ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.1890C>T (p.Leu630=)

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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 RCV003087648 SCV003472812 likely benign Hereditary hemochromatosis 2022-05-24 criteria provided, single submitter clinical testing

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