ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.541-18_541-8dup

dbSNP: rs1553177448
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000546563 SCV000630715 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2024-04-18 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004003799 SCV004819119 likely benign Hereditary pheochromocytoma-paraganglioma 2022-12-27 criteria provided, single submitter clinical testing

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