NM_006005.3(WFS1):c.2172G>A (p.Pro724=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002151404.5
Allele description [Variation Report for NM_006005.3(WFS1):c.2172G>A (p.Pro724=)]
NM_006005.3(WFS1):c.2172G>A (p.Pro724=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024