ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.918+9A>G

dbSNP: rs2145410020
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002220846 SCV002361529 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2022-11-23 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268607 SCV002551197 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004785482 SCV005405399 likely benign Familial cancer of breast 2024-08-22 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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