ClinVar Miner

Submissions for variant NM_003000.2(SDHB):c.541-9C>T (rs755367242)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000841519 SCV000983489 likely benign not provided 2018-04-02 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.
Invitae RCV000841519 SCV001081354 likely benign not provided 2018-12-05 criteria provided, single submitter clinical testing
Invitae RCV001472872 SCV001677013 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2020-01-25 criteria provided, single submitter clinical testing

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