| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912834 | 0.827 | 0.120 | 3 | 48572941 | missense variant | C/G;T | snv | 4.0E-06 | 6 | ||
| rs121912837 | 1.000 | 0.080 | 3 | 48573047 | missense variant | C/G;T | snv | 2 | |||
| rs121912848 | 3 | 48575125 | missense variant | C/A | snv | 1 |