ClinVar Miner

Submissions for variant NM_017882.3(CLN6):c.*141GT[8]

dbSNP: rs3837692
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 RCV000350982 SCV000393730 uncertain significance Neuronal Ceroid-Lipofuscinosis, Recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001597079 SCV001831512 benign not provided 2019-08-10 criteria provided, single submitter clinical testing

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