ClinVar Miner

Submissions for variant NM_013254.4(TBK1):c.1761-11C>T

gnomAD frequency: 0.00344  dbSNP: rs145696668
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001555840 SCV001777318 benign not provided 2021-10-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072083 SCV002405655 benign Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 2025-01-01 criteria provided, single submitter clinical testing

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