ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.789G>A (p.Lys263=)

dbSNP: rs2102228724
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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 RCV001805397 SCV002052614 likely benign Cardiomyopathy 2021-03-23 criteria provided, single submitter clinical testing

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