ClinVar Miner

Submissions for variant NM_017882.3(CLN6):c.876T>C (p.Gly292=)

dbSNP: rs916275768
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001718967 SCV000723014 likely benign not provided 2019-01-08 criteria provided, single submitter clinical testing
Invitae RCV001418405 SCV001620633 likely benign Neuronal ceroid lipofuscinosis 2024-01-29 criteria provided, single submitter clinical testing

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