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
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
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
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
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
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
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs9514828 0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2296651 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182