Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 15
rs9357271
BTBD9
0.776 0.160 6 38398097 intron variant T/C snv 0.38 8
rs733655
TMPRSS6
0.827 0.240 22 37099011 intron variant T/C snv 0.28 6
rs2280673
RAB6B
0.882 0.160 3 133839310 intron variant A/C;T snv 3
rs2858996
HFE
0.925 0.080 6 26093798 intron variant G/A;C;T snv 2
rs422982
SLC11A2
0.925 0.200 12 51012571 intron variant T/A;C snv 2
rs6564851 0.882 0.120 16 81230992 intergenic variant T/G snv 0.48 5
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs780246573
HFE ; LOC108783645
0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs80338880
TFR2
0.732 0.360 7 100633100 stop gained G/C snv 7.0E-06 12
rs797045145
HFE ; LOC108783645
0.807 0.240 6 26091479 stop gained G/A snv 6
rs121434375
HJV
0.851 0.080 1 146019672 stop gained T/A snv 4
rs80338882
TFR2
0.851 0.080 7 100630973 stop gained G/A snv 4.0E-06 1.4E-05 4
rs146519482
LOC108783645 ; HFE
0.925 0.080 6 26091475 stop gained G/C;T snv 4.5E-04 2
rs763369315
HAMP
1.000 0.080 19 35285003 stop gained C/A;T snv 4.0E-06 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 14