ClinVar Miner

Submissions for variant NM_017882.3(CLN6):c.*141GT[11]

dbSNP: rs3837692
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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 RCV000338546 SCV000393727 benign Neuronal Ceroid-Lipofuscinosis, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000338546 SCV000393731 uncertain significance Neuronal Ceroid-Lipofuscinosis, Recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001653554 SCV001868637 benign not provided 2019-08-18 criteria provided, single submitter clinical testing

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