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
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs9376090 6 135090090 intron variant T/C snv 0.19 3