ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.672T>C (p.Asp224=)

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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 RCV003780185 SCV004603635 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2023-01-18 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004805067 SCV005424052 likely benign Hereditary pheochromocytoma-paraganglioma 2024-03-24 criteria provided, single submitter clinical testing

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