Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2266788 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2075290 0.882 0.160 11 116782580 intron variant C/G;T snv 10
rs6589566 0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs12286037 1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs2160669 1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92 5
rs603446 1.000 0.040 11 116783719 intron variant C/T snv 0.33 2
rs121917821 0.925 0.080 11 116790814 stop gained G/A snv 4.0E-06 2
rs7118999 1.000 0.040 11 116774559 3 prime UTR variant C/A;T snv 1