| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 8 | ||
| rs62435145 | 1.000 | 0.040 | 7 | 1246931 | regulatory region variant | G/T | snv | 0.51 | 8 | ||
| rs3765209 | 0.851 | 0.040 | 21 | 15417030 | intron variant | C/T | snv | 0.31 | 7 | ||
| rs13146355 | 1.000 | 0.040 | 4 | 76490987 | intron variant | G/A | snv | 0.33 | 6 | ||
| rs1264347 | 1.000 | 0.040 | 6 | 30830920 | upstream gene variant | C/T | snv | 7.9E-02 | 4 | ||
| rs12922822 | 1.000 | 0.040 | 16 | 20356323 | upstream gene variant | C/A;T | snv | 4 | |||
| rs10084572 | 1.000 | 0.040 | 21 | 43992991 | downstream gene variant | T/A;C;G | snv | 3 | |||
| rs10941191 | 1.000 | 0.040 | 5 | 34504693 | intergenic variant | C/A;T | snv | 3 | |||
| rs11124945 | 1.000 | 0.040 | 2 | 43650017 | intron variant | A/G | snv | 0.21 | 3 | ||
| rs113296370 | 1.000 | 0.040 | 2 | 43636315 | upstream gene variant | A/C | snv | 0.17 | 3 | ||
| rs145590578 | 1.000 | 0.040 | 6 | 160236104 | intron variant | GTT/- | delins | 9.8E-02 | 3 | ||
| rs1556751 | 1.000 | 0.040 | 9 | 68818296 | intron variant | G/A | snv | 0.63 | 3 | ||
| rs1906436 | 1.000 | 0.040 | 15 | 53590245 | intron variant | T/C | snv | 0.32 | 3 | ||
| rs1974990 | 1.000 | 0.040 | 2 | 169790406 | non coding transcript exon variant | G/T | snv | 0.90 | 3 | ||
| rs200950799 | 1.000 | 0.040 | 12 | 17004185 | intergenic variant | C/T | snv | 1.1E-02 | 3 | ||
| rs2023463 | 1.000 | 0.040 | 6 | 29445226 | intron variant | C/T | snv | 7.6E-02 | 3 | ||
| rs2047866 | 1.000 | 0.040 | 15 | 75843853 | splice region variant | C/T | snv | 0.54 | 0.43 | 3 | |
| rs2105903 | 1.000 | 0.040 | 6 | 32427879 | intergenic variant | A/T | snv | 0.14 | 3 | ||
| rs2421556 | 1.000 | 0.040 | 2 | 73733254 | intron variant | G/C;T | snv | 3 | |||
| rs2542713 | 1.000 | 0.040 | 5 | 39385539 | intron variant | A/C;G | snv | 3 | |||
| rs2923008 | 1.000 | 0.040 | 6 | 31349134 | intron variant | G/A;T | snv | 3 | |||
| rs3132374 | 1.000 | 0.040 | 6 | 28900717 | downstream gene variant | C/G | snv | 5.3E-02 | 3 | ||
| rs3812035 | 1.000 | 0.040 | 5 | 177390142 | 3 prime UTR variant | G/A;T | snv | 3 | |||
| rs413988 | 1.000 | 0.040 | 5 | 698535 | intergenic variant | C/G;T | snv | 3 | |||
| rs4810479 | 1.000 | 0.040 | 20 | 45916409 | upstream gene variant | C/T | snv | 0.68 | 3 |