{{Rsnum
|rsid=199476371
|Chromosome=22
|Orientation=minus
|geno1=(CT;CT)
|geno2=(CT;TC)
|geno3=(TC;TC)
|Gene=ARSA
|position=50627338
|Gene_s=ARSA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199476371
|Reversed=1
|FwdREF=TC
|FwdALT=CT
|REF=GGA
|ALT=GAG
|RSPOS=51065765
|CHROM=22
|dbSNPBuildID=136
|SSR=0
|SAO=0
|VP=0x050368000000000002110800
|WGT=0
|VC=MNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.51065766_51065767delGAinsAG
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000003208.1; RCV000058959.1
|CLNDBN=Metachromatic leukodystrophy, severe; not provided
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=607574.0014; VAR_007249
|Disease=Metachromatic leukodystrophy; not provided
|GENEINFO=ARSA:410
|GENE_ID=410
|GENE_NAME=ARSA
}}{{PMID Auto
|PMID=7825603
|Title=Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic area.
|OA=1
}}