{{Rsnum
|rsid=4959270
|Gene=EXOC2
|Chromosome=6
|position=457748
|Orientation=plus
|GMAF=0.3737
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Condition=Hair Color
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 25.7 | 51.3 | 23.0
| HCB | 5.3 | 47.0 | 47.7
| JPT | 12.5 | 49.1 | 38.4
| YRI | 6.2 | 25.3 | 68.5
| ASW | 7.0 | 38.6 | 54.4
| CHB | 5.3 | 47.0 | 47.7
| CHD | 13.2 | 44.3 | 42.5
| GIH | 7.9 | 35.6 | 56.4
| LWK | 0.9 | 21.1 | 78.0
| MEX | 19.0 | 53.4 | 27.6
| MKK | 3.9 | 29.2 | 66.9
| TSI | 26.5 | 44.1 | 29.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=21197618
|Title=Model-based prediction of human hair color using DNA variants
|OA=1
}}
[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3057002/?tool=pubmed] EXOC2 (rs4959270 allelic OR for A vs. C: 0.56; 95% CI: [0.35–0.91]; P = 0.02) were most significantly associated with black hair color .

{{PMID Auto
|PMID=17952075
|Title=Genetic determinants of hair, eye and skin pigmentation in Europeans.
}}[https://uni.hi.is/apalsson/files/2011/10/PM_NG07.pdf]

{{PMID Auto
|PMID=18483556
|Title=A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
|OA=1
}}

{{PMID Auto
|PMID=19340012
|Title=Genome-wide association study of tanning phenotype in a population of European ancestry.
|OA=1
}}

{{PMID Auto
|PMID=20383147
|Title=Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}