ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1149A>G (p.Leu383=)

dbSNP: rs1567829755
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000781181 SCV000919063 likely benign not specified 2019-08-28 criteria provided, single submitter clinical testing

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