NM_003611.3(OFD1):c.2033C>G (p.Ala678Gly) AND History of neurodevelopmental disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 24, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000721044.2
Allele description
NM_003611.3(OFD1):c.2033C>G (p.Ala678Gly)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
Assertion and evidence details
Last Updated: Aug 23, 2022