ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.581-9dup

dbSNP: rs60664170
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000727625 SCV000854895 uncertain significance not provided 2018-01-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001523485 SCV001733195 benign Cohen syndrome 2024-01-31 criteria provided, single submitter clinical testing

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