| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2308321 | 0.653 | 0.480 | 10 | 129766800 | missense variant | A/G | snv | 9.3E-02 | 8.7E-02 | 29 | |
| rs2308327 | 0.790 | 0.280 | 10 | 129766906 | missense variant | A/G | snv | 9.4E-02 | 8.7E-02 | 10 | |
| rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 52 | |
| rs2069757 | 1.000 | 0.120 | 5 | 132662721 | intron variant | G/A | snv | 7.5E-02 | 1 | ||
| rs10881578 | 0.925 | 0.240 | 9 | 134340689 | intron variant | A/G | snv | 0.32 | 2 | ||
| rs7745098 | 1.000 | 0.120 | 6 | 135093866 | intron variant | C/G;T | snv | 2 | |||
| rs6928977 | 0.925 | 0.120 | 6 | 135305210 | intron variant | T/G | snv | 0.70 | 2 | ||
| rs11715604 | 0.851 | 0.160 | 3 | 136870707 | intron variant | A/G;T | snv | 4 | |||
| rs1002658 | 1.000 | 0.120 | 6 | 137660447 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs6439924 | 1.000 | 0.120 | 3 | 140450815 | intron variant | A/C | snv | 0.21 | 1 | ||
| rs2292779 | 0.851 | 0.320 | 8 | 140551294 | intron variant | G/C;T | snv | 0.57; 4.9E-06 | 4 | ||
| rs3212227 | 0.566 | 0.840 | 5 | 159315942 | 3 prime UTR variant | T/G | snv | 0.26 | 65 | ||
| rs568408 | 0.649 | 0.600 | 3 | 159995680 | 3 prime UTR variant | G/A | snv | 0.16 | 29 | ||
| rs73005220 | 0.851 | 0.160 | 19 | 16161878 | intron variant | A/G | snv | 3.9E-02 | 4 | ||
| rs1860661 | 0.882 | 0.120 | 19 | 1650135 | intron variant | A/C;G | snv | 6.7E-06; 0.54 | 3 | ||
| rs12638862 | 0.827 | 0.160 | 3 | 169759718 | downstream gene variant | A/G | snv | 0.24 | 10 | ||
| rs12621278 | 0.790 | 0.280 | 2 | 172446825 | intron variant | A/G | snv | 4.9E-02 | 7 | ||
| rs12488654 | 0.925 | 0.160 | 3 | 172524100 | upstream gene variant | G/A | snv | 0.16 | 2 | ||
| rs4918 | 0.763 | 0.400 | 3 | 186620593 | missense variant | G/A;C | snv | 0.67 | 12 | ||
| rs4459895 | 0.827 | 0.160 | 3 | 188236626 | intron variant | A/C | snv | 0.88 | 5 | ||
| rs1801177 | 0.742 | 0.240 | 8 | 19948197 | missense variant | G/A;C | snv | 1.4E-02; 2.0E-05 | 14 | ||
| rs1800890 | 0.658 | 0.400 | 1 | 206776020 | intron variant | A/T | snv | 0.32 | 29 | ||
| rs1800797 | 0.605 | 0.800 | 7 | 22726602 | non coding transcript exon variant | A/G | snv | 0.72 | 43 | ||
| rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
| rs149207840 | 0.851 | 0.160 | 2 | 230279864 | intron variant | CTGCCTC/-;CTGCCTCCTGCCTC | delins | 0.15 | 4 |