| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7482144 | 0.882 | 0.280 | 11 | 5254939 | 3 prime UTR variant | G/A | snv | 4 | |||
| rs118086209 | 1.000 | 0.120 | 11 | 86393453 | intron variant | T/C;G | snv | 1 | |||
| rs77301713 | 1.000 | 0.120 | 11 | 77121400 | intron variant | G/A | snv | 2.0E-02 | 1 | ||
| rs324011 | 0.742 | 0.360 | 12 | 57108399 | intron variant | C/T | snv | 0.32 | 12 | ||
| rs1059513 | 0.776 | 0.240 | 12 | 57095926 | 3 prime UTR variant | T/C | snv | 8.0E-02 | 11 | ||
| rs167769 | 0.827 | 0.280 | 12 | 57109992 | 5 prime UTR variant | C/T | snv | 0.31 | 5 | ||
| rs8008716 | 1.000 | 0.120 | 14 | 26656559 | intron variant | A/G | snv | 8.9E-02 | 1 | ||
| rs8041227 | 1.000 | 0.120 | 15 | 31246339 | intergenic variant | G/A | snv | 0.18 | 1 | ||
| rs12924112 | 1.000 | 0.120 | 16 | 11125863 | intron variant | T/A;G | snv | 1 | |||
| rs371915 | 1.000 | 0.120 | 16 | 84544635 | intron variant | A/C;G;T | snv | 1 | |||
| rs3744790 | 1.000 | 0.120 | 17 | 78897053 | intron variant | C/T | snv | 0.14 | 1 | ||
| rs9956738 | 1.000 | 0.120 | 18 | 52414603 | intron variant | A/G | snv | 4.6E-02 | 1 | ||
| rs3815700 | 1.000 | 0.120 | 19 | 32602346 | intron variant | T/C | snv | 0.19 | 1 | ||
| rs17004598 | 1.000 | 0.120 | 21 | 43658675 | intron variant | T/G | snv | 4.5E-02 | 1 | ||
| rs2075277 | 1.000 | 0.120 | 22 | 21028193 | 3 prime UTR variant | T/C | snv | 0.19 | 1 |