ClinVar Miner

Submissions for variant NM_006363.6(SEC23B):c.604-4dup

dbSNP: rs750339397
Minimum review status: Collection method:
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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 RCV002117852 SCV002410189 benign Congenital dyserythropoietic anemia, type II; Cowden syndrome 7 2025-01-24 criteria provided, single submitter clinical testing

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