Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1801278 | 0.637 | 0.560 | 2 | 226795828 | missense variant | C/G;T | snv | 4.0E-06; 5.2E-02 | 2 | ||
rs104893642 | 1.000 | 0.080 | 2 | 226796916 | missense variant | G/A;C | snv | 1.5E-05; 5.0E-06 | 1 | ||
rs1259467443 | 1.000 | 0.080 | 2 | 226796570 | inframe deletion | ACC/- | delins | 8.0E-06 | 7.0E-06 | 1 |