ClinVar Miner

Submissions for variant NM_014991.6(WDFY3):c.1153G>A (p.Ala385Thr)

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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 RCV001255807 SCV001432422 likely benign Microcephaly 18, primary, autosomal dominant no assertion criteria provided clinical testing

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