Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2855812 | 0.790 | 0.360 | 6 | 31504943 | intron variant | G/T | snv | 0.23 | 13 | ||
rs1042779 | 0.882 | 0.040 | 3 | 52786995 | missense variant | A/G | snv | 0.40 | 0.42 | 3 | |
rs10950398 | 1.000 | 0.040 | 7 | 12225245 | intron variant | G/A | snv | 0.52 | 2 | ||
rs2019065 | 1.000 | 0.040 | 3 | 52775509 | upstream gene variant | T/C | snv | 0.43 | 2 | ||
rs2286798 | 1.000 | 0.040 | 3 | 52787161 | intron variant | A/C | snv | 0.38 | 0.37 | 2 |