP2 | GRCh38.p7 | 16:69789993 | cacgcctgtaatccc[A/G]gcactttgagaggct | 11060 |
rs12446168 | snp | A/G | 0.365232 | 0.22186 | intron-variant | WWP2 | GRCh38.p7 | 16:69826567 | acagagtgagactcc[A/G]tctcaaaaaaaaaaa | 11060 |
rs12446197 | snp | A/G | 0.368324 | 0.220226 | intron-variant | WWP2 | GRCh38.p7 | 16:69820966 | GAGGCTGACAGCAGG[A/G]CCAGTGTGGTGCGTG | 11060 |
rs12446201 | snp | C/T | 0.467845 | 0.122652 | intron-variant | WWP2 | GRCh38.p7 | 16:69781683 | ttcattttgtgtttc[C/T]ataactggataatag | 11060 |
rs12447095 | snp | G/T | 0.489796 | 0.070696 | intron-variant | WWP2 | GRCh38.p7 | 16:69835860 | CAGGCTGGAATGTGG[G/T]GGCACGATCCTGGCT | 11060 |
rs12447388 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898180 | ttacaggcatctacc[A/C]ccatgcttggctagt | 11060 |
rs12447914 | snp | C/G | 0.492287 | 0.0616198 | intron-variant | WWP2 | GRCh38.p7 | 16:69850820 | tgttcttgtttgttt[C/G]tttgtttttgctGGG | 11060 |
rs12448486 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | WWP2 | GRCh38.p7 | 16:69768975 | GTAGCATGAGCCTGT[A/G]AAGAACAGGAGAATC | 11060 |
rs12448499 | snp | A/G | 0.474453 | 0.110094 | intron-variant | WWP2 | GRCh38.p7 | 16:69769251 | GAACCCGGGAGGTGG[A/G]GGTTTGCAGTGAGCC | 11060 |
rs12449259 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | WWP2 | GRCh38.p7 | 16:69829947 | aggcacacgccactg[C/T]gcccagctaattttt | 11060 |
rs12596679 | snp | A/G | 0.449853 | 0.150196 | intron-variant | WWP2 | GRCh38.p7 | 16:69788777 | taagagatttttgtc[A/G]ctttggtcactgtta | 11060 |
rs12598407 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | WWP2 | GRCh38.p7 | 16:69921599 | GTGCTAATGTTGCCC[A/G]TGATCATCGTGTATC | 11060 |
rs12598642 | snp | A/G | 0.365232 | 0.22186 | intron-variant | WWP2 | GRCh38.p7 | 16:69814869 | AGTTTTTCAGCTGGA[A/G]GATAAATAAAACTAC | 11060 |
rs12708902 | snp | A/G | 0.408188 | 0.193589 | intron-variant | WWP2 | GRCh38.p7 | 16:69934989 | CCAGTTCTGGGGAGG[A/G]GCGTCCCAGCGTCTG | 11060 |
rs12917755 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790974 | TTACATTATTGATTG[G/T]TTTTGTAGTCTTGAA | 11060 |
rs12917758 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790980 | TATTGATTGTTTTTG[C/T]AGTCTTGAAATATTT | 11060 |
rs12918890 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839183 | GGGGAGGGAGGTTCA[C/G]ATATGTGGTTTTGTA | 11060 |
rs12919094 | snp | A/G | 0.365646 | 0.221644 | intron-variant | WWP2 | GRCh38.p7 | 16:69809454 | TCAGGAGGGAATTCT[A/G]GGATGAGACAAATGC | 11060 |
rs12919904 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846050 | gccagactccatctc[A/C]aaaaaaaaaaaaaaa | 11060 |
rs12920039 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846047 | agagccagactccat[C/T]tcaaaaaaaaaaaaa | 11060 |
rs12920069 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826934 | acagagcgagactcc[A/C]cctcaaaaaaaaaaa | 11060 |
rs12920411 | snp | A/C/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826957 | AAAAAAAAAAAAAGG[A/C/G/T]GGGGGGGCGGAGAGA | 11060 |
rs12921025 | snp | C/T | 0.184521 | 0.241273 | intron-variant | WWP2 | GRCh38.p7 | 16:69788281 | ctgtgattgtgccac[C/T]gcactccagcccagg | 11060 |
rs12921131 | snp | G/T | 0.299916 | 0.244966 | intron-variant | WWP2 | GRCh38.p7 | 16:69826866 | ATGGTGTGAACCCGG[G/T]AGGCGGAGCTTGCAG | 11060 |
rs12921407 | snp | C/T | 0.364609 | 0.222182 | intron-variant | WWP2 | GRCh38.p7 | 16:69827030 | CCAGCACACATCTAC[C/T]TGTCCTTCATCTTTA | 11060 |
rs12922133 | snp | A/C | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69880014 | TTTTTCTTTATGGCC[A/C]CATTGGTTCTGCAGA | 11060 |
rs12922142 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784989 | acctgtaatcccagc[A/C]ctttgggaggttgag | 11060 |
rs12922147 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69805815 | tggtatctcactatg[C/T]tgcccaggttggGtg | 11060 |
rs12922291 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785060 | ggccaacatggcgaa[A/C]ccccatctctactaa | 11060 |
rs12922396 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830645 | TTGGGGGGCCGCGGG[A/G]AGGTGGAGTAAGCAG | 11060 |
rs12923161 | snp | G/T | 0 | 0 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909993 | tttgttgacttattg[G/T]ttttggctgtttttg | 11060 |
rs12923168 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910003 | tattgtttttggctg[G/T]ttttgtacttcattg | 11060 |
rs12923438 | snp | A/G | 0.405603 | 0.195673 | intron-variant | WWP2 | GRCh38.p7 | 16:69801198 | aaaaaaaaaaaaaaa[A/G]Caattttactttaat | 11060 |
rs12924193 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898215 | gtttttttagtagag[A/C]cagggtttcgccatg | 11060 |
rs12924486 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898321 | gtgtgagccaccact[C/T]ccagccAGttatttc | 11060 |
rs12924493 | snp | G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69840410 | CCCGGACTCTTCTTA[G/T]CTCCGTGGATCAGTA | 11060 |
rs12924526 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69928482 | CCTCCCTTGGGGACC[C/G]CAGAGCCCTTATCAG | 11060 |
rs12925429 | snp | A/G | 0.370365 | 0.219117 | intron-variant | WWP2 | GRCh38.p7 | 16:69767636 | GGCTGTCTGCAAAGA[A/G]GCAGGAGATGGAGGG | 11060 |
rs12925559 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898320 | ggtgtgagccaccac[C/T]cccagccAGttattt | 11060 |
rs12926035 | snp | C/G | 0.470618 | 0.117591 | intron-variant | WWP2 | GRCh38.p7 | 16:69776658 | atggagaaaccccgt[C/G]tctactaaaaataca | 11060 |
rs12926083 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923324 | TGTTGGGGGGGTGGG[G/T]GGGGTGCGTTCTGAT | 11060 |
rs12926263 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924634 | CCCTGAAGCCCTGGA[A/G]CCAGTTCCCCCTTCT | 11060 |
rs12926287 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862709 | GCCAGCCATGAAttc[C/T]ttttttttttttttt | 11060 |
rs12926494 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836968 | cattttggttgctta[A/G]gttggagtgccctgg | 11060 |
rs12926791 | snp | C/G | 0.364817 | 0.222075 | intron-variant | WWP2 | GRCh38.p7 | 16:69815643 | AATACACAAATTAGC[C/G]GGGTGTGGTGGCGGG | 11060 |
rs12927052 | snp | A/G | 0.409891 | 0.192184 | intron-variant | WWP2 | GRCh38.p7 | 16:69823140 | tgtctcaaaaaagaa[A/G]aaagtaaaaacaaaa | 11060 |
rs12927168 | snp | G/T | 0.409041 | 0.192888 | intron-variant | WWP2 | GRCh38.p7 | 16:69806753 | TTTTTACTTTAAATT[G/T]TTGCTATTTGTGTGT | 11060 |
rs12927431 | snp | A/G | 0.410737 | 0.191478 | intron-variant | WWP2 | GRCh38.p7 | 16:69823144 | tcaaaaaagaaaaaa[A/G]taaaaacaaaaacac | 11060 |
rs12929548 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789805 | ttttatttcccactt[C/G]tttACTTACGcattt | 11060 |
rs12930822 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807644 | aaaaaaaaaaaaaaa[A/G]gaaaAGAAAAAGGAA | 11060 |
rs12930878 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907971 | TTAagccgggtgcgg[G/T]ggctcactcctgtaa | 11060 |
rs12931741 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69865991 | ttttgttcgacactg[A/T]ggaaagaaagactta | 11060 |
rs12932078 | snp | A/G | 0.239037 | 0.24976 | intron-variant | WWP2 | GRCh38.p7 | 16:69934824 | TATCTCCAGCTTTTT[A/G]CATTTTTAGGTTACC | 11060 |
rs12932286 | snp | C/G | 0.248188 | 0.249993 | intron-variant | WWP2 | GRCh38.p7 | 16:69934708 | AAAGTCTGTGGCCCA[C/G]AGACCCTGGGCCCCC | 11060 |
rs12932715 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852095 | ttttgtaagaaactg[C/T]taaactgttttccaa | 11060 |
rs12932790 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824511 | ctccctccctccctt[C/T]ccccctccccctccc | 11060 |
rs12933062 | snp | A/T | 0.32955 | 0.237006 | intron-variant | WWP2 | GRCh38.p7 | 16:69778194 | TATATATATATATAT[A/T]TTTTTTTTTTTGAGA | 11060 |
rs12933101 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793919 | atCCTTGCttttttt[A/T]ttttttttttttttt | 11060 |
rs12933933 | snp | G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69795677 | ttttttttttttttg[G/T]gagagtctctctcca | 11060 |
rs12934211 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69774949 | actccagcctgggtg[A/C]cagagcaagactgtc | 11060 |
rs13329693 | snp | C/G | 0.0513262 | 0.151752 | intron-variant | WWP2 | GRCh38.p7 | 16:69857754 | gcagcctcgacctcc[C/G]aggctcaagtgatct | 11060 |
rs13329778 | snp | C/T | 0.00205705 | 0.0320046 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888082 | TCCCGAAGAACCTTC[C/T]GTTGTTGGTGTGACG | 11060 |
rs13329812 | snp | C/G | 0.00156375 | 0.0279182 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888127 | ACCCTTGAGTGTGAC[C/G]CCGAATCCCAACACG | 11060 |
rs13332047 | snp | C/T | 0.029116 | 0.117091 | intron-variant | WWP2 | GRCh38.p7 | 16:69776655 | aacatggagaaaccc[C/T]gtctctactaaaaat | 11060 |
rs13332544 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69880737 | CCTTGGCAGTGCAGT[C/T]GCTTGTGTTTCACGG | 11060 |
rs13333427 | snp | A/G | 0.160938 | 0.233598 | intron-variant | WWP2 | GRCh38.p7 | 16:69925838 | ATTTTGACACTGCCT[A/G]ACTCCCAAATGGATT | 11060 |
rs13333561 | snp | C/T | 0.046775 | 0.145601 | intron-variant | WWP2 | GRCh38.p7 | 16:69886801 | TCTGGCAAGTACATC[C/T]GTTCAATGATGGGAT | 11060 |
rs13334541 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WWP2 | GRCh38.p7 | 16:69842239 | GATTTCCAGAGATCT[C/T]GTAACTGACTCAGTA | 11060 |
rs13335267 | snp | C/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69891634 | TTTCATGATGCGTGC[C/T]CTGGTCACTCAGTTC | 11060 |
rs13335499 | snp | A/G | 0.046775 | 0.145601 | intron-variant | WWP2 | GRCh38.p7 | 16:69885092 | ACACCACTCTTTTAC[A/G]AACTCCTCCTACACA | 11060 |
rs13335500 | snp | G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69905905 | TTCTCTGAGCCTCAG[G/T]TTCCTCAGTGGTGAT | 11060 |
