NM_000517.6(HBA2):c.*82G>A AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 25, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000506995.2
Allele description [Variation Report for NM_000517.6(HBA2):c.*82G>A]
NM_000517.6(HBA2):c.*82G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Apr 23, 2022