ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.287-26A>G

gnomAD frequency: 0.00040  dbSNP: rs201397253
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000412023 SCV000488738 likely benign Paragangliomas 4 2016-05-31 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002267949 SCV002552207 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
University of Washington Department of Laboratory Medicine, University of Washington RCV000209378 SCV000265456 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

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