NM_006005.3(WFS1):c.482G>A (p.Arg161Gln) AND WFS1-Related Spectrum Disorders
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001154624.6
Allele description [Variation Report for NM_006005.3(WFS1):c.482G>A (p.Arg161Gln)]
NM_006005.3(WFS1):c.482G>A (p.Arg161Gln)
Condition(s)
- Name:
- WFS1-Related Spectrum Disorders
- Identifiers:
- MedGen: CN239410
Assertion and evidence details
Last Updated: Sep 16, 2024