Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs766914563 0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs368234815 0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs1015164 0.925 3 46410189 intron variant A/C;G;T snv 8
rs11157436 0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs10808739 0.882 8 64727703 intron variant G/A snv 0.24 6
rs11790131 0.882 0.080 9 19469848 intergenic variant G/A;T snv 6
rs143633948 0.882 0.080 6 131504454 intron variant G/A;C snv 6
rs2442719 0.882 0.120 6 31352761 intron variant C/T snv 0.53 6
rs35897606 0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 6
rs73084982 0.882 0.080 20 3430406 intergenic variant G/A snv 3.5E-02 6
rs73132848 0.882 0.080 3 8764738 intron variant G/A snv 9.3E-02 6
rs79709413 0.882 0.080 13 24740488 upstream gene variant G/T snv 4.7E-02 6
rs10892324 0.925 11 119032329 upstream gene variant T/A;G snv 5
rs11231017 0.925 11 62293877 downstream gene variant G/A snv 0.29 5
rs11649112 0.925 16 13267554 intron variant G/A snv 0.22 5
rs12460243 0.925 19 8066356 intron variant G/A snv 0.14 5
rs13064773 0.925 3 158893105 intergenic variant G/A snv 0.39 5
rs16823858 0.925 3 115559835 intron variant G/A;C snv 5