{{Rsnum
|rsid=386833434
|Chromosome=4
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=AGA
|position=177434418
|Gene_s=AGA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=4
|CLNACC=RCV000049362.1
|CLNALLE=1
|CLNDBN=Aspartylglycosaminuria
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0268225:208400:93
|CLNHGVS=NC_000004.11:g.178355572G>A
|CLNSIG=4
|Disease=Aspartylglycosaminuria
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=178355572
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833434
|GENEINFO=AGA:175
|GENE_ID=175
|GENE_NAME=AGA
}}{{PMID Auto
|PMID=11309371
|Title=Molecular pathogenesis of a disease: structural consequences of aspartylglucosaminuria mutations.
}}