Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1085307111 | 0.882 | 0.080 | 19 | 50793784 | missense variant | C/T | snv | 3 | |||
rs546603773 | 0.882 | 0.080 | 19 | 50791780 | missense variant | C/A;G;T | snv | 8.3E-06; 8.3E-06; 5.4E-05 | 3 |