ClinVar Miner

Submissions for variant NM_001395656.1(ROBO2):c.3327C>G (p.Cys1109Trp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005037201 SCV005657766 uncertain significance Vesicoureteral reflux 2 2024-03-01 criteria provided, single submitter clinical testing

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