Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs72743461 0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs10865710 0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1048990 0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182