ClinVar Miner

Submissions for variant NM_032856.5(WDR73):c.6_9del (p.Asp2fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV003447728 SCV004175403 likely pathogenic Galloway-Mowat syndrome 1 2023-06-09 criteria provided, single submitter clinical testing

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