| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1801581 | 0.925 | 0.080 | 1 | 94047009 | missense variant | C/A;T | snv | 2.8E-05; 3.0E-02 | 2 | ||
| rs76157638 | 0.851 | 0.080 | 1 | 94051698 | missense variant | C/G;T | snv | 4.4E-03; 4.0E-06 | 2 | ||
| rs61749409 | 0.882 | 0.080 | 1 | 94062710 | missense variant | G/A | snv | 4.4E-05 | 2.1E-05 | 2 | |
| rs61750120 | 0.882 | 0.160 | 1 | 94042767 | missense variant | G/A | snv | 1.2E-04 | 1.8E-04 | 3 | |
| rs62645944 | 0.807 | 0.080 | 1 | 94098794 | splice region variant | C/A | snv | 8.8E-05 | 6.3E-05 | 3 | |
| rs1801466 | 1.000 | 1 | 94010911 | missense variant | T/A | snv | 4.3E-02 | 4.1E-02 | 3 | ||
| rs201471607 | 0.851 | 0.080 | 1 | 94046943 | missense variant | T/C | snv | 1.4E-04 | 7.7E-05 | 4 | |
| rs61750200 | 0.790 | 0.080 | 1 | 94098928 | missense variant | G/A;T | snv | 1.1E-04; 8.0E-06 | 4 | ||
| rs281865404 | 0.851 | 0.080 | 1 | 94014675 | missense variant | GG/CA | mnv | 4 | |||
| rs560426 | 0.851 | 0.200 | 1 | 94087882 | intron variant | C/T | snv | 0.53 | 5 | ||
| rs61751374 | 0.776 | 0.160 | 1 | 94043413 | missense variant | G/A | snv | 1.7E-03 | 1.7E-03 | 5 | |
| rs768435443 | 0.807 | 0.080 | 1 | 94055128 | missense variant | A/G | snv | 4.0E-06 | 8 | ||
| rs1800553 | 0.742 | 0.240 | 1 | 94008251 | missense variant | C/T | snv | 4.7E-03 | 3.0E-03 | 13 |