NM_000132.4(F8):c.788-14T>G AND Abnormality of coagulation
- 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:
- RCV000851881.1
Allele description [Variation Report for NM_000132.4(F8):c.788-14T>G]
NM_000132.4(F8):c.788-14T>G
Condition(s)
- Name:
- Abnormality of coagulation
- Identifiers:
- MedGen: C1846821; Human Phenotype Ontology: HP:0001928
Assertion and evidence details
Last Updated: Apr 23, 2022