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
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
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214