| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1085307993 | 0.716 | 0.440 | 5 | 161331056 | missense variant | C/T | snv | 53 | |||
| rs1557055405 | 0.807 | 0.400 | X | 153743532 | missense variant | T/A | snv | 21 | |||
| rs1208636573 | 0.807 | 0.120 | 1 | 155612098 | stop gained | C/G;T | snv | 4.0E-06; 4.0E-06 | 15 | ||
| rs622288 | 0.807 | 0.120 | 1 | 155612848 | missense variant | C/T | snv | 3.6E-05 | 4.2E-05 | 15 | |
| rs587778779 | 0.807 | 0.240 | 2 | 218814379 | splice acceptor variant | G/A;T | snv | 14 | |||
| rs1057518760 | 1.000 | 0.080 | 2 | 240788182 | missense variant | C/T | snv | 4 |