Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs501220 0.882 0.160 6 25872797 intron variant C/A snv 0.20 4
rs2328893 0.882 0.160 6 25770011 intron variant A/G snv 0.57 3