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: CA267785638 437192
VCEP: Rett and Angelman-like Disorders VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_130838.1(UBE3A):c.876G>A (p.Lys292=) | Uncertain Significance | Angelman syndrome | 2021-05-10 | 1.0 | - | UBE3A |
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