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 | 34 | ||
rs75757892 | 6 | 7232156 | intron variant | C/T | snv | 0.12 | 3 | ||||
rs115024193 | 4 | 78793500 | intron variant | T/A | snv | 2.3E-02 | 2 |