Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1516725 0.925 0.120 3 186106215 intron variant T/C snv 0.86 5
rs7647305 1.000 0.080 3 186116501 intron variant T/C snv 0.74 4
rs9816226 1.000 0.080 3 186116710 intron variant A/T snv 0.82 3
rs73052033 3 186110676 intron variant T/C snv 0.15 1