Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs2306969 | 0.925 | 0.040 | 19 | 5851790 | intron variant | A/G | snv | 0.76 | 4 | ||
rs3732253 | 1.000 | 2 | 70448966 | 3 prime UTR variant | G/A | snv | 0.22 | 1 |