ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.732C>T (p.His244=)

dbSNP: rs1570944785
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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 RCV000925591 SCV001071134 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2024-07-15 criteria provided, single submitter clinical testing

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