| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4671393 | 0.790 | 0.400 | 2 | 60493816 | intron variant | A/C;G | snv | 11 | |||
| rs2416257 | 0.882 | 0.160 | 5 | 111099792 | intron variant | C/G;T | snv | 5 | |||
| rs7482144 | 0.882 | 0.280 | 11 | 5254939 | 3 prime UTR variant | G/A | snv | 4 | |||
| rs2296225 | 0.882 | 0.160 | 1 | 20704549 | missense variant | T/C;G | snv | 0.12; 4.0E-06 | 3 | ||
| rs489441 | 0.925 | 0.280 | 5 | 135158291 | intron variant | G/A;C;T | snv | 2 | |||
| rs118086209 | 1.000 | 0.120 | 11 | 86393453 | intron variant | T/C;G | snv | 1 | |||
| rs12924112 | 1.000 | 0.120 | 16 | 11125863 | intron variant | T/A;G | snv | 1 | |||
| rs2055376 | 1.000 | 0.120 | 5 | 116845732 | regulatory region variant | G/A;T | snv | 1 | |||
| rs252716 | 1.000 | 0.120 | 5 | 111089365 | intron variant | G/A;C | snv | 1 | |||
| rs2898261 | 1.000 | 0.120 | 8 | 11101029 | intron variant | G/A;T | snv | 1 | |||
| rs371915 | 1.000 | 0.120 | 16 | 84544635 | intron variant | A/C;G;T | snv | 1 | |||
| rs6799767 | 1.000 | 0.120 | 3 | 176312308 | intergenic variant | G/A;T | snv | 1 | |||
| rs77301713 | 1.000 | 0.120 | 11 | 77121400 | intron variant | G/A | snv | 2.0E-02 | 1 | ||
| rs61894547 | 0.882 | 0.160 | 11 | 76537586 | intron variant | C/T | snv | 3.1E-02 | 4 | ||
| rs77569859 | 1.000 | 0.120 | 2 | 31188421 | intron variant | T/C | snv | 4.1E-02 | 1 | ||
| rs17004598 | 1.000 | 0.120 | 21 | 43658675 | intron variant | T/G | snv | 4.5E-02 | 1 | ||
| rs9956738 | 1.000 | 0.120 | 18 | 52414603 | intron variant | A/G | snv | 4.6E-02 | 1 | ||
| rs149864795 | 1.000 | 0.120 | 2 | 31179541 | intron variant | G/A | snv | 4.8E-02 | 1 | ||
| rs6736278 | 1.000 | 0.120 | 2 | 31220009 | intron variant | C/T | snv | 5.4E-02 | 1 | ||
| rs599707 | 0.925 | 0.200 | 6 | 31840659 | downstream gene variant | C/T | snv | 7.6E-02 | 2 | ||
| rs1059513 | 0.776 | 0.240 | 12 | 57095926 | 3 prime UTR variant | T/C | snv | 8.0E-02 | 11 | ||
| rs11206830 | 1.000 | 0.120 | 1 | 56494451 | intron variant | C/T | snv | 8.7E-02 | 1 | ||
| rs8008716 | 1.000 | 0.120 | 14 | 26656559 | intron variant | A/G | snv | 8.9E-02 | 1 | ||
| rs28530674 | 1.000 | 0.120 | 1 | 18907640 | 3 prime UTR variant | A/G | snv | 0.11 | 1 | ||
| rs11819199 | 1.000 | 0.120 | 10 | 20576228 | intergenic variant | A/G | snv | 0.12 | 1 |