| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2057681 | 7 | 95308945 | intron variant | A/G | snv | 0.43 | 2 | ||||
| rs3917502 | 7 | 95316432 | intron variant | C/T | snv | 3.9E-02 | 1 | ||||
| rs3917510 | 7 | 95313808 | intron variant | T/G | snv | 6.2E-02 | 1 | ||||
| rs2237583 | 7 | 95320865 | intron variant | C/G;T | snv | 1 | |||||
| rs854572 | 7 | 95325384 | upstream gene variant | C/G | snv | 0.40 | 1 |