| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4299376 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 11 | |||
| rs4953023 | 0.925 | 0.040 | 2 | 43846861 | non coding transcript exon variant | G/A | snv | 6.9E-02 | 6 | ||
| rs6544718 | 0.882 | 0.120 | 2 | 43877786 | missense variant | T/A;C;G | snv | 0.84; 4.0E-06 | 4 | ||
| rs686030 | 9 | 15304784 | intron variant | C/A | snv | 0.88 | 3 |