DNA PATERNITY TESTING

Getting an early gender DNA test can be a fun activity for you, your family and friends! Especially as you make plans and get ready for your new baby. Our Gender Reveal test analyzes a simple blood draw sample to determine the gender of your unborn child. Gender Reveal testing is recommended as early as 8 weeks into pregnancy. This test can only be used for single pregnancies. This non-invasive prenatal test (NIPT) test has accuracy above 99%. This test analyzes the fetal DNA that circulates in maternal blood.

DNA testing can be used to determine if there is a biological relationship between two individuals. This is typically done by obtaining genetic material (DNA samples) from the two individuals via cheek swabs, then comparing these samples. 

A paternity test is used to determine if someone is the biological father of a child. It works by comparing the DNA of the alleged father to the DNA of the child. If possible, it is preferred to have the child’s mother participate in the Paternity Test as well, since she contributed 50% of her DNA to the child. 

This is an informational Paternity Test. Informational Paternity Test results cannot be used for any type of legal purpose, such as adding or removing a father’s name from the child’s birth certificate, child support, visitation, or other types of legal/verified situations. If you are not planning to use these test results for any type of legal reason, then this test can provide you answers and peace of mind. If you are looking for a Paternity Test that can be used for legal/other purposes, check out the Paternity Legal Test.

All tested parties may schedule an appointment or walk into one of our locations for testing. Our friendly Medical Assistants will collect the samples needed for the test. As an alternative, some store locations offer Home Collection Kits. If the Home Collection Kits are available for online purchase at your selected store, you will see a “Buy At Home Kit” button on this page. After you complete your purchase, a kit will be sent to the address(es) you designate and you can collect the samples yourself, then ship them directly to the lab for testing. 

The basic test kit contains collection supplies for 1 child and 1 alleged father. Test results from the Home Collection Kits are not legally admissible.

DNA testing can be used to determine if there is a biological relationship between two individuals. This is typically done by obtaining genetic material (DNA samples) from the two individuals via cheek swabs, then comparing these samples. 

A paternity test is used to determine if someone is the biological father of a child. It works by comparing the DNA of the alleged father to the DNA of the child. If possible, it is preferred to have the child’s mother participate in the Paternity Test as well, since she contributed 50% of her DNA to the child. 

The results from this paternity test can be used for legal purposes. Examples of legal settings that may require this type of test include (but are not limited to): 

• Adding or removing a father’s name from the child’s birth certificate
• Child support
• Adoption
• Child custody or visitation
• Medical, Social Security, or Military benefits
• Other types of legal/verified situations

If you are just looking for a Paternity Test that can provide answers and peace of mind, and you are not planning to use the results for any kind of legal purpose, check out the Informational Paternity Test (keep in mind that the results from the Informational Paternity Test are not legally admissible).

DNA testing can be used to determine if there is a biological relationship between two individuals. This is typically done by obtaining genetic material (DNA samples) from the two individuals, then comparing these samples. 

The Non-Invasive Prenatal Paternity Test can be used to determine the biological father of a child before the child is born. It requires a blood sample from the mother and a cheek swab from the alleged father. The fetal DNA is then separated from the mother’s DNA to create a DNA profile for the fetus. The DNA profile of the fetus is then tested against the alleged father’s DNA profile. This test can be performed at 7 weeks of pregnancy or later. 

The results from this non-invasive prenatal paternity test can be used for legal purposes.

DNA testing can be used to determine if there is a biological relationship between two individuals. This is typically done by obtaining genetic material (DNA samples) from the two individuals via cheek swabs, then comparing these samples. 

A maternity test is used to determine if someone is the biological mother of a child. It works by comparing the DNA of the alleged mother to the DNA of the child. 

This is an informational Maternity Test. Informational Maternity Test results cannot be used for any type of legal purpose. If you are not planning to use these test results for any type of legal reason, then this test can provide you answers and peace of mind. If you are looking for a Maternity Test that can be used for legal/other purposes, check out the Maternity Legal Test.

DNA testing can be used to determine if there is a biological relationship between two individuals. This is typically done by obtaining genetic material (DNA samples) from the two individuals via cheek swabs, then comparing these samples. 

A maternity test is used to determine if someone is the biological mother of a child. It works by comparing the DNA of the alleged mother to the DNA of the child. 

The results from this maternity test can be used for legal purposes. Examples of legal settings that may require this type of test include (but are not limited to): 

• Birth certificate issues
• Adoption
• Child custody or visitation
• Medical, Social Security, or Military benefits
• Other types of legal/verified situations

If you are just looking for a Maternity Test that can provide answers and peace of mind, and you are not planning to use the results for any kind of legal purpose, check out the Informational Maternity Test (keep in mind that the results from the Informational Maternity Test are not legally admissible).

