{{Rsnum
|rsid=80356708
|Chromosome=9
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=GRHPR
|position=37424864
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GRHPR
}}{{omim
|id=604296
|rsnum=80356708
|variant=0001
}}{{ClinVar
|rsid=80356708
|Reversed=0
|FwdREF=G
|FwdALT=
|REF=TG
|ALT=T
|RSPOS=37424858
|CHROM=9
|dbSNPBuildID=135
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=GRHPR:9380
|GENE_NAME=GRHPR
|GENE_ID=9380
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.37424861delG
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK2692; 604296.0001
|CLNSIG=5
|CLNCUI=C0268165; C0268165
|CLNDBN=Primary hyperoxaluria, type II
|Disease=Primary hyperoxaluria
|CLNACC=RCV000005990.2
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK2692:C0268165:260000:93599:40951006
}}{{PMID|10484776}} The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II.

{{PMID|14635115}} Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2.