Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10519068 0.925 0.120 15 60776505 intron variant G/A snv 0.22 2
rs10791824 0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs115288876 0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs117137535 0.882 0.120 9 137605991 intron variant G/A snv 2.7E-02 3
rs12186803 0.925 0.120 5 132704377 intron variant G/A;C snv 2
rs13360927 0.882 0.160 5 110700055 intron variant A/G snv 9.3E-02 3
rs13361382 0.882 0.160 5 110713253 intron variant G/A snv 9.3E-02 3
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1898671 0.851 0.160 5 111072304 intron variant C/T snv 0.25 5
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2853209 0.827 0.200 20 3670825 intron variant T/A snv 0.41 5
rs3024971 0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 7
rs324011 0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs35441874 0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs45613035 0.925 0.120 4 122219915 intron variant T/C snv 6.5E-02 2
rs4696480 0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs56375023 0.925 0.120 15 67156025 intron variant G/A snv 0.17 3
rs574456 0.882 0.160 2 140644133 intron variant A/T snv 8.1E-02 3
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs7216389 0.732 0.440 17 39913696 intron variant C/T snv 0.60 14