ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.98-81G>A

gnomAD frequency: 0.00067  dbSNP: rs45576939
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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000234340 SCV000285656 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2024-01-17 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001701710 SCV001477729 benign not provided 2020-08-25 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001701710 SCV002821449 likely benign not provided 2024-02-01 criteria provided, single submitter clinical testing TNNT2: BS1
Genome-Nilou Lab RCV003445717 SCV004173843 benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445718 SCV004173844 benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445716 SCV004173845 benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001701710 SCV001930709 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001701710 SCV001951531 likely benign not provided no assertion criteria provided clinical testing

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