NM_016239.4(MYO15A):c.7787+27G>T AND Autosomal recessive nonsyndromic hearing loss 3
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001779305.2
Allele description [Variation Report for NM_016239.4(MYO15A):c.7787+27G>T]
NM_016239.4(MYO15A):c.7787+27G>T
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024