ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2493-15C>T

dbSNP: rs1009398860
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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 RCV000582453 SCV000689340 likely benign Hereditary cancer-predisposing syndrome 2017-03-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002529226 SCV002999680 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-02-13 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004791612 SCV005406455 likely benign Familial cancer of breast 2024-09-05 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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