NM_001379180.1(ESRRB):c.577+15C>T AND Autosomal recessive nonsyndromic hearing loss 35
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000376138.5
Allele description [Variation Report for NM_001379180.1(ESRRB):c.577+15C>T]
NM_001379180.1(ESRRB):c.577+15C>T
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024