rs13335905 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | WWP2 | GRCh38.p7 | 16:69880075 | TTCTTCATGATGTTA[C/T]GTTATCAAAATAAAT | 11060 |
rs13336041 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69822469 | AGTTGTGACAGATGC[A/G]ATGGAGCAAAGTACA | 11060 |
rs13336410 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69928295 | GAGAAGCAGATTTGA[A/G]GGCTCAGGAACTTCC | 11060 |
rs13337996 | snp | C/T | 0.00506326 | 0.0500599 | intron-variant | WWP2 | GRCh38.p7 | 16:69795259 | GAAAAAAAATGCGGa[C/T]acacacacacacaca | 11060 |
rs13338223 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69886629 | gctgggtgtggtggc[A/G]cacacctgtaatcct | 11060 |
rs13338793 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | WWP2 | GRCh38.p7 | 16:69905055 | gctgatcagaccacg[C/T]ccaaataaggcagac | 11060 |
rs13338911 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69905137 | ctctaaagacttgcc[A/G]ctcacactgcttggc | 11060 |
rs13339493 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69769654 | TTGTTTGTAGTTGAT[A/G]TTTGAAGAGCTCTTA | 11060 |
rs13380481 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | WWP2 | GRCh38.p7 | 16:69901469 | ccagtctggggtgca[A/G]tggcgcgatctcagc | 11060 |
rs16959189 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | WWP2 | GRCh38.p7 | 16:69799471 | TCTGCCTCCACTACA[A/G]AGTTTAGCCCTCTTT | 11060 |
rs16959196 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | WWP2 | GRCh38.p7 | 16:69800459 | TTCATTTGCCCAGCC[A/G]ATATACTTTTGCTTT | 11060 |
rs16959200 | snp | C/T | 0.138207 | 0.223612 | intron-variant | WWP2 | GRCh38.p7 | 16:69803253 | AAAGTATATTCTAGA[C/T]GTCCTGACATTTTAT | 11060 |
rs16959260 | snp | A/G | 0.0429648 | 0.14013 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837798 | TGGGCGCCTTTAGGA[A/G]ATGACCTGGAAACAA | 11060 |
rs16959266 | snp | C/G | 0.32627 | 0.238082 | intron-variant | WWP2 | GRCh38.p7 | 16:69846869 | TTGCCTGGGTGGTGG[C/G]TCCCAAGTGTTCATT | 11060 |
rs16959270 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | WWP2 | GRCh38.p7 | 16:69849590 | GAGCAGTTGGTAAAT[A/G]TGGAATAGGATTGAG | 11060 |
rs16959271 | snp | A/G | 0.303938 | 0.244112 | intron-variant | WWP2 | GRCh38.p7 | 16:69849643 | CATTCTCCAAGCCAG[A/G]CGTTGAAAAGTAATC | 11060 |
rs16959272 | snp | A/C/T | 0.323434 | 0.238972 | intron-variant | WWP2 | GRCh38.p7 | 16:69849820 | CTCTTAAAAAAAAAA[A/C/T]CATGGAGATTAATTA | 11060 |
rs16959282 | snp | A/C/G | 0.0509478 | 0.151255 | intron-variant | WWP2 | GRCh38.p7 | 16:69858527 | GCGCCCTTTATCACA[A/C/G]CCGCCTTGTGCTTGC | 11060 |
rs17240793 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | WWP2 | GRCh38.p7 | 16:69810382 | GTTCTAGTCATCTCT[A/G]GGTAGAACCCAGCTT | 11060 |
rs17241731 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | WWP2 | GRCh38.p7 | 16:69859918 | GTCTGCTGTGGTACA[C/T]GACGACATACTTGAC | 11060 |
rs17300801 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | WWP2 | GRCh38.p7 | 16:69844989 | GGTCACTGTGCACAC[A/G]TGCTTATGACTGTAG | 11060 |
rs28396625 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837170 | ACTCAAGCAATCCAT[C/T]CTCCTTGGTCTCCCA | 11060 |
rs28405327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834549 | TTTTTTTTTTTGAGA[C/T]GGAGTTTCGCTCTTG | 11060 |
rs28427250 | snp | C/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69765237 | AAAAAAAGTTTCACC[C/T]TTTTGTCTTTTTTTT | 11060 |
rs28429826 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69873087 | TTGGTAAGTGACGCT[A/G]AGATAGTTTTCTAGT | 11060 |
rs28444781 | snp | A/G | 0.179744 | 0.239925 | intron-variant | WWP2 | GRCh38.p7 | 16:69889451 | TGGACCTGTGAATCA[A/G]ACAGCTCTGGGTTTG | 11060 |
rs28477934 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770551 | ATAATAAATCAGTAA[A/T]TGCAAATAAAGTGTT | 11060 |
rs28502677 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69768783 | ACGGGGCTTCCAATA[A/G]TGTACCTCCCTGCTC | 11060 |
rs28522432 | snp | A/G | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69894759 | CACTTTGGGGACCCA[A/G]TGCTCATTATCAATG | 11060 |
rs28523536 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69767532 | ATTATGTGTCACAGG[C/T]AGAAAGGGAATTTAC | 11060 |
rs28538568 | snp | C/T | 0.046775 | 0.145601 | intron-variant | WWP2 | GRCh38.p7 | 16:69888797 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 11060 |
rs28563078 | snp | C/G | 0.14933 | 0.228835 | intron-variant | WWP2 | GRCh38.p7 | 16:69807496 | TGGTGGTGTGTGCCT[C/G]TGGTCCCAGCTACTC | 11060 |
rs28564377 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834496 | TGCCACCTTCTTTTT[A/T]AAATTTTTTTATTTC | 11060 |
rs28576892 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69889940 | TCTCTTTATTCTATT[A/G]TTAAGCCACTTTCAT | 11060 |
rs28583989 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | WWP2 | GRCh38.p7 | 16:69874464 | CCTTTTTTGGCTGCG[C/T]ACTGCAGTTATGCAT | 11060 |
rs28610117 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69803643 | GGCAGGGCGCAGTGA[C/T]TTACACATGTAATCC | 11060 |
rs28611042 | snp | A/G | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69894912 | GGTTTCTTACATAAC[A/G]GAGGGCGTTGTGTTT | 11060 |
rs28624208 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | WWP2 | GRCh38.p7 | 16:69794124 | GGTTTCACCAAGTTG[A/G]CCAGGCTGGTTTCAA | 11060 |
rs28626641 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69872286 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAAGCTC | 11060 |
rs28634771 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69867919 | CAGCCATCACCCTGC[A/G]TTTGTCTGGGTGCTA | 11060 |
rs28651196 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69868844 | CTTCCCATGAAGTGG[A/G]AACTTTGAAATATTC | 11060 |
rs28673794 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69854382 | TTCGACTTTTCCTTT[C/T]GGATTCTGTTGGAAC | 11060 |
rs28753861 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | WWP2 | GRCh38.p7 | 16:69902818 | CCACTGAGGAGGAAC[A/G]GGAATCAGGAGGCTC | 11060 |
rs28756357 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69874092 | CTGTTCCTAAGATCC[A/G]TCTCTGAAGGGCAGT | 11060 |
rs28788800 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | WWP2 | GRCh38.p7 | 16:69801908 | TCTCTTTAAAAATGT[A/G]TCAATATATATTTAT | 11060 |
rs28803823 | snp | A/T | 0.021333 | 0.101051 | intron-variant | WWP2 | GRCh38.p7 | 16:69865411 | GCTGAATTTTAAGAG[A/T]TCTCTATCAATTCTA | 11060 |
rs28813707 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69876649 | GATTATAGGCGTGAG[C/G]CACTGTGCCCAGCCA | 11060 |
rs28845000 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808051 | CCACATCAAGACATA[A/G]CATATTTCTAGCATC | 11060 |
rs28867427 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69876921 | ACAGATGTGCTGTGA[C/T]CCAGGCTTTGTTGCT | 11060 |
rs28882509 | snp | G/T | 0.021333 | 0.101051 | intron-variant | WWP2 | GRCh38.p7 | 16:69865195 | GCTGGGACTACAGGC[G/T]CTTGCCACCATAACT | 11060 |
rs34016123 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844080 | GTTTGGATCTTTTTT[-/C]CCGTACCTTTATTAG | 11060 |
rs34029513 | in-del | -/TTCATTCA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849483 | TCATTCATTCATTCA[-/TTCATTCA]GTTATAATTAAGACA | 11060 |
rs34036455 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834055 | GGTCTTGTGTACCTC[-/A]AGCCCTTCTCCTGTA | 11060 |
rs34084672 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895341 | GTGAGAAAACAGTCC[-/T]TTTTGGTTGTTGTTT | 11060 |
rs34116436 | snp | C/T | 0.266819 | 0.249434 | intron-variant | WWP2 | GRCh38.p7 | 16:69907939 | GGAGGAGAGGGGTAG[C/T]CATAGAACCTGTGAC | 11060 |
rs34119313 | snp | G/T | 0.145978 | 0.227331 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933620 | GCAGTGCACAGCCTA[G/T]GCAACTGAGCATGGT | 11060 |
rs34147639 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775150 | GACTGGTAATACACT[-/G]GGGGGAAATTTAACA | 11060 |
rs34154307 | in-del | -/T | 0.490997 | 0.0664859 | intron-variant | WWP2 | GRCh38.p7 | 16:69824768 | CTTTGCACCTGTGGC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs34195470 | snp | A/G | 0.498813 | 0.0243321 | intron-variant | WWP2 | GRCh38.p7 | 16:69921787 | GTATTGAAACAGATT[A/G]TTTTGACTGGGCGCG | 11060 |
rs34196717 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822484 | ATGGAGCAAAGTACA[-/G]GGATGATCTGGGAAT | 11060 |
rs34223189 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783998 | ATTTAACAGCATCAG[-/T]TTCTCAAGTGTGGTC | 11060 |
rs34251036 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894242 | ACTATACCCAGGCTA[-/T]TTTTTTTTTTTTTTT | 11060 |
rs34269202 | in-del | -/A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69914100 | AAAAAAAAAAAAAAA[-/A/G]GAAAGTGATAAATTT | 11060 |
rs34284992 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825425 | CGAGATTCCATCTCC[-/A]AAAAAAAAAAAACCC | 11060 |
rs34308267 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917393 | TTTGCTAGCGGATGT[-/G]CCTGAGATTGGCTGT | 11060 |
rs34325481 | in-del | -/AC/ACAC | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69885102 | TTACAAACTCCTCCT[-/AC/ACAC]ACACACACACACACA | 11060 |
rs34378064 | snp | A/G | 0.489024 | 0.0732638 | intron-variant | WWP2 | GRCh38.p7 | 16:69848180 | GCGCAGTGGCTCAGC[A/G]TGCAGGCTGGGTGTA | 11060 |
rs34412638 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905930 | GGTGATGGTGATTCC[A/C]CCTTAAAGGATGAAG | 11060 |
rs34470069 | in-del | -/T | 0.48955 | 0.071525 | intron-variant | WWP2 | GRCh38.p7 | 16:69851177 | TAATTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG | 11060 |
rs34483596 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928960 | AGAGAGGTGCGAGGG[-/G]AAATGCAGCCACTCC | 11060 |
