Carrier Sickle Cell Anemia

Based on your genetics, your genetic predisposition for Sickle Cell Anemia is

Negative
Negative
Positive

What does this mean?

 Your genotype indicates that you do not carry the genetic mutation of Sickle cell anemia.

How Is Your Genetic Risk Calculated?

This result is based on the SNPs(single nucleotide polymorphism)that are associated with Sickle Cell Anemia.

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Limitations

This report does not diagnose any health conditions or provide medical advice. This should not be used as a diagnostic tool.
This result is limited to existing scientific research.
Please consult with a healthcare professional before making any major lifestyle changes or if you have any other concerns about your results.

What is Sickle Cell Anemia?

Sickle cell disease (SCD) is a group of inherited red blood cells disorders. People with this disorder have distorted red blood cells into a sickle, or crescent, shape. The abnormal hemoglobin causes red blood cells to become rigid, sticky and misshapen. The sickle cell gene is passed from generation to generation in a pattern of inheritance called autosomal recessive inheritance. SCD pathophysiology is extremely complex and can lead to numerous clinical complications, including painful vaso-occlusive crisis (VOC), end-organ damage, and a shortened lifespan.

Possible Inheritance Modes for Sickle Cell Anemia

There is one inheritance mode of Sickle Cell Anemia. Inheritance mode is how a gene will be passed down from parent to offspring.

Autosomal Recessive

The mutated gene is a recessive gene located on one of the non-sex chromosomes (autosomes). You can get the disease if inheritance both copies of abnormal mutation from your parent.

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