ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.5939+6C>T

gnomAD frequency: 0.00149  dbSNP: rs200393834
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000513735 SCV000610172 uncertain significance not provided 2017-03-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000513735 SCV001034960 benign not provided 2024-01-08 criteria provided, single submitter clinical testing
GeneDx RCV000513735 SCV001986829 likely benign not provided 2021-10-26 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000513735 SCV004137812 likely benign not provided 2022-08-01 criteria provided, single submitter clinical testing DOCK6: BP7
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000513735 SCV001797494 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000513735 SCV001965288 likely benign not provided no assertion criteria provided clinical testing

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