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: CA180890 177868
VCEP: RASopathy VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_030662.3(MAP2K2):c.401A>G (p.Tyr134Cys) | Pathogenic | cardiofaciocutaneous syndrome | 2018-12-10 | 1.0 | - | MAP2K2 |
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