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.
Patients
Find my answer
with genetic testing
Why am I sick?
How can I find my answer?
Why do I need genetic testing?
Genetic testing can help diagnose rare genetic diseases, which comprise about 80% of rare diseases.
When there is a limit to diagnosing with patient’s symptoms only, genetic information can help provide answers.
Accurate and rapid diagnosis enables appropriate treatment and care.
How do I get a genetic test?
-
01 You must visit a hospital or clinic. -
02 Your doctor will assess your medical condition and decide if a genetic test is necessary. -
03 A medical professional will collect your DNA sample. -
04 Your doctor will order 3billion’s genetic test. -
05 A clinical report will be provided with your doctor within 6 weeks. -
06 You doctor will share the results with you and will help you decide on the best treatment method and care plan.
어떻게 유전자검사를
받을 수 있나요?
받을 수 있나요?
-
STEP.1
환자가 병원에 방문합니다.
What does my test result mean?
-
When the test result is
PositiveThis 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
InconclusiveA 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
NegativeNo suspected variant was found to explain your current symptoms.
FAQs
