Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs597808 | 0.742 | 0.200 | 12 | 111535554 | intron variant | A/G | snv | 0.67 | 19 | ||
rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 10 | |||
rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
rs62621409 | 11 | 36437447 | missense variant | A/G | snv | 3.9E-02 | 3.5E-02 | 3 | |||
rs113931125 | 7 | 32906170 | intergenic variant | G/A | snv | 0.27 | 2 |