Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2974935 | 0.708 | 0.280 | 1 | 155212052 | non coding transcript exon variant | G/A;C;T | snv | 17 | |||
rs481519 | 0.708 | 0.280 | 3 | 27285723 | intron variant | C/A;T | snv | 17 | |||
rs56404467 | 0.708 | 0.280 | 13 | 32265853 | intron variant | G/A | snv | 1.3E-02 | 17 | ||
rs73110464 | 0.708 | 0.280 | 12 | 52918828 | intron variant | C/T | snv | 0.12 | 17 | ||
rs7725218 | 0.708 | 0.280 | 5 | 1282299 | intron variant | G/A | snv | 0.38 | 17 |