Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1259560536 1.000 0.040 20 3671756 missense variant T/C snv 7.0E-06 1
rs1402272180 1.000 0.040 1 243637661 missense variant C/T snv 7.0E-06 1
rs770462360 1.000 0.040 11 64839070 missense variant G/A snv 2.0E-05 1
rs1384093596 1.000 0.040 12 67657500 missense variant C/T snv 1
rs779221554 1.000 0.040 X 109430395 missense variant C/A;T snv 1
rs375412266 1.000 0.040 3 50617647 missense variant C/G;T snv 2.1E-04; 4.1E-06 1
rs17855787 1.000 0.040 17 50109341 missense variant G/A snv 1
rs371854396 1.000 0.040 1 20638098 missense variant C/G;T snv 1.6E-05; 4.0E-06 1
rs1466858740 1.000 0.040 16 24180881 missense variant G/A snv 1
rs1567176006 1.000 0.040 16 3602208 frameshift variant CT/- del 1
rs757496714 1.000 0.040 20 388189 missense variant C/T snv 4.0E-06 1
rs2291427 0.925 0.040 10 45440776 intron variant A/G;T snv 2
rs11548193 0.925 0.040 19 48799813 missense variant G/A;C snv 0.14 2
rs11670188 0.925 0.040 19 2014038 non coding transcript exon variant A/G snv 0.16 2
rs1210653597 0.925 0.120 9 21968756 missense variant T/C snv 2
rs1558650888 0.925 0.040 2 25234308 missense variant G/A snv 2
rs9642393 0.925 0.040 7 55177954 intron variant T/C snv 0.24 2
rs7325927 0.925 0.040 13 107823165 intron variant C/T snv 0.38 2
rs3829382 0.925 0.040 13 28003551 3 prime UTR variant G/T snv 0.46 2
rs11558961 0.925 0.040 17 44907319 3 prime UTR variant G/C;T snv 0.27; 1.2E-05 2
rs759927375 0.925 0.040 6 26020589 missense variant G/A;C snv 1.2E-05; 8.0E-06 2
rs1161136341 0.925 0.080 7 18591621 missense variant G/A snv 8.0E-06 1.4E-05 2
rs774238794 0.925 0.080 7 18644690 missense variant G/A;T snv 4.1E-05; 4.1E-06 2
rs8957 0.925 0.040 20 63742354 missense variant G/T snv 0.71 0.78 2
rs7732320 0.925 0.040 5 81423306 intron variant C/T snv 0.22 2