{{Rsnum
|rsid=82625
|Chromosome=10
|position=115756130
|Orientation=minus
|GMAF=0.06703
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.8 | 10.6 | 87.6
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 3.4 | 37.9 | 58.6
| ASW | 5.3 | 28.1 | 66.7
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 0.0 | 0.0
| LWK | 4.5 | 21.8 | 73.6
| MEX | 0.0 | 7.0 | 93.0
| MKK | 2.6 | 19.2 | 78.2
| TSI | 0.0 | 8.8 | 91.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22388998
|Trait=None
|Title=Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation.
|RiskAllele=
|Pval=0.000002
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}