Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5860563 | 1.000 | 0.080 | 4 | 99126006 | intron variant | -/A | delins | 3 | |||
rs58598658 | 0.925 | 0.080 | 13 | 73887725 | intron variant | -/A;AA | delins | 4 | |||
rs141424017 | 1.000 | 0.080 | 7 | 115311376 | intergenic variant | -/CAA | ins | 3 | |||
rs143894582 | 1.000 | 0.080 | 12 | 112469070 | intron variant | A/-;AA | delins | 1 | |||
rs3743832 | 1.000 | 0.080 | 16 | 9120023 | 3 prime UTR variant | A/C | snv | 0.55 | 4 | ||
rs1709819 | 1.000 | 0.080 | 21 | 37663813 | intron variant | A/C | snv | 0.59 | 3 | ||
rs1709820 | 1.000 | 0.080 | 21 | 37663669 | intron variant | A/C | snv | 0.57 | 3 | ||
rs1787396 | 1.000 | 0.080 | 21 | 37664185 | intron variant | A/C | snv | 0.57 | 3 | ||
rs1787398 | 1.000 | 0.080 | 21 | 37665202 | intron variant | A/C | snv | 0.57 | 3 | ||
rs2835836 | 1.000 | 0.080 | 21 | 37616885 | 3 prime UTR variant | A/C | snv | 0.26 | 3 | ||
rs4384980 | 1.000 | 0.080 | 3 | 182741281 | upstream gene variant | A/C | snv | 0.48 | 1 | ||
rs7183893 | 1.000 | 0.080 | 15 | 38704780 | intron variant | A/C | snv | 0.23 | 1 | ||
rs17028615 | 1.000 | 0.080 | 4 | 99150767 | intron variant | A/C;G | snv | 4 | |||
rs1709835 | 1.000 | 0.080 | 21 | 37665334 | intron variant | A/C;G | snv | 0.57 | 3 | ||
rs1787404 | 1.000 | 0.080 | 21 | 37677060 | intron variant | A/C;G | snv | 3 | |||
rs9378160 | 1.000 | 0.080 | 6 | 31500215 | intron variant | A/C;G | snv | 3 | |||
rs29230 | 0.807 | 0.440 | 6 | 29608616 | missense variant | A/C;G | snv | 4.1E-06; 0.18 | 1 | ||
rs12898370 | 1.000 | 0.080 | 15 | 77516256 | intergenic variant | A/C;T | snv | 3 | |||
rs1787395 | 1.000 | 0.080 | 21 | 37664176 | intron variant | A/C;T | snv | 3 | |||
rs6701037 | 1.000 | 0.080 | 1 | 175150943 | downstream gene variant | A/C;T | snv | 3 | |||
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 | ||
rs139438618 | 0.882 | 0.080 | 7 | 84008281 | intron variant | A/G | snv | 5.2E-02 | 4 | ||
rs1000579 | 1.000 | 0.080 | 4 | 4717767 | intron variant | A/G | snv | 0.44 | 3 | ||
rs10211296 | 1.000 | 0.080 | 2 | 165633833 | intron variant | A/G | snv | 0.34 | 3 |