{{Rsnum
|rsid=113994129
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=AGL
|position=99881329
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AGL
}}{{omim
|id=610860
|rsnum=113994129
|variant=0003
}}{{ClinVar
|rsid=113994129
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=99881329
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000605000002110100
|GENEINFO=AGL:178
|GENE_NAME=AGL
|GENE_ID=178
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.99881329G>A
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000642.2:c.2039G>A; NBK26372; 610860.0003
|CLNSIG=5
|CLNCUI=CN068470; C0017922
|CLNDBN=Glycogen storage disease IIIb; Glycogen storage disease type III
|Disease=Glycogen storage disease IIIb; Glycogen storage disease type III
|CLNACC=RCV000001154.2; RCV000020375.1
|Tags=PM;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1968740; NBK26372:C0017922:232400:ORPHA366:66937008
}}