ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.942C>A (p.Ser314=)

dbSNP: rs143627613
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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 RCV002144050 SCV002463333 likely benign Hereditary hemochromatosis 2021-10-02 criteria provided, single submitter clinical testing

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