ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.373-16C>T

gnomAD frequency: 0.00021  dbSNP: rs373508654
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001698320 SCV000534130 likely benign not provided 2018-04-06 criteria provided, single submitter clinical testing
Invitae RCV002060033 SCV002432121 likely benign Hypertrophic cardiomyopathy 2023-12-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502578 SCV002810188 likely benign Dilated cardiomyopathy 2A; Cardiomyopathy, familial restrictive, 1; Dilated cardiomyopathy 1FF; Hypertrophic cardiomyopathy 7 2022-04-26 criteria provided, single submitter clinical testing

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