ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.682+15C>T

gnomAD frequency: 0.00017  dbSNP: rs201450101
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000827221 SCV000968850 likely benign not provided 2018-05-15 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 RCV003509612 SCV004364099 likely benign Primary dilated cardiomyopathy 2023-11-15 criteria provided, single submitter clinical testing

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