ClinVar Miner

Submissions for variant NM_152594.3(SPRED1):c.854C>T (p.Pro285Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Service de Génétique Moléculaire, Hôpital Robert Debré RCV001261036 SCV001438437 uncertain significance Noonan syndrome no assertion criteria provided clinical testing

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