ClinVar Miner

Submissions for variant NM_007126.5(VCP):c.475C>G (p.Arg159Gly)

dbSNP: rs387906789
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000023065 SCV000044356 pathogenic Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 2010-12-09 no assertion criteria provided literature only

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