rs34489555 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925642 | ACCAGAGCAATTACA[-/G]GGTGATGGAGCTGGG | 11060 |
rs34492692 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835820 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 11060 |
rs34530549 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869452 | GGCTGAAGTGATCCT[-/C]CCTGCCTTGGCCTCC | 11060 |
rs34551082 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798913 | TGGGAGGTACAGATT[-/C]CCCTGTGGCACCTCC | 11060 |
rs34552795 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858835 | CTAGGTGTTCAAATT[-/A]CCCAAGTGATTATTG | 11060 |
rs34586049 | in-del | -/CT/TC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785223 | TTAGGTGTGTGAGAC[-/CT/TC]TSTCTCAAAAAAAAA | 11060 |
rs34586560 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788325 | GAGACCATGTCTCAG[-/A]AAAAAAAAATGTAAG | 11060 |
rs34598258 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815485 | AGACCCTGTCTCTTT[-/A]AAAAAAAAAAAAAAG | 11060 |
rs34605129 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848896 | CCAGTGATTTTTTTA[-/C]CATGGAAAAGTTTCA | 11060 |
rs34656454 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938045 | ATACGTATGGGTTTT[-/G]TTGTTGTCGTTATGA | 11060 |
rs34672996 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866558 | AAATGGAACCACACA[-/G]GGATTTGTCTTTTTG | 11060 |
rs34683525 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874215 | GGCAGCCTGTACTTT[-/A]ATATAACGTCTGCCC | 11060 |
rs34760758 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789759 | AACTTTTGCCTGTTT[-/A]CATTGGTGCAAGCTT | 11060 |
rs34761653 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916918 | CTGTAATCTCAGCAC[-/T]TTTGGGAGGCCGAGG | 11060 |
rs34763880 | snp | A/T | 0.0314385 | 0.121371 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772870 | TTCTGTTGACCTCTC[A/T]TGTGGGCAGCTAAGT | 11060 |
rs34777921 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820555 | GGCCCCCTGTCTCTT[-/A]AAAAAAAAAAAAAAT | 11060 |
rs34779902 | in-del | -/G | | | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910698 | CAGATGTGAGCCACT[-/G]GCGCCCAGCCTACTG | 11060 |
rs34794809 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819121 | TTTAGGATATATTCT[-/G]GGGATCCGACCATCT | 11060 |
rs34864771 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813679 | CACCATGTTGCCCAA[-/G]GCTGGTCTTAAACTT | 11060 |
rs34887959 | in-del | -/T/TT | 0.472573 | 0.208757 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923420 | GCATGAAGGCTGAGA[-/T/TT]TTTTTTTTAAAAGGC | 11060 |
rs34964009 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938041 | TTTTATACGTATGGG[-/TT]TTGTTGTTGTCGTTA | 11060 |
rs34974597 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904490 | CTCCTGCCTCAGTCT[-/C]CCTGAGTAGGTACGA | 11060 |
rs34978477 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829790 | AGGTTCCTAAAAGCA[-/G]GGGACAACGTCTGTT | 11060 |
rs34990976 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786866 | TAAGACAAACTATAC[C/G]CTGGTTGCAGTTGCT | 11060 |
rs35034230 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935609 | GGTTCCCGCACCAGC[-/T]TGGCTCTGCCCAGTC | 11060 |
rs35059847 | snp | C/G | 0.0002324 | 0.0107771 | missense | WWP2 | GRCh38.p7 | 16:69937640 | CAGCAAGCAGATCCA[C/G]TGGTTCTGGCAGGTG | 11060 |
rs35065241 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820856 | CACACACACACACAC[-/AC]GACGTTGAAAGAGTG | 11060 |
rs35075003 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763690 | AACAATTTATTGCTC[-/T]TTTCTTGTTTGCTGG | 11060 |
rs35110838 | in-del | -/CC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832313 | TGTCTCATCTAACTT[-/CC]CCCATCCCACCCCTG | 11060 |
rs35140828 | in-del | -/ATAT | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69777090 | TAAAACAGTATATGG[-/ATAT]ATATATACACATATG | 11060 |
rs35157080 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936145 | TCCTCTGGGTTCCCT[-/G]GGGGACAGTTCTAGA | 11060 |
rs35175050 | in-del | -/T/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851008 | GGTTTCACTCTTTAA[-/T/TT]TTTTTTTTTTTTTTT | 11060 |
rs35185233 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892229 | GTTCTGGGGTATATA[-/T]TTTGCAGAATGTGCA | 11060 |
rs35205098 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935013 | CGTCTGTATTTAACT[-/G]GGAAAGAGGGACACA | 11060 |
rs35218357 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827429 | GGTATGAATAATTTT[-/C]CCATGTTGTTGTATA | 11060 |
rs35273771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841082 | TCATTCAACACATAT[A/G]TATGTAATTGTATTC | 11060 |
rs35298127 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811753 | GCCAGACCCAGTCTC[-/A]AAAAAAATAAAAGAT | 11060 |
rs35326528 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925648 | GCAATTACAGGTGAT[-/G]GGAGCTGGGCAGCTG | 11060 |
rs35331872 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830103 | GGATTACAGGCACAT[-/G]GCCACCATGCCTGGC | 11060 |
rs35345467 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820640 | CTCCTCCCCAGCATT[-/C]CCCTGTTTCTCTTCT | 11060 |
rs35403363 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863523 | GGCGCCTGTAATCCC[-/C]AGCTACAAGGGAGGC | 11060 |
rs35408799 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798155 | CTACATGGGTTTACC[-/T]TTTCTTGGAAAGGAA | 11060 |
rs35448810 | in-del | -/TG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777037 | TCTTAAAACAGTATA[-/TG]TGTGTGTGTGTGTAT | 11060 |
rs35448987 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850223 | AACCCCGTCCCTACT[-/A]AAAATACAAAAAAAT | 11060 |
rs35463435 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939626 | GTCCAAGAGCTACTG[-/C]CCCCAAGTGTCCCCC | 11060 |
rs35469244 | snp | C/G | 0.117188 | 0.211804 | intron-variant | WWP2 | GRCh38.p7 | 16:69882065 | CTTCAAATGATCCAC[C/G]TGCTTTGGCCTCCGA | 11060 |
rs35474328 | in-del | -/TG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921831 | TAATCCCAGCACTTT[-/TG]GGGAGGCTGAGGCAG | 11060 |
rs35482172 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819734 | AAGGCATGTAATTCA[-/G]GGGATTTTAAAATGA | 11060 |
rs35485826 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899727 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 11060 |
rs35500537 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885697 | ACACCAGGGTGTGAA[-/T]TTAGGTGCTATATGA | 11060 |
rs35579205 | in-del | -/AA | 0.304937 | 0.243889 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838446 | GACCCTCCTTGACTT[-/AA]AAAAAAAAAAAAAAA | 11060 |
rs35580809 | in-del | -/G | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942170 | GTGATCTTGACCTCA[-/G]GGTCACGTAAGGGCT | 11060 |
rs35581644 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784673 | TCTGTGTGCTGAAAT[-/G]GGGCAGTACTCCAAA | 11060 |
rs35604394 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849345 | GGCTGCTTGATTGGG[-/C]AACTGCAGTTATTTA | 11060 |
rs35673651 | in-del | -/A/T/TA/TTA | 0.491987 | 0.0627894 | intron-variant | WWP2 | GRCh38.p7 | 16:69851026 | TTTTTTTTTTTTTTT[-/A/T/TA/TTA]GGACAGAGTCTCGCT | 11060 |
rs35714501 | in-del | -/ATTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849859 | TTATACATTGGTTTA[-/ATTA]TTTTGCATCAATTAA | 11060 |
rs35730603 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806281 | TATACCTAGTTGCTC[-/A]AAGATAGACTATTCC | 11060 |
rs35783119 | snp | G/T | 0.375 | 0.216506 | intron-variant | WWP2 | GRCh38.p7 | 16:69811979 | AATTAACAAAACTAA[G/T]AAATTTCCCGTTTTT | 11060 |
rs35791620 | in-del | -/A | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932274 | CAGGAGGTTGCAGTG[-/A]AGCCGAGATCGTGCC | 11060 |
rs35885048 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782257 | ACTGCACTCCAGCCC[-/G]GGGTGACAGAGCGAG | 11060 |
rs35926617 | multinucleotide-polymorphism | CT/GG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824509 | TCCCTCCCTCCCTCC[CT/GG]TCCCCCCTCCCCCTC | 11060 |
rs35928473 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883093 | GGAGGTGGAGGTTGC[-/A]AGTGAGCCAAGATCA | 11060 |
rs35940239 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875431 | TAATAAGACAACATG[-/A]AAGTTCACAGCATCA | 11060 |
rs35951179 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856329 | TGCAAAGGGGCACAA[-/G]GGAAATTTTGGGAGC | 11060 |
rs36055214 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769442 | CCATGGATTATATTG[-/A]AAAAAATTTTTTAAA | 11060 |
rs36095407 | in-del | -/C | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909282 | GACAGAAAGTTCTTT[-/C]CCACATGTGTCTCCT | 11060 |
rs41280902 | snp | A/C | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932880 | GAGAGAGCGCTGTGG[A/C]CCGCAGCGACCTCTC | 11060 |
rs41454046 | snp | A/G | 0.171057 | 0.237209 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909062 | TCTGGGAAACAAAAG[A/G]CGCATGGGAGGCCAA | 11060 |
rs55634572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69897706 | CAAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 11060 |
rs55635123 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | WWP2 | GRCh38.p7 | 16:69880675 | TGCTAATTACGAAAT[C/G]TTTGTCCAGTTTTGG | 11060 |
rs55693243 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803916 | CCGTCTCAAAAAAAA[-/A]TAAAGTAAAGGAATA | 11060 |
rs55749645 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801110 | AGAAGAATCGCTTGA[A/G]CCCGGGAGGTGGAGG | 11060 |
rs55825530 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811375 | ATTTTGGGAGGCTAA[A/G]GCAGGAGGTTTGCTT | 11060 |
rs55863174 | snp | C/G | 0.449726 | 0.150364 | intron-variant | WWP2 | GRCh38.p7 | 16:69786093 | TAGCACACTAGATTA[C/G]CTGTCTTTCTGCTGT | 11060 |
