| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs148050184 | 1.000 | 0.080 | X | 20172853 | missense variant | T/C;G | snv | 4.9E-05 | 1 | ||
| rs122454124 | 1.000 | 0.080 | X | 20209307 | missense variant | C/A | snv | 1 | |||
| rs879027948 | 1.000 | 0.080 | X | 20187928 | missense variant | G/A | snv | 1 | |||
| rs122454131 | 1.000 | 0.080 | X | 20186338 | missense variant | A/G | snv | 1 | |||
| rs28935171 | 1.000 | 0.080 | X | 20155435 | missense variant | C/T | snv | 1 | |||
| rs122454126 | 1.000 | 0.080 | X | 20204103 | missense variant | C/A;T | snv | 1 | |||
| rs122454130 | 1.000 | 0.080 | X | 20193514 | missense variant | A/T | snv | 1 | |||
| rs122454127 | 1.000 | 0.080 | X | 20195131 | missense variant | G/A | snv | 1 | |||
| rs122454125 | 1.000 | 0.080 | X | 20187923 | missense variant | A/C | snv | 1 | |||
| rs1271090915 | 1.000 | 0.080 | X | 20167743 | missense variant | T/C | snv | 1 | |||
| rs122454129 | 1.000 | 0.080 | X | 20175244 | missense variant | G/A | snv | 1 | |||
| rs387906703 | 1.000 | 0.080 | X | 20195128 | missense variant | T/A | snv | 1 |