ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.424-13_424-11dup

dbSNP: rs1365741915
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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 RCV002126305 SCV002451730 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2023-12-18 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465928 SCV002760334 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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