ClinVar Miner

Submissions for variant NM_001159699.2(FHL1):c.737-8C>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003741614 SCV004562710 likely benign Familial hemophagocytic lymphohistiocytosis type 1 2023-10-23 criteria provided, single submitter clinical testing

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