NM_005585.5(SMAD6):c.1026C>G (p.Arg342=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 2, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002381009.2
Allele description [Variation Report for NM_005585.5(SMAD6):c.1026C>G (p.Arg342=)]
NM_005585.5(SMAD6):c.1026C>G (p.Arg342=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024