ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.766-40C>T

gnomAD frequency: 0.00536  dbSNP: rs147408869
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000836342 SCV000978186 likely benign not provided 2018-06-12 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268333 SCV002552440 benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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