Disease: Primary Hyperoxaluria ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs180177321
rs180177321
Entrez Id: 9380
Gene Symbol: GRHPR
GRHPR
CUI: C0020501
Disease:
Primary Hyperoxaluria 		C 0.700 CausalMutation CLINVAR Ethnic differences in GRHPR mutations in patients with primary hyperoxaluria type 2. 24116921 2014