NM_017780.4(CHD7):c.6468C>T (p.Val2156=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001655612.2
Allele description [Variation Report for NM_017780.4(CHD7):c.6468C>T (p.Val2156=)]
NM_017780.4(CHD7):c.6468C>T (p.Val2156=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024