ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.424-37TTC[11]

dbSNP: rs34261028
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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 RCV002118535 SCV002450096 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2024-01-17 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002259170 SCV002527079 benign Hereditary cancer-predisposing syndrome 2022-01-03 criteria provided, single submitter curation

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