| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs863224451 | 0.701 | 0.440 | 17 | 7673796 | missense variant | C/A;G;T | snv | 20 | |||
| rs751478142 | 1.000 | 5 | 138570994 | missense variant | G/A | snv | 2.8E-05 | 1.4E-05 | 2 | ||
| rs772570880 | 1.000 | 5 | 138566715 | frameshift variant | CT/- | del | 6.3E-05 | 1 | |||
| rs765368797 | 1.000 | 5 | 138570987 | missense variant | T/C | snv | 4.0E-06 | 1 | |||
| rs993079710 | 1.000 | 17 | 7673244 | missense variant | C/T | snv | 1 |