NM_170707.4(LMNA):c.811-18del AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 11, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000612522.4
Allele description [Variation Report for NM_170707.4(LMNA):c.811-18del]
NM_170707.4(LMNA):c.811-18del
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Flagged submissions
Submission Accession | Submitter | Review Status (Assertion method) | Clinical Significance (Last evaluated) | Origin | Method | Citations |
---|---|---|---|---|---|---|
SCV000720950 | GeneDx | flagged submission Reason: This record appears to be redundant with a more recent record from the same submitter. Notes: SCV000720950 appears to be redundant with SCV000721068. (GeneDx Variant Classification (06012015)) | Likely benign (Jul 11, 2017) | germline | clinical testing |
Last Updated: Dec 9, 2023