NM_001711.6(BGN):c.111C>T (p.Asn37=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002489323.1
Allele description [Variation Report for NM_001711.6(BGN):c.111C>T (p.Asn37=)]
NM_001711.6(BGN):c.111C>T (p.Asn37=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024