ClinVar Miner

Submissions for variant NM_003907.3(EIF2B5):c.843+86A>G

gnomAD frequency: 0.02384  dbSNP: rs28584345
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001674086 SCV001885968 benign not provided 2021-05-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001674086 SCV005302595 benign not provided criteria provided, single submitter not provided

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