Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10468017 0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 10