Carrier Severe Combined Immunodeficiency Disease

Based on your genetics, your genetic predisposition for Severe Combined Immunodeficiency Disease is

Negative
Negative
Positive

What does this mean?

 Your genotype indicates that you do not carry the genetic mutation of Severe combined immunodeficiency disease.

How Is Your Genetic Risk Calculated?

This result is based on the SNPs(single nucleotide polymorphism)that are associated with Severe Combined Immunodeficiency Disease.

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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 Severe Combined Immunodeficiency Disease?

Severe combined immunodeficiencies (SCID) are a group of inherited disorders characterized by various abnormalities in the development and function of three specific types of white blood cells (T cells, B cells, and natural killer (NK) cells) that are involved in the immune system. Infants with SCID appear healthy at birth but are highly susceptible to severe infections. SCID may be caused by mutations in any of several genes and are usually inherited in an X-linked recessive (primarily affects male infants) or autosomal recessive manner.

Signs and Symptoms

Possible Inheritance Modes for Severe Combined Immunodeficiency Disease

There is one inheritance mode of Severe Combined Immunodeficiency Disease. 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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