{{Rsnum
|rsid=6151429
|Gene=ARSA
|Chromosome=22
|position=50625049
|Orientation=minus
|GMAF=0.03994
|Gene_s=ARSA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 82.3 | 17.7 | 0.0
| HCB | 92.7 | 7.3 | 0.0
| JPT | 97.3 | 2.7 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 92.7 | 7.3 | 0.0
| CHD | 94.5 | 5.5 | 0.0
| GIH | 82.2 | 17.8 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 94.8 | 5.2 | 0.0
| MKK | 96.2 | 3.8 | 0.0
| TSI | 81.4 | 16.7 | 2.0
| HapMapRevision=28
}}{{ClinVar
|ALT=C
|CAF=0.9601; 0.03994
|CHROM=22
|CLNACC=RCV000003190.1; RCV000020309.1
|CLNALLE=1
|CLNDBN=Arylsulfatase A pseudodeficiency; Metachromatic leukodystrophy
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=CN068604; NBK1130:C0023522:250100:512:396338004
|CLNHGVS=NC_000022.10:g.51063477T>C
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1130; 607574.0001
|COMMON=1
|Disease=Arylsulfatase A pseudodeficiency; Metachromatic leukodystrophy
|FwdALT=G
|FwdREF=A
|GENEINFO=ARSA:410
|GENE_ID=410
|GENE_NAME=ARSA
|REF=T
|RSPOS=51063477
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x050168000000150517110101
|WGT=0
|dbSNPBuildID=114
|rsid=6151429
}}

{{PMID Auto
|PMID=18454203
|Title=Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.
|OA=1
}}

{{PMID Auto
|PMID=24896259
|Title=Genome at Juncture of Early Human Migration: A Systematic Analysis of Two Whole Genomes and Thirteen Exomes from Kuwaiti Population Subgroup of Inferred Saudi Arabian Tribe Ancestry
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}