rs55871972 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69886374 | AGTATCTAGGTATCC[A/G]GCCTAGATACTTTGA | 11060 |
rs55887947 | snp | A/G | 0.472147 | 0.114677 | intron-variant | WWP2 | GRCh38.p7 | 16:69859440 | CATGCCTGTCATCCC[A/G]GTTACTCAGGAGGCT | 11060 |
rs55897481 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | WWP2 | GRCh38.p7 | 16:69869180 | GGCATGAGCCACTGT[A/G]TGCGGCCAACAGCTT | 11060 |
rs55921818 | snp | A/G | 0.106987 | 0.205054 | intron-variant | WWP2 | GRCh38.p7 | 16:69880231 | TGCTGGGATCCTATT[A/G]TCACAAAGACATTAA | 11060 |
rs55922317 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910585 | CAACTAATTTTTTGT[A/G]TTTTTAGTAGAGACA | 11060 |
rs55923742 | in-del | -/C/CAACAACAACAA/CAACAACAACAACAACAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783805 | CAACAACAACAACAA[lengthTooLong]AATATTAGAGTTGTG | 11060 |
rs55967108 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | WWP2 | GRCh38.p7 | 16:69908018 | GGCCAAGGTGGGTGG[A/G]TCGCTTGAGCTCAGG | 11060 |
rs55992518 | snp | C/T | 0.449853 | 0.150196 | intron-variant | WWP2 | GRCh38.p7 | 16:69787504 | CTGAAGTGGGAGGAT[C/T]GCTTGAGCCTGGGAG | 11060 |
rs55993175 | in-del | -/CA/CACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795294 | ACACACACACACACA[-/CA/CACA]TACACAGAGACATAG | 11060 |
rs56000913 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | WWP2 | GRCh38.p7 | 16:69805328 | GACGTGAGTCACTGC[A/G]CCCAGCCTGCTTGGT | 11060 |
rs56027108 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912992 | TATATATATATATAT[A/T]TATTTTTTTTTTTTT | 11060 |
rs56055115 | snp | G/T | 0.34989 | 0.229177 | intron-variant | WWP2 | GRCh38.p7 | 16:69913394 | GTGTTCCCAGCTACT[G/T]GGGAGGCTGAGGTGG | 11060 |
rs56057074 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912994 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 11060 |
rs56059021 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897696 | GGGTGGATCACAAGG[C/T]CAGGAGTTCGAGACC | 11060 |
rs56097386 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777858 | GATTGCCTGAGCTCA[A/G]GAGTTCCAGATCAGC | 11060 |
rs56105450 | in-del | -/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69802605 | TTTTCTTTCCTTTTG[-/T]TTTTTTTTTTTTTGA | 11060 |
rs56117028 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69851026 | TTTTTTTTTTTTTTT[A/T]GGACAGAGTCTCGCT | 11060 |
rs56136479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69835201 | GGCCTCTGTAGAGCC[A/G]TCTGCACAGCTGTAG | 11060 |
rs56140069 | snp | A/T | 0.172674 | 0.237741 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761420 | TCTACTAAAAATGCA[A/T]AAATTAGCCAGGCGT | 11060 |
rs56167956 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899463 | GGCCGGGTGCAATGG[C/T]TCATGCCTATAATCC | 11060 |
rs56180453 | snp | G/T | 0.0603597 | 0.1629 | intron-variant | WWP2 | GRCh38.p7 | 16:69883779 | CTATGGGTGAACCAG[G/T]TTGACTCAGAGGCTC | 11060 |
rs56180730 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897753 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCGGGT | 11060 |
rs56182388 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | WWP2 | GRCh38.p7 | 16:69906854 | CACCACACTCCAGCT[C/T]GGGCAACAGAGCAAG | 11060 |
rs56186702 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | WWP2 | GRCh38.p7 | 16:69819940 | TTTCCTGGACATTTT[A/G]TAGAAATGGAATCAT | 11060 |
rs56226752 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912955 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 11060 |
rs56282083 | snp | C/T | 0.450609 | 0.149185 | intron-variant | WWP2 | GRCh38.p7 | 16:69791825 | GTGCCTGGCCCCCAC[C/T]TCGGCCTCTTAAGGT | 11060 |
rs56295983 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855597 | GTATTAAATAGGGCA[A/G]TCAAGAGAGGTGTTG | 11060 |
rs56369384 | snp | C/T | 0.179105 | 0.239737 | intron-variant | WWP2 | GRCh38.p7 | 16:69828438 | ACAGCGCGATCTCAG[C/T]TCACCACAACCTCTG | 11060 |
rs56376857 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771978 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 11060 |
rs56377800 | snp | C/G | 0.0584853 | 0.160693 | intron-variant | WWP2 | GRCh38.p7 | 16:69895537 | GGGAGGCCGAGTCAG[C/G]AGGATTGGTTGAGTC | 11060 |
rs56398381 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791650 | CAGCCTCCTGAGTAG[C/T]TAGGACTTTAGGCAT | 11060 |
rs56801798 | in-del | -/TTAT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866316 | TATTTATTTATTTAT[-/TTAT]GGAGACGGAGTCTTC | 11060 |
rs57037249 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69915654 | GAAAGTGGTTGCCTT[C/T]GGGGAACAGGAGTCA | 11060 |
rs57082779 | in-del | -/TGTG | 0.447162 | 0.153712 | intron-variant | WWP2 | GRCh38.p7 | 16:69927437 | GACCCTGGGCCTGTG[-/TGTG]GCTGAATATGTCTGA | 11060 |
rs57123109 | in-del | -/AGC/CAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914430 | ATCCTTCTTCTCAGC[-/AGC/CAG]TGTAGAGCAGGACCT | 11060 |
rs57130040 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WWP2 | GRCh38.p7 | 16:69935762 | AGGAAGGCGGGTAGC[A/G]GTAGCAGAGTTTGAT | 11060 |
rs57154889 | snp | A/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69899246 | CACACTTGGTGGTTC[A/T]TGCCTGTAACTTTAG | 11060 |
rs57190436 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69920642 | AAAAAAAATGGAACC[A/G]AATGTTGTGGTGCAC | 11060 |
rs57201672 | in-del | -/AAAAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846065 | AAAAAAAAAAAAAAA[-/AAAAAA]GAATACTTATCTGGT | 11060 |
rs57359667 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848284 | GGAGAAACCCCATCT[C/T]TTCTAAAAATACAAA | 11060 |
rs57427510 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914100 | AAAAAAAAAAAAAAA[-/A]GAAAGTGATAAATTT | 11060 |
rs57518557 | snp | C/T | 0.448708 | 0.151707 | intron-variant | WWP2 | GRCh38.p7 | 16:69782257 | CACTGCACTCCAGCC[C/T]GGGTGACAGAGCGAG | 11060 |
rs57520353 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890139 | TTTTTTTTTTTTTTT[-/T]GTAGAGACAGGGTTT | 11060 |
rs57585852 | snp | A/C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69812476 | GCCCCCAACCCCCCC[A/C/T]CTTTTTTTTTTTTTT | 11060 |
rs57613728 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | WWP2 | GRCh38.p7 | 16:69927393 | GGACTCAGGACACCT[C/T]GGGTTCAGATCCACA | 11060 |
rs57651000 | in-del | -/T/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778192 | TATTTTTTTTTTTTT[-/T/TT]GAGAAATTTCAATAG | 11060 |
rs57674223 | in-del | -/CACACACA | 0.406641 | 0.194842 | intron-variant | WWP2 | GRCh38.p7 | 16:69868662 | ACACATACACATGTG[-/CACACACA]CACACACACACACAC | 11060 |
rs57805922 | in-del | -/A | 0.31721 | 0.240796 | intron-variant | WWP2 | GRCh38.p7 | 16:69832352 | TTTTATGAAAATCCC[-/A]GACATACTTCAACTA | 11060 |
rs57824734 | snp | C/T | 0.479014 | 0.100263 | intron-variant | WWP2 | GRCh38.p7 | 16:69778092 | ATATATATATATATA[C/T]ACACACACACACACA | 11060 |
rs57845663 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836535 | CTCAAATAGAACAGA[A/G]GAGGGTTATGTTCTC | 11060 |
rs57869957 | snp | A/G | 0.174932 | 0.238463 | intron-variant | WWP2 | GRCh38.p7 | 16:69915221 | TCCAGAAAAAAGAAA[A/G]AAGTTGTTACAAGTA | 11060 |
rs57904410 | in-del | -/GG/TG/TGC | 0.5 | 0 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923323 | TGTTGGGGGGGTGGG[-/GG/TG/TGC]GGGGGTGCGTTCTGA | 11060 |
rs57953452 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876367 | GGGTTTTTTTTTTTT[-/TT]CGTTTTTTGTTTTTG | 11060 |
rs58026486 | snp | A/C | 0.171057 | 0.237209 | intron-variant | WWP2 | GRCh38.p7 | 16:69878870 | ATGTGAATTTTAAAA[A/C]TGAGCTCTAGTGTGT | 11060 |
rs58153395 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69914334 | AGGCTCATCTGATTG[A/G]ATTTCTGAGTGCCAA | 11060 |
rs58163059 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778192 | TATATATATATATAT[A/T]TTTTTTTTTTTTTGA | 11060 |
rs58227376 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941224 | AGGTCATATTGAAAT[C/T]TTCAAGGTGACCATG | 11060 |
rs58236106 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899097 | TGGCTTGTCTTTTCA[-/A]TTTGCTTATGGTGCC | 11060 |
rs58342753 | snp | C/T | 0.0895391 | 0.191709 | intron-variant | WWP2 | GRCh38.p7 | 16:69939141 | ATGTTTTCTCTCGCC[C/T]TCTGGCGTCCTGGCT | 11060 |
rs58385119 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69836616 | AAATTTAAATTAAAT[G/T]AATTTATTTTTTGAG | 11060 |
rs58401894 | in-del | -/A | 0.317451 | 0.240729 | intron-variant | WWP2 | GRCh38.p7 | 16:69851824 | CTCTAGTAAAAATAC[-/A]AAAAAAAAATTAGCT | 11060 |
rs58483930 | in-del | -/CTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831827 | GGAAAAAAACAAAAC[-/CTT]TTTTTTTTTTTTTTT | 11060 |
rs58504050 | in-del | -/AA/AAAAAAA/AAAAAAAAAAAAAAAAAA | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69846070 | AAAAAAAAAAAAAAA[lengthTooLong]GAATACTTATCTGGT | 11060 |
rs58521765 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69914267 | CTCAAGTATCCAGAT[C/T]CAAACAGCTCACCAC | 11060 |
rs58722949 | snp | A/T | 0.106987 | 0.205054 | intron-variant | WWP2 | GRCh38.p7 | 16:69880021 | TTATGGCCACATTGG[A/T]TCTGCAGAGATAAAT | 11060 |
rs58813634 | in-del | -/T | 0.234401 | 0.249513 | intron-variant | WWP2 | GRCh38.p7 | 16:69900525 | TTTAATGTTGCCAAC[-/T]TTTTTTTTTTTCTTT | 11060 |
rs58892726 | snp | C/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69893321 | TGGCACAGAGTAGGC[C/T]CCCAAGACATGTTTG | 11060 |
rs58923591 | in-del | -/ACAAAACAAA/ACAAAACAAAACAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852011 | ACAAAACAAAACAAA[-/ACAAAACAAA/ACAAAACAAAACAAA]GTTTTTAACTTGCTT | 11060 |
