| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28933383 | 0.851 | 0.120 | 12 | 4912055 | missense variant | C/A;G;T | snv | 2 | |||
| rs118192162 | 0.851 | 0.120 | 19 | 38455359 | missense variant | A/C;G | snv | 2 | |||
| rs118192172 | 0.851 | 0.120 | 19 | 38457545 | missense variant | C/G;T | snv | 8.7E-05 | 1.1E-04 | 2 | |
| rs1800559 | 0.925 | 0.080 | 1 | 201060815 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs104894358 | 0.882 | 0.120 | 12 | 4912627 | stop gained | C/G;T | snv | 4.0E-06 | 1 | ||
| rs28928902 | 0.851 | 0.160 | 1 | 156136951 | missense variant | C/G;T | snv | 1.2E-05 | 1 | ||
| rs121913619 | 0.882 | 0.080 | 17 | 10650374 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs118192124 | 0.851 | 0.120 | 19 | 38500636 | missense variant | C/T | snv | 1 | |||
| rs121918592 | 0.882 | 0.080 | 19 | 38448712 | missense variant | G/A;C | snv | 1 | |||
| rs104894127 | 0.925 | 0.080 | 9 | 35685750 | missense variant | G/C | snv | 1 |