Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10198241 | 0.925 | 0.080 | 2 | 226115660 | intergenic variant | T/C | snv | 0.58 | 4 | ||
rs115357105 | 0.925 | 0.080 | 9 | 104376689 | intergenic variant | A/G | snv | 1.5E-02 | 4 | ||
rs11825659 | 0.925 | 0.080 | 11 | 133925624 | intron variant | A/G | snv | 0.12 | 4 | ||
rs12180309 | 0.925 | 0.080 | 6 | 91209048 | intergenic variant | C/T | snv | 1.9E-02 | 4 | ||
rs12544026 | 0.925 | 0.080 | 8 | 101819970 | intron variant | G/A | snv | 0.85 | 4 | ||
rs139438618 | 0.882 | 0.080 | 7 | 84008281 | intron variant | A/G | snv | 5.2E-02 | 4 | ||
rs2094081 | 0.925 | 0.080 | 1 | 38927359 | intron variant | G/A;C | snv | 4 | |||
rs55702914 | 0.925 | 0.080 | 2 | 197349672 | intergenic variant | C/G | snv | 0.37 | 4 | ||
rs58598658 | 0.925 | 0.080 | 13 | 73887725 | intron variant | -/A;AA | delins | 4 | |||
rs72737330 | 0.925 | 0.080 | 1 | 216600151 | intron variant | T/C | snv | 0.15 | 4 | ||
rs79246196 | 0.925 | 0.080 | 7 | 100185286 | intron variant | C/T | snv | 1.8E-02 | 4 | ||
rs12898460 | 0.882 | 0.080 | 15 | 38694612 | intron variant | C/T | snv | 0.23 | 3 | ||
rs12912251 | 0.882 | 0.080 | 15 | 38694167 | intron variant | G/T | snv | 0.25 | 3 |