Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs523349 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs2011077 0.807 0.080 5 177094455 intron variant C/T snv 0.19 8