Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050153 0.925 0.120 3 196049444 3 prime UTR variant G/A snv 2
rs10519068 0.925 0.120 15 60776505 intron variant G/A snv 0.22 2
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs10791824 0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs115288876 0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs11558538 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs11584340 0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 5
rs117137535 0.882 0.120 9 137605991 intron variant G/A snv 2.7E-02 3
rs1214598 0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12186803 0.925 0.120 5 132704377 intron variant G/A;C snv 2
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs1295685 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs13277355 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 3
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
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs138726443 0.790 0.200 1 152307547 stop gained G/A;C;T snv 2.8E-03; 4.0E-06; 1.6E-05 7
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs150597413 0.827 0.160 1 152305146 stop gained G/A;C;T snv 3.6E-05; 4.0E-06; 1.5E-03 5
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1555549674 0.882 0.240 17 42223402 missense variant T/G snv 6
rs167769 0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 5