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
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs1554286 0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs2058660 0.882 0.280 2 102437989 intron variant G/A snv 0.78 4