Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4149056 | 0.633 | 0.480 | 12 | 21178615 | missense variant | T/C | snv | 0.13 | 0.12 | 45 | |
rs4148323 | 0.701 | 0.440 | 2 | 233760498 | missense variant | G/A | snv | 2.2E-02 | 9.2E-03 | 22 | |
rs1042640 | 1.000 | 0.080 | 2 | 233772898 | 3 prime UTR variant | G/A;C;T | snv | 3 | |||
rs10929303 | 1.000 | 0.080 | 2 | 233772770 | 3 prime UTR variant | T/C | snv | 0.74 | 3 |