ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.4197C>T (p.Ile1399=)

gnomAD frequency: 0.00306  dbSNP: rs35583018
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000887610 SCV001031180 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV000887610 SCV001782750 likely benign not provided 2019-08-18 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000887610 SCV004137827 benign not provided 2023-03-01 criteria provided, single submitter clinical testing DOCK6: BP4, BP7, BS1, BS2

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