HGF, hepatocyte growth factor, 3082

N. diseases: 671; N. variants: 22
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853235
rs137853235
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C1842342
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)
T 0.700 CausalMutation CLINVAR
dbSNP: rs5745642
rs5745642
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0428472
Disease:
Serum HDL cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs5745642
rs5745642
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0392885
Disease:
High density lipoprotein measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs5745687
rs5745687
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C4522089
Disease:
Hepatocyte Growth Factor Measurement
T 0.700 GeneticVariation GWASCAT Genome-wide association study for endothelial growth factors. 25552591 2015
dbSNP: rs5745687
rs5745687
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C4522089
Disease:
Hepatocyte Growth Factor Measurement
C 0.700 GeneticVariation GWASCAT Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. 27989323 2017
dbSNP: rs5745695
rs5745695
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C2985280
Disease:
Blood Protein Measurement
A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs5745709
rs5745709
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0018099
Disease:
Gout
0.700 GeneticVariation GWASCAT Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences. 22179738 2012
dbSNP: rs5745709
rs5745709
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0003868
Disease:
Arthritis, Gouty
0.700 GeneticVariation GWASCAT Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences. 22179738 2012
dbSNP: rs984534
rs984534
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs12536657
rs12536657
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0020490
Disease:
Hyperopia
0.020 GeneticVariation BEFREE After correction for multiple testing, the SNPs rs12536657 (odds ratio [OR], 5.53; 95% confidence interval [CI], 1.14-26.76) and rs5745718 (OR, 2.24; 95% CI, 1.30-3.85) showed significant association with hypermetropia. 20005573 2010
dbSNP: rs12536657
rs12536657
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0020490
Disease:
Hyperopia
0.020 GeneticVariation BEFREE No association between rs12536657 and hyperopia was found through gender-adjusted logistic regression comparing the hyperopic children with either of the two control groups. 30863626 2019
dbSNP: rs17427817
rs17427817
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0017605
Disease:
Angle Closure Glaucoma
0.020 GeneticVariation BEFREE In a stratification analysis by ethnicity, rs12540393 and rs17427817 in HGF showed a nominal association with PACG in the Hui cohort, although significance was lost after correction. 30348125 2018
dbSNP: rs17427817
rs17427817
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0017605
Disease:
Angle Closure Glaucoma
0.020 GeneticVariation BEFREE Our study suggests that rs5745718 and rs17427817 are associated with a decreased risk of PACG in the Chinese Han population. 23585864 2013
dbSNP: rs17427817
rs17427817
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0017606
Disease:
Primary angle-closure glaucoma
0.020 GeneticVariation BEFREE In a stratification analysis by ethnicity, rs12540393 and rs17427817 in HGF showed a nominal association with PACG in the Hui cohort, although significance was lost after correction. 30348125 2018
dbSNP: rs17427817
rs17427817
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0017606
Disease:
Primary angle-closure glaucoma
0.020 GeneticVariation BEFREE Our study suggests that rs5745718 and rs17427817 are associated with a decreased risk of PACG in the Chinese Han population. 23585864 2013
dbSNP: rs10272030
rs10272030
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C4315867
Disease:
Moderate myopia
