{{Rsnum
|rsid=104894553
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ASPA
|position=3476371
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ASPA,SPATA22
}}{{omim
|id=608034
|rsnum=104894553
|variant=0012
}}{{ClinVar
|rsid=104894553
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=3379665
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ASPA:443
|GENE_NAME=ASPA
|GENE_ID=443
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.3379665G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608034.0012
|CLNSIG=5
|CLNCUI=CN068568
|CLNDBN=Canavan disease, mild
|Disease=Canavan disease
|CLNACC=RCV000002734.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN068568
}}