ClinVar Miner

Submissions for variant NM_002834.5(PTPN11):c.363A>G (p.Glu121=)

dbSNP: rs2135866636
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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 RCV001733382 SCV001983561 likely benign not specified 2021-09-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002539827 SCV003326492 likely benign RASopathy 2022-03-05 criteria provided, single submitter clinical testing

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