| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1868152 | 0.925 | 0.080 | 3 | 186502274 | intergenic variant | A/G;T | snv | 0.85 | 2 | ||
| rs779838446 | 0.925 | 0.080 | 8 | 42756217 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs111325002 | 1.000 | 0.080 | 3 | 96134788 | intergenic variant | A/G | snv | 8.6E-03 | 2 | ||
| rs150954431 | 1.000 | 0.080 | 12 | 124517777 | intron variant | C/T | snv | 1.6E-02 | 2 | ||
| rs2005290 | 1.000 | 0.080 | 17 | 3284718 | intron variant | C/G;T | snv | 2 | |||
| rs12071360 | 1.000 | 0.080 | 1 | 233608833 | intergenic variant | T/C | snv | 0.10 | 1 | ||
| rs1437134 | 1.000 | 0.080 | 16 | 69696523 | 3 prime UTR variant | A/G | snv | 0.66 | 1 | ||
| rs2229163 | 1.000 | 0.080 | 11 | 46385307 | synonymous variant | G/A | snv | 1.0E-02 | 3.9E-02 | 1 | |
| rs5374 | 1.000 | 0.080 | 18 | 77250689 | synonymous variant | T/C | snv | 0.57 | 0.57 | 1 | |
| rs6561333 | 1.000 | 0.080 | 13 | 46846177 | intron variant | T/C | snv | 0.60 | 1 | ||
| rs6713532 | 1.000 | 0.080 | 2 | 25161964 | intron variant | T/C | snv | 0.36 | 1 | ||
| rs6719226 | 1.000 | 0.080 | 2 | 25173143 | upstream gene variant | C/G | snv | 0.13 | 1 | ||
| rs6871510 | 1.000 | 0.080 | 5 | 79496521 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs6989250 | 1.000 | 0.080 | 8 | 53253835 | upstream gene variant | C/G;T | snv | 1 |