Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs10204525 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs4711998 0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs1682111 0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs61330082 0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13