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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!
Common Health Risks
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.
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.
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,
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Analyses 103 FDA Approved Drugs
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