rs3784262

Parent Gene: ALDH1A2

Importance: 3
Less common allele: C = 27%
More common allele: T = 73%
My Genotype: Log In
Risk Allele: A, A

Disease/Trait: Barrett's Esophagus

The A allele of rs3784262 is reported to be associated with Barrett's Esophagus (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined).

Disease/Trait: Esophageal Adenocarcinoma

The A allele of rs3784262 is reported to be associated with Esophageal Adenocarcinoma (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined).

Disease/Trait: Digestive System Disease

The A allele of rs3784262 is reported to be associated with Digestive System Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined).

Disease/Trait: Barrett's Esophagus

The A allele of rs3784262 is reported to be associated with Barrett's Esophagus (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Barrett's esophagus.