ClinVar Miner

Submissions for variant NM_015267.4(CUX2):c.760G>A (p.Glu254Lys)

dbSNP: rs1886461979
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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 RCV001353120 SCV001548288 benign Developmental and epileptic encephalopathy, 67 no assertion criteria provided clinical testing

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