ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.15G>A (p.Lys5=)

dbSNP: rs2140511623
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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 RCV001844577 SCV002103676 likely benign not specified 2022-02-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002543315 SCV003205601 likely benign RASopathy 2022-05-28 criteria provided, single submitter clinical testing

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