A prenatal paternity test checks for a match between the potential parent’s DNA and your baby while you’re still pregnant. To determine paternity, DNA is taken from the mother and potential father and examined with a series of lab tests called DNA sequencing.
Noninvasive prenatal paternity tests are available at laboratories. For people in the U.S., the American Pregnancy Association recommends labs with accreditation from The American Association of Blood Banks (AABB) because they meet high standards for testing performance.
Chorionic villus sampling (CVS) and amniocentesis tests are normally done at a health care provider’s office or an outpatient facility and sent to a lab for analysis.
The cost of a DNA test while you’re pregnant varies depending on the type of test. In the U.S., amniocentesis or CVS testing can cost over $500, while non-invasive tests are more expensive — around $1350 to $1750 depending on how quickly you want the results. Health insurance companies usually don’t cover this cost.
These tests are extremely precise. They show with 99.9 percent accuracy whether a male is the parent of the baby.
People who want to take a paternity test before birth have three options.
From week seven of pregnancy through the first trimester, you can get a noninvasive prenatal paternity test. During this test, DNA is collected from the mother by a blood draw and from the father with a cheek swab. The samples are analyzed to compare the baby’s and possible father’s DNA. In general, results are available after one week.
However, this test is not available for women carrying twins because the current technology can’t isolate DNA from both fetuses.
In this procedure, a small tissue sample is taken from the placenta through the cervix or abdomen. The sample is then compared to the potential father’s DNA. Generally, the test occurs between weeks 11 and 14 of pregnancy. Results can take several weeks.
Unlike NIPP, this invasive sampling procedure does pose a risk to the baby.
CVS can indicate whether a baby has a chromosomal condition like Down syndrome or genetic disorders like cystic fibrosis.
During amniocentesis, amniotic fluid is drawn with a needle from the pregnant parent’s abdomen. Then, the fluid sample is compared in a lab to DNA taken from the pregnant parent and potential father. This test typically takes place from weeks 15 to 20 of pregnancy. The results may not be available for several weeks.
Like CVS, this invasive sampling procedure does pose a risk to the baby.
You may prefer CVS or amniocentesis if:
Noninvasive prenatal paternity tests are considered by experts to be highly accurate and completely safe for both the pregnant parent and baby.
Amniocentesis and chorionic villus sampling are invasive paternity tests that carry more risks. Unless they’re needed to diagnose a severe genetic disorder, they are not usually recommended by health care providers.
Potential risks of chorionic villus sampling include:
Additionally, if you have any of the following conditions, your health care provider may recommend avoiding CVS:
After CVS, if you experience fluid leaking from your vagina, heavy vaginal bleeding, a fever, or contractions in your uterus, contact a health care provider right away.
Potential risks of amniocentesis can involve:
Prenatal paternity tests can help you get answers to important questions while you’re still pregnant. Consider your options and speak to your health care provider about which option suits your goals.
