ClinVar Miner

Submissions for variant NM_000364.4(TNNT2):c.84A>G (p.Arg28=) (rs370895664)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000526032 SCV000646906 likely benign Familial hypertrophic cardiomyopathy 2; Left ventricular noncompaction 6; Familial restrictive cardiomyopathy 3 2017-04-11 criteria provided, single submitter clinical testing

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