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
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs3135932 0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs1718119 0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs3764880 0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11