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Hypomorphic MC1R variants are the most prevalent genetic determinants of melanoma risk in the Caucasian population. However, the genetic background of wild‐type (WT) MC1R melanoma patients is poorly studied. To analyse the role of candidate common genetic variants on the melanoma risk and the naevi count in Spanish wild‐type MC1R melanoma patients. The present data suggest epistatic interaction among common variants related to melanocyte biology or pro‐inflammatory pathways might influence melanocytic proliferation in MC1R‐WT individuals.
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