Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs10911363 0.925 0.120 1 183580622 intron variant G/T snv 0.30 2
rs11168268
VDR
0.925 0.120 12 47858029 intron variant G/A snv 0.57 2
rs1477353313
ACR
0.925 0.120 22 50744085 missense variant T/G snv 2
rs1562444 0.925 0.120 11 92982683 3 prime UTR variant G/A snv 0.55 2
rs204989 0.925 0.120 6 32194075 intron variant G/A snv 0.21 2
rs2165667 0.925 0.040 4 186540475 intron variant A/G;T snv 2
rs540558 0.925 0.120 5 38844171 intron variant C/G snv 0.19 2
rs7033979 0.925 0.040 9 92461698 intron variant A/G;T snv 2
rs6074028 1.000 0.040 20 46126219 intron variant A/C;G snv 1
rs73115010 1.000 0.040 20 46124597 intron variant T/C snv 0.18 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs1385889785 1.000 0.040 1 157695436 missense variant G/C;T snv 4.0E-06; 4.0E-06 2
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs104895094 0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 5
rs28940580 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs3789604 0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs771184127 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 9
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs28936375 0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15
rs741761 0.882 0.200 15 74411588 missense variant T/A;C snv 1.8E-04; 0.35 3
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72