Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6932542 | 0.827 | 0.200 | 6 | 32412485 | downstream gene variant | A/G | snv | 0.55 | 5 | ||
rs805303 | 0.925 | 0.160 | 6 | 31648589 | intron variant | G/A | snv | 0.45 | 5 | ||
rs707928 | 0.827 | 0.320 | 6 | 31774813 | intron variant | A/G | snv | 0.47 | 4 | ||
rs1046089 | 0.882 | 0.200 | 6 | 31635190 | missense variant | G/A | snv | 0.36 | 0.40 | 3 | |
rs2763979 | 0.827 | 0.360 | 6 | 31826815 | upstream gene variant | C/T | snv | 0.45 | 3 | ||
rs805294 | 0.882 | 0.240 | 6 | 31720440 | intron variant | A/G | snv | 0.48 | 3 | ||
rs2242660 | 0.925 | 0.160 | 6 | 31629976 | intron variant | G/A | snv | 0.46 | 2 |