ClinVar Miner

Submissions for variant NM_033360.4(KRAS):c.*1758_*1759del

gnomAD frequency: 0.00456  dbSNP: rs535478558
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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 RCV000359373 SCV000377694 likely benign Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000264327 SCV000377695 likely benign Cardio-facio-cutaneous syndrome 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003389785 SCV004134568 benign not provided 2022-08-01 criteria provided, single submitter clinical testing KRAS: BS1, BS2

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