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: CA8622895 695335
VCEP: Platelet Disorders VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000212.3(ITGB3):c.197T>G (p.Leu66Arg) | Benign | Glanzmann thrombasthenia | 2023-12-19 | 2.0 | ClinGen Platelet Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2.1 | ITGB3 |
| View | NM_000212.3(ITGB3):c.197T>G (p.Leu66Arg) | Uncertain Significance | Glanzmann's thrombasthenia | 2021-08-20 | 1.0 | - | ITGB3 |
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