ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.3402T>G (p.Pro1134=)

dbSNP: rs2061308538
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Total submissions: 2
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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 RCV001290565 SCV001478640 likely benign not specified 2021-01-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002070111 SCV002359581 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-05-07 criteria provided, single submitter clinical testing

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