NM_000338.3(SLC12A1):c.2296-6G>T AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001288424.2
Allele description [Variation Report for NM_000338.3(SLC12A1):c.2296-6G>T]
NM_000338.3(SLC12A1):c.2296-6G>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024