rs3800569

Parent Gene: ATP6V0A4

Importance: 3
Less common allele: C = 20%
More common allele: T = 80%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Fetal Hemoglobin Measurement

The C allele of rs3800569 is reported to be associated with Fetal Hemoglobin Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with F-cell distribution.

Disease/Trait: Sickle Cell Anemia

The C allele of rs3800569 is reported to be associated with Sickle Cell Anemia (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with F-cell distribution.