Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17601696 | 10 | 121360522 | intergenic variant | C/T | snv | 6.0E-02 | 1 | ||||
rs10835211 | 1.000 | 0.080 | 11 | 27679818 | intron variant | G/A | snv | 0.19 | 1 |