ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.424-37TTC[7]

dbSNP: rs34261028
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001579364 SCV001158130 benign not provided 2021-01-22 criteria provided, single submitter clinical testing
Invitae RCV002068762 SCV002482938 benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2024-01-24 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268397 SCV002552152 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579364 SCV001806943 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001579364 SCV001925216 likely benign not provided no assertion criteria provided clinical testing

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