{{Rsnum
|rsid=74315458
|Chromosome=22
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ARSA
|position=50627374
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ARSA
}}{{omim
|id=607574
|rsnum=74315458
|variant=0010
}}{{ClinVar
|rsid=74315458
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=51065802
|CHROM=22
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=ARSA:410
|GENE_NAME=ARSA
|GENE_ID=410
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.51065802C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000003205.1; RCV000020316.1
|CLNDBN=Metachromatic leukodystrophy, late-onset; Metachromatic leukodystrophy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1130:C0023522:250100:512:396338004
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1130; 607574.0010
|Disease=Metachromatic leukodystrophy; Metachromatic leukodystrophy
}}{{PMID Auto
|PMID=1353340
|Title=Late-onset metachromatic leukodystrophy: molecular pathology in two siblings.
}}

{{PMID Auto
|PMID=15720392
|Title=Missense mutations as a cause of metachromatic leukodystrophy. Degradation of arylsulfatase A in the endoplasmic reticulum.
}}