| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104893633 | 0.925 | 0.080 | 2 | 73958201 | missense variant | G/T | snv | 4.0E-06 | 3 | ||
| rs28941785 | 1.000 | 0.080 | 1 | 70415987 | missense variant | C/A;T | snv | 4.0E-06; 6.5E-03 | 2 | ||
| rs28941786 | 1 | 70430388 | stop gained | C/G;T | snv | 8.0E-06; 4.0E-06 | 1 | ||||
| rs773107808 | 1 | 70432151 | stop gained | C/A;T | snv | 8.0E-06; 4.0E-06 | 1 |