| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs937337 | 1.000 | 0.040 | 14 | 52322041 | intron variant | G/A;C | snv | 0.93 | 1 | ||
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
| rs2723186 | 0.925 | 0.160 | 2 | 112917503 | intron variant | A/G;T | snv | 0.91 | 2 | ||
| rs4331426 | 0.925 | 0.080 | 18 | 22610832 | intergenic variant | G/A | snv | 0.86 | 2 | ||
| rs4148871 | 0.925 | 0.080 | 6 | 32835539 | intron variant | A/G | snv | 0.82 | 2 | ||
| rs1925714 | 1.000 | 0.040 | 1 | 228515588 | upstream gene variant | A/G | snv | 0.81 | 1 | ||
| rs1816702 | 0.827 | 0.120 | 4 | 153688371 | non coding transcript exon variant | T/C | snv | 0.79 | 6 | ||
| rs4149033 | 1.000 | 0.040 | 12 | 21164876 | intron variant | A/G | snv | 0.80 | 0.78 | 1 | |
| rs1861494 | 0.716 | 0.400 | 12 | 68157629 | intron variant | C/T | snv | 0.75 | 15 | ||
| rs776746 | 0.724 | 0.400 | 7 | 99672916 | splice acceptor variant | T/C | snv | 0.72 | 21 | ||
| rs5743810 | 0.689 | 0.360 | 4 | 38828729 | missense variant | A/G | snv | 0.73 | 0.72 | 21 | |
| rs5743899 | 0.807 | 0.160 | 11 | 1302334 | intron variant | C/T | snv | 0.71 | 6 | ||
| rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
| rs1495741 | 0.827 | 0.240 | 8 | 18415371 | regulatory region variant | G/A | snv | 0.71 | 9 | ||
| rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
| rs931924 | 1.000 | 0.040 | 5 | 25321925 | intron variant | C/T | snv | 0.70 | 1 | ||
| rs11958933 | 1.000 | 0.040 | 5 | 25323598 | intron variant | G/A | snv | 0.70 | 1 | ||
| rs1633256 | 1.000 | 0.040 | 1 | 159032767 | intron variant | A/G | snv | 0.70 | 1 | ||
| rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
| rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 | ||
| rs1327474 | 0.925 | 0.080 | 6 | 137219938 | upstream gene variant | C/T | snv | 0.67 | 2 | ||
| rs218916 | 1.000 | 0.040 | 8 | 89688709 | intron variant | C/T | snv | 0.67 | 2 | ||
| rs2287886 | 0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 | 9 | ||
| rs1101998 | 1.000 | 0.040 | 1 | 159029494 | intron variant | C/T | snv | 0.65 | 1 | ||
| rs4853542 | 1.000 | 0.040 | 2 | 191111876 | intron variant | A/G | snv | 0.65 | 1 |