Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs724159947 | 0.851 | 0.120 | 12 | 11869601 | missense variant | C/T | snv | 6 | |||
rs724159945 | 1.000 | 12 | 11885968 | missense variant | C/A;T | snv | 3 | ||||
rs724159946 | 1.000 | 12 | 11884541 | missense variant | G/A | snv | 7.0E-06 | 3 |