ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4185+31TG[3]

dbSNP: rs760098710
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001553440 SCV001774309 likely benign not provided 2020-07-02 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 10444347)
Labcorp Genetics (formerly Invitae), Labcorp RCV002067736 SCV002330564 likely benign Hereditary breast ovarian cancer syndrome 2022-09-18 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258134 SCV002538269 uncertain significance Hereditary cancer-predisposing syndrome 2021-08-16 criteria provided, single submitter curation
King Laboratory, University of Washington RCV001171477 SCV001251394 benign not specified 2019-09-01 no assertion criteria provided research

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