ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.9897A>G (p.Pro3299=)

gnomAD frequency: 0.00003  dbSNP: rs143405367
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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 RCV002098282 SCV002389595 likely benign Imerslund-Grasbeck syndrome 2022-06-05 criteria provided, single submitter clinical testing

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