ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.3873C>T (p.Cys1291=)

gnomAD frequency: 0.00019  dbSNP: rs200843111
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000932302 SCV001077984 benign not provided 2025-01-15 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000932302 SCV004011018 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing DOCK6: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV000932302 SCV005209428 likely benign not provided criteria provided, single submitter not provided

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