ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.4320A>G (p.Leu1440=)

dbSNP: rs2133637329
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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 RCV001397853 SCV001599613 likely benign Cohen syndrome 2020-10-06 criteria provided, single submitter clinical testing

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