Genotype testing identifies specific genetic variations. For instance, testing for sickle cell anemia involves determining if a person has two copies of the abnormal hemoglobin gene.
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Genotype testing identifies specific genetic variations. For instance, testing for sickle cell anemia involves determining if a person has two copies of the abnormal hemoglobin gene.
The genotype test determines an individual's genetic makeup regarding specific inherited traits or genetic conditions. It identifies genetic variations that can influence susceptibility to certain diseases or conditions.
A genotype test is crucial for understanding the risk of inheriting or passing on genetic conditions. It aids in family planning decisions and allows healthcare providers to provide tailored guidance or interventions based on genetic predispositions.
A genotype test can screen for various genetic conditions, including sickle cell disease, thalassemia, cystic fibrosis, and others. It helps assess the risk of inheriting these conditions and guides preventive measures or treatment plans.
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