rs58991135 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | WWP2 | GRCh38.p7 | 16:69918152 | CGAGATCGGCTTTCA[C/T]TTCTGCCCCCTTCAT | 11060 |
rs59001611 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935098 | CGTGGAGAACCCGGA[C/T]TGAGAAGCGGAGCCC | 11060 |
rs59057255 | snp | A/G | 0.117537 | 0.212022 | intron-variant | WWP2 | GRCh38.p7 | 16:69876226 | GCCTCCCAAAGTGCT[A/G]GGATTGTAGGCTTAA | 11060 |
rs59105082 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838987 | GAGGGATTTAGAGCA[C/G]TCTTTTTTGGGGGGG | 11060 |
rs59117950 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848282 | ATGGAGAAACCCCAT[C/T]TCTTCTAAAAATACA | 11060 |
rs59277595 | in-del | -/ATGTTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852677 | AAAATCTGGTTGTTC[-/ATGTTC]TTATTGTTGAGTTTT | 11060 |
rs59295610 | in-del | -/CACACACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912404 | ACACACACACACACA[-/CACACACA]GCCTCATGACTGCCT | 11060 |
rs59341411 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69783874 | GTGAGAGGATTGCTC[A/G]AGTCTAGGAGTTCAA | 11060 |
rs59441775 | in-del | -/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899751 | AAAAAAAAAAAAAAA[-/AA]TCAAGTTGTGGTTTA | 11060 |
rs59524086 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69785713 | CCCACTGCAACCTCC[A/G]CTTCCCGAGTTCAAG | 11060 |
rs59561303 | in-del | -/T | 0.486855 | 0.0799975 | intron-variant | WWP2 | GRCh38.p7 | 16:69803339 | TTCTATTTTTTTTTT[-/T]ACTTTGGAACATTTA | 11060 |
rs59609274 | in-del | -/AAAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899747 | AAAAAAAAAAAAAAA[-/AAAAA]TCAAGTTGTGGTTTA | 11060 |
rs59652261 | in-del | -/CACACA | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69912406 | ACACACACACACACA[-/CACACA]GCCTCATGACTGCCT | 11060 |
rs59740587 | snp | A/G | 0.181659 | 0.240478 | intron-variant | WWP2 | GRCh38.p7 | 16:69915105 | GATGTGGCCGAGAGA[A/G]GAAGGCCACTGCCAG | 11060 |
rs59771717 | in-del | -/ACACACAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883420 | CACACACACACACAC[-/ACACACAC]TCATTTACTCCTACT | 11060 |
rs59851738 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771978 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 11060 |
rs59908425 | in-del | -/TTATTTATTTAT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866308 | TATTTATTTATTTAT[-/TTATTTATTTAT]GGAGACGGAGTCTTC | 11060 |
rs59956274 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773197 | TCCTTTTTTTTTTTT[-/T]GAGATGACTCTCATG | 11060 |
rs60013671 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912611 | GGGGAAAGTGATAGT[C/T]TAAGAGAAAGAAACA | 11060 |
rs60073372 | in-del | -/GG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890548 | TTATAATTTGGGGGG[-/GG]AACAATGCAGAATCA | 11060 |
rs60137705 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | WWP2 | GRCh38.p7 | 16:69893698 | AGGCTTGCGCCACCA[C/T]GCCCAGCTAATTTTT | 11060 |
rs60162697 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825816 | ATTTTTTGTAGACAC[A/C]GGATCTCCCTATGTT | 11060 |
rs60219317 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69799898 | GTTTGTGGTCAGTGG[C/G]ATGGCCCATGGCGGT | 11060 |
rs60231938 | snp | A/G | 0.450859 | 0.148847 | intron-variant | WWP2 | GRCh38.p7 | 16:69796512 | TTGCGGCTCACTGCC[A/G]CTGCCCAGTAGTACC | 11060 |
rs60248492 | snp | C/G | 0.338523 | 0.233803 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909597 | TCCTTTTTTCCGTAC[C/G]TCCTGGAGGATGAAA | 11060 |
rs60340110 | in-del | -/T | 0.187685 | 0.242109 | intron-variant | WWP2 | GRCh38.p7 | 16:69880273 | CTGTGATTTTTTTTT[-/T]AGTGTTGATCACTTT | 11060 |
rs60476482 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69885247 | CATAGTGTTTTTTTT[A/T]AAATTGAGTAAAATG | 11060 |
rs60525790 | snp | G/T | 0.0748431 | 0.178382 | intron-variant | WWP2 | GRCh38.p7 | 16:69890542 | CTGTATGTTATAATT[G/T]GGGGGGAACAATGCA | 11060 |
rs60555123 | snp | C/T | 0.143622 | 0.226238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812478 | CCCCAACCCCCCCCC[C/T]TTTTTTTTTTTTTTA | 11060 |
rs60682617 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69830857 | ACCTGGGGTGGACTC[C/T]AGCCTGTGTGTGTCT | 11060 |
rs60683406 | snp | A/T | 0.0818113 | 0.184966 | intron-variant | WWP2 | GRCh38.p7 | 16:69882872 | AAGTTAATACAGCAG[A/T]CCGGGTGCGGTGGCT | 11060 |
rs60824446 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851388 | CTGATATTTTATTGT[C/T]TGCATAGTTTTGCCA | 11060 |
rs60941540 | snp | A/T | 0.49334 | 0.057322 | intron-variant | WWP2 | GRCh38.p7 | 16:69820126 | TAGTCCCAGCTACTC[A/T]GGAGGGTGAGGCAGG | 11060 |
rs60949042 | snp | C/T | 0.078151 | 0.181571 | intron-variant | WWP2 | GRCh38.p7 | 16:69899487 | ATAATCCCAGCACTT[C/T]GCGAGGCCGAGGCAG | 11060 |
rs61090597 | snp | A/C | 0.295854 | 0.245759 | intron-variant | WWP2 | GRCh38.p7 | 16:69842869 | AGATAGGGTTTTACC[A/C]TGTTGCCCAGGCTGG | 11060 |
rs61187943 | in-del | -/A/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875034 | TCAAAAAAAAAAAAA[-/A/AA]TTACAGCAAAAGTAT | 11060 |
rs61224211 | in-del | -/C | 0.306679 | 0.24349 | intron-variant | WWP2 | GRCh38.p7 | 16:69810307 | CTCTGAGGGGACATT[-/C]GCCCTGGCCATGGCT | 11060 |
rs61241672 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801120 | CTTGAACCCGGGAGG[C/T]GGAGGTTCCAGTGAG | 11060 |
rs61285331 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WWP2 | GRCh38.p7 | 16:69794953 | TGGGCAGTAGCTCAT[A/G]TTTGTAATCCCAGCA | 11060 |
rs61296923 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69801146 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 11060 |
rs61378072 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807616 | AGAGCAAGACCCTTT[C/T]TCCAAAAAAAAAAAA | 11060 |
rs61611907 | snp | C/T | 0.284733 | 0.247575 | intron-variant | WWP2 | GRCh38.p7 | 16:69913169 | AGTTGGGGTTACAGG[C/T]ACATGCCACCACGCC | 11060 |
rs61650147 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784116 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 11060 |
rs61664474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69907101 | TTTGCTTGTGGAAGC[A/G]GGTGTCAGAAGTTGG | 11060 |
rs62050038 | snp | A/T | 0.175254 | 0.238565 | intron-variant | WWP2 | GRCh38.p7 | 16:69768962 | CATTAGTGTTGGAGT[A/T]GCATGAGCCTGTGAA | 11060 |
rs62050039 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69770969 | GAAATCCTGTCTCTA[A/T]TAAAAAAAAAAAAAA | 11060 |
rs62050040 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69792131 | TGTGGGGTGTGACTG[C/T]GCGGTTTCCAGTTCC | 11060 |
rs62050041 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796004 | GGCCTGGACCAGAAC[A/T]AATTTTTTTTTCTTT | 11060 |
rs62050042 | snp | C/T | 0.232067 | 0.249356 | intron-variant | WWP2 | GRCh38.p7 | 16:69797844 | AGTGAGCCGAGATTG[C/T]GGCATTACACTCCAG | 11060 |
rs62050043 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69805142 | CCTCCTGGGTTCAAG[C/T]GATTCTCGTGCCTCA | 11060 |
rs62051384 | snp | C/T | 0.488606 | 0.0746142 | intron-variant | WWP2 | GRCh38.p7 | 16:69825279 | AAAATACAAAATTAG[C/T]TGGGCATGGTGGCAG | 11060 |
rs62051385 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69825413 | TGGGCAACAGAGCGA[A/G]ATTCCATCTCCAAAA | 11060 |
rs62051386 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825423 | AGCGAGATTCCATCT[A/C]CAAAAAAAAAAAACC | 11060 |
rs62051387 | snp | C/T | 0.488846 | 0.0738428 | intron-variant | WWP2 | GRCh38.p7 | 16:69826752 | AAAATTAGCCTAACA[C/T]GGTGAAACCCCGTCT | 11060 |
rs62051388 | snp | A/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827446 | CATGTTGTTGTATAC[A/G/T]CTTTATAATCACTAA | 11060 |
rs62051389 | snp | A/G | 0.488846 | 0.0738428 | intron-variant | WWP2 | GRCh38.p7 | 16:69828346 | CTGTCTTTCTTGCAA[A/G]GTCATCATCTATTAT | 11060 |
rs62051390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69830882 | GTGTCTGAGTTTCAG[A/G]GAACTGGGGAATGGA | 11060 |
rs62051391 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | WWP2 | GRCh38.p7 | 16:69848759 | GTGAACGCACATGAG[A/G]GAGTGTGTATGTGTG | 11060 |
rs62051417 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69863052 | TTCTCGGCATTTGGG[A/G]GAGATATGTCCCTAG | 11060 |
rs62053260 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69916716 | GCCTGGGTGTGGGGA[G/T]AGAGCTGTGGCATTC | 11060 |
rs62053261 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69919498 | CGTCCAGAATTGTGG[G/T]TGCTCTGGTTTCAAA | 11060 |
rs62053262 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | WWP2 | GRCh38.p7 | 16:69935396 | CCCTAGACTATTACT[C/G]ACCATTGGCCGCCAG | 11060 |
rs62053263 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937886 | TTGGGCCAGCTGGTG[C/T]GCAGGGACAGACCTG | 11060 |
rs62053264 | snp | A/G | 0.0410537 | 0.137264 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940870 | ATGAGAGGGGTTGAG[A/G]TCCCGAGCGCCACTC | 11060 |
rs63568562 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824768 | CTTTGCACCTGTGGC[G/T]TTTTTTTTTTTTTTT | 11060 |
rs66476556 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795274 | TACACACACACACAC[-/A]CACACACACACACAC | 11060 |
rs66476557 | snp | A/C | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69795274 | TACACACACACACAC[A/C]CACACACACACACAC | 11060 |
rs66601463 | in-del | -/T | 0.441977 | 0.16014 | intron-variant | WWP2 | GRCh38.p7 | 16:69786138 | TCTTTTTTTTTTTTT[-/T]CTTCTTTTTTTGAGA | 11060 |
rs66633306 | in-del | -/T | 0.313814 | 0.241719 | intron-variant | WWP2 | GRCh38.p7 | 16:69836293 | CTCCATCCTGCCTCC[-/T]TTTTTTTTTTTGTTT | 11060 |
rs66717971 | snp | A/C | 0.461592 | 0.133149 | intron-variant | WWP2 | GRCh38.p7 | 16:69934719 | CCCAGAGACCCTGGG[A/C]CCCCTCTTGACAAGT | 11060 |
