{{Rsnum
|rsid=267606764
|Chromosome=10
|position=97601925
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HOGA1
|Gene_s=HOGA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=G
|CHROM=10
|CLNACC=RCV000000051.1
|CLNALLE=1
|CLNDBN=Primary hyperoxaluria, type III
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C3150878:613616:416:93600
|CLNHGVS=NC_000010.10:g.99361682T>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613597.0006
|Disease=Primary hyperoxaluria
|FwdALT=G
|FwdREF=T
|GENEINFO=HOGA1:112817
|GENE_ID=112817
|GENE_NAME=HOGA1
|REF=T
|RSPOS=99361682
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606764
}}