| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2621416 | 0.882 | 0.280 | 6 | 32774091 | intergenic variant | T/C | snv | 0.26 | 1 | ||
| rs9268853 | 0.790 | 0.440 | 6 | 32461866 | intron variant | T/C | snv | 0.29 | 1 | ||
| rs6773854 | 1.000 | 0.120 | 3 | 187931631 | downstream gene variant | T/C | snv | 0.23 | 1 | ||
| rs121434629 | 0.763 | 0.320 | 7 | 6005918 | missense variant | C/A;T | snv | 1.6E-04; 8.1E-06 | 1 | ||
| rs121918459 | 0.662 | 0.440 | 12 | 112450368 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 2 | |
| rs11466782 | 0.925 | 0.120 | 5 | 157494947 | intron variant | A/G | snv | 0.10 | 3 | ||
| rs2466571 | 0.925 | 0.120 | 1 | 207766701 | intron variant | G/T | snv | 0.46 | 3 | ||
| rs751837 | 0.882 | 0.120 | 14 | 103018488 | intron variant | T/C | snv | 0.23 | 3 | ||
| rs1802710 | 14 | 100734308 | synonymous variant | T/A;C | snv | 0.63 | 3 | ||||
| rs867329357 | 0.925 | 0.120 | 13 | 102872275 | missense variant | G/A | snv | 4.0E-06 | 4.9E-05 | 3 | |
| rs1057519833 | 0.925 | 0.120 | 7 | 148809375 | missense variant | G/C | snv | 3 | |||
| rs2304240 | 0.882 | 0.200 | 19 | 10338716 | synonymous variant | A/G | snv | 0.81 | 0.85 | 3 | |
| rs10494879 | 0.925 | 0.120 | 1 | 206778859 | intron variant | C/A;G | snv | 0.36 | 3 | ||
| rs707824 | 0.925 | 0.120 | 6 | 14636732 | intergenic variant | T/C | snv | 0.74 | 3 | ||
| rs1257715362 | 0.925 | 0.120 | 4 | 85995065 | missense variant | A/G | snv | 7.0E-06 | 3 | ||
| rs1042752 | 0.925 | 0.120 | 11 | 111352386 | 3 prime UTR variant | A/G | snv | 0.39 | 3 | ||
| rs708486 | 0.925 | 0.120 | 14 | 52274253 | intron variant | A/G | snv | 0.35 | 3 | ||
| rs138228187 | 0.925 | 0.120 | 11 | 126292650 | missense variant | C/T | snv | 4.0E-05 | 1.4E-05 | 3 | |
| rs867830180 | 0.925 | 0.120 | 20 | 63695147 | missense variant | G/A;T | snv | 3 | |||
| rs1555525126 | 0.925 | 0.120 | 17 | 7673749 | missense variant | T/C | snv | 3 | |||
| rs1351687973 | 0.925 | 0.120 | 1 | 3731497 | missense variant | G/A | snv | 1.6E-05 | 3 | ||
| rs535311760 | 0.925 | 0.120 | 1 | 3730979 | missense variant | G/A | snv | 1.2E-05; 8.2E-06 | 3 | ||
| rs10190751 | 0.882 | 0.120 | 2 | 201141373 | splice acceptor variant | G/A | snv | 0.18 | 0.26 | 4 | |
| rs267601395 | 0.925 | 0.160 | 7 | 148811636 | missense variant | A/G;T | snv | 4 | |||
| rs6676671 | 0.882 | 0.160 | 1 | 206779403 | intron variant | T/A | snv | 0.32 | 4 |