NM_004840.3(ARHGEF6):c.169T>C (p.Cys57Arg) AND Intellectual disability, X-linked 46
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000990954.2
Allele description [Variation Report for NM_004840.3(ARHGEF6):c.169T>C (p.Cys57Arg)]
NM_004840.3(ARHGEF6):c.169T>C (p.Cys57Arg)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023