Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519804 | 1.000 | 0.040 | 14 | 104776711 | missense variant | G/T | snv | 1 | |||
rs397514644 | 0.925 | 0.040 | 14 | 104780190 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs397514645 | 1.000 | 14 | 104770805 | missense variant | T/G | snv | 1 |