ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.216-11T>C

dbSNP: rs2106135656
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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 RCV002197113 SCV002348913 likely benign Familial cancer of breast 2021-05-07 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002197113 SCV005405759 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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