ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.1422T>G (p.Thr474=)

dbSNP: rs2145927131
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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 RCV001472338 SCV001676468 likely benign Primary dilated cardiomyopathy 2023-06-15 criteria provided, single submitter clinical testing

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