ClinVar Miner

Submissions for variant NM_032856.5(WDR73):c.926ATGGAACACGGAGCCAAG[1] (p.309DGTRSQ[1])

dbSNP: rs11267906
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000989367 SCV001139664 benign Galloway-Mowat syndrome 1 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001672992 SCV001886444 benign not provided 2019-11-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001672992 SCV002422838 benign not provided 2025-02-02 criteria provided, single submitter clinical testing

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