| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs45487298 | 0.882 | 0.120 | 1 | 209706871 | intron variant | -/A | delins | 3 | |||
| rs5186 | 0.630 | 0.560 | 3 | 148742201 | 3 prime UTR variant | A/C | snv | 0.23 | 0.21 | 38 | |
| rs316019 | 0.790 | 0.360 | 6 | 160249250 | missense variant | A/C | snv | 0.90 | 0.89 | 8 | |
| rs3761581 | 0.851 | 0.160 | X | 129655744 | upstream gene variant | A/C | snv | 0.11 | 5 | ||
| rs4948878 | 1.000 | 0.040 | 10 | 44379373 | intron variant | A/C;G | snv | 2 | |||
| rs2270915 | 1.000 | 0.040 | 5 | 32786283 | missense variant | A/C;G;T | snv | 0.21 | 0.18 | 2 | |
| rs1047047 | 1.000 | 0.040 | 1 | 42153468 | synonymous variant | A/C;G;T | snv | 6.4E-05; 0.21; 4.0E-06 | 1 | ||
| rs3754701 | 0.882 | 0.120 | 2 | 237858561 | upstream gene variant | A/C;T | snv | 4 | |||
| rs12140311 | 1.000 | 0.040 | 1 | 16052230 | missense variant | A/C;T | snv | 8.0E-06; 9.6E-02 | 3 | ||
| rs2254524 | 1.000 | 0.040 | 21 | 46194555 | missense variant | A/C;T | snv | 0.66; 1.6E-05 | 2 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
| rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
| rs1137101 | 0.554 | 0.760 | 1 | 65592830 | missense variant | A/G | snv | 0.51 | 0.50 | 77 | |
| rs4994 | 0.578 | 0.640 | 8 | 37966280 | missense variant | A/G | snv | 0.11 | 9.2E-02 | 65 | |
| rs1137100 | 0.627 | 0.640 | 1 | 65570758 | missense variant | A/G | snv | 0.30 | 0.25 | 39 | |
| rs1801252 | 0.724 | 0.320 | 10 | 114044277 | missense variant | A/G | snv | 0.15 | 0.17 | 17 | |
| rs13333226 | 0.827 | 0.200 | 16 | 20354332 | intron variant | A/G | snv | 0.23 | 10 | ||
| rs2576178 | 0.790 | 0.160 | 10 | 88583641 | 5 prime UTR variant | A/G | snv | 0.29 | 9 | ||
| rs2106809 | 0.827 | 0.120 | X | 15599938 | intron variant | A/G | snv | 0.19 | 8 | ||
| rs2053044 | 1.000 | 0.040 | 5 | 148825809 | 5 prime UTR variant | A/G | snv | 0.59 | 5 | ||
| rs2070762 | 0.925 | 0.080 | 11 | 2165105 | intron variant | A/G | snv | 0.43 | 5 | ||
| rs1126742 | 0.925 | 0.040 | 1 | 46932824 | missense variant | A/G | snv | 0.17 | 0.20 | 4 | |
| rs4646188 | 0.925 | 0.120 | X | 15583220 | intron variant | A/G | snv | 9.1E-02 | 4 | ||
| rs758801521 | 0.882 | 0.160 | 8 | 26770618 | missense variant | A/G | snv | 4.0E-06 | 4 |