ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1340+7_1340+9del

dbSNP: rs1413352933
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000758986 SCV000887979 uncertain significance not provided 2018-05-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001461046 SCV001664930 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-12-21 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004788157 SCV005407085 likely benign Familial cancer of breast 2024-08-27 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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