rs121913051
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom.
|
19821824 |
2010 |
rs121913051
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Atypical hemolytic-uremic syndrome.
|
19846853 |
2009 |
rs121913055
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom.
|
19821824 |
2010 |
rs121913055
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Atypical hemolytic-uremic syndrome.
|
19846853 |
2009 |
rs460897
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Atypical hemolytic-uremic syndrome.
|
19846853 |
2009 |
rs460897
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom.
|
19821824 |
2010 |
rs1391815797
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.
|
14583443 |
2003 |
rs1391815797
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site.
|
11851332 |
2002 |
rs1391815797
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
|
10577907 |
1999 |
rs1391815797
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.
|
14978182 |
2004 |
rs1391815797
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries.
|
12960213 |
2003 |
rs1391815797
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Genetic studies into inherited and sporadic hemolytic uremic syndrome.
|
9551389 |
1998 |
rs1391815797
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
|
20513133 |
2010 |
rs1391815797
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
|
10762557 |
2000 |
rs145975787
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.
|
14978182 |
2004 |
rs145975787
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
|
10577907 |
1999 |
rs145975787
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
|
10762557 |
2000 |
rs145975787
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
|
20513133 |
2010 |
rs145975787
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries.
|
12960213 |
2003 |
rs145975787
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Genetic studies into inherited and sporadic hemolytic uremic syndrome.
|
9551389 |
1998 |
rs145975787
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site.
|
11851332 |
2002 |
rs145975787
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.
|
14583443 |
2003 |
rs148165372
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs149474608
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs1553270437
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|