| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387906676 | 1.000 | 0.080 | 10 | 121517394 | missense variant | C/G;T | snv | 1 | |||
| rs779326224 | 1.000 | 0.080 | 10 | 121520130 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387906676 | 1.000 | 0.080 | 10 | 121517394 | missense variant | C/G;T | snv | 1 | |||
| rs779326224 | 1.000 | 0.080 | 10 | 121520130 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 |