| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs146036912 | 0.925 | 0.080 | 4 | 108027727 | missense variant | T/C | snv | 6.8E-05 | 9.8E-05 | 2 | |
| rs137853102 | 1.000 | 0.080 | 4 | 108009797 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs137853101 | 1.000 | 0.080 | 4 | 107990050 | missense variant | G/A | snv | 1 |