| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2535629 | 0.827 | 0.040 | 3 | 52799203 | intron variant | G/A;C | snv | 2 | |||
| rs115714636 | 3 | 52796511 | missense variant | A/G | snv | 1.6E-03 | 6.4E-03 | 1 | |||
| rs736408 | 1.000 | 0.040 | 3 | 52801338 | intron variant | C/T | snv | 0.47 | 1 | ||
| rs2286797 | 1.000 | 0.080 | 3 | 52795617 | synonymous variant | G/A | snv | 4.5E-02 | 1.7E-02 | 1 | |
| rs4687552 | 0.925 | 0.080 | 3 | 52804386 | non coding transcript exon variant | T/C | snv | 0.33 | 1 |