NM_020638.3(FGF23):c.515_529del (p.Pro172_Arg176del) AND Autosomal dominant hypophosphatemic rickets
- Germline classification:
- Likely pathogenic (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003476889.1
Allele description [Variation Report for NM_020638.3(FGF23):c.515_529del (p.Pro172_Arg176del)]
NM_020638.3(FGF23):c.515_529del (p.Pro172_Arg176del)
Condition(s)
Assertion and evidence details
Last Updated: Jan 6, 2024