ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.229+15A>G

gnomAD frequency: 0.00029  dbSNP: rs370756162
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000600486 SCV000716847 likely benign not specified 2018-01-31 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 RCV002063035 SCV002376733 likely benign Primary dilated cardiomyopathy 2023-12-21 criteria provided, single submitter clinical testing

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