| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs16942333 | 15 | 88845033 | intron variant | A/G | snv | 3.3E-02 | 3 | ||||
| rs11854545 | 15 | 88825873 | intron variant | G/A;T | snv | 2 | |||||
| rs2280470 | 15 | 88852395 | intron variant | A/G | snv | 0.68 | 1 | ||||
| rs8041863 | 15 | 88816458 | intron variant | T/A;G | snv | 1 | |||||
| rs938609 | 15 | 88855400 | missense variant | T/A | snv | 0.51 | 0.52 | 1 | |||
| rs2351491 | 15 | 88854874 | synonymous variant | C/T | snv | 0.50 | 0.48 | 1 | |||
| rs16942341 | 15 | 88845674 | synonymous variant | C/T | snv | 3.8E-02 | 6.4E-02 | 1 | |||
| rs8026235 | 15 | 88806225 | intron variant | A/C | snv | 1.7E-02 | 1 |