NM_000260.4(MYO7A):c.2122A>G (p.Met708Val) AND Autosomal recessive nonsyndromic hearing loss 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001578681.2
Allele description [Variation Report for NM_000260.4(MYO7A):c.2122A>G (p.Met708Val)]
NM_000260.4(MYO7A):c.2122A>G (p.Met708Val)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024