VCP, valosin containing protein, 7415

N. diseases: 376; N. variants: 25
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909329
rs121909329
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		G 0.800 CausalMutation CLINVAR
dbSNP: rs121909330
rs121909330
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		C 0.800 GeneticVariation CLINVAR
dbSNP: rs121909331
rs121909331
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		T 0.800 CausalMutation CLINVAR
dbSNP: rs121909332
rs121909332
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		C 0.800 CausalMutation CLINVAR
dbSNP: rs387906789
rs387906789
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C3151403
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 		C 0.800 CausalMutation CLINVAR
dbSNP: rs864309502
rs864309502
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4225244
Disease:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y 		T 0.800 CausalMutation CLINVAR
dbSNP: rs121909329
rs121909329
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C3152097
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 14 WITHOUT FRONTOTEMPORAL DEMENTIA 		T 0.700 CausalMutation CLINVAR
dbSNP: rs387906790
rs387906790
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C3152097
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 14 WITHOUT FRONTOTEMPORAL DEMENTIA 		T 0.700 CausalMutation CLINVAR
dbSNP: rs397507560
rs397507560
Entrez Id: 2189;7415
Gene Symbol: FANCG;VCP
FANCG;VCP
CUI: C3469527
Disease:
fanconi anemia complementation group g 		G 0.700 CausalMutation CLINVAR
dbSNP: rs758407400
rs758407400
Entrez Id: 2189;7415
Gene Symbol: FANCG;VCP
FANCG;VCP
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs786204205
rs786204205
Entrez Id: 2189;7415
Gene Symbol: FANCG;VCP
FANCG;VCP
CUI: C0015625
Disease:
Fanconi Anemia 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs866101707
rs866101707
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C0002395
Disease:
Alzheimer's Disease 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs779834525
rs779834525
Entrez Id: 2189;7415
Gene Symbol: FANCG;VCP
FANCG;VCP
CUI: C0015625
Disease:
Fanconi Anemia 		A 0.700 CausalMutation CLINVAR Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9. 11093276 2000
dbSNP: rs779834525
rs779834525
Entrez Id: 2189;7415
Gene Symbol: FANCG;VCP
FANCG;VCP
CUI: C0015625
Disease:
Fanconi Anemia 		A 0.700 CausalMutation CLINVAR Functional analysis of patient-derived mutations in the Fanconi anemia gene, FANCG/XRCC9. 11438206 2001
dbSNP: rs397507560
rs397507560
Entrez Id: 2189;7415
Gene Symbol: FANCG;VCP
FANCG;VCP
CUI: C0015625
Disease:
Fanconi Anemia 		G 0.700 CausalMutation CLINVAR Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study. 12552564 2003
dbSNP: rs121909329
rs121909329
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		0.800 GeneticVariation UNIPROT Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
dbSNP: rs121909329
rs121909329
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C3151403
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 		T 0.800 CausalMutation CLINVAR Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
dbSNP: rs121909329
rs121909329
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		T 0.800 CausalMutation CLINVAR Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
dbSNP: rs121909330
rs121909330
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		0.800 GeneticVariation UNIPROT Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
dbSNP: rs121909330
rs121909330
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		A 0.800 CausalMutation CLINVAR Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
dbSNP: rs121909331
rs121909331
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		0.800 GeneticVariation UNIPROT Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
dbSNP: rs121909332
rs121909332
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		0.800 GeneticVariation UNIPROT Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
dbSNP: rs121909334
rs121909334
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		0.800 GeneticVariation UNIPROT Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
dbSNP: rs121909334
rs121909334
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C4551951
Disease:
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		T 0.800 CausalMutation CLINVAR Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
dbSNP: rs121909334
rs121909334
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C3151403
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 		T 0.800 CausalMutation CLINVAR Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004