ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.294A>G (p.Arg98=) (rs1568858567)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Health, Inc RCV000773674 SCV000907373 likely benign Cardiomyopathy 2018-08-05 criteria provided, single submitter clinical testing
Blueprint Genetics RCV000788503 SCV000927648 uncertain significance not provided 2018-04-23 criteria provided, single submitter clinical testing
Invitae RCV001448294 SCV001651380 likely benign Hypertrophic cardiomyopathy 2019-12-03 criteria provided, single submitter clinical testing

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