Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs324011 | 0.742 | 0.360 | 12 | 57108399 | intron variant | C/T | snv | 0.32 | 12 | ||
rs6967330 | 0.827 | 0.120 | 7 | 106018005 | missense variant | G/A | snv | 0.19 | 0.21 | 8 | |
rs2664538 | 0.827 | 0.200 | 20 | 46011586 | missense variant | A/G | snv | 6 |