{{Rsnum
|rsid=10518765
|Gene=UNC13C
|Chromosome=15
|position=54388434
|Orientation=plus
|GMAF=0.1387
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=UNC13C
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 61.1 | 36.3 | 2.7
| HCB | 88.1 | 11.9 | 0.0
| JPT | 83.2 | 16.8 | 0.0
| YRI | 89.8 | 9.5 | 0.7
| ASW | 86.0 | 10.5 | 3.5
| CHB | 88.1 | 11.9 | 0.0
| CHD | 88.8 | 11.2 | 0.0
| GIH | 69.3 | 26.7 | 4.0
| LWK | 77.3 | 22.7 | 0.0
| MEX | 60.3 | 36.2 | 3.4
| MKK | 76.9 | 21.2 | 1.9
| TSI | 60.8 | 35.3 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=17903293
|Trait=Select biomarker traits
|Title=Genome-wide association with select biomarker traits in the Framingham Heart Study
|RiskAllele=
|Pval=9.9999999999999995E-7
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto
|PMID=17052657
|Title=Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10518765
|overall_frequency_n=11
|overall_frequency_d=128
|overall_frequency=0.0859375
|n_genomes=8
|n_genomes_annotated=0
|n_haplomes=9
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}