NM_153700.2(STRC):c.4219-1G>A AND Autosomal recessive nonsyndromic hearing loss 16
- Germline classification:
- Likely pathogenic (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002467922.1
Allele description [Variation Report for NM_153700.2(STRC):c.4219-1G>A]
NM_153700.2(STRC):c.4219-1G>A
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024