ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.1074C>T (p.Pro358=)

dbSNP: rs780417157
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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 RCV003058641 SCV003448401 likely benign Hereditary hemochromatosis 2024-02-23 criteria provided, single submitter clinical testing

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