ClinVar Miner

Submissions for variant NM_001018005.2(TPM1):c.115-331C>T

gnomAD frequency: 0.00041  dbSNP: rs562829514
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000771282 SCV000903436 benign Cardiomyopathy 2018-04-08 criteria provided, single submitter clinical testing
GeneDx RCV001637126 SCV001849091 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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