Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 221 | ||
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 100 | |
rs5743708 | 0.525 | 0.800 | 4 | 153705165 | missense variant | G/A | snv | 1.7E-02 | 1.8E-02 | 97 | |
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 69 | |
rs3775291 | 0.602 | 0.640 | 4 | 186082920 | missense variant | C/G;T | snv | 1.2E-04; 0.28 | 51 | ||
rs2066844 | 0.587 | 0.520 | 16 | 50712015 | missense variant | C/T | snv | 2.6E-02 | 2.9E-02 | 49 | |
rs1065489 | 0.695 | 0.440 | 1 | 196740644 | missense variant | G/T | snv | 0.20 | 0.15 | 19 | |
rs762513613 | 0.752 | 0.280 | 1 | 161591315 | missense variant | A/G | snv | 4.2E-06 | 7.4E-06 | 11 | |
rs4794067 | 0.807 | 0.280 | 17 | 47731462 | upstream gene variant | T/A;C | snv | 0.25 | 7 | ||
rs3827440 | 0.851 | 0.120 | X | 79171491 | missense variant | T/A;C | snv | 5.5E-06; 0.51 | 6 | ||
rs3796508 | 0.827 | 0.120 | 4 | 38828495 | missense variant | C/T | snv | 1.2E-02 | 1.2E-02 | 6 | |
rs1475539937 | 0.882 | 0.120 | 3 | 52223085 | missense variant | A/G | snv | 4.0E-06 | 5 | ||
rs74315507 | 0.925 | 0.080 | 22 | 37232857 | missense variant | C/T | snv | 3 | |||
rs6876739 | 5 | 40938240 | intron variant | T/C | snv | 0.48 | 1 | ||||
rs373495105 | 19 | 11507836 | missense variant | C/A;G;T | snv | 2.0E-05; 2.8E-05 | 1 | ||||
rs1426866722 | 8 | 98774764 | missense variant | C/T | snv | 7.0E-06 | 1 |