ClinVar Miner

Submissions for variant NM_004946.3(DOCK2):c.2799+42206G>A

dbSNP: rs753446744
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001336757 SCV001530231 uncertain significance DOCK2 deficiency 2018-09-26 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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