DNA testing can be used to determine if there is a biological relationship between two individuals. This is typically done by obtaining genetic material (DNA samples) from the two individuals via cheek swabs, then comparing these samples. 

The Grandparent DNA Test (also called a Grandparentage Test) can be used to determine the likelihood of a child being your biological grandchild. This test compares the DNA from a child to the DNA of their biological mother, as well as the DNA from at least one biological paternal grandparent. This type of testing can be useful when an alleged father is unable or unwilling to participate in a paternity test.

Since the alleged father inherited half of his DNA from his mother (the child’s paternal grandmother) and half of his DNA from his father (the child’s paternal grandfather), it is preferable to include both biological paternal grandparents in this type of DNA family relationship test.

**Please note:  If both biological paternal grandparents and the child’s mother are not included in the Grandparent DNA Test, the test results may not always be conclusive.

This is an informational Grandparentage Test. Informational Grandparentage Test results cannot be used for any type of legal purpose. If you are not planning to use these test results for any type of legal reason, then this test can provide you answers and peace of mind. If you are looking for a Grandparentage Test that can be used for legal/other purposes, check out the Grandparentage Legal Test.

DNA testing can be used to determine if there is a biological relationship between two individuals. This is typically done by obtaining genetic material (DNA samples) from the two individuals via cheek swabs, then comparing these samples. 

The Grandparent DNA Test (also called a Grandparentage Test) can be used to determine the likelihood of a child being your biological grandchild. This test compares the DNA from a child to the DNA of their biological mother, as well as the DNA from at least one biological paternal grandparent. This type of testing can be useful when an alleged father is unable or unwilling to participate in a paternity test.

Since the alleged father inherited half of his DNA from his mother (the child’s paternal grandmother) and half of his DNA from his father (the child’s paternal grandfather), it is preferable to include both biological paternal grandparents in this type of DNA family relationship test.

**Please note:  If both biological paternal grandparents and the child’s mother are not included in the Grandparent DNA Test, the test results may not always be conclusive.

The results from this grandparentage test can be used for legal purposes. If you are just looking for a Grandparentage Test that can provide answers and peace of mind, and you are not planning to use the results for any kind of legal purpose, check out the Informational Grandparentage Test (keep in mind that the results from the Informational Grandparentage Test are not legally admissible).

DNA testing can be used to determine if there is a biological relationship between two individuals. This is typically done by obtaining genetic material (DNA samples) from the two individuals via cheek swabs, then comparing these samples. 

The Siblingship DNA Test compares the DNA from the sibling in question, a shared biological mother or father, and one or more known full or half-siblings to determine the likelihood of the unknown sibling being a full sibling, a half sibling, or unrelated.

**Please note: If a known parent is not included in the Siblingship DNA Test, the test results may not always be conclusive.

This is an informational Siblingship Test. Informational Siblingship Test results cannot be used for any type of legal purpose. If you are not planning to use these test results for any type of legal reason, then this test can provide you answers and peace of mind. If you are looking for a Siblingship Test that can be used for legal/other purposes, check out the Siblingship Legal Test.

DNA testing can be used to determine if there is a biological relationship between two individuals. This is typically done by obtaining genetic material (DNA samples) from the two individuals via cheek swabs, then comparing these samples. 

The Siblingship DNA Test compares the DNA from the sibling in question, a shared biological mother or father, and one or more known full or half-siblings to determine the likelihood of the unknown sibling being a full sibling, a half sibling, or unrelated.

**Please note: If a known parent is not included in the Siblingship DNA Test, the test results may not always be conclusive.

The results from this siblingship test can be used for legal purposes. If you are just looking for a Siblingship Test that can provide answers and peace of mind, and you are not planning to use the results for any kind of legal purpose, check out the Informational Siblingship Test (keep in mind that the results from the Informational Siblingship Test are not legally admissible).

Genes are passed down from parents to their children. Your genes determine your traits, such as eye color, hair color, blood type, height, and more. Your genes (in addition to other factors, such as age, weight, liver/kidney function, and more) can also affect how you respond to certain medications. 

This is because your genes determine the rate at which you metabolize, or “break down”, different medications. Poor metabolizers and intermediate metabolizers break down medications slowly, so they may experience side effects with standard doses. Extensive metabolizers break down medications at a normal rate, so they are less likely to experience side effects at standard doses. Ultra-rapid metabolizers break down medications rapidly, so they may not get enough medication at standard doses.

