| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12007229 | 1.000 | 0.120 | X | 67528513 | upstream gene variant | C/A | snv | 0.11 | 1 | ||
| rs2497931 | 1.000 | 0.120 | X | 67436434 | intergenic variant | A/C;T | snv | 1 | |||
| rs4485213 | 1.000 | 0.120 | 13 | 105256524 | intergenic variant | C/T | snv | 0.19 | 1 | ||
| rs951660 | 1.000 | 0.120 | 3 | 111919285 | intron variant | A/C | snv | 0.86 | 1 | ||
| rs10491487 | 1.000 | 0.120 | 5 | 81027549 | intron variant | T/G | snv | 8.2E-02 | 1 | ||
| rs26906 | 1.000 | 0.120 | 5 | 81069068 | intron variant | T/C | snv | 0.86 | 1 | ||
| rs290227 | 1.000 | 0.120 | 9 | 90874382 | intron variant | G/A | snv | 0.30 | 1 |