ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.2127C>T (p.Arg709=)

dbSNP: rs2486114706
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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 RCV002994867 SCV003299475 likely benign Hereditary hemochromatosis 2022-01-16 criteria provided, single submitter clinical testing

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