ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.1086+12_1086+13delinsTC

dbSNP: rs2145939546
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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 RCV002136006 SCV002454427 likely benign Primary dilated cardiomyopathy 2024-01-12 criteria provided, single submitter clinical testing

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