NM_007373.4(SHOC2):c.841+12G>A AND not provided
- 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:
- RCV001723705.2
Allele description [Variation Report for NM_007373.4(SHOC2):c.841+12G>A]
NM_007373.4(SHOC2):c.841+12G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 6, 2024