ClinVar Miner

Submissions for variant NM_203447.4(DOCK8):c.3234+15dup

dbSNP: rs375864618
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000267280 SCV000480266 uncertain significance Hyper-IgE syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005090628 SCV001724346 benign not provided 2024-10-22 criteria provided, single submitter clinical testing

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