ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2684C>A (p.Ser895Tyr)

dbSNP: rs1555573437
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503950 SCV000593772 uncertain significance not specified 2015-10-02 criteria provided, single submitter clinical testing

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