OMIM | 227240 |
Desc | SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5; SHEP5 |
Variant | |
Related | also |
OMIM | 606202 |
Desc | SOLUTE CARRIER FAMILY 45, MEMBER 2; SLC45A2 |
Variant | |
Related | also |
[PMID 17358008] Promoter polymorphisms in the MATP (SLC45A2) gene are associated with normal human skin color variation.
[PMID 18483556] A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
[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.