NM_004999.4(MYO6):c.406C>A (p.Arg136=) AND Autosomal recessive nonsyndromic hearing loss 37
- 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:
- RCV001159353.4
Allele description [Variation Report for NM_004999.4(MYO6):c.406C>A (p.Arg136=)]
NM_004999.4(MYO6):c.406C>A (p.Arg136=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023