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
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1800972 0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs11362 0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs1799946 0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13