ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.424-37TTC[6]

dbSNP: rs34261028
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Total submissions: 10
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243274 SCV000309332 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000402739 SCV000351423 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000307606 SCV000351424 uncertain significance Carney-Stratakis syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV001517903 SCV001726501 benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001580091 SCV001832144 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000243274 SCV002552163 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001580091 SCV003800432 likely benign not provided 2023-10-11 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003514341 SCV004362273 benign Paragangliomas 4 2022-08-17 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001580091 SCV001809642 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000243274 SCV001926430 benign not specified no assertion criteria provided clinical testing

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