NM_002193.4(INHBB):c.22G>A (p.Ala8Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004084716.1
Allele description [Variation Report for NM_002193.4(INHBB):c.22G>A (p.Ala8Thr)]
NM_002193.4(INHBB):c.22G>A (p.Ala8Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024