ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.1029G>A (p.Val343=)

dbSNP: rs758006460
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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 RCV001451081 SCV001654702 likely benign Primary dilated cardiomyopathy 2016-05-19 criteria provided, single submitter clinical testing

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