| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1456079929 | 0.851 | 0.120 | 11 | 101042001 | missense variant | C/A | snv | 8.0E-06 | 5 | ||
| rs1408080623 | 0.851 | 0.080 | 11 | 101128058 | missense variant | G/A | snv | 5 | |||
| rs776880789 | 0.925 | 0.080 | 11 | 101128241 | missense variant | G/C;T | snv | 4.7E-06; 4.7E-06 | 4 | ||
| rs1293387481 | 0.925 | 0.080 | 11 | 101062537 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs759862685 | 11 | 101127694 | missense variant | C/G;T | snv | 1.5E-04 | 1 |