ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2576-7T>A

dbSNP: rs759408257
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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 RCV000557285 SCV000633624 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2022-12-09 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000583224 SCV000689352 likely benign Hereditary cancer-predisposing syndrome 2016-11-06 criteria provided, single submitter clinical testing

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