Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519946 | 0.732 | 0.280 | 19 | 52212729 | missense variant | C/G;T | snv | 17 | |||
rs863225094 | 0.827 | 0.160 | 19 | 52213076 | missense variant | G/A | snv | 10 | |||
rs1057519947 | 0.790 | 0.160 | 19 | 52212730 | missense variant | G/A | snv | 9 | |||
rs786205228 | 0.827 | 0.080 | 19 | 52212718 | missense variant | C/G;T | snv | 3 | |||
rs1555791268 | 1.000 | 19 | 52212959 | missense variant | C/T | snv | 1 | ||||
rs786205227 | 1.000 | 19 | 52212726 | missense variant | C/T | snv | 1 |