| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs796052428 | 1.000 | 0.080 | 6 | 145627510 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs879745047 | 1.000 | 0.080 | 6 | 18121825 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs950907157 | 1.000 | 0.080 | 6 | 18122230 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs33949390 | 0.776 | 0.160 | 12 | 40320043 | missense variant | G/A;C;T | snv | 1.6E-04; 1.9E-03; 8.0E-06 | 9 | ||
| rs77369218 | 0.807 | 0.160 | 1 | 155235726 | missense variant | T/A | snv | 7 | |||
| rs514492 | 0.882 | 0.160 | 9 | 35062975 | splice region variant | C/T | snv | 0.75 | 0.75 | 3 | |
| rs143624519 | 0.724 | 0.240 | 17 | 45991484 | missense variant | G/A;T | snv | 1.5E-03; 1.2E-05 | 17 |