NM_001353921.2(ARHGEF9):c.1488G>A (p.Ser496=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002316549.9
Allele description [Variation Report for NM_001353921.2(ARHGEF9):c.1488G>A (p.Ser496=)]
NM_001353921.2(ARHGEF9):c.1488G>A (p.Ser496=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 26, 2024