NM_002137.4(HNRNPA2B1):c.476-19T>C AND Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003740707.2
Allele description [Variation Report for NM_002137.4(HNRNPA2B1):c.476-19T>C]
NM_002137.4(HNRNPA2B1):c.476-19T>C
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024