ClinVar Miner

Submissions for variant NM_033360.4(KRAS):c.*2391_*2392insC

gnomAD frequency: 0.00005  dbSNP: rs886049188
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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 RCV000277887 SCV000377672 uncertain significance Cardio-facio-cutaneous syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000330482 SCV000377673 uncertain significance Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing

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