{{Rsnum
|rsid=183211
|Gene=NSF
|Chromosome=17
|position=46710944
|Orientation=plus
|GMAF=0.4146
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NSF
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 2.7 | 38.9 | 58.4
| HCB | 40.4 | 45.6 | 14.0
| JPT | 54.0 | 38.9 | 7.1
| YRI | 17.1 | 47.3 | 35.6
| ASW | 29.8 | 40.4 | 29.8
| CHB | 40.4 | 45.6 | 14.0
| CHD | 39.4 | 43.1 | 17.4
| GIH | 2.0 | 23.8 | 74.3
| LWK | 19.1 | 41.8 | 39.1
| MEX | 22.4 | 48.3 | 29.3
| MKK | 12.8 | 42.3 | 44.9
| TSI | 13.9 | 44.6 | 41.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21812969
|Trait=None
|Title=Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
|RiskAllele=T
|Pval=3E-7
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23544013
  |Trait=Ovarian cancer in BRCA1 mutation carriers
  |Title=Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
  |RiskAllele=A
  |Pval=3E-8
  |OR=1.25
  |ORtxt=[1.16-1.35]
  |OA=1
}}

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