| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3856806 | 0.637 | 0.440 | 3 | 12434058 | synonymous variant | C/T | snv | 0.13 | 0.11 | 41 | |
| rs17366743 | 0.807 | 0.280 | 3 | 186854300 | missense variant | T/C | snv | 2.2E-02 | 2.1E-02 | 7 | |
| rs17058639 | 0.925 | 0.160 | 3 | 57896874 | splice region variant | C/T | snv | 0.30 | 0.24 | 2 | |
| rs200295620 | 0.925 | 0.160 | 3 | 168172398 | intergenic variant | T/-;TT | delins | 5.7E-03 | 2 | ||
| rs1043045 | 1.000 | 0.120 | 3 | 57928451 | 3 prime UTR variant | T/C | snv | 0.31 | 1 | ||
| rs1057719 | 1.000 | 0.120 | 3 | 57927987 | 3 prime UTR variant | A/G | snv | 0.31 | 1 | ||
| rs13064954 | 1.000 | 0.120 | 3 | 157136953 | downstream gene variant | G/A | snv | 7.9E-02 | 1 | ||
| rs9866141 | 1.000 | 0.120 | 3 | 157232790 | intron variant | C/A;T | snv | 4.7E-02 | 1 | ||
| rs8192678 | 0.667 | 0.440 | 4 | 23814039 | missense variant | C/T | snv | 0.31 | 0.26 | 28 | |
| rs2071559 | 0.667 | 0.680 | 4 | 55126199 | upstream gene variant | A/G | snv | 0.53 | 26 | ||
| rs1800592 | 0.807 | 0.200 | 4 | 140572807 | upstream gene variant | T/C | snv | 0.40 | 8 | ||
| rs140421861 | 1.000 | 0.120 | 4 | 73413512 | synonymous variant | C/T | snv | 1.1E-04 | 1.1E-04 | 1 | |
| rs4470583 | 1.000 | 0.120 | 4 | 161329780 | intergenic variant | A/G;T | snv | 1 | |||
| rs6856425 | 1.000 | 0.120 | 4 | 983130 | intron variant | T/C | snv | 7.6E-02 | 1 | ||
| rs1073203 | 0.882 | 0.160 | 5 | 125983763 | intron variant | C/G | snv | 0.15 | 4 | ||
| rs1372503923 | 0.925 | 0.160 | 5 | 53048731 | missense variant | A/C | snv | 3 | |||
| rs1145612 | 1.000 | 0.120 | 5 | 158271107 | upstream gene variant | C/A | snv | 0.49 | 1 | ||
| rs12656571 | 1.000 | 0.120 | 5 | 109742339 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs13163610 | 1.000 | 0.120 | 5 | 94213172 | intron variant | A/C | snv | 0.11 | 1 | ||
| rs148995025 | 1.000 | 0.120 | 5 | 7085094 | intron variant | A/G | snv | 8.9E-03 | 1 | ||
| rs17376456 | 1.000 | 0.120 | 5 | 94221997 | intron variant | A/G | snv | 8.7E-02 | 1 | ||
| rs17404956 | 1.000 | 0.120 | 5 | 166962488 | regulatory region variant | A/G | snv | 5.5E-02 | 1 | ||
| rs2300993 | 1.000 | 0.120 | 5 | 109702928 | intron variant | G/A | snv | 0.16 | 1 | ||
| rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
| rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 |