ClinVar Miner

Submissions for variant NM_001163809.2(WDR81):c.2980C>T (p.Arg994Trp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003147892 SCV003835320 uncertain significance Hydrocephalus, congenital, 3, with brain anomalies 2022-08-11 criteria provided, single submitter clinical testing
Baylor Genetics RCV003147891 SCV003835410 uncertain significance Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2 2022-08-11 criteria provided, single submitter clinical testing

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