ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.4895T>A (p.Ile1632Asn)

dbSNP: rs1373346977
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine RCV001258169 SCV001435057 uncertain significance Catecholaminergic polymorphic ventricular tachycardia 1 criteria provided, single submitter clinical testing

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