ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.1224C>A (p.Thr408=)

dbSNP: rs1438781560
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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 RCV002147309 SCV002414068 likely benign Hereditary hemochromatosis 2021-10-05 criteria provided, single submitter clinical testing

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