ClinVar Miner

Submissions for variant NM_002524.5(NRAS):c.111+18C>G

gnomAD frequency: 0.00002  dbSNP: rs756947288
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002202133 SCV002352521 likely benign RASopathy 2024-01-02 criteria provided, single submitter clinical testing

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