ClinVar Miner

Submissions for variant NM_007126.5(VCP):c.1194+9ATG[2]

dbSNP: rs886038581
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249024 SCV000311703 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058219 SCV002450250 likely benign Frontotemporal dementia and/or amyotrophic lateral sclerosis 6; Inclusion body myopathy with Paget disease of bone and frontotemporal dementia 2023-10-23 criteria provided, single submitter clinical testing

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