ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.885G>A (p.Gly295=)

dbSNP: rs2102212901
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001682532 SCV001905347 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799118 SCV002042863 likely benign Cardiomyopathy 2021-03-17 criteria provided, single submitter clinical testing
Invitae RCV001859432 SCV002240070 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2022-03-09 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451840 SCV004180476 likely benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451841 SCV004180477 likely benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451839 SCV004180478 likely benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing

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