ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.379+8A>G

dbSNP: rs1057520254
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000582716 SCV000689389 likely benign Hereditary cancer-predisposing syndrome 2016-06-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001493091 SCV001697713 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-04-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004787990 SCV005403051 likely benign Familial cancer of breast 2024-08-21 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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