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shop-by-goals-1Healthy BodyLearn how to work with your DNA to build a diet and fitness routine that gets results more quickly.
shop-by-goals-2Family PlanningGet screened for hereditary genetic conditions that may be passed on to your child.
shop-by-goals-3Cancer & Disease RiskDiscover your genetic risk level for hundreds of cancers & diseases that may impact your future.
shop-by-goals-4SkinGet personalised skincare tips and insights to reveal your brightest, most youthful skin.
shop-by-goals-5Success TraitsDiscover your child’s hidden genetic talents and help them achieve their highest potential.

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500+ Reports • 20 Categories

Your future child’s health starts with you. Get screened at home and gain valuable insights to help you make decisions that drastically improve the quality of your future family’s life.

Detailed, personalised reports that help you determine:

  • Your carrier risk for 160+ serious genetic diseases, including Alpha Thalassemia, Cystic Fibrosis, Sickle Cell Disease, and more

Plus, 500+ more reports including

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24%*of all individuals are estimated to be carriers of at least one genetic condition.*Source: Lazarin, Gabriel A et al. Official Journal of the American College of Medical Genetics (2013)
A must-do for all potential parents
Uncovering your and your partner’s carrier status before conceiving allows you to explore alternative options to ensure your child’s health.
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All family planning reports

