{{Rsnum
|rsid=199533
|Gene=NSF
|Chromosome=17
|position=46751565
|Orientation=minus
|GMAF=0.1084
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NSF
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 61.9 | 37.2 | 0.9
| HCB | 100.0 | 0.0 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 84.2 | 15.8 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 84.2 | 13.9 | 2.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 74.1 | 20.7 | 5.2
| MKK | 92.9 | 5.8 | 1.3
| TSI | 50.0 | 38.2 | 11.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19915575
|Trait=Parkinson's disease
|Title=Genome-wide association study reveals genetic risk underlying Parkinson's disease
|RiskAllele=T
|Pval=1E-14
|OR=1.28
|ORtxt=[NR]
|OA=1
}}

{{PMID Auto GWAS
|PMID=20711177
|Trait=None
|Title=Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
|RiskAllele=C
|Pval=0.000001
|OR=1.35
|ORtxt=[1.19-1.52]
|OA=1
}}

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