NM_006005.3(WFS1):c.1756G>A (p.Ala586Thr) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Aug 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003325164.2
Allele description [Variation Report for NM_006005.3(WFS1):c.1756G>A (p.Ala586Thr)]
NM_006005.3(WFS1):c.1756G>A (p.Ala586Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024