ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.2232C>G (p.Asp744Glu) (rs374362388)

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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 RCV000502318 SCV000593774 uncertain significance not specified 2016-10-25 criteria provided, single submitter clinical testing
Color RCV000583929 SCV000689324 uncertain significance Hereditary cancer-predisposing syndrome 2018-08-01 criteria provided, single submitter clinical testing

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