Paper Details

Paper Title

Points to consider for sharing variant-level information from clinical genetic testing with ClinVar.

Paper Journal Title

Cold Spring Harb Mol Case Stud

Paper Citation Count

Paper Publication Year

2018

Bio Mention

Human, genes, human, participants, patient, patients

Mesh Descriptor

Author Name	Affiliation
Danielle R Azzariti
Erin Rooney Riggs	Autism & Developmental Medicine Institute
Laura Lyman Rodriguez	National Human Genome Research Institute, National Institutes of Health
Laura Lyman Rodriguez	National Human Genome Research Institute, National Institutes of Health
Erin M Ramos	National Human Genome Research Institute, National Institutes of Health
Melissa J Landrum	National Center for Biotechnology Information, National Institutes of Health
Christa Lese Martin	Autism & Developmental Medicine Institute
Heidi L Rehm
Heidi L Rehm	Brigham & Women's Hospital and Harvard Medical School
Heidi L Rehm
Heidi L Rehm	Brigham & Women's Hospital and Harvard Medical School

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

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