HNF1B, HNF1 homeobox B, 6928

N. diseases: 279; N. variants: 72
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: rs7209295
rs7209295
Entrez Id: 6928;105371754
Gene Symbol: HNF1B;LOC105371754
HNF1B;LOC105371754
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