ClinVar Miner

Submissions for variant NM_007126.5(VCP):c.577-21_577-18del

dbSNP: rs763622603
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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 RCV000254424 SCV000311710 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058221 SCV002351486 likely benign Frontotemporal dementia and/or amyotrophic lateral sclerosis 6; Inclusion body myopathy with Paget disease of bone and frontotemporal dementia 2022-12-02 criteria provided, single submitter clinical testing

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