Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12188300 | 0.807 | 0.120 | 5 | 159402519 | intron variant | A/G;T | snv | 6 | |||
rs4921482 | 0.807 | 0.120 | 5 | 159337470 | intron variant | T/C;G | snv | 6 | |||
rs74817271 | 0.807 | 0.120 | 5 | 151090412 | intron variant | G/A | snv | 5.0E-02 | 6 | ||
rs10865331 | 0.827 | 0.120 | 2 | 62324337 | intergenic variant | A/G | snv | 0.57 | 5 | ||
rs33980500 | 0.742 | 0.200 | 6 | 111592059 | missense variant | C/T | snv | 8.6E-02 | 9.7E-02 | 3 | |
rs12191877 | 0.851 | 0.120 | 6 | 31285148 | intron variant | C/T | snv | 0.12 | 2 | ||
rs458017 | 0.925 | 0.080 | 6 | 111374888 | missense variant | T/C | snv | 5.9E-02 | 5.6E-02 | 2 | |
rs702873 | 0.882 | 0.120 | 2 | 60854407 | intron variant | C/T | snv | 0.35 | 2 |