ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.*700GAT[1]

dbSNP: rs60078732
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000403342 SCV000470880 benign Cohen syndrome 2016-06-14 criteria provided, single submitter clinical testing

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