ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.380-16A>T

dbSNP: rs769150213
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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 RCV000771621 SCV000904225 likely benign Hereditary cancer-predisposing syndrome 2017-10-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003768325 SCV004610226 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-12-18 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004788164 SCV005404010 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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