Although the rs26722(T) alllele is relatively rare, at least statistically it seems to be associated with darker eye, hair, and skin color, all other things being equal.[PMID 15714523]




[PMID 17999355] A genomewide association study of skin pigmentation in a South Asian population.

[PMID 18483556] A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.

[PMID 18806926] Association of the SLC45A2 gene with physiological human hair colour variation.

[PMID 19340012] Genome-wide association study of tanning phenotype in a population of European ancestry.

[PMID 19384953] Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians.

[PMID 20042077] Genetic determinants of hair and eye colours in the Scottish and Danish populations.




[PMID 23100201] A single-nucleotide polymorphism (SNP) multiplex system: the association of five SNPs with human eye and hair color in the Slovenian population and comparison using a Bayesian network and logistic regression model

rs26722

Parent Gene: SLC45A2

Importance: 1
Less common allele: T = 18%
More common allele: C = 82%
My Genotype: Log In