Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs2235076 | 0.925 | 0.080 | 6 | 102068385 | missense variant | G/A | snv | 1.8E-02 | 1.7E-02 | 2 | |
rs200533370 | 0.882 | 0.160 | X | 47574285 | missense variant | T/C | snv | 1.1E-03 | 1.4E-02 | 3 | |
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs28935468 | 0.732 | 0.240 | X | 154030912 | missense variant | G/A | snv | 17 | |||
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs587777164 | 0.882 | 0.080 | 14 | 62950522 | missense variant | C/T | snv | 3 | |||
rs61750240 | 0.752 | 0.240 | X | 154031020 | stop gained | G/A;C | snv | 5.5E-06 | 19 | ||
rs869312966 | 0.827 | 0.120 | 12 | 51806345 | missense variant | G/T | snv | 7 | |||
rs879255652 | 0.807 | 0.120 | 12 | 51790425 | stop gained | G/A;T | snv | 7 |