{{Rsnum
|rsid=113994128
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=AGL
|position=99875394
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AGL
}}{{omim
|id=610860
|rsnum=113994128
|variant=0013
}}{{ClinVar
|rsid=113994128
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=99875394
|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.99875394C>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000642.2:c.1222C>T; NBK26372; 610860.0013
|CLNSIG=5
|CLNCUI=CN068469; C0017922
|CLNDBN=Glycogen storage disease IIIa; Glycogen storage disease type III
|Disease=Glycogen storage disease IIIa; Glycogen storage disease type III
|CLNACC=RCV000001165.2; RCV000020372.1
|Tags=PM;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1968739; NBK26372:C0017922:232400:ORPHA366:66937008
}}