ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2258-2dup

dbSNP: rs2144680473
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002181185 SCV002476597 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2021-05-18 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004785521 SCV005407262 likely benign Familial cancer of breast 2024-09-04 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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