Gene: HFE ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.100 0.974 230 1997 2019
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.100 0.961 77 1997 2019
dbSNP: rs1800730
rs1800730
HFE ; LOC108783645
32 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 0.100 0.800 10 1999 2011
dbSNP: rs35201683
rs35201683
HFE
12 0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 0.030 1.000 3 2001 2003
dbSNP: rs780246573
rs780246573
HFE ; LOC108783645
12 0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 0.030 1.000 3 2001 2003
dbSNP: rs111033563
rs111033563
HFE ; LOC108783645
8 0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1167115018
rs1167115018
HFE ; LOC108783645
5 0.827 0.160 6 26092760 missense variant A/G snv 8.0E-06 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs146519482
rs146519482
HFE ; LOC108783645
2 0.925 0.080 6 26091475 stop gained G/C;T snv 4.5E-04 0.010 1.000 1 2002 2002
dbSNP: rs199916850
rs199916850
HFE ; LOC108783645
2 0.925 0.080 6 26091521 missense variant T/C snv 8.0E-06 1.4E-05 0.010 1.000 1 2008 2008
dbSNP: rs2858996
rs2858996
HFE
2 0.925 0.080 6 26093798 intron variant G/A;C;T snv 0.010 < 0.001 1 2011 2011
dbSNP: rs28934597
rs28934597
HFE ; LOC108783645
2 0.925 0.080 6 26091041 missense variant G/C snv 1.2E-05 7.0E-06 0.010 1.000 1 1999 1999
dbSNP: rs537002912
rs537002912
HFE
2 0.925 0.080 6 26093145 missense variant A/G snv 8.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs707889
rs707889
HFE
6 0.827 0.200 6 26095703 3 prime UTR variant G/A;T snv 0.010 < 0.001 1 2011 2011
dbSNP: rs748882267
rs748882267
HFE
2 0.925 0.080 6 26093156 missense variant C/G snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs781516027
rs781516027
HFE ; LOC108783645
3 0.882 0.080 6 26092744 missense variant C/G;T snv 8.0E-06; 3.6E-05 0.010 1.000 1 2014 2014