ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.365-16del

dbSNP: rs2469515156
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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 RCV002971048 SCV003281382 benign Familial cancer of breast 2022-06-12 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002971048 SCV005407069 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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