Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397509360
rs397509360
Entrez Id: 112817
Gene Symbol: HOGA1
HOGA1
CUI: C3150878
Disease:
Primary hyperoxaluria type III
T 0.700 CausalMutation CLINVAR Cellular degradation of 4-hydroxy-2-oxoglutarate aldolase leads to absolute deficiency in primary hyperoxaluria type 3. 27096395 2016
dbSNP: rs397509360
rs397509360
Entrez Id: 112817
Gene Symbol: HOGA1
HOGA1
CUI: C3150878
Disease:
Primary hyperoxaluria type III
T 0.700 CausalMutation CLINVAR Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria. 25644115 2015
dbSNP: rs397509360
rs397509360
Entrez Id: 112817
Gene Symbol: HOGA1
HOGA1
CUI: C3150878
Disease:
Primary hyperoxaluria type III
T 0.700 CausalMutation CLINVAR Performance evaluation of Sanger sequencing for the diagnosis of primary hyperoxaluria and comparison with targeted next generation sequencing. 25629080 2015
dbSNP: rs397509360
rs397509360
Entrez Id: 112817
Gene Symbol: HOGA1
HOGA1
CUI: C3150878
Disease:
Primary hyperoxaluria type III
T 0.700 CausalMutation CLINVAR 4-hydroxyglutamate is a biomarker for primary hyperoxaluria type 3. 24563386 2015
dbSNP: rs397509360
rs397509360
Entrez Id: 112817
Gene Symbol: HOGA1
HOGA1
CUI: C3150878
Disease:
Primary hyperoxaluria type III
T 0.700 CausalMutation CLINVAR 4-Hydroxy-2-oxoglutarate aldolase inactivity in primary hyperoxaluria type 3 and glyoxylate reductase inhibition. 22771891 2012
dbSNP: rs397509360
rs397509360
Entrez Id: 112817
Gene Symbol: HOGA1
HOGA1
CUI: C3150878
Disease:
Primary hyperoxaluria type III
T 0.700 CausalMutation CLINVAR The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3. 22391140 2012
dbSNP: rs397509360
rs397509360
Entrez Id: 112817
Gene Symbol: HOGA1
HOGA1
CUI: C3150878
Disease:
Primary hyperoxaluria type III
T 0.700 CausalMutation CLINVAR Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. 21896830 2011
dbSNP: rs397509360
rs397509360
Entrez Id: 112817
Gene Symbol: HOGA1
HOGA1
CUI: C3150878
Disease:
Primary hyperoxaluria type III
T 0.700 CausalMutation CLINVAR Mutations in DHDPSL are responsible for primary hyperoxaluria type III. 20797690 2010