NM_001379180.1(ESRRB):c.226G>A (p.Gly76Ser) AND Autosomal recessive nonsyndromic hearing loss 35
- 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:
- RCV001117009.4
Allele description [Variation Report for NM_001379180.1(ESRRB):c.226G>A (p.Gly76Ser)]
NM_001379180.1(ESRRB):c.226G>A (p.Gly76Ser)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023