ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.10830G>A (p.Leu3610=)

dbSNP: rs2492241240
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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 RCV003498970 SCV004261523 likely benign Cohen syndrome 2024-07-13 criteria provided, single submitter clinical testing

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