| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607165 | 0.708 | 0.520 | 16 | 89935679 | missense variant | G/A;C | snv | 18 | |||
| rs104893836 | 0.790 | 0.160 | 4 | 67754019 | missense variant | T/C | snv | 2.8E-03 | 2.3E-03 | 7 | |
| rs104893837 | 0.807 | 0.160 | 4 | 67740682 | missense variant | C/T | snv | 1.8E-03 | 1.3E-03 | 6 | |
| rs74315418 | 0.827 | 0.160 | 20 | 5314116 | missense variant | C/A;T | snv | 3.3E-04; 7.1E-04 | 5 | ||
| rs771470596 | 0.882 | 0.200 | 4 | 147539919 | missense variant | G/A;C | snv | 1.6E-05 | 4 | ||
| rs1800447 | 0.851 | 0.200 | 19 | 49016648 | missense variant | A/G | snv | 6.5E-02 | 7.6E-02 | 4 | |
| rs34349826 | 0.851 | 0.200 | 19 | 49016626 | missense variant | A/G | snv | 4.9E-02 | 7.5E-02 | 4 | |
| rs104894897 | 0.882 | 0.160 | X | 30304676 | missense variant | A/C | snv | 4 | |||
| rs78861628 | 0.851 | 0.160 | 20 | 5302393 | missense variant | G/A | snv | 3.9E-03 | 1.4E-02 | 4 | |
| rs104893844 | 0.882 | 0.160 | 4 | 67754068 | missense variant | C/T | snv | 3.6E-05 | 7.0E-06 | 4 | |
| rs74452732 | 0.851 | 0.160 | 4 | 67753825 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
| rs1363196459 | 0.882 | 0.040 | 4 | 147486001 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs148499544 | 0.882 | 0.160 | 4 | 67740670 | missense variant | A/C | snv | 8.0E-06 | 5.6E-05 | 3 | |
| rs970697573 | 0.882 | 0.040 | 19 | 19626965 | missense variant | C/T | snv | 3 | |||
| rs28935481 | 0.882 | 0.160 | X | 30304673 | missense variant | T/A;C | snv | 5.4E-06 | 3 | ||
| rs750566506 | 0.925 | 0.160 | 4 | 67754013 | missense variant | T/C | snv | 2 | |||
| rs1377173003 | 1.000 | 0.040 | 8 | 26770258 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
| rs149091975 | 1.000 | 0.040 | 2 | 120986480 | missense variant | G/A | snv | 4.3E-04 | 5.2E-04 | 1 |