NM_017780.4(CHD7):c.1565G>T (p.Gly522Val) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 2, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002317769.9
Allele description [Variation Report for NM_017780.4(CHD7):c.1565G>T (p.Gly522Val)]
NM_017780.4(CHD7):c.1565G>T (p.Gly522Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 13, 2024