Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 11 | ||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 10 | ||
rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 7 | ||
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 6 | ||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 6 | |||
rs3751812 | 0.882 | 0.160 | 16 | 53784548 | intron variant | G/T | snv | 0.30 | 4 | ||
rs7190492 | 1.000 | 0.080 | 16 | 53794840 | intron variant | A/G | snv | 0.68 | 3 | ||
rs8044769 | 0.851 | 0.200 | 16 | 53805223 | intron variant | T/A;C;G | snv | 3 |