Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C2676079
Disease:
METABOLIC SYNDROME, SUSCEPTIBILITY TO
T 0.700 SusceptibilityMutation CLINVAR