ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.364+7A>C

gnomAD frequency: 0.00001  dbSNP: rs1475396127
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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 RCV000758771 SCV000887594 uncertain significance not provided 2018-07-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001506326 SCV001711247 likely benign Familial cancer of breast 2024-01-19 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001506326 SCV005402889 likely benign Familial cancer of breast 2024-07-19 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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