ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.*67G>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002286307 SCV002576266 likely benign not provided 2020-07-18 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
CeGaT Center for Human Genetics Tuebingen RCV002286307 SCV002585703 benign not provided 2023-03-01 criteria provided, single submitter clinical testing DOCK6: BS1, BS2

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