| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs139262191 | 1.000 | 0.080 | 9 | 21077768 | missense variant | G/C;T | snv | 7.0E-04; 4.2E-04; 4.0E-06 | 1 | ||
| rs9333358 | 1.000 | 0.080 | 9 | 21078953 | upstream gene variant | T/C | snv | 0.20 | 1 | ||
| rs1051922 | 1.000 | 0.080 | 9 | 21077717 | synonymous variant | G/A | snv | 0.33 | 0.35 | 1 |