NM_001171.6(ABCC6):c.662+12C>T AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 27, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000613965.1
Allele description [Variation Report for NM_001171.6(ABCC6):c.662+12C>T]
NM_001171.6(ABCC6):c.662+12C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 14, 2024