Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs8040868 0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 17
rs6495308 0.851 0.160 15 78615314 intron variant T/C snv 0.29 8
rs1317286 0.925 0.120 15 78603787 intron variant A/G snv 0.30 6
rs3813567 1.000 0.080 15 78642209 intron variant G/A snv 0.77 2