ClinVar Miner

Submissions for variant NM_006393.3(NEBL):c.2473C>T (p.His825Tyr)

dbSNP: rs1554774990
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine RCV000656147 SCV000678341 uncertain significance Wolff-Parkinson-White pattern 2017-07-14 no assertion criteria provided research This variant was identified in an individual with Wolff-Parkinson-White syndrome

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