HNF4A, hepatocyte nuclear factor 4 alpha, 3172

N. diseases: 340; N. variants: 74
Disease: Hyperinsulinism due to HNF4A deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs776489992
rs776489992
Entrez Id: 3172
Gene Symbol: HNF4A
HNF4A
CUI: C4274078
Disease:
Hyperinsulinism due to HNF4A deficiency 		AGCT 0.700 GeneticVariation CLINVAR