Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs2571445 | 0.925 | 0.080 | 2 | 217818431 | missense variant | A/G;T | snv | 0.62 | 10 | ||
rs1496255 | 4 | 120683279 | downstream gene variant | G/A;T | snv | 4 | |||||
rs41434646 | 2 | 184295785 | intron variant | A/C;G | snv | 4.7E-03 | 3 |