ClinVar Miner

Submissions for variant NM_004656.4(BAP1):c.*45C>G

dbSNP: rs56898787
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000384140 SCV000445458 benign BAP1-related tumor predisposition syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001723946 SCV001950766 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268035 SCV002550576 benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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