Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs180177319
rs180177319
GRHPR
G 0.700 CausalMutation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015
dbSNP: rs180177319
rs180177319
GRHPR
G 0.700 CausalMutation CLINVAR Ethnic differences in GRHPR mutations in patients with primary hyperoxaluria type 2. 24116921

2014
dbSNP: rs180177319
rs180177319
GRHPR
G 0.700 CausalMutation CLINVAR Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2. 14635115

2003