Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
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
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38