ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.1257C>G (p.Gly419=)

dbSNP: rs2486126389
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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 RCV002862028 SCV003223057 likely benign Hereditary hemochromatosis 2022-07-31 criteria provided, single submitter clinical testing

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