NM_000488.4(SERPINC1):c.89T>A (p.Val30Glu) AND Thromboembolism
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000852239.9
Allele description [Variation Report for NM_000488.4(SERPINC1):c.89T>A (p.Val30Glu)]
NM_000488.4(SERPINC1):c.89T>A (p.Val30Glu)
Condition(s)
- Name:
- Thromboembolism
- Identifiers:
- MedGen: C0040038; Human Phenotype Ontology: HP:0001907
Assertion and evidence details
Last Updated: Jul 15, 2024