ClinVar Miner

Submissions for variant NM_000364.4(TNNT2):c.53-11_53-7del (rs45533739)

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Total submissions: 11
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000036600 SCV000060255 benign not specified 2006-11-07 criteria provided, single submitter clinical testing
GeneDx RCV000036600 SCV000209214 benign not specified 2013-09-25 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000036600 SCV000230138 benign not specified 2015-01-12 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000036600 SCV000305598 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000330905 SCV000353368 likely benign Left ventricular noncompaction cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000385533 SCV000353369 likely benign Familial restrictive cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000291224 SCV000353370 likely benign Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000327238 SCV000353371 likely benign Hypertrophic cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000646080 SCV000767837 benign not provided 2019-03-06 criteria provided, single submitter clinical testing
Color RCV000775982 SCV000910503 benign Cardiomyopathy 2018-03-09 criteria provided, single submitter clinical testing
Mendelics RCV000986505 SCV001135518 benign Familial hypertrophic cardiomyopathy 2 2019-05-28 criteria provided, single submitter clinical testing

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