| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 213 | |||
| rs71305152 | 0.882 | 0.040 | 8 | 105437494 | intron variant | -/TTTTCT | delins | 0.43 | 5 | ||
| rs374524467 | 0.827 | 0.040 | 4 | 110632961 | missense variant | A/C | snv | 8.0E-06 | 7.0E-06 | 5 | |
| rs865880036 | 0.827 | 0.040 | 15 | 37098156 | missense variant | A/C | snv | 1.3E-04 | 5 | ||
| rs2239647 | 0.851 | 0.080 | 14 | 32823537 | synonymous variant | A/C | snv | 0.60 | 0.65 | 3 | |
| rs9933544 | 0.882 | 0.040 | 16 | 24576962 | downstream gene variant | A/C | snv | 0.29 | 3 | ||
| rs730437 | 0.925 | 0.120 | 7 | 55147325 | intron variant | A/C | snv | 0.51 | 2 | ||
| rs201963 | 1.000 | 0.040 | 8 | 39721376 | intron variant | A/C | snv | 1 | |||
| rs3212112 | 1.000 | 0.040 | 14 | 103699345 | intron variant | A/C | snv | 7.1E-03 | 2.2E-02 | 1 | |
| rs4774756 | 1.000 | 0.040 | 15 | 55254859 | intron variant | A/C | snv | 0.66 | 1 | ||
| rs6010620 | 0.701 | 0.360 | 20 | 63678486 | intron variant | A/C;G | snv | 19 | |||
| rs17006625 | 0.925 | 0.080 | 3 | 20119604 | missense variant | A/C;G | snv | 4.0E-06; 3.3E-02 | 3 | ||
| rs11706832 | 1.000 | 0.040 | 3 | 66452557 | intron variant | A/C;G | snv | 1 | |||
| rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 110 | ||
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 484 | ||
| rs11571378 | 0.925 | 0.080 | 12 | 950115 | intron variant | A/C;T | snv | 2 | |||
| rs1345354331 | 1.000 | 0.040 | 3 | 49358221 | missense variant | A/C;T | snv | 6.8E-06; 6.8E-06 | 1 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 187 | |
| rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 107 | ||
| rs1801394 | 0.531 | 0.840 | 5 | 7870860 | missense variant | A/G | snv | 0.47 | 0.45 | 101 | |
| rs1136410 | 0.559 | 0.760 | 1 | 226367601 | missense variant | A/G | snv | 0.21 | 0.15 | 70 | |
| rs11615 | 0.572 | 0.640 | 19 | 45420395 | synonymous variant | A/G | snv | 0.50 | 0.55 | 62 | |
| rs1801275 | 0.581 | 0.680 | 16 | 27363079 | missense variant | A/G | snv | 0.25 | 0.36 | 57 | |
| rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 47 |