NM_001142800.2(EYS):c.6888T>C (p.His2296=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001474890.7
Allele description [Variation Report for NM_001142800.2(EYS):c.6888T>C (p.His2296=)]
NM_001142800.2(EYS):c.6888T>C (p.His2296=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024