ClinVar Miner

Submissions for variant NM_007126.5(VCP):c.1360-35A>G

gnomAD frequency: 0.75740  dbSNP: rs2258240
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249111 SCV000311706 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001610680 SCV001836221 benign not provided 2018-07-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002244627 SCV002514457 benign Charcot-Marie-Tooth disease type 2Y 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002244626 SCV002514458 benign Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002244625 SCV002514459 benign Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001610680 SCV005272581 benign not provided criteria provided, single submitter not provided

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