Disease: Primary hyperoxaluria type 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs180177304
rs180177304
Entrez Id: 9380
Gene Symbol: GRHPR
GRHPR
CUI: C0268165
Disease:
Primary hyperoxaluria type 2 		A 0.700 GeneticVariation CLINVAR Performance evaluation of Sanger sequencing for the diagnosis of primary hyperoxaluria and comparison with targeted next generation sequencing. 25629080 2015
dbSNP: rs180177304
rs180177304
Entrez Id: 9380
Gene Symbol: GRHPR
GRHPR
CUI: C0268165
Disease:
Primary hyperoxaluria type 2 		A 0.700 CausalMutation CLINVAR