ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.230-9A>G

gnomAD frequency: 0.00002  dbSNP: rs368172149
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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 RCV001494221 SCV001698872 likely benign Primary dilated cardiomyopathy 2020-08-21 criteria provided, single submitter clinical testing

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