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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_007126.5(VCP):c.*1001C>T	rs192556285	0.00482
NM_007126.5(VCP):c.*12C>T	rs62544156	0.00088
NM_007126.5(VCP):c.1584C>T (p.Ala528=)	rs147623367	0.00064
NM_007126.5(VCP):c.*4G>T	rs201091341	0.00052
NM_007126.5(VCP):c.2406T>C (p.Asp802=)	rs145508640	0.00032
NM_007126.5(VCP):c.*15C>T	rs762559031	0.00004
NM_007126.5(VCP):c.812-7C>G	rs764429197	0.00002

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