ClinVar Miner

Submissions for variant NM_002524.5(NRAS):c.176C>A (p.Ala59Asp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NIHR Bioresource Rare Diseases, University of Cambridge RCV001003789 SCV001162233 likely pathogenic Anemia no assertion criteria provided research
Service de Génétique Moléculaire, Hôpital Robert Debré RCV001261065 SCV001438467 likely pathogenic Noonan syndrome no assertion criteria provided clinical testing

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