ClinVar Miner

Submissions for variant NM_201525.4(ADGRG1):c.1925C>T (p.Ser642Phe)

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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 RCV001255739 SCV001432313 likely pathogenic Bilateral frontoparietal polymicrogyria no assertion criteria provided clinical testing

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