NM_001015877.2(PHF6):c.-47+8C>T AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 12, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000437613.1
Allele description [Variation Report for NM_001015877.2(PHF6):c.-47+8C>T]
NM_001015877.2(PHF6):c.-47+8C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2023