| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
| rs2230911 | 0.807 | 0.360 | 12 | 121177328 | missense variant | C/G | snv | 0.14 | 0.12 | 6 | |
| rs12137901 | 0.882 | 0.200 | 1 | 247417907 | intron variant | T/C | snv | 0.26 | 3 | ||
| rs7512998 | 0.882 | 0.200 | 1 | 247419919 | intron variant | C/T | snv | 0.83 | 3 | ||
| rs3806268 | 0.925 | 0.200 | 1 | 247424175 | synonymous variant | G/A;T | snv | 0.50; 4.8E-05 | 2 |