NM_000548.5(TSC2):c.4662+18G>A AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001729370.9
Allele description [Variation Report for NM_000548.5(TSC2):c.4662+18G>A]
NM_000548.5(TSC2):c.4662+18G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024