Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121434428 | 1.000 | 1 | 161209915 | missense variant | C/A | snv | 1 | ||||
rs121434427 | 1.000 | 1 | 161209912 | missense variant | G/A | snv | 1 | ||||
rs121434429 | 1.000 | 1 | 161213673 | missense variant | T/C | snv | 7.0E-06 | 1 |