What is carrier status and why is it the main reason for people buying a DNA health test?
Most carrier screening is for recessive disorders. It takes two genes—one from the mother and one from the father for a person to be affected. If a person has only one gene for a disorder, he or she is known as a carrier. Carriers often do not know that they have a gene for a disorder. They usually do not have symptoms.
Our carrier screening tells you whether you carry a gene for over 40 types of genetic disorders. When it is done before pregnancy, it allows you to find out your chances of having a child with a genetic disorder and make early health decisions.
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Normally, if both parents are carrier for a certain disease, there will be a 25% chance that their child will be affected and 50% chance will be a carrier.
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If you or/and your partner are carrier for certain inherited conditions, we can help to reduce or eliminate the chance of your child being affected by providing professional genetic counselling and fertility services.
WHO NEEDS A DNA TEST
Couple
A couple plans to start a family and wants to know the risk of passing on genetically linked diseases to their unborn child. Especially one of them or a close relative has a genetically linked illness.
Family
A parent wants to know his/her children’s health risks and potentials to make early healthcare and lifestyle decisions.
Self
Everyone who wants to live a better and healthier life. Our tests analyze your unique needs and provide actionable insights to optimize your diet and fitness routines. By knowing your health risks, you will get an idea on how to make health decisions.
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