NM_000053.4(ATP7B):c.3556+3A>G AND Wilson disease
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002695472.1
Allele description [Variation Report for NM_000053.4(ATP7B):c.3556+3A>G]
NM_000053.4(ATP7B):c.3556+3A>G
Condition(s)
Assertion and evidence details
Last Updated: Jan 6, 2024