ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.374+16C>T

dbSNP: rs141500917
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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 RCV002075802 SCV002388486 likely benign Primary dilated cardiomyopathy 2023-08-05 criteria provided, single submitter clinical testing

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