| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
| rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 | ||
| rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
| rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
| rs10754558 | 0.695 | 0.480 | 1 | 247448734 | 3 prime UTR variant | G/C;T | snv | 20 | |||
| rs1131498 | 0.732 | 0.360 | 1 | 169707345 | missense variant | A/G | snv | 0.21 | 0.22 | 13 | |
| rs1061624 | 0.776 | 0.320 | 1 | 12207208 | 3 prime UTR variant | A/G | snv | 0.48 | 8 | ||
| rs3024498 | 0.790 | 0.360 | 1 | 206768184 | 3 prime UTR variant | T/C | snv | 0.20 | 7 | ||
| rs2229238 | 0.851 | 0.080 | 1 | 154465420 | 3 prime UTR variant | T/A;C | snv | 0.80 | 5 | ||
| rs1052632 | 0.925 | 0.080 | 1 | 181051094 | non coding transcript exon variant | G/A;C | snv | 2 | |||
| rs1344800847 | 0.925 | 0.120 | 1 | 207569911 | missense variant | G/T | snv | 2 | |||
| rs3738467 | 0.925 | 0.120 | 1 | 207552816 | missense variant | G/T | snv | 1.4E-03 | 2 | ||
| rs10911362 | 1.000 | 0.040 | 1 | 183579857 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs1101998 | 1.000 | 0.040 | 1 | 159029494 | intron variant | C/T | snv | 0.65 | 1 | ||
| rs1633256 | 1.000 | 0.040 | 1 | 159032767 | intron variant | A/G | snv | 0.70 | 1 | ||
| rs1925714 | 1.000 | 0.040 | 1 | 228515588 | upstream gene variant | A/G | snv | 0.81 | 1 | ||
| rs2273346 | 1.000 | 0.040 | 1 | 11030840 | missense variant | A/G | snv | 5.0E-02 | 5.8E-02 | 1 | |
| rs3397 | 1.000 | 0.040 | 1 | 12207235 | 3 prime UTR variant | C/T | snv | 0.51 | 1 | ||
| rs411089 | 1.000 | 0.040 | 1 | 158255035 | intron variant | C/T | snv | 0.39 | 0.43 | 1 | |
| rs4240897 | 1.000 | 0.040 | 1 | 11982698 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs6676375 | 1.000 | 0.040 | 1 | 242711583 | intergenic variant | T/C | snv | 0.15 | 1 | ||
| rs6695096 | 1.000 | 0.040 | 1 | 11034982 | intron variant | C/A;T | snv | 1 | |||
| rs751273816 | 1.000 | 0.040 | 1 | 47373057 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs932347 | 1.000 | 0.040 | 1 | 209882285 | intergenic variant | C/T | snv | 0.15 | 1 | ||
| rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 |