Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066808 0.807 0.280 12 56344189 intron variant A/G snv 0.21 2
rs2066807 0.925 0.080 12 56346898 missense variant C/G snv 4.9E-02 4.6E-02 1
rs2066819 0.925 0.040 12 56356420 intron variant C/T snv 4.9E-02 4.5E-02 1