{{Rsnum
|rsid=104894548
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ASPA
|position=3483520
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ASPA,SPATA22
}}{{omim
|id=608034
|rsnum=104894548
|variant=0002
}}{{ClinVar
|rsid=104894548
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=3386814
|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.3386814T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608034.0002
|CLNSIG=5
|CLNCUI=C0206307
|CLNDBN=Spongy degeneration of central nervous system
|Disease=Spongy degeneration of central nervous system
|CLNACC=RCV000002724.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1234:C0206307:271900:141:80544005
}}