NM_001114753.3(ENG):c.578C>T (p.Thr193Met) AND Hereditary hemorrhagic telangiectasia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002231269.13
Allele description [Variation Report for NM_001114753.3(ENG):c.578C>T (p.Thr193Met)]
NM_001114753.3(ENG):c.578C>T (p.Thr193Met)
Condition(s)
- Name:
- Hereditary hemorrhagic telangiectasia (HHT)
- Synonyms:
- Osler Weber Rendu syndrome; ORW disease; Osler-Rendu-Weber disease; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0019180; MedGen: C0039445; OMIM: PS187300
Assertion and evidence details
Last Updated: Jul 15, 2024