ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.9331-3_9331-2insTTTTTTTTTTTGTTTTTT

dbSNP: rs2492091623
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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 RCV003006261 SCV003308583 likely benign Cohen syndrome 2022-02-14 criteria provided, single submitter clinical testing

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