rs66938317 | multinucleotide-polymorphism | AAA/GGG | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69826955 | AAAAAAAAAAAAAAA[AAA/GGG]GGCGGGGGGGAGAGA | 11060 |
rs67149019 | snp | C/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69826965 | AAAAAGGGGGGGGGG[C/G]GGAGAGAATAATGGA | 11060 |
rs68039170 | snp | C/T | 0.49263 | 0.0602539 | intron-variant | WWP2 | GRCh38.p7 | 16:69852186 | CTTCACCAGGTTTGA[C/T]GTAGTCCATTTTCTG | 11060 |
rs68161338 | snp | G/T | 0.368938 | 0.219895 | intron-variant | WWP2 | GRCh38.p7 | 16:69789875 | TGCTCAGTAAAAAAA[G/T]CCACATGTAACTTTT | 11060 |
rs71151133 | in-del | -/T | 0 | 0 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760514 | TTTTTTTTTTTTTTT[-/T]GTAGTTTTAGTAGAG | 11060 |
rs71151134 | in-del | -/T | 0.275999 | 0.248644 | intron-variant | WWP2 | GRCh38.p7 | 16:69769875 | CAAGTGATCAGTGTC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs71151135 | in-del | -/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69793936 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTGC | 11060 |
rs71151137 | in-del | -/CATT | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69806992 | ATTCATTCATTCATT[-/CATT]TATAGCTTTTCAGGT | 11060 |
rs71151138 | in-del | -/A | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69825436 | TCCAAAAAAAAAAAA[-/A]CCCCAAAAACCAAAA | 11060 |
rs71151139 | in-del | -/A | 0.367708 | 0.220556 | intron-variant | WWP2 | GRCh38.p7 | 16:69826268 | GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 11060 |
rs71151140 | in-del | -/A | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69827155 | ATGAAAAAAAAAAAA[-/A]CTACTGTGGAATTAA | 11060 |
rs71151141 | in-del | -/TTAT | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69866319 | TATTTATTTATTTAT[-/TTAT]GGAGACGGAGTCTTC | 11060 |
rs71384747 | snp | C/G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69826960 | AAAAAAAAAAAAAGG[C/G/T]GGGGGGGAGAGAATA | 11060 |
rs71385619 | in-del | -/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69811727 | TCACTGCAATCCAGT[-/C]TGGATGACAGAGCCA | 11060 |
rs71385620 | in-del | -/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69857382 | CAGGTGTGAGCCACC[-/C]ACGCCTGGCGTAACT | 11060 |
rs71385623 | in-del | -/CAG | 0.284733 | 0.247575 | intron-variant | WWP2 | GRCh38.p7 | 16:69914429 | TGCCATCCTTCTTCT[-/CAG]CAGCTGTAGAGCAGG | 11060 |
rs71385624 | in-del | -/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69928717 | AGTTCGAGACCAGCC[-/C]AGGACAACATAGCGA | 11060 |
rs71385625 | in-del | -/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69929177 | TGGGTGGCCACACCA[-/C]CCCCTCCCTCCGACC | 11060 |
rs71397988 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69807033 | CTGCATTTATCTTTG[G/T]CTTTTTTTTTTTGAG | 11060 |
rs71397990 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69817975 | GCAGTCGCTGGGTCA[A/G]AAGGTGGGCGTGTTT | 11060 |
rs71397991 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69863029 | GCCACCCCCGGCCTA[A/G]CCATGAATTCTCGGC | 11060 |
rs71397992 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69913299 | CGGCCTCCCAAAGTG[C/G]TGGGATTACAGGCGT | 11060 |
rs71397993 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69919907 | AAGTGATCCTCCCAC[C/T]TCAGCCCCCTCAAGT | 11060 |
rs71787048 | in-del | -/TATT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866801 | TTGCTTTCAGTTCCG[-/TATT]TATTTATTTATTTAT | 11060 |
rs71893412 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870315 | TTTTTTTTTTTTTTT[-/T]GGAGACACTCTCACT | 11060 |
rs72239290 | in-del | -/ATTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806954 | TCATTCATTCATTCA[-/ATTC]TTCATTCATTTATAG | 11060 |
rs72523665 | in-del | -/CT | 0.397452 | 0.201886 | intron-variant | WWP2 | GRCh38.p7 | 16:69917944 | TTGCGAATGTGCAGC[-/CT]CACGTGTTCTCTGTT | 11060 |
rs72626171 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814455 | TCAACACTATTTATA[A/T]ATATTTACAAATTCC | 11060 |
rs72783163 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | WWP2 | GRCh38.p7 | 16:69764346 | GCTGGGACTACAGGT[A/G]GGTGCCACCTCGCCT | 11060 |
rs72783165 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | WWP2 | GRCh38.p7 | 16:69765921 | TCCTGCCTCAGCCTC[C/G]GAAAGTGCTGAGATT | 11060 |
rs72783174 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | WWP2 | GRCh38.p7 | 16:69775775 | GTTCCTCTTCCTTAC[C/T]CCTCCCTAGTTCTTG | 11060 |
rs72783176 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | WWP2 | GRCh38.p7 | 16:69781097 | GTCACTAAAGTTTGT[A/G]TACAACCCCTGAATG | 11060 |
rs72783183 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69796017 | ACAAATTTTTTTTTC[C/T]TTCTTTTTTTTTTTG | 11060 |
rs72783184 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69798268 | GTAATTTCCCCAGAG[C/T]GAACAATTGCAAGCA | 11060 |
rs72783188 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | WWP2 | GRCh38.p7 | 16:69809391 | CAGAGACCCTGTTTC[C/T]GGATGCGAGACTGTC | 11060 |
rs72783189 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69819019 | TACATCTTGAAGCAG[C/T]GACAATTCTGTGTCA | 11060 |
rs72783195 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | WWP2 | GRCh38.p7 | 16:69821595 | GCAAAGGGTGATTCT[C/G]CTCCAAATGCTGAAT | 11060 |
rs72783198 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | WWP2 | GRCh38.p7 | 16:69822575 | TGTGTTCATGCATGT[A/G]TGTTTATCAAGGAAG | 11060 |
rs72785009 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | WWP2 | GRCh38.p7 | 16:69844670 | AGGCTGCAACAGGAA[A/G]TCGGATGCATTTTGG | 11060 |
rs72785012 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | WWP2 | GRCh38.p7 | 16:69844969 | TTTGCTGTTGCAGGT[A/G]TGAAGGTCACTGTGC | 11060 |
rs72785013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850620 | GACCGACGAAGTGGG[G/T]TTCAGGGATGTCACT | 11060 |
rs72785016 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851400 | TGTCTGCATAGTTTT[C/G]CCATTTCCAGAATGT | 11060 |
rs72785019 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | WWP2 | GRCh38.p7 | 16:69859094 | TGTAACAAATCACCA[C/T]AAACTCAGGGCTTAA | 11060 |
rs72785020 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69859696 | CTTCCCCCTGGCCCC[A/G]ACCCCTGCATTCCTT | 11060 |
rs72785024 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69863206 | TCTACAACTTTTGCT[A/C]ACTTTTACATTTTCT | 11060 |
rs72785026 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69866723 | GATGGGTTGCTTCTA[C/T]CTCTTGGCTATTGTG | 11060 |
rs72785029 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69867946 | GCTATTTTGGCCCAC[A/G]ATGTGTGGTTTCAGC | 11060 |
rs72785033 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69869462 | GATCCTCCTGCCTTG[A/G]CCTCCCAAGTACCTG | 11060 |
rs72785034 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | WWP2 | GRCh38.p7 | 16:69869575 | GGTCTCAAACTCTTG[A/G]GCTCAAGTGCCGTCC | 11060 |
rs72785037 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69870172 | TTAATCTACCTTTAG[A/G]GTTCCCATGTTAAAT | 11060 |
rs72785038 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | WWP2 | GRCh38.p7 | 16:69870212 | TATGTAAATGCATAG[C/T]ACACACAGTGCCTGG | 11060 |
rs72785040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69871571 | CTCTGGATTTGTTTA[C/G]TTGAAGTGGAAAAGT | 11060 |
rs72785045 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | WWP2 | GRCh38.p7 | 16:69877014 | AATGTTAAGTGAACA[C/T]TGGCTTCAACTTAAA | 11060 |
rs72785047 | snp | C/T | 0.106987 | 0.205054 | intron-variant | WWP2 | GRCh38.p7 | 16:69879385 | AACATTTCCCCCCAA[C/T]CTGACCGGCCCCCGC | 11060 |
rs72785048 | snp | C/T | 0.106987 | 0.205054 | intron-variant | WWP2 | GRCh38.p7 | 16:69879447 | TTCTGCATTTTCTTA[C/T]TCTAGATACCTCATA | 11060 |
rs72785052 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | WWP2 | GRCh38.p7 | 16:69880917 | CACACGCACCTAAGC[A/G]TCTTGGAACACACAG | 11060 |
rs72785055 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | WWP2 | GRCh38.p7 | 16:69882410 | TCTTTCTTTTGCTAG[A/G]TTATTGGGCTTATTG | 11060 |
rs72785057 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69884855 | AGTTGATATGGGGAG[A/G]TTTCTCTTTACAGAA | 11060 |
rs72785058 | snp | C/T | 0.131723 | 0.220251 | intron-variant | WWP2 | GRCh38.p7 | 16:69885968 | AGAAGAGGCAGTAGA[C/T]GATATCTCGAAGAGG | 11060 |
rs72785059 | snp | G/T | 0.065353 | 0.169134 | intron-variant | WWP2 | GRCh38.p7 | 16:69887117 | TAAGTGATCATCAAA[G/T]AGGTGAAGAGATGGT | 11060 |
rs72785064 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | WWP2 | GRCh38.p7 | 16:69896557 | AAATGATATCACATT[C/T]TCAGTGGCCCTTAAA | 11060 |
rs72785065 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | WWP2 | GRCh38.p7 | 16:69900839 | AGTGTTGCCAACCTC[C/T]ATTGAGGAGCTTTGG | 11060 |
rs72785067 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69914459 | GACCTTCACAATTCC[A/G]ATGGAAAATGATTTC | 11060 |
rs72785070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915656 | AAGTGGTTGCCTTCG[A/G]GGAACAGGAGTCAGC | 11060 |
rs72785073 | snp | A/G | 0.0618563 | 0.164627 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924328 | CCCATGTGTGGCTCC[A/G]GCACCCCTAGACGGG | 11060 |
rs73568154 | snp | A/T | 0.471863 | 0.115225 | intron-variant | WWP2 | GRCh38.p7 | 16:69850403 | AAAAAAAAAAAAAAA[A/T]GATGAAAAGTCAGGG | 11060 |
rs73572162 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | WWP2 | GRCh38.p7 | 16:69892045 | CTCTAGGTGCCATAC[A/G]GGCAGGGATTGTGTC | 11060 |
rs73572177 | snp | C/T | 0.361053 | 0.22398 | intron-variant | WWP2 | GRCh38.p7 | 16:69897824 | GAGGCAGAAGAATGG[C/T]TTGAACCAGGGAGGC | 11060 |
rs73572182 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69904855 | ACATCCCTACATGCT[A/G]TTTAATGGTGTTTGT | 11060 |
