NM_022489.4(INF2):c.*388A>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003326405.11
Allele description [Variation Report for NM_022489.4(INF2):c.*388A>G]
NM_022489.4(INF2):c.*388A>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024