Jeen’s carrier screening helps uncover inherited risks for peroxisomal disorders. It includes Zellweger spectrum disorders, rhizomelic chondrodysplasia punctata, and more.
Genes Tested
PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, GNPAT
Peroxisomal Disorders
Zellweger spectrum disorders
Rhizomelic chondrodysplasia punctata
Plus other peroxisome biogenesis disorders
1. Get your kit from us. Free next-day delivery of your Carrier Screening kit. Shipped after your free 30 minute genetic consultation and test choice is confirmed.
2. Easy returns. After your sample collection, send your sample in the pre-paid bag to the nearest depot (details in email). Lab turnaround time starts once it’s dispatched.
Turnaround Time:
17
-
21
days
Laboratory Location:
US
At Home Cheek Swab (Free): We send you the kit, you use the buccal swab for sample collection.
Jeen Clinic Network (+£40): 90+ locations across the UK. Flexible, affordable, and convenient blood draw.
Home Visit (+£65): A nurse comes to you for a convenient at-home blood draw.
Carrier screening is not routinely offered if you or your partner are more than 16 weeks pregnant. However, if there are specific circumstances and you’d like to explore whether an exception can be made, you’re welcome to book an appointment with one of our genetic counsellors.
Genetic testing with Jeen Health is only available to individuals aged 18 and over.
Please note: We do not routinely offer carrier screening if you or your partner are more than 16 weeks pregnant. If there are exceptional circumstances, you may book an appointment to discuss your options with a genetic counsellor.
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
7
-
10
days
7
-
10
days
17
-
21
days
7
-
10
days
2
-
4
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
7
-
10
days
7
-
10
days
17
-
21
days
7
-
10
days
2
-
4
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
17
-
21
days
Simple steps to check your Carrier Status with Jeen.
Buy your online genetic consult + carrier screening kit. It will prepare you for all the outcomes of your test.
Complete your consent form and we will book a 30-min call with our specialist.
Get your kit, collect sample with swab, package, sent and receive your results online.
A simple, low-cost option with flexible scheduling. For many patients, this is the quickest and most practical way to complete the test.
Genetic testing looks at your DNA to find changes or variants in your genes. These changes can tell us if you’re at risk for certain inherited conditions, like hereditary cancers or if you’re a carrier for a genetic condition.
It can reveal if you have a higher genetic risk for certain cancers (like breast, ovarian or bowel), if you’re a carrier for inherited conditions, or if you have a genetic condition that could impact your health or your family’s.
It’s simple — you speak with one of our expert Genetic Counsellors, receive a home kit in the post, collect a cheek swab, and send it back. Your DNA is analysed in a UK or US lab, and results are ready in under 4 weeks.
Yes. At Jeen Health, your data is encrypted and stored securely on our GDPR compliant servers, as well as with our vetted laboratories. Your results are only shared with you and your dedicated Genetic Counsellor, never with insurers or third parties.
Our team of expert Genetic Counsellors is here to help. Whether you're curious about testing, your results, or what’s right for you — we're just a message away.