Pharmacogenetic testing (also known as “pharmacogenomic testing” or “PGx”) is an exciting tool that can predict how you might respond to certain medications based on your genetic makeup. The Addiction PGx Panel analyzes genes associated with specific medications that are commonly prescribed to treat disorders related to addiction.

Genes are passed down from parents to their children. Your genes determine your traits, such as eye color, hair color, blood type, height, and more. Your genes (in addition to other factors, such as age, weight, liver/kidney function, and more) can also affect how you respond to certain medications. 

This is because your genes determine the rate at which you metabolize, or “break down”, different medications. Poor metabolizers and intermediate metabolizers break down medications slowly, so they may experience side effects with standard doses. Extensive metabolizers break down medications at a normal rate, so they are less likely to experience side effects at standard doses. Ultra-rapid metabolizers break down medications rapidly, so they may not get enough medication at standard doses.

Pharmacogenetic testing (also known as “pharmacogenomic testing” or “PGx”) is an exciting tool that can predict how you might respond to certain medications based on your genetic makeup. The ADHD PGx Panel analyzes different genes associated with specific medications that are commonly prescribed to treat ADHD.

Genes are passed down from parents to their children. Your genes determine your traits, such as eye color, hair color, blood type, height, and more. Your genes (in addition to other factors, such as age, weight, liver/kidney function, and more) can also affect how you respond to certain medications. 

This is because your genes determine the rate at which you metabolize, or “break down”, different medications. Poor metabolizers and intermediate metabolizers break down medications slowly, so they may experience side effects with standard doses. Extensive metabolizers break down medications at a normal rate, so they are less likely to experience side effects at standard doses. Ultra-rapid metabolizers break down medications rapidly, so they may not get enough medication at standard doses.

Pharmacogenetic testing (also known as “pharmacogenomic testing” or “PGx”) is an exciting tool that can predict how you might respond to certain medications based on your genetic makeup. The Mental Health PGx Panel analyzes different genes associated with specific medications that are commonly prescribed to treat mental health conditions.

Genes are passed down from parents to their children. Your genes determine your traits, such as eye color, hair color, blood type, height, and more. Your genes (in addition to other factors, such as age, weight, liver/kidney function, and more) can also affect how you respond to certain medications. 

This is because your genes determine the rate at which you metabolize, or “break down”, different medications. Poor metabolizers and intermediate metabolizers break down medications slowly, so they may experience side effects with standard doses. Extensive metabolizers break down medications at a normal rate, so they are less likely to experience side effects at standard doses. Ultra-rapid metabolizers break down medications rapidly, so they may not get enough medication at standard doses.

Pharmacogenetic testing (also known as “pharmacogenomic testing” or “PGx”) is an exciting tool that can predict how you might respond to certain medications based on your genetic makeup. The Comprehensive PGx Panel analyzes variations on different genes associated with various commonly prescribed medications.

Genes are passed down from parents to their children. Your genes determine your traits, such as eye color, hair color, blood type, height, and more. Your genes (in addition to other factors, such as age, weight, liver/kidney function, and more) can also affect how you respond to certain medications.

This is because your genes determine the rate at which you metabolize, or “break down”, different medications. Poor metabolizers and intermediate metabolizers break down medications slowly, so they may experience side effects with standard doses. Extensive metabolizers break down medications at a normal rate, so they are less likely to experience side effects at standard doses. Ultra-rapid metabolizers break down medications rapidly, so they may not get enough medication at standard doses.

Pharmacogenetic testing (also known as “pharmacogenomic testing” or “PGx”) is an exciting tool that can predict how you might respond to certain medications based on your genetic makeup. The Pain Management PGx Panel analyzes different genes associated with specific medications that are commonly prescribed in pain management.

The MTHFR Test looks for common changes (variants) in the MTHFR gene that may affect how your body processes folate (vitamin B9) and, in turn, how it helps manage homocysteine levels in the blood. It’s a simple genetic test that only needs to be done once because your DNA stays the same throughout your life. Many people consider this test when they have a personal or family history of elevated homocysteine, certain pregnancy-related concerns, or want additional insight into folate metabolism. 

The results of the MTHFR Test will indicate whether you have zero, one, or two copies of the most common MTHFR variants, and what that may mean in general terms. This test is informational and is not a diagnosis by itself.  The presence of a genetic variant may lead to next steps that could include dietary changes, supplements, and follow-up testing tailored to your individual needs.  Your healthcare provider can interpret your results alongside your symptoms, medical history, and other labs (such as homocysteine, folate, and B12).