ClinVar Miner

Submissions for variant NM_153252.5(BRWD3):c.1300T>C (p.Tyr434His)

gnomAD frequency: 0.00005  dbSNP: rs779094763
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502884 SCV000593783 likely benign not specified 2016-06-27 criteria provided, single submitter clinical testing
Ambry Genetics RCV000623943 SCV000741485 uncertain significance Inborn genetic diseases 2016-05-19 criteria provided, single submitter clinical testing

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