ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.9339C>T (p.Cys3113=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003081122 SCV003455464 likely benign Imerslund-Grasbeck syndrome 2024-10-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005045228 SCV005668492 likely benign Imerslund-Grasbeck syndrome type 1; Proteinuria, chronic benign 2024-06-18 criteria provided, single submitter clinical testing

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