Family Planning Panel
$29.00
/
Whole Genome Sequencing 30X
This product is only meant for customers who already purchased a Dante Genome Test
Family Planning Panel is used to identify genetic variants associated with various inherited diseases, including cystic fibrosis, Tay-Sachs disease, and sickle cell anemia, among others. The panel tests for known pathogenic variants in a wide range of genes and can provide information on carrier status.
This panel is recommended for individuals planning to start a family, particularly those of certain ethnic backgrounds with a higher risk of carrying specific genetic variants. Testing can help identify carrier status and inform family planning decisions, such as preimplantation genetic diagnosis or prenatal testing. It can also 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:
Family Planning Panel is used to identify genetic variants associated with various inherited diseases, including cystic fibrosis, Tay-Sachs disease, and sickle cell anemia, among others. The panel tests for known pathogenic variants in a wide range of genes and can provide information on carrier status.
This panel is recommended for individuals planning to start a family, particularly those of certain ethnic backgrounds with a higher risk of carrying specific genetic variants. Testing can help identify carrier status and inform family planning decisions, such as preimplantation genetic diagnosis or prenatal testing. It can also 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 290 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Fertility, Infertility
- Pregnancy loss
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