The SNP is associated with the following:

 

  • Fetal hemoglobin levels (P=7.00*10-35) (R)
  • F-cell distribution (P=2.00*10-7) (R).

Incomplete

 

rs11886868

Parent Gene: BCL11A

Importance: 5
Less common allele: T = 48%
More common allele: C = 52%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Fetal Hemoglobin Measurement

The T allele of rs11886868 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 Fetal hemoglobin levels.

Disease/Trait: Fetal Hemoglobin Measurement

rs11886868 is associated with Fetal Hemoglobin Measurement (R) . It is reported to have a 1.07 unit increase on F-cell distribution. No specific risk allele was identified in the study.

Disease/Trait: Sickle Cell Anemia

rs11886868 is associated with Sickle Cell Anemia (R) . It is reported to have a 1.07 unit increase on F-cell distribution. No specific risk allele was identified in the study.

Disease/Trait: Fetal Hemoglobin Measurement

rs11886868 is associated with Fetal Hemoglobin Measurement (R) . It is reported to have a 1.98 unit increase on F-cell distribution. No specific risk allele was identified in the study.

Disease/Trait: Sickle Cell Anemia

rs11886868 is associated with Sickle Cell Anemia (R) . It is reported to have a 1.98 unit increase on F-cell distribution. No specific risk allele was identified in the study.