| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 | |||
| rs29230 | 0.807 | 0.440 | 6 | 29608616 | missense variant | A/C;G | snv | 4.1E-06; 0.18 | 6 | ||
| rs2229902 | 0.851 | 0.160 | 3 | 7452730 | missense variant | A/T | snv | 0.31 | 0.30 | 4 | |
| rs45573936 | 1.000 | 0.120 | 6 | 44230625 | missense variant | T/C | snv | 1.8E-02 | 1.6E-02 | 1 |