rs4822983

Parent Gene: CHEK2

Importance: 2
Less common allele: T = 28%
More common allele: C = 72%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Esophageal Carcinoma

The T allele of rs4822983 is reported to be associated with Esophageal Carcinoma (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Esophageal cancer (squamous cell).

Disease/Trait: Squamous Cell Carcinoma

The T allele of rs4822983 is reported to be associated with Squamous Cell Carcinoma (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Esophageal cancer (squamous cell).