| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1799724 | 0.600 | 0.680 | 6 | 31574705 | upstream gene variant | C/T | snv | 8.5E-02 | 2 | ||
| rs9651118 | 0.683 | 0.480 | 1 | 11802157 | intron variant | T/C | snv | 0.18 | 2 | ||
| rs2853749 | 0.882 | 0.160 | 4 | 87976662 | intron variant | C/T | snv | 0.34 | 2 | ||
| rs767399782 | 0.925 | 0.120 | 19 | 6495736 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
| rs121918399 | 0.925 | 0.120 | 19 | 44907843 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs4846049 | 0.776 | 0.360 | 1 | 11790308 | 3 prime UTR variant | T/A;G | snv | 1 | |||
| rs3024490 | 0.742 | 0.520 | 1 | 206771966 | intron variant | A/C;G;T | snv | 1 | |||
| rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 1 | ||
| rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 1 | ||
| rs10431386 | 1.000 | 0.040 | 12 | 120691123 | intron variant | C/T | snv | 0.34 | 1 | ||
| rs1476413 | 0.790 | 0.360 | 1 | 11792243 | intron variant | C/G;T | snv | 4.0E-06; 0.26 | 0.23 | 1 | |
| rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 1 | |
| rs1057519583 | 0.882 | 0.160 | 10 | 103900115 | missense variant | C/G | snv | 1 | |||
| rs765462548 | 0.882 | 0.160 | 10 | 103898989 | missense variant | C/A;T | snv | 4.0E-06; 2.4E-05 | 1 | ||
| rs59007384 | 0.851 | 0.080 | 19 | 44893408 | intron variant | G/A;T | snv | 1 |