rs191164795
This variant is located in the SLC45A2 gene.
▶ClinVar annotation
Likely Benign★☆☆☆
1 submitter1 publicationAbout SLC45A2
This gene encodes a transporter protein that mediates melanin synthesis. The protein is expressed in a high percentage of melanoma cell lines. Mutations in this gene are a cause of oculocutaneous albinism type 4, and polymorphisms in this gene are associated with variations in skin and hair color. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
View all SLC45A2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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