ClinVar Miner

Submissions for variant NM_003001.5(SDHC):c.78-19C>A

dbSNP: rs144770080
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001927008 SCV002198337 likely benign Gastrointestinal stromal tumor; Paragangliomas 3 2024-01-19 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003738114 SCV004563737 likely benign not provided 2023-08-23 criteria provided, single submitter clinical testing

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