Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 25
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
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
rs2293607 0.807 0.200 3 169764547 non coding transcript exon variant T/A;C snv 6