ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.286+16C>T

gnomAD frequency: 0.00001  dbSNP: rs200305451
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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 RCV002126042 SCV002452276 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2024-10-30 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003320874 SCV004025227 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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