Why am I sick? How can I find my answer?
Of the many diseases in the world, more than 7,000 known rare diseases exist. It is difficult to get a diagnosis because each disease has limited information. 3billion helps patients overcome difficulties through 3billion's one-stop genetic testing.
Why do I need genetic testing?
80% of rare diseases are genetic
About 80% of rare diseases with genetic causes can be diagnosed with genetic tests.
Provides more accurate diagnosis
When it is difficult to diagnose with symptoms alone, genetic tests can help.
Faster diagnosis
Reduce the risk of severe and chronic conditions with treatments from fast diagnosis.
How do I get a genetic test?
- STEP 1You must visit a hospital or clinic.
- STEP 2Your doctor will assess your medical condition and decide if a genetic test is necessary.
- STEP 3A medical professional will collect your DNA sample.
- STEP 4Your doctor will order 3billion's genetic test.
- STEP 5A clinical report will be provided with your doctor within 5 weeks.
- STEP 6You doctor will share the results with you and will help you decide on the best treatment method and care plan.
What does my test result mean?
When the test result is Positive
This means that you most likely have a variant that causes disease. Your doctor will follow up with you based on these results.
When the test result is Inconclusive
A suspected variant that may explain the cause of your symptoms was detected, but there is no sufficient evidence yet. With additional clinical evidence, the variant can be re-classified as pathogenic or benign.
When the test result is Negative
No suspected variant was found to explain your current symptoms.
FAQs
- Is it possible to check if the patient’s family members also have the variants found in the patient?
- Can I share the report with my patient?
- How long does it take to get my report?
- Can patients order tests?