[카테고리:] FAQ

This test is suitable for individuals with a history of recurrent pregnancy loss, a family history of genetic disorders, or a previous child affected by a genetic condition. Even in the absence of symptoms, it can help identify underlying genetic risks and support informed planning for future children.

반복 유산을 경험했거나, 유전질환의 가족력 혹은 과거 유전질환을 가진 자녀의 병력이 있는 부모에게 고려할 수 있는 검사입니다. 현재 증상이 없더라도 잠재적인 유전질환 가능성을 확인하고, 향후 자녀의 유전질환 위험을 미리 확인하고 준비하기 위한 검사입니다.

Test pricing may vary depending on the type and quantity of tests. For detailed pricing, please inquire through the customer support page. 

3billion strictly complies with each country’s genomic data protection laws and medical device–related guidelines. In providing global services, we carefully review the regulatory and legal requirements of each country in advance, and where services are restricted by local regulations, we prioritize compliance with applicable local laws and guidelines. The final decision regarding service availability is…

All genomic data is de-identified to prevent individual identification and securely stored within 3billion’s security system. Retained data is strictly restricted to use for result accuracy verification, analysis quality management, service improvement, and medical research purposes only. 3billion adheres to the highest standards of security to protect children’s valuable genetic information and places the highest…