Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2469434 1.000 0.120 18 69876810 intron variant T/C snv 0.44 1
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 1