| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13256690 | 1.000 | 0.120 | 8 | 11481059 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
| rs1531577 | 1.000 | 0.120 | 8 | 11481052 | non coding transcript exon variant | C/T | snv | 0.71 | 1 | ||
| rs17416878 | 1.000 | 0.120 | 1 | 16120485 | downstream gene variant | A/G | snv | 0.24 | 1 | ||
| rs2244234 | 1.000 | 0.120 | 8 | 11478958 | upstream gene variant | T/G | snv | 0.83 | 1 | ||
| rs2254891 | 1.000 | 0.120 | 8 | 11483620 | upstream gene variant | G/A;C | snv | 1 | |||
| rs2409780 | 1.000 | 0.120 | 8 | 11480078 | intron variant | T/C | snv | 0.25 | 1 | ||
| rs2523790 | 1.000 | 0.120 | 6 | 29835873 | downstream gene variant | T/G | snv | 0.38 | 1 | ||
| rs2618473 | 1.000 | 0.120 | 8 | 11486618 | upstream gene variant | C/T | snv | 0.34 | 1 | ||
| rs2736335 | 1.000 | 0.120 | 8 | 11483978 | upstream gene variant | A/C;G;T | snv | 1 | |||
| rs2736338 | 1.000 | 0.120 | 8 | 11484374 | upstream gene variant | A/C;T | snv | 1 | |||
| rs34246750 | 1.000 | 0.120 | 14 | 52402039 | regulatory region variant | G/C | snv | 0.20 | 1 | ||
| rs35393613 | 1.000 | 0.120 | 8 | 11480957 | intron variant | C/A;G;T | snv | 1 | |||
| rs4872534 | 1.000 | 0.120 | 8 | 22710890 | intron variant | A/T | snv | 0.23 | 1 | ||
| rs6014819 | 1.000 | 0.120 | 20 | 56760851 | intergenic variant | G/A | snv | 0.26 | 1 | ||
| rs6025146 | 1.000 | 0.120 | 20 | 56760981 | intergenic variant | A/G | snv | 0.34 | 1 | ||
| rs6069865 | 1.000 | 0.120 | 20 | 56757888 | intergenic variant | T/C;G | snv | 1 | |||
| rs62489069 | 1.000 | 0.120 | 8 | 11480874 | intron variant | A/G | snv | 0.29 | 1 | ||
| rs8008348 | 1.000 | 0.120 | 14 | 52407427 | intergenic variant | A/G | snv | 0.34 | 1 | ||
| rs9485729 | 1.000 | 0.120 | 6 | 102688156 | intergenic variant | C/T | snv | 0.27 | 1 | ||
| rs7986087 | 1.000 | 0.120 | 13 | 95263491 | intron variant | C/T | snv | 9.7E-02 | 1 | ||
| rs868853 | 1.000 | 0.120 | 13 | 95302822 | upstream gene variant | C/T | snv | 0.85 | 1 | ||
| rs2293256 | 1.000 | 0.120 | 7 | 99460078 | splice region variant | G/A | snv | 5.8E-02 | 9.2E-02 | 1 | |
| rs750332 | 1.000 | 0.120 | 6 | 31639273 | intron variant | C/T | snv | 0.84 | 0.81 | 1 | |
| rs10100215 | 1.000 | 0.120 | 8 | 11504763 | intron variant | G/T | snv | 0.26 | 1 | ||
| rs11250141 | 1.000 | 0.120 | 8 | 11514632 | intron variant | G/A | snv | 0.48 | 1 |