Our genetic testing can reveal powerful insights about your health. We offer multiple options of Carrier Screening, Cancer Screening and NIPT.
Trusted specialists
Speak to our expert geneticists, design your personalised test
Get your test through the mail, easy oral self-swab
Get your detailed report and recommendations
Pre-conception screen of 1,008 genes for inherited recessive disease - for couples planning a pregnancy.
Chromosome-level analysis of all 46 chromosomes - detects numerical changes (aneuploidies) and large structural rearrangements. Useful for couples investigating recurrent miscarriage or fertility issues.
A simple oral-swab screen of your newborn for inherited conditions where early intervention changes outcomes - including treatable metabolic disorders, hearing impairment risk, and immune deficiencies.
Non-invasive prenatal screen from 9 weeks. 3 conditions.
Non-invasive prenatal screen from 10 weeks. 3 conditions, 2-4 working days from when your sample reaches the laboratory.
Non-invasive prenatal screen from 9 weeks. 9 conditions, 7-10 working day turnaround.
Non-invasive prenatal screen from 9 weeks with microdeletions. 13 conditions, 7-10 working days.
Non-invasive prenatal screen from 10 weeks. 30 conditions, 5-10 working day turnaround.
Non-invasive prenatal screen from 9 weeks. 12 conditions, 17-21 working day turnaround.
One of our most advanced non-invasive prenatal tests, screening for a broader range of chromosomal, genetic and rare conditions in your baby - including microdeletions and many monogenic disorders.
Comprehensive 50-gene hereditary cancer-risk panel.
13-gene panel focused on hereditary breast cancer predisposition.
13-gene panel focused on hereditary prostate cancer predisposition.
14-gene panel focused on hereditary ovarian cancer predisposition.
23-gene panel focused on hereditary colorectal cancer predisposition.
11-gene panel focused on hereditary pancreatic cancer predisposition.
Hereditary-cancer 50-gene panel bundled with our 1,008-variant carrier-screening panel - one counselling session, one report, one price. Best value when you want both.
A DNA medication-compatibility test (PGx) that screens 112+ medications across 14 therapy areas - find out which drugs are likely to work for you, which won't, and what doses to start at.
Genetic screening for autosomal-dominant and recessive polycystic kidney disease. Identifies pathogenic variants in PKD1, PKD2 and PKHD1 - useful for at-risk family members and reproductive planning.
Pre-conception screen of 1,008 genes for inherited recessive disease - for couples planning a pregnancy.
Chromosome-level analysis of all 46 chromosomes - detects numerical changes (aneuploidies) and large structural rearrangements. Useful for couples investigating recurrent miscarriage or fertility issues.
A simple oral-swab screen of your newborn for inherited conditions where early intervention changes outcomes - including treatable metabolic disorders, hearing impairment risk, and immune deficiencies.
Non-invasive prenatal screen from 9 weeks. 3 conditions.
Non-invasive prenatal screen from 10 weeks. 3 conditions, 2-4 working days from when your sample reaches the laboratory.
Non-invasive prenatal screen from 9 weeks. 9 conditions, 7-10 working day turnaround.
Non-invasive prenatal screen from 9 weeks with microdeletions. 13 conditions, 7-10 working days.
Non-invasive prenatal screen from 10 weeks. 30 conditions, 5-10 working day turnaround.
Non-invasive prenatal screen from 9 weeks. 12 conditions, 17-21 working day turnaround.
One of our most advanced non-invasive prenatal tests, screening for a broader range of chromosomal, genetic and rare conditions in your baby - including microdeletions and many monogenic disorders.
Comprehensive 50-gene hereditary cancer-risk panel.
13-gene panel focused on hereditary breast cancer predisposition.
13-gene panel focused on hereditary prostate cancer predisposition.
14-gene panel focused on hereditary ovarian cancer predisposition.
23-gene panel focused on hereditary colorectal cancer predisposition.
11-gene panel focused on hereditary pancreatic cancer predisposition.
Hereditary-cancer 50-gene panel bundled with our 1,008-variant carrier-screening panel - one counselling session, one report, one price. Best value when you want both.
A DNA medication-compatibility test (PGx) that screens 112+ medications across 14 therapy areas - find out which drugs are likely to work for you, which won't, and what doses to start at.
Genetic screening for autosomal-dominant and recessive polycystic kidney disease. Identifies pathogenic variants in PKD1, PKD2 and PKHD1 - useful for at-risk family members and reproductive planning.
Pre-conception screen of 1,008 genes for inherited recessive disease - for couples planning a pregnancy.
Chromosome-level analysis of all 46 chromosomes - detects numerical changes (aneuploidies) and large structural rearrangements. Useful for couples investigating recurrent miscarriage or fertility issues.
