ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.546G>A (p.Glu182=)

dbSNP: rs1567012356
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001201222 SCV001372313 likely benign not specified 2020-06-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002069300 SCV002393303 likely benign RASopathy 2022-09-27 criteria provided, single submitter clinical testing

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