Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2283265 0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs1076560 0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs1500 1.000 0.080 5 76981013 non coding transcript exon variant G/A;C snv 2