NM_080680.3(COL11A2):c.2682+26A>C AND Autosomal dominant nonsyndromic hearing loss 13
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001582885.2
Allele description [Variation Report for NM_080680.3(COL11A2):c.2682+26A>C]
NM_080680.3(COL11A2):c.2682+26A>C
Condition(s)
Assertion and evidence details
Last Updated: Mar 10, 2024