Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679475 0.925 0.120 4 121392885 intergenic variant A/C;G snv 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs17466626 0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs72743477 0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs1270942 0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs17759659 0.851 0.120 18 63291411 intron variant A/G snv 0.31 4
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs1015166 0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 2
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs17885785 0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs2066363 0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14