Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140948465 0.925 0.120 4 127930800 missense variant G/A;T snv 4.0E-06; 8.0E-06 2
rs587778809 0.925 0.120 4 127938781 splice donor variant A/T snv 8.0E-06 2.8E-05 2
rs724159970 0.925 0.120 4 127921733 stop gained C/A snv 4.0E-06 7.0E-06 2
rs724159971 0.925 0.120 4 127920743 stop gained G/A snv 2.0E-05 2.8E-05 2
rs727502800 0.925 0.120 4 127921860 missense variant C/G snv 2
rs267607235 1.000 0.120 4 127921639 missense variant G/A snv 2.0E-05 7.0E-06 2
rs1043984708 1.000 0.120 4 127920794 missense variant G/A;T snv 8.0E-06; 8.0E-06 1
rs1162750836 1.000 0.120 4 127942119 missense variant G/A snv 7.0E-06 1
rs118203975 1.000 0.120 4 127930752 missense variant C/T snv 1
rs118203976 1.000 0.120 4 127921588 missense variant C/T snv 4.0E-06 1
rs118203977 1.000 0.120 4 127930787 stop gained A/C;G snv 4.0E-06; 1.2E-05 1
rs118203978 1.000 0.120 4 127943829 missense variant T/C;G snv 4.0E-06 1
rs1275962600 1.000 0.120 4 127920793 missense variant C/T snv 7.0E-06 1
rs1439582451 1.000 0.120 4 127921926 frameshift variant C/- del 4.0E-06 1
rs1460276679 1.000 0.120 4 127921876 frameshift variant G/- delins 1.2E-05 1
rs1560776422 1.000 0.120 4 127957591 splice acceptor variant C/A snv 1
rs556661896 1.000 0.120 4 127942073 stop gained A/G;T snv 1
rs559155109 1.000 0.120 4 127920826 missense variant A/G snv 1.1E-04 1.4E-05 1
rs727502801 1.000 0.120 4 127932981 frameshift variant -/A ins 1.6E-05 1
rs749704755 1.000 0.120 4 127943775 missense variant C/A;T snv 8.0E-06; 4.0E-06 1
rs751696703 1.000 0.120 4 127942160 splice acceptor variant T/A snv 1
rs764549054 1.000 0.120 4 127920779 missense variant T/C snv 1.2E-05 7.0E-06 1
rs779838200 1.000 0.120 4 127957501 missense variant C/T snv 1.6E-05 1