NM_002203.4(ITGA2):c.1189G>A (p.Gly397Ser) AND Platelet-type bleeding disorder 9
- 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:
- RCV000289940.5
Allele description [Variation Report for NM_002203.4(ITGA2):c.1189G>A (p.Gly397Ser)]
NM_002203.4(ITGA2):c.1189G>A (p.Gly397Ser)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023