NM_006005.3(WFS1):c.1613T>C (p.Phe538Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 16, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000722408.1
Allele description [Variation Report for NM_006005.3(WFS1):c.1613T>C (p.Phe538Ser)]
NM_006005.3(WFS1):c.1613T>C (p.Phe538Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Feb 25, 2023