| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912550 | 0.827 | 0.120 | 7 | 128398557 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
| rs1042253 | 0.851 | 0.120 | 7 | 128398543 | synonymous variant | G/A | snv | 4.0E-06 | 4 | ||
| rs200729507 | 0.851 | 0.120 | 7 | 128396990 | missense variant | G/A;C;T | snv | 7.6E-05; 4.0E-06 | 4 | ||
| rs759995866 | 0.851 | 0.120 | 7 | 128398478 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
| rs137852534 | 0.851 | 0.120 | X | 78123196 | missense variant | T/C | snv | 1.1E-05 | 4 | ||
| rs137852538 | 0.925 | 0.080 | X | 78117385 | missense variant | A/T | snv | 3 |