[PMID 25837821] Inherited genetic variants associated with occurrence of multiple primary melanoma rs45430 Parent Gene: MX2 Importance: 4 Less common allele: C = 48% More common allele: T = 52% My Genotype: Log In Risk Allele: T Disease/Trait: Melanoma rs45430 is associated with Melanoma (R) . It is reported to increased association with Melanoma. No specific risk allele was identified in the study. Disease/Trait: Melanoma The T allele of rs45430 is reported to be associated with Melanoma (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Melanoma.