ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.93+17A>G

dbSNP: rs778826728
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000603396 SCV000726070 likely benign not specified 2017-12-20 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.
Color Diagnostics, LLC DBA Color Health RCV000775638 SCV000910013 likely benign Hereditary cancer-predisposing syndrome 2017-01-12 criteria provided, single submitter clinical testing
Invitae RCV002066521 SCV002346037 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-01-24 criteria provided, single submitter clinical testing

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