ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.2446+14_2446+15del

dbSNP: rs752528712
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000393301 SCV000361748 uncertain significance Megaloblastic anemia 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002059538 SCV002381898 likely benign Imerslund-Grasbeck syndrome 2023-05-02 criteria provided, single submitter clinical testing

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