Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4833095 | 0.662 | 0.480 | 4 | 38798089 | missense variant | T/C | snv | 0.38 | 0.44 | 28 | |
rs2155219 | 0.732 | 0.280 | 11 | 76588150 | upstream gene variant | G/T | snv | 0.52 | 14 | ||
rs7927894 | 0.742 | 0.320 | 11 | 76590272 | upstream gene variant | C/T | snv | 0.35 | 12 | ||
rs1837253 | 0.790 | 0.240 | 5 | 111066174 | upstream gene variant | T/C | snv | 0.72 | 10 | ||
rs1342326 | 0.790 | 0.360 | 9 | 6190076 | intergenic variant | A/C | snv | 0.21 | 9 | ||
rs928413 | 0.807 | 0.120 | 9 | 6213387 | upstream gene variant | G/A;C | snv | 7 | |||
rs1438673 | 0.882 | 0.120 | 5 | 111131801 | downstream gene variant | C/T | snv | 0.61 | 4 | ||
rs17294280 | 0.882 | 0.120 | 15 | 67175947 | intron variant | A/G | snv | 0.19 | 4 | ||
rs3853750 | 0.882 | 0.160 | 5 | 110818610 | intergenic variant | T/C | snv | 0.30 | 4 | ||
rs10197862 | 0.925 | 0.120 | 2 | 102350089 | intron variant | A/G | snv | 0.18 | 3 | ||
rs2069772 | 0.925 | 0.200 | 4 | 122451978 | intron variant | T/A;C | snv | 3 |