ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.1016-18G>A

gnomAD frequency: 0.00002  dbSNP: rs763917917
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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 RCV002595803 SCV003499086 likely benign Imerslund-Grasbeck syndrome 2024-03-25 criteria provided, single submitter clinical testing

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