ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.11019A>T (p.Thr3673=)

dbSNP: rs1588794390
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001448860 SCV001651963 likely benign Cohen syndrome 2021-11-11 criteria provided, single submitter clinical testing

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