| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6129653 | 0.925 | 0.120 | 20 | 40646963 | regulatory region variant | T/A;C | snv | 2 | |||
| rs7043516 | 1.000 | 0.080 | 9 | 97855151 | 3 prime UTR variant | A/C;T | snv | 2 | |||
| rs7554547 | 0.925 | 0.120 | 1 | 11913831 | non coding transcript exon variant | A/G;T | snv | 2 | |||
| rs7632427 | 0.925 | 0.160 | 3 | 89485227 | downstream gene variant | T/A;C | snv | 2 | |||
| rs908822 | 0.925 | 0.120 | 4 | 123985102 | regulatory region variant | C/A;T | snv | 2 | |||
| rs957448 | 0.925 | 0.120 | 8 | 94529074 | synonymous variant | A/G;T | snv | 0.33 | 2 | ||
| rs1030609 | 1.000 | 0.080 | 8 | 128727631 | intron variant | C/A;G | snv | 1 | |||
| rs10511145 | 1.000 | 0.080 | 3 | 89548529 | intergenic variant | C/A;T | snv | 1 | |||
| rs10779526 | 1.000 | 0.080 | 1 | 210178851 | intergenic variant | T/A;C;G | snv | 1 | |||
| rs12060567 | 1.000 | 0.080 | 1 | 210197245 | intergenic variant | G/A;C | snv | 1 | |||
| rs12548036 | 1.000 | 0.080 | 8 | 128935636 | intron variant | G/A;T | snv | 1 | |||
| rs126280 | 1.000 | 0.080 | 1 | 209846479 | intron variant | A/G;T | snv | 1 | |||
| rs1519841 | 1.000 | 0.080 | 8 | 128907554 | intron variant | T/C;G | snv | 1 | |||
| rs1575900 | 1.000 | 0.080 | 13 | 80102569 | intergenic variant | A/C;T | snv | 1 | |||
| rs17215941 | 1.000 | 0.080 | 13 | 80124853 | intron variant | T/A;C | snv | 1 | |||
| rs17352100 | 1.000 | 0.080 | 1 | 18625618 | intergenic variant | C/A;T | snv | 1 | |||
| rs1784394 | 1.000 | 0.080 | 11 | 134093321 | intron variant | T/C | snv | 1 | |||
| rs1854110 | 1.000 | 0.080 | 13 | 80127350 | intron variant | T/A;C;G | snv | 1 | |||
| rs1873149 | 1.000 | 0.080 | 15 | 63020229 | regulatory region variant | C/A;T | snv | 1 | |||
| rs2197111 | 1.000 | 0.080 | 8 | 129003469 | intron variant | A/C;G | snv | 1 | |||
| rs2294426 | 1.000 | 0.080 | 6 | 11729849 | intron variant | A/G;T | snv | 1 | |||
| rs2395855 | 1.000 | 0.080 | 8 | 128828493 | intron variant | T/A;C | snv | 1 | |||
| rs3789451 | 1.000 | 0.080 | 1 | 94120772 | intron variant | C/G;T | snv | 1 | |||
| rs3827712 | 1.000 | 0.080 | 1 | 94109615 | intron variant | T/C;G | snv | 1 | |||
| rs3857888 | 1.000 | 0.080 | 8 | 128812615 | intron variant | G/C;T | snv | 1 |