ClinVar Miner

Submissions for variant NM_033360.4(KRAS):c.*2626T>G

gnomAD frequency: 0.06273  dbSNP: rs61764370
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000384527 SCV000377660 likely benign Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV001511520 SCV001718782 benign RASopathy 2024-01-22 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001813459 SCV002060521 benign Noonan syndrome and Noonan-related syndrome 2017-11-01 criteria provided, single submitter clinical testing

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