| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs704017 | 0.776 | 0.080 | 10 | 79059375 | intron variant | A/G | snv | 0.55 | 1 | ||
| rs5275 | 0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv | 55 | |||
| rs2234922 | 0.630 | 0.440 | 1 | 225838705 | missense variant | A/G;T | snv | 0.19; 2.8E-05 | 42 | ||
| rs8192877 | 1.000 | 0.080 | 8 | 58491882 | intron variant | A/G;T | snv | 1 | |||
| rs11874392 | 0.763 | 0.080 | 18 | 48926786 | intron variant | A/T | snv | 0.50 | 2 | ||
| rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 18 | ||
| rs1800947 | 0.683 | 0.440 | 1 | 159713648 | splice region variant | C/A;G;T | snv | 4.4E-05; 5.1E-02; 4.0E-06 | 27 | ||
| rs762117133 | 1.000 | 0.080 | 5 | 112801324 | missense variant | C/A;T | snv | 2.4E-05 | 3 | ||
| rs150435881 | 1.000 | 0.080 | 10 | 94947853 | missense variant | C/A;T | snv | 4.0E-06; 5.6E-05 | 1 | ||
| rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
| rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
| rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 127 | |
| rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 117 | |||
| rs713598 | 0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 | 6 | |
| rs6747776 | 1.000 | 0.080 | 2 | 218860595 | intron variant | C/G | snv | 0.35 | 1 | ||
| rs20417 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 57 | |||
| rs35051736 | 1.000 | 0.080 | 20 | 54171650 | missense variant | C/G;T | snv | 4.0E-06; 3.0E-03 | 1 | ||
| rs1205 | 0.602 | 0.680 | 1 | 159712443 | 3 prime UTR variant | C/T | snv | 0.30 | 45 | ||
| rs1138272 | 0.611 | 0.600 | 11 | 67586108 | missense variant | C/T | snv | 5.9E-02 | 5.5E-02 | 42 | |
| rs58542926 | 0.630 | 0.440 | 19 | 19268740 | missense variant | C/T | snv | 6.5E-02 | 5.8E-02 | 38 | |
| rs9282861 | 0.658 | 0.440 | 16 | 28606193 | missense variant | C/T | snv | 31 | |||
| rs1042028 | 0.658 | 0.440 | 16 | 28606193 | missense variant | C/T | snv | 0.22 | 0.30 | 30 | |
| rs36053993 | 0.677 | 0.280 | 1 | 45331556 | missense variant | C/T | snv | 3.0E-03 | 3.3E-03 | 24 | |
| rs10936599 | 0.637 | 0.600 | 3 | 169774313 | synonymous variant | C/T | snv | 0.29 | 0.21 | 18 | |
| rs1799853 | 0.763 | 0.320 | 10 | 94942290 | missense variant | C/T | snv | 9.2E-02 | 8.9E-02 | 11 |