ClinVar Miner

Submissions for variant NM_013254.4(TBK1):c.1785A>G (p.Thr595=)

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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 RCV002937632 SCV003260487 likely benign Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 2022-08-10 criteria provided, single submitter clinical testing

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