The SNP is associated with the following:

 

 

  • Melanoma (P=9.00*10-10) (R).
  • Esophageal squamous cell carcinoma (P=4.00*10-13) (R).

rs13016963

Parent Gene: ALS2CR12, CASP8

Importance: 3
Less common allele: A = 36%
More common allele: G = 64%
My Genotype: Log In
Risk Allele: A, A

Disease/Trait: Esophageal Squamous Cell Carcinoma

The A allele of rs13016963 is reported to be associated with Esophageal Squamous Cell Carcinoma (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Esophageal squamous cell carcinoma.