NM_153676.4(USH1C):c.2547-1G>T AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 2, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000665878.1
Allele description [Variation Report for NM_153676.4(USH1C):c.2547-1G>T]
NM_153676.4(USH1C):c.2547-1G>T
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024