ClinVar Miner

Submissions for variant NM_003907.3(EIF2B5):c.72G>A (p.Pro24=)

dbSNP: rs1298889640
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000925813 SCV001071365 likely benign not provided 2023-09-19 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000925813 SCV005410460 uncertain significance not provided 2024-04-08 criteria provided, single submitter clinical testing

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