Blood (8)
  • Beta Thalassemia due to HBB mutation
  • Factor XI Deficiency due to F11 mutation
  • Fanconi Anemia due to FANCA mutation
  • Fanconi Anemia due to FANCC mutation
  • Fanconi Anemia due to FANCG mutation
  • Glucose-6-phosphate Dehydrogenase Deficiency due to G6PD mutation
  • Sickle Cell Disease due to HBB mutation
  • Hemophilia B due to F9 variant
Cardiovascular System (1)
  • Beta Thalassemia due to HBB mutation
Metabolic Disorders (10)
  • Bardet-Biedl Syndrome due to BBS1 mutation
  • Bardet-Biedl Syndrome due to BBS10 mutation
  • Bloom Syndrome due to BLM mutation
  • Cohen Syndrome due to VPS13B mutation
  • GRACILE Syndrome due to BCS1L mutation
  • Joubert Syndrome due to TMEM216 mutation
  • Nijmegen Breakage Syndrome due to NBN mutation
  • Pycnodysostosis due to CTSK mutation
  • Rhizomelic Chondrodysplasia Punctata due to PEX7 mutation
  • Zellweger Syndrome Spectrum due to PEX1 mutation
Eye & Ear (25)
  • Deafness due to PCDH15 mutation
  • Nonsyndromic Hearing Loss and Deafness due to GJB3 mutation
  • Pendred Syndrome due to SLC26A4 mutation
  • Nonsyndromic Hearing Loss and Deafness due to MT-RNR1 variant
  • Nonsyndromic Hearing Loss and Deafness due to GJB2 mutation
  • Usher Syndrome due to ADGRV1 (GPR98) mutation
  • Usher Syndrome due to CDH23 mutation
  • Usher Syndrome due to CIB2 mutation
  • Usher Syndrome due to CLRN1 mutation
  • Usher Syndrome due to MYO7A mutation
  • Usher Syndrome due to PCDH15 mutation
  • Usher Syndrome due to PDZD7 mutation
  • Usher Syndrome due to USH1C mutation
  • Usher Syndrome due to USH1G mutation
  • Usher Syndrome due to USH2A mutation
  • Usher Syndrome due to WHRN (DFNB31) mutation
  • Achromatopsia due to ATF6 mutation
  • Achromatopsia due to CNGA3 mutation
  • Achromatopsia due to CNGB3 mutation
  • Achromatopsia due to GNAT2 mutation
  • Achromatopsia due to PDE6C mutation
  • Achromatopsia due to PDE6H mutation
  • Choroideremia due to CHM mutation
  • Costeff Optic Atrophy Syndrome due to OPA3 mutation
  • X-linked Juvenile Retinoschisis due to RS1 mutation
Hormone Disorder (6)
  • Combined Pituitary Hormone Deficiency due to PROP1 mutation
  • Congenital Adrenal Hyperplasia due to CYP17A1 mutation
  • Hyperinsulinism due to ABCC8 mutation
  • Hyperinsulinism due to HADH mutation
  • Hyperinsulinism due to KCNJ11 mutation
  • Polyglandular Autoimmune Syndrome due to AIRE mutation
Metabolic System (58)
  • Acute Fatty Liver due to HADHA mutation
  • Alkaptonuria due to HGD mutation
  • Alkaptonuria due to HGD mutation
  • Alpha-Mannosidosis due to MAN2B1 mutation
  • Aspartylglycosaminuria due to AGA mutation
  • Biotinidase Deficiency due to BTD mutation
  • Carnitine Palmitoyltransferase Deficiency due to CPT1A mutation
  • Carnitine Palmitoyltransferase Deficiency due to CPT2 mutation
  • Citrullinemia due to ASS1 mutation
  • Citrullinemia due to SLC25A13 mutation
  • Congenital Disorder of Glycosylation due to MPI mutation
  • Congenital Disorder of Glycosylation due to PMM2 mutation
  • Cystinosis due to CTNS mutation
  • D-bifunctional Protein Deficiency due to HSD17B4 mutation
  • Dihydrolipoamide Dehydrogenase Deficiency due to DLD mutation
  • Dihydropyrimidine Dehydrogenase Deficiency due to DPYD mutation
  • Galactosemia due to GALT mutation
  • Gaucher Disease due to GBA mutation
  • Glutaric Acidemia due to GCDH mutation
  • Glycogen Storage Disease due to AGL mutation
  • Glycogen Storage Disease due to G6PC mutation
  • Glycogen Storage Disease due to PYGM mutation
  • Glycogen Storage Disease due to SLC37A4 mutation
  • Hereditary Fructose Intolerance due to ALDOB mutation
  • HFE-associated Hereditary Hemochromatosis due to HFE mutation
  • Homocystinuria due to CBS mutation
  • Isovaleric Acidemia due to IVD mutation
  • LCHAD Deficiency due to HADHA mutation
  • Maple Syrup Urine Disease due to BCKDHA mutation
  • Maple Syrup Urine Disease due to BCKDHB mutation
  • Maple Syrup Urine Disease due to DBT mutation
  • Maple Syrup Urine Disease due to DLD mutation
  • Medium Chain Acyl-CoA Dehydrogenase Deficiency due to ACADM mutation
  • MTHFR Deficiency due to MTHFR mutation
  • Mucolipidosis due to MCOLN1 mutation
  • Mucopolysaccharidosis due to IDUA mutation
  • Niemann-Pick Disease due to NPC1 mutation
