ClinVar Miner

Submissions for variant NM_025219.3(DNAJC5):c.237C>T (p.Tyr79=)

gnomAD frequency: 0.00009  dbSNP: rs149971662
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001698398 SCV000535062 likely benign not provided 2020-04-07 criteria provided, single submitter clinical testing
Invitae RCV000863600 SCV001004291 likely benign Neuronal ceroid lipofuscinosis 2023-12-30 criteria provided, single submitter clinical testing

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