Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 78 | ||
rs767685429 | 0.882 | 0.120 | 19 | 41332206 | missense variant | G/A;C | snv | 2.8E-05; 8.0E-06 | 3 | ||
rs2241716 | 1.000 | 0.080 | 19 | 41348181 | intron variant | C/T | snv | 4.0E-02 | 2 |