ClinVar Miner

Submissions for variant NM_030662.4(MAP2K2):c.534C>G (p.Leu178=)

gnomAD frequency: 0.00003  dbSNP: rs765573431
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000873415 SCV001015406 likely benign RASopathy 2023-07-07 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001251360 SCV001426931 benign not specified 2020-07-19 criteria provided, single submitter clinical testing

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