ClinVar Miner

Submissions for variant NM_006270.5(RRAS):c.454-19G>A

gnomAD frequency: 0.00002  dbSNP: rs776793181
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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 RCV001420789 SCV001623150 likely benign not specified 2024-12-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002070262 SCV002422983 likely benign Noonan syndrome 2024-10-21 criteria provided, single submitter clinical testing

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