  • Niemann-Pick Disease due to SMPD1 mutation
  • Phenylketonuria due to GCH1 mutation
  • Phenylketonuria due to GCHFR mutation
  • Phenylketonuria due to PAH mutation
  • Phenylketonuria due to PCBD1 mutation
  • Phenylketonuria due to PTS mutation
  • Phenylketonuria due to QDPR mutation
  • Pompe Disease due to GAA mutation
  • Primary Carnitine Deficiency due to SLC22A5 mutation
  • Primary Hyperoxaluria due to AGXT mutation
  • Primary Hyperoxaluria due to GRHPR mutation
  • Primary Hyperoxaluria due to HOGA1 mutation
  • Pseudocholinesterase Deficiency due to BCHE mutation
  • Short Chain Acyl-CoA Dehydrogenase Deficiency due to ACADS mutation
  • Trifunctional Protein Deficiency due to HADHA mutation
  • Tyrosinemia due to FAH mutation
  • Very Long Chain Acyl-CoA Dehydrogenase Deficiency due to ACADVL mutation
  • Wilson Disease due to ATP7B mutation
  • Methylmalonic Acidemia due to MMAA variant
  • Methylmalonic Acidemia due to MMAB variant
  • Methylmalonic Acidemia due to MMUT variant
Multiple Organ Systems (1)
  • Cystic Fibrosis due to CFTR mutation
Musculoskeletal System (15)
  • Achondrogenesis due to SLC26A2 mutation
  • Alpha-Sarcoglycanopathy due to SGCA mutation
  • Autosomal Recessive Hypophosphatasia due to ALPL mutation
  • Autosomal Recessive Muscular Dystrophy due to CAPN3 mutation
  • Autosomal Recessive Muscular Dystrophy due to CAV3 mutation
  • Autosomal Recessive Muscular Dystrophy due to DYSF mutation
  • Autosomal Recessive Muscular Dystrophy due to FKTN mutation
  • Beta-sarcoglycanopathy (Limb-girdle muscular dystrophy) due to SGCB mutation
  • Cartilage-hair Hypoplasia due to RMRP mutation
  • Diastrophic Dysplasia due to SLC26A2 mutation
  • Inclusion Body Myopathy due to GNE mutation
  • Nemaline Myopathy due to KLHL40 mutation
  • Nemaline Myopathy due to NEB mutation
  • Recessive Multiple Epiphyseal Dysplasia due to SLC26A2 mutation
  • Sulfate Transporter-related Osteochondrodysplasia due to SLC26A2 mutation
Nervous System (10)
  • Ataxia with Vitamin E Deficiency due to TTPA mutation
  • Ataxia-Telangiectasia due to ATM mutation
  • Canavan Disease due to ASPA mutation
  • Familial Dysautonomia due to ELP1 (IKBKAP) mutation
  • Hexosaminidase A Deficiency (Including Tay-Sachs Disease) due to HEXA mutation
  • Megalencephalic Leukoencephalopathy with Subcortical Cysts due to MLC1 mutation
  • Metachromatic Leukodystrophy due to ARSA mutation
  • Northern Epilepsy due to CLN8 mutation
  • Sjögren-Larsson Syndrome due to ALDH3A2 mutation
  • Smith-Lemli-Opitz Syndrome due to DHCR7 mutation
Neurometabolic Disorder (6)
  • Krabbe Disease due to GALC mutation
  • Neuronal Ceroid Lipofuscinosis due to CLN3 mutation
  • Neuronal Ceroid Lipofuscinosis due to CLN5 mutation
  • Neuronal Ceroid Lipofuscinosis due to PPT1 mutation
  • Neuronal Ceroid Lipofuscinosis due to TPP1 mutation
  • Salla Disease due to SLC17A5 mutation
Neuromuscular System (5)
  • Andermann Syndrome due to SLC12A6 mutation
  • Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) due to SACS mutation
  • Muscle-Eye-Brain Disease due to POMGNT1 mutation
  • Muscular dystrophy-dystroglycanopathy due to FKTN mutation
  • Segawa Syndrome due to TH mutation
Prenatal (1)
  • HELLP Syndrome due to HADHA mutation
Skin (4)
  • Herlitz Junctional Epidermolysis Bullosa due to LAMA3 mutation
  • Herlitz Junctional Epidermolysis Bullosa due to LAMB3 mutation
  • Herlitz Junctional Epidermolysis Bullosa due to LAMC2 mutation
  • Oculocutaneous Albinism due to TYR variant
Urinary System (10)
  • Autosomal Recessive Polycystic Kidney Disease due to PKHD1 mutation
  • Steroid-resistant Nephrotic Syndrome due to COQ8B (ADCK4) mutation
  • Steroid-resistant Nephrotic Syndrome due to CUBN mutation
  • Steroid-resistant Nephrotic Syndrome due to LAMB2 mutation
  • Steroid-resistant Nephrotic Syndrome due to LMX1B mutation
  • Steroid-resistant Nephrotic Syndrome due to NPHS1 mutation
  • Steroid-resistant Nephrotic Syndrome due to NPHS2 mutation
  • Steroid-resistant Nephrotic Syndrome due to PLCE1 mutation
  • Steroid-resistant Nephrotic Syndrome due to SMARCAL1 mutation
  • Steroid-resistant Nephrotic Syndrome due to WT1 mutation
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Received your report? We’re not going anywhere

