{{Rsnum
|rsid=119490108
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GRHPR
|position=37426545
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GRHPR
}}{{omim
|id=604296
|rsnum=119490108
|variant=0002
}}{{ClinVar
|rsid=119490108
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=37426542
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=GRHPR:9380
|GENE_NAME=GRHPR
|GENE_ID=9380
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.37426542C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604296.0002
|CLNSIG=5
|CLNCUI=C0268165
|CLNDBN=Primary hyperoxaluria, type II
|Disease=Primary hyperoxaluria
|CLNACC=RCV000005991.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK2692:C0268165:260000:93599:40951006
}}