{{Rsnum
|rsid=118203964
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=AGL
|position=99916492
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AGL,LOC101930120
}}{{omim
|id=610860
|rsnum=118203964
|variant=0009
}}{{ClinVar
|rsid=118203964
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=99916492
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060080a05000002110100
|GENEINFO=LOC101930120:101930120; AGL:178
|GENE_NAME=LOC101930120; AGL
|GENE_ID=101930120; 178
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.99916492G>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000642.2:c.4342G>C; 610860.0009
|CLNSIG=5
|CLNCUI=CN068469
|CLNDBN=Glycogen storage disease IIIa
|Disease=Glycogen storage disease IIIa
|CLNACC=RCV000001161.2
|Tags=PM;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1968739
}}