ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.593+33dup

gnomAD frequency: 0.95021  dbSNP: rs11409967
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001595341 SCV001828686 benign not provided 2021-05-27 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001658306 SCV001876435 benign Imerslund-Grasbeck syndrome type 1 2021-07-30 criteria provided, single submitter clinical testing

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