Source: ALL
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
0.700 | GeneticVariation | UNIPROT | Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. | 20513133 | 2010 |
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|
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 |
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|
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 |
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|
0.700 | GeneticVariation | UNIPROT | Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries. | 12960213 | 2003 |
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|
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 |
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|
0.700 | GeneticVariation | UNIPROT | Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome. | 10762557 | 2000 |
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|
0.700 | GeneticVariation | UNIPROT | Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome. | 10577907 | 1999 |
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|
0.700 | GeneticVariation | UNIPROT | Genetic studies into inherited and sporadic hemolytic uremic syndrome. | 9551389 | 1998 |