Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 7
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 6