NM_000186.4(CFH):c.1935G>A (p.Thr645=) AND Factor H deficiency
- Germline classification:
- Likely benign (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:
- RCV003451708.1
Allele description [Variation Report for NM_000186.4(CFH):c.1935G>A (p.Thr645=)]
NM_000186.4(CFH):c.1935G>A (p.Thr645=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024