| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs869320714 | 1.000 | 17 | 35557404 | missense variant | A/T | snv | 3 | ||||
| rs869320715 | 1.000 | 17 | 35557406 | missense variant | T/A | snv | 3 | ||||
| rs8073060 | 17 | 35548243 | missense variant | T/A | snv | 0.32 | 0.34 | 3 | |||
| rs145171343 | 17 | 35559745 | upstream gene variant | C/T | snv | 9.5E-03 | 2 | ||||
| rs7221322 | 17 | 35546753 | downstream gene variant | A/G | snv | 0.48 | 1 | ||||
| rs36064799 | 17 | 35553480 | non coding transcript exon variant | -/A | delins | 4.5E-02 | 7.5E-02 | 1 | |||
| rs10512472 | 17 | 35557785 | missense variant | T/C | snv | 0.21 | 0.19 | 1 | |||
| rs757188030 | 1.000 | 17 | 35557396 | missense variant | G/A;C | snv | 6.5E-06; 6.5E-06 | 1 | |||
| rs869320716 | 1.000 | 17 | 35557411 | missense variant | T/C | snv | 1 |