ClinVar Miner

Submissions for variant NM_000041.4(APOE):c.237-16_237-13del

dbSNP: rs377486301
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 RCV001579974 SCV002577291 likely benign not provided 2021-12-21 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579974 SCV001809243 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001699821 SCV001925106 benign not specified no assertion criteria provided clinical testing

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