ClinVar Miner

Submissions for variant NM_003085.5(SNCB):c.121+6T>C

gnomAD frequency: 0.97242  dbSNP: rs4868669
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001638123 SCV001848191 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810069 SCV002057505 benign Lewy body dementia 2021-07-15 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001528937 SCV001741539 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001528937 SCV001807251 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001528937 SCV001965621 benign not specified no assertion criteria provided clinical testing

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