Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs550057 | 0.925 | 0.080 | 9 | 133271182 | intron variant | T/A;C | snv | 11 | |||
rs3850625 | 1 | 201047168 | missense variant | G/A | snv | 0.12 | 8.9E-02 | 3 | |||
rs7024579 | 9 | 136208567 | 3 prime UTR variant | C/A;T | snv | 3 | |||||
rs2301343 | 2 | 40453009 | intron variant | T/G | snv | 0.22 | 2 |