{{Rsnum
|rsid = 28940893
|Gene = ARSA
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=22
|position=50625392
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ARSA
}}{{omim
|desc=ARYLSULFATASE A, ALLELE A
|id=607574
|rsnum=28940893
|variant=0004
}}
{{ neighbor
| rsid = 28940895
| distance = 54
}}

{{ClinVar
|rsid=28940893
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=51063820
|CHROM=22
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050368000000000402110100
|GENEINFO=ARSA:410
|GENE_NAME=ARSA
|GENE_ID=410
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.51063820G>A
|CLNSRC=Emory University; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=2598; NBK1130; 607574.0004
|CLNSIG=5
|CLNCUI=C0751276; C0751279; C0023522
|CLNDBN=Metachromatic leukodystrophy, juvenile type; Arylsulfatase a, allele a; Metachromatic leukodystrophy, adult type; Metachromatic leukodystrophy; not provided
|Disease=Metachromatic leukodystrophy; Arylsulfatase a; Metachromatic leukodystrophy; Metachromatic leukodystrophy; not provided
|CLNACC=RCV000003195.1; RCV000003196.1; RCV000003197.1; RCV000020314.1; RCV000078940.1
|Tags=RV;PM;PMC;S3D;SLO;HD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0751276:44359008; C0751279:24326000; NBK1130:C0023522:250100:512:396338004
}}

{{PMID Auto
|PMID=1670590
|Title=Molecular basis of different forms of metachromatic leukodystrophy.
}}

{{PMID Auto
|PMID=7866401
|Title=Molecular genetics of metachromatic leukodystrophy.
}}

{{PMID Auto
|PMID=8095918
|Title=Prevalence of common mutations in the arylsulphatase A gene in metachromatic leukodystrophy patients diagnosed in Britain.
}}

{{PMID Auto
|PMID=9090526
|Title=Metachromatic leukodystrophy: identification of the first deletion in exon 1 and of nine novel point mutations in the arylsulfatase A gene.
}}

{{PMID Auto
|PMID=11777924
|Title=Defective oligomerization of arylsulfatase a as a cause of its instability in lysosomes and metachromatic leukodystrophy.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}