0.010 GeneticVariation BEFREE Whereas the SNPs rs1743 (OR, 2.02; 95% CI, 1.19-3.43; P = .009), rs4732402 (OR, 2.03; 95% CI, 1.23-3.36; P = 0.005), rs12536657 (OR, 2.38; 95% CI, 1.40-4.05; P = 0.001), rs10272030 (OR, 2.22; 95% CI, 1.31-3.75; P = 0.003), and rs9642131 (OR, 2.44; 95% CI, 1.43-4.14; P = 0.001) showed significant association with low/moderate myopia. 20005573 2010
dbSNP: rs12536657
rs12536657
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C4315867
Disease:
Moderate myopia
0.010 GeneticVariation BEFREE Whereas the SNPs rs1743 (OR, 2.02; 95% CI, 1.19-3.43; P = .009), rs4732402 (OR, 2.03; 95% CI, 1.23-3.36; P = 0.005), rs12536657 (OR, 2.38; 95% CI, 1.40-4.05; P = 0.001), rs10272030 (OR, 2.22; 95% CI, 1.31-3.75; P = 0.003), and rs9642131 (OR, 2.44; 95% CI, 1.43-4.14; P = 0.001) showed significant association with low/moderate myopia. 20005573 2010
dbSNP: rs12540393
rs12540393
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0017605
Disease:
Angle Closure Glaucoma
0.010 GeneticVariation BEFREE In a stratification analysis by ethnicity, rs12540393 and rs17427817 in HGF showed a nominal association with PACG in the Hui cohort, although significance was lost after correction. 30348125 2018
dbSNP: rs12540393
rs12540393
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0017606
Disease:
Primary angle-closure glaucoma
0.010 GeneticVariation BEFREE In a stratification analysis by ethnicity, rs12540393 and rs17427817 in HGF showed a nominal association with PACG in the Hui cohort, although significance was lost after correction. 30348125 2018
dbSNP: rs1453208391
rs1453208391
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C1269955
Disease:
Tumor Cell Invasion
0.010 GeneticVariation BEFREE Upregulated genes included examples coding for secreted cytokines involved in tumour growth and invasion (S100P, HGF, MMP8, MMP9, PDGFC, IL1R2). 28214365 2017
dbSNP: rs1743
rs1743
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C4315867
Disease:
Moderate myopia
0.010 GeneticVariation BEFREE Whereas the SNPs rs1743 (OR, 2.02; 95% CI, 1.19-3.43; P = .009), rs4732402 (OR, 2.03; 95% CI, 1.23-3.36; P = 0.005), rs12536657 (OR, 2.38; 95% CI, 1.40-4.05; P = 0.001), rs10272030 (OR, 2.22; 95% CI, 1.31-3.75; P = 0.003), and rs9642131 (OR, 2.44; 95% CI, 1.43-4.14; P = 0.001) showed significant association with low/moderate myopia. 20005573 2010
dbSNP: rs2286194
rs2286194
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0022578
Disease:
Keratoconus
0.010 GeneticVariation BEFREE Ten tSNPs were genotyped.Following statistical analysis and multiple testing correction, a statistically significant association was found for the tSNP rs2286194 {p = 1.1×10-(3) Odds Ratio 0.52, 95% CI--0.35, 0.77} for keratoconus. 24416191 2014
dbSNP: rs2286194
rs2286194
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0271183
Disease:
Severe myopia
0.010 GeneticVariation BEFREE This study supports a strong association between the mild to moderate myopia group and the HGF SNP rs3735520 and the HGF haplotypes rs2286194-rs3735520-rs17501108 and rs12536657-rs2286194, and a moderate association of the extreme high myopia with rs2286194. 19471602 2009
dbSNP: rs3735520
rs3735520
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0271183
Disease:
Severe myopia
0.010 GeneticVariation BEFREE This study supports a strong association between the mild to moderate myopia group and the HGF SNP rs3735520 and the HGF haplotypes rs2286194-rs3735520-rs17501108 and rs12536657-rs2286194, and a moderate association of the extreme high myopia with rs2286194. 19471602 2009
dbSNP: rs3735520
rs3735520
Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0022578
Disease:
Keratoconus
0.010 GeneticVariation BEFREE SNPs rs4954218 (Near RAB3GAP1 (5')), rs4894535 (FNDC3B), rs2956540 (LOX), rs3735520 (Near HGF (5')), rs1324183 (MPDZ-NF1B), rs1536482 (RXRA-COL5A1), rs7044529 (COL5A1), rs2721051 (Near FOXO1 (3')), rs9938149 (BANP-ZNF469) and rs6050307 (VSX1) were assessed for their association with KC. 25675348 2015