ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.6647-19T>C

gnomAD frequency: 0.00001  dbSNP: rs535147712
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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 RCV003051373 SCV003450082 likely benign Imerslund-Grasbeck syndrome 2022-07-06 criteria provided, single submitter clinical testing

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