ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.4518T>G (p.Gly1506=)

dbSNP: rs1821779613
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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 RCV003605438 SCV004462066 likely benign Cohen syndrome 2025-01-24 criteria provided, single submitter clinical testing

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