| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs35947132 | 0.776 | 0.280 | 10 | 70600631 | missense variant | G/A | snv | 2.9E-02 | 2.9E-02 | 10 | |
| rs28933375 | 0.882 | 0.160 | 10 | 70598966 | missense variant | T/C | snv | 5.0E-03 | 7.5E-03 | 4 | |
| rs748409747 | 1.000 | 0.200 | 8 | 144505418 | missense variant | G/A;T | snv | 9.1E-06; 1.8E-05 | 2 | ||
| rs28933973 | 1.000 | 0.040 | 10 | 70599048 | missense variant | G/A | snv | 1.2E-05 | 2 | ||
| rs140148806 | 1.000 | 0.040 | 19 | 7645196 | splice acceptor variant | G/C | snv | 2.0E-04 | 2.3E-04 | 2 | |
| rs140184929 | 17 | 75831135 | missense variant | C/T | snv | 3.0E-04 | 1.3E-04 | 1 |