{{Rsnum
|rsid=113994127
|Chromosome=1
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AG)
|geno3=(AG;AG)
|Gene=AGL
|position=99851059
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AGL
}}{{omim
|id=610860
|rsnum=113994127
|variant=0004
}}{{ClinVar
|rsid=113994127
|Reversed=0
|FwdREF=AG
|FwdALT=
|REF=CAG
|ALT=C
|RSPOS=99851058
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050160401205000002110200
|GENEINFO=AGL:178
|GENE_NAME=AGL
|GENE_ID=178
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.99851059_99851060delAG
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNSRCID=NM_000642.2:c.17_18delAG; NM_000646.2:c.-175_-174delAG; NBK26372; 610860.0004
|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=RCV000001155.2; RCV000020374.1
|Tags=PM;SLO;NSF;REF;U5;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1968740; NBK26372:C0017922:232400:ORPHA366:66937008
|CLNORIGIN=1
}}