ClinVar Miner

Submissions for variant NM_005359.6(SMAD4):c.904+45dup

dbSNP: rs386387676
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001653936 SCV001871528 benign not provided 2019-11-19 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000584195 SCV002551318 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000584195 SCV000692034 benign not specified no assertion criteria provided clinical testing

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