ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.449+10C>G

gnomAD frequency: 0.00003  dbSNP: rs552910679
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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 RCV001324810 SCV001515776 likely benign Primary dilated cardiomyopathy 2023-02-02 criteria provided, single submitter clinical testing

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