| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912775 | 1.000 | 0.080 | 12 | 2550020 | missense variant | G/A | snv | 6.7E-04 | 3.6E-04 | 1 | |
| rs121912776 | 1.000 | 0.080 | 12 | 2115290 | missense variant | C/T | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912775 | 1.000 | 0.080 | 12 | 2550020 | missense variant | G/A | snv | 6.7E-04 | 3.6E-04 | 1 | |
| rs121912776 | 1.000 | 0.080 | 12 | 2115290 | missense variant | C/T | snv | 1 |