{{Rsnum
|rsid=113994133
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=AGL
|position=99916587
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AGL,LOC101930120
}}{{omim
|id=610860
|rsnum=113994133
|variant=0006
}}{{ClinVar
|rsid=113994133
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=99916587
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050160080005000002110100
|GENEINFO=LOC101930120:101930120; AGL:178
|GENE_NAME=LOC101930120; AGL
|GENE_ID=101930120; 178
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.99916398A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK26372; 610860.0006
|CLNSIG=5
|CLNCUI=CN068470; CN068469; C0017922
|CLNDBN=Glycogen storage disease IIIb; Glycogen storage disease IIIa; Glycogen storage disease type III
|Disease=Glycogen storage disease IIIb; Glycogen storage disease IIIa; Glycogen storage disease type III
|CLNACC=RCV000001157.2; RCV000001158.2; RCV000020379.1
|Tags=PM;SLO;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1968740; C1968739; NBK26372:C0017922:232400:ORPHA366:66937008
|CLNORIGIN=1
}}