| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
| rs850807 | 0.882 | 0.040 | 15 | 23652982 | intergenic variant | T/A;C | snv | 3 | |||
| rs941898 | 1.000 | 0.040 | 14 | 100133100 | intron variant | G/T | snv | 0.81 | 1 | ||
| rs12936442 | 1.000 | 0.040 | 17 | 3029815 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs802047 | 1.000 | 0.040 | 7 | 87328469 | intron variant | T/C | snv | 0.29 | 1 |