ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.10868-6T>C

dbSNP: rs2130933328
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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 RCV001487641 SCV001692136 likely benign Cohen syndrome 2021-02-05 criteria provided, single submitter clinical testing

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