ClinVar Miner

Submissions for variant NM_001318895.3(FHL2):c.513G>C (p.Thr171=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003620181 SCV004558364 likely benign Primary dilated cardiomyopathy 2024-01-28 criteria provided, single submitter clinical testing

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