| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2298991 | 1.000 | 0.040 | 4 | 109970856 | intron variant | T/A;G | snv | 1 | |||
| rs4698803 | 1.000 | 0.040 | 4 | 109993271 | missense variant | A/G;T | snv | 0.85 | 1 | ||
| rs6533485 | 1.000 | 0.040 | 4 | 110006407 | intron variant | G/C | snv | 0.61 | 1 | ||
| rs769047429 | 1.000 | 4 | 109999827 | frameshift variant | -/G | delins | 8.0E-06 | 1 | |||
| rs771293553 | 1.000 | 0.120 | 4 | 109913378 | missense variant | T/A;C | snv | 1 | |||
| rs778040733 | 1.000 | 0.080 | 4 | 109988662 | missense variant | T/C | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs887183646 | 1.000 | 0.080 | 4 | 109976079 | missense variant | C/T | snv | 3.2E-05 | 2.8E-05 | 1 | |
| rs902596253 | 1.000 | 0.080 | 4 | 109941062 | missense variant | C/T | snv | 1 |