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[We found no association of the homozygous 1580A, 1601C, 2166A, and 3507G genotypes with increased risks of melanoma. Exploratory analyses of subgroups of melanoma patients compared to all controls indicated no association of these genotypes with increased risks for development of multiple primary melanomas (n=28), a negative family history for melanoma (n=277), melanomas in individuals with a low number of nevi (n=273), melanomas in individuals older than 55 years (n=142), and melanomas thicker than 1 mm (n=126).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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