ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.5343-12del

dbSNP: rs745529365
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003505781 SCV004364956 benign Imerslund-Grasbeck syndrome 2023-10-10 criteria provided, single submitter clinical testing

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