Health All In One Genetic Health Risk Testing
Foresight Genetic Testing -Genetic Health Risk Testing
Nutrition Telomere Length Testing
Obesity Genetic Health Testing
Physical 
Youth 
The report results are based on the ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) clinical genetic testing database provided by the National Center for Bioinformatics. We use this database to evaluate together with Insight’s proprietary program analysis. Gene variation and disease-causing risk index correlate with genotype and disease risk. In addition, it is also supported by the GENOME-WIDE ASSOCIATION STUDY (GWAS), which lists the gene loci related to diseases or traits and the genes that cause abnormal biosynthesis of proteins in the body. As the evidence supports the particular gene, the higher the gene mutations, the higher the disease occurs.Total Guardian Cancer | Gene detection of cardiovascular and neurodegenerative diseases evaluated 34,286 related SNPs to detection of 29 types of cancer: Lung cancer| Liver cancer| Colorectal cancer| Breast cancer| Oral cancer| Prostate cancer| Stomach cancer| Pancreatic cancer| Esophageal cancer| Ovarian cancer| Cervical cancer| Endometrial cancer| Chronic lymphocytic leukemia| Acute myeloid leukemia| Chronic myeloid leukemia| Non-Hodgkin’s lymphoma| Multiple myeloma| Nasopharyngeal carcinoma Head and neck cancer| Thyroid cancer| Bladder cancer| Basal cell carcinoma| Melanoma| Testicular cancer| Renal cell carcinoma| Glioma| Meningiomas| Hodgkin's lymphoma| Chondrosarcoma. Detection of 37 cardiovascular diseases: Atrial septal defect | Familial dilated cardiomyopathy | Familial hypertrophic cardiomyopathy | Long QT syndrome | Short QT syndrome | AnkyrinB syndrome | Familial atrial fibrillation | Family Heart Block | Arrhythmogenic Right Ventricular Myocardial Disease | Ventricular Fibrillation | Sinus Syndrome | Brugada Syndrome | Wolff-Parkinson-White Syndrome | Catecholamine-Sensitive Polymorphic Ventricular Pulse | Stroke | Myocardial Infarction | Artery Atherosclerosis| Essential hypertension| Familial migraine| Coronary artery calcification| Coronary artery disease| Pulmonary hypertension| Thoracic aortic aneurysm| Thrombosis-prone disease| Pulmonary vein occlusive disease| Upper valve aortic valve stenosis| Hairy Cerebrovascular disease | Fabry disease | Gestational diabetes | Type 2 diabetes | Familial HDL deficiency | Familial hypercholesterolemia | Familial hypertriglyceridemia | Sitosterolemia | Hereditary folate malabsorption | Periodic paralysis of thyroid toxicity | Congenital hypothyroidism. Detection of 10 neurodegenerative diseases: Progressive supranuclear palsy | Frontotemporal dementia | Dementia with Lewy body | Alzheimer's disease | Late-stage Alzheimer's disease | Parkinson's disease | Huntington's disease | NOTCH3 gene abnormality Stroke and Vascular Dementia | Multiple System Degeneration | Amyotrophic Lateral Sclerosis
The report results are based on the ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) clinical genetic testing database provided by the National Center for Bioinformatics. We use this database to evaluate together with Insight’s proprietary program analysis. Gene variation and disease-causing risk index correlate with genotype and disease risk. In addition, it is also supported by the GENOME-WIDE ASSOCIATION STUDY (GWAS), which lists the gene loci related to diseases or traits and the genes that cause abnormal biosynthesis of proteins in the body. As the evidence supports the particular gene, the higher the gene mutations, the higher the disease occurs.Total Guardian Cancer | Gene detection of cardiovascular and neurodegenerative diseases evaluated 34,286 related SNPs to detection of 29 types of cancer: Lung cancer| Liver cancer| Colorectal cancer| Breast cancer| Oral cancer| Prostate cancer| Stomach cancer| Pancreatic cancer| Esophageal cancer| Ovarian cancer| Cervical cancer| Endometrial cancer| Chronic lymphocytic leukemia| Acute