| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 | |
| rs121909222 | 0.742 | 0.240 | 10 | 87933127 | missense variant | A/G | snv | 13 | |||
| rs3104746 | 0.790 | 0.120 | 16 | 52567188 | intron variant | T/A | snv | 8.6E-02 | 7 | ||
| rs11075995 | 0.882 | 0.080 | 16 | 53821379 | intron variant | A/T | snv | 0.77 | 5 | ||
| rs12493607 | 0.882 | 0.080 | 3 | 30641447 | intron variant | G/C;T | snv | 3 | |||
| rs6099128 | 0.925 | 20 | 56390288 | intron variant | T/G | snv | 0.13 | 2 | |||
| rs9436746 | 1.000 | 1 | 65442790 | intron variant | A/C | snv | 0.50 | 1 | |||
| rs9436748 | 1.000 | 1 | 65445989 | intron variant | G/A;T | snv | 0.33 | 1 | |||
| rs2070235 | 1.000 | 20 | 43702817 | missense variant | A/G | snv | 0.10 | 0.14 | 1 |