Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22