ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.*66G>A

gnomAD frequency: 0.01883  dbSNP: rs3729998
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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000381275 SCV000353312 likely benign Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000289254 SCV000353313 likely benign Left ventricular noncompaction cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000346573 SCV000353314 likely benign Hypertrophic cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000403791 SCV000353315 likely benign Familial restrictive cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001683177 SCV001899496 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445880 SCV004173706 benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445881 SCV004173707 benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445879 SCV004173708 benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing

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