| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs781754383 | 0.882 | 0.080 | 4 | 109960942 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 | 3 | ||
| rs121909497 | 0.925 | 0.080 | 11 | 102955390 | missense variant | A/G | snv | 3 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs781754383 | 0.882 | 0.080 | 4 | 109960942 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 | 3 | ||
| rs121909497 | 0.925 | 0.080 | 11 | 102955390 | missense variant | A/G | snv | 3 |