Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs780246573 0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs80338880 0.732 0.360 7 100633100 stop gained G/C snv 7.0E-06 12
rs1424266770 0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs11568350 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs1161457931 0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs1208663703 0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs9357271 0.776 0.160 6 38398097 intron variant T/C snv 0.38 8
rs111033563 0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 8
rs143396368
FXN
0.807 0.200 9 69072623 missense variant G/A;C snv 3.2E-05; 8.0E-06 7
rs707889
HFE
0.827 0.200 6 26095703 3 prime UTR variant G/A;T snv 6
rs199474387 0.807 0.240 6 29942870 missense variant G/C;T snv 6
rs11558492 0.827 0.200 1 231272345 missense variant A/G;T snv 0.16 5
rs1167115018 0.827 0.160 6 26092760 missense variant A/G snv 8.0E-06 7.0E-06 5
rs121434375
HJV
0.851 0.080 1 146019672 stop gained T/A snv 4
rs104893662 0.851 0.080 2 189571799 missense variant T/A;G snv 4
rs368420430 0.851 0.080 2 189564177 missense variant T/A;G snv 5.2E-05; 8.0E-06 4