Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs218264 | 4 | 54542708 | intergenic variant | A/G;T | snv | 3 | |||||
rs2519093 | 0.882 | 0.200 | 9 | 133266456 | intron variant | T/C | snv | 14 | |||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs9399136 | 6 | 135081201 | intron variant | T/C | snv | 0.18 | 4 | ||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 |