{{Rsnum
|rsid=337847
|Gene=ARSB
|Chromosome=5
|position=78964065
|Orientation=plus
|GMAF=0.1405
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ARSB
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 77.9 | 21.2 | 0.9
| HCB | 45.2 | 45.2 | 9.6
| JPT | 39.3 | 47.3 | 13.4
| YRI | 85.6 | 13.7 | 0.7
| ASW | 82.1 | 16.1 | 1.8
| CHB | 45.2 | 45.2 | 9.6
| CHD | 46.3 | 41.7 | 12.0
| GIH | 78.2 | 20.8 | 1.0
| LWK | 90.8 | 8.3 | 0.9
| MEX | 77.6 | 22.4 | 0.0
| MKK | 91.7 | 8.3 | 0.0
| TSI | 89.1 | 9.9 | 1.0
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19668339
|Trait=Hippocampal atrophy
|Title=Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
|RiskAllele=
|Pval=0.000007
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs337847
|overall_frequency_n=109
|overall_frequency_d=128
|overall_frequency=0.851562
|n_genomes=52
|n_genomes_annotated=0
|n_haplomes=91
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}