ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.504C>A (p.Gly168=)

dbSNP: rs1458709458
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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 RCV002141325 SCV002461560 likely benign Hereditary hemochromatosis 2020-11-06 criteria provided, single submitter clinical testing

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