| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1264347 | 1.000 | 0.040 | 6 | 30830920 | upstream gene variant | C/T | snv | 7.9E-02 | 4 | ||
| rs36217263 | 1.000 | 0.040 | 13 | 33015697 | upstream gene variant | A/- | del | 0.21 | 4 | ||
| rs3812035 | 1.000 | 0.040 | 5 | 177390142 | 3 prime UTR variant | G/A;T | snv | 4 | |||
| rs768925824 | 0.925 | 0.040 | 19 | 11110693 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
| rs891512 | 0.925 | 0.040 | 7 | 151011001 | intron variant | A/G | snv | 0.84 | 0.85 | 4 | |
| rs10084572 | 1.000 | 0.040 | 21 | 43992991 | downstream gene variant | T/A;C;G | snv | 3 | |||
| rs1052700 | 1.000 | 0.040 | 15 | 89665079 | 3 prime UTR variant | A/T | snv | 0.26 | 3 | ||
| rs10941191 | 1.000 | 0.040 | 5 | 34504693 | intergenic variant | C/A;T | snv | 3 | |||
| rs11071657 | 1.000 | 0.040 | 15 | 62141763 | regulatory region variant | A/G | snv | 0.31 | 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 | ||
| rs12107 | 1.000 | 0.040 | 22 | 36281936 | 3 prime UTR variant | G/A;T | snv | 3 | |||
| rs1228534100 | 1.000 | 0.040 | 12 | 120978892 | missense variant | G/A | snv | 7.0E-06 | 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 | ||
| rs192902098 | 1.000 | 0.040 | 13 | 27920235 | missense variant | C/A;G;T | snv | 2.6E-03; 3.4E-04; 5.6E-05 | 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 | ||
| rs2276047 | 1.000 | 0.040 | 11 | 72230337 | intron variant | A/G | snv | 0.28 | 0.33 | 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 |