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Paper Details

GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis.
J Thromb Haemost
16
2021
BTPD, ClinVar, GoldVariants, Thrombosis, bleeding, bleeding, thrombotic, and platelet disorders, genes, hemostatic diseases, patients, thrombotic, and platelet disorders
Author NameAffiliation
Karyn MegyUniversity of Cambridge
Karyn MegyCambridge University Hospitals
Kate DownesUniversity of Cambridge
Kate DownesCambridge University Hospitals NHS Foundation Trust
Kate DownesCambridge University Hospitals
Keith GomezRoyal Free London NHS Foundation Trust
Willem H OuwehandUniversity of Cambridge
Willem H OuwehandCambridge University Hospitals NHS Foundation Trust
Willem H OuwehandCambridge University Hospitals
Willem H OuwehandUniversity of Cambridge
Willem H OuwehandCambridge University Hospitals
Willem H OuwehandCambridge University Hospitals NHS Foundation Trust
Kathleen FresonCenter for Molecular and Vascular Biology
Kathleen FresonCenter for Molecular and Vascular Biology
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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