rs73572191 | snp | A/G | 0.0700422 | 0.173537 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910015 | CTGTTTTTGTACTTC[A/G]TTGGCAGAGTTGAGT | 11060 |
rs73572192 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910137 | CCCCAACCTATCCGC[C/T]GCACCCTGATCTAGG | 11060 |
rs73572193 | snp | G/T | 0.19334 | 0.243495 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910362 | ACACACTTGTACTTT[G/T]TGTACTTTATAACAT | 11060 |
rs73576131 | snp | G/T | 0.181659 | 0.240478 | intron-variant | WWP2 | GRCh38.p7 | 16:69916439 | GAAGTTTTTGAGCAG[G/T]AGTGTGACCGAAGGG | 11060 |
rs73576152 | snp | A/G | 0.175897 | 0.238765 | intron-variant | WWP2 | GRCh38.p7 | 16:69927237 | GCTGTGGCTGGGGCC[A/G]GCTCCCCAGGGCTCA | 11060 |
rs73576178 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933376 | GGGGATGGTGTTGGG[A/G]TCTGGGGGTGAAGGG | 11060 |
rs73579458 | snp | C/G | 0.434398 | 0.168811 | intron-variant | WWP2 | GRCh38.p7 | 16:69770861 | TGTGGGGCTGGGCGT[C/G]GTGGCTCACACCTGT | 11060 |
rs73579497 | snp | C/G | 0.450483 | 0.149354 | intron-variant | WWP2 | GRCh38.p7 | 16:69790247 | AACGAAATTCTATCT[C/G]AAAGAAAACAACAAA | 11060 |
rs73580162 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | WWP2 | GRCh38.p7 | 16:69934879 | GCCCAGAGAGGGCGC[A/G]CCAGTCCATGGGCGC | 11060 |
rs73580166 | snp | A/G | 0.029116 | 0.117091 | intron-variant | WWP2 | GRCh38.p7 | 16:69935084 | GAGGGTCCTGGGAGC[A/G]TGGAGAACCCGGATT | 11060 |
rs73580178 | snp | A/G | 0.183886 | 0.241099 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941182 | CAGCCTCCAACACGG[A/G]GACTCTGCCGTAACT | 11060 |
rs74027204 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69844314 | CTTAAGCTAGAACAG[C/T]GGTGGGCGAGGAATA | 11060 |
rs74027205 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69848932 | TCTTAGATAGTTTTC[C/T]TTCTCACTCCTTTAC | 11060 |
rs74027206 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69849124 | AGACAGCCTATCCCA[G/T]AAAGGAAAGAAAAAT | 11060 |
rs74027208 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69849438 | ATTGCCTCATTTCTG[G/T]TGCTGGGGAAGACAA | 11060 |
rs74027209 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69849482 | ATTTATTTATTTATT[C/T]ATTCATTCATTCATT | 11060 |
rs74027707 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | WWP2 | GRCh38.p7 | 16:69921474 | GGGAATCCCAGATTG[C/T]AGTCTCCTGTAATTC | 11060 |
rs74027708 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923509 | AGACTGTCAGTAAAG[A/G]CCTTTTTGGTCTGTT | 11060 |
rs74027734 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | WWP2 | GRCh38.p7 | 16:69928769 | AGAAAAAAAAGATAC[A/G]AGTCTAAGAAGAGGC | 11060 |
rs74027735 | snp | A/G | 0.00990075 | 0.0696588 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933187 | CGGGGCACCCTCTGC[A/G]TCGACGGACTCCTCG | 11060 |
rs74027736 | snp | A/T | 0.141596 | 0.225274 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933624 | TGCACAGCCTAGGCA[A/T]CTGAGCATGGTGACC | 11060 |
rs74029465 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69796948 | ATTGTAGGACTGTCA[C/T]CTTTCAGAAGAGTCT | 11060 |
rs74029466 | snp | A/G | 0.128976 | 0.218754 | intron-variant | WWP2 | GRCh38.p7 | 16:69797262 | GAAGAAGAAATGTAG[A/G]TGACTAACGACACAT | 11060 |
rs74029472 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69833872 | GATCAGTGGCCCTGC[A/G]GGGCCTGGCTGATGT | 11060 |
rs74029720 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | WWP2 | GRCh38.p7 | 16:69860566 | TCCAGGAAGAGAATG[C/T]CGGGCAAGTAGATCA | 11060 |
rs74029722 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | WWP2 | GRCh38.p7 | 16:69867790 | CTGACTGGCACTGCC[A/G]TTCTAACTGCTTTCT | 11060 |
rs74029723 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | WWP2 | GRCh38.p7 | 16:69868663 | CACATACACATGTGC[A/G]CACACACACACACAC | 11060 |
rs74029724 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69869924 | GGAGGTGGATCCTCC[C/T]AATGGGGAACTTTCT | 11060 |
rs74029725 | snp | G/T | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69871664 | GAACCAGCTTCTGTT[G/T]AGTCCAAAACTAGAG | 11060 |
rs74029728 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | WWP2 | GRCh38.p7 | 16:69872646 | ACTAAGTATTGTTGC[G/T]AAGAGCTGAGTCAGA | 11060 |
rs74029732 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | WWP2 | GRCh38.p7 | 16:69878753 | AATGTTCCATAATTC[A/G]TCTAACCATTCCTTA | 11060 |
rs74029733 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | WWP2 | GRCh38.p7 | 16:69882387 | AAACTCACCTATTCA[A/G]TCAAATATCTTTCTT | 11060 |
rs74029734 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69883400 | GTTCTAAGAATGTGC[A/G]CACACACACACACAC | 11060 |
rs74029735 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | WWP2 | GRCh38.p7 | 16:69885497 | AGGCTCTTACCTGTT[C/T]GTTAAGATCTAGCTT | 11060 |
rs74029736 | snp | A/C | 0.039522 | 0.134904 | intron-variant | WWP2 | GRCh38.p7 | 16:69885611 | AGTTATTATAATCTT[A/C]GGTTGAATTAGAGGA | 11060 |
rs74029737 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | WWP2 | GRCh38.p7 | 16:69889673 | GGCATGCTTCTGAAC[C/T]GGGAGGTGAAGTCCC | 11060 |
rs74029738 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | WWP2 | GRCh38.p7 | 16:69889833 | GTGTATCCTGTGAAC[C/T]GTTGTGATTCATAAA | 11060 |
rs74029740 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69895240 | AAACCAGGCGCTGCC[A/G]TTGAATTTCATTCCA | 11060 |
rs74029744 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69896792 | GTTTCTAAGGTGCTG[C/G]GGACTGCCCAGTTTC | 11060 |
rs74029746 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | WWP2 | GRCh38.p7 | 16:69899975 | CAATATTTATCTACA[A/G]TGTTATTTTTAAGGA | 11060 |
rs74029748 | snp | A/G | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69900001 | AAGGAATGAATACCC[A/G]TTATAGGAATAACAT | 11060 |
rs74029749 | snp | A/C | 0.0807149 | 0.183963 | intron-variant | WWP2 | GRCh38.p7 | 16:69902733 | TGAAAAATTGATACC[A/C]GTGTCACTTTCTTGG | 11060 |
rs74029751 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69905171 | GCTCTCTGAGCCTCT[C/T]CTGGTTCTGAGTGCT | 11060 |
rs74249227 | snp | C/T | 0.237303 | 0.249677 | intron-variant | WWP2 | GRCh38.p7 | 16:69892531 | TACCCTTTCCCAATC[C/T]ATTTTAACTTTTCTT | 11060 |
rs74320813 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69906367 | GTCAGCCACCGCACC[C/T]GGCCTTACGTATCTG | 11060 |
rs74338582 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | WWP2 | GRCh38.p7 | 16:69822075 | TCTCCCTTTGTTGCC[C/T]GAGCTGGTCTCAAAC | 11060 |
rs74342400 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | WWP2 | GRCh38.p7 | 16:69859816 | GCTGGAGAAGGCGCT[C/T]TGCTTCCAGGAGGTG | 11060 |
rs74370962 | snp | A/G | 0.110167 | 0.207236 | intron-variant | WWP2 | GRCh38.p7 | 16:69866503 | TGCAACCATCATCCC[A/G]CTTTCTCACTCAATT | 11060 |
rs74374911 | snp | G/T | | | missense | WWP2 | GRCh38.p7 | 16:69799211 | TTAGATTTAAAGGTC[G/T]GGAGCTGCCATACCT | 11060 |
rs74380942 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | WWP2 | GRCh38.p7 | 16:69780143 | GGTGTGGTTCCTTCC[C/T]GTCGTACTTTTATAC | 11060 |
rs74443425 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910416 | TCTGTGTACTGTGGC[C/T]TTTTTTTTTTTAGAC | 11060 |
rs74460098 | snp | A/C | | | missense | WWP2 | GRCh38.p7 | 16:69888207 | CTTCGGGTACACAGC[A/C]GCTCCCAGCGGCTGC | 11060 |
rs74463771 | snp | C/T | 0.149665 | 0.228982 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942015 | CCGGGGGTCTCCAAG[C/T]AGTTGCTGTGGGGTG | 11060 |
rs74464373 | snp | C/T | 0.084728 | 0.187577 | intron-variant | WWP2 | GRCh38.p7 | 16:69828198 | ACTGAAATGAGGACA[C/T]GAGTGCCCAATCCAC | 11060 |
rs74464813 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69829972 | ATTTTTTTTTTTTTT[C/T]CAGATAGAGTCTAAC | 11060 |
rs74467050 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69785644 | TTTTTTTTTTTTTTT[C/G]GAGACAGAGTCTTGC | 11060 |
rs74510080 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69785230 | GTGTGAGACTGTCTC[A/C]AAAAAAAAAAAAAGA | 11060 |
rs74554719 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69871182 | CCAGCTACTGGGGAG[C/G]CTGAGGTGGAAGGAT | 11060 |
rs74591285 | snp | A/G | 0.205417 | 0.245993 | intron-variant | WWP2 | GRCh38.p7 | 16:69821330 | AGCTGAGAGCTGTTG[A/G]AAAGAAAAGGTCCTT | 11060 |
rs74618581 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69903766 | AGCAAGAATCTGTCT[A/C]AAAAAAAAAAAAAAA | 11060 |
rs74620570 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69807367 | GTTTAATAATGAAAA[C/G]ATGTTTGCTTTGTAC | 11060 |
rs74644858 | snp | A/G | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69894044 | CAAGGTTCTCTTGGG[A/G]ATCTCATGGCTGTAT | 11060 |
rs74666562 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | WWP2 | GRCh38.p7 | 16:69937854 | TGGATGTGACAGGAG[G/T]TCGTCAGTGGTCAGC | 11060 |
rs74668609 | snp | G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69918860 | CTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTTG | 11060 |
rs74699651 | snp | A/G | 0.109461 | 0.206758 | intron-variant | WWP2 | GRCh38.p7 | 16:69860363 | CACACACTAGGTGCT[A/G]AGTCTCCAGAGGTTC | 11060 |
rs74726066 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827037 | ACATCTACTTGTCCT[G/T]CATCTTTAGCTCCCA | 11060 |
rs74761811 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69890140 | TTTTTTTTTTTTTTT[G/T]TAGAGACAGGGTTTT | 11060 |
rs74783350 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69922896 | TTTTTGCCACGACTC[C/T]TTTTTTTTTTTGAGA | 11060 |
rs74817807 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69926821 | CTCTGAAGACCCTGC[A/G]TCGTCAGTAGGCAGG | 11060 |
rs74865002 | snp | C/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69897432 | TTTTTAACCACCTCT[C/T]TTTAACCCCTTGATG | 11060 |
