ClinVar Miner

Submissions for variant NM_203447.4(DOCK8):c.3234+22_3234+27del

dbSNP: rs755800285
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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 RCV003762211 SCV002394406 likely benign Autosomal recessive hyper-IgE syndrome 2024-01-04 criteria provided, single submitter clinical testing

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