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Sarah Leigh, PhD


Committees, Working Groups & Task Teams

  • Cardiovascular Familial Hypercholesterolemia Variant Curation Expert Panel

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. If you have questions about the information contained on this website, please see a health care professional.
  • About ClinGen
  • ClinGen and ClinVar Partnership
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  • Working Groups & Expert Panels
  • Actionability
  • Ancestry and Diversity
  • Biocurator Working Group
  • Clinical Domain Working Groups
  • Community Curation Committee (C3)
  • Copy Number Variant Interpretation Guidelines
  • Data Platform
  • Dosage Sensitivity Curation
  • Education
  • EHR
  • CADRe (Consent & Disclosure Recommendations)
  • External Scientific Panel
  • Gene Curation
  • ​Genomic Variant
  • Lumping and Splitting
  • Sequence Variant Inter-Laboratory Discrepancy Resolution
  • Sequence Variant Interpretation
  • Somatic Cancer
  • Steering Committee

  • Clinical Domain Working Groups
  • Cardiovascular CDWG
  • Hearing Loss CDWG
  • Hemostasis/Thrombosis CDWG
  • Hereditary Cancer CDWG
  • Inborn Errors of Metabolism CDWG
  • Neurodevelopmental Disorders CDWG
  • RASopathy CDWG
  • Gene & Variant Expert Panels
  • Aminoacidopathy Gene Curation Expert Panel
  • Autism and Intellectual Disability Gene Curation Expert Panel
  • Brain Malformations Variant Curation Expert Panel
  • Breast and Ovarian Cancer Gene Curation Expert Panel
  • Brugada Syndrome Gene Curation Expert Panel
  • Cardiovascular Familial Hypercholesterolemia Variant Curation Expert Panel
  • Cardiovascular KCNQ1 Variant Curation Expert Panel
  • Cardiovascular LQTS Gene Curation Expert Panel
  • CDH1 Variant Curation Expert Panel
  • Coagulation Factor Deficiency Expert Panel
  • Colon Cancer and Polyposis Gene Curation Expert Panel
  • Congenital Creatine Deficiency Syndromes Variant Curation Expert Panel
  • Epilepsy Gene Curation Expert Panel
  • Familial Thoracic Aortic Aneurysm and Dissection Gene Curation Expert Panel
  • Fatty Acid Oxidation Gene Curation Expert Panel
  • Hearing Loss Gene Curation Expert Panel
  • Hearing Loss Variant Curation Expert Panel
  • Hemostasis/Thrombosis Gene Curation Expert Panel
  • Hereditary Breast Ovarian and Pancreatic Cancer Variant Curation Expert Panel
  • Hereditary Cancer Gene Curation Expert Panel
  • Hypertrophic Cardiomyopathy Gene Curation Expert Panel
  • Inherited Cardiomyopathy Variant Curation Expert Panel
  • Mitochondrial Disease Gene Curation Expert Panel
  • Mitochondrial Disease Variant Curation Expert Panel
  • Monogenic Diabetes Variant Curation Expert Panel
  • Myeloid Malignancy Variant Curation Expert Panel
  • PAH Variant Curation Expert Panel
  • Platelet Disorders Expert Panel
  • PTEN Variant Curation Expert Panel
  • RASopathy Gene Curation Expert Panel
  • RASopathy Variant Curation Expert Panel
  • Rett Angelman Variant Curation Expert Panel
  • Somatic/Germline Variant Curation Group
  • Storage Diseases Variant Curation Expert Panel
  • TP53 Variant Curation Expert Panel
  • VHL Variant Curation Expert Panel

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