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Jun 23, 2023 · Carrier screening determines if a person carries a nonworking copy of a gene associated with a specific genetic condition. People with one working copy and one nonworking copy of a gene are referred to as a "carrier" for the condition.
Oct 19, 2023 · People with one working copy and one nonworking copy of a gene are referred to as a "carrier" for the condition. They are typically not affected by the condition themselves.
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Are You a carrier of more than one genetic condition?
What does it mean to be a carrier for a genetic condition?
What is a carrier if a gene is not working?
Do you carry a gene for a genetic disorder?
If a result indicates that you carry a genetic condition, carrier screening will be offered for the other biological parent. If both parents are found to be carriers of the same condition, you'll be referred to the UCSF Prenatal Diagnostic Center to speak with a genetic counselor.
Since being a carrier for one or more genetic conditions is very common, anyone who is pregnant or planning to become pregnant should consider having genetic carrier screening. The results can provide you with important information about your chances to have a child with certain genetic conditions.
If you belong to an ethnic group or race that has a high rate of carriers for a specific genetic disorder, carrier screening for these disorders may be recommended. This also is called ethnic-based carrier screening.
Aug 21, 2019 · If you and your partner are both found to be carriers for the same genetic condition, there is a 25% (or 1 in 4) chance that the baby will inherit a nonworking copy of the gene from both parents.
Dec 19, 2022 · If you have a mutation in one of your own two sets of genes, you’re what’s known as a carrier: You’re carrying the genes for a genetic disorder but have no signs of the disease. Rarely, a condition (like Huntington’s disease) can be caused by a mutation in just one parent's genes.
