ClinVar Miner

Submissions for variant NM_025219.3(DNAJC5):c.351G>T (p.Thr117=)

dbSNP: rs775067598
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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 RCV001464893 SCV001668870 likely benign Neuronal ceroid lipofuscinosis 2023-03-08 criteria provided, single submitter clinical testing

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