{{Rsnum
|rsid=4426527
|Gene=AGXT
|Chromosome=2
|position=240878099
|Orientation=plus
|GMAF=0.1368
|Gene_s=AGXT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 64.6 | 31.0 | 4.4
| HCB | 82.5 | 16.8 | 0.7
| JPT | 82.1 | 17.9 | 0.0
| YRI | 97.3 | 2.0 | 0.7
| ASW | 75.4 | 24.6 | 0.0
| CHB | 82.5 | 16.8 | 0.7
| CHD | 88.1 | 11.0 | 0.9
| GIH | 82.2 | 16.8 | 1.0
| LWK | 90.9 | 8.2 | 0.9
| MEX | 67.2 | 31.0 | 1.7
| MKK | 87.2 | 12.2 | 0.6
| TSI | 71.0 | 25.0 | 4.0
| HapMapRevision=28
}}{{ClinVar
|ALT=G
|CAF=0.8632; 0.1368
|CHROM=2
|CLNACC=RCV000032682.1
|CLNALLE=1
|CLNDBN=Primary hyperoxaluria, type I
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1283:C0268164:259900:416:93598:65520001
|CLNHGVS=NC_000002.11:g.241817516A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604285.0014
|COMMON=1
|Disease=Primary hyperoxaluria
|FwdALT=G
|FwdREF=A
|GENEINFO=AGXT:189
|GENE_ID=189
|GENE_NAME=AGXT
|REF=A
|RSPOS=241817516
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000150516100101
|WGT=0
|dbSNPBuildID=111
|rsid=4426527
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}