ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2603G>A (p.Gly868Asp)

dbSNP: rs886048376
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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 RCV000656184 SCV000678378 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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