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: CA325653 18012
VCEP: Thrombosis VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000488.4(SERPINC1):c.89T>A (p.Val30Glu) | Pathogenic | antithrombin III deficiency | 2025-02-07 | 1.2 | ClinGen Thrombosis Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for SERPINC1 Version 1.1.0 | SERPINC1 |
| View | NM_000488.4(SERPINC1):c.89T>A (p.Val30Glu) | Pathogenic | antithrombin III deficiency | 2025-02-07 | 1.1 | - | SERPINC1 |
| View | NM_000488.4(SERPINC1):c.89T>A (p.Val30Glu) | Pathogenic | antithrombin III deficiency | 2024-10-02 | 1.0 | - | SERPINC1 |
Showing 1 to 3 of 3 rows