ClinVar Miner

Submissions for variant NM_007214.5(SEC63):c.*3031dup

dbSNP: rs34250899
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000381016 SCV000459384 uncertain significance Polycystic liver disease 1 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004695894 SCV005189180 uncertain significance not provided criteria provided, single submitter not provided

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