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Personal genetic testing

Personal Genetic Testing

Genetic insights for family planning, childhood health and adult health management. Explore four testing options and find the scope that suits your needs.

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01 · Personal genetics

Childhood Genetic Screening

Genetic insights for children and their families

Retail price¥2999

Screen for selected variants associated with single-gene disorders and review genetic information related to medication response, nutrition and metabolism. Results support informed discussions between families and healthcare professionals.

Who this test is for

For newborns and their families. We confirm the appropriate age range and test panel before testing.

Ask about Childhood Genetic Screening

What is included

Inherited Conditions

Selected panels cover conditions affecting the blood, immune, endocrine, nervous, muscular and urinary systems, as well as inherited metabolic disorders relevant to childhood health.

Medication Response

Explore genetic differences that may influence drug metabolism, effectiveness or adverse reactions. A clinician interprets these findings alongside the child’s age, medical history and other clinical information.

Nutrition and Inherited Traits

Review selected genetic findings related to nutrient metabolism and inherited traits. The genes tested and the evidence supporting each finding are defined in the agreed panel.

Report interpretation

The report explains relevant variants, the supporting evidence and what the results can tell you. Findings that warrant further investigation should be reviewed with a healthcare professional in the context of the child’s clinical information.

This service complements, rather than replaces, routine newborn screening, pediatric care and clinical diagnosis.

02 · Personal genetics

Preconception Genetic Screening

Carrier screening to inform family planning

Retail price¥2999

Identify selected variants associated with inherited conditions and assess carrier status before pregnancy. Individual and partner results provide a basis for genetic counseling and discussions of reproductive risk.

Who this test is for

For couples planning a pregnancy, including families with a history of inherited conditions or an affected child. Testing during pregnancy should first be discussed with a healthcare professional.

Ask about Preconception Genetic Screening

What is included

Screening for Inherited Conditions

The agreed panel covers selected single-gene disorders and variants relevant to the risk of an inherited condition in a child. Your test plan specifies the genes and variants included.

Interpreting Both Partners’ Results

Consider both partners’ carrier findings alongside family history to understand inheritance patterns and reproductive risk. A single result is interpreted in this wider context.

Genetic Counseling for Family Planning

A qualified professional can explain the meaning and limitations of the findings. If further assessment is indicated, a clinician will discuss the appropriate next steps.

Report interpretation

Interpretation brings together carrier status, partner results, inheritance patterns and personal and family history.

A carrier finding does not mean that the individual or a future child will necessarily have a condition. Clinical assessment remains important for risks outside the test panel.

03 · Personal genetics

Personal Health Genetics

Understand genetic susceptibility and medication response

Retail price¥2999

Bring genetic susceptibility and medication-response findings into the context of your family history, lifestyle and clinical information. The results can inform conversations with healthcare professionals about long-term health management.

Who this test is for

For adults interested in inherited susceptibility to health conditions and genetic factors that may affect medication response.

Ask about Personal Health Genetics

What is included

Cancer and Chronic Disease Susceptibility

Review selected genetic information associated with common cancers and chronic conditions, including gastric, colorectal and lung cancer where covered by the agreed panel.

Medication Response

Explore selected genes relevant to anti-infective, cancer, neuropsychiatric and cardiovascular treatments, with an explanation of how genetic differences may affect drug metabolism or response.

Putting Results in Context

Discuss the findings with a healthcare professional alongside your medical and family history and lifestyle, including whether further assessment or changes to health management are appropriate.

Report interpretation

The report explains genetic susceptibility separately from a disease diagnosis and sets out the scope of medication-related findings for professional interpretation.

Genetic susceptibility is not a diagnosis. Medication-related findings alone do not determine drug choice or dose; discuss any treatment changes with your clinician.

04 · Personal genetics

VIP Genetic Testing Package

An integrated approach to personal and family genetics

Retail price¥3999

Combine the testing areas covered by Childhood Genetic Screening, Preconception Genetic Screening and Personal Health Genetics in one plan. We confirm which inherited-condition, health, medication-response and nutrition modules are appropriate for the person being tested.

Who this test is for

For individuals and families seeking a broader view of inherited conditions, reproductive risk, disease susceptibility and medication response.

Ask about VIP Genetic Testing Package

What is included

Inherited Conditions and Reproductive Health

Review selected single-gene disorder variants and carrier findings to support childhood health discussions and genetic counseling for family planning.

Disease Susceptibility and Medication Response

Bring together selected findings on cancer and chronic disease susceptibility with medication-related genetic information for professional interpretation.

Nutrition and Inherited Traits

Include selected modules on nutrient metabolism and inherited traits. The agreed plan defines the tests, supporting evidence and report format.

Report interpretation

Results are organized by inherited conditions, health susceptibility, medication response and inherited traits, with an explanation of the uses and limitations of each area.

Confirm the exact test panel, sample requirements, fees and reporting service with our team before testing.

Inherited conditions

Inherited-condition testing

Childhood, preconception and VIP testing cover selected inherited conditions in the categories below. Contact us for the gene panel and testing scope appropriate to your needs.

Sample · Sequencing · Interpretation

From sample to report

  1. 01

    Choose a Panel and Submit a Sample

    Confirm the test panel and collection requirements with our team. Saliva is used where appropriate; collection requirements for newborns, children and other circumstances are assessed individually.

  2. 02

    DNA Extraction and Sequencing

    Samples undergo DNA extraction, library preparation and sequencing according to the agreed test plan, with quality assessment of both the sample and sequencing data.

  3. 03

    Genetic Analysis

    Relevant findings within the test panel are analyzed and annotated, then organized into the appropriate report sections.

  4. 04

    Understand Your Report

    A qualified professional explains the findings, the supporting evidence and the limits of interpretation. Results that require further investigation should be discussed with a clinician.

Test scope and interpretation

We confirm the test panel, eligible ages, sample requirements and report content before testing. Results should be interpreted by a qualified professional alongside personal and family history and clinical information. Consult your clinician about diagnosis, further investigations or medication changes.

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Find the right test for you and your family

Our team can explain the available tests, sample requirements and report interpretation.

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