[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.