Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs4553808 0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs121913459 0.672 0.160 9 130872896 missense variant C/T snv 25
rs749140677
VDR
0.752 0.240 12 47857185 missense variant G/A snv 8.0E-06 13
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs11568821 0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs12953 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs748843032 0.807 0.160 4 99594840 missense variant T/C snv 4.0E-06 8
rs36084323 0.807 0.280 2 241859444 upstream gene variant C/T snv 5.4E-02 8
rs9277534 0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 7
rs4693608 0.827 0.200 4 83320204 intron variant G/A;C snv 6
rs2056626 0.882 0.080 1 167451188 intron variant T/G snv 0.30 5
rs4845618 0.851 0.160 1 154427539 intron variant G/T snv 0.53 5
rs987870 0.851 0.160 6 33075103 intron variant A/G snv 0.19 4
rs2278293 0.882 0.040 7 128400698 non coding transcript exon variant C/T snv 0.47 3
rs7588571 0.882 0.040 2 79161461 intron variant G/A snv 0.49 3
rs11545566 0.882 0.080 1 179293868 5 prime UTR variant G/A snv 0.24 3
rs17114808 0.925 0.040 10 102631528 3 prime UTR variant C/A;G;T snv 2
rs17114803 1.000 0.040 10 102627177 splice region variant T/C snv 0.16 0.15 1