ClinVar Miner

Submissions for variant NM_004946.3(DOCK2):c.3497C>T (p.Thr1166Ile)

dbSNP: rs1253821966
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001313911 SCV001504422 uncertain significance DOCK2 deficiency 2021-08-27 criteria provided, single submitter clinical testing

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