| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 | ||
| rs370640837 | 1.000 | 0.120 | 2 | 215019657 | missense variant | G/A;T | snv | 1.8E-04 | 1 | ||
| rs1187237313 | 1.000 | 0.120 | 7 | 20727052 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs757430763 | 1.000 | 0.120 | 4 | 8061051 | missense variant | C/T | snv | 4.4E-05 | 1 | ||
| rs61732239 | 1.000 | 0.120 | 20 | 44625622 | missense variant | C/G;T | snv | 1.0E-03 | 1 | ||
| rs200567888 | 1.000 | 0.120 | 3 | 89210327 | missense variant | G/T | snv | 1.2E-03 | 9.8E-04 | 1 | |
| rs772906202 | 1.000 | 0.120 | 19 | 15110668 | missense variant | G/A | snv | 3.1E-05 | 7.0E-06 | 1 | |
| rs762846821 | 0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 | 1 |