NM_016203.4(PRKAG2):c.*1040dup AND Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome
- Germline classification:
- Uncertain significance (3 submissions)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000272481.13
Allele description [Variation Report for NM_016203.4(PRKAG2):c.*1040dup]
NM_016203.4(PRKAG2):c.*1040dup
Condition(s)
- Name:
- Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome
- Identifiers:
- MedGen: CN239247
Assertion and evidence details
Last Updated: Sep 29, 2024