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
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs3775290 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15
rs4074 0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5743314 0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs5998152 0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
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
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs910049 0.776 0.400 6 32347950 intron variant T/C snv 0.76 8
rs9380516 0.925 0.120 6 35534425 TF binding site variant T/C snv 0.85 2