ClinVar Miner

Submissions for variant NM_017882.3(CLN6):c.*141GT[13]

dbSNP: rs3837692
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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 RCV000279536 SCV000393729 likely benign Neuronal Ceroid-Lipofuscinosis, Recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001709592 SCV001936788 benign not provided 2019-08-10 criteria provided, single submitter clinical testing

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