ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2906-7T>C

dbSNP: rs1237575383
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000875557 SCV001018001 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2023-09-21 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001190780 SCV001358364 likely benign Hereditary cancer-predisposing syndrome 2021-05-05 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799003 SCV002043630 uncertain significance Breast and/or ovarian cancer 2020-06-17 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV001190780 SCV002533657 uncertain significance Hereditary cancer-predisposing syndrome 2021-07-07 criteria provided, single submitter curation

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