ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.2799A>G (p.Gln933=)

dbSNP: rs1818831444
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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 RCV001493265 SCV001697888 likely benign Cohen syndrome 2022-09-12 criteria provided, single submitter clinical testing

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