NM_004560.4(ROR2):c.1589G>A (p.Arg530Gln) AND Autosomal recessive Robinow syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000279061.5
Allele description [Variation Report for NM_004560.4(ROR2):c.1589G>A (p.Arg530Gln)]
NM_004560.4(ROR2):c.1589G>A (p.Arg530Gln)
Condition(s)
Assertion and evidence details
Last Updated: Aug 4, 2024