| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs398123392 | 0.882 | 0.160 | 6 | 31861259 | missense variant | T/C;G | snv | 1.1E-04 | 2 | ||
| rs104893983 | 0.882 | 0.160 | 6 | 31860510 | missense variant | C/T | snv | 8.0E-06 | 2 | ||
| rs104893985 | 0.925 | 0.160 | 6 | 31862112 | missense variant | G/A | snv | 2.4E-05 | 7.0E-06 | 1 | |
| rs193922915 | 0.925 | 0.160 | 6 | 31859879 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs28940583 | 0.882 | 0.160 | 6 | 31860588 | missense variant | C/T | snv | 5.6E-05 | 1.7E-04 | 1 | |
| rs104893978 | 0.925 | 0.160 | 6 | 31860519 | missense variant | A/G | snv | 1.4E-05 | 1 |