Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs696 0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs34557412 0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 15
rs5754100 0.882 22 21561877 intron variant T/C snv 0.18 5