NM_007373.4(SHOC2):c.52G>C (p.Val18Leu) AND RASopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002628416.2
Allele description
NM_007373.4(SHOC2):c.52G>C (p.Val18Leu)
Condition(s)
- Name:
- RASopathy
- Synonyms:
- rasopathies; Noonan spectrum disorder
- Identifiers:
- MONDO: MONDO:0021060; MedGen: C5555857
Assertion and evidence details
Last Updated: May 19, 2024