ClinVar Miner

Submissions for variant NM_017882.3(CLN6):c.297+19del

dbSNP: rs61224699
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
GeneDx RCV000187083 SCV000240658 benign not specified 2013-04-25 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV001522609 SCV001732184 benign Neuronal ceroid lipofuscinosis 2024-01-29 criteria provided, single submitter clinical testing

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