NM_000260.4(MYO7A):c.5945-9G>C AND Autosomal dominant nonsyndromic hearing loss 11
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001111848.4
Allele description [Variation Report for NM_000260.4(MYO7A):c.5945-9G>C]
NM_000260.4(MYO7A):c.5945-9G>C
Condition(s)
Assertion and evidence details
Last Updated: Jun 17, 2024