ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.4869G>A (p.Ala1623=)

gnomAD frequency: 0.00107  dbSNP: rs187249194
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000974303 SCV001122121 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
GeneDx RCV000974303 SCV001770938 likely benign not provided 2020-12-23 criteria provided, single submitter clinical testing

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