{{Rsnum
|rsid=11986414
|Chromosome=8
|position=1798784
|Orientation=plus
|GMAF=0.2677
|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 | 4.4 | 31.0 | 64.6
| HCB | 9.5 | 38.7 | 51.8
| JPT | 12.4 | 45.1 | 42.5
| YRI | 2.1 | 19.2 | 78.8
| ASW | 1.8 | 8.8 | 89.5
| CHB | 9.5 | 38.7 | 51.8
| CHD | 12.8 | 44.0 | 43.1
| GIH | 5.0 | 27.7 | 67.3
| LWK | 0.9 | 11.0 | 88.1
| MEX | 19.0 | 41.4 | 39.7
| MKK | 3.8 | 19.9 | 76.3
| TSI | 5.9 | 29.4 | 64.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=22388998
|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
|OA=1
}}

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