| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
| rs11552822 | 1.000 | 9 | 21971109 | missense variant | C/A;T | snv | 4.3E-06 | 2 | |||
| rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 2 | |||
| rs747621669 | 9 | 21970988 | missense variant | C/T | snv | 4.1E-06 | 1 | ||||
| rs121912657 | 0.683 | 0.480 | 17 | 7673806 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs762846821 | 0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 | 1 | ||
| rs879253942 | 0.677 | 0.400 | 17 | 7673826 | missense variant | A/G | snv | 1 |