Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28936415 0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs80338701 0.776 0.360 16 8811088 stop gained C/A;T snv 4.4E-05; 5.4E-06 13
rs376754460 0.807 0.280 16 8801859 missense variant G/A;C;T snv 8.0E-06 12
rs190521996 0.790 0.320 16 8811660 missense variant T/C snv 2.9E-04 4.1E-04 12
rs141498002 0.827 0.280 16 8811099 stop gained G/A;T snv 1.1E-04; 5.2E-06 8
rs80338700 0.851 0.200 16 8806398 missense variant C/G;T snv 4.0E-06; 2.4E-05 7
rs80338708 1.000 0.080 16 8847794 missense variant C/G;T snv 1.3E-04; 4.4E-05 3
rs937726878 0.882 0.240 16 8797949 splice donor variant G/T snv 1.4E-05 7.0E-06 3
rs80338707 0.925 0.080 16 8847775 missense variant G/A;C snv 6.8E-05; 4.0E-06 2
rs80338709 0.925 0.080 16 8847806 missense variant G/C snv 6.0E-05 2.7E-04 2
rs148032587 0.925 0.080 16 8811173 missense variant G/A snv 1.6E-04 1.3E-04 2
rs370160676 1.000 0.080 16 8847715 non coding transcript exon variant T/C;G snv 4.0E-06; 4.0E-06 1
rs104894534 1.000 0.080 16 8801863 missense variant T/C snv 1
rs398123309 1.000 0.080 16 8813090 missense variant G/A;C snv 4.0E-06 1
rs139716296 1.000 0.080 16 8804845 splice donor variant T/C snv 6.8E-05 7.0E-05 1
rs1057517110 0.925 0.160 16 8811086 missense variant T/C snv 1
rs1274794195 1.000 0.080 16 8811636 splice acceptor variant GAAA/- delins 4.0E-06 1
rs200503569 1.000 0.080 16 8806383 missense variant C/T snv 1.2E-05 7.0E-06 1
rs104894527 1.000 0.080 16 8804781 missense variant G/T snv 7.0E-06 1
rs532870929 1.000 0.080 16 8813087 missense variant T/C snv 3.6E-05 1.4E-05 1
rs80338704 1.000 0.080 16 8813030 missense variant A/G snv 4.0E-06 1.4E-05 1
rs1060499598 1.000 0.080 16 8804844 splice donor variant G/A snv 1.2E-05 2.1E-05 1
rs104894530 1.000 0.080 16 8811080 missense variant G/C snv 1
rs1057516372 1.000 0.080 16 8806314 splice acceptor variant A/G snv 4.0E-06 1
rs150719105 1.000 0.080 16 8811161 missense variant T/C snv 1.6E-04 6.3E-05 1