ClinVar Miner

Submissions for variant NM_000410.4(HFE):c.76+9G>T

dbSNP: rs2113726940
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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 RCV002212860 SCV002360982 likely benign Hereditary hemochromatosis 2021-11-11 criteria provided, single submitter clinical testing

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