| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 5 | |
| rs11709077 | 0.925 | 0.120 | 3 | 12295008 | intron variant | G/A | snv | 8.8E-02 | 3 | ||
| rs17036328 | 1.000 | 0.040 | 3 | 12348985 | intron variant | T/C | snv | 0.14 | 3 | ||
| rs1171114 | 1.000 | 0.040 | 6 | 83517927 | intron variant | T/C | snv | 0.59 | 2 | ||
| rs6490117 | 1.000 | 0.040 | 12 | 117161544 | intron variant | C/A;G | snv | 2 | |||
| rs652722 | 1.000 | 0.040 | 11 | 31883988 | intron variant | C/T | snv | 0.32 | 2 | ||
| rs6559921 | 1.000 | 0.040 | 9 | 86257124 | intron variant | A/T | snv | 0.26 | 2 | ||
| rs845084 | 1.000 | 0.040 | 10 | 123460520 | intron variant | G/A | snv | 0.26 | 2 |