Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs180697792 | 1.000 | 0.040 | 17 | 69298289 | intron variant | G/A | snv | 2 | |||
rs573431210 | 17 | 69280242 | intron variant | T/G | snv | 1.2E-02 | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs180697792 | 1.000 | 0.040 | 17 | 69298289 | intron variant | G/A | snv | 2 | |||
rs573431210 | 17 | 69280242 | intron variant | T/G | snv | 1.2E-02 | 1 |