ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.9432G>A (p.Lys3144=) (rs367780360)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Integrated Genetics/Laboratory Corporation of America RCV000781824 SCV000920171 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Invitae RCV000869621 SCV001011061 likely benign Catecholaminergic polymorphic ventricular tachycardia 2019-12-31 criteria provided, single submitter clinical testing
Color RCV001184514 SCV001350496 likely benign Cardiomyopathy 2019-06-18 criteria provided, single submitter clinical testing

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