ClinVar Miner

Submissions for variant NM_006270.5(RRAS):c.345-4G>A

gnomAD frequency: 0.00029  dbSNP: rs377672475
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000873816 SCV001015886 likely benign Noonan syndrome 2024-01-31 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002265907 SCV002548407 benign not specified 2022-05-07 criteria provided, single submitter clinical testing

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