FGF2, fibroblast growth factor 2, 2247

N. diseases: 635; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs308403
rs308403
Entrez Id: 2247
Gene Symbol: FGF2
FGF2
CUI: C0205682
Disease:
Waist-Hip Ratio
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10518406
rs10518406
Entrez Id: 2247
Gene Symbol: FGF2
FGF2
CUI: C1305855
Disease:
Body mass index
G 0.700 GeneticVariation GWASCAT Genetic studies of body mass index yield new insights for obesity biology. 25673413 2015
dbSNP: rs308379
rs308379
Entrez Id: 2247
Gene Symbol: FGF2
FGF2
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Multivariate Cox proportional analysis revealed that the FGF2 rs308379 A allele (hazard ratio(HR)=1.663, p=0.004) and advanced tumor stage (HR=3.430, p<0.001) were independent prognostic factors for overall survival in patients with HCC. 30952770 2019
dbSNP: rs308379
rs308379
Entrez Id: 2247
Gene Symbol: FGF2
FGF2
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE Multivariate Cox proportional analysis revealed that the FGF2 rs308379 A allele (hazard ratio(HR)=1.663, p=0.004) and advanced tumor stage (HR=3.430, p<0.001) were independent prognostic factors for overall survival in patients with HCC. 30952770 2019
dbSNP: rs308442
rs308442
Entrez Id: 2247
Gene Symbol: FGF2
FGF2
CUI: C0029456
Disease:
Osteoporosis
0.010 GeneticVariation BEFREE Thus, the rs308442 locus of <i>FGF-2</i> gene is closely correlated to osteoporosis in this Zhuang ethnic Chinese cohort, and the TA may be the risk genotype of osteoporosis. 28653999 2017
dbSNP: rs167428
rs167428
Entrez Id: 2247
Gene Symbol: FGF2
FGF2
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Subsequent replication study successfully validated one SNP (rs167428) associated with fat mass (P(combine) = 3.46 × 10(-5)). eQTL analyses revealed that SNPs associated with obesity also affected FGF2 expression. 26879180 2016
dbSNP: rs1405250454
rs1405250454
Entrez Id: 2247
Gene Symbol: FGF2
FGF2
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis
0.010 GeneticVariation BEFREE The ALS-mouse model over-expressing a mutant human SOD1 (G93A) gene closely mimics human ALS disease. 22542539 2012
dbSNP: rs1449683
rs1449683
Entrez Id: 2247
Gene Symbol: FGF2
FGF2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Here, we selected four commonly studied polymorphisms in VEGF, rs3025039 (known as +936 C/T), rs1109324, rs154765 and rs833052, one polymorphism at the promoter of the VEGFR1 (-710 C/T) and another in the FGF2, rs1449683, gene to explore their association with BC susceptibility. 22315135 2012
dbSNP: rs1449683
rs1449683
Entrez Id: 2247
Gene Symbol: FGF2
FGF2
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Here, we selected four commonly studied polymorphisms in VEGF, rs3025039 (known as +936 C/T), rs1109324, rs154765 and rs833052, one polymorphism at the promoter of the VEGFR1 (-710 C/T) and another in the FGF2, rs1449683, gene to explore their association with BC susceptibility. 22315135 2012