NM_000186.4(CFH):c.33G>T (p.Met11Ile) AND Factor H deficiency
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003449561.1
Allele description [Variation Report for NM_000186.4(CFH):c.33G>T (p.Met11Ile)]
NM_000186.4(CFH):c.33G>T (p.Met11Ile)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024