Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10204525 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs1054690270 0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs10932029 0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs11003123 0.827 0.200 10 52771774 upstream gene variant G/A snv 0.30 6
rs12304647 0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs13347 0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs1358379 0.882 0.160 6 71403739 intron variant T/C snv 6.2E-02 3
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs2896019 0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5
rs3820998 0.882 0.120 2 161138615 intron variant C/A;T snv 3
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs4656942 0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs485618 0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54 4
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs705382 0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs7536540 0.882 0.160 1 65058899 intron variant C/G;T snv 0.65 3