ClinVar archives and aggregates information about relationships among variation and human health. Submission to ClinVar · Sources of data in ClinVar · About · Variation report

25 јан 2024 · ClinVar is a freely accessible, public archive of reports of human variations classified for diseases and drug responses, with supporting ...

ClinVar is a a freely accessible, public archive of reports of the relationships among human variations and phenotypes hosted by the National Center for ...

20 ној 2017 · ClinVar (1,2) is a freely available, public archive of human genetic variants and interpretations of their significance to disease. It is ...

Welcome to ClinVar Miner! The content on this website is current as of 3 June 2024. On that date, ClinVar had 4,393,252 submissions on 2,966,675 variants.

28 ној 2019 · ClinVar is a freely available, public archive of human genetic variants and interpretations of their relationships to diseases and other ...

ClinVar is a public archive with free access to reports on the relationships between human variations and phenotypes, with supporting evidence.

ClinVar accessions submissions reporting human variation, interpretations of the relationship of that variation to human health and the evidence supporting each ...

ClinVar aggregates information about genomic variation and its relationship to human health. Contact us at 'clinvar@ncbi.nlm.nih.gov' with any questions or ... README.md · Issues 5 · Pull requests 0

Simple ClinVar was developed to provide gene- and disease-wise summary statistic based on all available genetic variants from ClinVar. How many missense ...