NM_006939.4(SOS2):c.3489+19C>T AND Noonan syndrome 9
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002061987.16
Allele description [Variation Report for NM_006939.4(SOS2):c.3489+19C>T]
NM_006939.4(SOS2):c.3489+19C>T
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024