ClinVar Miner

Submissions for variant NM_203447.4(DOCK8):c.5962-22_5962-9del

dbSNP: rs35071801
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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 RCV003761334 SCV001678308 likely benign Autosomal recessive hyper-IgE syndrome 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV001567086 SCV001790713 likely benign not provided 2020-09-28 criteria provided, single submitter clinical testing

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