Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs786204929 0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213