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Please note this is a beta version of the ClinGen Evidence Repository. This resource is intended to provide access to variant level evidence used and applied by ClinGen Variant Curation Expert Panels in the classification of variants. In this beta version, the evidence is limited to curation notes and referenced literature (PMIDs).

For general information about ClinGen Expert Panels and Variant Curation please visit: Clinical Domain Working Groups. For specific inquiries regarding a variant classification or evidence curation (e.g. population database queried, segregation counts or other evidence used) or to submit general comments about the evidence repo, please email us.

The resource is undergoing updates and tesing. Should you encounter any issues regarding the data displayed, lack of functionality or other problems, please let us know so we can rectify these accordingly. Your help in this regard is greatly appreciated.

Evidence Repository

Expert curated classifications for variants' pathogenicity.

News

V1.0.8 NEW-FEATURE: Tab-delimited data dump and Guideline UI (2019-04-15)
V1.0.7 BUG-FIX: Minor bug fixes and improvements (2019-01-24)
V1.0.6 NEW-FEATURE: New guidelines (2018-12-04)
V1.0.5 NEW-FEATURE: Support for non CAR variants (2018-11-15)
V1.0.4 NEW-FEATURE: Capture/Show variant specific evidence (2018-10-25)
The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. If you have questions about the information contained on this website, please see a health care professional.
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