If you and your partner are carriers of the same mutation, our test includes a complimentary 1-on-1 consultation to support you through any next steps, including:

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Seeking Professional AdviceOur genetic counsellors help interpret your results and recommend next steps to help protect mother and child.
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Exploring Alternate OptionsIVF and pre-implantation testing can help mitigate the risk of your child inheriting a genetic disorder.
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Planning AheadIf your pregnancy or delivery requires specialist care, our counsellors can help you prepare safely for what’s to come.

Protecting your family is priceless

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Don’t just take our word for it,see what our customers have to say
goals.familyPlanning.testimonials.1.name-card
Sharon“Shocked yet grateful for my Family Planning results”No one in my family has ever had Thalassemia, so when I found out I’m a carrier I was shocked and upset. Now I’m happy to know so I can start reviewing options with my gyno, as I hope to get pregnant soon.
goals.familyPlanning.testimonials.2.name-card
Carrie“Feeling more prepared for my baby than ever”I was anxious to discover I’m a carrier for Deafness (I’m pregnant). When I did my consult, the counsellor was really helpful and understanding, so now I feel ready to handle whatever may happen when my child is born.
goals.familyPlanning.testimonials.3.name-card
Sebastian“Good for you – and your kids, too”I bought CircleDNA as a gift for me & my partner – it was a surprise to find we each carry 2-3 diseases. It’s made us take a closer look at our health, and actually we’re considering getting CircleDNA for our future kids now, too.
goals.familyPlanning.testimonials.3.name-card
Sebastian“Good for you – and your kids, too”I bought CircleDNA as a gift for me & my partner – it was a surprise to find we each carry 2-3 diseases. It’s made us take a closer look at our health, and actually we’re considering getting CircleDNA for our future kids now, too.
goals.familyPlanning.testimonials.1.name-card
Sharon“Shocked yet grateful for my Family Planning results”No one in my family has ever had Thalassemia, so when I found out I’m a carrier I was shocked and upset. Now I’m happy to know so I can start reviewing options with my gyno, as I hope to get pregnant soon.
goals.familyPlanning.testimonials.2.name-card
Carrie“Feeling more prepared for my baby than ever”I was anxious to discover I’m a carrier for Deafness (I’m pregnant). When I did my consult, the counsellor was really helpful and understanding, so now I feel ready to handle whatever may happen when my child is born.
goals.familyPlanning.testimonials.3.name-card
Sebastian“Good for you – and your kids, too”I bought CircleDNA as a gift for me & my partner – it was a surprise to find we each carry 2-3 diseases. It’s made us take a closer look at our health, and actually we’re considering getting CircleDNA for our future kids now, too.
goals.familyPlanning.testimonials.1.name-card
Sharon“Shocked yet grateful for my Family Planning results”No one in my family has ever had Thalassemia, so when I found out I’m a carrier I was shocked and upset. Now I’m happy to know so I can start reviewing options with my gyno, as I hope to get pregnant soon.
goals.familyPlanning.testimonials.2.name-card
Carrie“Feeling more prepared for my baby than ever”I was anxious to discover I’m a carrier for Deafness (I’m pregnant). When I did my consult, the counsellor was really helpful and understanding, so now I feel ready to handle whatever may happen when my child is born.
goals.familyPlanning.testimonials.3.name-card
Sebastian“Good for you – and your kids, too”I bought CircleDNA as a gift for me & my partner – it was a surprise to find we each carry 2-3 diseases. It’s made us take a closer look at our health, and actually we’re considering getting CircleDNA for our future kids now, too.
What sets CircleDNA apart?
goals.common.usp.accuracy.title
Validated 99.9% Analytical AccuracyOur unique Whole Exome Sequencing (WES) technology conducts a full scan on all your protein-coding genes, providing you with comprehensive and accurate results.
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Encrypted Secured DataYour privacy and data security is our top priority. We do not sell, lease, or rent your data to any third party. We adhere to leading international security standard ISO-27001.
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Complimentary 1-on-1 ConsultationDeep dive into your results with our health professionals with a complimentary 1-on-1 phone consultation.
goals.common.usp.saliva_collection.title
Simple and Convenient Saliva CollectionAll kits include a non-invasive, FDA-approved saliva collection swab and test tube, with free delivery both ways.
goals.common.usp.accuracy.title
Validated 99.9% Analytical AccuracyOur unique Whole Exome Sequencing (WES) technology conducts a full scan on all your protein-coding genes, providing you with comprehensive and accurate results.
goals.common.usp.encryption.title
Encrypted Secured DataYour privacy and data security is our top priority. We do not sell, lease, or rent your data to any third party. We adhere to leading international security standard ISO-27001.
goals.common.usp.consultation.title
Complimentary 1-on-1 ConsultationDeep dive into your results with our health professionals with a complimentary 1-on-1 phone consultation.
goals.common.usp.saliva_collection.title
Simple and Convenient Saliva CollectionAll kits include a non-invasive, FDA-approved saliva collection swab and test tube, with free delivery both ways.
goals.common.usp.accuracy.title
Validated 99.9% Analytical AccuracyOur unique Whole Exome Sequencing (WES) technology conducts a full scan on all your protein-coding genes, providing you with comprehensive and accurate results.
goals.common.usp.encryption.title
Encrypted Secured DataYour privacy and data security is our top priority. We do not sell, lease, or rent your data to any third party. We adhere to leading international security standard ISO-27001.
goals.common.usp.consultation.title
Complimentary 1-on-1 ConsultationDeep dive into your results with our health professionals with a complimentary 1-on-1 phone consultation.
What sets CircleDNA apart?
goals.common.usp.saliva_collection.title
Simple and Convenient Saliva Collection
goals.common.usp.accuracy.title
Validated 99.9% Analytical Accuracy
goals.common.usp.consultation.title
Complimentary 1-on-1 Consultation
goals.common.usp.encryption.titleyour privacy is safe with usEncrypted Secured DataYour privacy and data security is our top priority. We do not sell, lease, or rent your data to any third party. We adhere to leading international security standard ISO-27001.

