ClinVar Miner

Submissions for variant NM_004656.4(BAP1):c.932-151G>A

dbSNP: rs1705120040
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV002272729 SCV002556823 pathogenic Uveal melanoma 2021-04-27 criteria provided, single submitter clinical testing
Baylor Genetics RCV003464427 SCV004214923 uncertain significance BAP1-related tumor predisposition syndrome 2022-10-02 criteria provided, single submitter clinical testing

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