| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1351361600 | 1.000 | 0.160 | 5 | 33944733 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs749979474 | 1.000 | 0.160 | 11 | 89284852 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1351361600 | 1.000 | 0.160 | 5 | 33944733 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs749979474 | 1.000 | 0.160 | 11 | 89284852 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 1 |