| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80358192 | 0.807 | 0.080 | 1 | 36098332 | missense variant | A/C;G | snv | 4.6E-05 | 6 | ||
| rs80358191 | 0.882 | 0.080 | 1 | 36098318 | missense variant | G/T | snv | 3 | |||
| rs201235688 | 0.925 | 0.080 | 1 | 36098380 | missense variant | C/A;T | snv | 1.2E-03 | 2 | ||
| rs727504229 | 0.925 | 0.080 | 1 | 36098317 | missense variant | TG/AC | mnv | 2 | |||
| rs145553904 | 1.000 | 0.080 | 1 | 36097957 | missense variant | G/A | snv | 1.4E-03 | 1.4E-03 | 1 | |
| rs199786966 | 1.000 | 0.080 | 1 | 36098612 | missense variant | C/G | snv | 4.0E-04 | 3.3E-04 | 1 | |
| rs369487110 | 1.000 | 0.080 | 1 | 36098770 | missense variant | C/G;T | snv | 4.1E-06; 1.1E-04 | 4.9E-05 | 1 |