ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.200-29C>G

gnomAD frequency: 0.00690  dbSNP: rs45449197
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000168962 SCV000305592 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001610479 SCV001835976 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445603 SCV004173816 benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445604 SCV004173817 benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003445602 SCV004173818 benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000168962 SCV001959161 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000168962 SCV001971962 benign not specified no assertion criteria provided clinical testing

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