ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.7429+15A>T

dbSNP: rs1002318603
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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 RCV002177948 SCV002347948 likely benign Cohen syndrome 2022-02-24 criteria provided, single submitter clinical testing

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