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Paper Details

Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants.
J Am Heart Assoc
22
2020
59, MYBPC3, Participants, cardiac actionable genes, cardiac genes, cardiomyopathy, human, participants, patient, person, whole genome sequence
Author NameAffiliation
Tess D PottingerCenter for Genetic Medicine Northwestern University Feinberg School of Medicine Chicago IL.
Megan J PuckelwartzCenter for Genetic Medicine Northwestern University Feinberg School of Medicine Chicago IL.
Megan J PuckelwartzDepartment of Pharmacology Northwestern University Feinberg School of Medicine Chicago IL.
Jennifer A PachecoCenter for Genetic Medicine Northwestern University Feinberg School of Medicine Chicago IL.
Laura J Rasmussen-TorvikDepartment of Preventive Medicine Northwestern University Feinberg School of Medicine Chicago IL.
Laura J Rasmussen-TorvikDepartment of Preventive Medicine Northwestern University Feinberg School of Medicine Chicago IL.
Maureen E SmithCenter for Genetic Medicine Northwestern University Feinberg School of Medicine Chicago IL.
Rex L ChisholmCenter for Genetic Medicine Northwestern University Feinberg School of Medicine Chicago IL.
Rex L ChisholmDepartment of Cell and Molecular Biology Northwestern University Feinberg School of Medicine Chicago IL.
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink