List of variants in gene VCP reported as benign by PreventionGenetics, part of Exact Sciences

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_007126.5(VCP):c.1360-35A>G	rs2258240	0.75740
NM_007126.5(VCP):c.811+3G>A	rs514492	0.75591
NM_007126.5(VCP):c.1695+8A>G	rs684562	0.54947
NM_007126.5(VCP):c.129+47G>A	rs10972300	0.17835
NM_007126.5(VCP):c.1092C>T (p.Asp364=)	rs61752947	0.00619
NM_007126.5(VCP):c.1360-14C>G	rs144304208	0.00311
NM_007126.5(VCP):c.1704A>G (p.Gln568=)	rs142577424	0.00296
NM_007126.5(VCP):c.384T>C (p.Gly128=)	rs367703031	0.00003
NM_007126.5(VCP):c.1082-18_1082-8dup	rs11272867

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