ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.1569-1G>C

dbSNP: rs1574756672
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen RCV001730131 SCV001977029 likely pathogenic Familial cancer of breast 2021-10-12 criteria provided, single submitter clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003238378 SCV002009153 pathogenic not provided 2021-11-03 criteria provided, single submitter clinical testing

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