Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1940709 | 1.000 | 0.040 | 11 | 112978997 | intron variant | G/A | snv | 0.30 | 2 | ||
| rs1940728 | 1.000 | 0.040 | 11 | 112981473 | intron variant | G/A;T | snv | 0.44 | 2 | ||
| rs72995548 | 1.000 | 0.040 | 11 | 113268199 | non coding transcript exon variant | C/T | snv | 3.5E-02 | 2 |