| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28520091 | 1.000 | 0.040 | 4 | 7844513 | intron variant | C/A;G;T | snv | 2 | |||
| rs28795989 | 1.000 | 0.040 | 4 | 7889818 | intron variant | A/C;G | snv | 2 | |||
| rs7663205 | 1.000 | 0.040 | 4 | 7887369 | intron variant | C/T | snv | 0.45 | 1 | ||
| rs10505100 | 1.000 | 0.040 | 8 | 107266388 | intron variant | C/A | snv | 0.13 | 1 | ||
| rs31918 | 1.000 | 0.040 | 5 | 14820818 | intron variant | C/T | snv | 0.29 | 2 | ||
| rs61394862 | 1.000 | 0.040 | 5 | 14850985 | intron variant | C/G;T | snv | 1 | |||
| rs11217878 | 1.000 | 0.040 | 11 | 120469674 | intron variant | G/A | snv | 0.20 | 2 | ||
| rs58073046 | 1.000 | 0.040 | 11 | 120377784 | intron variant | A/G | snv | 8.7E-02 | 2 | ||
| rs1020338837 | 1.000 | 0.040 | 3 | 28340470 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
| rs566095092 | 1.000 | 0.040 | 3 | 28336841 | missense variant | T/C | snv | 4.0E-06 | 2.1E-05 | 1 | |
| rs548246291 | 1.000 | 0.040 | 1 | 1232945 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 | 1 | |
| rs372487178 | 0.925 | 0.040 | 11 | 62616748 | missense variant | C/T | snv | 2.1E-05 | 2 | ||
| rs1401907822 | 1.000 | 0.040 | 5 | 177608566 | missense variant | G/A | snv | 1 | |||
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
| rs4141671 | 1.000 | 0.040 | 10 | 58578993 | intron variant | T/C | snv | 0.49 | 2 | ||
| rs2093210 | 1.000 | 0.040 | 14 | 60490561 | intron variant | C/T | snv | 0.45 | 4 | ||
| rs33912345 | 0.807 | 0.200 | 14 | 60509819 | missense variant | C/A;G | snv | 0.53 | 7 | ||
| rs9309969 | 1.000 | 0.040 | 3 | 85085406 | intron variant | T/C;G | snv | 2 | |||
| rs9284802 | 1.000 | 0.040 | 3 | 85046615 | intron variant | G/A | snv | 0.44 | 1 | ||
| rs4977756 | 0.683 | 0.440 | 9 | 22068653 | intron variant | G/A | snv | 0.64 | 24 | ||
| rs564398 | 0.716 | 0.360 | 9 | 22029548 | 3 prime UTR variant | T/C | snv | 0.31 | 0.28 | 18 | |
| rs2157719 | 0.708 | 0.360 | 9 | 22033367 | non coding transcript exon variant | C/T | snv | 0.71 | 17 | ||
| rs1412829 | 0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 | 14 | ||
| rs7865618 | 0.776 | 0.240 | 9 | 22031006 | non coding transcript exon variant | G/A;T | snv | 11 |