ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.6184A>G (p.Asn2062Asp)

dbSNP: rs754400139
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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 RCV001878338 SCV002118524 uncertain significance Cohen syndrome 2021-09-07 criteria provided, single submitter clinical testing

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