ClinVar Miner

Submissions for variant NM_004985.5(KRAS):c.-176CGG[4]

dbSNP: rs886049200
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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 RCV000267881 SCV000377758 uncertain significance Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000323287 SCV000377759 uncertain significance Cardio-facio-cutaneous syndrome 2016-06-14 criteria provided, single submitter clinical testing

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