ClinVar Miner

Submissions for variant NM_001128929.3(ROBO2):c.*3923C>T

gnomAD frequency: 0.04891  dbSNP: rs10865561
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000316645 SCV000484063 benign Vesicoureteral reflux 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716414 SCV005298285 benign not provided criteria provided, single submitter not provided

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