ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.73-11A>C

gnomAD frequency: 0.00002  dbSNP: rs927103985
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001810677 SCV001477715 likely benign not provided 2020-04-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002070106 SCV002336134 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2024-07-19 criteria provided, single submitter clinical testing

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