GHRL, ghrelin and obestatin prepropeptide, 51738

N. diseases: 183; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4684677
rs4684677
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0040128
Disease:
Thyroid Diseases
0.010 GeneticVariation BEFREE The association between rs4684677 T/A polymorphism in preproghrelin gene and predisposition to autoimmune thyroid diseases in children. 25868387 2015