ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.*250_*252dup

dbSNP: rs71274940
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000342191 SCV000470873 likely benign Cohen syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001653728 SCV001865140 benign not provided 2019-07-11 criteria provided, single submitter clinical testing

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