Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs193107685 0.851 0.160 7 74123572 downstream gene variant T/C snv 1.0E-02 4
rs201802880 0.882 0.200 7 74779296 missense variant G/A snv 1.1E-03 4
rs204990 0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs204994 0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 4
rs2422345 0.851 0.160 1 173368608 upstream gene variant G/A snv 0.63 4
rs2523589 0.851 0.200 6 31359557 upstream gene variant G/A;T snv 4
rs2596560 0.851 0.280 6 31387541 intergenic variant T/C snv 0.22 4
rs3115553 0.851 0.200 6 32278050 intron variant C/T snv 0.25 4
rs3129943 0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
rs3129963 0.851 0.280 6 32412431 downstream gene variant A/G snv 0.17 4
rs3130299 0.851 0.240 6 32235760 regulatory region variant A/G snv 0.24 4
rs3135394 0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 4
rs3766379 0.851 0.320 1 160837925 intron variant T/C snv 0.57 4
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 4
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs4937333 0.882 0.120 11 128460625 3 prime UTR variant T/C snv 0.45 4
rs4958880 0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs5029924 0.851 0.200 6 137866361 intron variant C/T snv 0.13 4
rs5029937 0.882 0.160 6 137874014 intron variant G/T snv 0.13 4
rs540386 0.851 0.200 11 36503743 intron variant C/G;T snv 4
rs5754467 0.851 0.160 22 21630805 upstream gene variant A/G;T snv 4
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 4
rs744600 0.851 0.160 2 190700031 intron variant G/T snv 0.60 4
rs76246107 0.851 0.160 19 49618017 intron variant G/A snv 7.7E-02 4
rs7929541 0.851 0.160 11 633689 upstream gene variant T/C snv 0.34 4