Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1744297 | 14 | 104102135 | intron variant | T/C | snv | 0.86 | 12 | ||||
rs17450273 | 12 | 102967601 | intergenic variant | C/A;T | snv | 4 | |||||
rs13244654 | 7 | 56079263 | intron variant | T/C | snv | 0.48 | 4 | ||||
rs62149891 | 2 | 61877999 | intron variant | A/G | snv | 1.0E-01 | 3 |