| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 6 | ||
| rs1789924 | 0.925 | 0.160 | 4 | 99353129 | upstream gene variant | C/G;T | snv | 1 | |||
| rs971074 | 0.925 | 0.040 | 4 | 99420704 | synonymous variant | C/T | snv | 0.12 | 0.13 | 1 | |
| rs1494961 | 0.925 | 0.160 | 4 | 83453327 | missense variant | C/T | snv | 0.56 | 0.60 | 1 | |
| rs4767364 | 0.807 | 0.160 | 12 | 112083644 | intron variant | G/A | snv | 0.45 | 1 |