NM_001352514.2(HLCS):c.2121+11T>A AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 31, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000445315.1
Allele description [Variation Report for NM_001352514.2(HLCS):c.2121+11T>A]
NM_001352514.2(HLCS):c.2121+11T>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024