ClinVar Miner

Submissions for variant NM_006493.4(CLN5):c.63G>A (p.Arg21=)

dbSNP: rs1338752072
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001492562 SCV001697176 likely benign Neuronal ceroid lipofuscinosis 2023-10-03 criteria provided, single submitter clinical testing

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