Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
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
rs7248488 0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs8103163 0.882 0.120 19 21991950 intron variant A/C snv 0.59 4
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1805034 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 12
rs10088262 0.925 0.160 8 123753462 intergenic variant A/G snv 0.56 2
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62