ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.5982C>T (p.Asp1994=)

gnomAD frequency: 0.00001  dbSNP: rs759538241
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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 RCV001495338 SCV001700018 likely benign Cohen syndrome 2022-07-12 criteria provided, single submitter clinical testing

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