ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.33+10G>A

dbSNP: rs2486148755
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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 RCV002881129 SCV003233932 likely benign Hereditary hemochromatosis 2022-09-11 criteria provided, single submitter clinical testing

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