ClinVar Miner

Submissions for variant NM_015021.3(ZNF292):c.4862del (p.Asn1621fs)

dbSNP: rs2127867444
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Génétique des Maladies du Développement, Hospices Civils de Lyon RCV001806689 SCV002025266 likely pathogenic Intellectual developmental disorder, autosomal dominant 64 no assertion criteria provided clinical testing

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