ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.147A>G (p.Pro49=)

dbSNP: rs2101541448
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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 RCV001458027 SCV001661842 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2019-12-19 criteria provided, single submitter clinical testing

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