ClinVar Miner

Submissions for variant NM_032856.5(WDR73):c.706_719dup (p.Ser240fs)

dbSNP: rs1596050297
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München RCV000995911 SCV001150308 pathogenic Galloway-Mowat syndrome 1 2019-12-30 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002275179 SCV002563271 pathogenic not provided 2020-01-01 criteria provided, single submitter clinical testing

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