NM_001079668.3(NKX2-1):c.*579C>G AND Benign hereditary chorea
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000362328.5
Allele description [Variation Report for NM_001079668.3(NKX2-1):c.*579C>G]
NM_001079668.3(NKX2-1):c.*579C>G
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023