ClinVar Miner

Submissions for variant NM_001379403.1(WDR26):c.1082A>G (p.His361Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV002280298 SCV002568321 likely pathogenic Skraban-Deardorff syndrome 2022-04-29 criteria provided, single submitter clinical testing PS2, PM2, PP2

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