ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.1795-9T>G (rs777006706)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662553 SCV000785136 likely benign Fanconi anemia, complementation group J; Neoplasm of ovary 2017-05-15 criteria provided, single submitter clinical testing
GeneDx RCV000615895 SCV000731023 likely benign not specified 2018-01-03 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000552644 SCV000633575 likely benign Familial cancer of breast; Fanconi anemia, complementation group J 2017-06-15 criteria provided, single submitter clinical testing

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