ClinVar Miner

Submissions for variant NM_002524.5(NRAS):c.273G>A (p.Ala91=)

gnomAD frequency: 0.00001  dbSNP: rs1429502684
Minimum review status: Collection method:
Minimum conflict level:
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002111089 SCV002381217 likely benign RASopathy 2023-03-22 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003403684 SCV004122862 likely benign not specified 2023-10-13 criteria provided, single submitter clinical testing

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