ClinVar Miner

Submissions for variant NM_000143.4(FH):c.1143C>T (p.Thr381=)

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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 RCV005073546 SCV005705989 likely benign not provided 2024-06-03 criteria provided, single submitter clinical testing

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