| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs193922399 | 1.000 | 0.120 | 11 | 17404527 | missense variant | A/C | snv | 1 | |||
| rs193922401 | 1.000 | 0.120 | 11 | 17395914 | missense variant | C/A;T | snv | 1 | |||
| rs193922403 | 1.000 | 0.120 | 11 | 17395215 | missense variant | G/A;C | snv | 1.9E-04 | 1 | ||
| rs193922406 | 1.000 | 0.120 | 11 | 17393752 | missense variant | A/C | snv | 1 | |||
| rs193922407 | 1.000 | 0.120 | 11 | 17393741 | missense variant | C/T | snv | 1 | |||
| rs984164636 | 1.000 | 0.120 | 11 | 17461720 | missense variant | T/C | snv | 1 | |||
| rs193922565 | 1.000 | 0.120 | 11 | 17388087 | missense variant | A/G | snv | 1 | |||
| rs534808921 | 1.000 | 0.120 | 11 | 17387967 | missense variant | C/A | snv | 1.2E-05 | 1 |