A simple oral-swab screen of your newborn for inherited conditions where early intervention changes outcomes - including treatable metabolic disorders, hearing impairment risk, and immune deficiencies.
Non-invasive prenatal screen from 9 weeks. 3 conditions.
Non-invasive prenatal screen from 10 weeks. 3 conditions, 2-4 working days from when your sample reaches the laboratory.
Non-invasive prenatal screen from 9 weeks. 9 conditions, 7-10 working day turnaround.
Non-invasive prenatal screen from 9 weeks with microdeletions. 13 conditions, 7-10 working days.
Non-invasive prenatal screen from 10 weeks. 30 conditions, 5-10 working day turnaround.
Non-invasive prenatal screen from 9 weeks. 12 conditions, 17-21 working day turnaround.
One of our most advanced non-invasive prenatal tests, screening for a broader range of chromosomal, genetic and rare conditions in your baby - including microdeletions and many monogenic disorders.
Comprehensive 50-gene hereditary cancer-risk panel.
13-gene panel focused on hereditary breast cancer predisposition.
13-gene panel focused on hereditary prostate cancer predisposition.
14-gene panel focused on hereditary ovarian cancer predisposition.
23-gene panel focused on hereditary colorectal cancer predisposition.
11-gene panel focused on hereditary pancreatic cancer predisposition.
Hereditary-cancer 50-gene panel bundled with our 1,008-variant carrier-screening panel - one counselling session, one report, one price. Best value when you want both.
A DNA medication-compatibility test (PGx) that screens 112+ medications across 14 therapy areas - find out which drugs are likely to work for you, which won't, and what doses to start at.
Genetic screening for autosomal-dominant and recessive polycystic kidney disease. Identifies pathogenic variants in PKD1, PKD2 and PKHD1 - useful for at-risk family members and reproductive planning.
At Jeen, we focus on health, not hair colour. Our genetic testing uses 50x sequencing depth (NGS) for greater accuracy and confidence in detecting inherited conditions.
DNA is broken into small fragments, sequenced, and computationally assemble into the full genome.
Sequencing depth is how many times your DNA is read. Higher depth = more accurate results, lower depth = risk of missed mutations.
Larger genomes (like humans) need more sequencing reads. That’s why high-depth testing matters-it ensures nothing is missed.
Not all genetic tests are created equal. At Jeen, we use 50x sequencing coverage, which means each section of your DNA is read around 50 times. Here’s why it makes a difference:
Bigger genome → more data needed
Higher depth → better accuracy
Balance cost vs. detail!
Have questions? We’re here to help. Genetic testing can feel overwhelming, but it doesn’t have to be. Our genetic counsellors are here to walk you through your options, explain the science in plain English, and help you decide if testing is right for you.
Sensitivity and specificity help you understand how reliable a test is. A test with high sensitivity catches more true positives, and one with high specificity avoids false alarms. Together, they help ensure your results are trustworthy.
Not quite. Even highly accurate tests need interpretation. A genetic counsellor helps explain what your result means for you and your family - and whether you need any follow-up or additional screening.
These metrics help determine a test's accuracy. High sensitivity ensures most carriers are identified, while high specificity ensures non-carriers aren't misdiagnosed. Together, they provide a comprehensive view of a test's reliability.
Sensitivity measures how well a test identifies true positives among all who have the condition, while PPV assesses the likelihood that a positive test result is a true positive. Sensitivity is intrinsic to the test, whereas PPV is influenced by the condition's prevalence in the population.
Several things can influence test accuracy - including how common the gene variant is in the population (prevalence), the quality of the lab, and even how the sample was collected. That’s why expert-designed tests and genetic counselling matter.
Test stats like sensitivity or PPV can change based on the population being tested, the condition being looked for, and how the test is used. That’s why context matters - Jeen’s team explains your results in a way that fits your unique case.
Yes. A test designed to catch all potential cases (high sensitivity) might also capture individuals without the condition, leading to false positives and thus lower specificity. Balancing both metrics is crucial for accurate testing.
Yes – and it’s a key part of your journey with Jeen. Our genetic counsellors are here to help you understand what your results mean and guide you through everything, including terms like sensitivity and specificity. You’ll have a counselling session before your test to explain what we’re looking for and what the results could mean. If your result shows something unusual, we’ll contact you and arrange a follow-up session. Even if your results are normal, you're always welcome to book another session if you'd like to talk them through with our team.
The statistics and clinical claims on this page are supported by the following authoritative sources.
Pick the appointment that suits you and choose a time - no account needed.
Trouble loading? Open the booking page.
Our team of expert specialists is here to help - whether you're curious about testing, your results, or what's right for you. We're just a message away.
