NM_006005.3(WFS1):c.2511G>T (p.Trp837Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 6, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003494281.1
Allele description [Variation Report for NM_006005.3(WFS1):c.2511G>T (p.Trp837Cys)]
NM_006005.3(WFS1):c.2511G>T (p.Trp837Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 14, 2024