NM_006005.3(WFS1):c.712+8C>T AND Wolfram syndrome 1
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002509107.3
Allele description [Variation Report for NM_006005.3(WFS1):c.712+8C>T]
NM_006005.3(WFS1):c.712+8C>T
Condition(s)
Assertion and evidence details
Last Updated: Jul 15, 2024