Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 30 | ||
rs2571445 | 0.925 | 0.080 | 2 | 217818431 | missense variant | A/G;T | snv | 0.62 | 10 | ||
rs72681869 | 14 | 50188639 | missense variant | G/A;C | snv | 4.0E-06; 4.1E-03 | 6 | ||||
rs12779675 | 10 | 27908597 | intron variant | G/A;C | snv | 2 |