ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.1032C>T (p.Asp344=)

dbSNP: rs759106464
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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 RCV001414597 SCV001616736 likely benign Primary dilated cardiomyopathy 2019-08-02 criteria provided, single submitter clinical testing

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