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Congratulations! Your Colour of Circle is…
Sunshine Yellow!
You have a bright, positive attitude towards life and bring sunshine to everyone around you! You are caring and compassionate and your family means the world to you. You always put their wellbeing first. Sometimes to an extent where you forget about your own.
Keep reading to learn more about the genetic reports we recommend, based on your health goals assessment!
As a Sunshine Yellow Circler, You should consider focusing on...
Family Planning
163 reports
Common Health Risks
8 reports
Ancestry
15 reports
Diet
15 reports
Nutrition
20 reports
Protect Your Family, Right From the Start.
Pregnant or thinking of starting a family? Take the first step towards securing your family's health with Circle Family Planning DNA test - specially designed to provide genetic insights on whether you and your partner carry inherited conditions that might be passed on to your unborn child.
Many of us are carriers of inherited conditions and simply don’t know it. Over 80% of children with inherited conditions are born to parents with no known family history. If you and your partner are carriers of the same condition, there are important steps you can take if you are planning a pregnancy or are already pregnant.
The best gift you will ever receive is the peace of mind and assurance in the health of your child. Discover actionable insights that help you protect your family’s health, based on your DNA.
Your Family Planning DNA Report Includes
Your Carrier Status
A full breakdown of your carrier status for 163 hereditary conditions so you can work with your doctor to prepare for the health of your future family.
Which Genes Were Tested
A breakdown of which mutations were analysed and detected in your DNA sample and how we determined your result.
Valuable Insights
Your healthcare provider can advise on exploring alternative options for family planning if you and your partner are carriers of the same mutation.
Information About Your Results
Educational insights into each condition so that you can confidently make informed decisions for your family.
What Your Results Will Tell You
Negative
If you are negative for a condition, it means that you have a significantly reduced risk of being a carrier of that disease.
Positive
If you are positive for a condition, it means that you tested positive as a carrier of a genetic disease. This does not guarantee that your children will or will not inherit that condition.
If You’re Planning a Pregnancy
If you are positive for a condition, it means that you tested positive as a carrier of a genetic disease. This does not guarantee that your children will or will not inherit that condition.
Pursue In Vitro Fertilisation
During the in vitro fertilisation (IVF) process, a fertility specialist can look at the genes of several of your embryos and choose only those that will not be affected by the inherited condition to place in your womb. This is called pre-implantation genetic testing for monogenic/single gene diseases, or PGT-M.
Consider Other Options
If both prospective parents are carriers for mutations in the same gene, you can greatly reduce the risk of having an affected child by finding an egg or sperm donor that is not a carrier for the same condition. Adoption is another option.
If You’re Already Pregnant
Diagnostic tests such as chorionic villus sampling (CVS) or amniocentesis can determine if an inherited disease was passed on to your child. Whether or not you decide to pursue diagnostic testing, there are options you can discuss with your healthcare provider if you find out you and your partner are both carriers for the same inherited condition.
Speak to a Specialist
Knowing your child requires a certain type of care before birth means you can involve the right kind of specialist long before delivery. For some inherited conditions, there are treatments that can make a big difference in outcome if they are used early.
Find the Right Place to Deliver
Depending on what your baby is at risk for, you might want to seek out a specialised facility that is equipped to manage newborns with inherited conditions.
Surround Yourself with Support
You may simply want to talk with one of our genetic counsellors or work with a support group to understand what could lie ahead.
Understand Your Risk for 163 Hereditary Conditions
All 163 Family Planning Reports
Achondrogenesis due to SLC26A2 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, Acute Fatty Liver due to HADHA mutation, Alkaptonuria due to HGD mutation, Alpha Thalassemia due to HBA1 mutation, Alpha Thalassemia due to HBA2 mutation, Alpha-1 Antitrypsin Deficiency due to SERPINA1 mutation, Alpha-Mannosidosis due to MAN2B1 mutation, Alpha-Sarcoglycanopathy due to SGCA mutation,Andermann Syndrome due to SLC12A6 mutation, Aspartylglycosaminuria due to AGA mutation, Ataxia with Vitamin E Deficiency due to TTPA mutation, Ataxia-Telangiectasia due to ATM mutation, Autosomal Recessive Hypophosphatasia due to ALPL mutation, Autosomal Recessive Muscular Dsytrophy due to CAPN3 mutation, Autosomal Recessive Muscular Dsytrophy due to CAV3 mutation, Autosomal Recessive Muscular Dsytrophy due to DYSF mutation, Autosomal Recessive Muscular Dsytrophy due to FKTN mutation, Autosomal Recessive Polycystic Kidney Disease due to PKHD1 mutation, Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) due to SACS mutation, Bardet-Biedl Syndrome due to BBS1 mutation, Bardet-Biedl Syndrome due to BBS10 mutation, Beta Thalassemia due to HBB mutation, Beta-sarcoglycanopathy (Limb-girdle muscular dystrophy) due to SGCB mutation, Biotinidase Deficiency due to BTD mutation, Bloom Syndrome due to BLM mutation, Canavan Disease due to ASPA mutation,
View Full List of Conditions
Why Circle Family Planning DNA Test
Results You Can Trust
Circle Family Planning DNA test has been developed and designed by our team of leading scientists to be highly accurate and comprehensive. Our advanced Whole Exome Sequencing (WES) technology allows us to detect more than 99% of mutations for the vast majority of conditions we screen for, regardless of ethnicity, so you can confidently make informed decisions for your family.
Results To Guide Your Approach To A Healthy Pregnancy
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