Data Sharing For Clinicians

Learn how to share variant interpretations and suppporting observations from your clinic with ClinVar.

Clinicians looking to share genetic variant information and supporting phenotype information from their patients can submit data to ClinVar or inform their patients about enrolling in ClinGen's patient registry GenomeConnect. GenomeConnect participants are consented for broad data sharing with databases such as ClinVar.


ClinVar Submission

While clinical and research laboratories make up the majority of ClinVar submitters, we encourage clinicians to share their own variant interpretations and supporting phenotype data. Two ClinVar submission use cases for clinicians are outlined here.

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Empower your patients to engage in genetics and health data sharing through ClinGen's patient registry, GenomeConnect.

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