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rs1569328

Parent Gene: FOS

Importance: 3
Less common allele: T = 11%
More common allele: C = 89%
My Genotype: Log In
Risk Allele: G, A

Disease/Trait: Crohn's Disease

rs1569328 is associated with Crohn's Disease (R). It is reported to association with Crohn's disease. No specific risk allele was identified in the study.

Disease/Trait: Inflammatory Bowel Disease

The G allele of rs1569328 is reported to be associated with Inflammatory Bowel Disease (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Inflammatory bowel disease (EA).

Disease/Trait: Crohn's Disease

The A allele of rs1569328 is reported to be associated with Crohn's Disease (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Crohn's disease (EA).