| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs751416416 | 0.882 | 0.120 | 8 | 53250920 | missense variant | C/A;T | snv | 8.3E-06; 4.1E-06 | 5 | ||
| rs594242 | 1.000 | 0.040 | 13 | 46883917 | intron variant | C/A;G | snv | 3 | |||
| rs1439050 | 0.925 | 0.080 | 9 | 84673278 | intron variant | G/A;T | snv | 2 | |||
| rs2268115 | 1.000 | 0.040 | 12 | 13716791 | intron variant | G/A;T | snv | 1 |