ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.7774T>C (p.Leu2592=)

dbSNP: rs761019645
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001804681 SCV002051989 likely benign Cardiomyopathy 2021-05-17 criteria provided, single submitter clinical testing

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