{{Rsnum
|rsid=121908529
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=AGXT
|position=240871433
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AGXT
}}{{omim
|id=604285
|rsnum=121908529
|variant=0002
}}{{ClinVar
|rsid=121908529
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=241810850
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000040002110100
|GENEINFO=AGXT:189
|GENE_NAME=AGXT
|GENE_ID=189
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.241810850G>A
|CLNORIGIN=1
|CLNSRCID=
604285.0002; 604285.0013
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000032681.1
|Tags=PM;S3D;SLO;VLD;OTHERKG;LSD;OM
|CLNDBN=Primary hyperoxaluria, type I
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1283:C0268164:259900:416:93598:65520001
|CLNSRC=OMIM Allelic Variant
|Disease=Primary hyperoxaluria
}}