ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.795G>A (p.Lys265=)

dbSNP: rs1658577208
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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 RCV001181215 SCV001346315 likely benign Cardiomyopathy 2019-06-30 criteria provided, single submitter clinical testing

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