Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 16
rs1689510 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14