| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9728619 | 0.925 | 0.120 | 1 | 145698627 | intron variant | A/G | snv | 0.51 | 3 | ||
| rs12129861 | 0.925 | 0.120 | 1 | 145709377 | upstream gene variant | C/T | snv | 0.43 | 3 | ||
| rs900347 | 0.925 | 0.120 | 1 | 145708339 | upstream gene variant | C/G;T | snv | 2 | |||
| rs9659930 | 0.925 | 0.120 | 1 | 145704365 | intron variant | C/G | snv | 0.18 | 2 | ||
| rs1298954 | 0.925 | 0.120 | 1 | 145704906 | intron variant | C/T | snv | 0.44 | 2 | ||
| rs882210 | 0.925 | 0.120 | 1 | 145702119 | intron variant | C/G | snv | 4.8E-02 | 2 | ||
| rs1797052 | 1 | 145707383 | 5 prime UTR variant | A/G;T | snv | 1 |