| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12734001 | 1.000 | 0.080 | 1 | 202421786 | intron variant | C/T | snv | 3.5E-05 | 2 | ||
| rs12734338 | 0.925 | 0.120 | 1 | 202500595 | intron variant | T/C | snv | 2 | |||
| rs3817222 | 1.000 | 0.080 | 1 | 202495632 | missense variant | C/T | snv | 3.6E-05 | 7.0E-06 | 1 | |
| rs12739262 | 1 | 202422615 | splice region variant | C/T | snv | 1.5E-04 | 7.0E-05 | 1 |