| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs36053993 | 0.677 | 0.280 | 1 | 45331556 | missense variant | C/T | snv | 3.0E-03 | 3.3E-03 | 31 | |
| rs150766139 | 0.742 | 0.320 | 16 | 2046238 | stop gained | G/A | snv | 1.4E-03 | 1.4E-03 | 13 | |
| rs483352909 | 0.752 | 0.160 | 12 | 132673664 | missense variant | G/A;C | snv | 1.6E-05 | 11 | ||
| rs63751310 | 0.851 | 0.200 | 3 | 37048595 | stop gained | C/T | snv | 6 | |||
| rs587780749 | 0.925 | 0.160 | 1 | 45332443 | missense variant | C/A;T | snv | 5.6E-05; 8.0E-06 | 5 | ||
| rs121908380 | 0.882 | 0.160 | 1 | 45333449 | stop gained | G/A;T | snv | 1.4E-03; 1.2E-04 | 4 | ||
| rs34126013 | 0.925 | 0.160 | 1 | 45332458 | missense variant | G/A | snv | 6.8E-05 | 2.1E-05 | 3 |