Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1136666
rs1136666
Entrez Id: 2597;112268089
Gene Symbol: GAPDH;LOC112268089
GAPDH;LOC112268089
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE This study confirmed that the rs1136666 CC allele of theGAPDH increased the risk of PD, particularly in older male patients. 29886133 2018
dbSNP: rs143455013
rs143455013
Entrez Id: 2597
Gene Symbol: GAPDH
GAPDH
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE Importantly, loss of DJ-1 function upon knock down (KD) or expression of the PD associated form L166P resulted in the absence of HMW DJ-1 complexes. 29016861 2017
dbSNP: rs760555162
rs760555162
Entrez Id: 2597
Gene Symbol: GAPDH
GAPDH
CUI: C0271650
Disease:
Impaired glucose tolerance
0.010 GeneticVariation BEFREE Using physiological tests and a biophysics approach based on nuclear magnetic resonance (NMR), we unexpectedly found that SOD1(G93A) ALS mice suffered from severe glucose intolerance, which was counteracted by high intensity swimming but not moderate intensity running exercise. 29104532 2017
dbSNP: rs760555162
rs760555162
Entrez Id: 2597
Gene Symbol: GAPDH
GAPDH
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis
0.010 GeneticVariation BEFREE Using physiological tests and a biophysics approach based on nuclear magnetic resonance (NMR), we unexpectedly found that SOD1(G93A) ALS mice suffered from severe glucose intolerance, which was counteracted by high intensity swimming but not moderate intensity running exercise. 29104532 2017
dbSNP: rs1060619
rs1060619
Entrez Id: 2597;112268089
Gene Symbol: GAPDH;LOC112268089
GAPDH;LOC112268089
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE While for the rs1060619 locus, the minor allele conferred increased risk for PD (allelic contrast, OR = 1.41, 95% CI: 1.14-1.75, corrected P = 0.007; additive model, OR = 1.43, 95% CI: 1.15-1.79, corrected P = 0.002). 26258539 2015
dbSNP: rs1448135344
rs1448135344
Entrez Id: 2597
Gene Symbol: GAPDH
GAPDH
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE High-dose vitamin C impairs tumor growth in Apc/Kras(G12D) mutant mice. 26541605 2015
dbSNP: rs3741918
rs3741918
Entrez Id: 2597;112268089
Gene Symbol: GAPDH;LOC112268089
GAPDH;LOC112268089
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE The minor allele of rs3741918 was associated with decreased risk of sporadic PD (allelic contrast, OR = 0.74, 95% CI: 0.59-0.93, corrected P = 0.028; additive model, OR = 0.73, 95% CI: 0.58-0.92, corrected P = 0.018). 26258539 2015
dbSNP: rs11549340
rs11549340
Entrez Id: 2597
Gene Symbol: GAPDH
GAPDH
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Most of the patients (82.8%) had a KRAS wild type tumor; a p.Gly12Cys was found in three patients and a p.Gly12Val mutation in one. 22668015 2012
dbSNP: rs1060620
rs1060620
Entrez Id: 2597;112268089
Gene Symbol: GAPDH;LOC112268089
GAPDH;LOC112268089
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE When the two family datasets were examined, none of the SNPs were significant in NE families, but two SNPs were associated with AD in Caribbean Hispanics: rs740850 in NCAPD2 (p = 0.0097) and rs1060620 in GAPDH (p = 0.042). 18340469 2008
dbSNP: rs763539313
rs763539313
Entrez Id: 2597
Gene Symbol: GAPDH
GAPDH
CUI: C0001430
Disease:
Adenoma
0.010 GeneticVariation BEFREE Association of Lys173Arg polymorphism with CYP11B2 expression in normal adrenal glands and aldosterone-producing adenomas. 16118341 2005