ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.601-32A>C

gnomAD frequency: 0.73965  dbSNP: rs1104859
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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 RCV000242651 SCV000305599 benign not specified criteria provided, single submitter clinical testing
Mendelics RCV000986504 SCV001135517 benign Hypertrophic cardiomyopathy 2 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001658184 SCV001874612 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838564 SCV002098604 benign Dilated cardiomyopathy 1D 2021-09-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838565 SCV002098605 benign Cardiomyopathy, familial restrictive, 3 2021-09-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000986504 SCV002098606 benign Hypertrophic cardiomyopathy 2 2021-09-10 criteria provided, single submitter clinical testing

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