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Order your kit today
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Collect your sample at home with our easy-to-use saliva swab and return to our accredited labs
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Receive your report via the Circle app within 18 business days
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Book your 1-on-1 consultation with our health professional

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Got questions? Get answers

Check out our frequently asked questions below, or contact us for more information.
What is CircleDNA?
CircleDNA is the world’s most comprehensive DNA test that enables you to take full control of your health by understanding your genetic blueprint, so you can make informed decisions about your health with full confidence. This at-home test provides 500+ reports about your diet, nutrition, sports, cancer and disease risks, carrier conditions and much more with a simple saliva swab. The results are delivered within 18 business days in an easy-to-use mobile app.
What can I do if I find out that I’m a carrier for a genetic disease?
Talk to a genetic counselor: They can help you understand the implications of being a carrier and the risk of passing the disorder to your children. They can also guide you through your options for testing and family planning.Consider genetic testing: This test can determine if your partner is also a carrier for the same disorder. If you both carry a mutation in the same gene, there is a 25% chance your child could inherit the disorder. If only one of you carries the mutation, there is a 50% chance your child will also be a carrier. It is also important to inform close family members about the test so they can understand their risk.Explore family planning options: If you and your partner are both carriers, you have several options for family planning, including in vitro fertilization with preimplantation genetic diagnosis (PGD), adoption, or using a sperm or egg donor who is not a carrier.
How does CircleDNA test for my carrier status?
CircleDNA offers carrier screening to detect disease-causing mutations associated with 161 conditions. Although this test is not a diagnostic test, the mutations detected are interpreted using the same clinical-grade standards as those used by physicians. The mutations are classified according to the guidelines recommended by the American College of Medical Genetics and Genomics. CircleDNA's whole exome sequencing technology scans all protein-coding genes, allowing it to detect both known and novel disease-causing mutations.
How are my data and privacy protected?
CircleDNA adheres to the leading international security standard, ISO-27001, as we implement physical, technical, and administrative measures to prevent any unauthorized access to, or disclosure of, your sensitive information. All connections are encrypted with Secure Socket Layer (SSL) technology. We do not sell, lease, or rent your personal information to any third party without your explicit consent. Your data will also never be shared with anyone outside of CircleDNA for marketing or other purposes. You are the only individual or party who is able to authorize how your information is used, stored, and shared with others.
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Carrier screening is highly recommended for both parents
Our comprehensive carrier screening includes:
Family Planning
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160+reports
Discover your carrier status while learning more about each disease, and explore actionable next steps.

Of the diseases screened...

116shorten lifespan
Cystic FibrosisLife expectancy up to 35 yrs
Ataxia-TelangiectasiaMedian age of death at 22 yrs
Andermann SyndromeFatal before the age of 40
71carry a significant risk for intellectual disability
Phenylalanine Hydroxylase Deficiency
Smith-Lemli-Opitz Syndrome
Hyperinsulinism
38are treatable if caught early
Gracile SyndromeFrom birth to 4 months of age
D-bifunctional Protein DeficiencyFrom birth to 4 months of age
CitrullinemiaLongest lifespan known as 17 days without management
38are treatable if caught early
Gracile SyndromeFrom birth to 4 months of age
D-bifunctional Protein DeficiencyFrom birth to 4 months of age
CitrullinemiaLongest lifespan known as 17 days without management
116shorten lifespan
Cystic FibrosisLife expectancy up to 35 yrs
Ataxia-TelangiectasiaMedian age of death at 22 yrs
Andermann SyndromeFatal before the age of 40
71carry a significant risk for intellectual disability
Phenylalanine Hydroxylase Deficiency
Smith-Lemli-Opitz Syndrome
Hyperinsulinism
38are treatable if caught early
Gracile SyndromeFrom birth to 4 months of age
D-bifunctional Protein DeficiencyFrom birth to 4 months of age
CitrullinemiaLongest lifespan known as 17 days without management
116shorten lifespan
Cystic FibrosisLife expectancy up to 35 yrs
Ataxia-TelangiectasiaMedian age of death at 22 yrs
Andermann SyndromeFatal before the age of 40
71carry a significant risk for intellectual disability
Phenylalanine Hydroxylase Deficiency
Smith-Lemli-Opitz Syndrome
Hyperinsulinism
38are treatable if caught early
Gracile SyndromeFrom birth to 4 months of age
D-bifunctional Protein DeficiencyFrom birth to 4 months of age
CitrullinemiaLongest lifespan known as 17 days without management
SkinLearn what skin problems you may be predisposed to and how to prevent them.
AncestryGet a detailed breakdown of your ancestral roots.
Success TraitsA summary of the traits that form the basis of who you are.
Disease & Cancer ScreeningGet an overview of your genetic health risks & take early action.
Diet & FitnessFind out which diet types and fitness routines are best suited to you.
Drug ResponseUncover a breakdown of your body's response to drugs and medication.