ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.*729AACA[4]

dbSNP: rs371820097
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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 RCV000386250 SCV000440589 uncertain significance Noonan syndrome with multiple lentigines 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000291851 SCV000440590 uncertain significance Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694703 SCV005187524 uncertain significance not provided criteria provided, single submitter not provided

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