ClinVar Miner

Submissions for variant NM_007126.5(VCP):c.372A>G (p.Glu124=)

dbSNP: rs1587128887
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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 RCV001505470 SCV001710376 likely benign Frontotemporal dementia and/or amyotrophic lateral sclerosis 6; Inclusion body myopathy with Paget disease of bone and frontotemporal dementia 2022-07-06 criteria provided, single submitter clinical testing

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