HNF4A, hepatocyte nuclear factor 4 alpha, 3172

N. diseases: 340; N. variants: 74
Disease: Serum HDL cholesterol measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800961
rs1800961
Entrez Id: 3172
Gene Symbol: HNF4A
HNF4A
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		T 0.700 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs1800961
rs1800961
Entrez Id: 3172
Gene Symbol: HNF4A
HNF4A
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs1800961
rs1800961
Entrez Id: 3172
Gene Symbol: HNF4A
HNF4A
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs1800961
rs1800961
Entrez Id: 3172
Gene Symbol: HNF4A
HNF4A
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		T 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906 2009