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
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14