| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs67507747 | 0.827 | 0.160 | 17 | 50194032 | missense variant | C/A;G;T | snv | 5 | |||
| rs66883877 | 0.882 | 0.160 | 7 | 94419499 | missense variant | G/A;C;T | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs121912986 | 0.882 | 0.200 | 4 | 87610957 | missense variant | C/A;T | snv | 4.0E-06 | 3 | ||
| rs72651645 | 0.925 | 0.160 | 17 | 50191463 | missense variant | C/T | snv | 2 | |||
| rs72651638 | 1.000 | 0.080 | 17 | 50191850 | missense variant | C/T | snv | 1 | |||
| rs749422119 | 1.000 | 0.080 | 6 | 7568548 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs201185673 | 1.000 | 0.080 | 4 | 185506632 | missense variant | G/A | snv | 3.0E-04 | 1.4E-04 | 1 |