ClinVar Miner

Submissions for variant NM_030662.4(MAP2K2):c.529-5T>C

gnomAD frequency: 0.00001  dbSNP: rs766943752
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000247121 SCV000314696 likely benign not specified criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000247121 SCV000699638 likely benign not specified 2025-04-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001487659 SCV001692155 likely benign RASopathy 2024-04-29 criteria provided, single submitter clinical testing

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