{{Rsnum
|rsid=976683
|Gene=NLGN1
|Chromosome=3
|position=173767581
|Orientation=minus
|GMAF=0.4601
|Gene_s=NLGN1
|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 | 53.6 | 40.2 | 6.2
| HCB | 12.5 | 46.3 | 41.2
| JPT | 13.3 | 42.5 | 44.2
| YRI | 14.3 | 42.9 | 42.9
| ASW | 15.8 | 52.6 | 31.6
| CHB | 12.5 | 46.3 | 41.2
| CHD | 9.2 | 45.0 | 45.9
| GIH | 16.8 | 52.5 | 30.7
| LWK | 12.7 | 50.9 | 36.4
| MEX | 36.2 | 51.7 | 12.1
| MKK | 18.1 | 43.9 | 38.1
| TSI | 47.1 | 43.1 | 9.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=23929743
|Title=Genome-Wide Analysis of Blood Pressure Variability and Ischemic Stroke
}}

{{PMID Auto
|PMID=20070850
|Title=Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
|OA=1
}}

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