Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6903608 | 0.742 | 0.400 | 6 | 32460508 | intron variant | C/G;T | snv | 5 | |||
rs9269081 | 0.851 | 0.280 | 6 | 32473323 | intron variant | A/C | snv | 0.69 | 2 | ||
rs3781093 | 0.882 | 0.120 | 10 | 8059964 | intron variant | T/C | snv | 0.19 | 1 | ||
rs204999 | 0.763 | 0.480 | 6 | 32142202 | intergenic variant | A/G | snv | 0.28 | 12 | ||
rs9268542 | 0.851 | 0.280 | 6 | 32416944 | intergenic variant | A/G | snv | 0.35 | 3 | ||
rs2858870 | 0.851 | 0.280 | 6 | 32604474 | intergenic variant | T/A;C | snv | 2 | |||
rs9268528 | 0.851 | 0.280 | 6 | 32415331 | regulatory region variant | A/G | snv | 0.34 | 3 |