Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121918134 | 1.000 | 3 | 49022497 | missense variant | G/A;C | snv | 4.0E-06 | 1 | |||
rs121918135 | 1.000 | 3 | 49022903 | missense variant | G/C | snv | 1 | ||||
rs138275059 | 1.000 | 3 | 49023111 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 1 |