NM_017841.4(SDHAF2):c.206G>A (p.Arg69His) AND Hereditary pheochromocytoma-paraganglioma
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000792983.6
Allele description [Variation Report for NM_017841.4(SDHAF2):c.206G>A (p.Arg69His)]
NM_017841.4(SDHAF2):c.206G>A (p.Arg69His)
Condition(s)
- Name:
- Hereditary pheochromocytoma-paraganglioma
- Synonyms:
- Hereditary Paraganglioma-Pheochromocytoma Syndromes; Hereditary Paragangliomas and Pheochromocytomas
- Identifiers:
- MONDO: MONDO:0017366; MedGen: C1708353
Assertion and evidence details
Last Updated: May 1, 2024