NM_000518.5(HBB):c.324C>T (p.Gly108=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 28, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000507146.13
Allele description [Variation Report for NM_000518.5(HBB):c.324C>T (p.Gly108=)]
NM_000518.5(HBB):c.324C>T (p.Gly108=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Venous malformation
Venous malformationMedGen
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024