| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80356611 | 0.790 | 0.240 | 11 | 17387943 | missense variant | C/A;G;T | snv | 4.0E-06 | 10 | ||
| rs1441649062 | 0.851 | 0.080 | 7 | 44149822 | missense variant | G/A | snv | 4.0E-06 | 4 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80356611 | 0.790 | 0.240 | 11 | 17387943 | missense variant | C/A;G;T | snv | 4.0E-06 | 10 | ||
| rs1441649062 | 0.851 | 0.080 | 7 | 44149822 | missense variant | G/A | snv | 4.0E-06 | 4 |