| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10062929 | 1.000 | 0.120 | 5 | 111072481 | intron variant | C/A | snv | 0.13 | 1 | ||
| rs3744790 | 1.000 | 0.120 | 17 | 78897053 | intron variant | C/T | snv | 0.14 | 1 | ||
| rs8041227 | 1.000 | 0.120 | 15 | 31246339 | intergenic variant | G/A | snv | 0.18 | 1 | ||
| rs2075277 | 1.000 | 0.120 | 22 | 21028193 | 3 prime UTR variant | T/C | snv | 0.19 | 1 | ||
| rs3815700 | 1.000 | 0.120 | 19 | 32602346 | intron variant | T/C | snv | 0.19 | 1 | ||
| rs9399137 | 0.851 | 0.320 | 6 | 135097880 | intron variant | T/C | snv | 0.20 | 13 | ||
| rs11495981 | 1.000 | 0.120 | 7 | 28137682 | intron variant | C/T | snv | 0.29 | 2 | ||
| rs167769 | 0.827 | 0.280 | 12 | 57109992 | 5 prime UTR variant | C/T | snv | 0.31 | 5 | ||
| rs324011 | 0.742 | 0.360 | 12 | 57108399 | intron variant | C/T | snv | 0.32 | 12 | ||
| rs2000260 | 1.000 | 0.120 | 1 | 108130783 | downstream gene variant | A/G | snv | 0.37 | 1 | ||
| rs3806933 | 0.807 | 0.360 | 5 | 111071044 | 5 prime UTR variant | C/A;T | snv | 0.40 | 7 | ||
| rs1986734 | 1.000 | 0.120 | 4 | 76499631 | intron variant | C/T | snv | 0.43 | 3 | ||
| rs3806932 | 0.925 | 0.160 | 5 | 111069977 | upstream gene variant | A/G | snv | 0.51 | 3 | ||
| rs2155219 | 0.732 | 0.280 | 11 | 76588150 | upstream gene variant | G/T | snv | 0.52 | 14 | ||
| rs4240384 | 1.000 | 0.120 | 5 | 124955709 | intron variant | T/C | snv | 0.85 | 1 |