NM_002137.4(HNRNPA2B1):c.578-18C>T AND Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002612510.2
Allele description [Variation Report for NM_002137.4(HNRNPA2B1):c.578-18C>T]
NM_002137.4(HNRNPA2B1):c.578-18C>T
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024