NM_006005.3(WFS1):c.1761G>C (p.Arg587=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 17, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000424281.1
Allele description [Variation Report for NM_006005.3(WFS1):c.1761G>C (p.Arg587=)]
NM_006005.3(WFS1):c.1761G>C (p.Arg587=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024