Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519861 | 0.776 | 0.080 | 7 | 55181398 | missense variant | T/A | snv | 15 | |||
rs2036527 | 0.851 | 0.080 | 15 | 78559273 | regulatory region variant | G/A | snv | 0.29 | 12 | ||
rs56113850 | 0.807 | 0.080 | 19 | 40847202 | intron variant | T/C | snv | 0.52 | 10 | ||
rs6495309 | 0.807 | 0.080 | 15 | 78622903 | upstream gene variant | C/A;T | snv | 10 | |||
rs10937405 | 0.807 | 0.080 | 3 | 189665394 | intron variant | C/T | snv | 0.38 | 9 | ||
rs1458974438 | 0.807 | 0.080 | 19 | 1206957 | missense variant | G/A | snv | 9 | |||
rs10519203 | 0.851 | 0.080 | 15 | 78521704 | intron variant | G/A | snv | 0.67 | 8 | ||
rs1062980 | 0.827 | 0.080 | 15 | 78500185 | 3 prime UTR variant | T/C | snv | 0.39 | 8 | ||
rs12910984 | 0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv | 8 | |||
rs146795390 | 0.827 | 0.080 | 7 | 55191776 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 8 | |
rs2036534 | 0.827 | 0.080 | 15 | 78534606 | 3 prime UTR variant | T/C | snv | 0.26 | 8 | ||
rs6183 | 0.827 | 0.080 | 5 | 42718990 | missense variant | C/A | snv | 2.3E-03 | 7.4E-04 | 8 | |
rs1057519784 | 0.827 | 0.080 | 2 | 29220765 | missense variant | G/T | snv | 7 | |||
rs1489759 | 0.882 | 0.080 | 4 | 144553321 | intron variant | A/G | snv | 0.43 | 7 | ||
rs2568494 | 0.851 | 0.080 | 15 | 78448622 | intron variant | G/A | snv | 0.36 | 7 | ||
rs7689420 | 0.851 | 0.080 | 4 | 144647200 | non coding transcript exon variant | T/C | snv | 0.79 | 7 | ||
rs931794 | 0.851 | 0.080 | 15 | 78533838 | 3 prime UTR variant | G/A;C | snv | 7 | |||
rs938682 | 0.851 | 0.080 | 15 | 78604205 | intron variant | G/A | snv | 0.72 | 7 | ||
rs1057519729 | 0.827 | 0.080 | 15 | 66435113 | missense variant | A/C | snv | 6 | |||
rs11637630 | 0.882 | 0.080 | 15 | 78607377 | intron variant | G/A | snv | 0.71 | 6 | ||
rs12894467 | 0.807 | 0.080 | 14 | 101041390 | non coding transcript exon variant | C/T | snv | 0.51 | 0.50 | 6 | |
rs1389500636 | 0.827 | 0.080 | 7 | 55156796 | missense variant | G/A | snv | 6 | |||
rs171140 | 0.807 | 0.080 | 19 | 45361744 | non coding transcript exon variant | C/A | snv | 0.58 | 0.64 | 6 | |
rs2131877 | 0.827 | 0.080 | 3 | 195137645 | intron variant | G/A | snv | 0.20 | 6 | ||
rs2233947 | 0.851 | 0.080 | 6 | 31139278 | non coding transcript exon variant | C/T | snv | 9.3E-03 | 6 |