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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs17375018 0.790 0.360 1 67189464 intron variant G/A snv 0.29 7
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5