List of variants in gene VCP reported as likely pathogenic for Frontotemporal dementia and/or amyotrophic lateral sclerosis 6

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_007126.5(VCP):c.572G>A (p.Arg191Gln)	rs121909334	0.00002
NM_007126.5(VCP):c.283C>T (p.Arg95Cys)	rs121909332
NM_007126.5(VCP):c.463C>T (p.Arg155Cys)	rs121909330
NM_007126.5(VCP):c.466G>A (p.Gly156Ser)
NM_007126.5(VCP):c.475C>T (p.Arg159Cys)	rs387906789
NM_007126.5(VCP):c.572G>C (p.Arg191Pro)	rs121909334

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