Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs13347 0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs1049305 0.925 0.160 7 30924207 3 prime UTR variant G/C snv 0.52 4
rs485618 0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54 4
rs1059122 0.882 0.160 4 88726273 3 prime UTR variant T/A snv 0.46 3
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs1545224 0.925 0.120 2 88124297 3 prime UTR variant A/G snv 0.18 2
rs887304 0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 2
rs3017895 1.000 0.080 4 88728340 3 prime UTR variant A/G snv 0.19 1
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs26311 1.000 0.080 3 10291242 5 prime UTR variant C/G snv 0.16 1
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs769217
CAT
0.742 0.440 11 34461361 synonymous variant C/T snv 0.25 0.22 12
rs2233682 0.827 0.240 19 9838476 synonymous variant G/A snv 3.7E-02 6.3E-02 5
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs2289030 0.882 0.120 12 94834510 non coding transcript exon variant G/C snv 9.7E-02 6.3E-02 6
rs3106796 0.882 0.160 2 188985047 non coding transcript exon variant A/G snv 0.35 3
rs3859501 0.882 0.120 19 53788157 non coding transcript exon variant A/C snv 0.43 3
rs675520 0.925 0.080 6 137672095 non coding transcript exon variant A/G;T snv 2