{{Rsnum
|rsid=80338819
|Chromosome=22
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ARSA
|position=50626676
|Gene_s=ARSA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=22
|CLNACC=RCV000020322.1
|CLNALLE=1
|CLNDBN=Metachromatic leukodystrophy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1130:C0023522:250100:512:396338004
|CLNHGVS=NC_000022.10:g.51065104C>G
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1130
|Disease=Metachromatic leukodystrophy
|FwdALT=C
|FwdREF=G
|GENEINFO=ARSA:410
|GENE_ID=410
|GENE_NAME=ARSA
|REF=C
|RSPOS=51065104
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=131
|rsid=80338819
}}{{PMID Auto
|PMID=15720392
|Title=Missense mutations as a cause of metachromatic leukodystrophy. Degradation of arylsulfatase A in the endoplasmic reticulum.
}}