| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121918117 | 0.851 | 0.160 | 7 | 30969116 | stop gained | G/A;T | snv | 1.8E-04 | 4 | ||
| rs137853223 | 0.851 | 0.160 | 17 | 63917337 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
| rs137904970 | 0.925 | 0.120 | 9 | 136200607 | missense variant | C/T | snv | 3.2E-05 | 1.4E-05 | 2 | |
| rs749318884 | 0.925 | 0.120 | 1 | 180248431 | missense variant | G/A | snv | 8.4E-05 | 3.5E-05 | 2 | |
| rs763850922 | 0.925 | 0.120 | 17 | 63917760 | splice region variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 2 |