Routine biochemical tests are used to assess mother’s and child’s health. These tests are suggested by doctors on routine basis to every pregnant woman. These tests give information on various health conditions that might complicate the pregnancy.
Identifying the risk factors is the first step in screening for birth defects.Abnormal ultrasound findings along with NT Scan and maternal serum screening give a risk for chromosomal abnormalities.
A positive test result indicates a risk that the baby has for being affected with an abnormality. It does not confirm the diagnosis as there are chances of false positives also. A diagnostic test must be done in order to confirm a positive result.
False Positive Results (FPRs) show the presence of a particular condition even if it is not present.FPRs may arise if there is a history of multiple miscarriages, in cases of twin pregnancy or if the mother conceived in her mid-40s.
A non-invasive test (NIPS or Non-Invasive Prenatal Screening) or an invasive procedure (amniocentesis or CVS) can be done to collect cells of the baby.Confirmation of Maternal Serum screening test results is done by karyotype, QF-PCR, FISH or microarray on this sample.
Swab your cheeks; your genetic information is hidden within your saliva. We process your saliva to decipher your genetic information corresponding to a particular health/lifestyle condition. Further, the genetic information is analyzed, interpreted and translated into a simple language by our scientific experts, to generate a personalized clinical report.
Early Detection
Detecting today is the key to a Healthy tomorrow. Take relevant and preventive measures to act fast on a given condition before it's too late.
Planning
Helping you to plan next steps accordingly. Beneficial for high risk individuals and their families through on-time monitoring combined with targeted diagnosis.
Diagnosis
A crucial piece of information to Doctors for targeted diagnosis based on your genetic makeup, saving time, effort and health insurance.
Power to "YOU"
Your secret to Health is within you. Genetic testing gives "YOU" the power to make decisions and adopt changes in lifestyle for a healthy living
Personalized Health
Once you know your genes, you have the power to use that secret to get personalized insights into your Diet, Exercises, Medicines etc. All unique to "YOU" and your
health.
Time Saving
Saving a lot of time and effort with exhaustive coverage on genes and advancement in technology, Genetic testing has become quite convinient and viable.
Cost Effective
We are on a mission to serve masses even in resource limited areas and bring economically viable healthcare solutions for all.
Genetic Counseling
With certified genetic counselors on board, they take you through your genes with a case to case pre and post test genetic counseling support as a part of each test offering.
You can avail genetic counseling free of cost with all of our products in our Personalized Health segment. Pre and post test counseling is included as a part of your product. It helps you to understand your report in a much better way and also guides you to take on recommendations to help you live a healthy Life.
All the tests in the Personalized Health Segment are recommended for a healthy individual looking to improve their personal lifestyle and enable them to take informed decisions for a healthy tomorrow. While being healthy, let's get healthy on a personal note.
Genes2Me perform over 1600 different laboratory tests. Test ranges from routine testing to cancer diagnostic test and next generation advanced genetic testing.
Genes2Me offers laboratory testing in different fields of Biochemistry, Clinical Pathology, Immunology, Microbiology, Pharmacogenomics, Cardiology, Neurology, Oncology, Genetic conditions, Pre and post natal screening, High resolution HLA typing, Rarer blood group typing, Inherited cancer and many more.
A few blood tests do require fasting prior to having your blood drawn. But for Genetic tests, fasting is not required. Please contact us to understand the requirements of specific testing.
All routine tests are completed and reported within about 24-48 hours of receiving the sample for testing, and certain tests take several days to weeks for reporting. Genetic test will take at least 15-20 days for reports. To know the status of the report, you can call directly at 1800 121 4030 or Sign up to our website to download reports.
Oncology is a branch of medical science that deals with the study, diagnosis and treatment of tumors and cancers. Cancer arises mostly by mutation in oncogenes, tumor suppressors gene, where abnormal cells divide in an uncontrolled way in the body.
Genes2Me provide a comprehensive panel to analyze your genetic predisposition to various mutations responsible for cancer. We test the risk assessment for Lung, Breast, Colorectal, Pancreatic, Thyroid, Bladder, Ovarian, and Testicular cancer.
BRCA stands for BReast CAncer which is usually classified into Breast cancer type 1 and type 2. There are two genes, namely, BRCA1 and BRCA2 which are found in every normal individual. But any genetic variation or mutation occurring in either of these two genes can lead to the incidence of breast, ovarian, and to a lesser extent other cancers such as prostate cancer, pancreatic cancer, and melanoma.
You can book your test simply by giving a call at 1800 121 4030. Online booking is also available just by submitting a form at contact us page (https://www.genes2me.com/contact-us).
You can book your appointment for expert advice with our doctors and counselors by submitting a form at contact us page (https://www.genes2me.com/contact-us).
Genes2Me provide free home sample collection facility at PAN India. Our trained phlebotomist (person who collects the blood sample) would visit your home to collect the sample.
Genes2Me know the importance of your security and privacy. The information collected from you is strictly confidential and not be disclosed to any third party. We protect the information against loss, misuse, alteration or pilferage and extremely serious measures are taken to minimize the risks.
Our Client is our Priority.
The information listed below will be considered private and confidential:
Your medical record as reported by your doctors, nurses, and others
Conversations with your doctor, nurse, healthcare about your care or treatment
Personal information about you with us
Billing information about you at a doctor’s office, clinic or hospital
Contact us if you think your rights are violated through email (contact@genes2me.com) or call (1800 121 4030). As we won’t share any sort of information with any third party until we receive confirmation from our client.
Easily proceed for the payment via following below mentioned steps.
Step 1: Register yourself with Genes2Me as a Doctor/Patient. Click on Login/Signup
Step 2: Buy test/product through test category of Genetics, Mother and Child Care, Diagnostics and Oncology
Step 3: Product is added to your shopping cart, now proceed for payment
Step 4: Check your checklist and proceed towards checkout & pay
Step 5: Fill your card details (credit/debit) and wait till you receive transaction status as "Success" or "Failure" .
Once you made the payment, an acknowledgment message will appear on screen ‘Success’ on the successful transaction and ‘Failure’ for a failed transaction. Furthermore, Transactions ID will appear on the
acknowledgment message, which you can save and quote for the transaction related queries.
You will receive an email acknowledgement on provided email ID & mobile number, while make the payment.
In such a case, you need to drop an email (contact@genes2me.com) or call (1800 121 4030) Genes2me to register your query.
