ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.424-11C>G

gnomAD frequency: 0.00001  dbSNP: rs199523383
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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 RCV002157137 SCV002334852 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2024-12-26 criteria provided, single submitter clinical testing

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