ClinVar Miner

Submissions for variant NM_002524.4(NRAS):c.-208T>A

gnomAD frequency: 0.01703  dbSNP: rs2273267
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000288966 SCV000347401 likely benign Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001582914 SCV001811257 likely benign not provided 2019-07-24 criteria provided, single submitter clinical testing

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