ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.51C>T (p.Thr17=)

dbSNP: rs550555402
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002075283 SCV002378069 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2021-07-17 criteria provided, single submitter clinical testing

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