ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.1107C>A (p.Pro369=)

dbSNP: rs371533709
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000614702 SCV000728021 likely benign not specified 2018-02-26 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV002528690 SCV003296471 likely benign Primary dilated cardiomyopathy 2022-07-31 criteria provided, single submitter clinical testing

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