Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113561019 1.000 0.080 3 9756791 missense variant G/A;T snv 3.9E-03; 4.0E-06 2
rs11777210 1.000 0.080 8 1979843 intron variant C/G;T snv 2
rs1374712964 1.000 0.080 1 45332028 missense variant T/C snv 2
rs1400826115 1.000 0.080 3 9756770 missense variant A/G snv 4.0E-06 2
rs2279398 1.000 0.080 5 177503768 3 prime UTR variant C/T snv 2.7E-02 2
rs2015 0.925 0.120 19 38878729 3 prime UTR variant T/G snv 0.47 3
rs664589 0.925 0.080 11 65501878 non coding transcript exon variant C/G snv 6.0E-02 3.8E-02 4
rs41291957 0.882 0.200 5 149428827 intron variant G/A snv 0.12 7
rs1126616 0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26 8
rs121908568 0.807 0.160 17 65536495 stop gained G/A snv 8
rs13278062 0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 8
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs3138053 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 10
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs7708392 0.732 0.400 5 151077924 intron variant G/C snv 0.44 12
rs9138 0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 14
rs201745983 0.752 0.200 12 111783219 missense variant G/A snv 6.8E-05 7.7E-05 14
rs2682818 0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 14
rs2066842 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 15
rs2276466 0.732 0.320 16 13949318 3 prime UTR variant C/A;G snv 15
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 15
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 15