NM_002109.6(HARS1):c.522+1G>A AND Usher syndrome type 3B
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002236505.3
Allele description [Variation Report for NM_002109.6(HARS1):c.522+1G>A]
NM_002109.6(HARS1):c.522+1G>A
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024