| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 39 | |
| rs151344517 | 0.742 | 0.320 | 18 | 12337505 | missense variant | C/T | snv | 31 | |||
| rs1042636 | 0.672 | 0.360 | 3 | 122284922 | missense variant | A/G | snv | 0.15 | 9.0E-02 | 23 | |
| rs104893689 | 0.790 | 0.200 | 3 | 122261589 | missense variant | G/A;C | snv | 10 | |||
| rs1057518933 | 0.851 | 0.160 | 3 | 122284403 | missense variant | G/A | snv | 5 | |||
| rs121909262 | 0.851 | 0.120 | 3 | 122254304 | missense variant | C/G;T | snv | 5 | |||
| rs397507481 | 0.882 | 0.240 | 7 | 140754206 | missense variant | G/C;T | snv | 4 | |||
| rs121434597 | 0.851 | 0.120 | 3 | 46898691 | missense variant | A/G | snv | 4 | |||
| rs201858689 | 0.882 | 0.120 | 3 | 122284257 | missense variant | G/T | snv | 2.8E-05 | 3 |