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: CA115846 2900
VCEP: Platelet Disorders VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000419.3(ITGA2B):c.1787T>C | Pathogenic | Glanzmann thrombasthenia | 2023-11-03 | 1.2 | ClinGen Platelet Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2.1 | ITGA2B |
| View | NM_000419.3(ITGA2B):c.1787T>C | Pathogenic | Glanzmann thrombasthenia | 2023-11-03 | 1.1 | ClinGen Platelet Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2.1 | N/A |
| View | NM_000419.3(ITGA2B):c.1787T>C | Pathogenic | Glanzmann thrombasthenia | 2023-10-17 | 1.0 | ClinGen Platelet Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2.1 | N/A |
Showing 1 to 3 of 3 rows