ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.215+7A>C

dbSNP: rs1241658352
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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 RCV002157022 SCV002334789 likely benign Familial cancer of breast 2024-06-25 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002157022 SCV005407188 likely benign Familial cancer of breast 2024-07-18 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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