NM_177398.4(LMX1A):c.331del (p.Gln111fs) AND Autosomal dominant nonsyndromic hearing loss 7
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- May 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002251019.1
Allele description [Variation Report for NM_177398.4(LMX1A):c.331del (p.Gln111fs)]
NM_177398.4(LMX1A):c.331del (p.Gln111fs)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023