NM_000208.4(INSR):c.653-23TC[13] AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001817443.4
Allele description [Variation Report for NM_000208.4(INSR):c.653-23TC[13]]
NM_000208.4(INSR):c.653-23TC[13]
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 17, 2024