Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2291720 1.000 0.080 3 23195698 intron variant A/G snv 2.8E-02 1
rs1495130 1.000 0.080 3 23199518 intron variant C/G snv 0.11 1