The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries.
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Curation History
Variant: CA137387 4927
VCEP: Hearing Loss VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_022124.5(CDH23):c.3625A>G (p.Thr1209Ala) | Benign | Usher syndrome | 2019-07-17 | 1.0 | - | CDH23 |
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