| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs122453114 | 1.000 | 0.120 | X | 153693586 | missense variant | G/C | snv | 1 | |||
| rs781899045 | 1.000 | 0.080 | X | 153695191 | missense variant | G/A | snv | 1.4E-05 | 3.8E-05 | 1 | |
| rs145438966 | 1.000 | 0.080 | X | 153694800 | missense variant | A/G | snv | 1.6E-03 | 3.7E-04 | 1 | |
| rs868950793 | X | 153688666 | missense variant | C/A;G;T | snv | 1.6E-05; 3.3E-05 | 3.9E-05 | 1 |