| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2743173 | 1.000 | 0.080 | 20 | 8264646 | intron variant | T/A;C;G | snv | 1 | |||
| rs4299396 | 1.000 | 0.080 | 20 | 8934668 | intron variant | A/T | snv | 0.30 | 1 | ||
| rs6888451 | 1.000 | 0.080 | 5 | 149744371 | intron variant | C/G;T | snv | 1 | |||
| rs13170573 | 1.000 | 0.080 | 5 | 156327182 | 5 prime UTR variant | C/A;G;T | snv | 1 | |||
| rs199803244 | 1.000 | 0.080 | 12 | 27501430 | intron variant | -/C;CAAAC | ins | 1 | |||
| rs12415421 | 1.000 | 0.080 | 10 | 17391921 | intron variant | C/T | snv | 5.4E-02 | 1 | ||
| rs1880242 | 1.000 | 0.080 | 7 | 22719988 | intron variant | G/T | snv | 0.60 | 1 | ||
| rs4849682 | 1.000 | 0.080 | 2 | 118185307 | intron variant | C/T | snv | 0.20 | 1 | ||
| rs11211631 | 1.000 | 0.080 | 1 | 47918069 | intron variant | A/C | snv | 0.46 | 1 | ||
| rs74472562 | 1.000 | 0.080 | 11 | 44741205 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs251864 | 1.000 | 0.080 | 19 | 39406653 | upstream gene variant | A/G;T | snv | 1 | |||
| rs17879933 | 1.000 | 0.080 | 19 | 39409277 | 3 prime UTR variant | TT/-;TTT | delins | 0.11 | 1 | ||
| rs11126184 | 0.925 | 0.080 | 2 | 68425042 | intergenic variant | C/A | snv | 0.55 | 2 | ||
| rs9902709 | 0.925 | 0.080 | 17 | 42185329 | intron variant | A/G | snv | 3.4E-02 | 0.13 | 2 | |
| rs1409986 | 1.000 | 0.080 | 1 | 70865815 | missense variant | A/G | snv | 0.94 | 0.94 | 2 | |
| rs5417 | 1.000 | 0.080 | 17 | 7281743 | 5 prime UTR variant | C/A;T | snv | 2 | |||
| rs3746083 | 0.925 | 0.160 | 19 | 39408027 | synonymous variant | C/A;G;T | snv | 4.0E-06; 3.5E-02 | 2 | ||
| rs1024610 | 0.882 | 0.200 | 17 | 34253212 | upstream gene variant | T/A | snv | 0.85 | 3 | ||
| rs7030789 | 0.925 | 0.080 | 9 | 110973232 | intron variant | A/G | snv | 0.68 | 3 | ||
| rs4751440 | 0.925 | 0.120 | 10 | 127552592 | missense variant | G/A;C | snv | 1.6E-05; 9.4E-02 | 3 | ||
| rs2586886 | 1.000 | 0.080 | 2 | 26709163 | intron variant | C/G;T | snv | 4 | |||
| rs878855328 | 0.882 | 0.120 | 1 | 11117039 | missense variant | C/T | snv | 4 | |||
| rs3774262 | 0.851 | 0.200 | 3 | 186854025 | intron variant | G/A | snv | 0.10 | 5 | ||
| rs1054135 | 0.851 | 0.240 | 8 | 81478525 | 3 prime UTR variant | C/T | snv | 0.17 | 5 | ||
| rs1063537 | 0.807 | 0.320 | 3 | 186856286 | 3 prime UTR variant | C/T | snv | 9.6E-02 | 6 |