NM_000186.4(CFH):c.459G>A (p.Glu153=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002638723.2
Allele description [Variation Report for NM_000186.4(CFH):c.459G>A (p.Glu153=)]
NM_000186.4(CFH):c.459G>A (p.Glu153=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024