ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.*2155_*2156del

dbSNP: rs398064261
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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 RCV000278358 SCV000448522 uncertain significance Carcinoma of pancreas 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004695784 SCV005190330 uncertain significance not provided criteria provided, single submitter not provided

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