ClinVar Miner

Submissions for variant NM_025132.4(WDR19):c.2897A>G (p.Asp966Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Cologne University RCV003232886 SCV003929421 uncertain significance Senior-Loken syndrome 8 2023-04-25 criteria provided, single submitter clinical testing

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