NM_205849.3(FAM9B):c.6G>T (p.Ala2=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003440939.6
Allele description
NM_205849.3(FAM9B):c.6G>T (p.Ala2=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 17, 2024