ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.4548G>A (p.Thr1516=)

gnomAD frequency: 0.00064  dbSNP: rs377755210
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
PreventionGenetics, part of Exact Sciences RCV000247428 SCV000313655 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000905870 SCV001050471 benign not provided 2024-11-05 criteria provided, single submitter clinical testing

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