| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12722502 | 0.882 | 0.080 | 10 | 6051176 | intron variant | C/T | snv | 7.8E-03 | 4 | ||
| rs2033784 | 1.000 | 0.080 | 15 | 67157322 | intron variant | A/G | snv | 0.35 | 4 | ||
| rs2381416 | 1.000 | 0.080 | 9 | 6193455 | upstream gene variant | C/A | snv | 0.65 | 4 | ||
| rs61894547 | 0.882 | 0.160 | 11 | 76537586 | intron variant | C/T | snv | 3.1E-02 | 4 | ||
| rs10455025 | 1.000 | 0.080 | 5 | 111069301 | upstream gene variant | A/C | snv | 0.24 | 3 | ||
| rs12952581 | 0.925 | 0.080 | 17 | 49370984 | intron variant | G/A | snv | 0.42 | 0.28 | 3 | |
| rs61840192 | 1.000 | 0.080 | 10 | 9001441 | intergenic variant | G/A;C;T | snv | 3 | |||
| rs7918084 | 1.000 | 0.080 | 10 | 92669710 | non coding transcript exon variant | C/T | snv | 0.60 | 3 | ||
| rs11603634 | 1.000 | 0.080 | 11 | 1142570 | intergenic variant | A/G | snv | 0.38 | 2 | ||
| rs4594881 | 1.000 | 0.080 | 5 | 35846713 | intergenic variant | G/T | snv | 0.28 | 2 | ||
| rs9807989 | 1.000 | 0.080 | 2 | 102354740 | intron variant | T/C;G | snv | 0.46 | 2 |