ClinVar Miner

Submissions for variant NM_145716.4(SSBP3):c.729dup (p.Gly244fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine RCV003128005 SCV003804073 uncertain significance Developmental disorder 2022-01-13 criteria provided, single submitter clinical testing

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