Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs4149117 0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs75961395 0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 10
rs1051861187 0.827 0.080 7 87409385 missense variant A/G snv 6
rs57749775 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs5743314 0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs10433937 0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs104894630 0.882 0.120 17 10692805 missense variant G/A snv 4
rs11465817 0.882 0.120 1 67255414 intron variant C/A;T snv 4