Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 24 | |||||
rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 22 | |||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 22 | |||
rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 18 | |||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 15 | |||
rs1801020 | 1.000 | 0.040 | 5 | 177409531 | 5 prime UTR variant | A/G | snv | 0.65 | 0.67 | 8 | |
rs1801690 | 0.925 | 0.120 | 17 | 66212167 | missense variant | C/G | snv | 4.8E-02 | 4.0E-02 | 6 | |
rs2731672 | 5 | 177415473 | intron variant | T/C | snv | 0.66 | 6 | ||||
rs2545801 | 5 | 177414338 | intron variant | T/C | snv | 0.56 | 5 | ||||
rs2289252 | 1.000 | 0.040 | 4 | 186286227 | non coding transcript exon variant | C/T | snv | 0.35 | 4 | ||
rs710446 | 0.925 | 0.120 | 3 | 186742138 | missense variant | T/C | snv | 0.42 | 0.44 | 4 | |
rs7447593 | 5 | 177397136 | non coding transcript exon variant | C/G;T | snv | 4 | |||||
rs12644950 | 4 | 154616169 | upstream gene variant | G/A | snv | 0.25 | 3 | ||||
rs1593 | 4 | 186274397 | 3 prime UTR variant | T/A;G | snv | 3 | |||||
rs1042445 | 3 | 186677647 | missense variant | C/A;T | snv | 0.27 | 3 | ||||
rs16860992 | 1.000 | 0.080 | 3 | 186676249 | intron variant | G/C;T | snv | 3 | |||
rs9898 | 0.925 | 0.160 | 3 | 186672838 | missense variant | C/T | snv | 0.38 | 0.43 | 3 | |
rs2304595 | 1.000 | 0.040 | 4 | 186251126 | non coding transcript exon variant | G/A | snv | 0.36 | 3 | ||
rs2228243 | 1.000 | 0.080 | 3 | 186677324 | missense variant | A/G;T | snv | 0.20; 4.0E-06 | 3 | ||
rs4253421 | 4 | 186283783 | intron variant | A/C;G;T | snv | 2 | |||||
rs2287694 | 5 | 177433292 | intron variant | T/C | snv | 8.5E-02 | 2 | ||||
rs2050190 | 1.000 | 0.120 | 6 | 32371299 | intron variant | A/G | snv | 0.35 | 2 | ||
rs2469184 | 15 | 86648746 | intron variant | A/G | snv | 0.54 | 1 | ||||
rs7962629 | 12 | 7059466 | intron variant | A/G | snv | 0.13 | 1 | ||||
rs56810541 | 4 | 186279396 | intron variant | A/T | snv | 0.35 | 1 |