| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11819199 | 1.000 | 0.120 | 10 | 20576228 | intergenic variant | A/G | snv | 0.12 | 1 | ||
| rs2000260 | 1.000 | 0.120 | 1 | 108130783 | downstream gene variant | A/G | snv | 0.37 | 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 | |||
| rs6799767 | 1.000 | 0.120 | 3 | 176312308 | intergenic variant | G/A;T | snv | 1 | |||
| rs8041227 | 1.000 | 0.120 | 15 | 31246339 | intergenic variant | G/A | snv | 0.18 | 1 | ||
| rs3815700 | 1.000 | 0.120 | 19 | 32602346 | intron variant | T/C | snv | 0.19 | 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 | ||
| rs77569859 | 1.000 | 0.120 | 2 | 31188421 | intron variant | T/C | snv | 4.1E-02 | 1 | ||
| rs77301713 | 1.000 | 0.120 | 11 | 77121400 | intron variant | G/A | snv | 2.0E-02 | 1 | ||
| rs118086209 | 1.000 | 0.120 | 11 | 86393453 | intron variant | T/C;G | snv | 1 | |||
| rs3744790 | 1.000 | 0.120 | 17 | 78897053 | intron variant | C/T | snv | 0.14 | 1 | ||
| rs12924112 | 1.000 | 0.120 | 16 | 11125863 | intron variant | T/A;G | snv | 1 | |||
| rs9956738 | 1.000 | 0.120 | 18 | 52414603 | intron variant | A/G | snv | 4.6E-02 | 1 | ||
| rs28530674 | 1.000 | 0.120 | 1 | 18907640 | 3 prime UTR variant | A/G | snv | 0.11 | 1 | ||
| rs8008716 | 1.000 | 0.120 | 14 | 26656559 | intron variant | A/G | snv | 8.9E-02 | 1 | ||
| rs4240384 | 1.000 | 0.120 | 5 | 124955709 | intron variant | T/C | snv | 0.85 | 1 | ||
| rs371915 | 1.000 | 0.120 | 16 | 84544635 | intron variant | A/C;G;T | snv | 1 | |||
| rs2075277 | 1.000 | 0.120 | 22 | 21028193 | 3 prime UTR variant | T/C | snv | 0.19 | 1 | ||
| rs11206830 | 1.000 | 0.120 | 1 | 56494451 | intron variant | C/T | snv | 8.7E-02 | 1 | ||
| rs17004598 | 1.000 | 0.120 | 21 | 43658675 | intron variant | T/G | snv | 4.5E-02 | 1 | ||
| rs10062929 | 1.000 | 0.120 | 5 | 111072481 | intron variant | C/A | snv | 0.13 | 1 | ||
| rs2898261 | 1.000 | 0.120 | 8 | 11101029 | intron variant | G/A;T | snv | 1 | |||
| rs599707 | 0.925 | 0.200 | 6 | 31840659 | downstream gene variant | C/T | snv | 7.6E-02 | 2 |