ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.351G>A (p.Glu117=)

dbSNP: rs1659436211
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001608760 SCV001833165 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV002070482 SCV002391386 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2021-07-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451833 SCV004181452 benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451834 SCV004181453 benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451832 SCV004181454 benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing

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