Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs60600003 0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs73316435 0.882 17 47252111 upstream gene variant C/A;T snv 5