ClinVar Miner

Submissions for variant NM_001128929.3(ROBO2):c.73G>A (p.Val25Met)

dbSNP: rs78834776
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000611343 SCV000743808 benign Vesicoureteral reflux 2 2016-05-19 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000611343 SCV000734292 benign Vesicoureteral reflux 2 no assertion criteria provided clinical testing
PreventionGenetics, part of Exact Sciences RCV003965298 SCV004795978 benign ROBO2-related disorder 2020-11-18 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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