Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs10046 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246