NM_000518.5(HBB):c.-273T>C AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000860863.19
Allele description [Variation Report for NM_000518.5(HBB):c.-273T>C]
NM_000518.5(HBB):c.-273T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024