ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.861C>T (p.Leu287=)

gnomAD frequency: 0.00001  dbSNP: rs746457439
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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 RCV001454874 SCV001658613 likely benign Primary dilated cardiomyopathy 2020-08-15 criteria provided, single submitter clinical testing

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