ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.164-50G>A

dbSNP: rs3729843
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243455 SCV000305591 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001711664 SCV001939266 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445813 SCV004173823 benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445814 SCV004173824 benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445812 SCV004173825 benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711664 SCV005288659 benign not provided criteria provided, single submitter not provided

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