ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.2160+5G>A

gnomAD frequency: 0.00405  dbSNP: rs150276162
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000970354 SCV001117926 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000970354 SCV001822655 likely benign not provided 2020-10-09 criteria provided, single submitter clinical testing
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille RCV001252476 SCV001428233 likely benign Intellectual disability 2019-01-01 no assertion criteria provided clinical testing

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