ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.765+13G>A

gnomAD frequency: 0.00002  dbSNP: rs115561881
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000245434 SCV000309335 benign not specified criteria provided, single submitter clinical testing
Counsyl RCV000411316 SCV000489459 likely benign Paragangliomas 4 2016-10-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058131 SCV002404794 benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2025-01-06 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV000411316 SCV004015418 benign Paragangliomas 4 2023-07-07 criteria provided, single submitter clinical testing

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