Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv 3
rs9514828 0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs9380516 0.925 0.120 6 35534425 TF binding site variant T/C snv 0.85 2
rs910049 0.776 0.400 6 32347950 intron variant T/C snv 0.76 8
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs897206619
HFE
0.882 0.120 6 26093128 missense variant C/T snv 3.5E-05 3
rs887304 0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 2
rs886277 1.000 0.080 11 2418537 missense variant T/C snv 0.44 0.47 1
rs843720 0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs843645 0.827 0.120 2 54247527 intron variant T/A;G snv 0.19 5
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs8021276 0.925 0.080 14 92110162 upstream gene variant A/G;T snv 2
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs769217
CAT
0.742 0.440 11 34461361 synonymous variant C/T snv 0.25 0.22 12
rs767864210 0.882 0.120 4 94657500 missense variant G/A;T snv 8.0E-05 2.1E-05 3
rs7664413 0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25 7
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs75961395 0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 10
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs757075712 0.763 0.200 10 58390856 missense variant C/T snv 1.6E-05 1.4E-05 15
rs755284374
HFE
0.882 0.120 6 26093122 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs7536540 0.882 0.160 1 65058899 intron variant C/G;T snv 0.65 3
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs747432300 0.925 0.120 8 144504357 missense variant C/A;T snv 8.1E-06; 1.2E-04 2