Female infertility Panel
Female infertility Panel
Prix habituel
€29.00 EUR
Prix habituel
Prix soldé
€29.00 EUR
Prix unitaire
par
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This product is only meant for customers who already purchased a MyGenome Test
The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major female infertility conditions
Female infertility panel is used to identify genetic variants associated with female infertility, which can be caused by a variety of factors, including hormonal imbalances, structural abnormalities, and genetic mutations. This panel tests for genetic variants that are known to affect reproductive function, such as genes involved in follicle development, hormone production, and oocyte maturation.
This panel is designed for women who are experiencing difficulty conceiving or who have a family history of infertility. Genetic testing can provide information on the underlying causes of infertility, as well as inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
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The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major female infertility conditions
Female infertility panel is used to identify genetic variants associated with female infertility, which can be caused by a variety of factors, including hormonal imbalances, structural abnormalities, and genetic mutations. This panel tests for genetic variants that are known to affect reproductive function, such as genes involved in follicle development, hormone production, and oocyte maturation.
This panel is designed for women who are experiencing difficulty conceiving or who have a family history of infertility. Genetic testing can provide information on the underlying causes of infertility, as well as inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 120 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Autoimmune Polyendocrine Syndrome
- Primary Ciliary Dyskinesia
- Pituitary Hormone Deficiency
Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.