| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607165 | 0.708 | 0.520 | 16 | 89935679 | missense variant | G/A;C | snv | 18 | |||
| rs201439531 | 0.827 | 0.200 | 10 | 49664880 | missense variant | C/G | snv | 7.0E-06 | 11 | ||
| rs769234940 | 0.827 | 0.200 | 10 | 49627735 | missense variant | C/T | snv | 1.6E-05 | 2.8E-05 | 11 | |
| rs1555216163 | 0.851 | 0.160 | 12 | 80717084 | frameshift variant | AGTTCTCACC/- | delins | 4 | |||
| rs1565864693 | 0.851 | 0.160 | 12 | 80717346 | missense variant | C/T | snv | 4 | |||
| rs1569484022 | 1.000 | 0.120 | MT | 5667 | non coding transcript exon variant | G/A | snv | 1 |