myeloid leukemia| Chronic myeloid leukemia| Non-Hodgkin’s lymphoma| Multiple myeloma| Nasopharyngeal carcinoma Head and neck cancer| Thyroid cancer| Bladder cancer| Basal cell carcinoma| Melanoma| Testicular cancer| Renal cell carcinoma| Glioma| Meningiomas| Hodgkin's lymphoma| Chondrosarcoma. Detection of 37 cardiovascular diseases: Atrial septal defect | Familial dilated cardiomyopathy | Familial hypertrophic cardiomyopathy | Long QT syndrome | Short QT syndrome | AnkyrinB syndrome | Familial atrial fibrillation | Family Heart Block | Arrhythmogenic Right Ventricular Myocardial Disease | Ventricular Fibrillation | Sinus Syndrome | Brugada Syndrome | Wolff-Parkinson-White Syndrome | Catecholamine-Sensitive Polymorphic Ventricular Pulse | Stroke | Myocardial Infarction | Artery Atherosclerosis| Essential hypertension| Familial migraine| Coronary artery calcification| Coronary artery disease| Pulmonary hypertension| Thoracic aortic aneurysm| Thrombosis-prone disease| Pulmonary vein occlusive disease| Upper valve aortic valve stenosis| Hairy Cerebrovascular disease | Fabry disease | Gestational diabetes | Type 2 diabetes | Familial HDL deficiency | Familial hypercholesterolemia | Familial hypertriglyceridemia | Sitosterolemia | Hereditary folate malabsorption | Periodic paralysis of thyroid toxicity | Congenital hypothyroidism. Detection of 10 neurodegenerative diseases: Progressive supranuclear palsy | Frontotemporal dementia | Dementia with Lewy body | Alzheimer's disease | Late-stage Alzheimer's disease | Parkinson's disease | Huntington's disease | NOTCH3 gene abnormality Stroke and Vascular Dementia | Multiple System Degeneration | Amyotrophic Lateral SclerosisReference:
DNA is involved in the control of cell growth and division. "Telomere" (TELOMERE) is an important indicator to protect DNA stability because it is a region of repetitive DNA sequences at the end of a chromosome.According to research, telomere length is related to human age and pattern of life. Each time a cell divides, the telomeres become slightly shorter. Eventually, they become too short, and the cell can no longer divide and function; finally, the cell dies. Therefore, detecting the telomere will indicate the actual age, which is the indicator of ้healthcare and beauty guidelines | healthy food | lifestyle improvement, and cell youth.
"Obesity is a chronic disease," says the World Health OrganizationAccurate obesity type analysis helps you easily master fitness methods! !Fitness typeThis gene is involved in fat breakdown and regulation of energy balance in the body. Those with abnormal genetic results are more likely to cause fat accumulation to be distributed above the waist and hips. .Beer bellyPeople with abnormal results of this gene have inhibited fat breakdown, resulting in excessive fat accumulation in internal organs. However, the abdominal adipose tissue of the human body is more likely to become a preferential site for fat deposition, especially in men than in women, resulting in a "beer belly" obese body.Prone to diabetesFor those with abnormal genetic results, the fat mainly accumulates in the waist and buttocks. Women are also affected by natural estrogen so that fat accumulates in the lower abdomen and buttocks at the same time, resulting in an obese body mainly below the buttocks, forming a "pear" figure, which is easy to cause second type diabetes.Puff typeThose in the high-risk group due to genetic results have higher fasting blood lipids, and the fat is not easily metabolized, resulting in an excessively high BMI. Both visceral fat and subcutaneous fat tend to exceed the standard.Slow metabolizerPeople with abnormal genetic results have a higher probability of developing obesity, type 2 diabetes, hypertension, hyperlipidemia and other obesity-related metabolic diseases.Fitness guidelines to help you lose weight tailor-made!Fat is not a blessing, health and thinner more!
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