One test. 67 insights into your DNA.

Introducing CarrierCheck™, a simple genetic test to get you started on your family planning journey

Order Now
 
box2x

CarrierCheck can help you discover how your DNA may affect your future children.

Just like traits such as eye color and height, genetic conditions can also run in families. CarrierCheck gives you insight into your carrier status for 67 inherited conditions. While carriers are usually healthy, knowing your status can help you learn more about your family’s genetics and what the risks might be for future generations.

Through our partnership with Helix, you will also gain access to Helix’s full range of tests so you can continue your DNA exploration.

CarrierCheck is simple to order and easy to understand.

CarrierCheck is quick and easy to order online, and we’ll mail your DNA kit directly to you. A genetic counseling session and customized test report are also included with every order to help you understand your results.

CarrierCheck is purchased through the Helix marketplace. To place your order, you will be leaving the Sema4 website.

If you have a personal or family history of certain medical conditions, CarrierCheck may not be right for you. This test is not appropriate for you if you are pregnant or trying to get pregnant. Medical experts, such as the American College of Obstetricians and Gynecologists, recommend a more comprehensive carrier screen that includes conditions like spinal muscular atrophy if you are trying to have a child.

Once you place your order, a doctor will review the health information you provide to confirm that CarrierCheck is appropriate for you. If your test request is not approved for any reason, you will not be charged.

How does CarrierCheck work?

  1. After purchasing CarrierCheck, create a Sema4 account to provide your health history.
  2. A doctor reviews your health history information to confirm that CarrierCheck is appropriate for you. If your test request is not approved for any reason, you will not be charged.
  3. Helix sends a DNA kit to your home. Provide a saliva sample and mail the kit back.
  4. Helix sequences your entire exome at their lab. If this is the first product you have ordered from Helix, this will take about 6 to 10 weeks. You can track the status of your test online. Once your results are ready, you will receive an email.
  5. Schedule a consultation with a genetic counselor to learn more about your results.

  6. View, print, and share your customized results report online.

What does CarrierCheck screen for?

CarrierCheck analyzes your DNA to see if you are a carrier of gene variants (or changes) associated with 67 inherited conditions. It can help you understand more about how your DNA may affect your future children.

  • 3-methylcrotonyl-CoA carboxylase deficiency (MCCC1-related)
  • 3-methylcrotonyl-CoA carboxylase deficiency (MCCC2-related)
  • Andermann syndrome
  • Autosomal recessive polycystic kidney disease
  • Autosomal recessive spastic ataxia of Charlevoix-Saguenay
  • Beta thalassemia and other beta-globin-related hemoglobinopathies
  • Bloom syndrome
  • Canavan disease
  • Carnitine palmitoyltransferase II deficiency
  • Citrullinemia, type 1
  • Combined malonic and methylmalonic aciduria
  • Combined pituitary hormone deficiency 2
  • Congenital disorder of glycosylation, type Ia
  • Cystic fibrosis
  • D-bifunctional protein deficiency
  • Dihydrolipoamide dehydrogenase deficiency
  • Familial dysautonomia
  • Fanconi anemia, group C
  • Galactokinase deficiency
  • Galactosemia
  • Glutaric acidemia, type I
  • Glycogen storage disease, type Ia
  • Glycogen storage disease, type Ib
  • Glycogen storage disease, type II
  • Glycogen storage disease, type III
  • GRACILE syndrome and other BCS1L-related disorders
  • Hemoglobin C disease
  • Hereditary fructose intolerance
  • Inclusion body myopathy 2
  • Isovaleric acidemia
  • Krabbe disease
  • Leber congenital amaurosis 10 and other CEP290-related ciliopathies
  • Leber congenital amaurosis 8, retinitis pigmentosa 12, and pigmented paravenous chorioretinal atrophy
  • Leigh syndrome, French-Canadian type
  • Limb-girdle muscular dystrophy, type 2A
  • Limb-girdle muscular dystrophy, type 2D
  • Limb-girdle muscular dystrophy, type 2E
  • Limb-girdle muscular dystrophy, Type 2I
  • Maple syrup urine disease, type 1b
  • Medium chain acyl-CoA dehydrogenase deficiency
  • Metachromatic leukodystrophy
  • Methylmalonic aciduria and homocystinuria, cobalamin C type
  • Mucolipidosis IV
  • Mucopolysaccharidosis, type IVb and GM1 gangliosidosis
  • Neuronal ceroid-lipofuscinosis (CLN5-related)
  • Neuronal ceroid-lipofuscinosis (PPT1-related)
  • Niemann-Pick disease, type A/B
  • Nijmegen breakage syndrome
  • Non-syndromic hearing loss (GJB2-related)
  • Pendred syndrome
  • Phenylalanine hydroxylase deficiency
  • Primary ciliary dyskinesia (DNAI1-related)
  • Primary hyperoxaluria, type 1
  • Primary hyperoxaluria, type 2
  • Retinitis pigmentosa 26
  • Rhizomelic chondrodysplasia punctata, type 1
  • Salla disease
  • Sandhoff disease
  • Sickle cell disease
  • Sjogren-Larsson syndrome
  • Sulfate transporter-related osteochondrodysplasia
  • Tay-Sachs disease
  • Tyrosinemia, type I
  • Usher syndrome, type IF
  • Usher syndrome, type III
  • Wilson disease
  • Zellweger syndrome spectrum (PEX1-related)
Have more questions about CarrierCheck?
Read FAQ
A negative test result reduces, but doesn’t eliminate, your risk of being a carrier for these genetic conditions.

The information provided by CarrierCheck isn’t comprehensive. If you have been diagnosed with a particular medical condition, or if a medical condition runs in your family, speak with a genetic counselor to discuss which genetic test may be most appropriate for you.


CT License #: CL-830