Health ❯ Healthcare ❯ Genetics

Genetic Testing

23andMe BRCA Testing Adverse Drug Reactions Polygenic Risk Score Hereditary Cancer Risk ApoE4 Mutation Consumer Genetics BRCA Newborn Screening Disease Penetrance Cancer Markers Patient Advocacy Consumer Services Consumer Health User Data Protection Genetic Data Privacy Apolipoprotein E (ApoE4) Rare Diseases Young-Onset Colorectal Cancer Polygenic Risk Scores Monogenic Diabetes User Privacy Patient Awareness Personalized Medicine Genetic Risk Factors Alzheimer's Disease Risk Prediction Medication Side Effects BRCA Genes Blood Group Genotyping Statistical Methods Genetic Disorders PI3K Pathway Mutations BRCA1 and BRCA2 Ancestry-Specific Data Local Ancestry Inference APOL1 Gene Variants Parental Screening Hereditary Conditions Disparities in Genetic Testing BRCA Mutations Spinal Muscular Atrophy NHS Initiatives Genetic Parentage Hereditary Cancer Testing Whole Exome Sequencing Risk Assessment Variants of Uncertain Significance Cardiovascular Risk Assessment Inherited Syndromes Cancer Genetics Inherited Conditions Preimplantation Genetic Testing Cancer Predisposition Syndromes Chromosomal Abnormalities

gnomAD Adds Local Ancestry Frequencies to Improve Genetic Test Accuracy

A Nature Communications study reports frequency estimates that reflect mixed ancestry can move some variants over ACMG thresholds.

Genetic Risk Score Flags Future Breast Cancer Risk After DCIS or LCIS

Mount Sinai Team Publishes AI ‘Penetrance’ Scores to Gauge Disease Risk From Rare Variants

Researchers Propose Widening Preventive Mastectomy Access to Avert 6,500 UK Breast Cancer Cases a Year

UK Regulator Probes Pancreatitis Cases Linked to GLP-1 Weight-Loss Drugs

Study Finds Fewer than Half of Womb Cancer Patients Complete Lynch Syndrome Blood Tests