ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.7680T>C (p.Ala2560=)

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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 RCV005158982 SCV005789629 likely benign Imerslund-Grasbeck syndrome 2024-05-03 criteria provided, single submitter clinical testing

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