Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs7270101 0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs12304647 0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs16851720 0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs1140409 0.925 0.080 17 64500552 missense variant A/C snv 5.4E-02 5.0E-02 2
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs4074 0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv 3
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs2679757 0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs57749775 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2
rs675520 0.925 0.080 6 137672095 non coding transcript exon variant A/G;T snv 2