| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 62 | ||
| rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 43 | ||
| rs121913273 | 0.605 | 0.440 | 3 | 179218294 | missense variant | G/A;C | snv | 22 | |||
| rs2699887 | 0.763 | 0.280 | 3 | 179148620 | intron variant | C/T | snv | 0.18 | 11 | ||
| rs6443624 | 0.776 | 0.200 | 3 | 179179886 | intron variant | C/A | snv | 0.30 | 8 | ||
| rs17849071 | 0.776 | 0.160 | 3 | 179218439 | intron variant | T/G | snv | 7.9E-02 | 8 | ||
| rs121913274 | 0.645 | 0.320 | 3 | 179218304 | missense variant | A/C;G;T | snv | 4 | |||
| rs7646409 | 0.882 | 0.040 | 3 | 179182405 | intron variant | T/C | snv | 0.26 | 4 | ||
| rs6443626 | 0.851 | 0.200 | 3 | 179237995 | 3 prime UTR variant | T/C | snv | 0.24 | 4 | ||
| rs17849079 | 0.882 | 0.120 | 3 | 179234232 | synonymous variant | C/T | snv | 2.1E-02 | 1.5E-02 | 3 | |
| rs121913282 | 0.882 | 0.040 | 3 | 179221072 | missense variant | A/C | snv | 3 | |||
| rs9866361 | 0.882 | 0.040 | 3 | 179190061 | intron variant | G/A | snv | 0.24 | 3 | ||
| rs3976507 | 0.882 | 0.120 | 3 | 179239995 | 3 prime UTR variant | C/T | snv | 0.19 | 0.24 | 3 | |
| rs587777790 | 0.732 | 0.280 | 3 | 179199690 | missense variant | G/A | snv | 2 | |||
| rs778184105 | 3 | 179199098 | missense variant | C/A | snv | 4.1E-06 | 2 | ||||
| rs2677764 | 0.925 | 0.080 | 3 | 179206019 | intron variant | C/A;T | snv | 2 | |||
| rs9838411 | 0.925 | 0.080 | 3 | 179169899 | intron variant | G/A | snv | 0.25 | 2 | ||
| rs397517202 | 0.851 | 0.320 | 3 | 179234230 | missense variant | A/G | snv | 2 | |||
| rs141178472 | 0.925 | 0.080 | 3 | 179234393 | 3 prime UTR variant | T/C | snv | 3.0E-03 | 3.3E-03 | 2 | |
| rs863225460 | 0.882 | 0.200 | 3 | 179199160 | missense variant | T/A | snv | 2 | |||
| rs1442481831 | 0.925 | 0.080 | 3 | 179203635 | missense variant | T/C | snv | 2 | |||
| rs1607237 | 1.000 | 0.040 | 3 | 179232509 | intron variant | C/T | snv | 0.68 | 1 | ||
| rs4855094 | 1.000 | 0.040 | 3 | 179160189 | intron variant | G/A | snv | 0.10 | 1 | ||
| rs71310379 | 3 | 179199003 | missense variant | C/A | snv | 4.4E-05 | 4.2E-05 | 1 | |||
| rs121913272 | 0.752 | 0.400 | 3 | 179210192 | missense variant | T/C;G | snv | 1 |