ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.2962G>C (p.Gly988Arg)

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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 RCV001255795 SCV001432409 likely benign Greig cephalopolysyndactyly syndrome no assertion criteria provided clinical testing

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