rs74872275 | snp | A/G | 0.0165278 | 0.0893908 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838424 | TCTTGGCGTAATAGA[A/G]GAGGGAGACCCTCCT | 11060 |
rs74895198 | in-del | -/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780267 | TGCCTTTTTTTTTTT[-/TTT]CCCCTCTTGGCATTA | 11060 |
rs74926774 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | WWP2 | GRCh38.p7 | 16:69794789 | GAAAAAAACCAAAAA[A/G]TTAAACAAACAAAAA | 11060 |
rs74932735 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | WWP2 | GRCh38.p7 | 16:69776500 | CTTATCTAAGCTCTA[A/G]AGATTGTTACCTAGA | 11060 |
rs74944669 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69849660 | GTTGAAAAGTAATCA[G/T]GGCTGGGCATGGTGG | 11060 |
rs74956818 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | WWP2 | GRCh38.p7 | 16:69765452 | CTTCAATTTTATTAG[A/C]GAAGGGCACATTGAT | 11060 |
rs74990353 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | WWP2 | GRCh38.p7 | 16:69780493 | CTCCCTCTGCAAATG[C/T]CTGGGAGTAGAATCC | 11060 |
rs75031249 | snp | A/G | 0.299158 | 0.245119 | intron-variant | WWP2 | GRCh38.p7 | 16:69850109 | GATGAAAAGTCGGCC[A/G]GGCGCAGTGGCTCAC | 11060 |
rs75109048 | snp | A/G | 0.030665 | 0.119967 | intron-variant | WWP2 | GRCh38.p7 | 16:69890316 | AAAGTCCTGTTCCAC[A/G]TACCTTTGTACCTCA | 11060 |
rs75117285 | snp | A/T | 0.0966517 | 0.197444 | intron-variant | WWP2 | GRCh38.p7 | 16:69856297 | TGAAGATGTGGGGGC[A/T]TTGGAGGAGGGATTG | 11060 |
rs75132335 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921845 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACTTGAG | 11060 |
rs75135913 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69860829 | CAACATAGCAAGACT[C/T]GATCTCTAGTTAAAA | 11060 |
rs75146240 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69810427 | TCAGTTTTTTAACAT[C/T]TTTTTTTTTTTTTTT | 11060 |
rs75146396 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69857242 | CCGAGTAGCTGGGCG[C/T]GCTCCACCACGCTCA | 11060 |
rs75147526 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69871183 | CAGCTACTGGGGAGG[C/T]TGAGGTGGAAGGATC | 11060 |
rs75168081 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | WWP2 | GRCh38.p7 | 16:69937418 | AAAGCAGGGACTTAC[A/C]TTACCCATATTATTA | 11060 |
rs75191689 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | WWP2 | GRCh38.p7 | 16:69792278 | ACTGATCTCTGAAAA[A/G]CATAGTATAATAAAA | 11060 |
rs75226973 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69771950 | CTAAAAGTCTTTTTA[G/T]TCTTTTTTTTTTTTT | 11060 |
rs75230278 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926042 | TGGTGACTCTGGAAA[C/T]GCATCGCTGCTAGTT | 11060 |
rs75255448 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | WWP2 | GRCh38.p7 | 16:69907470 | CAACTTCTCCTAGAC[A/G]GTACCCAAAAGTAGA | 11060 |
rs75279003 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69811919 | TTTCTTTCATCCCTA[A/T]ATACTGATGTGTCTG | 11060 |
rs75323448 | snp | C/T | 0.00225761 | 0.0335218 | intron-variant | WWP2 | GRCh38.p7 | 16:69936284 | TGACACGGTAGACAT[C/T]TCCCCACTTGGTCTC | 11060 |
rs75343511 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69809836 | GAAGGGGAGAGAGAG[A/G]AAAAGAAAAAAGAAA | 11060 |
rs75392779 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | WWP2 | GRCh38.p7 | 16:69930029 | TCAAAGTCCCTCATG[A/G]GCTCTGCAGAGACAA | 11060 |
rs75436961 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69826742 | AAAAAAAAAAAAAAT[A/T]AGCCTAACACGGTGA | 11060 |
rs75483657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69849446 | ATTTCTGTTGCTGGG[A/G]AAGACAATGGAATAA | 11060 |
rs75491847 | snp | C/T | 0.332337 | 0.236052 | intron-variant | WWP2 | GRCh38.p7 | 16:69849074 | AAGCCTAACCGTCTC[C/T]GGTGAGCTCTAAATA | 11060 |
rs75498986 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | WWP2 | GRCh38.p7 | 16:69917033 | AGACTCTGTCTCAAA[A/G]CAAAACAAAACCAAA | 11060 |
rs75549727 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69856159 | AAGTAACTTAACAAC[A/G]TGAATGACTCTTAAA | 11060 |
rs75559999 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69835821 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT | 11060 |
rs75627846 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69905491 | GAACTTTTTGAGTTC[C/T]GACATGATGCTTAAA | 11060 |
rs75631340 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | WWP2 | GRCh38.p7 | 16:69813890 | CCAACATAATCCAAT[A/G]TAGGTAAAATTTACT | 11060 |
rs75639409 | snp | C/T | 0.121717 | 0.214577 | intron-variant | WWP2 | GRCh38.p7 | 16:69796068 | ACAATTGGCAAAATA[C/T]GAATAAAGTCTGTAA | 11060 |
rs75656721 | snp | C/T | 0.00175323 | 0.0295557 | intron-variant | WWP2 | GRCh38.p7 | 16:69799321 | TGAAGGGGGTGCCGA[C/T]GTGATTCTTGGGTGG | 11060 |
rs75683664 | snp | C/T | 0.206336 | 0.246157 | intron-variant | WWP2 | GRCh38.p7 | 16:69903910 | ACTGAAAAATGAGCG[C/T]ACTAGTATTAGGGCT | 11060 |
rs75694192 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | WWP2 | GRCh38.p7 | 16:69843291 | TTGTTATACGTATTA[A/C]AAATGACGTAATGTT | 11060 |
rs75694396 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69864740 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTGGCT | 11060 |
rs75782863 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69845914 | AATTAGCCAGGCATG[A/G]TGGTGTGTGCCTATA | 11060 |
rs75876862 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | WWP2 | GRCh38.p7 | 16:69835069 | GCTTGTGAGCTTCCT[A/G]TATGCTAACTCAGAT | 11060 |
rs75905191 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | WWP2 | GRCh38.p7 | 16:69881673 | AAATAAAACAAAAAG[A/G]ACCTGTGGTTTTAAA | 11060 |
rs75918479 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | WWP2 | GRCh38.p7 | 16:69797306 | AACCTTGCTGGTAAT[C/G]GAAGAACAGCAATAG | 11060 |
rs75920310 | snp | A/T | 0.0629771 | 0.165899 | intron-variant | WWP2 | GRCh38.p7 | 16:69853786 | ACAAGGTGAAGGGTA[A/T]GGAGGGAGGGGGGTA | 11060 |
rs75943235 | snp | C/T | 0.0205511 | 0.0992634 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941318 | GACCCCCAGGCAGCC[C/T]CTTGGACTGGTCCCG | 11060 |
rs75979388 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69844489 | ACTTAATTTGGGGCT[C/T]AAAGTCAGATTCAGC | 11060 |
rs76023406 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826965 | AAAAAGGGGGGGGGG[-/C]GGAGAGAATAATGGA | 11060 |
rs76046080 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861848 | TGGAAACTGGCCCAG[C/T]TCCACTGAATTTTTT | 11060 |
rs76050961 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69863855 | TTACTTAGCATAATG[C/T]GGTTGTGATTCACCT | 11060 |
rs76061922 | snp | A/C | 0.0372196 | 0.131242 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940729 | CTTGAGGGACCCAGA[A/C]CTTTGGGTCCAAGAG | 11060 |
rs76094505 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | WWP2 | GRCh38.p7 | 16:69818539 | AACCTCCAGTGAGGT[A/G]TTCTGCTGCTCTGCT | 11060 |
rs76125541 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69870678 | TCTGTTTCTCTGTCT[C/G]GAGAGGGGTGATCTT | 11060 |
rs76126453 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | WWP2 | GRCh38.p7 | 16:69872720 | GAGCCAGGTAACTAC[G/T]TGGGGGTGTGCAGGG | 11060 |
rs76170784 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69892627 | CAGCCTCAGCCTCAC[C/G]GGCTCAAGTGATCCT | 11060 |
rs76195560 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | WWP2 | GRCh38.p7 | 16:69875755 | ATTCAGGCCTACTTC[C/T]TATTCTAGCTCTCTT | 11060 |
rs76202767 | snp | A/G | 0.106633 | 0.204807 | intron-variant | WWP2 | GRCh38.p7 | 16:69850658 | GAGGGTACAGCATGA[A/G]TGAAGGCAAGGAGGA | 11060 |
rs76225953 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69895857 | ACCATTCTTTGAGTA[G/T]CATCAGATTAAAGGA | 11060 |
rs76309079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921665 | TTGCCGTCTTGTGTC[A/G]TGTTCCTGCTGGGAC | 11060 |
rs76310379 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | WWP2 | GRCh38.p7 | 16:69901025 | TCCTTCGGGGAAGGA[C/T]TGAGTTTAACACATT | 11060 |
rs76384477 | snp | A/G | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923968 | ATTTTTTTCAGTAAT[A/G]ATTCAACGTGATTTG | 11060 |
rs76394580 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926039 | AGGTGGTGACTCTGG[A/C]AACGCATCGCTGCTA | 11060 |
rs76409767 | snp | A/G | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69793394 | TTCACTGGGACTGTA[A/G]CATTGCATTAGAGAA | 11060 |
rs76419401 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69903768 | CAAGAATCTGTCTCA[A/C]AAAAAAAAAAAAAGA | 11060 |
rs76464903 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | WWP2 | GRCh38.p7 | 16:69883588 | TTCAACTTTAAGTTC[C/T]GGGGTACGTGTACAG | 11060 |
rs76467397 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | WWP2 | GRCh38.p7 | 16:69863140 | CCTGAATCACATTCC[C/T]ATCCACATTCTTGCT | 11060 |
rs76499841 | snp | A/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69784937 | AGTTTTTTTTTTTTT[A/T]AAAGAAAAGAAAGAG | 11060 |
rs76507959 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909593 | GTTTTCCTTTTTTCC[A/G]TACCTCCTGGAGGAT | 11060 |
rs76525403 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | WWP2 | GRCh38.p7 | 16:69897510 | TCATTCCCTGTATAC[A/G]GTGATACATGGAACT | 11060 |
rs76525814 | snp | A/T | 0.121717 | 0.214577 | intron-variant | WWP2 | GRCh38.p7 | 16:69804725 | ACTCCCCATGCCCCC[A/T]AAAAAATCTCTTGAG | 11060 |
rs76531346 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925365 | TTTATTTTTTATTGA[C/T]TGATTGATTTTTTCA | 11060 |
rs76533226 | snp | C/G | 0.123105 | 0.215401 | intron-variant | WWP2 | GRCh38.p7 | 16:69797423 | CTATGTAGAGTGGGA[C/G]AGTGACCTTGCCTCT | 11060 |