ClinVar Miner

Submissions for variant NM_203447.4(DOCK8):c.5962-18_5962-9del

dbSNP: rs35071801
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001546044 SCV001765489 likely benign not provided 2020-06-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003761396 SCV004452490 likely benign Autosomal recessive hyper-IgE syndrome 2023-06-30 criteria provided, single submitter clinical testing

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