ClinVar Miner

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

dbSNP: rs386387676
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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 RCV001653935 SCV001866388 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000582477 SCV002551320 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000582477 SCV000692033 benign not specified no assertion criteria provided clinical testing

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