NGF, nerve growth factor, 4803

N. diseases: 616; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11102930
rs11102930
Entrez Id: 4803;112840934
Gene Symbol: NGF;NGF-AS1
NGF;NGF-AS1
CUI: C0017661
Disease:
IGA Glomerulonephritis
0.010 GeneticVariation BEFREE The genotyping data of 197 patients and 289 control subjects revealed significant association between NGF SNP rs11102930 and presence of IgAN. 21178826 2011
dbSNP: rs6330
rs6330
Entrez Id: 4803;112840934
Gene Symbol: NGF;NGF-AS1
NGF;NGF-AS1
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE Regarding the functional roles of neurotrophin polymorphisms as they relate to executive dysfunction, the NGF gene rs6330 might influence the inhibition task in Japanese patients with early-stage AD or A-MCI. 22301435 2011
dbSNP: rs6330
rs6330
Entrez Id: 4803;112840934
Gene Symbol: NGF;NGF-AS1
NGF;NGF-AS1
CUI: C2748208
Disease:
Executive dysfunction
0.010 GeneticVariation BEFREE Regarding the functional roles of neurotrophin polymorphisms as they relate to executive dysfunction, the NGF gene rs6330 might influence the inhibition task in Japanese patients with early-stage AD or A-MCI. 22301435 2011
dbSNP: rs6330
rs6330
Entrez Id: 4803;112840934
Gene Symbol: NGF;NGF-AS1
NGF;NGF-AS1
CUI: C0011265
Disease:
Presenile dementia
0.010 GeneticVariation BEFREE Among 200 outpatients with dementia and MCI whose NGF SNP rs6330 genotype was identified, those with A-MCI (n = 35) and early-stage AD (n = 67) were recruited and divided into three groups according to genotype (C/C: n = 58, C/T: n = 39, T/T: n = 5). 22301435 2011
dbSNP: rs6330
rs6330
Entrez Id: 4803;112840934
Gene Symbol: NGF;NGF-AS1
NGF;NGF-AS1
CUI: C0497327
Disease:
Dementia
0.010 GeneticVariation BEFREE Among 200 outpatients with dementia and MCI whose NGF SNP rs6330 genotype was identified, those with A-MCI (n = 35) and early-stage AD (n = 67) were recruited and divided into three groups according to genotype (C/C: n = 58, C/T: n = 39, T/T: n = 5). 22301435 2011
dbSNP: rs11466112
rs11466112
Entrez Id: 4803;112840934
Gene Symbol: NGF;NGF-AS1
NGF;NGF-AS1
CUI: C0234229
Disease:
Deep pain
0.010 GeneticVariation BEFREE We have previously identified a homozygous missense (R221W) mutation in the NGFB gene in patients with loss of deep pain perception. 19038341 2009