Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1534891 0.827 0.200 22 38299094 intron variant T/C snv 0.90 5
rs316019 0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs6898743
GHR
0.776 0.160 5 42602390 intron variant C/G snv 0.78 9
rs2320615 0.925 0.080 4 163148797 intron variant A/G snv 0.78 3
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs413812 1.000 0.080 4 170588298 intron variant T/C snv 0.76 1
rs2014300 0.851 0.080 21 34985564 intron variant A/G;T snv 0.75 5
rs10931936 0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs26279 0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70 9
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs738722 0.882 0.120 22 28734024 intron variant T/C snv 0.67 4
rs2236142 0.827 0.120 22 28741956 5 prime UTR variant G/C snv 0.66 6
rs861530 0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs4462560 0.851 0.080 15 75355623 3 prime UTR variant G/C snv 0.64 5
rs10058728 1.000 0.080 5 149524529 intron variant A/T snv 0.64 2
rs4711998 0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs115510139 0.827 0.120 2 237331726 intron variant A/T snv 0.60 6
rs13016963 0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25