{{Rsnum
|rsid=180177191
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=AGXT
|position=240868893
|Gene_s=AGXT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=180177191
|Reversed=0
|FwdREF=C
|FwdALT=A,G,T
|REF=C
|ALT=A,G,T
|RSPOS=241808310
|CHROM=2
|GMAF=0.0009
|dbSNPBuildID=135
|SSR=0
|SAO=0
|VP=0x050360000a01000016110104
|GENEINFO=AGXT:189
|GENE_NAME=AGXT
|GENE_ID=189
|WGT=1
|VC=SNV
|CLNALLE=3
|CLNHGVS=NC_000002.11:g.241808310C>T
|CLNSIG=5
|CLNCUI=259900
|CLNDBN=Primary hyperoxaluria, type I
|Tags=PM;S3D;SLO;NSM;REF;KGPhase1;KGPROD;OTHERKG;LSD;OM;NOV
|CAF=0.9991; 0.0009183; .
|CLNDSDB=OMIM
|CLNDSDBID=259900
|COMMON=0
|Disease=Primary hyperoxaluria
}}