| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
| rs8054556 | 0.925 | 0.080 | 16 | 29946895 | intron variant | G/A;C;T | snv | 4 | |||
| rs2057884 | 1.000 | 0.040 | 7 | 105289803 | intron variant | T/C | snv | 0.59 | 2 | ||
| rs2526882 | 1.000 | 0.040 | 14 | 70907985 | synonymous variant | G/A;C | snv | 0.62 | 2 | ||
| rs7235891 | 1.000 | 0.040 | 18 | 55787543 | intron variant | T/C | snv | 0.55 | 2 |