rs738722

Parent Gene: CHEK2

Importance: 3
Less common allele: T = 30%
More common allele: C = 70%
My Genotype: Log In
Risk Allele: T, T, T

Disease/Trait: Esophageal Carcinoma

The T allele of rs738722 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 and gastric cancer (ESCC).

Disease/Trait: Optic Cup Area Measurement

The T allele of rs738722 is reported to be associated with Optic Cup Area Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Optic cup area (EA).

Disease/Trait: Optic Cup Area Measurement

The T allele of rs738722 is reported to be associated with Optic Cup Area Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Optic cup area.