ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.6201G>A (p.Glu2067=)

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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 RCV002819116 SCV003200423 likely benign Imerslund-Grasbeck syndrome 2022-07-05 criteria provided, single submitter clinical testing

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