ClinVar Miner

Submissions for variant NM_002524.5(NRAS):c.450+12C>T

gnomAD frequency: 0.00001  dbSNP: rs749906475
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003539398 SCV004269193 likely benign RASopathy 2023-01-27 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001699996 SCV001924129 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001699996 SCV001930222 likely benign not provided no assertion criteria provided clinical testing

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