ClinVar Miner

Submissions for variant NM_033360.4(KRAS):c.*633T>C

gnomAD frequency: 0.48177  dbSNP: rs9266
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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 RCV000398489 SCV000377729 likely benign Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001813461 SCV002060523 benign Noonan syndrome and Noonan-related syndrome 2021-07-13 criteria provided, single submitter clinical testing

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