ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.10033-17C>T

gnomAD frequency: 0.00271  dbSNP: rs188241873
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002117905 SCV002402566 benign Imerslund-Grasbeck syndrome 2024-12-17 criteria provided, single submitter clinical testing
GeneDx RCV002285533 SCV002575306 likely benign not provided 2020-03-31 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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