| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4652 | 0.752 | 0.200 | 14 | 55138318 | missense variant | A/C | snv | 4.1E-06; 0.45 | 0.57 | 12 | |
| rs3745297 | 0.790 | 0.120 | 19 | 49154952 | missense variant | A/C | snv | 0.41 | 0.38 | 10 | |
| rs58034145 | 0.827 | 0.160 | 1 | 156134830 | missense variant | A/C | snv | 10 | |||
| rs3763313 | 0.807 | 0.320 | 6 | 32408694 | upstream gene variant | A/C | snv | 0.21 | 7 | ||
| rs730881098 | 0.882 | 0.040 | 1 | 201365613 | missense variant | A/C | snv | 3 | |||
| rs777064945 | 1.000 | 0.040 | 6 | 38722928 | missense variant | A/C;G | snv | 4.1E-06; 8.3E-06 | 1 | ||
| rs9268494 | 0.882 | 0.200 | 6 | 32407575 | non coding transcript exon variant | A/C;T | snv | 0.32 | 3 | ||
| rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
| rs3746444 | 0.514 | 0.760 | 20 | 34990448 | mature miRNA variant | A/G | snv | 0.20 | 0.19 | 105 | |
| rs1801252 | 0.724 | 0.320 | 10 | 114044277 | missense variant | A/G | snv | 0.15 | 0.17 | 17 | |
| rs1805105 | 0.776 | 0.280 | 16 | 346264 | synonymous variant | A/G | snv | 0.61 | 0.69 | 11 | |
| rs2306969 | 0.925 | 0.040 | 19 | 5851790 | intron variant | A/G | snv | 0.76 | 4 | ||
| rs1241664568 | 1.000 | 0.040 | 11 | 64320661 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
| rs151080979 | 1.000 | 0.040 | 12 | 69610255 | missense variant | A/G | snv | 4.9E-03 | 4.0E-03 | 1 | |
| rs373850074 | 1.000 | 0.040 | 4 | 94654525 | missense variant | A/G | snv | 1.2E-04 | 7.0E-05 | 1 | |
| rs56165849 | 1.000 | 0.040 | 10 | 86681952 | intron variant | A/G | snv | 0.50 | 1 | ||
| rs59065411 | 1.000 | 0.040 | 1 | 156115207 | missense variant | A/G | snv | 1 | |||
| rs6660685 | 1.000 | 0.040 | 1 | 16020493 | intron variant | A/G | snv | 0.70 | 1 | ||
| rs74676849 | 1.000 | 0.040 | 7 | 11849866 | intergenic variant | A/G | snv | 2.6E-02 | 1 | ||
| rs756636226 | 1.000 | 0.040 | 11 | 64321644 | missense variant | A/G | snv | 5.4E-05 | 4.9E-05 | 1 | |
| rs886039024 | 1.000 | 0.040 | 15 | 63060900 | missense variant | A/G | snv | 1 | |||
| rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
| rs57045855 | 0.882 | 0.040 | 1 | 156134464 | missense variant | A/G;T | snv | 6 | |||
| rs9034 | 0.827 | 0.200 | 7 | 106249610 | 3 prime UTR variant | A/G;T | snv | 5 | |||
| rs267607155 | 0.925 | 0.040 | 2 | 178782980 | missense variant | A/G;T | snv | 3 |