| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1293762 | 1.000 | 0.080 | 12 | 112993031 | intron variant | T/G | snv | 0.67 | 1 | ||
| rs1293767 | 1.000 | 0.080 | 12 | 112987349 | missense variant | C/A;G;T | snv | 3.3E-05; 0.76 | 1 | ||
| rs15895 | 1.000 | 0.040 | 12 | 113010483 | stop lost | A/G;T | snv | 0.75 | 1 | ||
| rs739901 | 1.000 | 0.040 | 12 | 112977858 | intron variant | C/A | snv | 0.18 | 1 |