Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
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
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs222747 0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
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
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs11171739 0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 10
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111