ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.201-36G>T

gnomAD frequency: 0.95416  dbSNP: rs1022580
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Total submissions: 9
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252587 SCV000309328 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001636774 SCV000605074 benign not provided 2020-04-22 criteria provided, single submitter clinical testing
GeneDx RCV001636774 SCV001848099 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807164 SCV002054687 benign Gastrointestinal stromal tumor 2021-07-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807165 SCV002054688 benign Mitochondrial complex 2 deficiency, nuclear type 4 2021-07-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807163 SCV002054689 benign Paragangliomas 4 2021-07-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807162 SCV002054690 benign Pheochromocytoma 2021-07-15 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV001807163 SCV004015412 benign Paragangliomas 4 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001636774 SCV005285511 benign not provided criteria provided, single submitter not provided

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