Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113533135 1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs1532002 1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2