ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.775-19G>A

gnomAD frequency: 0.00048  dbSNP: rs189646218
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001697423 SCV000714678 likely benign not provided 2018-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002062818 SCV002372580 likely benign Primary dilated cardiomyopathy 2024-01-25 criteria provided, single submitter clinical testing

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