NM_001164508.2(NEB):c.11806-7C>A AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000246177.5
Allele description [Variation Report for NM_001164508.2(NEB):c.11806-7C>A]
NM_001164508.2(NEB):c.11806-7C>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024