ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.1833-8T>A

gnomAD frequency: 0.00708  dbSNP: rs7252321
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000881454 SCV001024632 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV000881454 SCV001802950 likely benign not provided 2020-10-18 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000881454 SCV001798227 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000881454 SCV001920077 likely benign not provided no assertion criteria provided clinical testing

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