ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.2301+18A>G

dbSNP: rs202001092
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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 RCV002201247 SCV002482967 benign Imerslund-Grasbeck syndrome 2025-01-22 criteria provided, single submitter clinical testing

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