{{Rsnum
|rsid=10121009
|Gene=UNC13B
|Chromosome=9
|position=35269822
|Orientation=plus
|GMAF=0.3485
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=UNC13B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 63.0 | 31.5 | 5.6
| HCB | 33.3 | 47.4 | 19.3
| JPT | 36.7 | 43.1 | 20.2
| YRI | 19.0 | 46.3 | 34.7
| ASW | 22.8 | 63.2 | 14.0
| CHB | 33.3 | 47.4 | 19.3
| CHD | 26.4 | 50.9 | 22.6
| GIH | 60.0 | 33.0 | 7.0
| LWK | 21.3 | 46.3 | 32.4
| MEX | 54.5 | 41.8 | 3.6
| MKK | 41.9 | 43.2 | 14.8
| TSI | 58.0 | 39.0 | 3.0
| 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=A
|Pval=0.000003
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=18633107
|Title=G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes.
|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}}
{{on chip | NatGeo2}}