Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 43 | ||
rs2872507 | 0.752 | 0.360 | 17 | 39884510 | intergenic variant | G/A;T | snv | 12 | |||
rs7927894 | 0.742 | 0.320 | 11 | 76590272 | upstream gene variant | C/T | snv | 0.35 | 12 | ||
rs2305480 | 0.763 | 0.280 | 17 | 39905943 | missense variant | G/A | snv | 0.40 | 0.35 | 10 | |
rs4794820 | 0.790 | 0.160 | 17 | 39933091 | intron variant | A/G;T | snv | 9 | |||
rs928413 | 0.807 | 0.120 | 9 | 6213387 | upstream gene variant | G/A;C | snv | 7 | |||
rs1558641 | 0.925 | 0.080 | 2 | 102149405 | intron variant | G/A | snv | 0.13 | 3 |