ClinVar Miner

Submissions for variant NM_032856.5(WDR73):c.41+262G>A

gnomAD frequency: 0.00888  dbSNP: rs147776100
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001585391 SCV001819284 likely benign not provided 2020-11-02 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495944 SCV002804322 likely benign Galloway-Mowat syndrome 1 2021-07-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001585391 SCV005213336 likely benign not provided criteria provided, single submitter not provided

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