{{Rsnum
|rsid=180177259
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=AGXT
|position=240875165
|Gene_s=AGXT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=180177259
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=241814582
|CHROM=2
|dbSNPBuildID=135
|SSR=0
|SAO=0
|VP=0x050360000601000002110100
|GENEINFO=AGXT:189
|GENE_NAME=AGXT
|GENE_ID=189
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.241814582G>A
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604285.0010; 604285.0010
|CLNSIG=1
|CLNCUI=C0268164; C0268164
|CLNDBN=Primary hyperoxaluria, type I
|Disease=Primary hyperoxaluria
|CLNACC=SCV000026185.1; SCV000026185.1
|Tags=PM;S3D;SLO;NSN;REF;OTHERKG;LSD;OM
}}